5112 NP_001070868 P588A not found in SNVbox database
5164 NP_001070868 D603Y not found in SNVbox database
5751 NP_001070868 P454H not found in SNVbox database
6788 NP_001070868 W566S not found in SNVbox database
7017 NP_705833 P139T not found in SNVbox database
8798 NP_109597 R205K not found in SNVbox database
9064 NP_705833 P330S not found in SNVbox database
276 NP_001070868 Q272R not found in SNVbox database
780 NP_705833 V753G not found in SNVbox database
1181 NP_001070868 D434Y not found in SNVbox database
3444 NP_705833 A370V not found in SNVbox database
3907 NP_001070868 H419N not found in SNVbox database
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:58862760 G>A maps to NM_130786.3 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr19:58863736 A>G maps to NM_130786.3 H175H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A6S8-01A-12D-A32B-08 chr10:52573648 A>G maps to NM_138932.2 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6XC-01A-12D-A32B-08 chr10:52575966 G>A maps to NM_138932.2 R314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr16:7383040 C>T maps to NM_145891.2 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:7568363 C>T maps to NM_145891.2 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YN-01A-11D-A34A-08 chr16:7645561 C>T maps to NM_145891.2 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5143-01A-01D-1468-08 chr12:9243976 G>A maps to NM_000014.4 T763T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TS-01A-12D-A33T-08 chr12:53703026 G>C maps to NM_015665.5 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6X4-01A-51D-A32B-08 chr12:125603202 G>A maps to NM_023928.3 W338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6IZ-01A-11D-A31L-08 chr1:12785440 G>A maps to NM_001103170.1 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U6-01A-12D-A33T-08 chr1:12779670 C>T maps to NM_001103170.1 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5397-01A-01D-1893-08 chr1:12711260 G>A maps to NM_001013630.1 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8161-01A-11D-2253-08 chr1:12726319 C>A maps to NM_001013630.1 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MY-01A-11D-A26M-08 chr6:44269150 C>G maps to NM_020745.2 L883L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7877-01A-11D-2395-08 chr6:44270855 C>T maps to NM_020745.2 L734L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:41107180 C>T maps to NM_001136042.2 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7J3-01A-21D-A34J-08 chr4:57221382 A>G maps to NM_181806.2 Y356Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr11:105967613 C>T maps to NM_015423.2 R304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XA-01A-11D-A26M-08 chr17:79094024 G>A maps to NM_001080395.2 D1237D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:79093213 C>T maps to NM_001080395.2 T1350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:79093231 C>T maps to NM_001080395.2 T1344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:107555450 C>A did not map to a codon.
Sequencing variant TCGA-E1-A7YH-01A-11D-A34A-08 chr9:107602686 G>A maps to NM_005502.3 C309C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:67197726 G>T maps to NM_080282.3 I363I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:67189380 C>T maps to NM_080282.3 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:215838766 C>A did not map to a codon.
Sequencing variant TCGA-HT-7855-01A-11D-2395-08 chr2:215843554 G>A maps to NM_173076.2 Y1650Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:215809801 C>T maps to NM_173076.2 P2422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:48312580 C>T maps to NM_152701.3 H1106H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:48313910 C>T maps to NM_152701.3 L1550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7Z3-01A-11D-A34J-08 chr7:48319514 A>G maps to NM_152701.3 Q2908Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7616-01A-11D-2253-08 chr7:48556329 T>C maps to NM_152701.3 T4550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr7:48411940 A>T maps to NM_152701.3 S3660S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7854-01A-11D-2253-08 chr7:48506640 C>T maps to NM_152701.3 Q4302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CZ-01A-11D-A32B-08 chr7:48682919 T>C maps to NM_152701.3 C4958C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UR-01A-11D-A33T-08 chr9:139905167 C>T maps to ENST00000355090 K2056K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A6MO-01A-11D-A33T-08 chr9:139907685 G>T maps to ENST00000355090 L1575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:2333210 G>A maps to NM_001089.2 C1337C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:2367362 G>T maps to NM_001089.2 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7637-01A-11D-2086-08 chr16:2374515 G>A maps to NM_001089.2 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A87Q-01A-11D-A36O-08 chr16:2376170 G>A maps to NM_001089.2 N53N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr1:94486866 G>A maps to NM_000350.2 P1649P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7857-01A-11D-2395-08 chr1:94528251 G>T maps to NM_000350.2 G606G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr1:94512530 G>A maps to NM_000350.2 Y954Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:67246064 A>T maps to ENST00000392677 S1583S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:67124789 G>A maps to NM_080284.2 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:67079047 G>A maps to NM_080284.2 L1528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:67081188 G>A maps to NM_080284.2 D1388D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:67130868 C>A maps to NM_080284.2 G159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr17:67111541 A>G maps to NM_080284.2 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A669-01A-12D-A31L-08 chr19:1056089 C>T maps to NM_019112.3 R1422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:1043734 C>A maps to NM_019112.3 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr19:1042062 G>A maps to NM_019112.3 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr19:1044691 C>T maps to NM_019112.3 D388D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YO-01A-11D-A34A-08 chr19:1049301 C>T maps to NM_019112.3 G806G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7681-01A-11D-2395-08 chr17:66914236 G>A maps to NM_007168.2 R626R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:66979977 G>A maps to NM_080283.3 S1504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:66982384 G>A maps to NM_080283.3 N1376N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A6S2-01A-21D-A32B-08 chr17:67023789 C>T maps to NM_080283.3 V594V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr17:66982396 C>T maps to NM_080283.3 A1372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6666-01A-11D-1893-08 chr7:87183088 T>C maps to NM_000927.3 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6405-01A-11D-1705-08 chr7:87178714 C>T maps to NM_000927.3 T558T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TS-01A-12D-A33T-08 chr7:87145839 C>T maps to NM_000927.3 T1023T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5304-01A-01D-1468-08 chr1:229685029 C>G maps to NM_012089.2 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:20784922 T>A maps to NM_001163941.1 P1097P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr7:20767946 G>A maps to NM_001163941.1 S912S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:220078890 G>A maps to NM_005689.2 A468A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:74282212 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:74289278 A>C did not map to a codon.
Sequencing variant TCGA-FG-A710-01A-12D-A33T-08 chr23:74290345 C>A did not map to a codon.
Sequencing variant TCGA-P5-A5EW-01A-11D-A27K-08 chr23:74291460 C>A did not map to a codon.
Sequencing variant TCGA-TQ-A7RW-01A-11D-A33T-08 chr23:74282267 T>C did not map to a codon.
Sequencing variant TCGA-E1-A7YN-01A-11D-A34A-08 chr16:16162083 C>T maps to ENST00000399408 F583F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr6:43400461 C>T maps to NM_033450.2 C205C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A87Q-01A-11D-A36O-08 chr6:43415636 C>T maps to NM_033450.2 D1279D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7690-01A-11D-2253-08 chr16:48211012 C>T maps to NM_032583.3 S1120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A847-01A-11D-A36O-08 chr16:48218515 C>T maps to NM_032583.3 A1031A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5140-01A-01D-1468-08 chr16:48174761 G>A maps to NM_033226.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:48120674 C>A maps to NM_033226.2 E1231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:48120657 T>C maps to NM_033226.2 R1236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5319-01A-01D-1893-08 chr16:48162528 G>A maps to NM_033226.2 T452T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RH-01A-12D-A34A-08 chr16:48117858 A>G maps to NM_033226.2 V1318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:101560196 C>A maps to NM_000392.3 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6410-01A-11D-1893-08 chr10:101594196 C>T maps to NM_000392.3 L1107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:48750832 C>T maps to NM_003786.3 R805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:48753804 C>T maps to NM_003786.3 V1078V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6542-01A-11D-1893-08 chr17:48733299 C>T maps to NM_003786.3 C51C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CY-01A-11D-A32B-08 chr17:48755184 G>A maps to NM_003786.3 E1153E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KM-01A-11D-A27K-08 chr13:95840745 G>A maps to NM_005845.3 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:183677557 T>C maps to NM_005688.2 G815G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R4-01A-12D-A34J-08 chr16:16276376 G>A maps to NM_001171.5 F713F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64V-01A-11D-A29Q-08 chr12:22012588 C>A maps to NM_005691.2 L812L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:22005069 C>T maps to NM_005691.2 W910*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:22001152 C>A maps to NM_005691.2 E933*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr12:22001087 G>A maps to NM_005691.2 D954D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153005566 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:152991416 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:152991338 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153005668 C>T did not map to a codon.
Sequencing variant TCGA-DU-A76O-01A-11D-A32B-08 chr12:40013105 T>C maps to NM_005164.3 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UU-01A-12D-A34A-08 chr4:146032139 C>T maps to NM_002940.2 R212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr6:30558336 C>G maps to NM_001025091.1 A799A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:150921060 C>A maps to NM_005692.3 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6542-01A-11D-1893-08 chr7:150911220 G>A maps to NM_005692.3 D597D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66D-01A-11D-A31L-08 chr3:183908940 G>A maps to NM_018358.2 P489P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:183905480 C>T maps to NM_018358.2 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CY-01A-11D-A32B-08 chr3:183908940 G>A maps to NM_018358.2 P489P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr21:43708162 C>T maps to NM_004915.3 R380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:43704781 C>T maps to NM_004915.3 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:43711732 C>T maps to NM_004915.3 G552G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr21:43704747 C>T maps to NM_004915.3 C271C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:44051082 C>T maps to NM_022436.2 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EZ-01A-11D-A27K-08 chr2:44050051 G>A maps to NM_022436.2 S449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:27351332 C>T maps to NM_032604.3 Q47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr3:111705807 A>C maps to NM_018394.2 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:27893162 G>A maps to NM_198147.2 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7881-01A-11D-2395-08 chr17:27893249 G>A maps to NM_198147.2 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:89719109 C>T maps to NM_152924.4 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:89719100 C>A maps to NM_152924.4 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:89659563 T>C maps to NM_152924.4 N2N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TD-01A-12D-A34A-08 chr3:43759312 C>T maps to NM_016006.4 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:204255866 G>A did not map to a codon.
Sequencing variant TCGA-DU-A76K-01A-11D-A33T-08 chr2:204259425 G>A maps to ENST00000295851 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84H-01A-11D-A36O-08 chr2:204281775 G>A maps to ENST00000295851 P446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7470-01A-12D-2086-08 chr3:100489773 T>C maps to ENST00000471714 Q1509Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:133729607 T>G maps to NM_007313.2 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:133753947 C>T maps to NM_007313.2 R492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85A-01A-21D-A36O-08 chr1:179078463 C>T maps to NM_007314.3 R646R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CY-01A-11D-A32B-08 chr4:8055950 C>T maps to NM_001130083.1 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5390-01A-02D-1468-08 chr7:150554514 C>T maps to ENST00000416793 Y319Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8010-01A-11D-2395-08 chr7:150555012 C>T maps to ENST00000416793 V485V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr17:915190 G>A maps to NM_021962.2 Q666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:107781844 C>A maps to NM_139166.4 E192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A617-01A-11D-A29Q-08 chr11:34184210 G>A maps to NM_145804.2 S710S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:38175456 G>A maps to NM_001607.3 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:38164582 C>T maps to NM_001607.3 G410G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:47329191 G>T maps to NM_006111.2 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:35512703 T>C did not map to a codon.
Sequencing variant TCGA-FG-A6J3-01A-11D-A31L-08 chr17:35454874 T>A maps to NM_198834.1 K2204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CV-01A-11D-A31L-08 chr17:35641872 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:109577713 C>A maps to NM_001093.3 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:109614052 G>A maps to NM_001093.3 P474P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr12:109644645 C>T maps to NM_001093.3 P1015P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TD-01A-12D-A34A-08 chr12:109644573 A>G maps to NM_001093.3 K991K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8113-01A-11D-2395-08 chr12:109690902 C>T maps to NM_001093.3 T1995T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:112174795 C>T maps to NM_001136538.1 R599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7490-01A-11D-2024-08 chr12:112193512 G>A maps to NM_001136538.1 P1032P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:128631413 C>A maps to NM_014049.4 A610A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:128627875 C>T maps to NM_014049.4 D473D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:76205768 G>A maps to ENST00000370834 W224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8110-01A-11D-2395-08 chr12:121176334 G>A did not map to a codon.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr15:89386880 T>C did not map to a codon.
Sequencing variant TCGA-E1-A7YK-01A-11D-A34A-08 chr15:89392714 A>G maps to NM_013227.3 E593E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:195022729 G>A maps to NM_012287.5 G430G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7015-01A-11D-2024-08 chr1:226349373 G>A maps to NM_022735.3 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YY-01A-11D-A34J-08 chr10:27499971 C>T maps to ENST00000375888 Q334Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5965-01B-11D-1893-08 chr10:27524037 A>C maps to ENST00000375888 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:32483421 G>A maps to NM_001094.4 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:156757854 G>A maps to NM_017419.2 S407S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:44104851 C>T maps to NM_032592.3 D415D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr11:44089248 G>T maps to NM_032592.3 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7603-01A-21D-2086-08 chr16:67694141 C>T maps to NM_001082486.1 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:61570880 C>T maps to NM_000789.3 Y999Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8163-01A-11D-2253-08 chr17:61557163 C>T maps to NM_000789.3 Y182Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr23:15580078 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:15609979 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:15618960 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:15584453 A>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:15596322 C>T did not map to a codon.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr23:15609936 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:6312495 G>T maps to NM_133492.2 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr19:6312224 G>A maps to NM_133492.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:100490881 G>A maps to NM_000665.3 S324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6188-01A-11D-1893-08 chr14:23550989 C>T maps to NM_014977.3 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:23549096 C>A maps to NM_014977.3 G541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5277-01A-01D-1468-08 chr17:40030157 G>A maps to ENST00000401700 Q894*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TS-01A-11D-A289-08 chr17:40065857 G>A maps to ENST00000401700 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:135616829 G>T did not map to a codon.
Sequencing variant TCGA-DU-7294-01A-11D-2024-08 chr7:96747044 C>A maps to NM_020186.2 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:55069582 C>A maps to NM_015547.3 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7854-01A-11D-2253-08 chr20:44472286 C>G maps to NM_005469.3 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8188-01A-11D-2253-08 chr23:23748658 G>T did not map to a codon.
Sequencing variant TCGA-P5-A72Z-01A-11D-A32B-08 chr23:23723124 G>A did not map to a codon.
Sequencing variant TCGA-P5-A781-01A-11D-A32B-08 chr23:23723893 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:73951966 A>G maps to NM_004035.6 Y200Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6404-01A-11D-1705-08 chr4:8396381 G>A maps to NM_003501.2 R382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6689-01A-11D-1893-08 chr11:47264837 G>A maps to NM_001610.2 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7304-01A-12D-2086-08 chr3:132051044 C>T maps to NM_001134194.1 R105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TC-01A-21D-A34J-08 chr12:6749666 G>A maps to NM_032489.2 R367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66D-01A-11D-A31L-08 chr23:70823727 A>T did not map to a codon.
Sequencing variant TCGA-E1-A7Z2-01A-21D-A34J-08 chr23:70828952 G>A did not map to a codon.
Sequencing variant TCGA-EZ-7264-01A-11D-2024-08 chr23:70824012 G>A did not map to a codon.
Sequencing variant TCGA-TM-A84H-01A-11D-A36O-08 chr23:70824519 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:125547890 C>T maps to NM_001612.5 Q118Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7302-01A-11D-2086-08 chr15:78475122 C>T maps to NM_015162.4 W223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A6S8-01A-12D-A32B-08 chr15:78474343 G>A maps to NM_015162.4 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85E-01A-11D-A36O-08 chr15:78474350 C>T maps to NM_015162.4 W344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:185684329 G>A maps to NM_001995.2 G504G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr4:185724473 C>A maps to NM_001995.2 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UU-01A-12D-A34A-08 chr23:108887277 G>A did not map to a codon.
Sequencing variant TCGA-DU-5847-01A-11D-1705-08 chr23:108921234 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:108917674 C>A did not map to a codon.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr23:108926515 G>C did not map to a codon.
Sequencing variant TCGA-FG-A87N-01A-11D-A36O-08 chr23:108902735 G>T did not map to a codon.
Sequencing variant TCGA-HT-A74K-01A-11D-A32B-08 chr23:108911383 T>C did not map to a codon.
Sequencing variant TCGA-RY-A83Y-01A-11D-A36O-08 chr5:131309075 G>A maps to NM_001009185.1 H362H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr16:20635525 G>A maps to NM_052956.2 A513A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6402-01A-11D-1705-08 chr16:20476847 C>T maps to NM_001010845.2 R63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr16:20477030 C>T maps to NM_001010845.2 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8563-01A-11D-2395-08 chr16:20492161 G>A maps to NM_001010845.2 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A840-01A-11D-A36O-08 chr16:20576154 G>A maps to NM_182617.3 R5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6186-01A-12D-2024-08 chr12:7477157 G>A maps to NM_001080454.1 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TI-01A-11D-A33T-08 chr16:20451156 C>G maps to NM_017888.2 Y524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:33501897 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:81532986 G>A maps to NM_024560.2 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74K-01A-11D-A32B-08 chr12:81503359 C>T maps to NM_024560.2 N111N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr1:229568327 G>A maps to NM_001100.3 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:90701148 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:5568062 G>A maps to NM_001101.3 C217C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64V-01A-11D-A29Q-08 chr15:35086922 G>A maps to NM_005159.4 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A86X-01A-11D-A36O-08 chr17:79478120 G>A maps to NM_001614.2 C272C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7605-01A-11D-2086-08 chr2:74146596 C>T maps to NM_001615.3 I342I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr9:111617664 C>T maps to NM_006686.3 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:18149676 C>T maps to NM_030812.2 C58C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr1:18152413 C>T maps to NM_030812.2 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YL-01A-11D-A34A-08 chr19:8808925 G>A maps to NM_178525.3 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:69387792 G>T maps to NM_001130004.1 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr11:66330633 C>T maps to NM_001104.1 S892S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:58698848 G>A maps to NM_018477.2 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr2:65467017 T>C maps to NM_001005386.2 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4942-01A-01D-1468-08 chr2:114699854 C>T maps to NM_005721.3 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:152517445 G>A maps to NM_020445.4 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:53911753 G>A maps to NM_022899.4 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4938-01B-11D-1893-08 chr23:127186135 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:127185264 G>A did not map to a codon.
Sequencing variant TCGA-DU-A6S8-01A-12D-A32B-08 chr23:127185636 C>T did not map to a codon.
Sequencing variant TCGA-HT-7477-01B-11D-A289-08 chr23:127185375 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:2938558 C>T maps to NM_080431.4 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5270-01A-02D-1468-08 chr12:52370108 A>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:158395159 C>T maps to NM_145259.2 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7015-01A-11D-2024-08 chr2:158443696 A>G did not map to a codon.
Sequencing variant TCGA-FG-7637-01A-11D-2086-08 chr2:158401020 G>A maps to NM_145259.2 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85E-01A-11D-A36O-08 chr3:38519420 C>T maps to NM_001106.3 N110N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:52314610 G>A maps to NM_001077401.1 A482A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:43249742 C>T maps to NM_000022.2 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4938-01B-11D-1893-08 chr4:123336615 A>T maps to NM_139243.3 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:58889777 C>A maps to NM_001110.2 E739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:127797170 G>A maps to NM_003474.4 H247H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:155029697 C>T maps to NM_207197.1 R395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:156940492 G>A maps to ENST00000430702 D231D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A87Q-01A-11D-A36O-08 chr8:39624683 G>A maps to NM_001464.3 C433C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7477-01B-11D-A289-08 chr8:39624671 T>C maps to NM_001464.3 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U8-01A-21D-A33T-08 chr8:39666967 T>C maps to NM_001464.3 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5965-01B-11D-1893-08 chr14:70991444 G>A maps to NM_003814.4 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:87795161 C>T maps to NM_021723.3 L698L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66B-01A-11D-A29Q-08 chr8:24181516 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:24170972 G>A maps to NM_014265.4 E152E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr8:24187574 C>T maps to NM_014265.4 D350D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YL-01A-11D-A34A-08 chr8:24197030 G>A maps to NM_014265.4 K540K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7686-01A-11D-2253-08 chr8:24201056 A>G maps to NM_014265.4 G650G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8320-01A-11D-2395-08 chr8:24193002 C>T maps to NM_014265.4 C472C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A77W-01A-11D-A32B-08 chr8:24199149 G>A maps to NM_014265.4 S570S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:120438760 G>A maps to NM_021794.2 Q67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7304-01A-12D-2086-08 chr1:120437549 G>A maps to NM_021794.2 C470C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5273-01A-01D-1468-08 chr8:39091489 G>C maps to NM_145004.5 V569V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-HT-7480-01A-11D-2086-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr8:24350111 T>A did not map to a codon.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr8:24350562 A>T maps to ENST00000380789 R555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6J3-01A-11D-A31L-08 chr8:38934857 G>A maps to NM_003816.2 V603V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:24256481 G>A maps to NM_014479.3 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:8651766 G>A maps to NM_030957.2 V724V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:8651775 G>A maps to NM_030957.2 Y721Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6188-01A-11D-1893-08 chr5:33648938 G>A maps to NM_030955.2 C489C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UR-01A-11D-A33T-08 chr5:33588802 C>T maps to NM_030955.2 P922P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:33577232 A>G maps to NM_030955.2 I966I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7602-01A-21D-2086-08 chr5:33576464 G>A maps to NM_030955.2 P1222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U1-01A-21D-A33T-08 chr5:33576785 C>T maps to NM_030955.2 S1115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:72520572 C>T maps to NM_139155.2 P1215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:72468456 C>T maps to NM_139155.2 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr11:130341227 G>A maps to NM_139055.2 G676G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KK-01A-11D-A27K-08 chr11:130332500 C>T maps to NM_139055.2 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:5190118 C>A maps to NM_139056.2 T361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:5235132 G>A maps to NM_139056.2 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr5:5239325 C>T maps to NM_139056.2 N739N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RP-01A-21D-A34A-08 chr5:5242304 G>A did not map to a codon.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr15:100657166 G>A maps to NM_139057.2 V591V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CF-01A-11D-A36O-08 chr15:100695506 G>A maps to NM_139057.2 D400D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr16:77401349 G>A maps to NM_199355.2 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7298-01A-11D-2024-08 chr5:129039954 C>A maps to NM_133638.3 G1055G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8163-01A-11D-2253-08 chr5:129037125 A>G maps to NM_133638.3 K994K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A61C-01A-11D-A29Q-08 chr5:129070794 C>G maps to NM_133638.3 P1155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IZ-01A-11D-A34A-08 chr5:178541200 G>A maps to NM_014244.4 N1101N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr12:43840497 G>A maps to ENST00000389420 H699H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A70Z-01A-12D-A33T-08 chr12:43884231 G>A maps to ENST00000389420 D361D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:73149301 G>A maps to NM_014243.1 L1057L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr4:73434465 G>C maps to NM_014243.1 S5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WL-01A-21D-A33T-08 chr21:28296757 C>A maps to NM_007038.3 G803*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:64748587 C>A maps to NM_197941.2 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XC-01A-11D-A26M-08 chr15:79059039 A>G maps to ENST00000258883 N1071N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64V-01A-11D-A29Q-08 chr15:79092722 G>A maps to ENST00000258883 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:79060601 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:130284491 C>T maps to NM_007037.4 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:64601049 G>A maps to NM_182920.1 Q1046*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7CF-01A-11D-A32B-08 chr3:64640135 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:18680456 C>T maps to NM_001040272.4 I428I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:18777289 C>T maps to NM_001040272.4 Y1021Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:18795490 C>T maps to NM_001040272.4 Y1258Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:18661964 C>T maps to NM_001040272.4 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:18777745 C>T maps to NM_001040272.4 A1173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A618-01A-11D-A29Q-08 chr9:18829916 G>A maps to NM_001040272.4 V1397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7489-01A-11D-2024-08 chr9:18776968 C>T maps to NM_001040272.4 D914D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:136412158 G>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:84657497 C>T maps to NM_207517.2 Q1258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:150525643 C>T maps to ENST00000369039 Q117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:1507279 C>T maps to NM_213604.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr1:154560601 G>A maps to ENST00000292205 N1049N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:154574232 G>A maps to ENST00000292205 D338D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:154562662 C>T maps to ENST00000292205 K874K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64W-01A-11D-A29Q-08 chr10:1405303 C>T maps to NM_018702.2 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr1:33585651 C>T maps to ENST00000373441 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CV-01A-11D-A31L-08 chr7:140374050 C>T maps to NM_052853.3 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:41206295 C>T maps to NM_024876.3 T318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:45724576 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:45719376 C>T maps to NM_021116.2 H656H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A614-01A-11D-A29Q-08 chr7:45717490 G>A maps to NM_021116.2 S543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7636-01A-11D-2086-08 chr1:167870981 C>T maps to NM_018417.4 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7471-01A-11D-2253-08 chr1:167870911 G>A maps to NM_018417.4 R142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U5-01A-12D-A33T-08 chr1:167849748 G>A maps to NM_018417.4 C373C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7C4-01A-11D-A32B-08 chr1:167802328 T>G maps to NM_018417.4 R1163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:7817085 G>A maps to NM_020546.2 L997L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:7789843 C>T maps to NM_020546.2 R853R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr5:7520912 C>T maps to NM_020546.2 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A72U-01A-31D-A32B-08 chr5:7520912 C>T maps to NM_020546.2 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QY-01A-11D-A34A-08 chr5:7520963 C>T maps to NM_020546.2 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:25050826 G>T maps to NM_004036.3 L792L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R8-01A-11D-A34J-08 chr2:25141328 G>A maps to NM_004036.3 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr14:24791274 G>A maps to NM_139247.3 N861N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:24798657 G>A maps to NM_139247.3 D433D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A780-01A-12D-A32B-08 chr14:24793575 C>T maps to NM_139247.3 T615T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A83X-01A-11D-A36O-08 chr14:24787934 C>T maps to NM_139247.3 P1002P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WH-A86K-01A-11D-A36O-08 chr14:24787934 C>T maps to NM_139247.3 P1002P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:123038540 C>A maps to NM_183357.2 E746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr3:123036942 G>A maps to NM_183357.2 R760*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr16:50347882 C>G maps to NM_001114.3 P922P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7487-01A-11D-2024-08 chr8:131922057 G>A maps to NM_001115.2 S512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:4027577 G>A maps to NM_001116.3 N911N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84S-01A-11D-A36O-08 chr16:4016306 G>A maps to NM_001116.3 I1177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A617-01A-11D-A29Q-08 chr4:2877686 G>A maps to NM_014189.2 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8161-01A-11D-2253-08 chr2:70904916 G>C maps to NM_001185054.1 P492P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:111892061 G>T did not map to a codon.
Sequencing variant TCGA-VV-A86M-01A-11D-A36O-08 chr10:111892081 C>G maps to NM_016824.3 L584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5396-01A-02D-1468-08 chr4:100205753 G>A maps to NM_000667.3 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7013-01A-11D-2024-08 chr4:100205898 C>T maps to NM_000667.3 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QZ-01A-12D-A34J-08 chr4:100208067 T>C maps to NM_000667.3 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr4:100237087 C>T maps to NM_000668.4 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EZ-01A-11D-A27K-08 chr4:100264167 G>A maps to NM_000669.3 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TZ-01A-21D-A32B-08 chr4:100266126 C>G maps to NM_000669.3 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6X5-01A-12D-A32B-08 chr4:100047869 T>C maps to ENST00000505590 V350V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:99996152 C>A maps to NM_000671.3 V291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:67369315 T>G maps to NM_144650.2 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:3504689 G>A maps to NM_018269.3 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CV-01A-11D-A31L-08 chr2:3517684 G>T maps to NM_018269.3 Y61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:202917538 C>A maps to NM_015999.3 E51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A6YH-01A-21D-A32B-08 chr1:202915645 G>A maps to NM_015999.3 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:49508535 G>A maps to NM_181442.1 N905N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7015-01A-11D-2024-08 chr20:49508436 A>G maps to NM_181442.1 T938T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A710-01A-12D-A33T-08 chr20:49509062 G>A maps to NM_181442.1 R730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:77894586 C>T maps to NM_014913.3 Q431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:203098112 C>T maps to NM_001048230.1 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IY-01A-11D-A34A-08 chr17:15878190 C>G maps to NM_000676.2 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:114078565 C>T maps to NM_138430.3 W291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RH-01A-12D-A34A-08 chr13:114107557 G>A maps to NM_138430.3 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7483-01A-11D-2024-08 chr20:4202426 G>T maps to NM_000678.3 R488R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr2:96781414 C>T maps to NM_000682.5 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5141-01A-01D-1468-08 chr5:148206921 C>T maps to NM_000024.5 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:67047314 C>T maps to NM_001619.3 Y149Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:67049161 G>A maps to NM_001619.3 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A70Z-01A-12D-A33T-08 chr22:26057596 C>T maps to NM_005160.3 Q107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:60881368 G>A maps to NM_175573.1 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:40745934 C>T maps to ENST00000428371 R512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr1:244581039 T>C maps to NM_001126.3 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EU-01A-11D-A27K-08 chr7:44151919 G>A maps to NM_001129.3 T739T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8161-01A-11D-2253-08 chr19:3061201 G>A maps to NM_198969.1 D94D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:88036336 C>T maps to NM_001166693.1 P784P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:87968379 G>A maps to NM_001166693.1 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64W-01A-11D-A29Q-08 chr23:148068961 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:148037906 T>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:148035175 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:148037454 G>A did not map to a codon.
Sequencing variant TCGA-DU-6403-01A-11D-1705-08 chr23:148069036 G>T did not map to a codon.
Sequencing variant TCGA-DU-7009-01A-11D-2024-08 chr23:148037322 C>T did not map to a codon.
Sequencing variant TCGA-HT-7681-01A-11D-2395-08 chr23:148049221 G>T did not map to a codon.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr23:148048317 A>C did not map to a codon.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr23:148035252 G>A did not map to a codon.
Sequencing variant TCGA-HT-7880-01A-11D-2395-08 chr23:148037447 A>G did not map to a codon.
Sequencing variant TCGA-S9-A6TS-01A-12D-A33T-08 chr23:148048607 T>C did not map to a codon.
Sequencing variant TCGA-S9-A6TV-01A-12D-A34J-08 chr23:148038125 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:100210418 G>T maps to NM_001025108.1 P593P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76O-01A-11D-A32B-08 chr2:100623318 A>G maps to NM_001025108.1 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YD-01A-11D-A34A-08 chr5:132216760 A>T maps to NM_014423.3 L1161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84S-01A-11D-A36O-08 chr5:132262878 A>G maps to NM_014423.3 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:64779663 T>C maps to ENST00000422803 C352C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6IZ-01A-11D-A31L-08 chr2:64796312 G>A maps to ENST00000422803 K725K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7611-01A-11D-2395-08 chr2:236626275 G>T maps to NM_001037131.1 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CA-01A-11D-A36O-08 chr2:236659028 C>T maps to NM_001037131.1 I190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6X4-01A-51D-A32B-08 chr10:88769469 C>T maps to NM_133447.1 D487D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5319-01A-01D-1893-08 chr12:58126703 G>A maps to NM_001122772.1 C536C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R2-01A-21D-A34J-08 chr12:58135802 G>A maps to NM_014770.2 R18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-8125-01A-11D-2253-08 chr10:75457305 G>A maps to NM_001144000.1 Q70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8114-01A-11D-2395-08 chr10:51769669 C>T maps to NM_001077665.2 T595T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YJ-01A-11D-A34A-08 chr15:86940657 G>A maps to NM_152336.2 W766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8106-01A-11D-2395-08 chr15:86838483 A>C did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr15:86800127 G>A maps to NM_152336.2 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:228399559 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:100160219 C>A maps to NM_006076.4 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:100162562 C>A maps to NM_006076.4 P465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:100353532 G>A did not map to a codon.
Sequencing variant TCGA-CS-5390-01A-02D-1468-08 chr1:15904230 G>A maps to NM_024758.3 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:161587375 C>T maps to NM_020133.2 K84K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:6605222 C>T maps to NM_018361.3 R207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:84465729 G>A maps to NM_032717.3 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7US-01A-11D-A33T-08 chr15:78805579 C>G maps to NM_001013619.2 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RJ-01A-11D-A33T-08 chr1:978951 C>T maps to NM_198576.2 C546C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CF-01A-11D-A36O-08 chr1:230845897 C>A maps to NM_000029.3 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IQ-01A-21D-A34A-08 chr9:88201793 A>G maps to ENST00000395847 H995H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr23:115303725 G>A did not map to a codon.
Sequencing variant TCGA-FG-A70Y-01A-12D-A34J-08 chr23:115304313 G>C did not map to a codon.
Sequencing variant TCGA-P5-A731-01A-11D-A32B-08 chr23:115303786 A>G did not map to a codon.
Sequencing variant TCGA-R8-A6MK-01A-11D-A32B-08 chr5:35037112 G>A maps to NM_031900.3 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A77X-01A-11D-A32B-08 chr4:109675775 C>G maps to NM_031279.3 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6666-01A-11D-1893-08 chr5:177652384 C>A maps to NM_153373.2 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr1:247021039 C>T maps to ENST00000428671 P1441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr20:32873404 G>A maps to NM_000687.2 I336I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7884-01B-11D-2395-08 chr1:27875776 C>T maps to NM_001029882.2 P950P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr6:135787391 G>A maps to NM_017651.4 N103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5141-01A-01D-1468-08 chr11:62289981 G>A maps to NM_001620.1 D3969D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:62290341 G>A maps to NM_001620.1 I3849I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:62287035 A>G maps to NM_001620.1 A4951A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5318-01A-01D-1468-08 chr11:62299209 C>T maps to NM_001620.1 E893E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr11:62294253 C>T maps to NM_001620.1 K2545K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A711-01A-21D-A33T-08 chr11:62289339 G>A maps to NM_001620.1 D4183D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr11:62287401 G>A maps to NM_001620.1 D4829D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TY-01A-12D-A32B-08 chr11:62287083 C>T maps to NM_001620.1 P4935P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7J3-01A-21D-A34J-08 chr11:62301030 A>G maps to NM_001620.1 G286G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RM-01A-11D-A33T-08 chr11:62297886 C>T maps to NM_001620.1 G1334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W9-A837-01A-11D-A36O-08 chr11:62300246 G>A maps to NM_001620.1 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:105420881 G>A maps to NM_138420.2 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:105416924 C>T maps to NM_138420.2 L1621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:105411293 C>T maps to NM_138420.2 V3498V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:105416411 G>A maps to NM_138420.2 D1792D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:105419258 G>A maps to NM_138420.2 F843F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6405-01A-11D-1705-08 chr14:105420968 C>T maps to NM_138420.2 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr14:105414215 C>T maps to NM_138420.2 G2524G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A70Z-01A-12D-A33T-08 chr14:105413441 G>A maps to NM_138420.2 D2782D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A87Q-01A-11D-A36O-08 chr14:105419204 C>T maps to NM_138420.2 P861P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7469-01A-11D-2253-08 chr14:105421332 G>A maps to NM_138420.2 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7487-01A-11D-2024-08 chr14:105420365 G>A maps to NM_138420.2 G474G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CW-01A-11D-A32B-08 chr14:105418742 C>T maps to NM_138420.2 K1015K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7C3-01A-11D-A32B-08 chr14:105418754 C>T maps to NM_138420.2 S1011S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U6-01A-12D-A33T-08 chr7:17379701 A>T maps to NM_001621.4 G751G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84B-01A-11D-A36O-08 chr7:17379425 C>T maps to NM_001621.4 F659F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A75L-01A-11D-A32B-08 chr5:353937 G>A maps to NM_020731.3 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:434144 C>T maps to NM_020731.3 P452P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7607-01A-11D-2086-08 chr5:413499 G>A maps to NM_020731.3 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7676-01A-11D-2395-08 chr5:423983 C>G maps to NM_020731.3 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74H-01A-11D-A32B-08 chr5:413481 C>T maps to NM_020731.3 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5281-01A-01D-1468-08 chr12:8757942 G>A maps to NM_020661.2 R99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:129272656 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:129290549 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:129265658 C>A did not map to a codon.
Sequencing variant TCGA-DU-A7T6-01A-11D-A33T-08 chr23:129290462 C>G did not map to a codon.
Sequencing variant TCGA-FG-A6J3-01A-11D-A31L-08 chr23:129274524 T>A did not map to a codon.
Sequencing variant TCGA-DU-5874-01A-11D-1705-08 chr10:71880313 C>T maps to NM_032797.5 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:21328397 C>A maps to NM_144704.2 C134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:143654484 A>G maps to NM_016108.2 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:106969006 C>A maps to NM_001624.2 S900S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:106978131 G>T maps to NM_001624.2 E1146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:106969186 A>G maps to NM_001624.2 E960E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7298-01A-11D-2024-08 chr1:26650672 C>T maps to NM_001039775.3 W1569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr1:26650747 C>T maps to NM_001039775.3 V1544V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5142-01A-01D-1468-08 chr1:159035846 G>A maps to NM_004833.1 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RS-01A-12D-A33T-08 chr7:6049110 G>A maps to NM_006303.3 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7013-01A-11D-2024-08 chr17:6329142 C>T maps to NM_014336.3 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr17:6331636 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:55183013 C>A maps to ENST00000427138 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:55193475 G>A maps to ENST00000427138 T804T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:151674766 G>A maps to NM_005100.3 Q1747Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:86087013 C>T maps to NM_006738.4 R164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:86227998 G>A maps to NM_006738.4 L1732L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7684-01A-11D-2253-08 chr15:86287024 G>A maps to NM_006738.4 K2791K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7CF-01A-11D-A32B-08 chr15:86287009 G>A maps to NM_006738.4 K2786K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A6S6-01A-21D-A32B-08 chr23:119037474 A>T did not map to a codon.
Sequencing variant TCGA-CS-6188-01A-11D-1893-08 chr9:112900625 C>T maps to NM_007203.4 D934D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:112899575 G>A maps to NM_007203.4 K584K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:112899206 C>T maps to NM_007203.4 A461A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8320-01A-11D-2395-08 chr9:112898642 C>T maps to NM_007203.4 H273H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr23:49957835 G>T did not map to a codon.
Sequencing variant TCGA-DU-5872-01A-11D-1705-08 chr23:49957596 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:49963373 G>C did not map to a codon.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr23:49958080 T>C did not map to a codon.
Sequencing variant TCGA-HT-7470-01A-12D-2086-08 chr23:49958836 C>T did not map to a codon.
Sequencing variant TCGA-HT-7601-01A-11D-2086-08 chr23:49957503 G>C did not map to a codon.
Sequencing variant TCGA-HT-7882-01A-11D-2395-08 chr23:49958223 G>A did not map to a codon.
Sequencing variant TCGA-VM-A8C8-01A-11D-A36O-08 chr23:49961551 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:131490379 G>T maps to ENST00000431975 G180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:15484808 G>A maps to NM_005858.2 Y53Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:91708646 G>A maps to NM_005751.4 Q2400Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:91715583 C>T maps to NM_005751.4 R3023*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr7:91631133 G>T maps to NM_005751.4 E635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr7:91737806 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:109814754 G>A maps to NM_001145128.2 S1851S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:109366028 C>T maps to NM_152763.3 Q710Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr7:134212704 C>T maps to NM_020299.4 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5964-01A-11D-1705-08 chr10:5144388 C>T maps to NM_003739.4 R223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5277-01A-01D-1468-08 chr10:4881967 C>T maps to NM_001040177.1 C210C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:4877926 C>T maps to NM_001040177.1 R129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QY-01A-11D-A34A-08 chr1:19630775 A>G maps to NM_003689.2 D341D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:40744859 C>T maps to NM_001626.3 Q220Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:53532472 G>A maps to ENST00000425875 D26D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr23:55042059 C>T did not map to a codon.
Sequencing variant TCGA-HW-A5KL-01A-11D-A27K-08 chr23:55052377 G>A did not map to a codon.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr15:58254314 G>A maps to NM_003888.2 G382G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7873-01B-11D-2395-08 chr15:101425494 C>T maps to NM_000693.2 H41H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7CF-01A-11D-A32B-08 chr9:38396183 C>A maps to NM_000692.3 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:125828945 C>A maps to ENST00000273450 E740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W9-A837-01A-11D-A36O-08 chr3:125831671 G>A maps to ENST00000273450 R722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7015-01A-11D-2024-08 chr17:19641634 C>T did not map to a codon.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr17:19646620 G>A maps to NM_000691.4 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:67430844 G>A maps to NM_001031615.1 H333H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6400-01A-12D-1705-08 chr11:67433864 G>A maps to NM_001031615.1 C53C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8158-01A-11D-2253-08 chr1:19209802 G>A maps to NM_003748.3 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7486-01A-11D-2024-08 chr6:135239870 C>T maps to NM_022568.3 K382K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:165638675 A>G maps to NM_000696.3 N314N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:34178814 G>A maps to NM_032834.3 Q129Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:38714921 C>A maps to NM_001013620.3 C443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:52602698 A>G maps to NM_001004127.2 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:110970861 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:110928325 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:110925384 G>A did not map to a codon.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr23:110952272 G>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:183960346 C>T maps to NM_005787.5 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:63872049 G>T maps to ENST00000263440 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:77825381 G>T maps to NM_024079.4 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:29754875 C>T maps to NM_004304.3 R353R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:102100176 G>A maps to NM_017621.3 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5304-01A-01D-1468-08 chr19:36501794 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:73829482 C>T maps to NM_015120.4 L4095L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:73677139 T>A maps to NM_015120.4 T1161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:73717915 G>T maps to NM_015120.4 E2943*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:73717090 C>T maps to NM_015120.4 R2668*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DU-6392-01A-11D-1705-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-DU-6392-01A-11D-1705-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr17:7976178 G>A maps to NM_001139.2 I672I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:4539074 C>T maps to NM_001140.3 P380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A780-01A-12D-A32B-08 chr17:4534927 C>T maps to NM_001140.3 R652R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84I-01A-11D-A36O-08 chr17:4540427 G>A maps to NM_001140.3 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:45878106 G>A maps to NM_000698.2 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XB-01A-11D-A26M-08 chr18:56203629 G>A maps to NM_052947.3 D1263D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:56205159 T>C maps to NM_052947.3 P753P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:56202618 G>T maps to NM_052947.3 P1600P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7009-01A-11D-2024-08 chr18:56203278 T>C maps to NM_052947.3 Q1380Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8161-01A-11D-2253-08 chr18:56246387 C>T maps to NM_052947.3 P540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:85382936 C>T maps to NM_020778.4 R345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7006-01A-11D-2024-08 chr15:85383196 G>A maps to NM_020778.4 G431G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr15:85382931 G>A did not map to a codon.
Sequencing variant TCGA-HW-8320-01A-11D-2395-08 chr2:233274353 G>A maps to NM_031313.2 A457A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4943-01A-01D-1468-08 chr2:202609062 G>A maps to NM_020919.3 H696H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:202622248 G>A maps to NM_020919.3 S449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8105-01A-11D-2395-08 chr2:202619250 G>A maps to NM_020919.3 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RG-01A-11D-A33T-08 chr2:202626335 G>A maps to NM_020919.3 N127N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:202467965 G>A maps to NM_001168221.1 C117C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:202172322 G>A maps to NM_139163.2 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:202494501 C>T maps to ENST00000409099 K214K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A70Z-01A-12D-A33T-08 chr11:44286676 G>A maps to NM_021926.3 C321C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:33520543 G>A maps to NM_152462.2 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76O-01A-11D-A32B-08 chr17:33521272 C>T maps to NM_152462.2 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:11188668 G>A maps to NM_054028.1 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:11189076 C>T maps to NM_054028.1 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5874-01A-11D-1705-08 chr17:7385398 G>A maps to NM_001102614.1 Q32Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr9:116840417 C>T maps to NM_001633.3 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TR-01A-11D-A289-08 chr11:46563767 C>T maps to ENST00000458649 W600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A614-01A-11D-A29Q-08 chr11:46431878 C>G maps to ENST00000458649 L1052L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:96350566 G>A maps to NM_152435.2 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:11316259 C>T did not map to a codon.
Sequencing variant TCGA-E1-A7YV-01A-11D-A34J-08 chr23:11317074 G>A did not map to a codon.
Sequencing variant TCGA-TQ-A7RS-01A-12D-A33T-08 chr23:11316388 A>T did not map to a codon.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr16:56396892 G>A maps to NM_001144.4 D620D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:53819520 G>T maps to NM_020547.2 G224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7856-01A-11D-2395-08 chr12:53825208 C>T maps to NM_020547.2 G558G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7290-01A-11D-2024-08 chr11:118074284 C>G maps to NM_001098526.1 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:110050172 G>A maps to NM_020703.2 N454N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:110050379 G>A maps to NM_020703.2 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr1:110050352 G>A maps to NM_020703.2 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr23:109459854 A>G did not map to a codon.
Sequencing variant TCGA-DH-5144-01A-01D-1468-08 chr23:109444268 T>C did not map to a codon.
Sequencing variant TCGA-E1-A7YY-01A-11D-A34J-08 chr23:109459809 C>T did not map to a codon.
Sequencing variant TCGA-TQ-A7RS-01A-12D-A33T-08 chr23:109561294 G>A did not map to a codon.
Sequencing variant TCGA-VW-A8FI-01A-11D-A36O-08 chr2:128628857 A>G maps to NM_031445.2 N161N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:112054487 C>A did not map to a codon.
Sequencing variant TCGA-EZ-7264-01A-11D-2024-08 chr23:112058787 T>C did not map to a codon.
Sequencing variant TCGA-HT-7690-01A-11D-2253-08 chr23:112022265 C>A did not map to a codon.
Sequencing variant TCGA-P5-A5F6-01A-11D-A289-08 chr23:112058795 C>T did not map to a codon.
Sequencing variant TCGA-QH-A6CW-01A-11D-A32B-08 chr23:112048275 C>G did not map to a codon.
Sequencing variant TCGA-VW-A7QS-01A-12D-A33T-08 chr23:112058795 C>T did not map to a codon.
Sequencing variant TCGA-S9-A7IZ-01A-11D-A34A-08 chr11:94532856 G>A maps to NM_130847.2 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:134085260 G>A maps to ENST00000514516 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8185-01A-11D-2253-08 chr1:115216304 G>A maps to NM_000036.2 C713C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:10521709 C>T maps to NM_000480.2 D554D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5ET-01A-11D-A27K-08 chr17:66246611 G>A did not map to a codon.
Sequencing variant TCGA-FG-A6J3-01A-11D-A31L-08 chr2:112536311 G>C maps to NM_022662.2 L1775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:140074824 G>A maps to NM_013366.3 D566D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:121756219 G>A maps to NM_016237.4 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:121783769 C>T maps to NM_016237.4 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:121773352 G>A maps to NM_016237.4 H311H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7467-01A-11D-2024-08 chr12:121769170 G>A maps to NM_016237.4 H337H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8563-01A-11D-2395-08 chr12:121790074 C>G maps to NM_016237.4 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:77272761 C>T maps to NM_015305.3 W459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8320-01A-11D-2395-08 chr8:108306211 A>G maps to NM_001146.3 R330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CF-01A-11D-A36O-08 chr8:108334250 T>G maps to NM_001146.3 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:896547 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:868968 G>A maps to NM_015985.2 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:129870902 T>C maps to NM_012098.2 R36R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A711-01A-21D-A33T-08 chr9:129854000 C>T maps to NM_012098.2 W410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7472-01A-11D-2024-08 chr9:129854132 C>G maps to NM_012098.2 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:11249978 C>T maps to NM_021146.2 Q115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr8:41554023 C>T maps to ENST00000415018 P939P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr8:41577304 G>A maps to ENST00000415018 Y327Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7C3-01A-11D-A32B-08 chr8:41530254 C>T maps to ENST00000415018 A1571A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XD-01A-11D-A27K-08 chr4:114278386 T>C maps to NM_001148.4 I2871I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr4:114280345 C>T maps to NM_001148.4 T3524T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:114288728 G>A maps to NM_001148.4 S3680S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:114120207 A>G maps to NM_001148.4 Q109Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:114274546 A>G maps to NM_001148.4 E1591E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7Z6-01A-11D-A34J-08 chr4:114239725 C>T maps to NM_001148.4 G950G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:61835997 A>G maps to NM_020987.2 S1547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:61828938 G>T maps to NM_020987.2 A3900A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7606-01A-11D-2086-08 chr10:61958112 T>C maps to NM_020987.2 L558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr10:61832502 T>C maps to NM_020987.2 Q2712Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:65218320 G>A maps to NM_182703.3 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8161-01A-11D-2253-08 chr17:4088254 C>G maps to NM_016376.3 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:14713082 C>A did not map to a codon.
Sequencing variant TCGA-CS-6666-01A-11D-1893-08 chr5:139866583 T>A maps to ENST00000253810 P728P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5277-01A-01D-1468-08 chr5:139917068 C>T maps to ENST00000253810 R2392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:139887504 C>A maps to ENST00000253810 T1229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XG-01A-11D-A27K-08 chr7:91981896 C>T maps to NM_019004.1 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7857-01A-11D-2395-08 chr11:113267964 C>T maps to NM_178510.1 D286D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XF-01A-11D-A27K-08 chr12:133313476 A>C did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:241468875 G>A maps to ENST00000401804 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6396-01A-11D-1705-08 chr5:72849255 T>C maps to NM_023039.4 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TS-01A-11D-A289-08 chr16:89357150 C>T maps to NM_013275.4 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YN-01A-11D-A34A-08 chr16:89348856 G>A maps to NM_013275.4 R1365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr16:89347171 C>T maps to NM_013275.4 P1926P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:9263873 C>T maps to NM_015208.3 H1917H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:9258859 C>T maps to NM_015208.3 D1865D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74H-01A-11D-A32B-08 chr1:70779455 T>C maps to NM_030816.4 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:5927717 G>A maps to NM_001009941.2 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5281-01A-01D-1468-08 chr4:73957065 T>A maps to NM_032217.3 P2093P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:73964216 C>A maps to NM_032217.3 E1532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7300-01A-21D-2086-08 chr4:74012997 T>C maps to NM_032217.3 Q573Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr4:74021733 A>G did not map to a codon.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr4:73942822 T>C did not map to a codon.
Sequencing variant TCGA-QH-A65R-01A-21D-A31L-08 chr4:73944452 A>C maps to NM_032217.3 T2438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CY-01A-11D-A32B-08 chr4:73957007 C>A maps to NM_032217.3 G2113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TX-01A-21D-A32B-08 chr4:74000832 C>T did not map to a codon.
Sequencing variant TCGA-HT-A4DV-01A-11D-A26M-08 chr2:97506179 T>A maps to NM_144994.7 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EZ-7264-01A-11D-2024-08 chr19:33096833 A>G maps to NM_032139.2 N800N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A710-01A-12D-A33T-08 chr18:21226218 G>A maps to NM_173505.2 Y55Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U6-01A-12D-A33T-08 chr18:21199493 C>T did not map to a codon.
Sequencing variant TCGA-DU-A5TS-01A-11D-A289-08 chr10:37508225 G>T maps to ENST00000374660 E1259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A736-01A-11D-A32B-08 chr10:37454052 G>A maps to ENST00000374660 K622K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6402-01A-11D-1705-08 chr18:14763802 G>A maps to NM_001145029.1 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R2-01A-21D-A34J-08 chr18:14791431 G>C maps to NM_001145029.1 V589V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UR-01A-11D-A33T-08 chr5:94014526 A>G maps to NM_032290.3 E614E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A710-01A-12D-A33T-08 chr5:79855580 C>T maps to NM_001004441.2 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7CA-01A-21D-A33T-08 chr5:79855466 A>G maps to NM_001004441.2 Y124Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74O-01A-11D-A32B-08 chr2:97853076 C>T maps to NM_001164315.1 D694D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TR-01A-11D-A289-08 chr5:132149636 G>T maps to NM_175873.4 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:94231652 C>A maps to NM_017704.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7856-01A-11D-2395-08 chr12:56645996 A>G maps to NM_173595.3 S491S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7C3-01A-11D-A32B-08 chr7:117874918 G>A maps to ENST00000357099 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:35051219 C>T maps to NM_015245.2 I978I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YN-01A-11D-A34A-08 chr12:5708775 G>A maps to ENST00000356134 R704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:26556045 C>T maps to NM_031418.2 R305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7009-01A-11D-2024-08 chr12:101437334 T>A maps to ENST00000392977 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:22261164 C>T maps to NM_213599.2 Y271Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:45810503 C>A maps to NM_001142679.1 T678T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:45814909 C>A maps to NM_001142679.1 S758S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7489-01A-11D-2024-08 chr12:45797220 G>T did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:242148713 C>T maps to NM_001001891.3 F418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:17441160 C>T maps to NM_020959.2 Q382Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UR-01A-11D-A33T-08 chr11:418475 C>T maps to NM_001012302.2 W748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7470-01A-12D-2086-08 chr11:429779 G>A maps to NM_001012302.2 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:90347137 C>T maps to NM_001150.2 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr2:69297778 A>G maps to NM_032208.2 R99R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CZ-01A-11D-A32B-08 chr10:46122442 A>G maps to NM_001128324.1 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr9:75773610 C>T maps to NM_000700.1 Q23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:169105787 C>T maps to NM_007193.3 R288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7686-01A-11D-2253-08 chr4:169105804 T>C maps to NM_007193.3 Y293Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U9-01A-11D-A32B-08 chr4:169100461 T>C maps to NM_007193.3 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A780-01A-12D-A32B-08 chr15:60644016 T>C maps to NM_001002858.2 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XA-01A-11D-A26M-08 chr4:79531253 T>C maps to NM_005139.2 C319C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:70031689 C>T maps to NM_001153.3 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:150514014 G>A maps to NM_001155.4 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr1:150957081 C>T maps to NM_003568.2 D134D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7601-01A-11D-2086-08 chr7:36570026 C>A maps to NM_001177506.1 E507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RH-01A-12D-A34A-08 chr17:41004013 G>A maps to NM_003734.2 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A617-01A-11D-A29Q-08 chr2:201478595 G>A maps to NM_001159.3 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:71768514 C>T maps to ENST00000423132 Q811Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:50309176 C>T maps to NM_014203.2 D900D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:50285228 T>C maps to NM_014203.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:50309431 C>T maps to NM_014203.2 F926F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F4-01A-11D-A289-08 chr11:986943 C>T maps to ENST00000332231 N375N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:33966766 T>C maps to NM_001030006.1 D475D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:2116214 C>T maps to ENST00000355272 S688S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7013-01A-11D-2024-08 chr5:115177766 C>T maps to NM_001284.2 H11H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TP-01A-11D-A289-08 chr1:114442616 G>A maps to NM_006594.2 N341N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:29346644 C>A maps to NM_005503.3 Y186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:6417021 C>T maps to ENST00000389906 A653A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:41015669 C>T maps to NM_004307.1 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:41015609 C>T maps to NM_004307.1 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7601-01A-11D-2086-08 chr4:41015609 C>T maps to NM_004307.1 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:112176147 A>G maps to NM_001127510.2 P1619P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F6-A8O4-01A-11D-A36O-08 chr5:112176255 A>C maps to NM_001127510.2 T1655T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:1462050 C>T maps to NM_005883.2 G576G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5965-01B-11D-1893-08 chr1:159557755 G>A maps to NM_001639.3 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5847-01A-11D-1705-08 chr23:55033525 A>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:55026891 C>T did not map to a codon.
Sequencing variant TCGA-HT-7857-01A-11D-2395-08 chr23:55033115 C>T did not map to a codon.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr23:55033741 G>T did not map to a codon.
Sequencing variant TCGA-TQ-A7RJ-01A-11D-A33T-08 chr23:55033215 C>G did not map to a codon.
Sequencing variant TCGA-HT-A615-01A-11D-A29Q-08 chr11:43343604 C>T maps to NM_001142930.1 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8188-01A-11D-2253-08 chr11:57003347 A>G maps to NM_005161.4 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YL-01A-11D-A34A-08 chr11:129996637 C>T maps to NM_001642.2 F378F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A70Z-01A-12D-A33T-08 chr11:116691768 G>A maps to NM_000482.3 D335D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5140-01A-01D-1468-08 chr2:21228171 G>A maps to NM_000384.2 I3856I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5847-01A-11D-1705-08 chr2:21226161 C>T maps to NM_000384.2 R4044R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:21231045 C>T maps to NM_000384.2 L2898L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:21236128 G>A maps to NM_000384.2 Y1373Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7302-01A-11D-2086-08 chr2:21227212 G>A maps to NM_000384.2 A4005A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EZ-7264-01A-11D-2024-08 chr2:21234702 C>T maps to NM_000384.2 G1679G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7604-01A-11D-2086-08 chr2:21230554 A>C maps to NM_000384.2 L3062*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A614-01A-11D-A29Q-08 chr2:21230418 G>A maps to NM_000384.2 N3107N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A86X-01A-11D-A36O-08 chr2:21245797 G>A maps to NM_000384.2 H907H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RH-01A-12D-A34A-08 chr2:21236128 G>T maps to NM_000384.2 Y1373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RR-01A-21D-A34A-08 chr2:21229827 C>T maps to NM_000384.2 L3304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:28507306 C>T maps to NM_018690.2 G315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:41029258 G>C maps to NM_006789.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7018-01A-11D-2024-08 chr22:39387536 C>T maps to ENST00000402182 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:39425373 G>A maps to NM_152426.3 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84L-01A-11D-A36O-08 chr22:39448227 G>A maps to NM_145298.5 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr19:45411903 G>A maps to NM_000041.2 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A858-01A-11D-A36O-08 chr17:64224314 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:36661286 G>A maps to NM_145343.2 Q151Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A83Z-01A-11D-A36O-08 chr22:36537769 C>T maps to NM_145640.2 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6396-01A-11D-1705-08 chr22:36587385 G>A maps to ENST00000332987 R261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:36122597 G>A maps to NM_030642.1 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84J-01A-11D-A36O-08 chr22:36116678 G>A maps to NM_030642.1 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8158-01A-11D-2253-08 chr23:23899065 T>A did not map to a codon.
Sequencing variant TCGA-WY-A859-01A-12D-A36O-08 chr23:23899025 G>T did not map to a codon.
Sequencing variant TCGA-CS-4938-01B-11D-1893-08 chr3:57291435 A>G maps to NM_012096.2 K470K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:57274503 T>C maps to NM_012096.2 C99C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:57294735 C>T maps to NM_012096.2 S592S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:57303714 A>C maps to NM_012096.2 *710Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:57303660 G>A maps to NM_012096.2 Q692Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7490-01A-11D-2024-08 chr16:88876923 G>A maps to NM_000485.2 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A710-01A-12D-A33T-08 chr1:154294527 C>T maps to NM_080429.2 N75N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:33442894 G>T maps to NM_004925.3 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr18:24445620 C>A did not map to a codon.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr18:24442316 G>A maps to NM_001650.4 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4943-01A-01D-1468-08 chr5:115351038 T>C maps to NM_173800.4 T847T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5303-01A-01D-1468-08 chr5:115336873 C>T maps to NM_173800.4 G586G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr5:115298644 C>T maps to NM_173800.4 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RR-01A-21D-A34A-08 chr5:115327922 A>G maps to NM_173800.4 T403T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RH-01A-12D-A34A-08 chr15:35193057 G>A maps to NM_014691.2 L670L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:66765079 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:66766151 G>A did not map to a codon.
Sequencing variant TCGA-DU-6406-01A-11D-1705-08 chr23:66765160 A>T did not map to a codon.
Sequencing variant TCGA-DU-7309-01A-11D-2086-08 chr23:66765382 T>C did not map to a codon.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr23:66863187 G>C did not map to a codon.
Sequencing variant TCGA-S9-A6TS-01A-12D-A33T-08 chr23:66931474 A>G did not map to a codon.
Sequencing variant TCGA-S9-A6U5-01A-12D-A33T-08 chr23:66765615 A>G did not map to a codon.
Sequencing variant TCGA-S9-A7J0-01A-11D-A34A-08 chr23:66765160 A>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:47422623 G>T did not map to a codon.
Sequencing variant TCGA-DH-5143-01A-01D-1468-08 chr11:72410501 C>A maps to NM_001040118.2 E800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:72408650 C>T maps to NM_001040118.2 E927E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6IZ-01A-11D-A31L-08 chr11:72398485 G>A maps to NM_001040118.2 Q1395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RM-01A-11D-A33T-08 chr4:36179547 A>G maps to NM_015230.2 V586V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:141039453 C>T maps to NM_022481.5 R1053R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr8:143694471 G>A maps to NM_015193.3 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:228285650 C>G maps to NM_001024228.1 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A72Z-01A-11D-A32B-08 chr4:153791962 A>G maps to NM_001025595.1 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:131904948 T>C maps to ENST00000356962 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:121304886 C>T maps to NM_001012659.1 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:107211821 C>T maps to NM_018011.3 E177E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8191-01A-11D-2253-08 chr15:32917834 G>C did not map to a codon.
Sequencing variant TCGA-VM-A8CA-01A-11D-A36O-08 chr10:32150340 T>C maps to NM_018287.5 Q310Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8166-01A-11D-2253-08 chr6:129959562 A>T maps to NM_033515.2 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:110485283 C>T did not map to a codon.
Sequencing variant TCGA-E1-A7YH-01A-11D-A34A-08 chr10:24909112 G>A maps to NM_020824.3 R571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A780-01A-12D-A32B-08 chr10:24890932 G>A maps to NM_020824.3 R941*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4938-01B-11D-1893-08 chr10:49791050 G>A maps to ENST00000417912 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:49662147 C>T maps to ENST00000417912 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:86921844 C>T maps to NM_001025616.2 T739T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A83Y-01A-11D-A36O-08 chr2:69046418 C>T maps to NM_001007231.2 R390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:142281517 G>T maps to NM_015071.4 G206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TJ-01A-11D-A34J-08 chr17:43475374 G>A maps to ENST00000428638 H594H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RK-01A-11D-A33T-08 chr1:94651005 T>G maps to NM_004815.3 T604T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:119128598 C>T maps to NM_020754.2 A634A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7686-01A-11D-2253-08 chr11:128839035 G>A maps to NM_001142685.1 H2010H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CH-01A-12D-A36O-08 chr11:128848707 C>G maps to NM_001142685.1 R679R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:36272094 C>T maps to ENST00000007510 H342H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7881-01A-11D-2395-08 chr19:36268761 T>G maps to ENST00000007510 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TZ-01A-21D-A32B-08 chr19:36268614 G>A maps to ENST00000007510 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr23:130217832 C>T did not map to a codon.
Sequencing variant TCGA-FG-A6J3-01A-11D-A31L-08 chr23:130220044 C>A did not map to a codon.
Sequencing variant TCGA-QH-A65X-01A-11D-A32B-08 chr23:130220335 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:145773467 G>A maps to NM_025251.1 F334F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5144-01A-01D-1468-08 chr23:153175535 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153176002 G>A did not map to a codon.
Sequencing variant TCGA-KT-A7W1-01A-11D-A34A-08 chr23:153173282 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:32563099 C>T maps to NM_001030055.1 S1075S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66D-01A-11D-A31L-08 chr23:11157493 G>C did not map to a codon.
Sequencing variant TCGA-HT-A615-01A-11D-A29Q-08 chr23:11174685 C>T did not map to a codon.
Sequencing variant TCGA-S9-A7J0-01A-11D-A34A-08 chr23:11157234 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:57872424 G>A maps to ENST00000393797 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7877-01A-11D-2395-08 chr12:15095521 G>A maps to NM_001175.4 D180D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:42396803 G>A maps to NM_199002.1 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7301-01A-11D-2086-08 chr19:42396178 C>T maps to NM_199002.1 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YQ-01A-11D-A34J-08 chr19:42396887 G>A maps to NM_199002.1 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:1817378 C>T maps to ENST00000398564 Y239Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:1882008 C>T maps to ENST00000398564 G1066G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R7-01A-11D-A289-08 chr8:1877526 A>T maps to ENST00000398564 T1024T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:17961054 C>T maps to NM_018125.3 H581H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:17934327 G>A maps to NM_018125.3 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:17949528 G>A maps to NM_018125.3 A353A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr1:156916462 G>C maps to NM_198236.1 L895L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr11:120355175 C>T maps to NM_015313.2 C1528C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A730-01A-11D-A32B-08 chr11:120350734 G>A maps to NM_015313.2 W1278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:8216238 G>T did not map to a codon.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr17:8216516 C>T maps to NM_173728.3 F293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A735-01A-11D-A32B-08 chr19:7531820 G>A maps to NM_001130955.1 T786T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:16535348 C>A maps to NM_153213.3 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:16535420 C>A maps to NM_153213.3 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85A-01A-21D-A36O-08 chr1:16528978 G>A maps to NM_153213.3 H666H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr7:143884336 C>T maps to NM_001003702.2 E380E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84M-01A-11D-A36O-08 chr5:148989207 G>A maps to NM_001001669.2 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64P-01A-11D-A29Q-08 chr2:131797916 C>A maps to NM_015320.2 I336I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66G-01A-21D-A31L-08 chr23:135750294 C>T did not map to a codon.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr23:135825809 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:135750300 C>T did not map to a codon.
Sequencing variant TCGA-DU-7290-01A-11D-2024-08 chr23:135862896 T>A did not map to a codon.
Sequencing variant TCGA-KT-A7W1-01A-11D-A34A-08 chr23:135825937 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:111932993 C>A maps to NM_001113511.1 T586T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:62875506 C>A did not map to a codon.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr23:62917173 T>G did not map to a codon.
Sequencing variant TCGA-HT-7877-01A-11D-2395-08 chr23:62893976 G>A did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr23:62857962 C>T did not map to a codon.
Sequencing variant TCGA-S9-A6U2-01A-21D-A33T-08 chr23:62857998 G>T did not map to a codon.
Sequencing variant TCGA-DB-5275-01A-01D-1468-08 chr1:27100206 C>T maps to NM_006015.4 R1335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:27056261 C>T maps to NM_006015.4 Q420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6410-01A-11D-1893-08 chr1:27101341 G>T maps to NM_006015.4 E1542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7304-01A-12D-2086-08 chr1:27087502 C>T maps to NM_006015.4 R693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7637-01A-11D-2086-08 chr1:27100380 C>T maps to NM_006015.4 Q1365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7468-01A-11D-2024-08 chr1:27105549 C>T maps to NM_006015.4 R1721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7611-01A-11D-2395-08 chr1:27056285 C>T maps to NM_006015.4 Q428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A735-01A-11D-A32B-08 chr1:27101373 G>A maps to NM_006015.4 Q1552Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A780-01A-12D-A32B-08 chr1:27101118 C>T maps to NM_006015.4 P1467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84S-01A-11D-A36O-08 chr1:27101005 C>T maps to NM_006015.4 Q1430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66F-01A-11D-A29Q-08 chr6:157495230 C>T maps to ENST00000367148 Q1026*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:157454309 C>T maps to ENST00000367148 Y827Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:157517440 C>T maps to ENST00000367148 Y1375Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7290-01A-11D-2024-08 chr6:157454204 T>A maps to ENST00000367148 Y792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A75M-01A-11D-A32B-08 chr12:46246182 C>A maps to NM_152641.2 S1426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5303-01A-01D-1468-08 chr12:46242661 C>T maps to NM_152641.2 R542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:74884147 C>T maps to ENST00000395077 N471N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:34622472 C>A maps to NM_001017363.1 G307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:34623515 C>T maps to NM_001017363.1 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TV-01A-12D-A34J-08 chr9:34623536 C>T maps to NM_001017363.1 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:58831662 C>T maps to NM_002892.3 I952I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:58831192 C>T maps to NM_002892.3 R796*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:235377286 C>T maps to NM_016374.5 E546E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:63817057 C>T maps to NM_032199.2 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:63851261 T>C maps to NM_032199.2 S680S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:49004628 T>C maps to NM_006321.2 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:175793459 C>T maps to NM_173664.4 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:175793445 C>T maps to NM_173664.4 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76K-01A-11D-A33T-08 chr13:50204750 C>T maps to NM_138450.5 H56H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:160395142 G>A maps to NM_025047.2 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:41477480 C>T maps to NM_001661.3 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:69151035 C>T maps to NM_006407.3 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:153591514 G>A maps to NM_152522.4 W154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5273-01A-01D-1468-08 chr6:109294620 T>C maps to NM_032131.4 H836H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A89V-01A-11D-A36O-08 chr6:109286253 G>A maps to NM_032131.4 W786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8158-01A-11D-2253-08 chr10:23292318 C>T maps to NM_173081.3 N569N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KT-A74X-01A-11D-A32B-08 chr10:23326257 G>A maps to NM_173081.3 A823A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:28196636 C>T maps to NM_018076.2 K855K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8113-01A-11D-2395-08 chr16:31470907 G>A maps to ENST00000408912 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr19:19162909 C>T maps to ENST00000392336 D253D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A83X-01A-11D-A36O-08 chr2:232141450 G>T maps to ENST00000359743 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5390-01A-02D-1468-08 chr23:100808651 G>A did not map to a codon.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr23:100910838 T>A did not map to a codon.
Sequencing variant TCGA-FG-7638-01B-11D-2086-08 chr23:100912541 C>T did not map to a codon.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr23:101857470 T>A did not map to a codon.
Sequencing variant TCGA-S9-A6WM-01A-12D-A33T-08 chr23:101858273 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:80873695 G>A maps to NM_014862.3 S623S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8015-01B-11D-A289-08 chr15:80845027 C>A maps to NM_014862.3 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6X8-01A-12D-A32B-08 chr15:80767430 G>T maps to NM_014862.3 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8186-01A-11D-2253-08 chr11:13402767 T>C maps to ENST00000403290 P528P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:27521252 T>C maps to NM_020183.3 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5275-01A-01D-1468-08 chr3:35758846 T>C maps to ENST00000458225 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:69495965 C>T did not map to a codon.
Sequencing variant TCGA-HT-8012-01A-11D-2395-08 chr23:69500074 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:4624309 C>T maps to ENST00000412477 D423D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr17:4619833 G>C maps to ENST00000412477 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WN-01A-12D-A33T-08 chr19:18119538 G>A maps to NM_015683.1 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:4891207 G>A maps to NM_001080523.1 Y293Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CZ-01A-11D-A32B-08 chr19:4891573 G>A maps to NM_001080523.1 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A75K-01A-11D-A32B-08 chr23:2827920 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:2836235 G>A did not map to a codon.
Sequencing variant TCGA-DU-A6S7-01A-21D-A32B-08 chr23:2825455 G>A did not map to a codon.
Sequencing variant TCGA-E1-A7YH-01A-11D-A34A-08 chr23:2836161 G>A did not map to a codon.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr23:2836027 G>A did not map to a codon.
Sequencing variant TCGA-DB-A64P-01A-11D-A29Q-08 chr23:2853193 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:2867534 C>T did not map to a codon.
Sequencing variant TCGA-E1-5318-01A-01D-1468-08 chr23:2867630 G>A did not map to a codon.
Sequencing variant TCGA-FG-A711-01A-21D-A33T-08 chr23:2854889 T>C did not map to a codon.
Sequencing variant TCGA-DU-7300-01A-21D-2086-08 chr23:3021882 C>T did not map to a codon.
Sequencing variant TCGA-DB-A75K-01A-11D-A32B-08 chr23:2933250 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:2951114 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:2924664 C>T did not map to a codon.
Sequencing variant TCGA-DH-A7US-01A-11D-A33T-08 chr5:149677436 C>T maps to NM_001012301.2 W350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VV-A829-01A-21D-A36O-08 chr4:114899933 G>A maps to NM_024590.3 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:3681426 G>A maps to NM_004314.2 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8111-01A-11D-2395-08 chr11:3681543 C>T maps to NM_004314.2 Y265Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5849-01A-11D-1705-08 chr4:77018806 C>T maps to NM_001130016.1 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7475-01A-11D-2024-08 chr4:77018800 A>G maps to NM_001130016.1 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:231125861 G>T maps to NM_022786.1 G101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr22:19960525 G>A maps to NM_001670.2 H824H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5396-01A-02D-1468-08 chr10:104650299 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:131124477 C>A maps to NM_018482.2 G755*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:131191541 C>T maps to NM_018482.2 Q238Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:9496442 C>T maps to NM_003887.2 G432G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6405-01A-11D-1705-08 chr2:239344636 C>A maps to NM_001040445.1 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7Z3-01A-11D-A34J-08 chr23:15306082 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:63444765 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:63445175 G>T did not map to a codon.
Sequencing variant TCGA-FG-A6J3-01A-11D-A31L-08 chr23:63444339 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:76397591 G>A maps to NM_080868.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:177142709 G>A maps to NM_080874.3 N142N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr15:101170213 C>T maps to NM_198243.2 R262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr23:15272892 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:15266935 A>G did not map to a codon.
Sequencing variant TCGA-FG-A87Q-01A-11D-A36O-08 chr23:15287956 C>T did not map to a codon.
Sequencing variant TCGA-TQ-A7RQ-01A-11D-A33T-08 chr23:15268607 A>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:101296418 G>A maps to NM_006828.2 R136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:155449531 T>C maps to ENST00000368346 G1043G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:37985944 C>T maps to NM_004674.3 T434T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7US-01A-11D-A33T-08 chr23:1743283 G>A did not map to a codon.
Sequencing variant TCGA-DB-A64W-01A-11D-A29Q-08 chr23:1551212 G>A did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr23:1536975 C>T did not map to a codon.
Sequencing variant TCGA-TM-A84J-01A-11D-A36O-08 chr7:97482449 T>C maps to NM_183356.3 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:62563618 G>A maps to NM_004318.3 H160H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:197072571 C>A maps to NM_018136.4 G1937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:197059197 C>T maps to NM_018136.4 L3282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:197074287 G>A maps to NM_018136.4 Q1365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:197071585 G>A maps to NM_018136.4 A2265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:197059133 G>A maps to NM_018136.4 R3304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr9:95228796 G>A maps to NM_017680.4 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7610-01A-21D-2086-08 chr3:130732930 C>T maps to ENST00000514044 E695E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CX-01A-11D-A32B-08 chr2:96789807 C>T maps to NM_001002036.3 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A73M-01A-11D-A32B-08 chr2:96799704 G>A maps to NM_001002036.3 Y112Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85E-01A-11D-A36O-08 chr2:96799704 G>A maps to NM_001002036.3 Y112Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:176913102 C>T maps to ENST00000281881 V775V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YO-01A-11D-A34A-08 chr1:176853604 G>A maps to ENST00000281881 H1040H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WN-01A-12D-A33T-08 chr1:176915087 G>A maps to ENST00000281881 A749A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr9:119413977 G>A maps to ENST00000313400 D967D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:31017710 G>A maps to ENST00000375687 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8162-01A-21D-2253-08 chr20:31023106 C>T maps to ENST00000375687 D864D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7695-01A-11D-2253-08 chr2:25972672 C>T maps to NM_018263.4 R584R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RW-01A-11D-A33T-08 chr18:31326456 C>T maps to NM_030632.1 C2215C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:124340562 A>G maps to NM_014109.3 T1245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7902-01A-12D-2395-08 chr2:23985166 C>G maps to NM_017552.1 R1102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:1421518 C>T maps to NM_031921.4 I331I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6690-01A-11D-1893-08 chr1:1431190 G>T maps to NM_031921.4 L647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr1:1386074 C>T maps to NM_001039211.2 D4D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:123503323 C>T maps to NM_001001976.1 K476K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:123658439 C>T maps to NM_007041.2 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:123658450 C>A maps to NM_007041.2 E283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A72U-01A-31D-A32B-08 chr2:175979597 T>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:39917986 G>T maps to NM_182810.1 E146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:161790921 A>G maps to NM_007348.2 A386A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr6:32088574 G>A maps to NM_004381.4 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YK-01A-11D-A34A-08 chr6:32087598 A>G did not map to a codon.
Sequencing variant TCGA-S9-A7R2-01A-21D-A34J-08 chr6:32089120 G>C maps to NM_004381.4 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8109-01A-11D-2395-08 chr12:14634096 T>C maps to NM_018179.3 V1086V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TP-01A-11D-A289-08 chr16:10551309 G>T maps to NM_024997.2 E426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6670-01A-11D-1893-08 chr11:64674137 T>C maps to ENST00000421419 R994R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:64664286 G>A maps to ENST00000421419 D1737D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:64662654 G>T maps to ENST00000421419 I1871I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7007-01A-11D-2024-08 chr11:64677553 C>A maps to ENST00000421419 L607L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5ET-01A-11D-A27K-08 chr11:64665786 C>T maps to ENST00000421419 G1575G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr14:96757938 A>G maps to NM_018036.5 H1859H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A6S8-01A-12D-A32B-08 chr14:96795933 T>A maps to NM_018036.5 R590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:107381353 G>T did not map to a codon.
Sequencing variant TCGA-TQ-A7RO-01A-11D-A33T-08 chr23:107381180 G>A did not map to a codon.
Sequencing variant TCGA-TM-A84B-01A-11D-A36O-08 chr19:10659650 C>T maps to NM_032885.4 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5390-01A-02D-1468-08 chr6:106764040 G>A maps to NM_004849.2 R15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6404-01A-11D-1705-08 chr6:106764058 G>A maps to NM_004849.2 R9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7677-01A-11D-2253-08 chr2:220088459 G>A maps to NM_024085.3 S482S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:150714128 C>T maps to NM_173681.5 S761S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:216209587 C>T maps to NM_004044.6 N438N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:108163492 G>A maps to NM_000051.3 V1528V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:108153588 T>C maps to NM_000051.3 N1243N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:108163423 C>T maps to NM_000051.3 A1505A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F6-A8O3-01A-11D-A36O-08 chr11:108124758 C>A maps to NM_000051.3 S706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:81069744 C>T maps to NM_015251.2 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:81077071 C>A maps to NM_015251.2 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7854-01A-11D-2253-08 chr12:7050145 C>T maps to NM_001940.3 H1106H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:25967017 A>G maps to NM_024490.3 I383I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:160076221 C>T maps to NM_025153.2 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:160033804 G>A maps to NM_025153.2 R1043*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RC-01A-11D-A289-08 chr5:160039780 G>A maps to NM_025153.2 T935T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KK-01A-11D-A27K-08 chr5:160049523 G>T maps to NM_025153.2 T563T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7CA-01A-21D-A33T-08 chr4:47514778 T>C maps to NM_020453.3 N74N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:113514617 G>A maps to NM_032189.3 A915A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:182635855 C>A maps to NM_014616.1 I1166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5871-01A-12D-1705-08 chr23:138850562 T>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:138882242 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:138864819 C>A did not map to a codon.
Sequencing variant TCGA-HT-7690-01A-11D-2253-08 chr23:138857057 T>C did not map to a codon.
Sequencing variant TCGA-HT-8010-01A-11D-2395-08 chr23:138886674 G>C did not map to a codon.
Sequencing variant TCGA-TM-A7C3-01A-11D-A32B-08 chr23:138864752 A>G did not map to a codon.
Sequencing variant TCGA-TQ-A7RI-01A-11D-A33T-08 chr23:138879423 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:19770597 G>A maps to NM_020410.2 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:17322536 G>A maps to NM_022089.2 G492G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5318-01A-01D-1468-08 chr3:194170982 G>A maps to NM_024524.3 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:193081987 G>A maps to NM_198505.2 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TA-01A-11D-A33T-08 chr3:193036785 A>C maps to NM_198505.2 L676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:42489539 G>T maps to ENST00000441343 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr1:160136481 C>T maps to NM_144699.3 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:160147441 C>T maps to NM_144699.3 Y908Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:119500593 T>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:119509349 A>G did not map to a codon.
Sequencing variant TCGA-E1-A7YO-01A-11D-A34A-08 chr23:119496053 C>T did not map to a codon.
Sequencing variant TCGA-FG-A87Q-01A-11D-A36O-08 chr23:119500505 G>A did not map to a codon.
Sequencing variant TCGA-R8-A6MK-01A-11D-A32B-08 chr16:28909639 G>A maps to NM_173201.3 K544K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:110764193 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:110783172 T>C maps to NM_170665.3 C909C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A75P-01A-11D-A32B-08 chr17:3844558 C>A maps to NM_174953.1 P602P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:3844864 C>T maps to NM_174953.1 E543E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:3832729 C>T maps to NM_174953.1 E918E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5395-01A-01D-1468-08 chr3:10452377 C>T maps to NM_001001331.2 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:10420080 G>A maps to NM_001001331.2 D352D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:10413735 C>A did not map to a codon.
Sequencing variant TCGA-VW-A8FI-01A-11D-A36O-08 chr3:10417230 C>T maps to NM_001001331.2 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XD-01A-11D-A27K-08 chr23:152813392 C>T did not map to a codon.
Sequencing variant TCGA-DU-5874-01A-11D-1705-08 chr23:152845600 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:152827664 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:152821651 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:152806913 G>A did not map to a codon.
Sequencing variant TCGA-DU-7300-01A-21D-2086-08 chr23:152827613 G>A did not map to a codon.
Sequencing variant TCGA-DU-A7T6-01A-11D-A33T-08 chr23:152826215 C>T did not map to a codon.
Sequencing variant TCGA-FG-8186-01A-11D-2253-08 chr23:152807341 G>A did not map to a codon.
Sequencing variant TCGA-HT-7686-01A-11D-2253-08 chr23:152826159 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:84472888 G>A maps to ENST00000416219 E368E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:84497224 C>T maps to ENST00000416219 L939L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4942-01A-01D-1468-08 chr19:36054146 C>T maps to NM_000704.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:36053483 C>T maps to NM_000704.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8165-01A-11D-2253-08 chr19:36046428 G>C maps to NM_000704.2 V690V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr19:36045931 C>T maps to NM_000704.2 L791L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr19:36046392 C>T maps to NM_000704.2 A702A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:43667330 G>A maps to NM_001001937.1 I309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:43668132 A>G maps to NM_001001937.1 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5853-01A-11D-1893-08 chr12:57036471 G>C maps to NM_001686.3 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:43036037 A>G maps to NM_001165877.1 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5281-01A-01D-1468-08 chr21:35288046 G>A maps to NM_001697.2 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153663812 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153660610 G>T did not map to a codon.
Sequencing variant TCGA-RY-A83Z-01A-11D-A36O-08 chr23:153664055 A>T did not map to a codon.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr5:81613926 G>A maps to NM_001017971.1 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:40458972 C>T did not map to a codon.
Sequencing variant TCGA-S9-A6WO-01A-21D-A34A-08 chr7:138444520 G>A maps to NM_130840.2 D205D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:87111267 C>T maps to NM_152565.1 R21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:113517136 C>A maps to NM_001690.3 P446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A75M-01A-11D-A32B-08 chr23:77266952 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:77294366 T>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:77266735 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:77244935 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:77267081 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:77254147 G>T did not map to a codon.
Sequencing variant TCGA-E1-5318-01A-01D-1468-08 chr23:77301815 T>G did not map to a codon.
Sequencing variant TCGA-HT-A74K-01A-11D-A32B-08 chr23:77267106 G>A did not map to a codon.
Sequencing variant TCGA-S9-A6TS-01A-12D-A33T-08 chr23:77254081 G>A did not map to a codon.
Sequencing variant TCGA-TM-A7CF-01A-11D-A32B-08 chr23:77301959 T>C did not map to a codon.
Sequencing variant TCGA-WY-A859-01A-12D-A36O-08 chr23:77245263 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:52585454 G>A maps to NM_000053.2 Q7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:42445620 C>T maps to NM_006095.2 L1028L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr13:26411308 C>A maps to NM_016529.4 T921T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:26043136 C>T maps to NM_016529.4 G33G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6395-01A-12D-1705-08 chr13:26125549 C>A maps to NM_016529.4 G322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr13:26273414 G>A maps to NM_016529.4 A772A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:154303298 C>T maps to NM_020452.3 C66C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr19:1785265 G>A maps to NM_138813.2 L1142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6403-01A-11D-1705-08 chr19:1785227 G>A maps to NM_138813.2 Y1154Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr19:1785488 G>A maps to NM_138813.2 C1124C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:50273578 G>A maps to NM_006045.1 N468N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:50221542 G>A maps to NM_006045.1 Y940Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64O-01A-11D-A29Q-08 chr18:77134066 C>T maps to NM_198531.3 Y1080Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:77105534 G>A maps to NM_198531.3 L860L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:47101573 G>T maps to NM_022745.3 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:28564458 G>A maps to NM_016311.3 Q97Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A75M-01A-11D-A32B-08 chr3:142238508 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:142168413 G>A maps to NM_001184.3 R2598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WQ-01A-12D-A34A-08 chr3:142281244 C>T maps to NM_001184.3 V333V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7C5-01A-11D-A32B-08 chr20:3615006 C>T maps to NM_139321.2 Q1305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:117040978 G>T maps to NM_207303.2 E739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:117226751 C>T maps to NM_207303.2 V1162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:117061553 G>A did not map to a codon.
Sequencing variant TCGA-CS-4943-01A-01D-1468-08 chr23:76829759 G>C did not map to a codon.
Sequencing variant TCGA-DB-5273-01A-01D-1468-08 chr23:76939963 G>A did not map to a codon.
Sequencing variant TCGA-DB-5281-01A-01D-1468-08 chr23:76940082 C>T did not map to a codon.
Sequencing variant TCGA-DB-A4XB-01A-11D-A26M-08 chr23:76855198 A>G did not map to a codon.
Sequencing variant TCGA-DB-A4XD-01A-11D-A27K-08 chr23:76940499 T>C did not map to a codon.
Sequencing variant TCGA-DB-A64S-01A-11D-A29Q-08 chr23:76888812 C>T did not map to a codon.
Sequencing variant TCGA-DB-A64S-01A-11D-A29Q-08 chr23:76939873 G>A did not map to a codon.
Sequencing variant TCGA-DB-A75O-01A-11D-A32B-08 chr23:76875969 T>C did not map to a codon.
Sequencing variant TCGA-DH-5142-01A-01D-1468-08 chr23:76890085 T>C did not map to a codon.
Sequencing variant TCGA-DH-5144-01A-01D-1468-08 chr23:76949413 A>G did not map to a codon.
Sequencing variant TCGA-DH-A66D-01A-11D-A31L-08 chr23:76939840 C>A did not map to a codon.
Sequencing variant TCGA-DU-5853-01A-11D-1893-08 chr23:76845410 C>T did not map to a codon.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr23:76764101 G>T did not map to a codon.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr23:76909628 G>A did not map to a codon.
Sequencing variant TCGA-DU-5872-01A-11D-1705-08 chr23:76813105 T>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:76939694 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:76776352 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:76918941 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:76776889 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:76875918 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:76776884 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:76907779 C>T did not map to a codon.
Sequencing variant TCGA-DU-6396-01A-11D-1705-08 chr23:76909628 G>A did not map to a codon.
Sequencing variant TCGA-DU-6408-01A-11D-1705-08 chr23:76874370 A>C did not map to a codon.
Sequencing variant TCGA-DU-6408-01A-11D-1705-08 chr23:76874432 A>C did not map to a codon.
Sequencing variant TCGA-DU-7007-01A-11D-2024-08 chr23:76814312 G>A did not map to a codon.
Sequencing variant TCGA-DU-7011-01A-11D-2024-08 chr23:76939495 G>A did not map to a codon.
Sequencing variant TCGA-DU-7011-01A-11D-2024-08 chr23:76849193 G>A did not map to a codon.
Sequencing variant TCGA-DU-7309-01A-11D-2086-08 chr23:76813013 C>A did not map to a codon.
Sequencing variant TCGA-DU-8163-01A-11D-2253-08 chr23:76814187 A>C did not map to a codon.
Sequencing variant TCGA-DU-8166-01A-11D-2253-08 chr23:76940086 T>C did not map to a codon.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr23:76909628 G>A did not map to a codon.
Sequencing variant TCGA-DU-A5TP-01A-11D-A289-08 chr23:76938406 G>A did not map to a codon.
Sequencing variant TCGA-DU-A5TR-01A-11D-A289-08 chr23:76875910 T>C did not map to a codon.
Sequencing variant TCGA-DU-A76O-01A-11D-A32B-08 chr23:76874350 C>A did not map to a codon.
Sequencing variant TCGA-DU-A76O-01A-11D-A32B-08 chr23:76938028 G>A did not map to a codon.
Sequencing variant TCGA-DU-A76O-01A-11D-A32B-08 chr23:76890193 C>T did not map to a codon.
Sequencing variant TCGA-DU-A7T8-01A-21D-A34J-08 chr23:76939374 G>T did not map to a codon.
Sequencing variant TCGA-E1-5304-01A-01D-1468-08 chr23:76814312 G>A did not map to a codon.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr23:76939495 G>A did not map to a codon.
Sequencing variant TCGA-E1-A7YE-01A-11D-A34A-08 chr23:76813055 C>G did not map to a codon.
Sequencing variant TCGA-E1-A7YH-01A-11D-A34A-08 chr23:76875999 C>T did not map to a codon.
Sequencing variant TCGA-E1-A7YI-01A-11D-A34A-08 chr23:76909646 T>A did not map to a codon.
Sequencing variant TCGA-E1-A7YK-01A-11D-A34A-08 chr23:76889114 A>G did not map to a codon.
Sequencing variant TCGA-E1-A7YK-01A-11D-A34A-08 chr23:76889174 A>G did not map to a codon.
Sequencing variant TCGA-E1-A7Z4-01A-11D-A34J-08 chr23:76938561 G>C did not map to a codon.
Sequencing variant TCGA-FG-5963-01A-11D-1705-08 chr23:76813114 C>T did not map to a codon.
Sequencing variant TCGA-FG-5965-01B-11D-1893-08 chr23:76889171 A>T did not map to a codon.
Sequencing variant TCGA-FG-6689-01A-11D-1893-08 chr23:76912103 G>C did not map to a codon.
Sequencing variant TCGA-FG-6690-01A-11D-1893-08 chr23:76939521 A>T did not map to a codon.
Sequencing variant TCGA-FG-7638-01B-11D-2086-08 chr23:76937356 T>C did not map to a codon.
Sequencing variant TCGA-FG-8182-01A-11D-2253-08 chr23:76845301 A>G did not map to a codon.
Sequencing variant TCGA-FG-8191-01A-11D-2253-08 chr23:76909628 G>A did not map to a codon.
Sequencing variant TCGA-FG-A4MX-01A-11D-A26M-08 chr23:76855964 A>C did not map to a codon.
Sequencing variant TCGA-FG-A70Y-01A-12D-A34J-08 chr23:76909628 G>A did not map to a codon.
Sequencing variant TCGA-FG-A713-01A-11D-A32B-08 chr23:76944309 C>T did not map to a codon.
Sequencing variant TCGA-HT-7475-01A-11D-2024-08 chr23:76813075 T>C did not map to a codon.
Sequencing variant TCGA-HT-7477-01B-11D-A289-08 chr23:76940499 T>G did not map to a codon.
Sequencing variant TCGA-HT-7478-01A-11D-2024-08 chr23:76813081 A>G did not map to a codon.
Sequencing variant TCGA-HT-7482-01A-11D-2024-08 chr23:76849220 T>C did not map to a codon.
Sequencing variant TCGA-HT-7483-01A-11D-2024-08 chr23:76814318 T>C did not map to a codon.
Sequencing variant TCGA-HT-7485-01A-11D-2024-08 chr23:76940488 T>A did not map to a codon.
Sequencing variant TCGA-HT-7603-01A-21D-2086-08 chr23:76909628 G>A did not map to a codon.
Sequencing variant TCGA-HT-7610-01A-21D-2086-08 chr23:76890082 A>C did not map to a codon.
Sequencing variant TCGA-HT-7690-01A-11D-2253-08 chr23:76849220 T>C did not map to a codon.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr23:76813057 C>T did not map to a codon.
Sequencing variant TCGA-HT-7880-01A-11D-2395-08 chr23:76938787 G>T did not map to a codon.
Sequencing variant TCGA-HT-7880-01A-11D-2395-08 chr23:76937899 T>A did not map to a codon.
Sequencing variant TCGA-HT-7902-01A-12D-2395-08 chr23:76849195 A>G did not map to a codon.
Sequencing variant TCGA-HT-8013-01A-11D-2395-08 chr23:76939234 C>A did not map to a codon.
Sequencing variant TCGA-HT-8018-01A-11D-2395-08 chr23:76931744 T>C did not map to a codon.
Sequencing variant TCGA-HT-8563-01A-11D-2395-08 chr23:76890194 C>G did not map to a codon.
Sequencing variant TCGA-HT-A5R5-01A-11D-A289-08 chr23:76939553 C>G did not map to a codon.
Sequencing variant TCGA-HT-A5R5-01A-11D-A289-08 chr23:76937080 C>A did not map to a codon.
Sequencing variant TCGA-HT-A614-01A-11D-A29Q-08 chr23:76938919 G>A did not map to a codon.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr23:76939696 C>A did not map to a codon.
Sequencing variant TCGA-HT-A74J-01A-12D-A32B-08 chr23:76938028 G>A did not map to a codon.
Sequencing variant TCGA-HW-8319-01A-11D-2395-08 chr23:76940430 C>T did not map to a codon.
Sequencing variant TCGA-HW-A5KL-01A-11D-A27K-08 chr23:76939960 A>G did not map to a codon.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr23:76937037 G>C did not map to a codon.
Sequencing variant TCGA-P5-A5F1-01A-11D-A289-08 chr23:76938787 G>A did not map to a codon.
Sequencing variant TCGA-P5-A72W-01A-11D-A32B-08 chr23:76890124 C>T did not map to a codon.
Sequencing variant TCGA-P5-A736-01A-11D-A32B-08 chr23:76829759 G>C did not map to a codon.
Sequencing variant TCGA-QH-A6X8-01A-12D-A32B-08 chr23:76855028 T>C did not map to a codon.
Sequencing variant TCGA-QH-A870-01A-11D-A36O-08 chr23:76939353 G>C did not map to a codon.
Sequencing variant TCGA-S9-A6TS-01A-12D-A33T-08 chr23:76812937 G>A did not map to a codon.
Sequencing variant TCGA-S9-A6TV-01A-12D-A34J-08 chr23:76829786 C>G did not map to a codon.
Sequencing variant TCGA-S9-A6U8-01A-21D-A33T-08 chr23:76813105 T>C did not map to a codon.
Sequencing variant TCGA-S9-A6UA-01A-12D-A33T-08 chr23:76920267 C>T did not map to a codon.
Sequencing variant TCGA-S9-A6WG-01A-11D-A33T-08 chr23:76875919 G>A did not map to a codon.
Sequencing variant TCGA-S9-A6WO-01A-21D-A34A-08 chr23:76939958 C>T did not map to a codon.
Sequencing variant TCGA-S9-A7R7-01A-11D-A34J-08 chr23:76939999 G>A did not map to a codon.
Sequencing variant TCGA-S9-A7R8-01A-11D-A34J-08 chr23:76938343 T>C did not map to a codon.
Sequencing variant TCGA-TM-A7C4-01A-11D-A32B-08 chr23:76920260 G>T did not map to a codon.
Sequencing variant TCGA-TM-A7C4-01A-11D-A32B-08 chr23:76940429 C>T did not map to a codon.
Sequencing variant TCGA-TM-A84L-01A-11D-A36O-08 chr23:76938325 G>A did not map to a codon.
Sequencing variant TCGA-TQ-A7RH-01A-12D-A34A-08 chr23:76849195 A>G did not map to a codon.
Sequencing variant TCGA-TQ-A7RJ-01A-11D-A33T-08 chr23:76912143 C>G did not map to a codon.
Sequencing variant TCGA-TQ-A7RJ-01A-11D-A33T-08 chr23:76938582 G>C did not map to a codon.
Sequencing variant TCGA-TQ-A7RK-01A-11D-A33T-08 chr23:76909613 G>A did not map to a codon.
Sequencing variant TCGA-VM-A8C8-01A-11D-A36O-08 chr23:76938787 G>A did not map to a codon.
Sequencing variant TCGA-VV-A86M-01A-11D-A36O-08 chr23:76940453 T>G did not map to a codon.
Sequencing variant TCGA-WY-A85A-01A-21D-A36O-08 chr23:76855050 T>G did not map to a codon.
Sequencing variant TCGA-WY-A85B-01A-11D-A36O-08 chr23:76845303 C>T did not map to a codon.
Sequencing variant TCGA-WY-A85D-01A-11D-A36O-08 chr23:76814252 G>A did not map to a codon.
Sequencing variant TCGA-WY-A85E-01A-11D-A36O-08 chr23:76938296 A>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:16327653 G>A maps to NM_000332.3 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:16306646 G>A maps to NM_000332.3 D787D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6405-01A-11D-1705-08 chr12:111908029 A>G maps to NM_002973.3 Y1066Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CB-01A-11D-A36O-08 chr12:111895131 C>T maps to NM_002973.3 A1134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64W-01A-11D-A29Q-08 chr16:28847393 A>G maps to NM_148414.1 A1012A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:28844585 G>A maps to NM_148414.1 E622E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:28846455 C>A maps to NM_148414.1 S837S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6690-01A-11D-1893-08 chr16:28846973 T>C maps to NM_148414.1 P930P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr23:13337541 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:63973905 C>T maps to NM_001177387.1 Q423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:54961319 C>T maps to NM_198437.1 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5276-01A-01D-1468-08 chr19:57744017 C>T maps to NM_001015878.1 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:70229954 C>T maps to NM_015570.2 Q478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:32615648 C>T maps to NM_015060.1 S551S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6XA-01A-12D-A32B-08 chr7:32582853 C>T maps to NM_015060.1 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:99439404 G>A maps to NM_021732.2 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr12:63543860 C>T maps to NM_000706.3 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153171512 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153171564 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153171771 G>T did not map to a codon.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr23:153172154 C>T did not map to a codon.
Sequencing variant TCGA-S9-A6WI-01A-21D-A33T-08 chr23:153171400 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:69459753 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:63532577 G>A maps to NM_004655.3 S667S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65V-01A-11D-A29Q-08 chr17:63533497 G>A maps to NM_004655.3 Y552Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:41748812 C>T maps to NM_021913.3 F446F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CS-01A-11D-A31L-08 chr7:99565784 G>A maps to NM_001185.3 D202D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:79170553 G>A maps to ENST00000269392 Q619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:831741 C>T maps to NM_001700.3 C207C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WH-A86K-01A-11D-A36O-08 chr19:831864 G>A maps to NM_001700.3 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:235647670 G>A maps to ENST00000366599 N215N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VW-A7QS-01A-12D-A33T-08 chr1:235617569 C>T maps to ENST00000366599 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:193149590 G>A maps to NM_003783.3 R368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:41033235 C>T maps to NM_033172.1 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RR-01A-21D-A34A-08 chr21:41033274 G>A maps to NM_033172.1 Q263Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:62450245 T>C maps to NM_006577.5 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7015-01A-11D-2024-08 chr3:182987918 G>A maps to NM_032047.4 W111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7J0-01A-11D-A34A-08 chr2:232263161 C>T maps to NM_145236.2 F244F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:58022540 G>A maps to NM_001478.3 R319R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A870-01A-11D-A36O-08 chr17:47241555 C>T maps to NM_153446.2 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:668482 C>T maps to NM_173593.3 F928F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8012-01A-11D-2395-08 chr12:665814 C>T maps to NM_173593.3 R721R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8110-01A-11D-2395-08 chr9:33135342 G>A maps to NM_001497.3 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F6-A8O3-01A-11D-A36O-08 chr1:161143659 C>T maps to NM_003779.3 K223K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:118935106 G>A maps to NM_212543.1 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RP-01A-21D-A34A-08 chr3:118935160 C>T maps to NM_212543.1 R276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TB-01A-11D-A33T-08 chr21:42613771 C>T maps to NM_012105.3 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:90660618 C>T maps to NM_001170794.1 V402V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8188-01A-11D-2253-08 chr6:90661004 G>A maps to NM_001170794.1 Q274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7607-01A-11D-2086-08 chr10:121432113 G>A maps to NM_004281.3 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:38065262 T>A maps to NM_004874.2 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74O-01A-11D-A32B-08 chr21:11098731 C>T maps to NM_181704.1 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A6S3-01A-12D-A32B-08 chr21:11049594 A>G maps to NM_182482.2 C102C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:32203080 G>A maps to NM_001703.2 I976I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6188-01A-11D-1893-08 chr6:70048900 C>T maps to NM_001704.2 N1094N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:70071115 T>C maps to NM_001704.2 N1317N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74H-01A-11D-A32B-08 chr17:79059506 G>A maps to NM_017451.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:97944810 G>A maps to NM_018842.4 H200H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr16:1395341 G>A maps to NM_003933.4 W713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YE-01A-11D-A34A-08 chr6:33543652 G>A maps to ENST00000360661 Y43Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr20:17716422 C>T maps to NM_001159495.1 H87H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:91182143 G>A maps to NM_020063.1 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:129321275 G>A maps to NM_003658.4 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr5:17275507 C>T maps to NM_006317.3 D61D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7677-01A-11D-2253-08 chr6:31506617 C>T maps to ENST00000417556 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:31600227 C>T maps to NM_080686.2 L1260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:31605082 C>T maps to NM_080686.2 R2105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:31599926 A>G maps to NM_080686.2 R1159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7Z6-01A-11D-A34J-08 chr6:31599147 C>T maps to NM_080686.2 R900*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7J0-01A-11D-A34A-08 chr6:31604006 C>T maps to NM_080686.2 P1882P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:134371212 C>T maps to NM_013318.3 T2214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:134354637 G>T did not map to a codon.
Sequencing variant TCGA-E1-A7YS-01A-11D-A34A-08 chr9:134334664 C>T maps to NM_013318.3 S442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:171510588 C>T maps to ENST00000392078 D1328D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:171482311 G>A did not map to a codon.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr6:31612930 C>G maps to ENST00000404765 R387R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5141-01A-01D-1468-08 chr6:31630381 A>C maps to NM_033177.3 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7495-01A-11D-2024-08 chr19:49459500 C>T maps to NM_138761.3 R94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:56995054 C>T maps to NM_013449.3 Q1403Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:160239234 G>T maps to NM_013450.2 P1280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A781-01A-11D-A32B-08 chr11:27077072 A>G maps to NM_003986.2 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7477-01B-11D-A289-08 chr4:123664897 A>G maps to NM_152618.2 T617T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:33380507 G>A did not map to a codon.
Sequencing variant TCGA-FG-A711-01A-21D-A33T-08 chr19:45322334 G>A maps to NM_005581.3 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:94049656 G>A maps to NM_003567.2 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:59115388 G>A maps to ENST00000407086 S664S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:59469377 C>T maps to ENST00000407086 S930S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:59112047 A>G maps to ENST00000407086 Q583Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5964-01A-11D-1705-08 chr17:58967053 A>G did not map to a codon.
Sequencing variant TCGA-QH-A6X8-01A-12D-A32B-08 chr17:59024688 T>C maps to ENST00000407086 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:25002835 G>T maps to NM_001178093.1 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr2:60679727 C>T maps to NM_018014.3 S768S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85D-01A-11D-A36O-08 chr2:60687796 G>T maps to NM_022893.3 V750V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:99642371 C>T maps to NM_138576.2 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R9-01A-11D-A289-08 chr14:99641423 C>T maps to NM_138576.2 A583A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:52402055 G>A maps to NM_020396.2 R202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr22:18185019 T>G maps to NM_015367.2 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:187447457 C>T maps to NM_001706.4 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A75K-01A-11D-A32B-08 chr1:147092732 A>G maps to NM_004326.2 P924P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WL-01A-21D-A33T-08 chr1:147092747 G>A maps to NM_004326.2 P929P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:118773030 G>T maps to NM_182557.2 S474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YN-01A-11D-A34A-08 chr6:136594290 G>A maps to NM_014739.2 N629N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4942-01A-01D-1468-08 chr23:39923698 C>T did not map to a codon.
Sequencing variant TCGA-CS-5397-01A-01D-1893-08 chr23:39932303 G>A did not map to a codon.
Sequencing variant TCGA-DH-A66G-01A-21D-A31L-08 chr23:39933902 C>A did not map to a codon.
Sequencing variant TCGA-DH-A7UV-01A-12D-A34A-08 chr23:39913576 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:39933020 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:39932794 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:39922013 C>A did not map to a codon.
Sequencing variant TCGA-DU-6403-01A-11D-1705-08 chr23:39933842 G>T did not map to a codon.
Sequencing variant TCGA-DU-6403-01A-11D-1705-08 chr23:39933841 C>T did not map to a codon.
Sequencing variant TCGA-HT-7472-01A-11D-2024-08 chr23:39934220 C>G did not map to a codon.
Sequencing variant TCGA-HT-7610-01A-21D-2086-08 chr23:39931689 G>A did not map to a codon.
Sequencing variant TCGA-HT-7611-01A-11D-2395-08 chr23:39932879 G>T did not map to a codon.
Sequencing variant TCGA-QH-A6XA-01A-12D-A32B-08 chr23:39933590 C>T did not map to a codon.
Sequencing variant TCGA-TQ-A7RQ-01A-11D-A33T-08 chr23:39922918 C>A did not map to a codon.
Sequencing variant TCGA-VV-A829-01A-21D-A36O-08 chr23:39911567 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:129139262 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:129184751 A>G did not map to a codon.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr23:129147462 G>A did not map to a codon.
Sequencing variant TCGA-P5-A780-01A-12D-A32B-08 chr23:129190021 T>C did not map to a codon.
Sequencing variant TCGA-QH-A6X9-01A-12D-A32B-08 chr23:129189970 C>T did not map to a codon.
Sequencing variant TCGA-S9-A6TW-01A-12D-A32B-08 chr23:129149823 G>T did not map to a codon.
Sequencing variant TCGA-TQ-A7RS-01A-12D-A33T-08 chr23:129149178 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:23603636 C>T maps to NM_004327.3 Y554Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8158-01A-11D-2253-08 chr22:23631728 C>G maps to NM_004327.3 S876S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U2-01A-21D-A33T-08 chr22:23656795 T>C maps to NM_004327.3 F1207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:96730333 C>T maps to NM_000710.2 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5277-01A-01D-1468-08 chr14:96706766 A>G maps to NM_000623.3 Q34Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A6S3-01A-12D-A32B-08 chr14:96707057 C>T maps to NM_000623.3 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:27679426 G>A maps to NM_001143810.1 R311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:40970837 G>A maps to NM_003766.3 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8012-01A-11D-2395-08 chr14:101005289 C>T maps to NM_020836.3 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5390-01A-02D-1468-08 chr23:18221652 G>T did not map to a codon.
Sequencing variant TCGA-DB-5281-01A-01D-1468-08 chr23:18234678 C>T did not map to a codon.
Sequencing variant TCGA-DB-A64V-01A-11D-A29Q-08 chr23:18183207 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:18195786 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:18234727 C>T did not map to a codon.
Sequencing variant TCGA-FG-5965-01B-11D-1893-08 chr23:18189325 T>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:107390798 C>T maps to NM_001080450.2 V532V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:107390912 C>T maps to NM_001080450.2 P494P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7634-01A-11D-2086-08 chr6:107391125 G>A maps to NM_001080450.2 F423F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:42119621 G>A maps to NM_207406.3 N506N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:56846619 C>T maps to NM_152731.2 I4I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8106-01A-11D-2395-08 chr11:61724344 T>C maps to NM_001139443.1 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A4DS-01A-11D-A26M-08 chr19:12866568 C>T maps to NM_017682.2 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr12:70048983 G>A maps to NM_032735.2 S570S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:102318099 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:102317980 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:102564672 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:102471114 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:14743743 G>A maps to NM_016561.2 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:133118939 C>T maps to NM_003571.2 R5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr23:152770258 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:152770098 C>A did not map to a codon.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr23:152773770 C>T did not map to a codon.
Sequencing variant TCGA-P5-A77W-01A-11D-A32B-08 chr23:152773796 G>A did not map to a codon.
Sequencing variant TCGA-TQ-A7RU-01A-21D-A34A-08 chr23:152770283 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:102005006 A>G did not map to a codon.
Sequencing variant TCGA-TM-A84H-01A-11D-A36O-08 chr23:102004757 C>T did not map to a codon.
Sequencing variant TCGA-DB-A64V-01A-11D-A29Q-08 chr9:95481528 C>T maps to NM_001003800.1 Q466Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:127825746 G>A maps to NM_139343.1 R202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A70Z-01A-12D-A33T-08 chr12:51717862 G>A maps to NM_016293.2 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:22479051 G>T maps to NM_018688.4 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RJ-01A-11D-A33T-08 chr11:102206865 G>A maps to NM_182962.1 T498T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:32688446 C>T maps to NM_016252.3 Q1647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8186-01A-11D-2253-08 chr19:53793156 C>T maps to NM_033341.3 Q157Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr8:11414293 C>T maps to ENST00000427279 Y300Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:28601164 G>T maps to NM_000386.2 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:97964315 G>A maps to NM_013314.3 Q292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:56113372 C>T maps to NM_001487.3 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A87N-01A-11D-A36O-08 chr19:40953795 C>T maps to NM_000713.2 *207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr1:169347581 A>G maps to NM_003666.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MY-01A-11D-A26M-08 chr10:22618233 A>G maps to NM_005180.6 E248E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:22052379 C>T maps to NM_006129.4 F529F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr8:22037986 C>T maps to NM_006129.4 P356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:69093134 C>T maps to NM_014482.1 Q301Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YM-01A-11D-A34A-08 chr2:69093100 G>A maps to NM_014482.1 R313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:50659371 A>G did not map to a codon.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr4:79792135 A>G maps to NM_198892.1 Q477Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr4:79793823 G>A maps to NM_198892.1 P555P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YN-01A-11D-A34A-08 chr4:81967315 C>T maps to NM_001201.2 A247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RC-01A-11D-A289-08 chr4:81967783 C>T maps to NM_001201.2 C403C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7855-01A-11D-2395-08 chr6:7727730 G>A maps to NM_001718.4 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:34125701 C>T maps to NM_133468.3 Y581Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6396-01A-11D-1705-08 chr10:88679127 C>T maps to NM_004329.2 P356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:203329607 C>A maps to NM_001204.6 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84B-01A-11D-A36O-08 chr10:43292065 C>T maps to NM_014753.3 N458N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:15527468 A>T did not map to a codon.
Sequencing variant TCGA-S9-A7J3-01A-21D-A34J-08 chr23:15561244 T>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:83931980 C>T maps to NM_001717.3 L674L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:16727881 G>A maps to NM_017637.5 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IX-01A-12D-A34A-08 chr9:16727915 A>C maps to NM_017637.5 L70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5962-01B-11D-1893-08 chr5:172578698 T>C did not map to a codon.
Sequencing variant TCGA-HT-7692-01A-12D-2253-08 chr5:172587004 G>A maps to NM_013979.2 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:13603267 T>C maps to NM_148894.2 E1752E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:13605907 C>T maps to NM_148894.2 S872S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:13604563 C>T maps to NM_148894.2 A1320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:13615172 C>T maps to NM_148894.2 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:13601605 A>G maps to NM_148894.2 I2306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EX-01A-12D-A289-08 chr4:13603084 G>A maps to NM_148894.2 S1813S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EZ-01A-11D-A27K-08 chr4:13602745 T>G maps to NM_148894.2 A1926A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YJ-01A-11D-A34A-08 chr6:3140629 C>T maps to NM_004332.2 C225C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6689-01A-11D-1893-08 chr20:36953196 C>T maps to NM_001725.2 R323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7469-01A-11D-2253-08 chr20:36952336 C>T maps to NM_001725.2 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TD-01A-12D-A34A-08 chr20:31606095 C>T maps to NM_025227.1 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UU-01A-12D-A34A-08 chr22:32813108 C>T maps to NM_174932.2 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5143-01A-01D-1468-08 chr1:220240685 T>C maps to NM_006085.4 K144K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:65978370 T>A maps to ENST00000321892 S3036S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65R-01A-21D-A31L-08 chr17:65941666 C>T maps to ENST00000321892 P2407P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RJ-01A-11D-A33T-08 chr17:65899907 A>G maps to ENST00000321892 L975L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:41201146 G>T maps to ENST00000471181 T1821T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:41244757 A>G maps to ENST00000471181 P930P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:136901412 G>T maps to NM_007371.3 A559A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:92446487 T>C maps to ENST00000347608 S513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R7-01A-11D-A34J-08 chr2:28521235 G>A maps to NM_004899.3 Q322Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7882-01A-11D-2395-08 chr14:105688183 G>A maps to NM_001519.2 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:36295757 C>A maps to NM_032352.3 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:9785585 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:9776066 C>A maps to NM_001003694.1 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr3:9781282 C>T maps to NM_001003694.1 C400C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:36178154 C>T maps to NM_015695.2 R677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr23:135574305 C>T did not map to a codon.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr23:135572457 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:55814690 A>G maps to NM_032430.1 E347E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:1464846 C>T maps to NM_003957.2 D254D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:40568685 G>T maps to NM_018963.3 T2103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:79973206 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:79932252 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:79932199 C>A did not map to a codon.
Sequencing variant TCGA-HT-7691-01A-11D-2253-08 chr23:79932311 G>A did not map to a codon.
Sequencing variant TCGA-P5-A5EX-01A-12D-A289-08 chr23:79942475 A>G did not map to a codon.
Sequencing variant TCGA-TQ-A7RM-01A-11D-A33T-08 chr23:79932814 G>A did not map to a codon.
Sequencing variant TCGA-DU-7007-01A-11D-2024-08 chr1:32842100 G>T maps to NM_001143888.1 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr3:49699984 C>T maps to NM_003458.3 S3569S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5140-01A-01D-1468-08 chr16:3640689 G>A maps to NM_032444.2 Y983Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:3639669 T>C maps to NM_032444.2 S1323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:3645674 G>A maps to NM_032444.2 G648G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RB-01A-11D-A289-08 chr16:3640626 G>A maps to NM_032444.2 P1004P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A859-01A-12D-A36O-08 chr16:3632639 G>A maps to NM_032444.2 G1736G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-HT-8564-01A-11D-2395-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-HT-8564-01A-11D-2395-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-S9-A6U9-01A-11D-A32B-08 chr14:93730193 C>T maps to NM_001002860.2 S436S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:92612768 A>G maps to NM_183242.3 E321E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8158-01A-11D-2253-08 chr1:92606708 G>T maps to NM_183242.3 G291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr3:15686763 C>A maps to NM_000060.2 G467G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:111369363 C>T maps to NM_017589.2 W46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr23:100613412 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:100615565 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:100604906 C>A did not map to a codon.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr23:100630145 C>T did not map to a codon.
Sequencing variant TCGA-P5-A5F4-01A-11D-A289-08 chr23:100615677 C>T did not map to a codon.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr23:100617591 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:26463634 C>T maps to NM_007049.3 D198D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YM-01A-11D-A34A-08 chr6:26393182 C>T maps to NM_001197237.1 H520H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:26408055 C>T maps to NM_007048.5 D197D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr6:32362766 G>A maps to ENST00000468270 Q372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85E-01A-11D-A36O-08 chr5:180432370 G>A maps to NM_197975.2 K300K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:180377168 G>A maps to NM_001040462.2 G376G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A72U-01A-31D-A32B-08 chr5:180376260 C>T maps to NM_001040462.2 H286H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr10:103281442 G>A maps to NM_033637.2 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:111408164 C>A maps to NM_004336.3 E721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr2:111398885 G>A maps to NM_004336.3 N927N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr15:40509801 C>T maps to ENST00000412359 S942S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr17:56402927 C>T maps to NM_004758.2 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:115894780 C>A maps to NM_018017.2 E516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:98741969 C>T maps to NM_015652.2 R275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:124457659 G>A maps to NM_001010912.1 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:21804299 C>A maps to NM_207371.3 G818*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:5803399 G>A maps to NM_017782.4 Q2380Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:5788960 C>T maps to NM_017782.4 L1193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr10:5782301 G>A maps to NM_017782.4 P723P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:102748107 C>A maps to NM_021830.4 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:104573025 C>T maps to NM_001083913.1 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5395-01A-01D-1468-08 chr10:120489878 C>T maps to NM_153810.4 W137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:120450774 G>A did not map to a codon.
Sequencing variant TCGA-S9-A6WD-01A-12D-A33T-08 chr10:120450871 T>C maps to NM_153810.4 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:11908609 C>T maps to NM_153256.3 D73D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YO-01A-11D-A34A-08 chr10:73521532 G>A maps to NM_022153.1 H111H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:33135325 A>G maps to ENST00000375025 K517K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:33137575 C>A maps to ENST00000375025 I583I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:50315726 C>T maps to NM_001031746.3 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:103753314 G>A maps to NM_024541.2 R419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VW-A8FI-01A-11D-A36O-08 chr10:103753314 G>A maps to NM_024541.2 R419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:105974144 C>T maps to ENST00000389588 Q152Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr10:105990459 G>A maps to ENST00000389588 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WL-01A-21D-A33T-08 chr10:105942138 G>A maps to ENST00000389588 S759S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:124697270 G>A maps to NM_024942.3 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:128147786 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:134743223 C>T maps to ENST00000368586 K317K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8563-01A-11D-2395-08 chr10:134752145 G>A maps to ENST00000368586 N161N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:8951034 C>T maps to NM_020643.2 W71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:8948648 G>A maps to NM_020643.2 Q133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A72Z-01A-11D-A32B-08 chr11:8943015 C>T maps to NM_020643.2 Q417Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:68029757 C>T maps to NM_022338.3 K235K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:558621 C>T maps to NM_173573.2 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:128774419 C>T maps to NM_145013.1 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:30354442 C>T maps to NM_152316.1 Q153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:47074067 C>T maps to NM_001003677.1 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5319-01A-01D-1893-08 chr11:122774731 G>A maps to NM_024806.2 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CX-01A-11D-A32B-08 chr11:122817280 G>A maps to NM_024806.2 Q570Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:61252176 C>T maps to NM_145017.2 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TS-01A-12D-A33T-08 chr11:66555676 T>G maps to ENST00000360962 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7603-01A-21D-2086-08 chr11:82644344 A>G maps to NM_145018.3 G655G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KJ-01A-12D-A27K-08 chr11:82643882 A>T maps to NM_145018.3 G501G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:61549093 C>A maps to NM_001127392.1 S938S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:27070658 C>T maps to NM_018164.2 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:91347826 G>A maps to NM_152638.2 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:110922991 G>A maps to NM_013300.2 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:4600385 G>T maps to NM_020374.2 P485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64W-01A-11D-A29Q-08 chr12:40041652 C>A maps to NM_001031748.2 C148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:40078671 A>G maps to NM_001031748.2 G430G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:40020149 C>T maps to NM_001031748.2 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:88379744 G>A maps to NM_152589.1 H336H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr12:112617094 G>C maps to NM_001109662.2 V3526V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:112667651 T>C maps to NM_001109662.2 Q1951Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:112673463 G>A maps to NM_001109662.2 L1685L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:112621022 G>A maps to NM_001109662.2 N3437N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr12:112647837 G>A maps to NM_001109662.2 A2444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85C-01A-11D-A36O-08 chr12:112605176 G>A maps to NM_001109662.2 Q3988*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:64746764 A>C maps to NM_001170633.1 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr12:64746732 G>C maps to NM_001170633.1 S119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr12:97082741 G>A maps to ENST00000342887 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WG-01A-11D-A33T-08 chr12:97051790 C>T maps to ENST00000342887 H169H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:80647270 C>T maps to NM_173591.3 C428C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8113-01A-11D-2395-08 chr12:80749687 C>T maps to NM_173591.3 G1913G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85C-01A-11D-A36O-08 chr12:80732943 T>C maps to NM_173591.3 T1641T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7US-01A-11D-A33T-08 chr12:31814955 C>T maps to NM_001135864.1 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6IZ-01A-11D-A31L-08 chr12:93100523 G>A maps to NM_001037671.3 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:46946550 G>A maps to NM_025113.2 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WM-01A-12D-A33T-08 chr13:73320714 C>T maps to ENST00000377815 I376I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WM-01A-12D-A33T-08 chr13:73319292 C>G maps to ENST00000377815 S289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:57082682 G>A maps to NM_017799.3 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:90770308 C>T maps to NM_017970.2 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:90755213 C>T maps to NM_017970.2 S835S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84S-01A-11D-A36O-08 chr14:90784398 T>C maps to NM_017970.2 Q41Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:45700409 G>A maps to NM_018353.4 R510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YS-01A-11D-A34A-08 chr14:45702021 T>C maps to NM_018353.4 G450G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:74824283 G>A maps to NM_018228.2 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:74823873 C>T maps to NM_018228.2 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YJ-01A-11D-A34A-08 chr14:76621050 C>T maps to NM_017926.2 D115D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7681-01A-11D-2395-08 chr14:76668099 G>A maps to NM_017926.2 W452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr14:81380709 G>A maps to NM_152446.3 R64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:91655378 G>T maps to NM_001102368.1 E354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:77318753 C>T maps to NM_194287.2 F258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:99182650 C>T maps to NM_182560.2 C41C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5395-01A-01D-1468-08 chr14:50472372 G>A maps to NM_001012706.1 R49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:45370112 C>T maps to NM_001017923.1 R159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:58605245 G>T maps to ENST00000438670 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84B-01A-11D-A36O-08 chr14:60908816 A>G maps to NM_174978.2 N512N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:74205451 G>A maps to NM_001043318.1 G420G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6XA-01A-12D-A32B-08 chr14:74196469 C>T maps to NM_001043318.1 P656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:74516427 G>A maps to NM_025057.2 K272K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WN-01A-12D-A33T-08 chr14:74516766 A>G maps to NM_025057.2 A385A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6186-01A-12D-2024-08 chr14:95932396 C>T maps to NM_152592.3 Q166Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:95912287 G>A maps to NM_152592.3 D530D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:95906100 C>T maps to NM_152592.3 P698P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:65056007 G>A maps to NM_172365.1 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr15:24924469 T>A maps to NM_018958.2 C1152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7857-01A-11D-2395-08 chr15:24921604 C>T maps to NM_018958.2 D197D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7882-01A-11D-2395-08 chr15:24921091 T>A maps to NM_018958.2 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:81429026 C>A maps to ENST00000458088 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:75498565 G>A maps to NM_015492.4 E59E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QZ-01A-12D-A34J-08 chr15:75498580 G>A maps to NM_015492.4 A64A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-S9-A7J0-01A-11D-A34A-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:37100620 G>A maps to NM_001130010.1 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CW-01A-11D-A32B-08 chr15:90167941 C>T maps to NM_152259.3 L1467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:65871754 T>C maps to ENST00000420799 E552E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84T-01A-11D-A36O-08 chr15:65885871 C>A maps to ENST00000420799 E330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YL-01A-11D-A34A-08 chr15:34647756 C>T maps to ENST00000438749 G506G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R7-01A-11D-A289-08 chr15:34646896 C>A maps to ENST00000438749 I432I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:40855058 G>A maps to NM_001080791.1 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:73848683 G>A maps to NM_001042367.1 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:15680613 G>A maps to NM_033201.2 K181K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7902-01A-12D-2395-08 chr16:81095241 C>A maps to NM_152337.2 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RJ-01A-11D-A33T-08 chr16:29827953 C>T maps to NM_024516.3 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:8729110 C>T maps to NM_024109.2 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7857-01A-11D-2395-08 chr16:89785501 G>A maps to NM_004913.2 Y36Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:4794892 C>T maps to NM_139170.2 H308H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr16:1889338 G>A maps to NM_001163560.2 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85C-01A-11D-A36O-08 chr16:49433164 C>T maps to NM_144602.2 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YL-01A-11D-A34A-08 chr16:58149205 G>A maps to NM_013242.2 Y144Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr16:67701891 A>G maps to NM_001012984.2 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:19725640 A>G maps to NM_001012991.2 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr16:19726119 C>A maps to NM_001012991.2 E80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TB-01A-11D-A33T-08 chr16:19718261 G>A maps to NM_001012991.2 N449N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7009-01A-11D-2024-08 chr17:72959891 C>T maps to NM_030630.2 E110E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:29226233 G>A maps to NM_024683.3 Q346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:10614223 C>T maps to NM_020233.4 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:45425208 C>T maps to NM_152347.4 R185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A89V-01A-11D-A36O-08 chr17:8136302 T>C maps to NM_025099.5 Q622Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:57289831 T>C maps to NM_018149.6 N630N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A736-01A-11D-A32B-08 chr17:57290559 A>C maps to NM_018149.6 T792T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:7329069 C>T maps to NM_175734.4 H21H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:30666926 G>A maps to NM_022344.2 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7477-01B-11D-A289-08 chr17:71243389 C>T maps to NM_017941.4 C580C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:7162167 C>A maps to NM_203414.1 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:5114137 G>A maps to NM_207103.2 D132D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr18:13645352 G>A maps to NM_181481.3 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:33557431 T>C maps to NM_031446.3 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:77797334 C>T maps to NM_024805.2 Y69Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7478-01A-11D-2024-08 chr18:77794644 G>C maps to NM_024805.2 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:47010025 G>A maps to NM_001035005.3 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:20950205 C>T maps to NM_032933.4 Q168Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:1231116 C>T maps to ENST00000382477 P399P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:3547268 C>T did not map to a codon.
Multiple mappings detected for codon TCGA-FG-A713-01A-11D-A32B-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr19:12841861 G>A maps to NM_024038.2 D148D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:16612322 C>T maps to NM_032207.2 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:36499481 G>A maps to ENST00000455847 C212C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7857-01A-11D-2395-08 chr19:50981246 C>G maps to ENST00000376920 S59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8114-01A-11D-2395-08 chr2:68270035 T>G maps to ENST00000407324 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:22987482 C>T maps to NM_000491.3 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84R-01A-21D-A36O-08 chr13:24892992 G>A maps to NM_178540.3 G68G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-KT-A7W1-01A-11D-A34A-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:7241912 T>C maps to ENST00000290575 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:244756881 T>C did not map to a codon.
Sequencing variant TCGA-TQ-A7RO-01A-11D-A33T-08 chr1:244756808 G>A maps to NM_001130957.1 R744R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7475-01A-11D-2024-08 chr1:111494469 G>A maps to NM_018372.3 R346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5874-01A-11D-1705-08 chr1:200880751 C>T maps to NM_018265.2 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:200877870 G>A maps to NM_018265.2 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:200869239 G>A maps to NM_018265.2 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7607-01A-11D-2086-08 chr1:200880682 C>T maps to NM_018265.2 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:169773304 G>A maps to NM_018186.2 Q134Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:169366575 G>A maps to ENST00000367806 H423H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7881-01A-11D-2395-08 chr1:169394120 G>A maps to ENST00000367806 Y15Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr1:220870063 C>T maps to NM_024709.4 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85E-01A-11D-A36O-08 chr1:179478531 T>A maps to NM_144696.4 L830L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:11018797 G>T maps to NM_001170754.1 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:170964534 C>T maps to NM_001163629.1 C400C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:247737602 A>G maps to NM_145278.3 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:116666973 C>T maps to NM_152367.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:112020050 G>A did not map to a codon.
Alternatively spliced codon TCGA-DU-6392-01A-11D-1705-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HW-7486-01A-11D-2024-08 chr1:57185711 A>G maps to NM_001004303.4 I716I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7Z3-01A-11D-A34J-08 chr1:27278346 C>T maps to NM_152365.2 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:75039104 C>T maps to NM_001002912.4 V763V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RC-01A-11D-A289-08 chr1:75038486 A>C maps to NM_001002912.4 G969G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7C3-01A-11D-A32B-08 chr1:75038690 C>T maps to NM_001002912.4 K901K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:55119693 C>T maps to ENST00000454855 I365I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84O-01A-11D-A36O-08 chr1:55118673 G>A maps to ENST00000454855 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8322-01A-11D-2395-08 chr1:206243207 G>A maps to NM_001007544.1 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:11775174 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:234510122 T>C maps to ENST00000424237 C121C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:228288867 C>T maps to NM_024319.2 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6X9-01A-12D-A32B-08 chr1:28206167 C>T maps to NM_001105556.1 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:25573045 G>A maps to NM_020317.3 Q137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:25569196 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:25573442 G>A maps to NM_020317.3 Y4Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A669-01A-12D-A31L-08 chr1:223568628 C>T maps to NM_152610.2 S604S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A843-01A-11D-A36O-08 chr1:223567707 C>T maps to NM_152610.2 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:156706422 G>T did not map to a codon.
Sequencing variant TCGA-F6-A8O4-01A-11D-A36O-08 chr1:156262834 T>C maps to NM_144580.1 *407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F6-A8O4-01A-11D-A36O-08 chr1:111891190 A>G maps to NM_181643.4 K104K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7856-01A-11D-2395-08 chr1:16559498 G>A maps to NM_030907.3 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:172558791 C>T maps to ENST00000367723 Q1003*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A8XE-01A-11D-A36O-08 chr1:172579032 C>T maps to ENST00000367723 G1285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:229462699 C>A maps to NM_145257.3 E141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:31912541 C>A maps to ENST00000437789 T494T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7475-01A-11D-2024-08 chr6:31911097 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:9510425 C>T maps to NM_012261.3 Q268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:61574939 C>T maps to NM_017896.2 R137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:42826273 C>T maps to NM_016470.6 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A669-01A-12D-A31L-08 chr20:31035488 C>T maps to NM_080616.3 V407V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:31873890 G>A maps to NM_033197.2 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr20:35445841 G>A maps to NM_080627.2 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EX-01A-12D-A289-08 chr20:35445830 G>T maps to NM_080627.2 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:35507460 A>G maps to NM_080628.1 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:35748187 G>T maps to ENST00000343811 R787R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7483-01A-11D-2024-08 chr20:62493606 C>T maps to NM_080622.3 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CA-01A-11D-A36O-08 chr20:60987731 G>A maps to NM_080833.2 H608H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr20:31656778 C>T maps to NM_182658.1 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-8125-01A-11D-2253-08 chr20:31659935 C>T maps to NM_182658.1 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:31695610 C>T maps to NM_182519.2 D602D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr20:31671677 G>A maps to NM_182519.2 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7006-01A-11D-2024-08 chr20:3236734 G>A maps to NM_001009984.1 Q1060*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:62187486 G>A maps to NM_024059.2 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6689-01A-11D-1893-08 chr20:61428540 C>G maps to NM_018270.4 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:20180468 C>T maps to ENST00000389655 R622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WL-01A-21D-A33T-08 chr20:20056148 T>C maps to ENST00000389655 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:3734740 G>A maps to NM_001039140.1 Y188Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:34828308 C>T maps to NM_015511.3 R173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XD-01A-11D-A27K-08 chr20:744512 G>A maps to NM_033409.3 C234C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7680-01A-11D-2253-08 chr20:745935 G>A maps to NM_033409.3 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:17970727 T>C maps to NM_052865.2 I337I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7006-01A-11D-2024-08 chr20:18794626 G>A maps to NM_178483.2 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:270253 G>A maps to NM_153269.1 Q45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:45941951 C>T maps to ENST00000443468 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TR-01A-11D-A289-08 chr21:45953632 T>C maps to ENST00000443468 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RP-01A-21D-A34A-08 chr21:45949681 A>T maps to ENST00000443468 Y265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RP-01A-21D-A34A-08 chr21:45949705 A>G maps to ENST00000443468 D257D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:30532335 C>T maps to NM_020152.2 Y169Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:30521513 T>C maps to NM_020152.2 D125D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:37398093 C>T maps to NM_001163857.1 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:19431880 G>A maps to NM_173793.4 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:43309426 G>A maps to NM_015500.1 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:73809209 G>A maps to ENST00000334126 G941G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WP-01A-12D-A34A-08 chr11:73806411 C>T maps to ENST00000334126 E1007E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A75L-01A-11D-A32B-08 chr2:27799756 G>A maps to NM_032266.3 E106E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7606-01A-11D-2086-08 chr2:27804532 T>C maps to NM_032266.3 S1698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7684-01A-11D-2253-08 chr2:27799837 A>T maps to NM_032266.3 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:27001096 C>T maps to NM_017877.3 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7616-01A-11D-2253-08 chr2:27438347 G>A maps to NM_080592.3 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IZ-01A-11D-A34A-08 chr2:44931419 A>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:26672922 C>T maps to NM_145038.2 C523C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8165-01A-11D-2253-08 chr2:106690447 C>G maps to NM_032411.2 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A61B-01A-11D-A29Q-08 chr2:27360156 G>A maps to NM_178553.3 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:241835228 G>T maps to NM_001085437.1 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5142-01A-01D-1468-08 chr2:219232560 C>T maps to NM_198559.1 F346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:55408812 A>G maps to NM_152385.2 S358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:74787406 G>A maps to NM_138804.3 D431D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74K-01A-11D-A32B-08 chr2:211019255 A>G maps to NM_152519.2 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:73456647 G>T maps to NM_032319.1 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:73455930 G>A maps to NM_032319.1 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6J3-01A-11D-A31L-08 chr2:26798817 C>T maps to NM_001105519.1 Y41Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr2:29295045 G>A maps to NM_001029883.1 D694D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7J0-01A-11D-A34A-08 chr2:29295876 A>G maps to NM_001029883.1 A417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8189-01B-11D-A289-08 chr2:170518797 G>T maps to NM_001085447.1 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:74042504 T>A maps to NM_001080474.1 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U0-01A-12D-A32B-08 chr2:74042528 C>T maps to NM_001080474.1 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:242815104 G>A maps to NM_173821.2 T466T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4938-01B-11D-1893-08 chr19:6686852 G>A maps to NM_000064.2 Q1184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:6714040 G>T maps to NM_000064.2 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:6686755 C>T did not map to a codon.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr19:6678248 G>T maps to NM_000064.2 I1588I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5302-01A-01D-1468-08 chr19:6697495 G>A maps to NM_000064.2 T885T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7489-01A-11D-2024-08 chr19:6709692 A>G did not map to a codon.
Sequencing variant TCGA-S9-A6TX-01A-21D-A32B-08 chr19:6697471 C>T maps to NM_000064.2 S893S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R8-01A-11D-A34J-08 chr19:6677967 G>A maps to NM_000064.2 D1639D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:119449126 G>A maps to NM_033364.3 Q307Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7605-01A-11D-2086-08 chr3:119465993 C>T maps to NM_033364.3 S645S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YE-01A-11D-A34A-08 chr3:194790668 G>A maps to NM_152531.4 A319A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5962-01B-11D-1893-08 chr3:118870124 C>T maps to NM_152539.2 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A730-01A-11D-A32B-08 chr3:118865902 G>A maps to NM_152539.2 Q289Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TY-01A-12D-A32B-08 chr3:118865134 C>T maps to NM_152539.2 D33D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:8672544 C>T maps to NM_015931.1 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:37458931 C>T maps to NM_178339.2 Q59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7290-01A-11D-2024-08 chr3:161063917 G>T maps to NM_001040100.1 S65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:56675538 G>A maps to ENST00000447900 T819T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr3:56667650 C>T maps to ENST00000447900 E1056E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:69053623 C>T maps to ENST00000383701 E175E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6290-01A-11D-1705-08 chr3:184870437 G>A maps to NM_001025266.1 C58C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:57832851 C>T maps to NM_032313.2 V566V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:100445676 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:113540639 C>T maps to NM_018392.4 E186E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U8-01A-21D-A33T-08 chr4:113540264 T>C maps to NM_018392.4 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:121958552 C>T maps to NM_024574.3 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7475-01A-11D-2024-08 chr4:71201799 T>C maps to NM_033122.3 N348N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WD-01A-12D-A33T-08 chr4:71201163 C>G maps to NM_033122.3 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:99055574 C>A maps to NM_174952.2 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6XC-01A-12D-A32B-08 chr4:71024190 G>A maps to NM_214711.3 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:184614138 C>T maps to NM_021942.4 G692G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:184601407 C>A maps to NM_021942.4 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:123722523 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:123794415 G>A maps to NM_001735.2 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8110-01A-11D-2395-08 chr9:123812512 C>T maps to NM_001735.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:133295379 C>T maps to NM_020199.2 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7641-01B-11D-2253-08 chr5:134782789 G>A maps to NM_130848.2 Y3Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr5:175763803 A>C maps to ENST00000443967 T732T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5141-01A-01D-1468-08 chr5:43506029 C>T maps to NM_198566.2 W251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7855-01A-11D-2395-08 chr5:43488035 T>C maps to NM_198566.2 E565E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:154200009 G>A maps to NM_032385.3 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:172535772 C>T maps to NM_153607.2 R457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:37196094 G>A maps to NM_023073.3 R1226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:37121768 T>C maps to NM_023073.3 K2991K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:125967479 C>A maps to NM_207408.1 C18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr5:41149346 A>G maps to NM_001115131.1 C873C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:41176733 G>T maps to NM_001115131.1 V337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr5:41149448 G>A maps to NM_001115131.1 D839D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr5:41159280 G>A maps to NM_001115131.1 R587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:34214828 C>T maps to NM_178508.3 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7882-01A-11D-2395-08 chr6:32261387 C>T maps to ENST00000447241 T354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5396-01A-02D-1468-08 chr6:43193849 C>T maps to ENST00000509253 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:33669179 G>T maps to NM_032340.2 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KT-A7W1-01A-11D-A34A-08 chr6:33665459 G>T maps to NM_032340.2 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:35754806 C>T maps to NM_001010886.3 D44D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64U-01A-11D-A29Q-08 chr6:30618836 G>T maps to NM_001161376.1 E362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7290-01A-11D-2024-08 chr6:47846863 G>A maps to NM_001013732.3 I572I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CZ-01A-11D-A32B-08 chr6:47846106 G>A maps to NM_001013732.3 R825*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A89Z-01A-11D-A36O-08 chr6:4069946 A>G maps to NM_173563.1 C170C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:97681831 G>A maps to NM_198468.2 R403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:121427276 G>A maps to ENST00000275159 G1160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:127796863 C>T maps to NM_001012279.2 P769P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YQ-01A-11D-A34J-08 chr6:151789764 A>G maps to NM_024573.1 G282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:74073390 C>T maps to NM_001017361.2 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:36298233 G>A maps to NM_001010903.4 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RP-01A-21D-A34A-08 chr6:31691584 C>A maps to NM_138272.1 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:31734932 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:31743782 G>A maps to NM_025258.2 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:24714602 G>A maps to NM_030939.4 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7Z4-01A-11D-A34J-08 chr6:24718869 T>C maps to NM_030939.4 K9K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:35716619 T>C maps to NM_145028.3 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8011-01A-11D-2395-08 chr6:151914324 C>T maps to ENST00000367290 D459D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:2594055 C>A maps to NM_152743.3 E4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YD-01A-11D-A34A-08 chr7:2582923 C>G maps to NM_152743.3 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7691-01A-11D-2253-08 chr7:2583294 C>A maps to NM_152743.3 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7T6-01A-11D-A33T-08 chr7:6844657 G>A maps to NM_198097.3 C339C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:25176354 G>A maps to NM_138811.3 R337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84Q-01A-11D-A36O-08 chr7:25194756 G>A maps to NM_138811.3 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5397-01A-01D-1893-08 chr7:142637544 G>A maps to NM_178829.4 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr7:129856217 C>T maps to NM_145268.3 R215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:134851539 C>T maps to NM_024033.2 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5275-01A-01D-1468-08 chr7:120629720 C>T maps to NM_024913.4 R16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66F-01A-11D-A29Q-08 chr7:120629720 C>T maps to NM_024913.4 R16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85E-01A-11D-A36O-08 chr7:120740099 G>T maps to NM_024913.4 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:112461819 G>A maps to NM_152556.2 D399D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:89909124 G>T maps to NM_001039706.2 V430V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A70Z-01A-12D-A33T-08 chr7:6370434 C>T maps to NM_001037163.1 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YJ-01A-11D-A34A-08 chr1:57347156 C>T maps to NM_000562.2 Y168Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:57415266 G>A maps to NM_000066.2 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:57425740 C>T maps to NM_000066.2 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8322-01A-11D-2395-08 chr1:57417780 C>T maps to NM_000066.2 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RM-01A-11D-A33T-08 chr1:57397486 C>T maps to NM_000066.2 R539R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8013-01A-11D-2395-08 chr8:42401644 C>T maps to NM_001135675.1 D10D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr8:33357851 C>T maps to NM_001102401.1 R472R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:67428263 A>T maps to NM_152765.3 K193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7677-01A-11D-2253-08 chr8:27891082 G>T maps to ENST00000341513 I581I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:39341682 G>A maps to NM_001737.3 C101C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76L-01A-11D-A32B-08 chr5:39308392 T>C maps to NM_001737.3 E393E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr5:39364518 T>A maps to NM_001737.3 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6XC-01A-12D-A32B-08 chr9:27284732 C>T maps to NM_020641.2 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:104238210 G>A maps to NM_032342.1 I388I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr9:112963590 C>T maps to NM_001012993.2 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6UA-01A-12D-A33T-08 chr9:100667128 C>T maps to NM_016481.3 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:139741208 G>A maps to NM_001080482.2 S781S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:139741106 C>T maps to NM_001080482.2 R747R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QW-01A-11D-A34A-08 chr9:34611083 G>A maps to NM_148179.1 C70C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr9:34381049 G>A maps to NM_032596.3 C184C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:97563234 C>T maps to NM_001193329.1 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:5361187 C>A did not map to a codon.
Sequencing variant TCGA-TQ-A7RP-01A-21D-A34A-08 chr9:27565530 G>A maps to NM_018325.2 Q168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U2-01A-21D-A33T-08 chr9:90500145 G>A maps to NM_178828.4 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:139722959 C>T maps to NM_001173988.1 R110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A75K-01A-11D-A32B-08 chr8:86249203 A>G maps to NM_001738.3 H108H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7677-01A-11D-2253-08 chr19:49143393 G>A maps to NM_001217.3 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr8:86180768 A>G maps to NM_198584.2 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:87969993 G>A maps to NM_001739.1 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:87921776 G>T maps to NM_001739.1 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:66886637 C>T maps to NM_005182.2 C180C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YH-01A-11D-A34A-08 chr8:61121346 C>T maps to NM_004056.4 Q290Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:35675905 C>T maps to NM_001216.2 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TY-01A-12D-A32B-08 chr9:35676352 G>A maps to NM_001216.2 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R3-01A-11D-A34J-08 chr1:227152915 C>T maps to NM_020247.4 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr22:24479227 G>A maps to NM_012295.3 T932T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6X9-01A-12D-A32B-08 chr22:24466845 G>A maps to NM_012295.3 E776E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:20837318 C>T maps to NM_001100619.2 V630V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7294-01A-11D-2024-08 chr18:20837288 C>T maps to NM_001100619.2 H620H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6188-01A-11D-1893-08 chr11:67287315 G>A maps to NM_016366.2 D195D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A6S3-01A-12D-A32B-08 chr11:67287396 C>T maps to NM_016366.2 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:48543904 C>T maps to NM_019855.3 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:21739838 T>C maps to NM_138644.1 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:65141175 C>T maps to ENST00000371073 N940N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TS-01A-11D-A289-08 chr9:140946555 G>A maps to ENST00000277549 G1242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8185-01A-11D-2253-08 chr9:140946549 C>G maps to ENST00000277549 S1240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:2774793 G>A maps to NM_199460.2 L1530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YL-01A-11D-A34A-08 chr3:53769490 C>T maps to NM_001128840.1 A904A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A780-01A-12D-A32B-08 chr3:53694204 C>T maps to NM_001128840.1 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr1:181707519 C>T maps to ENST00000357570 D1190D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7472-01A-11D-2024-08 chr1:181754901 C>A maps to ENST00000357570 I1911I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr23:49088175 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:49062225 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:49063465 C>T did not map to a codon.
Sequencing variant TCGA-HT-7608-01A-11D-2086-08 chr23:49063293 C>T did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr23:49088266 G>A did not map to a codon.
Sequencing variant TCGA-R8-A73M-01A-11D-A32B-08 chr23:49071866 C>T did not map to a codon.
Sequencing variant TCGA-DU-6393-01A-11D-1705-08 chr17:48669422 C>T maps to NM_018896.3 V960V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6397-01A-11D-1705-08 chr17:48703622 A>G maps to NM_018896.3 L2215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7605-01A-11D-2086-08 chr17:48652950 G>A maps to NM_018896.3 T396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A6MK-01A-11D-A32B-08 chr17:48646632 G>A maps to NM_018896.3 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IZ-01A-11D-A34A-08 chr17:48649290 C>T maps to NM_018896.3 N213N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7J0-01A-11D-A34A-08 chr17:48703991 C>T maps to NM_018896.3 S2338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RN-01A-11D-A33T-08 chr17:48677186 G>A maps to NM_018896.3 L1219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:1266972 C>A maps to NM_021098.2 I1762I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:1250549 C>T maps to NM_021098.2 Y366Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr16:1250282 G>A maps to NM_021098.2 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:40054158 G>A maps to NM_021096.3 P665P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:201029851 G>T maps to NM_000069.2 T1116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:201018172 A>T maps to NM_000069.2 P1432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QZ-01A-12D-A34J-08 chr1:201010634 G>A maps to NM_000069.2 L1711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5142-01A-01D-1468-08 chr7:81624210 G>A maps to NM_000722.2 F569F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:81588628 G>A maps to NM_000722.2 R1041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr7:81598289 C>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:50417155 C>T maps to ENST00000435965 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:50405101 G>A maps to ENST00000435965 D763D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5965-01B-11D-1893-08 chr3:50417430 C>T maps to ENST00000435965 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74O-01A-11D-A32B-08 chr3:50405101 G>A maps to ENST00000435965 D763D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5303-01A-01D-1468-08 chr3:55052338 C>T maps to NM_018398.2 C994C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr12:1995490 G>A maps to NM_172364.4 D297D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:152729006 C>T maps to NM_000726.3 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KT-A7W1-01A-11D-A34A-08 chr22:36960616 G>A maps to NM_006078.3 D251D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7Z6-01A-11D-A34J-08 chr1:174973949 G>A maps to NM_014412.2 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:27454414 C>T maps to NM_004341.3 G789G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:115111117 C>T maps to NM_014333.3 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7873-01B-11D-2395-08 chr3:85984925 C>G maps to NM_153184.3 S230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:62452064 G>A maps to ENST00000383709 D1172D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:122047654 C>T maps to NM_001167940.1 P899P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:122111439 C>T maps to NM_001167940.1 V725V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr7:121965554 C>G maps to NM_001167940.1 L1235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WD-01A-12D-A33T-08 chr7:122261561 G>A maps to NM_001167940.1 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:91094330 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:91072447 G>A maps to NM_004929.2 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:54115880 G>A maps to NM_020898.2 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:54118438 G>A maps to NM_020898.2 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:46925798 C>A maps to ENST00000448105 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YU-01A-11D-A34J-08 chr17:46919110 G>A maps to ENST00000448105 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7473-01A-11D-2024-08 chr7:93072937 C>G maps to NM_001164737.1 R294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4943-01A-01D-1468-08 chr2:188225388 T>G maps to NM_005795.4 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:134618792 G>T maps to NM_033138.3 E425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A843-01A-11D-A36O-08 chr10:105215288 G>A maps to NM_001001412.3 D257D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:5567215 C>T maps to NM_005185.2 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8110-01A-11D-2395-08 chr7:71571178 G>A maps to NM_031468.3 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:13051398 G>A maps to NM_004343.3 K249K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:16593274 G>A maps to NM_145046.3 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6J3-01A-11D-A31L-08 chr19:16594776 C>T maps to NM_145046.3 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:128409142 C>T maps to ENST00000342367 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:12595235 C>T maps to NM_153498.2 S35S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DU-6392-01A-11D-1705-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:209779783 C>T maps to NM_020439.2 Y185Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:209781260 C>T maps to NM_020439.2 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RP-01A-21D-A34A-08 chr7:44323781 G>A maps to NM_001220.4 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7620-01A-11D-2253-08 chr4:114436308 G>A maps to ENST00000515496 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:110784899 C>T maps to NM_001744.4 C208C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:49896834 G>A maps to NM_024046.3 G474G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R7-01A-11D-A34J-08 chr3:49899246 C>T maps to NM_024046.3 K93K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8319-01A-11D-2395-08 chr9:138713008 G>A maps to ENST00000409386 F1177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IS-01A-11D-A34A-08 chr9:138713203 G>A maps to ENST00000409386 S1112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:200730021 A>G maps to ENST00000236925 E65E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:7725162 C>A maps to NM_015215.2 V852V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:67696121 T>C maps to NM_018448.3 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:85628937 C>A maps to NM_001747.2 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:241536167 C>T maps to NM_023083.3 Q518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:30959397 G>A maps to ENST00000295055 R565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:30980985 G>A maps to ENST00000295055 G264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5302-01A-01D-1468-08 chr2:30966406 C>T maps to ENST00000295055 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8163-01A-11D-2253-08 chr1:223900425 C>G maps to NM_001748.4 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:110494307 C>T did not map to a codon.
Sequencing variant TCGA-P5-A780-01A-12D-A32B-08 chr23:110497568 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:230891087 C>T maps to NM_006615.2 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:230895264 C>A maps to NM_006615.2 C97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7616-01A-11D-2253-08 chr19:36631957 C>G maps to NM_001749.2 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:55601249 C>T maps to NM_032330.1 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7294-01A-11D-2024-08 chr16:55600781 A>G maps to NM_032330.1 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A711-01A-21D-A33T-08 chr12:30906346 C>T maps to NM_001002259.1 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8105-01A-11D-2395-08 chr12:75692507 G>A maps to NM_032606.3 R354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:18891729 C>T maps to NM_033328.2 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:18891390 C>A maps to NM_033328.2 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QZ-01A-12D-A34J-08 chr12:18891210 T>A maps to NM_033328.2 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:19712003 G>A maps to ENST00000375145 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66D-01A-11D-A31L-08 chr7:2968245 G>A maps to NM_032415.4 D580D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:2984157 G>A maps to NM_032415.4 H124H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WO-01A-21D-A34A-08 chr7:2983875 C>T maps to NM_032415.4 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:78163619 C>T maps to NM_024110.2 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5280-01A-01D-1468-08 chr11:104915358 G>A maps to NM_001017534.1 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76K-01A-11D-A33T-08 chr5:40852927 G>A maps to NM_032587.3 R498R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:139264249 G>A maps to NM_052813.4 I343I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7C4-01A-11D-A32B-08 chr13:111296776 A>G maps to NM_024537.2 F457F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:38318392 G>T maps to NM_007359.4 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CU-01A-11D-A31L-08 chr17:38324148 G>A maps to NM_007359.4 P566P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:40915860 A>G maps to NM_170589.3 T1159T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DU-6392-01A-11D-1705-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:94157498 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:94175011 C>T maps to NM_022900.4 N544N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr23:41393958 G>T did not map to a codon.
Sequencing variant TCGA-TQ-A7RM-01A-11D-A33T-08 chr23:41383252 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:73499249 G>A maps to NM_020753.3 G635G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TS-01A-11D-A289-08 chr17:73498547 C>G maps to NM_020753.3 P869P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8185-01A-11D-2253-08 chr17:73502704 G>T maps to NM_020753.3 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KM-01A-11D-A27K-08 chr17:73497956 G>A maps to NM_020753.3 C1066C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A83Y-01A-11D-A36O-08 chr17:73498193 T>C maps to NM_020753.3 S987S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:104897598 A>G maps to NM_033292.2 C362C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:15166059 C>A maps to NM_012114.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:104819403 C>A did not map to a codon.
Sequencing variant TCGA-E1-A7YQ-01A-11D-A34J-08 chr11:104815485 G>T maps to NM_001225.3 G376G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:104869615 T>C maps to NM_001136112.1 T377T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:116269611 C>A did not map to a codon.
Sequencing variant TCGA-DH-A66D-01A-11D-A31L-08 chr3:122002555 C>T maps to NM_001178065.1 C595C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7486-01A-11D-2024-08 chr3:122003578 G>A maps to NM_001178065.1 Q936Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:10699520 C>T maps to NM_001079843.1 S1586S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:10715762 G>A maps to NM_001079843.1 S536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TZ-01A-21D-A32B-08 chr1:10710808 G>A maps to NM_001079843.1 N940N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W9-A837-01A-11D-A36O-08 chr11:34473714 A>G maps to NM_001752.3 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:65788616 G>A maps to NM_053054.3 G577G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YN-01A-11D-A34A-08 chr11:65788324 C>T maps to NM_053054.3 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U6-01A-12D-A33T-08 chr11:65787823 C>T maps to NM_053054.3 T676T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CZ-01A-11D-A32B-08 chr5:134345081 C>T maps to NM_178019.2 R280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr16:88958663 C>T maps to NM_005187.5 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6IZ-01A-11D-A31L-08 chr11:119103189 G>A maps to NM_005188.2 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:105389182 A>G maps to NM_170662.3 D861D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A615-01A-11D-A29Q-08 chr19:45284224 C>T maps to NM_012116.3 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:107399539 C>T maps to NM_024814.2 R465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:24897111 G>A maps to NM_001039771.2 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6690-01A-11D-1893-08 chr20:54573804 G>A maps to NM_080617.4 N138N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8110-01A-11D-2395-08 chr20:54579017 C>T maps to NM_080617.4 K70K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A780-01A-12D-A32B-08 chr20:54573642 C>T maps to NM_080617.4 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5871-01A-12D-1705-08 chr21:37518617 G>A maps to NM_001236.3 E214E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:169923299 C>A maps to NM_032783.4 G153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R1-01A-12D-A34J-08 chr9:70871888 C>T maps to NM_201453.2 Y161Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:77758261 C>T maps to NM_005189.2 C340C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:77808426 C>T maps to NM_003655.2 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:77808612 C>T maps to NM_003655.2 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:39262894 G>A maps to NM_014292.3 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VW-A8FI-01A-11D-A36O-08 chr22:39262561 G>A maps to NM_014292.3 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:77768487 G>A maps to NM_020649.2 T372T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:14038836 G>A maps to NM_017721.4 V816V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:14034192 G>A maps to NM_017721.4 R563R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YU-01A-11D-A34J-08 chr19:14024099 C>T maps to NM_017721.4 Y166Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:97769580 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:70531162 C>T maps to NM_018237.2 G833G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YJ-01A-11D-A34A-08 chr10:70509371 C>T maps to NM_018237.2 R350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:57134064 G>T maps to NM_133459.3 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr18:57136831 G>A maps to NM_133459.3 D91D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WQ-01A-12D-A34A-08 chr18:57136752 G>A maps to NM_133459.3 R118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:131605001 G>A maps to NM_004059.4 D44D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8110-01A-11D-2395-08 chr3:42907139 A>G maps to NM_001296.4 K382K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R7-01A-11D-A289-08 chr3:42906980 C>T maps to NM_001296.4 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:66564466 G>A maps to NM_024781.2 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:35660848 G>T maps to NM_174923.2 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6667-01A-12D-2024-08 chr2:219895548 G>A maps to NM_194302.2 C341C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:219884250 G>T maps to NM_194302.2 T1150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EZ-7264-01A-11D-2024-08 chr2:219900290 C>T maps to NM_194302.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7490-01A-11D-2024-08 chr2:219868813 C>T maps to NM_194302.2 K1805K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84H-01A-11D-A36O-08 chr2:219894927 T>C maps to NM_194302.2 V388V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84R-01A-21D-A36O-08 chr4:110603876 A>G maps to NM_017918.4 E197E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6400-01A-12D-1705-08 chr16:58292427 G>A did not map to a codon.
Sequencing variant TCGA-DU-7300-01A-21D-2086-08 chr16:58287906 A>G maps to NM_014157.3 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr22:21988387 C>T maps to NM_152612.2 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85D-01A-11D-A36O-08 chr22:21989104 C>T maps to NM_152612.2 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:48921960 G>A did not map to a codon.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr19:33444649 C>T maps to NM_032816.3 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr22:42221754 C>A maps to NM_024821.2 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:57741391 G>A maps to NM_032269.5 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:109411017 C>A maps to NM_144978.1 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YL-01A-11D-A34A-08 chr17:16593776 C>T maps to NM_014695.1 Y21Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7J0-01A-11D-A34A-08 chr17:16610780 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:76922405 C>T maps to NM_020879.2 C851C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:76912053 G>A maps to NM_020879.2 L700L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:76871011 C>T maps to NM_020879.2 Q82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A614-01A-11D-A29Q-08 chr4:24875311 T>C maps to NM_001130726.2 K85K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A83X-01A-11D-A36O-08 chr2:197541383 C>T maps to NM_001080539.1 R457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5276-01A-01D-1468-08 chr4:77250101 G>A maps to NM_001042784.1 H983H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:77305272 C>A maps to NM_001042784.1 E232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr4:77255305 A>T maps to NM_001042784.1 A893A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7467-01A-11D-2024-08 chr4:77317544 A>G maps to NM_001042784.1 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5847-01A-11D-1705-08 chr19:11462649 G>A did not map to a codon.
Sequencing variant TCGA-DH-A7UR-01A-11D-A33T-08 chr23:133379729 G>T did not map to a codon.
Sequencing variant TCGA-DU-5872-01A-11D-1705-08 chr23:133379652 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:133379663 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:93646191 G>A maps to NM_206886.2 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:26597550 G>T maps to NM_022778.2 E566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:26582025 G>A maps to NM_022778.2 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8182-01A-11D-2253-08 chr23:49105640 C>T did not map to a codon.
Sequencing variant TCGA-FG-8189-01B-11D-A289-08 chr23:49093731 T>G did not map to a codon.
Sequencing variant TCGA-FG-A6IZ-01A-11D-A31L-08 chr23:49093691 C>T did not map to a codon.
Sequencing variant TCGA-HT-8012-01A-11D-2395-08 chr1:3677957 C>G maps to NM_152492.2 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7469-01A-11D-2253-08 chr1:43032077 C>T maps to NM_001080850.2 R263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7007-01A-11D-2024-08 chr15:74554907 C>T maps to ENST00000321288 Q308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8105-01A-11D-2395-08 chr15:74623085 G>A maps to ENST00000321288 L716L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:96273468 T>C maps to NM_182496.2 E365E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:180334612 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:180377293 C>T maps to NM_181426.1 E228E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:180337713 C>T maps to NM_181426.1 L681L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:78023946 C>T maps to NM_017950.2 Q342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr12:94769687 G>A maps to NM_001042399.1 R303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:61833659 C>T maps to NM_020198.2 P296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7476-01A-11D-2024-08 chr3:113172504 C>G maps to NM_144718.3 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IQ-01A-21D-A34A-08 chr3:113172642 C>T maps to NM_144718.3 W604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CS-01A-11D-A31L-08 chr12:102433744 T>C maps to NM_016053.2 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr3:107096616 C>T maps to NM_032600.2 D61D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:40950137 G>A maps to NM_001040431.1 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A6MO-01A-11D-A33T-08 chr12:119909927 C>T maps to NM_178499.3 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr16:3085392 G>A maps to NM_001103175.1 D35D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7609-01A-11D-2086-08 chr5:150565606 G>A maps to NM_015621.2 R158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8186-01A-11D-2253-08 chr13:52439603 G>A maps to NM_031290.2 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:32637484 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:37319368 C>T maps to ENST00000379187 R171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:100614353 C>A maps to NM_019083.2 S475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr19:46915401 G>A maps to NM_032040.3 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr19:46914993 G>A maps to NM_032040.3 N358N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RG-01A-11D-A33T-08 chr19:46915065 A>G maps to NM_032040.3 N334N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:112337933 G>A maps to ENST00000447230 R696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:56419886 C>T maps to NM_001080433.1 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RJ-01A-11D-A33T-08 chr2:56420285 C>T maps to NM_001080433.1 F317F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:66359607 G>T maps to NM_018219.2 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84S-01A-11D-A36O-08 chr2:55566773 T>C maps to ENST00000436346 K448K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7874-01A-11D-2395-08 chr11:64112394 G>A maps to NM_032251.5 R794R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:91780359 C>T maps to NM_001080414.2 T600T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr14:91806239 G>A maps to NM_001080414.2 D204D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:28605514 A>G maps to NM_018318.3 E343E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:124421700 C>T maps to NM_025140.1 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CH-01A-12D-A36O-08 chr5:169015539 A>G maps to NM_017785.4 Q40Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XF-01A-11D-A27K-08 chr9:36170044 C>A maps to NM_005893.2 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6X5-01A-12D-A32B-08 chr9:36170641 C>T maps to NM_005893.2 G381G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:42305083 T>C maps to NM_000729.4 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:26483460 G>T maps to NM_000730.2 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:26490891 G>A maps to NM_000730.2 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6402-01A-11D-1705-08 chr4:26483466 G>A maps to NM_000730.2 Y360Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85C-01A-11D-A36O-08 chr4:26483532 G>A maps to NM_000730.2 Y338Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr11:6292256 C>T maps to NM_176875.2 N276N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7882-01A-11D-2395-08 chr11:6292256 C>T maps to NM_176875.2 N276N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8185-01A-11D-2253-08 chr17:32612838 C>T maps to NM_002986.2 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:34199457 G>A maps to NM_002985.2 R67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UV-01A-12D-A34A-08 chr23:50085215 A>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:50085329 A>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:50054132 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:50031780 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:50053091 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:50053115 G>A did not map to a codon.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr23:50051783 G>A did not map to a codon.
Sequencing variant TCGA-FG-A87Q-01A-11D-A36O-08 chr23:50054450 T>A did not map to a codon.
Sequencing variant TCGA-HT-7686-01A-11D-2253-08 chr23:50055580 T>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:100009528 T>C maps to NM_005190.3 K56K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:2498891 C>T maps to NM_001761.2 A377A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5142-01A-01D-1468-08 chr4:78081990 A>T maps to NM_004354.2 K132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:97817679 G>A maps to NM_001134375.1 Q278Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7855-01A-11D-2395-08 chr5:159707583 G>A maps to NM_024565.5 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:1323365 G>T maps to NM_030937.4 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A713-01A-11D-A32B-08 chr12:49087745 T>C maps to NM_001240.2 Q417Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7471-01A-11D-2253-08 chr12:49087564 C>A maps to NM_001240.2 E478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:135711149 C>T maps to NM_058241.2 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:35819080 A>G maps to NM_145012.4 K163K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:167549771 T>G maps to NM_004367.5 Y18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:167549744 C>T maps to NM_004367.5 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A711-01A-21D-A33T-08 chr6:167550305 C>T maps to NM_004367.5 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr17:38711758 G>A maps to NM_001838.3 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:38711143 G>A maps to NM_001838.3 I329I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EZ-01A-11D-A27K-08 chr17:38711203 G>A maps to NM_001838.3 D309D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7637-01A-11D-2086-08 chr3:45942528 C>T maps to NM_031200.2 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A73M-01A-11D-A32B-08 chr3:132319325 C>T maps to NM_178445.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RW-01A-11D-A33T-08 chr4:139966531 T>A maps to NM_012118.2 I400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A6MK-01A-11D-A32B-08 chr11:66368005 C>T maps to NM_005125.1 Q159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:69991023 C>T maps to NM_006431.2 D357D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:10254885 G>A maps to NM_012073.3 K89K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UV-01A-12D-A34A-08 chr17:33258004 G>T maps to NM_006584.3 V471V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7620-01A-11D-2253-08 chr2:73478418 C>G maps to NM_006429.3 Y423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:30439248 A>G maps to NM_006585.2 N175N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr22:17073094 G>A maps to NM_014406.4 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84O-01A-11D-A36O-08 chr22:17073350 C>T maps to NM_014406.4 E30E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:74468751 G>T did not map to a codon.
Sequencing variant TCGA-DU-8166-01A-11D-2253-08 chr6:74472142 G>A maps to NM_133493.3 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8182-01A-11D-2253-08 chr6:74491007 T>C maps to NM_133493.3 D643D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:836122 C>T maps to NM_139030.3 Y18Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:7653810 A>C maps to NM_004244.4 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr12:7635287 G>A maps to NM_004244.4 V1066V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RH-01A-12D-A34A-08 chr12:7635290 G>A maps to NM_004244.4 F1065F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:7556245 A>G maps to ENST00000416109 I441I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:7527242 G>A maps to ENST00000416109 S1078S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6J3-01A-11D-A31L-08 chr12:7521535 G>T maps to ENST00000416109 A1365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RC-01A-11D-A289-08 chr12:7527056 G>A maps to ENST00000416109 D1140D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F0-01A-11D-A289-08 chr12:7526162 G>A maps to ENST00000416109 N1171N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:66478852 C>T maps to NM_005582.2 T606T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:66481845 C>A did not map to a codon.
Sequencing variant TCGA-FG-A87Q-01A-11D-A36O-08 chr16:28944768 G>A maps to NM_001178098.1 K258K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5395-01A-01D-1468-08 chr1:158226759 C>T maps to NM_001763.2 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:158227280 G>A maps to NM_001763.2 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RW-01A-11D-A33T-08 chr1:158226058 T>C maps to NM_001763.2 H197H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr1:158299223 C>T maps to NM_001764.2 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7J0-01A-11D-A34A-08 chr1:158151455 T>C maps to NM_001766.3 Y91Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8319-01A-11D-2395-08 chr1:158325318 G>A maps to NM_030893.3 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CF-01A-11D-A36O-08 chr1:158325644 C>T maps to NM_030893.3 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5853-01A-11D-1893-08 chr3:112064082 C>T maps to NM_001004196.2 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XG-01A-11D-A27K-08 chr19:7809892 G>A maps to NM_021155.3 H278H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:7809027 C>T maps to NM_021155.3 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CA-01A-11D-A36O-08 chr19:7809880 G>A maps to NM_021155.3 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:35835804 C>A maps to NM_001771.3 I703I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:35827140 G>A maps to NM_001771.3 K205K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7294-01A-11D-2024-08 chr19:35832000 T>C maps to NM_001771.3 S489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A87Q-01A-11D-A36O-08 chr19:35837089 G>A maps to NM_001771.3 P788P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr1:160811430 C>A maps to NM_001166663.1 E108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7480-01A-11D-2086-08 chr1:160811090 G>A maps to NM_001166663.1 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7680-01A-11D-2253-08 chr1:160811159 G>A maps to NM_001166663.1 Y170Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr11:66084108 G>A maps to NM_020404.2 R130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:204599532 G>A maps to NM_006139.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:47471061 A>G maps to NM_012120.2 E17E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TS-01A-11D-A289-08 chr6:47575764 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:30364964 G>A maps to NM_006110.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7854-01A-11D-2253-08 chr17:72473593 C>T maps to NM_007261.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:72540829 G>A maps to NM_006678.3 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr17:72613293 G>A maps to ENST00000426295 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr17:72613302 T>C maps to ENST00000426295 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7858-01A-11D-2395-08 chr17:72521998 C>T maps to NM_174892.2 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:49840408 T>C maps to NM_001774.2 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5319-01A-01D-1893-08 chr11:118211222 C>T maps to NM_000732.4 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65V-01A-11D-A29Q-08 chr20:44751285 A>G maps to NM_001250.4 E98E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5870-01A-11D-1705-08 chr23:135741430 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:135741286 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:60889371 C>T maps to NM_014207.3 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8320-01A-11D-2395-08 chr1:207500165 G>A maps to NM_001114752.1 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:7484214 G>A maps to NM_001251.2 Q254Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A73M-01A-11D-A32B-08 chr17:7484226 G>A maps to NM_001251.2 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:80274542 C>A maps to NM_006137.6 E133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TZ-01A-21D-A32B-08 chr9:35618217 C>A did not map to a codon.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr5:149782732 G>A maps to NM_001025159.1 N256N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RW-01A-11D-A33T-08 chr5:149792210 G>A maps to NM_001025159.1 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7Z4-01A-11D-A34J-08 chr17:62007605 G>C maps to NM_001039933.1 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr11:44640200 G>A maps to NM_002231.3 E218E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr11:44621760 C>T maps to NM_002231.3 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:14131768 G>T maps to NM_004233.3 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:14135455 G>T maps to NM_004233.3 E203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr20:23065098 G>A maps to NM_012072.3 D577D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7881-01A-11D-2395-08 chr20:23065824 C>T maps to NM_012072.3 Q335Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6668-01A-11D-1893-08 chr19:14508024 C>T maps to NM_078481.2 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IY-01A-11D-A34A-08 chr19:14499538 C>T maps to NM_078481.2 N33N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RC-01A-11D-A289-08 chr23:2656283 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:149945939 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:149963701 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:149963704 C>T did not map to a codon.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr23:149938822 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:43021270 G>A maps to NM_138477.2 T865T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:43023930 C>T maps to NM_138477.2 L542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5397-01A-01D-1893-08 chr1:100818539 G>T maps to NM_033312.2 G10G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:100908488 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:99285969 G>A maps to NM_033331.2 Y328Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:43825272 G>A maps to NM_001255.2 E98E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6410-01A-11D-1893-08 chr1:43824984 G>A maps to NM_001255.2 K33K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr1:43826261 C>A maps to NM_001255.2 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4942-01A-01D-1468-08 chr5:54436229 G>A maps to NM_001170402.1 C164C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:137548860 G>A maps to NM_004661.3 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:3778367 G>A maps to NM_021873.2 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:137627772 C>T maps to NM_001790.3 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:45232099 G>A maps to NM_001114091.1 Q299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R3-01A-11D-A34J-08 chr17:45216209 A>C maps to NM_001114091.1 V539V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R7-01A-11D-A34J-08 chr17:45216209 A>C maps to NM_001114091.1 V539V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7C4-01A-11D-A32B-08 chr17:45234391 A>G maps to NM_001114091.1 D243D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:10502250 G>A maps to NM_007065.3 G371G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4944-01A-01D-1468-08 chr1:227348327 T>C maps to ENST00000366766 K203K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:103418838 G>A maps to NM_006035.3 C1056C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:103465942 C>T maps to NM_006035.3 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:103434649 G>A maps to NM_006035.3 Y762Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:103406240 C>T maps to NM_006035.3 K1545K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:103410309 G>A maps to NM_006035.3 S1442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6690-01A-11D-1893-08 chr14:103430858 G>A maps to NM_006035.3 D902D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A75K-01A-11D-A32B-08 chr11:64595068 A>G maps to NM_017525.2 N1360N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YD-01A-11D-A34A-08 chr11:64603245 C>T maps to NM_017525.2 S582S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A8XE-01A-11D-A36O-08 chr11:64597513 G>A maps to NM_017525.2 R1132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:71282024 G>A maps to NM_012121.4 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4943-01A-01D-1468-08 chr22:19470283 C>T maps to NM_001178010.1 D92D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:19483524 C>T maps to NM_001178010.1 Y220Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:19496190 C>A maps to NM_001178010.1 I430I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WP-01A-12D-A34A-08 chr17:38451606 G>A did not map to a codon.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr1:91989861 T>G maps to NM_001134420.1 L532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:21946037 G>A maps to NM_018719.4 Q264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:45152199 G>A maps to NM_022842.3 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:45134804 G>A maps to NM_022842.3 Q531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:45132743 G>A maps to NM_022842.3 V638V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:54605591 G>A maps to NM_201546.2 D317D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:68847373 C>T maps to NM_004360.3 N432N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:24509871 G>A maps to NM_006727.3 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:65032516 C>T maps to NM_001797.2 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5851-01A-13D-1893-08 chr5:21752211 G>A maps to NM_004061.3 F673F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:21854855 C>T maps to NM_004061.3 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A61B-01A-11D-A29Q-08 chr5:21752318 G>A maps to NM_004061.3 R638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TX-01A-21D-A32B-08 chr16:82892058 G>A maps to ENST00000268613 E46E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5964-01A-11D-1705-08 chr16:89261355 G>A maps to NM_004933.2 A746A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85D-01A-11D-A36O-08 chr16:66945163 C>T maps to NM_004062.2 G615G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:95183095 C>A maps to NM_001144663.1 E301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TG-01A-21D-A34J-08 chr8:95178175 A>G maps to NM_001144663.1 H365H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7490-01A-11D-2024-08 chr8:95182643 G>A maps to NM_001144663.1 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7J0-01A-11D-A34A-08 chr8:95188825 G>A maps to NM_001144663.1 R123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:25727733 A>T maps to NM_001792.3 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:25572621 G>A maps to NM_001792.3 V447V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5141-01A-01D-1468-08 chr18:59174699 G>A maps to NM_031891.2 E308E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A60L-01A-12D-A31L-08 chr20:44803599 G>A maps to NM_021248.1 Q678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr20:44838992 G>A maps to NM_021248.1 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:73544137 C>A maps to ENST00000398860 I1826I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:73571131 C>T maps to ENST00000398860 N3051N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:73206144 G>A maps to ENST00000398860 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A72W-01A-11D-A32B-08 chr10:73450309 C>T maps to ENST00000398860 G720G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr14:23523983 C>T maps to NM_022478.3 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RJ-01A-11D-A33T-08 chr20:58564209 C>T maps to NM_177980.2 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:60427859 C>T maps to NM_001794.2 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7604-01A-11D-2086-08 chr20:60498708 G>T maps to NM_001794.2 V525V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr20:60503308 C>T maps to NM_001794.2 N611N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A840-01A-11D-A36O-08 chr20:60427937 C>T maps to NM_001794.2 D287D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr16:66424459 C>T maps to NM_001795.3 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr5:31323106 C>T maps to NM_004932.2 R689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6405-01A-11D-1705-08 chr5:31323147 G>T maps to NM_004932.2 R702R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7T6-01A-11D-A33T-08 chr16:61687748 G>T maps to NM_001796.2 V721V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr16:62055207 G>A maps to NM_001796.2 Q34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr16:62055201 G>A maps to NM_001796.2 Q36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr5:26881406 T>G maps to NM_016279.3 A736A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8011-01A-11D-2395-08 chr10:85970773 G>A maps to NM_033100.2 V446V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7US-01A-11D-A33T-08 chr5:176016159 C>T maps to NM_001171976.1 A995A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:176003071 C>A maps to NM_001171976.1 A360A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:176011939 C>A maps to NM_001171976.1 A886A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:176016105 C>T maps to NM_001171976.1 D977D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr5:176011567 G>A maps to NM_001171976.1 P762P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WM-01A-12D-A33T-08 chr5:175995742 C>T maps to NM_001171976.1 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:105662782 C>T maps to NM_152750.4 D655D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr7:105669000 G>A maps to NM_152750.4 T759T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YL-01A-11D-A34A-08 chr11:618781 G>A maps to NM_021924.4 Q593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RF-01A-11D-A33T-08 chr11:621208 G>A maps to NM_021924.4 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CD-01A-11D-A36O-08 chr11:618737 T>C maps to NM_021924.4 A607A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:62545440 C>T maps to NM_001786.4 Q72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A87N-01A-11D-A36O-08 chr1:1573135 G>A maps to ENST00000401097 I482I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:40027398 G>A maps to NM_003718.4 A471A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:40133840 A>G maps to NM_003718.4 P1267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:90613514 G>T maps to NM_012395.2 G316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr7:90377063 T>C maps to NM_012395.2 Y128Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7490-01A-11D-2024-08 chr7:90613504 T>A maps to NM_012395.2 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8191-01A-11D-2253-08 chr23:47082980 C>T did not map to a codon.
Sequencing variant TCGA-CS-6670-01A-11D-1893-08 chr1:205492348 C>T maps to NM_212503.2 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:110953231 C>T did not map to a codon.
Sequencing variant TCGA-DB-A4XG-01A-11D-A27K-08 chr9:123342217 A>G maps to NM_018249.4 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:123290157 C>A maps to NM_018249.4 E309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr9:123253596 G>A maps to NM_018249.4 D490D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:68550441 C>T maps to NM_001799.3 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:39440540 G>A maps to ENST00000395035 N121N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:39440588 G>A maps to ENST00000395035 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:18668630 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:18643245 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:18622862 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:18622548 C>A did not map to a codon.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr23:18646677 C>A did not map to a codon.
Sequencing variant TCGA-TM-A7C4-01A-11D-A32B-08 chr23:18600036 A>G did not map to a codon.
Sequencing variant TCGA-DH-5142-01A-01D-1468-08 chr12:12871756 A>C did not map to a codon.
Sequencing variant TCGA-TQ-A7RH-01A-12D-A34A-08 chr9:21971028 C>T maps to NM_001195132.1 W110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RU-01A-21D-A34A-08 chr9:21994136 C>T did not map to a codon.
Sequencing variant TCGA-P5-A5EZ-01A-11D-A27K-08 chr4:184367508 G>A maps to NM_017632.2 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R2-01A-21D-A34J-08 chr4:184367379 G>A maps to NM_017632.2 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:22006081 G>A maps to NM_004936.3 D107D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CZ-01A-11D-A32B-08 chr1:51436139 C>T maps to NM_078626.2 Q34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A83Y-01A-11D-A36O-08 chr1:51439738 G>T maps to NM_078626.2 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8186-01A-11D-2253-08 chr14:54884630 C>T maps to NM_005192.3 R172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7Z2-01A-21D-A34J-08 chr11:125887049 G>A maps to ENST00000392693 N287N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:15510967 C>T maps to ENST00000455584 Q708Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:15522424 C>T maps to ENST00000261644 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7298-01A-11D-2024-08 chr17:15510997 C>A did not map to a codon.
Sequencing variant TCGA-TM-A84B-01A-11D-A36O-08 chr17:15341349 G>A maps to ENST00000395926 Q67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:85560114 T>A maps to NM_001263.3 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:5155837 C>T maps to NM_003818.2 N68N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr6:31083951 G>A maps to NM_001264.4 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:28537430 G>A maps to NM_001265.3 Q255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:72673429 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:72667185 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:72667385 C>T did not map to a codon.
Sequencing variant TCGA-FG-A6J3-01A-11D-A31L-08 chr23:72667534 C>A did not map to a codon.
Sequencing variant TCGA-S9-A6WQ-01A-12D-A34A-08 chr23:72667523 G>A did not map to a codon.
Sequencing variant TCGA-TQ-A7RQ-01A-11D-A33T-08 chr23:72667178 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:4952498 G>A did not map to a codon.
Sequencing variant TCGA-HT-A615-01A-11D-A29Q-08 chr16:80718588 G>A maps to NM_152342.2 N154N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R2-01A-21D-A34J-08 chr16:80646693 G>A maps to NM_152342.2 I349I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A6ML-01A-11D-A32B-08 chr19:45028280 G>T maps to NM_001102597.1 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:42083693 A>G maps to NM_001098506.1 K69K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:42213701 C>T maps to NM_004363.2 H56H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6401-01A-11D-1705-08 chr19:42224878 G>A maps to NM_004363.2 S603S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:42187994 C>T did not map to a codon.
Sequencing variant TCGA-S9-A7R7-01A-11D-A34J-08 chr19:42187806 G>A maps to NM_006890.3 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66B-01A-11D-A29Q-08 chr14:23588123 G>A maps to NM_001805.2 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:37454685 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:17690297 C>T maps to NM_017424.2 K90K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:18028273 G>A maps to ENST00000400579 A1078A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CY-01A-11D-A32B-08 chr9:135946994 C>T maps to NM_001807.3 P705P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:51736375 G>A maps to NM_001971.5 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:15789913 C>T maps to ENST00000375924 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:15802638 C>T maps to ENST00000442979 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:11363272 C>T maps to NM_006561.3 Y406Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:3282218 C>T maps to NM_021938.3 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:46774547 G>A maps to NM_014246.1 V2441V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:46765669 G>A maps to NM_014246.1 Y2597Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A6S7-01A-21D-A32B-08 chr22:46780467 G>A maps to NM_014246.1 A2285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr22:46776724 G>A maps to NM_014246.1 R2406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr22:46806346 G>A maps to NM_014246.1 D1627D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:109795907 A>G maps to NM_001408.2 E1069E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:109794053 C>T maps to NM_001408.2 A451A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7T6-01A-11D-A33T-08 chr1:109792761 T>C maps to NM_001408.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7T6-01A-11D-A33T-08 chr1:109792764 C>T maps to NM_001408.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr1:109801231 C>T maps to NM_001408.2 H1163H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr3:48690584 C>T maps to NM_001407.2 R1828R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:48679323 G>A maps to NM_001407.2 C2928C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7695-01A-11D-2253-08 chr3:48684251 G>A maps to NM_001407.2 Y2413Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UR-01A-11D-A33T-08 chr16:90038171 T>C maps to NM_145039.3 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:104068632 T>C maps to NM_001813.2 Q1338Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:214811345 T>C did not map to a codon.
Sequencing variant TCGA-FG-A87N-01A-11D-A36O-08 chr1:214818124 A>T maps to NM_016343.3 K1738*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:100356227 G>A did not map to a codon.
Sequencing variant TCGA-QH-A6X5-01A-12D-A32B-08 chr23:100400089 A>G did not map to a codon.
Sequencing variant TCGA-E1-A7YO-01A-11D-A34A-08 chr1:173776587 G>A maps to NM_001127181.2 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:42341981 G>T maps to NM_024053.3 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:25038366 C>A maps to NM_024322.2 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:49448777 T>A maps to NM_018132.3 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr16:67863713 G>A maps to NM_025082.3 D380D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:123886324 G>A maps to NM_007018.4 T589T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr9:123858805 C>T maps to NM_007018.4 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5143-01A-01D-1468-08 chr4:56823425 T>C maps to NM_025009.3 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:56877582 C>A maps to NM_025009.3 I837I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7J3-01A-21D-A34J-08 chr15:49031240 C>T maps to NM_001194998.1 G1446G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:117261582 T>G maps to NM_014956.4 A675A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:13103523 C>T maps to NM_032142.3 L2296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:13095649 G>T maps to NM_032142.3 E2135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:13052932 C>A maps to NM_032142.3 S1011S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A713-01A-11D-A32B-08 chr18:13100326 A>G maps to NM_032142.3 R2229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:34091113 C>T maps to NM_007186.3 I1639I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KK-01A-11D-A27K-08 chr20:34059912 T>C maps to NM_007186.3 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:88500546 G>A maps to NM_025114.3 R908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:88514814 C>A maps to NM_025114.3 E440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:179989221 G>A maps to NM_014810.4 L771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:180064776 C>T maps to NM_014810.4 D2877D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:180044226 C>T maps to NM_014810.4 R1880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:180056828 C>T maps to NM_014810.4 I2134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:180012258 G>A maps to NM_014810.4 L1477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:95546133 C>T maps to NM_014679.3 R81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7309-01A-11D-2086-08 chr2:65296820 A>G maps to NM_015147.2 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7C4-01A-11D-A32B-08 chr2:65298754 C>G maps to NM_015147.2 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7616-01A-11D-2253-08 chr3:101446273 G>A maps to ENST00000327230 K78K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WI-01A-21D-A33T-08 chr3:101484295 C>T maps to ENST00000327230 S859S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:111726100 A>G maps to NM_001007794.1 K341K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:14722361 C>T maps to NM_005454.2 E103E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:182412564 C>T maps to NM_001030311.2 Q407Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr16:66974477 G>A maps to NM_003869.5 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4X9-01A-11D-A26M-08 chr16:67006755 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:66997235 C>T maps to NM_024922.5 H79H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:67005217 T>C maps to NM_024922.5 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:55905557 G>A maps to NM_001143685.1 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:55907779 C>T maps to NM_001143685.1 W81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr16:67034836 C>T maps to ENST00000326686 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5143-01A-01D-1468-08 chr18:580650 G>T maps to NM_004066.1 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RI-01A-11D-A33T-08 chr23:151997186 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:196659280 C>T maps to NM_000186.3 C416C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:196884206 T>A maps to NM_006684.2 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76R-01A-11D-A32B-08 chr1:196871560 T>C maps to NM_006684.2 C24C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5144-01A-01D-1468-08 chr11:65623201 C>T did not map to a codon.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr23:47487018 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:47485821 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:47486267 G>A did not map to a codon.
Sequencing variant TCGA-RY-A83Z-01A-11D-A36O-08 chr23:47485790 G>A did not map to a codon.
Sequencing variant TCGA-DU-7309-01A-11D-2086-08 chr19:49557631 G>T maps to ENST00000377280 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A618-01A-11D-A29Q-08 chr2:27325299 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:54996914 T>C maps to NM_006568.2 Y131Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WN-01A-12D-A33T-08 chr14:54989228 A>G maps to NM_006568.2 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:41247770 G>A maps to NM_024111.3 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CX-01A-11D-A32B-08 chr21:37785364 G>A maps to NM_005441.2 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr3:14157998 G>A maps to NM_144636.2 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:113343848 C>T maps to ENST00000409719 N72N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:98209390 A>G maps to NM_001270.2 D1159D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:146736230 G>T maps to NM_004284.3 E243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:93467604 T>C maps to NM_001271.3 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7J0-01A-11D-A34A-08 chr15:93522489 G>A maps to NM_001271.3 L951L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YI-01A-11D-A34A-08 chr17:7814263 C>T maps to NM_001005271.2 Q2011*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:6711197 A>G maps to ENST00000309577 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:6700692 G>A maps to ENST00000309577 Y1093Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:6702686 G>A maps to ENST00000309577 V803V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:6171833 C>T did not map to a codon.
Sequencing variant TCGA-E1-A7YS-01A-11D-A34A-08 chr1:6194807 G>A maps to NM_015557.2 N994N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr1:6202325 G>A maps to NM_015557.2 R766R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:40050061 G>T maps to NM_032221.3 S1738*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5303-01A-01D-1468-08 chr20:40045242 C>T maps to NM_032221.3 A2157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A73M-01A-11D-A32B-08 chr20:40102093 C>G maps to NM_032221.3 R844R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:61654158 T>C maps to NM_017780.2 H56H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:61750300 T>C maps to NM_017780.2 Y1420Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A6S8-01A-12D-A32B-08 chr14:21897260 T>C maps to NM_001170629.1 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr14:21861839 T>G maps to NM_001170629.1 P2038P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IS-01A-11D-A34A-08 chr16:53288442 C>T maps to ENST00000219084 R1319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7469-01A-11D-2253-08 chr20:5905693 G>A maps to NM_001819.2 *678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:883218 G>T maps to NM_001142676.1 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:203188358 C>T maps to NM_003465.2 E338E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:85218761 C>A did not map to a codon.
Sequencing variant TCGA-FG-A87Q-01A-11D-A36O-08 chr23:85119688 C>T did not map to a codon.
Sequencing variant TCGA-QH-A870-01A-11D-A36O-08 chr23:85218742 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:89712450 C>T maps to NM_001083314.1 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65S-01A-11D-A29Q-08 chr16:89720316 A>G maps to NM_002768.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:87294955 G>A maps to NM_014043.3 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:78971128 C>T maps to NM_024591.4 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6403-01A-11D-1705-08 chr7:29535575 G>A maps to NM_004067.2 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:220404122 C>T maps to NM_024536.5 E770E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66D-01A-11D-A31L-08 chr23:109924806 C>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:109924727 C>T did not map to a codon.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr23:110002886 A>T did not map to a codon.
Sequencing variant TCGA-R8-A6MO-01A-11D-A33T-08 chr23:109931821 C>A did not map to a codon.
Sequencing variant TCGA-TQ-A7RM-01A-11D-A33T-08 chr23:109937507 C>A did not map to a codon.
Sequencing variant TCGA-HT-7467-01A-11D-2024-08 chr11:62677197 G>A maps to NM_000738.2 Q459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:34354989 C>T maps to NM_012125.3 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:34355584 C>T maps to NM_012125.3 R223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:175618429 G>A maps to NM_001039523.2 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CF-01A-11D-A36O-08 chr2:175619021 A>G maps to NM_001039523.2 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7300-01A-21D-2086-08 chr8:27321506 T>G maps to NM_000742.3 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:78893831 G>A maps to NM_000743.4 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6395-01A-12D-1705-08 chr15:78893606 A>G maps to NM_000743.4 N459N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7471-01A-11D-2253-08 chr15:78894482 C>T maps to NM_000743.4 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:61981022 G>A maps to NM_000744.5 A580A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:61978113 C>T maps to NM_000744.5 P620P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:61981751 C>T maps to NM_000744.5 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:42552707 C>T maps to NM_000749.3 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:233405400 G>A maps to NM_005199.4 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr11:45672218 G>A maps to NM_003654.4 D85D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr2:101009736 C>A maps to NM_004854.3 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IS-01A-11D-A34A-08 chr12:105151331 C>T maps to NM_018413.5 H270H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5277-01A-01D-1468-08 chr10:125801889 G>A maps to NM_015892.3 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr10:125804255 G>A maps to NM_015892.3 H242H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6UA-01A-12D-A33T-08 chr10:125805698 C>T maps to NM_015892.3 Q10Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6186-01A-12D-2024-08 chr16:71570879 C>T maps to NM_001166395.1 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:75513168 C>A maps to NM_021615.4 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:24497011 G>A maps to NM_031422.4 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:129521468 T>C maps to NM_175856.4 N878N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr15:78398160 C>T maps to NM_006383.2 E154E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85E-01A-11D-A36O-08 chr19:16284256 G>A maps to NM_054113.2 H10H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6670-01A-11D-1893-08 chr19:42791393 T>G did not map to a codon.
Sequencing variant TCGA-DH-A7UR-01A-11D-A33T-08 chr19:42797277 C>T maps to NM_015125.3 R1214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7US-01A-11D-A33T-08 chr19:42791827 G>A maps to NM_015125.3 W238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7638-01B-11D-2086-08 chr19:42793430 G>A maps to NM_015125.3 A411A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7480-01A-11D-2086-08 chr19:42796450 G>T did not map to a codon.
Sequencing variant TCGA-HT-7616-01A-11D-2253-08 chr19:42795389 C>T maps to NM_015125.3 Q824*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7875-01A-11D-2395-08 chr19:42796330 C>T maps to NM_015125.3 Q994*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F0-01A-11D-A289-08 chr19:42791827 G>A maps to NM_015125.3 W238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F0-01A-11D-A289-08 chr19:42796878 C>T maps to NM_015125.3 Q1113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A86X-01A-11D-A36O-08 chr19:42791392 G>A did not map to a codon.
Sequencing variant TCGA-S9-A6UB-01A-21D-A33T-08 chr19:42792002 G>A maps to NM_015125.3 W269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IY-01A-11D-A34A-08 chr19:42791852 C>T maps to NM_015125.3 Q247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RI-01A-11D-A33T-08 chr19:42791852 C>T maps to NM_015125.3 Q247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:9911603 G>T maps to ENST00000430427 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr16:10997736 C>T maps to NM_000246.3 R308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8106-01A-11D-2395-08 chr16:11002909 G>A maps to NM_000246.3 A894A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CV-01A-11D-A31L-08 chr19:19654988 C>T maps to NM_153221.2 A545A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A710-01A-12D-A33T-08 chr2:175243708 T>C maps to NM_004882.3 E142E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr12:120128189 C>T maps to ENST00000392521 A1984A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:71522665 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:130931345 C>T maps to NM_012127.2 E760E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr2:113513831 T>G maps to NM_152515.3 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:66599865 C>T maps to NM_016951.2 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R2-01A-21D-A34J-08 chr15:43990946 C>T maps to ENST00000424065 R405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7T6-01A-11D-A33T-08 chr5:80547052 G>A maps to NM_001825.2 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:122125202 C>A maps to NM_015282.2 E1283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:122106111 G>A maps to NM_015282.2 V1463V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:33592887 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:86939128 G>A maps to NM_001285.3 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QZ-01A-12D-A34J-08 chr1:86959230 A>T maps to NM_001285.3 V543V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7874-01A-11D-2395-08 chr1:86919121 C>T maps to NM_006536.5 S742S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8C8-01A-11D-A36O-08 chr1:87031501 C>T maps to ENST00000263723 N251N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:143039109 G>A maps to NM_000083.2 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:184073304 C>A maps to NM_004366.4 E395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr4:170601231 C>T maps to NM_173872.2 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VW-A7QS-01A-12D-A33T-08 chr4:170610266 G>A maps to NM_173872.2 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:10176404 C>A did not map to a codon.
Sequencing variant TCGA-DU-7011-01A-11D-2024-08 chr23:10180552 C>T did not map to a codon.
Sequencing variant TCGA-RY-A83Z-01A-11D-A36O-08 chr23:10176603 G>A did not map to a codon.
Sequencing variant TCGA-S9-A6UA-01A-12D-A33T-08 chr23:10176377 C>T did not map to a codon.
Sequencing variant TCGA-TQ-A7RF-01A-11D-A33T-08 chr23:10181804 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:49856786 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:49846430 T>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:49851516 T>A did not map to a codon.
Sequencing variant TCGA-TM-A7C4-01A-11D-A32B-08 chr23:49851228 C>T did not map to a codon.
Sequencing variant TCGA-TQ-A7RM-01A-11D-A33T-08 chr23:49851212 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:11888654 C>T maps to ENST00000376496 N365N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:1504418 G>A maps to ENST00000382745 G382G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:16353029 G>T did not map to a codon.
Sequencing variant TCGA-DU-8163-01A-11D-2253-08 chr1:16352609 A>G maps to NM_004070.3 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:16376348 T>C maps to NM_000085.3 C302C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:16377037 C>A maps to NM_000085.3 T332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7019-01A-11D-2024-08 chr1:16378308 C>T maps to NM_000085.3 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8163-01A-11D-2253-08 chr1:16378295 A>C maps to NM_000085.3 P463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A711-01A-21D-A33T-08 chr1:16375045 C>T maps to NM_000085.3 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7856-01A-11D-2395-08 chr1:16377497 G>A maps to NM_000085.3 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7881-01A-11D-2395-08 chr21:37833826 C>T maps to NM_001146077.1 W56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YE-01A-11D-A34A-08 chr3:190127815 A>C maps to NM_006580.3 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:106171574 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:106171566 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:106171741 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:184240732 C>T maps to NM_001111319.1 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:113650927 C>A maps to NM_001101389.1 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr7:73245692 C>T maps to NM_001305.3 C54C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:73245992 C>T maps to NM_001305.3 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr16:3065806 C>T maps to NM_021195.4 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6UA-01A-12D-A33T-08 chr16:3065625 G>A maps to NM_021195.4 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7605-01A-11D-2086-08 chr17:7163695 C>T maps to NM_001185022.1 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:51871825 C>T maps to NM_152353.2 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:6978459 G>A maps to NM_182906.2 D288D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr14:38724435 G>A maps to NM_175060.1 D264D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr14:38724726 G>A maps to NM_175060.1 N167N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:11066885 C>T maps to ENST00000409790 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7T6-01A-11D-A33T-08 chr16:69988451 C>T maps to NM_182619.2 N144N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:10228125 T>A maps to NM_016511.2 K174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76R-01A-11D-A32B-08 chr12:10145810 G>A maps to NM_016509.3 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:8278155 G>A did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:71043765 G>A maps to NM_173535.2 N249N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8C8-01A-11D-A36O-08 chr19:7794296 G>A maps to NM_198492.3 D279D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7CF-01A-11D-A32B-08 chr12:8612214 T>G maps to NM_001007033.1 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:154528181 G>T did not map to a codon.
Sequencing variant TCGA-HT-7620-01A-11D-2253-08 chr23:154508570 A>C did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr9:139889177 G>A maps to NM_004669.2 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7605-01A-11D-2086-08 chr1:25140629 A>G maps to NM_013943.2 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:122862244 G>A maps to ENST00000302528 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6J1-01A-11D-A31L-08 chr12:122845628 G>A maps to ENST00000302528 N294N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WE-01A-12D-A33T-08 chr12:122817532 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:73814803 C>T maps to NM_003388.4 D995D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:73770799 C>T maps to NM_003388.4 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:73790596 G>A maps to NM_003388.4 S622S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:73811412 C>T maps to NM_003388.4 N910N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WH-A86K-01A-11D-A36O-08 chr7:73768331 C>A maps to NM_003388.4 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:36508318 G>A maps to NM_015526.2 S495S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:201722763 G>T maps to NM_001162407.1 Y241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:155233071 G>A maps to ENST00000368361 F479F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6407-01A-13D-1705-08 chr5:178039444 C>T maps to NM_020666.2 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CV-01A-11D-A31L-08 chr5:178030706 G>A maps to NM_020666.2 R453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:77569212 T>C maps to NM_006493.2 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:1728702 C>T maps to NM_018941.3 N277N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:10566360 C>T maps to NM_052964.2 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:10560052 G>A maps to NM_052964.2 D141D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7875-01A-11D-2395-08 chr4:56301647 T>C maps to NM_004898.2 Q825Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:65472480 C>T maps to NM_006660.3 Q47Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:150659372 A>G maps to NM_001195794.1 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CZ-01A-11D-A32B-08 chr4:17528504 C>T maps to NM_001079827.2 R167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:36213592 C>A maps to NM_022111.3 E848*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:9795562 C>T maps to NM_001009566.1 T615T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RH-01A-12D-A34A-08 chr3:140281989 C>T maps to NM_022131.2 P809P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RU-01A-21D-A34A-08 chr3:140178465 C>T maps to NM_022131.2 D359D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:36199091 T>C maps to NM_007096.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:57760371 T>C maps to NM_004859.3 Y1290Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:19213860 G>T maps to NM_007098.3 R610R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:19207450 C>T maps to NM_007098.3 E954E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YV-01A-11D-A34J-08 chr22:19175591 C>A maps to NM_007098.3 L1445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7875-01A-11D-2395-08 chr8:27472226 A>G maps to NM_001831.2 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7604-01A-11D-2086-08 chr18:618008 G>A maps to NM_199167.1 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr8:62371029 C>T maps to NM_173519.2 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5393-01A-01D-1468-08 chr6:123332252 A>G maps to NM_001010852.2 Q171Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U1-01A-21D-A33T-08 chr14:24974843 G>A maps to NM_001836.2 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6666-01A-11D-1893-08 chr16:81641213 G>T maps to NM_198390.2 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:47834232 C>T maps to NM_016308.2 Y88Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CE-01A-11D-A36O-08 chr5:79029293 C>A maps to NM_153610.3 S1569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:72247448 G>A maps to NM_032649.5 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:72173217 C>T maps to NM_018235.2 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:47942778 C>T did not map to a codon.
Sequencing variant TCGA-DB-A75P-01A-11D-A32B-08 chr23:150912422 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:150912735 C>T did not map to a codon.
Sequencing variant TCGA-DU-7298-01A-11D-2024-08 chr23:150909278 C>G did not map to a codon.
Sequencing variant TCGA-S9-A89V-01A-11D-A36O-08 chr23:150912516 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:98999889 C>T maps to NM_001298.2 N145N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr2:99006189 C>T maps to NM_001298.2 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:57951324 A>G maps to NM_001297.4 C671C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8105-01A-11D-2395-08 chr16:57918280 G>A maps to NM_001297.4 T1181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YD-01A-11D-A34A-08 chr8:87683307 A>G maps to NM_019098.4 P119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6X9-01A-12D-A32B-08 chr8:87645033 A>G maps to NM_019098.4 F422F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:224872496 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:26515347 C>A maps to ENST00000374253 T599T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:21627187 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:21579606 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:21609229 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:21609292 A>G did not map to a codon.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr23:21627465 C>A did not map to a codon.
Sequencing variant TCGA-DU-7019-01A-11D-2024-08 chr23:21534626 G>T did not map to a codon.
Sequencing variant TCGA-TQ-A7RN-01A-11D-A33T-08 chr23:21627188 A>G did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr19:11660567 C>T maps to NM_001299.4 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:95367781 A>G maps to NM_001839.3 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:97494866 G>A maps to NM_017623.4 A685A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:97474382 C>A maps to NM_020184.3 T678T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5144-01A-01D-1468-08 chr16:58622798 C>T maps to NM_016284.3 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:58559182 C>T maps to NM_016284.3 A2228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7858-01A-11D-2395-08 chr16:58564251 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:70726545 G>T did not map to a codon.
Sequencing variant TCGA-KT-A74X-01A-11D-A32B-08 chr7:135073581 T>C maps to NM_001190848.1 G564G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:17089982 C>A maps to NM_013354.5 G228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:17102652 C>T maps to NM_013354.5 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:154250244 C>A maps to NM_004779.4 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:40120333 C>T maps to NM_033133.4 D84D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:42902285 G>A maps to NM_006586.3 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7695-01A-11D-2253-08 chr6:88854090 A>G maps to NM_016083.4 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:246829044 C>T maps to NM_152609.2 C672C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8320-01A-11D-2395-08 chr17:40956251 A>T maps to NM_173478.2 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8182-01A-11D-2253-08 chr9:17236519 G>A maps to NM_017738.2 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7300-01A-21D-2086-08 chr12:41333260 G>A maps to NM_001843.2 G451G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IX-01A-12D-A34A-08 chr12:41422974 G>A maps to NM_001843.2 A978A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:74316425 T>C maps to NM_020872.1 T936T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:74347324 T>C maps to NM_020872.1 L728L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:3095606 C>T maps to NM_175607.1 S976S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:3078899 C>T maps to NM_175607.1 T660T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F6-A8O4-01A-11D-A36O-08 chr3:2967439 G>A maps to NM_175607.1 R445R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr7:147600795 C>T maps to NM_014141.5 D746D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr7:147259308 C>T maps to NM_014141.5 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A60K-01A-11D-A29Q-08 chr9:39086826 G>C maps to NM_033655.3 Y1080*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7638-01B-11D-2086-08 chr16:76482069 C>T maps to NM_033401.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85D-01A-11D-A36O-08 chr16:76389359 T>C maps to NM_033401.3 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A4DV-01A-11D-A26M-08 chr2:125204402 G>A maps to NM_130773.2 W269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:7842842 C>T maps to NM_001037144.4 Q314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:7849173 C>T maps to NM_001037144.4 D621D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7C3-01A-11D-A32B-08 chr17:7850970 C>T maps to NM_001037144.4 D692D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:40717043 C>T maps to NM_001042532.2 G456G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr7:51287613 T>G maps to ENST00000395542 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:51096640 G>A maps to ENST00000395542 R800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:51085262 C>T maps to ENST00000395542 V1339V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:51152917 A>G maps to ENST00000395542 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr7:51287613 T>G maps to ENST00000395542 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7290-01A-11D-2024-08 chr7:51287613 T>G maps to ENST00000395542 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr7:51096965 T>C maps to ENST00000395542 K691K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8011-01A-11D-2395-08 chr7:51097052 C>T maps to ENST00000395542 A662A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:165561492 C>T maps to ENST00000392717 P411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5305-01A-01D-1893-08 chr13:46092960 T>C maps to NM_031431.2 N665N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:70516637 G>A maps to NM_015386.2 I638I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WD-01A-12D-A33T-08 chr16:70546309 T>C maps to NM_015386.2 K190K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr7:107204266 G>C maps to NM_006348.3 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:107052969 G>A maps to NM_006348.3 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5303-01A-01D-1468-08 chr7:107002755 T>C maps to NM_006348.3 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7616-01A-11D-2253-08 chr7:106851542 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:23404665 G>A maps to NM_153603.3 I630I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:23428436 A>G maps to NM_153603.3 H381H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:23400309 T>C maps to NM_153603.3 R748R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YI-01A-11D-A34A-08 chr1:103355016 C>T maps to NM_080629.2 G1498G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:75844496 T>C maps to ENST00000322507 V1823V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:121279064 G>T did not map to a codon.
Sequencing variant TCGA-DU-7007-01A-11D-2024-08 chr8:121290391 A>T maps to NM_021110.1 K1086*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66F-01A-11D-A29Q-08 chr9:101832035 G>A maps to NM_001855.3 A1345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:101748294 C>T maps to NM_001855.3 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8158-01A-11D-2253-08 chr9:101778340 T>C maps to NM_001855.3 P529P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6UA-01A-12D-A33T-08 chr9:101765778 C>T maps to NM_001855.3 S370S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:32157669 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:32119489 C>T maps to NM_001856.3 R1504R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YQ-01A-11D-A34J-08 chr1:32157244 T>G did not map to a codon.
Sequencing variant TCGA-DU-6403-01A-11D-1705-08 chr10:105793847 A>G maps to NM_000494.3 Y1337Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F1-01A-11D-A289-08 chr10:105836080 G>A maps to NM_000494.3 H103H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:46911188 C>T maps to ENST00000359759 P1121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:46932213 C>T maps to ENST00000359759 L1723L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5395-01A-01D-1468-08 chr6:70866053 G>A maps to NM_001858.4 G705G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66G-01A-21D-A31L-08 chr6:70866563 A>G maps to NM_001858.4 G747G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6186-01A-12D-2024-08 chr17:48270360 G>A maps to NM_000088.3 G605G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5962-01B-11D-1893-08 chr17:48264127 G>A maps to NM_000088.3 L1229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WP-01A-12D-A34A-08 chr17:48263207 G>C maps to NM_000088.3 S1393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6188-01A-11D-1893-08 chr7:94043556 C>T maps to NM_000089.3 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:94039588 C>T maps to NM_000089.3 S357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A780-01A-12D-A32B-08 chr7:94041966 T>C maps to NM_000089.3 I492I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6XC-01A-12D-A32B-08 chr7:94038131 C>T maps to NM_000089.3 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:61937230 A>G did not map to a codon.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr20:61951524 G>A maps to ENST00000326996 R1024R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr20:61960982 G>A maps to ENST00000326996 G1321G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7486-01A-11D-2024-08 chr6:56044618 G>A maps to NM_030820.3 R133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XD-01A-11D-A27K-08 chr8:139768054 C>T maps to NM_152888.1 A640A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:139788213 C>A maps to NM_152888.1 E600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8165-01A-11D-2253-08 chr8:139793187 G>A maps to NM_152888.1 D544D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A6S7-01A-21D-A32B-08 chr8:139890317 G>A maps to NM_152888.1 H111H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:86304297 C>T maps to NM_152890.5 E1217E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85C-01A-11D-A36O-08 chr1:86591608 A>T maps to NM_152890.5 L137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr9:116931262 C>T maps to NM_032888.2 T476T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:116999976 C>T maps to NM_032888.2 P903P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:7476094 C>A did not map to a codon.
Sequencing variant TCGA-P5-A733-01A-11D-A32B-08 chr12:48372073 C>T maps to NM_001844.4 S1001S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7J2-01A-11D-A34A-08 chr12:48380872 C>T maps to NM_001844.4 P451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7C3-01A-11D-A32B-08 chr12:48377905 A>G maps to NM_001844.4 D635D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A858-01A-11D-A36O-08 chr12:48373308 T>C maps to NM_001844.4 G906G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr2:189867064 C>T maps to NM_000090.3 F811F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:110861233 G>A maps to NM_001845.4 Q219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7467-01A-11D-2024-08 chr13:110813711 C>T maps to NM_001845.4 T1489T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U5-01A-12D-A33T-08 chr13:110895027 T>C maps to NM_001845.4 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:111118374 C>T maps to NM_001846.2 A668A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7007-01A-11D-2024-08 chr13:111147701 C>T maps to NM_001846.2 H1216H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5281-01A-01D-1468-08 chr2:228153926 G>A maps to NM_000091.4 K981K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:228012193 C>T maps to ENST00000396625 W2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7C5-01A-11D-A32B-08 chr2:227886827 C>T maps to ENST00000396625 A1384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XG-01A-11D-A27K-08 chr23:107823772 G>T did not map to a codon.
Sequencing variant TCGA-DH-5144-01A-01D-1468-08 chr23:107930899 A>G did not map to a codon.
Sequencing variant TCGA-DU-5851-01A-13D-1893-08 chr23:107840716 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:107925049 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:107869005 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:107936009 A>G did not map to a codon.
Sequencing variant TCGA-DU-7007-01A-11D-2024-08 chr23:107938507 A>T did not map to a codon.
Sequencing variant TCGA-E1-5319-01A-01D-1893-08 chr23:107816842 C>T did not map to a codon.
Sequencing variant TCGA-E1-A7Z6-01A-11D-A34J-08 chr23:107938634 T>C did not map to a codon.
Sequencing variant TCGA-FG-A70Z-01A-12D-A33T-08 chr23:107683419 A>T did not map to a codon.
Sequencing variant TCGA-FN-7833-01A-11D-2086-08 chr23:107821210 A>T did not map to a codon.
Sequencing variant TCGA-WY-A858-01A-11D-A36O-08 chr23:107938544 G>T did not map to a codon.
Sequencing variant TCGA-CS-5396-01A-02D-1468-08 chr23:107406178 C>T did not map to a codon.
Sequencing variant TCGA-DB-5277-01A-01D-1468-08 chr23:107454951 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:107554054 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:107436902 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:107420133 C>A did not map to a codon.
Sequencing variant TCGA-FG-5962-01B-11D-1893-08 chr23:107402953 C>T did not map to a codon.
Sequencing variant TCGA-TQ-A7RH-01A-12D-A34A-08 chr23:107417808 G>T did not map to a codon.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr9:137591839 C>T maps to NM_000093.3 N121N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YV-01A-11D-A34J-08 chr9:137712050 C>T maps to NM_000093.3 S1512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A617-01A-11D-A29Q-08 chr9:137704485 C>T maps to NM_000093.3 S1260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RK-01A-11D-A33T-08 chr9:137591839 C>T maps to NM_000093.3 N121N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:189918929 T>C maps to NM_000393.3 P800P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-7675-01A-11D-2086-08 chr2:189933562 C>T maps to NM_000393.3 G402G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65V-01A-11D-A29Q-08 chr2:189898825 G>A maps to NM_000393.3 G1490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8C8-01A-11D-A36O-08 chr19:10079132 C>T maps to NM_015719.3 P1414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5853-01A-11D-1893-08 chr21:47409673 A>G maps to NM_001848.2 K304K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:47423034 C>T maps to NM_001848.2 D812D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7300-01A-21D-2086-08 chr21:47409673 A>G maps to NM_001848.2 K304K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr21:47423449 C>T maps to NM_001848.2 D870D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:47549204 C>T maps to NM_058174.2 Q853*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:47532001 G>A maps to NM_001849.3 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6403-01A-11D-1705-08 chr2:238277602 G>A maps to NM_004369.3 D1501D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8011-01A-11D-2395-08 chr2:238249143 G>A maps to NM_004369.3 N2805N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8C8-01A-11D-A36O-08 chr2:238280789 G>A maps to NM_004369.3 S1290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CW-01A-11D-A32B-08 chr3:130188153 C>T maps to ENST00000312481 Q2436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:48609475 A>G maps to NM_000094.3 G2342G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TC-01A-21D-A34J-08 chr3:48621039 A>G maps to NM_000094.3 S1450S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:36564677 G>A maps to NM_005202.2 R202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:70944297 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:71003926 G>A maps to NM_001851.4 D213D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:40777350 C>A maps to NM_001852.3 G152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:61458646 G>A did not map to a codon.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr2:3691638 C>T maps to ENST00000418971 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VW-A8FI-01A-11D-A36O-08 chr18:346799 C>T maps to NM_130386.2 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A89Z-01A-11D-A36O-08 chr3:15520492 T>C maps to NM_005677.3 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TS-01A-12D-A33T-08 chr15:75631003 G>A maps to NM_017828.3 K53K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76R-01A-11D-A32B-08 chr8:146076588 C>T maps to NM_001081003.1 R45R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TU-01A-12D-A32B-08 chr11:36302378 C>T maps to NM_014186.3 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5849-01A-11D-1705-08 chr1:160268751 T>C maps to NM_001098398.1 L629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:160275248 G>A maps to NM_001098398.1 N556N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:139079975 C>T maps to NM_004766.2 A719A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:139092101 G>A maps to NM_004766.2 G349G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:83984280 G>A maps to ENST00000503682 Q256Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:99688569 G>T maps to NM_006833.4 E178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:6833965 C>T maps to NM_001164093.1 D48D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:84194770 C>A did not map to a codon.
Sequencing variant TCGA-WY-A85E-01A-11D-A36O-08 chr4:47605645 G>A maps to NM_006587.2 I860I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:100897183 G>A maps to NM_052820.3 Y124Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7695-01A-11D-2253-08 chr9:100897159 C>T maps to NM_052820.3 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:4412703 C>T maps to NM_024535.3 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:101489458 C>T maps to NM_078470.4 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:73931072 G>A maps to NM_173827.2 N164N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr20:30231297 T>C maps to NM_032609.2 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:85814834 G>A maps to NM_006067.4 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YH-01A-11D-A34A-08 chr2:98264495 G>A maps to NM_001862.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RP-01A-21D-A34A-08 chr19:36145572 G>A maps to ENST00000392201 W86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WQ-01A-12D-A34A-08 chr23:77160726 G>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:19548727 C>T maps to NM_014711.4 N579N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:19543862 T>C maps to NM_014711.4 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr16:19547383 G>A maps to NM_014711.4 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:130020366 G>A maps to NM_001868.2 R2R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:129909567 C>T maps to NM_001869.2 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A89Z-01A-11D-A36O-08 chr7:129962407 C>T maps to NM_016352.3 T386T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:68430255 G>A maps to NM_020361.4 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5142-01A-01D-1468-08 chr19:17039028 C>A maps to ENST00000443236 E1111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:46638872 G>A maps to NM_001872.3 R236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:28750623 A>C maps to NM_001304.4 G586G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:166414349 C>T maps to NM_001873.2 R381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F6-A8O3-01A-11D-A36O-08 chr15:83218294 A>G maps to ENST00000261723 A443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A6MO-01A-11D-A33T-08 chr4:15055830 T>C maps to NM_001177382.1 F817F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:93999627 G>T maps to NM_014912.4 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A6MO-01A-11D-A33T-08 chr5:173380276 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:75122676 G>A maps to NM_001030005.2 E153E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64O-01A-11D-A29Q-08 chr3:194062519 G>C maps to NM_001080513.2 V304V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7601-01A-11D-2086-08 chr16:57147303 C>G maps to NM_152727.5 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr8:87559940 T>C maps to NM_003909.3 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RG-01A-11D-A33T-08 chr8:87568560 C>T maps to NM_003909.3 Q496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5394-01A-01D-1468-08 chr14:24543955 C>T maps to NM_006032.2 R208R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85E-01A-11D-A36O-08 chr14:24542244 C>A maps to NM_006032.2 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TW-01A-12D-A32B-08 chr3:9754443 G>A maps to ENST00000383832 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EZ-7264-01A-11D-2024-08 chr2:211471548 C>T maps to NM_001122633.1 G698G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5965-01B-11D-1893-08 chr2:211525380 T>A did not map to a codon.
Sequencing variant TCGA-FG-A87N-01A-11D-A36O-08 chr8:145626337 G>A maps to NM_013291.2 H173H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7J3-01A-21D-A34J-08 chr2:9607903 C>T maps to NM_016207.2 Q619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:99048352 G>T maps to NM_006693.2 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:99051746 C>T maps to NM_006693.2 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:99042454 C>T maps to NM_006693.2 C49C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:69650590 C>T maps to ENST00000266679 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7601-01A-11D-2086-08 chr11:61183776 A>G maps to NM_024811.3 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7604-01A-11D-2086-08 chr11:61178543 G>A maps to NM_024811.3 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:51009824 C>T maps to NM_152245.2 A573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr22:51011380 G>C maps to NM_152245.2 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:50209544 G>A maps to NM_152359.2 E406E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr19:50203967 G>A maps to NM_152359.2 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7298-01A-11D-2024-08 chr7:29134735 C>T maps to NM_031311.3 W142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74O-01A-11D-A32B-08 chr7:29160566 T>C maps to NM_031311.3 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5140-01A-01D-1468-08 chr23:88009307 C>G did not map to a codon.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr23:88009268 T>A did not map to a codon.
Sequencing variant TCGA-QH-A6CV-01A-11D-A31L-08 chr23:88008524 A>C did not map to a codon.
Sequencing variant TCGA-RY-A83Y-01A-11D-A36O-08 chr23:88008825 A>G did not map to a codon.
Sequencing variant TCGA-DB-A4XB-01A-11D-A26M-08 chr20:2775985 G>A maps to NM_019609.4 H599H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:2774976 G>T maps to NM_019609.4 T688T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5322-01A-01D-1468-08 chr10:125526578 G>C maps to NM_198148.2 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:8616084 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:8608504 G>A maps to NM_001014447.2 A316A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A77X-01A-11D-A32B-08 chr4:8616092 C>T maps to NM_001014447.2 S457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:207753902 C>T maps to NM_000651.4 L1721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr1:207793264 G>A maps to NM_000651.4 S2369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U8-01A-21D-A33T-08 chr1:207758073 G>T maps to NM_000651.4 E1795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7489-01A-11D-2024-08 chr1:207890948 G>T maps to NM_175710.1 E519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:207640204 G>A maps to NM_001006658.2 W131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:156670686 A>C maps to NM_001878.3 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:1710038 G>A maps to NM_020825.3 P796P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8319-01A-11D-2395-08 chr16:1706071 C>T maps to NM_020825.3 D438D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:197325985 C>T maps to NM_201253.2 I338I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:197326117 C>A maps to NM_201253.2 V382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6689-01A-11D-1893-08 chr1:197390658 G>A maps to NM_201253.2 W567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:208440060 C>T maps to NM_134442.3 Q205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:35736701 G>A maps to NM_006368.4 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6396-01A-11D-1705-08 chr19:4171093 C>G maps to NM_032607.1 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YE-01A-11D-A34A-08 chr22:50320924 G>A maps to NM_001135101.1 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8106-01A-11D-2395-08 chr5:76259211 G>A maps to NM_001882.3 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr7:30695574 G>A maps to ENST00000348438 R322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:36749445 C>A maps to NM_016441.2 P806P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A845-01A-11D-A36O-08 chr2:36737264 T>C maps to NM_016441.2 Y547Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:105954545 C>T maps to NM_001311.4 C28C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr14:105945492 G>A maps to ENST00000483017 W222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:1389270 G>A maps to NM_175918.3 T324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7299-01A-21D-2024-08 chr6:49663636 A>G maps to ENST00000211238 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:84872223 C>T maps to NM_031476.3 N41N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85E-01A-11D-A36O-08 chr16:84888388 C>T maps to NM_031476.3 C221C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:21304087 G>A maps to NM_005207.3 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:18710375 G>A maps to NM_004750.4 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:1314992 G>A did not map to a codon.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr23:1321389 G>A did not map to a codon.
Sequencing variant TCGA-HT-8105-01A-11D-2395-08 chr23:1317466 G>T did not map to a codon.
Sequencing variant TCGA-VW-A7QS-01A-12D-A33T-08 chr23:1325395 G>A did not map to a codon.
Sequencing variant TCGA-HW-7495-01A-11D-2024-08 chr17:29112982 T>C maps to NM_015986.3 G342G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:159683347 G>A maps to NM_000567.2 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr10:99696062 G>A maps to NM_018058.4 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VW-A8FI-01A-11D-A36O-08 chr10:99640051 C>T maps to NM_018058.4 K591K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:122722467 C>T maps to NM_019604.2 N87N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R9-01A-11D-A289-08 chr19:18871030 C>T maps to NM_001098482.1 A309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr19:18879356 G>A maps to NM_001098482.1 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W9-A837-01A-11D-A36O-08 chr19:18888092 C>T maps to NM_001098482.1 I618I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A614-01A-11D-A29Q-08 chr1:153924629 C>A maps to NM_181715.2 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8C8-01A-11D-A36O-08 chr1:153924029 G>C maps to NM_181715.2 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A615-01A-11D-A29Q-08 chr11:45891722 C>T maps to NM_021117.3 G459G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr22:25623852 C>T maps to NM_000496.2 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76K-01A-11D-A33T-08 chr22:25599759 C>T maps to NM_004076.3 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr22:25603097 C>T maps to NM_004076.3 D185D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-8125-01A-11D-2253-08 chr3:97596596 C>T maps to ENST00000182096 Q239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:209007576 C>A maps to NM_005210.3 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:151133381 G>A maps to NM_144727.1 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:34975778 G>T maps to ENST00000416217 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A615-01A-11D-A29Q-08 chr23:151908874 G>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:115276642 G>A maps to NM_001130523.1 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:115267899 G>A maps to NM_001130523.1 S580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:115267954 C>T did not map to a codon.
Sequencing variant TCGA-TM-A84Q-01A-11D-A36O-08 chr1:115282475 T>C maps to NM_001130523.1 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:149435685 C>T maps to NM_005211.3 V819V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:149437133 C>T maps to NM_005211.3 Q718Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7T6-01A-11D-A33T-08 chr5:131409572 C>T maps to NM_000758.2 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CV-01A-11D-A31L-08 chr5:131409548 T>G maps to NM_000758.2 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:1413222 C>T did not map to a codon.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr23:1404768 A>G did not map to a codon.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr23:1409321 G>A did not map to a codon.
Sequencing variant TCGA-E1-A7YD-01A-11D-A34A-08 chr23:1422831 C>A did not map to a codon.
Sequencing variant TCGA-F6-A8O4-01A-11D-A36O-08 chr23:1409340 C>T did not map to a codon.
Sequencing variant TCGA-HT-A5RB-01A-11D-A289-08 chr23:1413342 G>A did not map to a codon.
Sequencing variant TCGA-QH-A6CZ-01A-11D-A32B-08 chr23:1413279 C>T did not map to a codon.
Sequencing variant TCGA-S9-A7R8-01A-11D-A34J-08 chr23:1407749 G>A did not map to a codon.
Sequencing variant TCGA-HT-A614-01A-11D-A29Q-08 chr17:38172559 C>T maps to NM_000759.3 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A6MO-01A-11D-A33T-08 chr1:36932095 C>T maps to NM_156039.3 W818*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:19316022 C>T maps to NM_018371.4 K255K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:43655965 G>A maps to NM_018590.3 K301K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QW-01A-11D-A34A-08 chr17:61987184 G>A maps to NM_022579.1 D185D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:2967740 C>A maps to NM_033225.5 G2183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7Z4-01A-11D-A34J-08 chr8:2910029 T>C maps to NM_033225.5 Q2538Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:34090741 G>A maps to ENST00000373381 S1763S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:34042962 G>A maps to ENST00000373381 S2463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:34052209 G>A maps to ENST00000373381 I2275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:34083158 G>A maps to ENST00000373381 G1922G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6666-01A-11D-1893-08 chr8:113697869 C>T maps to NM_198123.1 W749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64R-01A-11D-A29Q-08 chr8:113364707 A>G maps to NM_198123.1 I2064I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:113347558 G>A maps to NM_198123.1 H2388H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:113529311 A>T maps to NM_198123.1 I1569I. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DU-6392-01A-11D-1705-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DU-7015-01A-11D-2024-08 chr8:113277703 A>G maps to NM_198123.1 N3208N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7609-01A-11D-2086-08 chr8:113504736 T>C maps to NM_198123.1 R1753R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85E-01A-11D-A36O-08 chr4:71115133 C>A maps to NM_005212.2 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:1978307 G>A maps to NM_001319.6 K64K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:1980184 C>T maps to NM_001319.6 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:122950077 G>A maps to NM_001044723.1 Q452Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:469368 G>A maps to NM_177559.2 D259D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:31634613 C>T maps to ENST00000375885 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:68107747 C>T maps to ENST00000389042 Q1231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:166535948 C>T maps to ENST00000409420 R514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7692-01A-12D-2253-08 chr20:18168087 G>A maps to NM_020536.4 L778L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A87Q-01A-11D-A36O-08 chr20:23669405 C>T maps to NM_001899.2 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8C8-01A-11D-A36O-08 chr20:23667835 G>A maps to NM_001899.2 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:100081696 A>T did not map to a codon.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr23:100077400 A>T did not map to a codon.
Sequencing variant TCGA-P5-A72U-01A-31D-A32B-08 chr23:100075433 C>T did not map to a codon.
Sequencing variant TCGA-DU-7006-01A-11D-2024-08 chr23:120009415 C>A did not map to a codon.
Sequencing variant TCGA-FG-A713-01A-11D-A32B-08 chr23:120008869 C>T did not map to a codon.
Sequencing variant TCGA-S9-A6TZ-01A-21D-A32B-08 chr23:120009260 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153881750 G>A did not map to a codon.
Sequencing variant TCGA-HT-8012-01A-11D-2395-08 chr23:153881576 C>T did not map to a codon.
Sequencing variant TCGA-FG-6689-01A-11D-1893-08 chr18:19996738 G>A maps to NM_172241.2 Q346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:39771383 G>T maps to ENST00000396158 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:39790250 G>T maps to ENST00000396158 G560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7CA-01A-21D-A33T-08 chr14:39763256 C>G maps to ENST00000396158 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RV-01A-21D-A34A-08 chr10:126682515 G>A maps to NM_022802.2 G813G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:219268071 C>T maps to NM_021198.1 R197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:38022345 C>A maps to NM_001008392.1 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:138264966 G>A maps to ENST00000355078 E644E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:80801375 C>T maps to ENST00000402739 I610I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:68139105 G>A maps to NM_013266.2 S512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74J-01A-12D-A32B-08 chr3:41274829 A>G did not map to a codon.
Sequencing variant TCGA-HW-8320-01A-11D-2395-08 chr20:36431346 C>A maps to NM_030877.3 C370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:57577604 A>T maps to NM_001085458.1 R820R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:57569567 C>T maps to NM_001085458.1 D440D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QZ-01A-12D-A34J-08 chr11:57564167 T>C maps to NM_001085458.1 G220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:11364910 G>T maps to NM_001332.2 I423I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:3560040 C>T maps to NM_001031681.2 H211H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:3559989 C>T maps to NM_001031681.2 Y194Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64U-01A-11D-A29Q-08 chr23:16608917 A>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:16688715 C>A did not map to a codon.
Sequencing variant TCGA-DU-5851-01A-13D-1893-08 chr11:10783516 C>T maps to NM_014633.3 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6404-01A-11D-1705-08 chr14:25043507 G>A maps to NM_001911.2 Y179Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A845-01A-11D-A36O-08 chr14:25043624 C>T maps to NM_001911.2 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84S-01A-11D-A36O-08 chr9:99800202 G>C maps to NM_001333.2 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6666-01A-11D-1893-08 chr4:156847188 C>G maps to NM_001334.2 *322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:70275271 G>A maps to NM_001184740.1 R344R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:117424356 G>T maps to NM_033427.2 S740S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:117432639 T>A maps to NM_033427.2 K204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:112999760 A>G maps to NM_018704.2 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5142-01A-01D-1468-08 chr10:16883004 C>T maps to NM_001081.3 T3235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66G-01A-21D-A31L-08 chr10:16982103 T>C maps to NM_001081.3 G1825G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:17147574 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:17083136 C>T maps to NM_001081.3 Q1304Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:17164792 C>T did not map to a codon.
Sequencing variant TCGA-FG-8187-01A-11D-2253-08 chr10:16992024 G>A maps to NM_001081.3 G1685G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74K-01A-11D-A32B-08 chr10:16941018 T>C maps to NM_001081.3 G2858G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7CA-01A-21D-A33T-08 chr10:17110715 T>C maps to NM_001081.3 T893T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:104184301 G>A maps to NM_024040.2 D78D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:35324207 G>A maps to NM_001198778.1 Y317Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr13:113891148 T>C maps to NM_001008895.1 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6670-01A-11D-1893-08 chr23:119691895 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:119693957 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:119678007 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:119672533 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:119674286 G>T did not map to a codon.
Sequencing variant TCGA-DU-7009-01A-11D-2024-08 chr23:119708421 A>G did not map to a codon.
Sequencing variant TCGA-FG-A87N-01A-11D-A36O-08 chr23:119673127 A>G did not map to a codon.
Sequencing variant TCGA-HT-A615-01A-11D-A29Q-08 chr23:119669686 C>G did not map to a codon.
Sequencing variant TCGA-HT-A61B-01A-11D-A29Q-08 chr23:119694139 C>G did not map to a codon.
Sequencing variant TCGA-S9-A6TZ-01A-21D-A32B-08 chr23:119674328 A>T did not map to a codon.
Sequencing variant TCGA-S9-A6WM-01A-12D-A33T-08 chr23:119677612 T>A did not map to a codon.
Sequencing variant TCGA-S9-A6WN-01A-12D-A33T-08 chr23:119678006 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:43010901 G>A maps to NM_001168370.1 S1208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:43181529 C>T maps to ENST00000354495 N1856N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:43172549 C>T maps to ENST00000354495 S1468S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:101891754 C>T maps to ENST00000360264 G1328G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:101838848 C>T maps to ENST00000360264 N407N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7Z2-01A-21D-A34J-08 chr7:101459364 C>T maps to ENST00000360264 Q19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr12:111748298 C>A maps to NM_015267.3 I571I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YQ-01A-11D-A34J-08 chr12:111758083 G>A maps to NM_015267.3 A757A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr12:111729276 C>T maps to NM_015267.3 P119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A6MK-01A-11D-A32B-08 chr12:111748436 G>A maps to NM_015267.3 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A72U-01A-31D-A32B-08 chr10:124594346 G>A maps to NM_022034.4 N419N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:180851515 G>A maps to NM_020943.2 R38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7882-01A-11D-2395-08 chr2:180810176 A>G maps to NM_020943.2 N802N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RW-01A-11D-A33T-08 chr2:180810419 T>C maps to NM_020943.2 G721G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8182-01A-11D-2253-08 chr17:36958969 C>T maps to NM_017748.3 R382R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:107299982 T>C maps to NM_152434.2 K325K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76L-01A-11D-A32B-08 chr3:39307574 G>A maps to NM_001171174.1 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:18919456 G>A maps to NM_001338.3 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7T6-01A-11D-A33T-08 chr4:74735500 C>G maps to NM_001511.2 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr4:74863730 G>A maps to NM_002994.3 D108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RM-01A-11D-A33T-08 chr4:74702738 G>A maps to NM_002993.3 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YJ-01A-11D-A34A-08 chr2:219029010 G>A maps to NM_000634.2 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65X-01A-11D-A32B-08 chr2:219029664 C>T maps to NM_000634.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A89V-01A-11D-A36O-08 chr2:218999634 C>T maps to NM_001168298.1 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:70836748 C>T did not map to a codon.
Sequencing variant TCGA-HT-7695-01A-11D-2253-08 chr23:70837108 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:136872918 G>A maps to NM_001008540.1 D197D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:45988626 G>A maps to NM_006564.1 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:237489830 G>A maps to NM_020311.2 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:30577668 T>A did not map to a codon.
Sequencing variant TCGA-DU-6407-01A-13D-1705-08 chr23:30578232 T>C did not map to a codon.
Sequencing variant TCGA-DU-5847-01A-11D-1705-08 chr23:35985794 C>T did not map to a codon.
Sequencing variant TCGA-FG-8186-01A-11D-2253-08 chr23:35966454 G>A did not map to a codon.
Sequencing variant TCGA-FG-8186-01A-11D-2253-08 chr23:35993796 C>A did not map to a codon.
Sequencing variant TCGA-RY-A83Z-01A-11D-A36O-08 chr23:35959494 C>G did not map to a codon.
Sequencing variant TCGA-S9-A6WP-01A-12D-A34A-08 chr23:35985739 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:19983520 C>A did not map to a codon.
Sequencing variant TCGA-DU-6401-01A-11D-1705-08 chr23:19983582 G>T did not map to a codon.
Sequencing variant TCGA-DU-8165-01A-11D-2253-08 chr23:19955646 A>C did not map to a codon.
Sequencing variant TCGA-DU-A7T6-01A-11D-A33T-08 chr23:19953960 C>T did not map to a codon.
Sequencing variant TCGA-DB-A64W-01A-11D-A29Q-08 chr23:75397597 A>T did not map to a codon.
Sequencing variant TCGA-HW-8319-01A-11D-2395-08 chr23:75396759 C>G did not map to a codon.
Sequencing variant TCGA-E1-A7Z3-01A-11D-A34J-08 chr23:40506560 C>T did not map to a codon.
Sequencing variant TCGA-P5-A77W-01A-11D-A32B-08 chr23:40495932 G>A did not map to a codon.
Sequencing variant TCGA-TQ-A7RW-01A-11D-A33T-08 chr23:148627359 G>A did not map to a codon.
Sequencing variant TCGA-DU-5847-01A-11D-1705-08 chr23:149100913 T>A did not map to a codon.
Sequencing variant TCGA-TQ-A7RW-01A-11D-A33T-08 chr23:149101908 C>T did not map to a codon.
Sequencing variant TCGA-S9-A7R3-01A-11D-A34J-08 chr23:106459932 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:134305082 G>T did not map to a codon.
Sequencing variant TCGA-DU-8166-01A-11D-2253-08 chr23:134303694 G>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:118694316 G>T did not map to a codon.
Sequencing variant TCGA-DH-A66D-01A-11D-A31L-08 chr23:105882864 A>T did not map to a codon.
Sequencing variant TCGA-DU-5854-01A-11D-1705-08 chr23:105855369 G>A did not map to a codon.
Sequencing variant TCGA-QH-A6X8-01A-12D-A32B-08 chr23:105905387 C>T did not map to a codon.
Sequencing variant TCGA-DH-A7UR-01A-11D-A33T-08 chr23:23953454 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:23953346 C>A did not map to a codon.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr23:23956784 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:36162798 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:36090058 C>A did not map to a codon.
Sequencing variant TCGA-DU-6407-01A-13D-1705-08 chr23:36091354 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:115592987 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:70325978 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:139038580 C>T did not map to a codon.
Sequencing variant TCGA-DU-A6S8-01A-12D-A32B-08 chr23:139038427 T>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:7761607 C>T maps to NM_144607.4 Y52Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:37642786 C>T did not map to a codon.
Sequencing variant TCGA-DU-6403-01A-11D-1705-08 chr23:37660586 G>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:22958207 C>T maps to NM_014608.2 D617D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:22940757 T>C maps to NM_014608.2 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:156757834 C>T maps to ENST00000442283 L773L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A75K-01A-11D-A32B-08 chr23:83126516 A>G did not map to a codon.
Sequencing variant TCGA-DH-A66D-01A-11D-A31L-08 chr23:83129567 T>G did not map to a codon.
Sequencing variant TCGA-DU-A6S8-01A-12D-A32B-08 chr23:83128412 C>T did not map to a codon.
Sequencing variant TCGA-E1-A7YD-01A-11D-A34A-08 chr23:83129601 T>C did not map to a codon.
Sequencing variant TCGA-E1-A7YH-01A-11D-A34A-08 chr23:83127918 A>G did not map to a codon.
Sequencing variant TCGA-E1-A7YH-01A-11D-A34A-08 chr23:83128299 G>T did not map to a codon.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr23:83129575 G>T did not map to a codon.
Sequencing variant TCGA-P5-A5F4-01A-11D-A289-08 chr23:83116195 T>C did not map to a codon.
Sequencing variant TCGA-E1-A7YO-01A-11D-A34A-08 chr15:74630910 C>T did not map to a codon.
Sequencing variant TCGA-S9-A6WD-01A-12D-A33T-08 chr15:74637577 C>T maps to NM_000781.2 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:143957746 G>A maps to ENST00000377675 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:75014931 G>A maps to NM_000499.3 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5318-01A-01D-1468-08 chr15:75012967 G>C maps to NM_000499.3 V467V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XF-01A-11D-A27K-08 chr2:72361955 G>A maps to NM_019885.2 D265D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:72359682 G>A maps to NM_019885.2 P404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:219679380 G>A maps to NM_000784.3 R459R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:127944963 C>A did not map to a codon.
Sequencing variant TCGA-F6-A8O3-01A-11D-A36O-08 chr10:96480295 T>C did not map to a codon.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr10:96535296 G>C did not map to a codon.
Sequencing variant TCGA-DU-8161-01A-11D-2253-08 chr10:96818193 A>G maps to NM_000770.3 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YL-01A-11D-A34A-08 chr10:96824642 G>A maps to NM_000770.3 R186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:42523853 C>T maps to NM_000106.4 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YN-01A-11D-A34A-08 chr7:99367746 C>A maps to NM_017460.3 E144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6X4-01A-51D-A32B-08 chr7:99453217 C>T maps to NM_022820.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr7:99250312 T>C maps to NM_000777.3 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:100166438 G>A did not map to a codon.
Sequencing variant TCGA-DB-A75L-01A-11D-A32B-08 chr1:47603304 C>T maps to NM_001010969.2 Q50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:47603165 C>A maps to NM_001010969.2 V3V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84J-01A-11D-A36O-08 chr1:47608993 C>T maps to NM_001010969.2 H188H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:47283691 C>T maps to NM_001099772.1 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7873-01B-11D-2395-08 chr1:47279203 C>T maps to NM_001099772.1 C182C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A77X-01A-11D-A32B-08 chr19:16040276 G>A maps to NM_021187.3 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8162-01A-21D-2253-08 chr19:15791262 C>T maps to NM_023944.2 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8013-01A-11D-2395-08 chr19:16006352 G>A maps to NM_001082.3 C102C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U0-01A-12D-A32B-08 chr19:16006352 G>A maps to NM_001082.3 C102C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:47548007 C>T maps to NM_178134.2 R123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7J0-01A-11D-A34A-08 chr7:91747892 C>A maps to NM_000786.3 E375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr8:59409692 G>A maps to NM_000780.3 N126N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:65528284 C>A maps to NM_004820.3 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WH-A86K-01A-11D-A36O-08 chr8:65527679 G>A maps to NM_004820.3 D320D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:77528396 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:77528524 G>A did not map to a codon.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr23:77528953 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:49281517 G>T maps to NM_020377.2 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7858-01A-11D-2395-08 chr17:76694916 C>T maps to NM_004762.2 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:158300427 C>T maps to NM_004288.4 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6408-01A-11D-1705-08 chr17:20135589 G>A maps to NM_001033553.1 E741E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:59730236 C>A maps to NM_014992.1 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A713-01A-11D-A32B-08 chr14:59797961 G>A maps to NM_014992.1 S532S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QZ-01A-12D-A34J-08 chr14:59798009 C>A maps to NM_014992.1 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YD-01A-11D-A34A-08 chr6:39828774 C>A maps to ENST00000398904 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YI-01A-11D-A34A-08 chr6:39828702 G>A did not map to a codon.
Sequencing variant TCGA-CS-5397-01A-01D-1893-08 chr1:57756660 G>A maps to ENST00000371231 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7US-01A-11D-A33T-08 chr9:124528874 C>G maps to ENST00000408936 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:124522546 C>T maps to ENST00000408936 R333R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:124525894 C>T maps to ENST00000408936 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:85769295 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:85403937 G>A did not map to a codon.
Sequencing variant TCGA-P5-A781-01A-11D-A32B-08 chr23:85906100 A>G did not map to a codon.
Sequencing variant TCGA-QH-A6X8-01A-12D-A32B-08 chr23:86069791 C>G did not map to a codon.
Sequencing variant TCGA-RY-A83X-01A-11D-A36O-08 chr23:85404018 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:59113638 C>T maps to NM_016651.5 F766F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:59112615 C>T maps to NM_016651.5 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:6452453 G>A maps to NM_139179.3 C519C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8C8-01A-11D-A36O-08 chr11:61110296 C>T maps to NM_015533.3 D282D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7487-01A-11D-2024-08 chr12:109294235 C>T maps to NM_001917.4 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:90313592 C>T maps to NM_004938.2 N878N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:90272949 C>T maps to NM_004938.2 R611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TI-01A-11D-A33T-08 chr9:90322026 C>T maps to NM_004938.2 N1347N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RI-01A-11D-A33T-08 chr9:90283583 C>T maps to NM_004938.2 R666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-8125-01A-11D-2253-08 chr19:3964721 C>T maps to NM_001348.1 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7304-01A-12D-2086-08 chr2:159660848 A>G maps to NM_001017920.2 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7854-01A-11D-2253-08 chr6:33287899 C>T maps to NM_001350.4 E451E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:1422372 C>T maps to NM_018959.2 D147D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:121976431 A>G maps to NM_014618.2 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:121930123 G>A maps to NM_014618.2 N508N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7J0-01A-11D-A34A-08 chr9:121929631 T>C maps to NM_014618.2 A672A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:136505009 C>T maps to NM_000787.3 Q128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7007-01A-11D-2024-08 chr9:136501813 G>A maps to NM_000787.3 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:37857347 G>T maps to NM_024345.3 G389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:24588927 C>A maps to NM_025230.4 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5847-01A-11D-1705-08 chr23:125685929 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:125685395 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:125685777 C>T did not map to a codon.
Sequencing variant TCGA-DU-8158-01A-11D-2253-08 chr23:125686451 G>A did not map to a codon.
Sequencing variant TCGA-HT-A5RC-01A-11D-A289-08 chr23:125686252 G>A did not map to a codon.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr23:125299119 C>T did not map to a codon.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr23:125298903 C>G did not map to a codon.
Sequencing variant TCGA-E1-A7YQ-01A-11D-A34J-08 chr23:125299246 G>A did not map to a codon.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr23:125299119 C>T did not map to a codon.
Sequencing variant TCGA-HW-A5KL-01A-11D-A27K-08 chr23:125299671 G>A did not map to a codon.
Sequencing variant TCGA-S9-A6U0-01A-12D-A32B-08 chr23:125299211 G>T did not map to a codon.
Sequencing variant TCGA-S9-A7IZ-01A-11D-A34A-08 chr23:125298905 C>T did not map to a codon.
Sequencing variant TCGA-S9-A7R8-01A-11D-A34J-08 chr23:125298549 C>T did not map to a codon.
Sequencing variant TCGA-TM-A84H-01A-11D-A36O-08 chr23:125299815 G>A did not map to a codon.
Sequencing variant TCGA-TQ-A7RJ-01A-11D-A33T-08 chr23:125299761 C>T did not map to a codon.
Sequencing variant TCGA-TQ-A7RP-01A-21D-A34A-08 chr23:125298842 C>T did not map to a codon.
Sequencing variant TCGA-WY-A85E-01A-11D-A36O-08 chr23:125299772 C>T did not map to a codon.
Sequencing variant TCGA-HT-7616-01A-11D-2253-08 chr2:172337524 A>C maps to NM_025000.3 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:41984210 G>A maps to NM_001029955.3 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7011-01A-11D-2024-08 chr4:41984363 C>A maps to NM_001029955.3 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64Q-01A-11D-A29Q-08 chr1:167956740 T>C maps to ENST00000367840 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6667-01A-12D-2024-08 chr23:27999087 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:27998290 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:27998473 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:27999352 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:27997793 C>T did not map to a codon.
Sequencing variant TCGA-DU-6400-01A-12D-1705-08 chr23:27998599 C>A did not map to a codon.
Sequencing variant TCGA-DU-A6S8-01A-12D-A32B-08 chr23:27998105 C>A did not map to a codon.
Sequencing variant TCGA-DU-A7T6-01A-11D-A33T-08 chr23:27998065 G>C did not map to a codon.
Sequencing variant TCGA-E1-A7YH-01A-11D-A34A-08 chr23:27998603 G>A did not map to a codon.
Sequencing variant TCGA-E1-A7YQ-01A-11D-A34J-08 chr23:27998162 C>G did not map to a codon.
Sequencing variant TCGA-S9-A7QY-01A-11D-A34A-08 chr23:27998609 C>T did not map to a codon.
Sequencing variant TCGA-QH-A6XC-01A-12D-A32B-08 chr23:27765734 C>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:98600528 G>A maps to ENST00000326857 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IS-01A-11D-A34A-08 chr11:31312191 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:6643930 C>T maps to NM_003737.2 E2992E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TZ-01A-21D-A32B-08 chr11:6650969 G>A maps to NM_003737.2 V1656V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:155219765 G>T maps to NM_017639.3 T1445T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr4:155287389 C>T maps to NM_017639.3 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr4:155254332 C>A maps to NM_017639.3 G510G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7605-01A-11D-2086-08 chr4:155163899 T>C maps to NM_017639.3 K1867K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr4:155176789 G>A maps to NM_017639.3 N1819N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr4:155287389 C>T maps to NM_017639.3 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6XC-01A-12D-A32B-08 chr4:155176690 G>A maps to NM_017639.3 Y1852Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WQ-01A-12D-A34A-08 chr4:155176789 G>A maps to NM_017639.3 N1819N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:36362371 C>T maps to NM_004734.4 Q703Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8106-01A-11D-2395-08 chr4:151153980 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:115594911 C>A maps to NM_014881.3 *1041L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RH-01A-12D-A34A-08 chr10:115609944 C>A maps to NM_014881.3 E307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr12:91546925 G>A maps to NM_133503.2 N231N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5853-01A-11D-1893-08 chr1:155013045 C>T maps to NM_152494.3 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:155005151 T>A maps to NM_144622.2 K178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84J-01A-11D-A36O-08 chr1:155004068 C>T maps to NM_144622.2 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RO-01A-11D-A33T-08 chr13:95121240 G>A maps to NM_001129889.1 C118C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:183814218 C>T maps to NM_001012732.1 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:74595113 G>A maps to NM_004082.4 L667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7875-01A-11D-2395-08 chr12:57928085 G>A maps to ENST00000434715 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:182683486 G>A maps to NM_020640.2 Q20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:114135035 A>G maps to NM_001014283.1 I81I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:52729855 C>T maps to ENST00000451288 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KT-A7W1-01A-11D-A34A-08 chr11:102937265 T>C maps to NM_032299.3 K124K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:110653598 C>T did not map to a codon.
Sequencing variant TCGA-DU-A7T6-01A-11D-A33T-08 chr23:110644390 G>A did not map to a codon.
Sequencing variant TCGA-DU-5849-01A-11D-1705-08 chr19:17425149 C>T maps to NM_024050.5 R30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:31696256 C>A maps to NM_013974.1 G148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:50530955 G>A maps to NM_000790.3 A472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:50530982 G>T maps to NM_000790.3 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:38099826 G>T maps to NM_001164232.1 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YN-01A-11D-A34A-08 chr11:103908726 C>T maps to NM_001001711.2 R393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5322-01A-01D-1468-08 chr1:15956988 G>A maps to NM_032341.4 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:30860314 C>T maps to NM_013994.2 I365I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr1:162746048 C>A maps to NM_006182.2 I724I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:3171367 G>A maps to NM_023935.1 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6J3-01A-11D-A31L-08 chr22:24313559 T>C maps to NM_001084393.1 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YE-01A-11D-A34A-08 chr11:108577516 T>A maps to NM_004398.2 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5396-01A-02D-1468-08 chr12:31236925 T>C maps to NM_030653.3 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:31236769 T>C maps to NM_030653.3 C56C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:31244759 C>T maps to NM_030653.3 I399I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:31255887 C>T maps to NM_030653.3 G797G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5319-01A-01D-1893-08 chr12:31244795 C>T maps to NM_030653.3 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:118577330 T>C maps to NM_006773.3 D159D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A669-01A-12D-A31L-08 chr16:70400655 T>C maps to NM_018332.3 D304D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr16:70400562 C>T maps to NM_018332.3 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KT-A7W1-01A-11D-A34A-08 chr16:70404223 G>A maps to NM_018332.3 A373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A669-01A-12D-A31L-08 chr16:70363826 C>T maps to NM_007242.4 N293N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:70349947 C>T maps to NM_007242.4 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:70738644 T>C maps to NM_004728.2 I650I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:49224260 G>T maps to NM_004818.2 I818I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:94528947 G>T maps to NM_020414.3 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6186-01A-12D-2024-08 chr23:134706885 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:134711349 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:134711195 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:134681060 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:134707897 A>G did not map to a codon.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr23:134709029 T>A did not map to a codon.
Sequencing variant TCGA-DU-8158-01A-11D-2253-08 chr23:134711344 A>G did not map to a codon.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr23:134715063 G>A did not map to a codon.
Sequencing variant TCGA-S9-A7QY-01A-11D-A34A-08 chr23:134707957 C>T did not map to a codon.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr23:41204457 C>T did not map to a codon.
Sequencing variant TCGA-FG-8186-01A-11D-2253-08 chr23:41202024 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:55086458 C>T maps to NM_024415.2 R410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A730-01A-11D-A32B-08 chr5:176940446 C>T maps to NM_016222.2 P379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr17:61864441 G>A maps to NM_203499.1 K11K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:74104639 C>T maps to NM_018665.2 H4H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:134109456 G>A maps to ENST00000452510 E173E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7676-01A-11D-2395-08 chr12:132624719 C>T maps to NM_175066.3 A566A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8105-01A-11D-2395-08 chr12:132626152 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:35986131 A>G maps to NM_007010.3 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:23018281 C>T did not map to a codon.
Sequencing variant TCGA-P5-A731-01A-11D-A32B-08 chr12:113614882 A>G maps to NM_001111322.1 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85D-01A-11D-A36O-08 chr12:113599732 G>A maps to NM_001111322.1 S755S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:124094551 G>A maps to NM_020936.1 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R1-01A-12D-A34J-08 chr7:44613433 C>T did not map to a codon.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr11:686995 G>A maps to NM_021008.2 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:91033201 G>A maps to NM_001359.1 W161*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DU-6392-01A-11D-1705-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:461020 C>T maps to NM_020664.3 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:35278291 G>A maps to NM_022047.3 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:90025468 C>T maps to NM_207514.1 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:6794286 G>T maps to NM_001925.1 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6666-01A-11D-1893-08 chr20:29956512 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:100615991 C>T maps to NM_206918.2 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7014-01A-11D-2024-08 chr6:18249992 A>C maps to NM_003472.3 A217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:126146101 G>A maps to NM_020946.1 G556G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:126520031 G>A maps to NM_020946.1 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:126371737 C>A maps to NM_020946.1 G248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6400-01A-12D-1705-08 chr9:126319962 C>T maps to NM_020946.1 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:140287480 C>T maps to NM_015689.3 S365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:140244524 G>A maps to NM_015689.3 H740H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:115166214 G>A maps to ENST00000393274 Q286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:115153702 G>A maps to ENST00000393274 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CW-01A-11D-A32B-08 chr1:115137091 A>T did not map to a codon.
Sequencing variant TCGA-TM-A84J-01A-11D-A36O-08 chr1:115130508 A>G maps to ENST00000393274 H832H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:142176403 C>T maps to NM_014957.2 Q477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A781-01A-11D-A32B-08 chr8:142185446 C>T maps to NM_014957.2 S728S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W9-A837-01A-11D-A36O-08 chr8:142178541 C>T maps to NM_014957.2 G651G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:66031163 C>T maps to ENST00000443035 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:153909041 G>A maps to NM_014856.2 S805S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr1:153907308 C>T maps to NM_014856.2 Q900Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8186-01A-11D-2253-08 chr1:153907308 C>T maps to NM_014856.2 Q900Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A711-01A-21D-A33T-08 chr1:153907308 C>T maps to NM_014856.2 Q900Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A77W-01A-11D-A32B-08 chr1:153907308 C>T maps to NM_014856.2 Q900Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TV-01A-12D-A34J-08 chr1:153907308 C>T maps to NM_014856.2 Q900Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RJ-01A-11D-A33T-08 chr1:153907308 C>T maps to NM_014856.2 Q900Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RQ-01A-11D-A33T-08 chr1:153907308 C>T maps to NM_014856.2 Q900Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:9164958 A>G maps to NM_015213.2 P1126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr12:31605200 G>A maps to NM_144973.3 N434N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QY-01A-11D-A34A-08 chr12:31632835 C>T maps to NM_144973.3 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XF-01A-11D-A27K-08 chr12:100656177 A>C maps to ENST00000422147 Y188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5270-01A-02D-1468-08 chr22:32293559 C>T maps to NM_001136029.1 G1423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:32242866 G>A maps to NM_001136029.1 T1014T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8563-01A-11D-2395-08 chr22:24179852 G>A maps to NM_001135751.1 D172D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:3782427 G>A maps to ENST00000430539 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YV-01A-11D-A34J-08 chr7:24784275 C>A maps to NM_001127453.1 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7607-01A-11D-2086-08 chr7:24789216 G>A maps to NM_001127453.1 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:117169037 G>T maps to NM_015404.3 S611S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65R-01A-21D-A31L-08 chr9:117266883 G>A maps to NM_015404.3 H66H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:145540575 G>A maps to NM_012079.4 Y417Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr8:145541794 C>T maps to NM_012079.4 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8165-01A-11D-2253-08 chr23:69421804 G>A did not map to a codon.
Sequencing variant TCGA-FG-5965-01B-11D-1893-08 chr23:69424363 T>A did not map to a codon.
Sequencing variant TCGA-VW-A7QS-01A-12D-A33T-08 chr23:69424319 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:19122583 C>T maps to NM_022719.2 E380E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8319-01A-11D-2395-08 chr22:19026632 G>A maps to NM_005137.2 D466D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:56335064 T>C maps to NM_201554.1 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:14797356 C>T did not map to a codon.
Sequencing variant TCGA-CS-4942-01A-01D-1468-08 chr13:42763201 C>T maps to NM_178009.2 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:50119029 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:50144081 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:50125502 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:50144082 G>A did not map to a codon.
Sequencing variant TCGA-E1-5319-01A-01D-1893-08 chr23:50213437 T>C did not map to a codon.
Sequencing variant TCGA-HT-7874-01A-11D-2395-08 chr23:50127814 A>C did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr23:50147115 G>A did not map to a codon.
Sequencing variant TCGA-TQ-A7RJ-01A-11D-A33T-08 chr23:50136277 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:55319718 G>A maps to NM_014762.3 N403N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:55337187 G>A maps to NM_014762.3 Y237Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr1:55337127 G>A maps to NM_014762.3 H257H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74J-01A-12D-A32B-08 chr11:71152481 A>C maps to NM_001360.2 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:24464263 C>T maps to NM_198083.3 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:9674948 G>A maps to ENST00000330255 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F4-01A-11D-A289-08 chr23:2161262 T>C did not map to a codon.
Sequencing variant TCGA-KT-A74X-01A-11D-A32B-08 chr10:12131002 C>T maps to NM_018706.5 R246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:54579474 T>C maps to NM_019030.2 Q507Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7686-01A-11D-2253-08 chr5:54577280 G>C maps to NM_019030.2 L676L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:47889409 G>A maps to NM_138615.2 G750G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr3:47891360 C>T maps to NM_138615.2 D1112D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:47865950 G>A did not map to a codon.
Sequencing variant TCGA-S9-A6UB-01A-21D-A33T-08 chr19:47883202 C>T maps to NM_014681.5 A981A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7620-01A-11D-2253-08 chr20:37634880 C>T maps to NM_021931.3 Y368Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A75L-01A-11D-A32B-08 chr3:154032921 T>C maps to NM_020865.2 Q172Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:72141253 C>T maps to NM_014003.3 S872S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:72130082 G>A maps to NM_014003.3 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr16:72133710 C>T maps to NM_014003.3 Y347Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:39053083 G>A maps to NM_198963.1 C973C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:41568555 G>T maps to NM_004941.1 E111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:140967805 C>T maps to ENST00000398557 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5143-01A-01D-1468-08 chr23:96639007 A>T did not map to a codon.
Sequencing variant TCGA-FG-A6J3-01A-11D-A31L-08 chr23:96173533 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:95577791 G>A maps to NM_177438.2 G706G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64R-01A-11D-A29Q-08 chr20:61527923 C>T maps to NM_033081.2 R671R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7884-01B-11D-2395-08 chr20:61511991 C>T maps to NM_033081.2 P1772P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5277-01A-01D-1468-08 chr21:47978200 T>C maps to ENST00000318711 I1289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:47969686 C>T maps to ENST00000318711 I843I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6410-01A-11D-1893-08 chr21:47952056 G>T maps to ENST00000318711 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr21:47916994 G>A maps to ENST00000318711 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IZ-01A-11D-A34A-08 chr21:47918600 C>T maps to ENST00000318711 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:51126252 C>T maps to NM_173602.2 I1305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:51097979 G>T maps to NM_173602.2 G795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76K-01A-11D-A33T-08 chr12:51138417 C>T maps to NM_173602.2 C1509C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:465044 C>T maps to NM_014974.2 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:429982 C>T maps to NM_014974.2 A620A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:323450 G>T maps to NM_014974.2 A1495A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:486832 C>T maps to NM_014974.2 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A72Z-01A-11D-A32B-08 chr10:518417 G>A maps to NM_014974.2 R77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:2717756 G>A maps to NM_145173.3 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QZ-01A-12D-A34J-08 chr3:122578990 A>G maps to NM_032839.2 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:233199424 C>T maps to NM_152383.4 Q792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74K-01A-11D-A32B-08 chr1:223178728 G>A maps to NM_032890.2 T1330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RO-01A-11D-A33T-08 chr15:40655852 G>A maps to NM_033510.1 E49E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153993730 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153994249 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:154004498 C>A did not map to a codon.
Sequencing variant TCGA-FG-A60L-01A-12D-A31L-08 chr23:153994500 A>C did not map to a codon.
Sequencing variant TCGA-P5-A72U-01A-31D-A32B-08 chr4:107845810 C>T maps to NM_014421.2 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr8:12946018 A>C maps to NM_182643.2 P1423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7607-01A-11D-2086-08 chr8:12957909 G>A maps to NM_182643.2 L646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CY-01A-11D-A32B-08 chr8:13357010 G>A maps to NM_182643.2 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8163-01A-11D-2253-08 chr3:196812551 G>A maps to NM_004087.2 I612I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7008-01A-11D-2024-08 chr11:83676478 G>A maps to NM_001142699.1 H363H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5144-01A-01D-1468-08 chr23:69670625 C>T did not map to a codon.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr23:69717041 C>G did not map to a codon.
Sequencing variant TCGA-HT-A615-01A-11D-A29Q-08 chr23:69669654 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:7100195 C>T maps to NM_001365.3 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:79628941 G>A maps to NM_004747.3 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:79603265 G>A maps to NM_004747.3 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6395-01A-12D-1705-08 chr18:3879576 G>A maps to NM_004746.2 N164N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7609-01A-11D-2086-08 chr8:1626415 C>T maps to ENST00000357934 A717A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7US-01A-11D-A33T-08 chr20:35060260 C>A maps to ENST00000339266 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TD-01A-12D-A34A-08 chr14:101201220 C>T maps to NM_003836.5 D380D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CU-01A-11D-A31L-08 chr14:101200587 C>T maps to NM_003836.5 I169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5ET-01A-11D-A27K-08 chr6:170594118 A>C maps to NM_005618.3 G379G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:41228900 G>A maps to NM_019074.3 S572S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:96639118 G>A maps to NM_005222.3 W214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:124336137 G>A maps to ENST00000368915 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A72U-01A-31D-A32B-08 chr10:124392719 C>T maps to ENST00000368915 C2137C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WI-01A-21D-A33T-08 chr10:124333278 G>A did not map to a codon.
Sequencing variant TCGA-FG-8187-01A-11D-2253-08 chr1:46977832 G>A maps to NM_147192.2 Q272Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5397-01A-01D-1893-08 chr23:31747755 G>A did not map to a codon.
Sequencing variant TCGA-DB-A75K-01A-11D-A32B-08 chr23:31241161 A>T did not map to a codon.
Sequencing variant TCGA-DB-A75L-01A-11D-A32B-08 chr23:31947767 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:31986617 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:32456420 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:31196870 A>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:31645872 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:32382808 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:32429868 C>A did not map to a codon.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr23:32380908 C>T did not map to a codon.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr23:32867884 C>T did not map to a codon.
Sequencing variant TCGA-DU-A7T6-01A-11D-A33T-08 chr23:31854864 G>C did not map to a codon.
Sequencing variant TCGA-FG-A4MY-01A-11D-A26M-08 chr23:32456487 C>T did not map to a codon.
Sequencing variant TCGA-HT-A5R5-01A-11D-A289-08 chr23:31747793 T>C did not map to a codon.
Sequencing variant TCGA-KT-A7W1-01A-11D-A34A-08 chr23:32834681 G>A did not map to a codon.
Sequencing variant TCGA-S9-A7QW-01A-11D-A34A-08 chr23:32456372 C>T did not map to a codon.
Sequencing variant TCGA-TM-A84H-01A-11D-A36O-08 chr23:32459326 G>A did not map to a codon.
Sequencing variant TCGA-DU-8158-01A-11D-2253-08 chr5:78359456 C>A maps to NM_013391.2 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7294-01A-11D-2024-08 chr19:46275946 G>A maps to NM_004409.3 H432H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr9:1056822 C>T maps to NM_181872.4 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7616-01A-11D-2253-08 chr9:977180 C>G maps to NM_021240.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5141-01A-01D-1468-08 chr19:42353196 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:118484953 G>A maps to NM_005509.4 W1144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:52434365 T>C maps to ENST00000273600 S4298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:52417475 G>A maps to ENST00000273600 A2672A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr3:52420204 G>A maps to ENST00000273600 R2885R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YS-01A-11D-A34A-08 chr3:52420321 G>A maps to ENST00000273600 L2924L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr3:52380762 C>T maps to ENST00000273600 D644D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr3:52407043 C>T maps to ENST00000273600 G2320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CZ-01A-11D-A32B-08 chr3:52397072 C>G maps to ENST00000273600 L1719L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:124285902 G>A maps to NM_207437.3 V728V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7007-01A-11D-2024-08 chr12:124332563 C>T maps to NM_207437.3 T1839T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7019-01A-11D-2024-08 chr12:124335565 C>T maps to NM_207437.3 P1960P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76O-01A-11D-A32B-08 chr12:124267720 G>A maps to NM_207437.3 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7634-01A-11D-2086-08 chr12:124358199 C>T maps to NM_207437.3 Y2509Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:21789967 C>T maps to NM_003777.3 R2983*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:21654887 C>T maps to NM_003777.3 R1337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr7:21721267 C>T maps to NM_003777.3 D1816D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7495-01A-11D-2024-08 chr7:21639634 G>A maps to NM_003777.3 G966G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U0-01A-12D-A32B-08 chr7:21640403 C>T maps to NM_003777.3 H1037H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:76482146 C>T maps to ENST00000389840 S2376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:76548827 A>G maps to ENST00000389840 I746I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:76455115 T>C maps to ENST00000389840 Q3262Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YJ-01A-11D-A34A-08 chr17:76503839 G>A maps to ENST00000389840 H1424H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A6YH-01A-21D-A32B-08 chr17:76533485 C>T maps to ENST00000389840 V918V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A89Z-01A-11D-A36O-08 chr17:76497399 C>T maps to ENST00000389840 W1769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84H-01A-11D-A36O-08 chr17:76464784 G>A maps to ENST00000389840 R2884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr17:7643863 C>T maps to NM_020877.2 R501R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:7671222 C>T maps to NM_020877.2 L1227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:7643818 G>T maps to NM_020877.2 P486P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:7662913 G>T maps to NM_020877.2 G875*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7605-01A-11D-2086-08 chr17:7708391 G>A maps to NM_020877.2 R3100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr17:7637983 G>A maps to NM_020877.2 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:20955877 C>A maps to NM_017539.1 L3817L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:20975278 C>T maps to NM_017539.1 S3309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7309-01A-11D-2086-08 chr16:20990738 C>T maps to NM_017539.1 T2663T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr16:21049262 C>T maps to NM_017539.1 S1590S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TX-01A-21D-A32B-08 chr16:21145635 C>T maps to NM_017539.1 E342E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5390-01A-02D-1468-08 chr5:13841809 G>A maps to NM_001369.2 F1825F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5849-01A-11D-1705-08 chr5:13736039 C>G maps to NM_001369.2 V3819V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:13891147 C>T maps to NM_001369.2 T838T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5305-01A-01D-1893-08 chr5:13751312 G>T maps to NM_001369.2 T3695T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8109-01A-11D-2395-08 chr5:13919349 A>G maps to NM_001369.2 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A89Z-01A-11D-A36O-08 chr5:13758952 A>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:84804520 C>T maps to NM_001370.1 R689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F0-01A-11D-A289-08 chr2:84784901 T>G maps to NM_001370.1 L549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A75K-01A-11D-A32B-08 chr2:196756528 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:196729637 C>T maps to NM_018897.2 E2247E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:196728881 G>A maps to NM_018897.2 D2499D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:196674468 C>T maps to NM_018897.2 A3296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76R-01A-11D-A32B-08 chr2:196728872 C>T maps to NM_018897.2 Q2502Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RU-01A-21D-A34A-08 chr2:196619148 G>A maps to NM_018897.2 Y3892Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5390-01A-02D-1468-08 chr6:38980112 G>A maps to ENST00000327475 L4486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:38705718 C>T maps to ENST00000327475 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:38905957 G>A maps to ENST00000327475 T3912T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6395-01A-12D-1705-08 chr6:38893889 T>A maps to ENST00000327475 I3662I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RQ-01A-11D-A33T-08 chr6:38891793 G>A maps to ENST00000327475 T3594T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:11790176 C>T maps to NM_001372.3 N3669N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7T6-01A-11D-A33T-08 chr17:11607665 C>T maps to NM_001372.3 G1766G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YN-01A-11D-A34A-08 chr17:11573025 C>T maps to NM_001372.3 R1090*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7641-01B-11D-2253-08 chr17:11671915 C>T maps to NM_001372.3 F2439F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8189-01B-11D-A289-08 chr17:11835359 G>A maps to NM_001372.3 T4045T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr17:11660880 G>A maps to NM_001372.3 P2289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:34514423 C>T maps to NM_012144.2 D534D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:34996466 C>T maps to NM_001135005.1 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5849-01A-11D-1705-08 chr22:41257197 C>T maps to NM_145174.1 E267E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:41257828 G>T maps to NM_145174.1 S57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8563-01A-11D-2395-08 chr2:183593667 C>T maps to NM_018981.1 R194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:6700035 G>A maps to NM_018198.3 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr1:6697341 G>A maps to NM_018198.3 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:180705836 G>A maps to NM_145261.3 Q35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:65845090 G>T maps to ENST00000371069 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:65855118 G>A maps to ENST00000371069 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8182-01A-11D-2253-08 chr1:65858363 T>G maps to ENST00000371069 A573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74K-01A-11D-A32B-08 chr1:65871610 G>A maps to ENST00000371069 P762P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr17:40133942 G>A maps to NM_003315.3 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A75K-01A-11D-A32B-08 chr23:153631306 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:84878086 C>A maps to NM_021233.2 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TY-01A-12D-A32B-08 chr2:230453156 C>T maps to NM_139072.3 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:6541319 C>A maps to NM_144666.2 T591T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:6587818 C>T maps to NM_144666.2 L3737L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:6524150 C>T maps to NM_144666.2 Y305Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:32854483 G>T maps to ENST00000381000 G80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WE-01A-12D-A33T-08 chr12:32884345 G>A maps to ENST00000381000 R432R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:10886448 C>T maps to NM_001005361.2 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:10904444 G>T maps to NM_001005361.2 G348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:10939812 C>T maps to NM_001005361.2 D720D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:101646232 C>A maps to ENST00000342239 E1172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:10265643 A>G maps to NM_001130823.1 I527I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:10277309 G>A maps to NM_001130823.1 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:10270409 G>A maps to NM_001130823.1 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:10265688 C>T maps to NM_001130823.1 A512A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8321-01A-11D-2395-08 chr2:25457208 C>T maps to NM_175629.1 W893*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65X-01A-11D-A32B-08 chr2:25497831 C>T maps to NM_175629.1 W206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RJ-01A-11D-A33T-08 chr2:25467116 G>A maps to NM_175629.1 C586C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WH-A86K-01A-11D-A36O-08 chr2:25470555 C>T maps to NM_175629.1 W306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:31395664 C>T maps to NM_006892.3 R840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr20:31368260 G>A maps to NM_006892.3 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:129245736 T>C maps to ENST00000398025 D1876D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:128850977 C>T maps to ENST00000398025 D724D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66G-01A-21D-A31L-08 chr23:117700015 T>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:117718714 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:117752684 G>A did not map to a codon.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr23:117773443 T>A did not map to a codon.
Sequencing variant TCGA-HT-8012-01A-11D-2395-08 chr23:117752577 C>A did not map to a codon.
Sequencing variant TCGA-HW-8320-01A-11D-2395-08 chr23:117695459 G>A did not map to a codon.
Sequencing variant TCGA-P5-A77W-01A-11D-A32B-08 chr23:117744240 C>T did not map to a codon.
Sequencing variant TCGA-S9-A7R2-01A-21D-A34J-08 chr23:117739299 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:169141090 C>T maps to NM_004946.2 H573H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A870-01A-11D-A36O-08 chr5:169116336 G>A maps to NM_004946.2 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WP-01A-12D-A34A-08 chr5:169111327 C>T maps to NM_004946.2 Y245Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:51264829 C>T maps to NM_004947.4 D498D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:51127791 C>T maps to NM_004947.4 D241D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:111617248 G>A maps to ENST00000428084 N213N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6405-01A-11D-1705-08 chr8:25216577 G>A did not map to a codon.
Multiple mappings detected for codon TCGA-FG-A60K-01A-11D-A29Q-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr19:11347157 G>A maps to ENST00000319867 N752N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RK-01A-11D-A33T-08 chr19:11346349 G>T maps to ENST00000319867 R826R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:63128775 G>A maps to ENST00000371140 Q22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7301-01A-11D-2086-08 chr1:62995073 A>G maps to ENST00000371140 L1219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:328086 G>A maps to NM_203447.3 T320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:379792 C>T maps to NM_203447.3 F821F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YM-01A-11D-A34A-08 chr9:325673 C>T maps to NM_203447.3 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7495-01A-11D-2024-08 chr9:289508 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:99457447 G>A maps to ENST00000428223 L1858L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RM-01A-11D-A33T-08 chr13:99532923 G>A maps to ENST00000428223 Y916Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:176931112 C>T maps to NM_024872.2 R454R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QY-01A-11D-A34A-08 chr18:67406222 C>T maps to NM_152721.5 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7Z6-01A-11D-A34J-08 chr9:131708673 A>G maps to NM_014908.3 Y303Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7470-01A-12D-2086-08 chr6:83839855 C>T maps to NM_015018.2 Q786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:37583874 T>C maps to NM_005128.2 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:37618054 C>T maps to NM_005128.2 I1259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:2216347 G>A maps to ENST00000221482 P664P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:2216560 G>A maps to ENST00000221482 T735T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:118971439 G>T maps to NM_001382.3 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr16:68026418 G>A maps to NM_022355.2 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:38713066 G>A maps to NM_001135155.1 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:44437629 T>C maps to NM_001384.4 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:49562424 C>A maps to ENST00000449701 G111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7882-01A-11D-2395-08 chr2:116497432 G>A maps to NM_020868.3 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr11:66276619 C>T maps to NM_005700.3 F704F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:162903927 A>G maps to NM_001935.3 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:65739320 G>A maps to NM_197960.2 S866S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:4714096 G>A maps to ENST00000357909 Y182Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:4697660 G>A maps to ENST00000357909 I438I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr12:7867928 G>A maps to NM_199286.2 W78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8321-01A-11D-2395-08 chr12:7867803 G>A maps to NM_199286.2 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr7:34978934 T>A maps to NM_015283.1 A566A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EZ-7264-01A-11D-2024-08 chr12:63994084 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:98186448 A>G maps to NM_001160301.1 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5143-01A-01D-1468-08 chr8:105459568 C>A maps to NM_001385.2 G196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5144-01A-01D-1468-08 chr8:26484190 C>T maps to NM_001197293.1 C284C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:134015523 C>A maps to NM_006426.2 Y395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:134013929 C>T maps to NM_006426.2 N294N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YK-01A-11D-A34A-08 chr1:111674062 C>T maps to NM_178454.4 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:113890728 G>A maps to NM_000796.3 C37C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:9784207 G>A maps to NM_000798.4 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:31796680 C>T maps to NM_004147.3 R40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:100503522 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:100492742 A>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:100486729 C>T did not map to a codon.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr23:100490938 G>A did not map to a codon.
Sequencing variant TCGA-HT-7485-01A-11D-2024-08 chr18:28725702 G>A maps to NM_024421.2 D270D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WD-01A-12D-A33T-08 chr18:28710644 C>T maps to NM_024421.2 E839E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RJ-01A-11D-A33T-08 chr18:28728467 G>A maps to NM_024421.2 C255C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A87Q-01A-11D-A36O-08 chr18:28662323 C>T maps to ENST00000438199 K394K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:28588260 G>A maps to NM_001941.3 P498P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:28588281 G>A maps to NM_001941.3 N491N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6XC-01A-12D-A32B-08 chr18:28598766 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:41516604 G>A maps to NM_001389.3 Y1024Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:41719791 C>A maps to NM_001389.3 G339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5318-01A-01D-1468-08 chr11:117308780 G>T maps to NM_020693.2 S1481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:38390257 G>A maps to NM_018962.2 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A6S6-01A-21D-A32B-08 chr18:65179103 C>T maps to NM_032160.2 G924G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YU-01A-11D-A34J-08 chr18:65178395 A>C maps to NM_032160.2 S1160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:28935224 C>T maps to NM_001942.2 H1022H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr18:28934738 A>G maps to NM_001942.2 S860S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr18:28923926 C>T maps to NM_001942.2 N620N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6668-01A-11D-1893-08 chr18:29102121 C>T maps to NM_001943.3 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5847-01A-11D-1705-08 chr18:29099848 C>T maps to NM_001943.3 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7603-01A-21D-2086-08 chr18:29126612 T>C maps to NM_001943.3 F1088F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6J3-01A-11D-A31L-08 chr18:29054363 T>C maps to NM_001944.2 S794S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:28993014 T>G maps to NM_001134453.1 A879A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EU-01A-11D-A27K-08 chr18:28993041 T>A maps to NM_001134453.1 P888P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A89Z-01A-11D-A36O-08 chr18:28986301 T>A maps to NM_001134453.1 I633I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6188-01A-11D-1893-08 chr6:7571617 G>A maps to NM_004415.2 L568L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:7567604 C>T maps to NM_004415.2 Q355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:7583867 C>T maps to NM_004415.2 L2125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr6:7583353 C>A maps to NM_004415.2 T1953T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CZ-01A-11D-A32B-08 chr6:7572216 C>T maps to NM_004415.2 C682C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WH-A86K-01A-11D-A36O-08 chr6:7581049 G>T maps to NM_004415.2 E1543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6400-01A-12D-1705-08 chr4:88534156 T>C maps to NM_014208.3 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:56397209 C>T maps to ENST00000361203 V5469V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:56401696 C>T maps to ENST00000361203 Q5339Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:56391169 G>A maps to ENST00000361203 R5829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A72Z-01A-11D-A32B-08 chr6:56374647 G>A maps to ENST00000361203 I6057I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YE-01A-11D-A34A-08 chr1:205126502 G>A maps to NM_015375.2 T750T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr1:205138720 G>A maps to NM_015375.2 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:118264321 A>G maps to NM_173666.2 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:122289444 C>T maps to NM_138287.3 R693R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TB-01A-11D-A33T-08 chr3:122287625 A>G maps to NM_138287.3 E230E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A61B-01A-11D-A29Q-08 chr17:7150175 T>C maps to NM_015343.4 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:45434272 C>T maps to NM_175940.1 F595F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:45427308 C>T maps to NM_175940.1 H105H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6J1-01A-11D-A31L-08 chr15:45442842 T>C maps to NM_175940.1 P944P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RJ-01A-11D-A33T-08 chr15:45445611 C>A maps to NM_175940.1 Y1153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:45386443 G>A maps to NM_014080.4 C1517C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6403-01A-11D-1705-08 chr15:45401121 G>A maps to NM_014080.4 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr15:45389889 G>A maps to NM_014080.4 F1205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:45408870 T>C maps to NM_207581.3 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:76818214 G>A maps to NM_001003892.1 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr10:76803651 G>A maps to NM_001003892.1 Y108Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7475-01A-11D-2024-08 chr10:76803656 G>A maps to NM_001003892.1 Q107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:68071994 G>A maps to NM_017803.3 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A847-01A-11D-A36O-08 chr7:107214149 T>C maps to NM_181581.1 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:76854613 G>T maps to ENST00000356369 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7606-01A-11D-2086-08 chr6:348773 G>T maps to ENST00000457386 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7857-01A-11D-2395-08 chr6:348271 C>T maps to ENST00000457386 Q145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RW-01A-11D-A33T-08 chr6:348219 C>G maps to ENST00000457386 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8109-01A-11D-2395-08 chr1:167096395 G>A maps to NM_001080426.1 T676T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:52088294 G>A maps to NM_001947.3 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:52088115 G>A maps to NM_001947.3 D264D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr11:1578530 C>T maps to NM_004420.2 P365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:152915525 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:152914911 G>A did not map to a codon.
Sequencing variant TCGA-HW-7491-01A-11D-2024-08 chr17:7132712 T>C maps to NM_004422.2 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:46570553 G>A maps to NM_017653.3 F627F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:102478324 C>T maps to NM_001376.4 L2244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A711-01A-21D-A33T-08 chr2:172585348 C>T maps to NM_001378.1 C460C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6670-01A-11D-1893-08 chr11:103056993 T>C maps to NM_001080463.1 S2219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:103107183 T>C maps to NM_001080463.1 C3245C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:103026220 C>T maps to NM_001080463.1 A1245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:103048400 T>C maps to NM_001080463.1 C1997C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A75L-01A-11D-A32B-08 chr2:44031781 A>T maps to NM_001193464.1 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr20:33122559 C>T maps to ENST00000374846 R122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:71908240 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:71795212 G>A did not map to a codon.
Sequencing variant TCGA-S9-A6WM-01A-12D-A33T-08 chr2:71709085 G>A maps to NM_001130987.1 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WO-01A-21D-A34A-08 chr2:71797732 G>A maps to NM_001130987.1 W1030*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VV-A829-01A-21D-A36O-08 chr2:71896840 C>T maps to NM_001130987.1 L1917L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5144-01A-01D-1468-08 chr15:55731773 T>C maps to NM_130810.2 L263L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DU-6392-01A-11D-1705-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:108366850 C>T maps to NM_014648.3 Y618Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76R-01A-11D-A32B-08 chr3:108353773 C>T maps to NM_014648.3 C291C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RM-01A-11D-A33T-08 chr3:108351852 G>A maps to NM_014648.3 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YD-01A-11D-A34A-08 chr6:20488346 C>T maps to NM_001949.3 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YE-01A-11D-A34A-08 chr8:86115376 A>G maps to ENST00000256117 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:2284591 G>A maps to NM_004424.3 Q534Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A730-01A-11D-A32B-08 chr3:121554192 G>T maps to NM_018456.4 E21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:23556016 C>T maps to NM_001083614.1 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7475-01A-11D-2024-08 chr5:158140056 G>A maps to NM_024007.3 H430H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr5:158158157 G>A maps to NM_024007.3 N348N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A87Q-01A-11D-A36O-08 chr8:25747367 C>T maps to NM_022659.2 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:233349248 C>A maps to NM_004826.2 E373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:127611166 C>T maps to NM_001139510.1 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A60L-01A-12D-A31L-08 chr1:150482461 C>A maps to ENST00000369049 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:95277057 T>C maps to NM_001393.3 R303R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:95263330 G>A maps to NM_001393.3 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:172482123 C>T maps to ENST00000392692 N375N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:172525558 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:139164319 G>T maps to NM_001195037.2 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7015-01A-11D-2024-08 chr23:68836452 C>T did not map to a codon.
Sequencing variant TCGA-S9-A89Z-01A-11D-A36O-08 chr23:65835829 T>C did not map to a codon.
Sequencing variant TCGA-HT-7469-01A-11D-2253-08 chr2:109547446 C>T maps to ENST00000376651 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CX-01A-11D-A32B-08 chr2:109527457 G>A maps to ENST00000376651 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84O-01A-11D-A36O-08 chr2:109526914 C>G did not map to a codon.
Sequencing variant TCGA-S9-A7J0-01A-11D-A34A-08 chr1:236645900 C>T maps to NM_145861.2 D200D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YS-01A-11D-A34A-08 chr15:74964116 T>A did not map to a codon.
Sequencing variant TCGA-TM-A84B-01A-11D-A36O-08 chr16:67913853 T>C maps to NM_014329.3 A641A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:33703439 G>A maps to NM_018217.2 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YJ-01A-11D-A34A-08 chr20:33703559 G>T maps to NM_018217.2 Y471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr1:184695448 T>C maps to NM_025191.3 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:184723756 G>T maps to NM_025191.3 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:184688654 A>G maps to NM_025191.3 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:184663406 C>T maps to NM_025191.3 Q863Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YU-01A-11D-A34J-08 chr1:184692990 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:83433158 G>A maps to NM_005711.3 C123C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7J2-01A-11D-A34A-08 chr6:12296197 G>A maps to NM_001955.4 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5395-01A-01D-1468-08 chr4:148407183 G>T maps to NM_001957.3 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:93258691 A>G maps to NM_003566.3 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:144663399 G>A maps to NM_032378.4 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr19:3977233 G>A maps to NM_001961.3 L788L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7882-01A-11D-2395-08 chr8:49643960 G>A maps to NM_024593.3 R54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:3788264 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:28380514 G>T maps to NM_198529.3 E515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8185-01A-11D-2253-08 chr17:28409943 C>T maps to NM_198529.3 Y1154Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TV-01A-12D-A34J-08 chr17:28405523 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:44022454 G>A maps to NM_022785.3 D779D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A710-01A-12D-A33T-08 chr22:44079701 G>A maps to NM_022785.3 N392N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:16963024 C>T maps to NM_181723.2 R397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:19974982 G>T maps to NM_144715.3 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:52334249 G>A maps to NM_018100.3 V419V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7CA-01A-21D-A33T-08 chr6:52288805 T>C maps to NM_018100.3 R42R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:44091869 C>A did not map to a codon.
Sequencing variant TCGA-HW-A5KL-01A-11D-A27K-08 chr23:44120531 C>T did not map to a codon.
Sequencing variant TCGA-S9-A7J3-01A-21D-A34J-08 chr23:44109648 C>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:155103871 C>T maps to NM_004428.2 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:155039406 T>C maps to NM_182689.1 H105H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:68060408 A>G did not map to a codon.
Sequencing variant TCGA-E1-A7YI-01A-11D-A34A-08 chr23:68060347 G>A did not map to a codon.
Sequencing variant TCGA-CS-5396-01A-02D-1468-08 chr13:107147325 T>A maps to NM_004093.2 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr14:23828663 T>G maps to NM_005864.2 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:82443884 G>A maps to NM_024580.5 R970R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:42942370 C>T maps to NM_004247.3 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YQ-01A-11D-A34J-08 chr4:110932546 C>A maps to NM_001963.4 S1187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A8XE-01A-11D-A36O-08 chr4:110932373 T>C maps to NM_001963.4 T1129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A72U-01A-31D-A32B-08 chr9:139563047 C>T maps to NM_201446.1 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:38435282 C>T maps to ENST00000354891 G737G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7477-01B-11D-A289-08 chr5:38338819 C>T maps to ENST00000354891 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A70Z-01A-12D-A33T-08 chr7:55273103 C>T maps to NM_005228.3 Q1143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr7:55260472 G>A maps to NM_005228.3 W880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WQ-01A-12D-A34A-08 chr7:55270223 C>T maps to NM_005228.3 P1059P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:41306599 C>A maps to NM_053046.2 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:34419871 G>A maps to NM_022073.3 C29C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:34398307 G>A maps to NM_022073.3 H196H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr5:137803724 G>A maps to NM_001964.2 S529S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6IZ-01A-11D-A31L-08 chr2:73519640 A>G maps to NM_001965.3 D238D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UR-01A-11D-A33T-08 chr2:63272231 C>T maps to NM_015252.3 R1174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr2:63182657 T>C maps to NM_015252.3 L810L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:64622266 C>T maps to NM_006795.2 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KT-A7W1-01A-11D-A34A-08 chr11:64622119 G>A maps to NM_006795.2 A430A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:31489452 C>T maps to NM_014600.2 D497D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:31467292 C>A maps to NM_014600.2 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6670-01A-11D-1893-08 chr3:184910181 G>A maps to NM_001966.3 S668S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:184910835 G>T maps to NM_001966.3 Y450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:140685394 C>T maps to NM_024757.4 I826I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64U-01A-11D-A29Q-08 chr6:31848859 C>T maps to ENST00000395728 G1126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:125452283 C>T maps to ENST00000278903 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CE-01A-11D-A36O-08 chr11:125453433 C>G maps to ENST00000278903 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XB-01A-11D-A26M-08 chr23:20156712 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:20150321 T>C did not map to a codon.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr23:20156718 C>T did not map to a codon.
Sequencing variant TCGA-DU-A5TP-01A-11D-A289-08 chr23:20156712 C>T did not map to a codon.
Sequencing variant TCGA-HT-7609-01A-11D-2086-08 chr23:20156728 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:6078265 G>A maps to NM_014413.3 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A8XE-01A-11D-A36O-08 chr2:88874642 T>C maps to NM_004836.5 E786E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5304-01A-01D-1468-08 chr15:40258022 G>A maps to NM_001013703.2 K332K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RQ-01A-11D-A33T-08 chr15:40257950 C>T maps to NM_001013703.2 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7608-01A-11D-2086-08 chr12:124111688 G>A maps to NM_001414.3 H128H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:183855491 C>T maps to NM_003907.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr8:141595387 C>T maps to NM_012154.3 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:36474596 C>A maps to NM_024852.2 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:36299617 C>T maps to NM_017629.2 I469I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:24084145 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:120819203 C>T maps to NM_003750.2 E451E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr10:120796751 G>A maps to NM_003750.2 D1266D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CB-01A-11D-A36O-08 chr7:2403385 A>G maps to ENST00000314800 E330E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XF-01A-11D-A27K-08 chr1:32688224 G>A maps to NM_003757.2 K30K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7019-01A-11D-2024-08 chr22:38270461 C>T maps to ENST00000262832 R322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:7481532 T>C maps to NM_001416.2 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:7480799 C>T maps to NM_001416.2 R255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YS-01A-11D-A34A-08 chr3:184046466 C>T maps to NM_001194947.1 P1341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:10820604 T>C maps to ENST00000429377 E937E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:10824814 T>C maps to ENST00000429377 R353R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:21137324 C>T maps to NM_001198801.1 P1530P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr1:21268143 G>A maps to NM_001198801.1 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84M-01A-11D-A36O-08 chr1:21205842 G>A maps to NM_001198801.1 Y845Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A61C-01A-11D-A29Q-08 chr14:103802434 G>A maps to NM_183004.3 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WM-01A-12D-A33T-08 chr17:7214423 A>T maps to NM_001143760.1 K115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:100013243 C>T maps to NM_015904.3 C1092C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A710-01A-12D-A33T-08 chr17:12908352 T>C maps to NM_018127.6 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7300-01A-21D-2086-08 chr19:852924 C>T maps to NM_001972.2 H39H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:8032573 C>T maps to ENST00000351593 E204E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6J1-01A-11D-A31L-08 chr19:8038657 A>G maps to ENST00000351593 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EZ-01A-11D-A27K-08 chr9:23701563 G>A maps to ENST00000359598 R204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:41525482 G>A maps to NM_172373.3 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:139981790 C>A maps to ENST00000379550 G282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:129208063 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:129205191 A>G did not map to a codon.
Sequencing variant TCGA-P5-A735-01A-11D-A32B-08 chr23:129205310 C>T did not map to a codon.
Sequencing variant TCGA-S9-A7J3-01A-21D-A34J-08 chr23:129203476 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:37770992 G>A maps to NM_052906.3 F194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:37771271 G>A maps to NM_052906.3 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:37769951 C>A maps to NM_052906.3 V541V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr22:37770332 G>A maps to NM_052906.3 A414A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:47497219 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:47496427 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:47497275 C>T did not map to a codon.
Sequencing variant TCGA-VW-A8FI-01A-11D-A36O-08 chr23:47500628 A>G did not map to a codon.
Sequencing variant TCGA-E1-5318-01A-01D-1468-08 chr19:18557616 G>A maps to NM_006532.3 N491N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RR-01A-21D-A34A-08 chr20:45002148 G>A maps to ENST00000439931 H447H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:141446678 C>T maps to NM_153702.3 R33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:85617290 C>T maps to NM_001135023.1 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7490-01A-11D-2024-08 chr2:85617290 C>T maps to NM_001135023.1 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:73456971 T>C maps to ENST00000358929 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:53139924 G>T maps to ENST00000370918 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:110972808 G>A maps to NM_024090.2 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:60053413 G>T maps to NM_024930.2 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A61B-01A-11D-A29Q-08 chr18:33738839 G>T maps to ENST00000442325 G568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr1:79392753 T>A maps to NM_022159.3 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7616-01A-11D-2253-08 chr1:79470842 G>C maps to NM_022159.3 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RC-01A-11D-A289-08 chr1:79470884 C>T maps to NM_022159.3 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153609119 A>T did not map to a codon.
Sequencing variant TCGA-TQ-A7RJ-01A-11D-A33T-08 chr23:153608069 G>A did not map to a codon.
Sequencing variant TCGA-TQ-A7RQ-01A-11D-A33T-08 chr23:153608122 C>T did not map to a codon.
Sequencing variant TCGA-HT-7677-01A-11D-2253-08 chr12:7083746 C>T maps to ENST00000261406 R101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RF-01A-11D-A33T-08 chr22:29629639 G>A maps to NM_133455.2 G317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:100357547 G>A maps to NM_001008707.1 E196E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8322-01A-11D-2395-08 chr14:89160702 A>T maps to ENST00000380664 P829P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YE-01A-11D-A34A-08 chr16:10631920 C>T maps to NM_001424.4 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:6904077 C>A maps to ENST00000381407 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TT-01A-11D-A289-08 chr19:6937658 G>A maps to ENST00000381407 T887T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:119305194 G>A maps to NM_004098.3 K153K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F4-01A-11D-A289-08 chr10:119303011 G>C maps to NM_004098.3 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:119600594 G>A maps to NM_001426.3 N366N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr4:71510352 C>T maps to NM_031889.2 T1070T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:71500101 G>A maps to NM_031889.2 Q96Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr9:130587088 G>A maps to NM_001114753.1 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U2-01A-21D-A33T-08 chr17:77078144 G>A maps to NM_001042573.1 K346K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:691267 C>T maps to ENST00000319815 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:129765464 G>T did not map to a codon.
Sequencing variant TCGA-TQ-A7RM-01A-11D-A33T-08 chr23:129843237 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:111441426 T>C maps to NM_001977.3 Y544Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr4:111397843 C>T maps to NM_001977.3 R92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KM-01A-11D-A27K-08 chr4:111464024 G>A maps to NM_001977.3 A642A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:120612989 C>T maps to NM_006209.3 R300R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6401-01A-11D-1705-08 chr8:120596282 A>G maps to NM_006209.3 P510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6666-01A-11D-1893-08 chr6:46129356 G>A maps to NM_021572.4 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YI-01A-11D-A34A-08 chr6:46135855 C>T maps to NM_021572.4 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:77709176 C>T maps to NM_178543.3 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr1:150599963 G>A maps to NM_207042.1 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6UB-01A-21D-A33T-08 chr10:97583114 C>T maps to NM_001098175.1 N53N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:40457482 C>T maps to NM_001248.2 Y250Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr10:101464241 T>C maps to NM_020354.3 H539H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:110352716 G>T did not map to a codon.
Sequencing variant TCGA-DB-A64V-01A-11D-A29Q-08 chr22:41566475 T>C maps to NM_001429.3 H1451H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:41566460 T>C maps to NM_001429.3 Y1446Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr12:132466656 G>T maps to ENST00000333577 P557P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7680-01A-11D-2253-08 chr12:132547140 G>A maps to ENST00000333577 Q2779Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7684-01A-11D-2253-08 chr12:132547140 G>A maps to ENST00000333577 Q2779Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7874-01A-11D-2395-08 chr12:132466833 G>A maps to ENST00000333577 Q616Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5ET-01A-11D-A27K-08 chr12:132547107 G>A maps to ENST00000333577 Q2768Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A733-01A-11D-A32B-08 chr12:132549241 A>G maps to ENST00000333577 K2824K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7J0-01A-11D-A34A-08 chr12:132551994 C>T maps to ENST00000333577 P2982P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:46603892 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:29344861 C>A maps to NM_001166005.1 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr20:34770233 G>A maps to NM_012156.2 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TT-01A-11D-A289-08 chr6:131188676 T>C maps to NM_001431.3 S884S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A6MO-01A-11D-A33T-08 chr6:131222115 C>T maps to NM_001431.3 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:5397137 G>A maps to NM_012307.2 A920A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:111570339 G>A maps to NM_022140.3 Q360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:120889206 C>A maps to NM_020909.3 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:120799599 G>T maps to NM_020909.3 E67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:43512938 C>A maps to NM_000119.2 G29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:43503646 G>A maps to NM_000119.2 D202D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:21938862 G>A maps to ENST00000265800 R369R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:149522543 G>A maps to NM_015630.3 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr2:149528636 A>G maps to NM_015630.3 T467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:37960396 G>A maps to NM_017549.3 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:143088765 G>A maps to NM_005232.4 H933H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A6S6-01A-21D-A32B-08 chr7:143096027 C>T maps to NM_005232.4 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:16456914 C>A did not map to a codon.
Sequencing variant TCGA-E1-5304-01A-01D-1468-08 chr3:89448614 G>T maps to NM_005233.5 E527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YE-01A-11D-A34A-08 chr3:89390201 T>C maps to NM_005233.5 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:222294739 G>A maps to NM_004438.3 N876N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:66201669 C>T maps to NM_004439.5 T944T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WD-01A-12D-A33T-08 chr4:66213864 A>G maps to NM_004439.5 F855F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A8XE-01A-11D-A36O-08 chr4:66197689 C>T maps to ENST00000511294 E1004E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:97367131 C>T maps to ENST00000514100 D385D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:93953251 C>T maps to NM_004440.3 V963V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:22903302 C>T maps to NM_020526.3 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A4DS-01A-11D-A26M-08 chr1:22924292 G>A maps to NM_020526.3 A685A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:134881020 C>T maps to NM_004441.4 D528D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:23111558 C>T maps to ENST00000400191 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:184295233 C>T maps to NM_004443.3 Y486Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:184290521 C>T maps to NM_004443.3 D138D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A618-01A-11D-A29Q-08 chr7:100421496 C>A maps to NM_004444.4 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6393-01A-11D-1705-08 chr7:142564302 G>A maps to NM_004445.3 P509P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8191-01A-11D-2253-08 chr7:142562151 G>A maps to NM_004445.3 E198E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7611-01A-11D-2395-08 chr7:142568142 C>T maps to NM_004445.3 G928G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr7:142561053 G>T maps to NM_004445.3 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WM-01A-12D-A33T-08 chr1:92528674 C>T maps to NM_173567.4 D307D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R2-01A-21D-A34J-08 chr3:37032872 G>A maps to NM_014805.3 R566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr17:48616600 C>T maps to NM_017957.2 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6188-01A-11D-1893-08 chr8:144942252 G>A maps to NM_031308.1 D1723D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr8:144942234 G>A maps to NM_031308.1 F1729F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:144943347 C>T maps to NM_031308.1 V1358V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:144947319 C>T maps to NM_031308.1 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:144940548 C>T maps to NM_031308.1 V2291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7606-01A-11D-2086-08 chr8:144940575 C>T maps to NM_031308.1 S2282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EU-01A-11D-A27K-08 chr8:144942912 G>A maps to NM_031308.1 S1503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64W-01A-11D-A29Q-08 chr1:220142261 T>A maps to NM_004446.2 G1475G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:220206994 A>G maps to NM_004446.2 D79D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7606-01A-11D-2086-08 chr19:16487939 C>T maps to ENST00000455140 P791P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5393-01A-01D-1468-08 chr19:55597451 G>A maps to NM_133180.2 W514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:55590425 G>A did not map to a codon.
Sequencing variant TCGA-S9-A6WQ-01A-12D-A34A-08 chr23:48687674 G>A did not map to a codon.
Sequencing variant TCGA-S9-A7R8-01A-11D-A34J-08 chr23:48688181 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:37865569 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:65349794 C>A maps to ENST00000506030 I883I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr5:65338966 C>A maps to ENST00000506030 R457R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:56487332 C>T maps to NM_001982.2 C493C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CV-01A-11D-A31L-08 chr2:212652795 T>C maps to NM_005235.2 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:1291147 G>T maps to NM_178040.2 E645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YW-01A-11D-A34J-08 chr3:56026188 G>A maps to ENST00000460849 D717D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr3:56026257 G>A maps to ENST00000460849 D694D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8182-01A-11D-2253-08 chr19:45916940 A>T maps to NM_202001.2 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YL-01A-11D-A34A-08 chr10:50669555 G>A maps to NM_000124.2 A1275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:71427038 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:71425009 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:71428205 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:71426139 G>A did not map to a codon.
Sequencing variant TCGA-TM-A84F-01A-11D-A36O-08 chr4:75248409 C>T maps to NM_001432.2 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8161-01A-11D-2253-08 chr21:39755663 G>A maps to NM_001136154.1 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:172324044 C>T maps to NM_001031711.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:34144847 G>A maps to ENST00000447986 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:44804806 C>T maps to NM_024066.1 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:44687262 G>T maps to NM_024066.1 G327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:62122803 G>A maps to NM_001433.3 G856G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr17:62144065 C>T maps to NM_001433.3 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A669-01A-12D-A31L-08 chr16:23716445 G>A maps to NM_033266.3 C252C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:23702330 G>A maps to NM_033266.3 R916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RJ-01A-11D-A33T-08 chr14:53113131 A>G maps to NM_014584.1 C391C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:19153730 C>T maps to NM_052911.2 Q358Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5144-01A-01D-1468-08 chr12:53680350 A>G maps to NM_012291.4 L1277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:53685847 A>G maps to NM_012291.4 L1924L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7603-01A-21D-2086-08 chr1:6488428 C>T maps to NM_031475.2 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6UA-01A-12D-A33T-08 chr1:6504599 G>A maps to NM_031475.2 P350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:64083219 C>T maps to NM_004451.3 R352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8011-01A-11D-2395-08 chr14:76905887 C>T maps to NM_004452.3 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XF-01A-11D-A27K-08 chr23:103495292 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:103499525 T>C did not map to a codon.
Sequencing variant TCGA-DU-7018-01A-11D-2024-08 chr23:103499229 C>A did not map to a codon.
Sequencing variant TCGA-S9-A6TZ-01A-21D-A32B-08 chr23:103495450 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:67630707 C>T maps to NM_019002.3 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84B-01A-11D-A36O-08 chr2:67631742 C>T maps to NM_019002.3 S643S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:76580229 A>G maps to NM_000126.3 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:159624691 G>T maps to NM_004453.2 E412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8111-01A-11D-2395-08 chr4:159603572 G>A maps to NM_004453.2 K134K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7Z3-01A-11D-A34J-08 chr19:44030436 G>A maps to NM_014297.3 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:204115783 G>A maps to NM_018208.2 N209N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:14027792 C>T maps to NM_004956.4 Q17Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RW-01A-11D-A33T-08 chr4:5798787 G>A maps to NM_153717.2 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:74003885 C>T maps to NM_001988.2 P1800P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:74006602 G>A maps to NM_001988.2 R895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr17:74003588 G>T maps to NM_001988.2 A1899A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A83X-01A-11D-A36O-08 chr17:74004206 C>T maps to NM_001988.2 T1693T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7879-01A-11D-2395-08 chr22:29694856 C>T maps to NM_013986.3 R523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:242024776 C>T maps to NM_006027.4 I338I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr4:56734653 G>T maps to NM_018261.3 E190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5303-01A-01D-1468-08 chr6:564074 G>A maps to NM_018303.4 R583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74H-01A-11D-A32B-08 chr7:133602452 G>A maps to NM_021807.3 Q663Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8019-01A-21D-2395-08 chr10:94700481 A>T did not map to a codon.
Sequencing variant TCGA-FG-8191-01A-11D-2253-08 chr17:74084887 G>T maps to NM_001145297.2 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:231472243 C>T maps to NM_175876.3 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:108381793 C>T maps to NM_015065.2 Q1480Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr11:108381247 G>A maps to NM_015065.2 N1662N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WE-01A-12D-A33T-08 chr11:108409779 A>G maps to NM_015065.2 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:44219461 C>T maps to NM_000401.3 Y496Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:26357052 C>A maps to NM_004455.2 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr1:26349415 C>T maps to NM_004455.2 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KK-01A-11D-A27K-08 chr1:26360305 C>T maps to NM_004455.2 N546N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:28573839 G>A maps to NM_001440.2 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:28574067 C>T maps to NM_001440.2 D164D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A75P-01A-11D-A32B-08 chr8:72211441 G>A maps to NM_000503.4 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RW-01A-11D-A33T-08 chr8:72127634 A>G maps to NM_000503.4 S528S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YN-01A-11D-A34A-08 chr6:133789765 G>A maps to ENST00000452339 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7677-01A-11D-2253-08 chr6:133783470 A>T did not map to a codon.
Sequencing variant TCGA-HT-7475-01A-11D-2024-08 chr17:40869992 C>A did not map to a codon.
Sequencing variant TCGA-DB-A64W-01A-11D-A29Q-08 chr6:159188409 G>A maps to NM_001111077.1 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:159190827 G>A maps to NM_001111077.1 S413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:159187957 G>A maps to NM_001111077.1 F583F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:113803536 G>A maps to NM_000504.3 K391K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:6318783 C>T maps to NM_000129.3 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:94998762 G>A maps to NM_001993.4 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7610-01A-21D-2086-08 chr1:169519049 G>A maps to ENST00000367796 Q534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:113772784 C>A maps to NM_000131.3 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5396-01A-02D-1468-08 chr23:154176083 G>T did not map to a codon.
Sequencing variant TCGA-DB-A4XF-01A-11D-A27K-08 chr23:154194744 C>T did not map to a codon.
Sequencing variant TCGA-DH-A66G-01A-21D-A31L-08 chr23:154132780 C>A did not map to a codon.
Sequencing variant TCGA-DH-A66G-01A-21D-A31L-08 chr23:154132779 C>A did not map to a codon.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr23:154065951 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:154158778 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:154133298 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:154133204 T>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:154159625 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:154088873 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:154132705 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:154091390 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:154156920 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:154194306 T>C did not map to a codon.
Sequencing variant TCGA-E1-A7YE-01A-11D-A34A-08 chr23:154091432 A>C did not map to a codon.
Sequencing variant TCGA-FG-A70Z-01A-12D-A33T-08 chr23:154157637 C>T did not map to a codon.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr23:154159215 T>C did not map to a codon.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr23:154250802 A>G did not map to a codon.
Sequencing variant TCGA-QH-A6CS-01A-11D-A31L-08 chr23:154130441 C>T did not map to a codon.
Sequencing variant TCGA-TM-A84H-01A-11D-A36O-08 chr23:154157390 G>C did not map to a codon.
Sequencing variant TCGA-TQ-A7RQ-01A-11D-A33T-08 chr23:154158010 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:138630555 G>T did not map to a codon.
Sequencing variant TCGA-FG-A6IZ-01A-11D-A31L-08 chr23:138643993 C>T did not map to a codon.
Sequencing variant TCGA-S9-A6TZ-01A-21D-A32B-08 chr23:138643010 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:57337036 C>T did not map to a codon.
Sequencing variant TCGA-HT-A614-01A-11D-A29Q-08 chr23:57358191 C>T did not map to a codon.
Sequencing variant TCGA-FG-8188-01A-11D-2253-08 chr4:120243251 C>T maps to NM_000134.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:61608151 C>A maps to NM_004265.2 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WH-A86K-01A-11D-A36O-08 chr17:72875554 G>C maps to ENST00000310226 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7880-01A-11D-2395-08 chr15:80452127 C>T maps to NM_000137.1 Q75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8163-01A-11D-2253-08 chr2:96071500 G>A maps to NM_016044.2 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8110-01A-11D-2395-08 chr3:138341216 G>A maps to NM_001033030.1 W134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6X4-01A-51D-A32B-08 chr3:138351878 T>G maps to NM_001033030.1 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:207078477 G>T maps to NM_005449.4 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:14563962 G>A maps to NM_031453.2 R237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6667-01A-12D-2024-08 chr19:1881346 A>G maps to NM_031213.3 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:74489669 G>A maps to NM_016014.2 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A669-01A-12D-A31L-08 chr12:47629727 A>G maps to NM_138371.1 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:57613949 G>A maps to NM_152678.2 G606G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:47799935 C>T maps to NM_030802.3 E129E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:203630267 C>A maps to NM_173511.3 I517I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5393-01A-01D-1468-08 chr11:126126562 C>G maps to NM_024556.3 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:208477940 G>T maps to ENST00000272839 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5397-01A-01D-1893-08 chr9:96326728 C>T maps to ENST00000333936 C1116C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:96214349 C>T maps to ENST00000333936 D51D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:96305687 C>T maps to ENST00000333936 D726D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8109-01A-11D-2395-08 chr9:96324504 T>A maps to ENST00000333936 V1016V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr23:54209050 G>A did not map to a codon.
Sequencing variant TCGA-DH-A7UR-01A-11D-A33T-08 chr23:54161405 A>C did not map to a codon.
Sequencing variant TCGA-S9-A7QX-01A-11D-A34A-08 chr23:54209077 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:133919927 G>T did not map to a codon.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr13:25743873 T>C maps to NM_152704.2 Q628Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5393-01A-01D-1468-08 chr23:63411384 G>A did not map to a codon.
Sequencing variant TCGA-DU-5871-01A-12D-1705-08 chr23:63411821 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:63410255 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:63410129 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:63410756 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:63412963 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:63410720 G>A did not map to a codon.
Sequencing variant TCGA-DU-7298-01A-11D-2024-08 chr23:63410719 C>T did not map to a codon.
Sequencing variant TCGA-HW-8321-01A-11D-2395-08 chr23:63412956 A>G did not map to a codon.
Sequencing variant TCGA-P5-A781-01A-11D-A32B-08 chr23:63411229 C>T did not map to a codon.
Sequencing variant TCGA-QH-A65S-01A-11D-A29Q-08 chr23:63412446 A>G did not map to a codon.
Sequencing variant TCGA-FG-8186-01A-11D-2253-08 chr2:131521708 C>T maps to NM_001105195.1 N688N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KK-01A-11D-A27K-08 chr2:131521799 C>T maps to NM_001105195.1 Q719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7603-01A-21D-2086-08 chr13:51825994 C>T maps to NM_145019.2 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5280-01A-01D-1468-08 chr2:225266431 A>G maps to NM_001122779.1 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7CA-01A-21D-A33T-08 chr19:17531344 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:22985426 T>C maps to NM_032581.3 V449V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:201887580 A>G maps to NM_173822.3 Y42Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YK-01A-11D-A34A-08 chr23:134156372 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:184764287 G>A maps to NM_052966.2 S870S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:184772784 A>G maps to NM_052966.2 F496F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8189-01B-11D-A289-08 chr1:184863334 T>C maps to NM_052966.2 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85C-01A-11D-A36O-08 chr1:184777345 A>G maps to NM_052966.2 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5141-01A-01D-1468-08 chr9:130270473 G>A maps to NM_022833.2 Y480Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:130269156 G>A maps to NM_022833.2 T736T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6X9-01A-12D-A32B-08 chr19:17653072 C>T maps to ENST00000335393 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6407-01A-13D-1705-08 chr5:16475173 C>T maps to NM_001034850.1 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A711-01A-21D-A33T-08 chr17:40761318 G>A maps to NM_178126.3 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:71234658 T>C maps to NM_001162529.1 D624D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UR-01A-11D-A33T-08 chr10:61012752 C>T maps to ENST00000442566 E489E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6405-01A-11D-1705-08 chr5:175526031 A>G maps to NM_001079529.2 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7470-01A-12D-2086-08 chr5:175533579 C>A maps to NM_001079529.2 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:6235764 C>T maps to NM_032127.3 A825A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:116590681 G>A maps to NM_020940.3 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:74413269 T>C maps to NM_152445.1 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R7-01A-11D-A34J-08 chr14:75538367 C>T maps to NM_024643.2 S364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:32713255 C>T maps to NM_032648.2 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7636-01A-11D-2086-08 chr5:74130349 T>G maps to NM_015566.1 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7US-01A-11D-A33T-08 chr15:98982907 G>A maps to NM_182562.2 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:15256191 G>T maps to NM_001010924.1 P465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:187627517 C>T maps to NM_177454.3 R817*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7C5-01A-11D-A32B-08 chr5:93386526 A>C maps to NM_032042.5 L73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:84383807 G>T maps to NM_139076.2 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:75720697 G>A maps to NM_032181.2 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RW-01A-11D-A33T-08 chr1:36788036 C>A maps to NM_018166.1 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TD-01A-12D-A34A-08 chr2:29259477 C>T maps to NM_199280.2 F830F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MX-01A-11D-A26M-08 chr2:29222092 G>A maps to NM_199280.2 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7602-01A-21D-2086-08 chr2:29240087 G>A maps to NM_199280.2 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:45432169 T>C maps to ENST00000361462 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7Z6-01A-11D-A34J-08 chr11:82444516 G>C maps to NM_175885.3 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:49992708 T>C maps to NM_032130.2 V731V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:91230487 A>G maps to NM_001145065.1 Q351Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RP-01A-21D-A34A-08 chr4:91549202 C>T maps to NM_001145065.1 D584D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8185-01A-11D-2253-08 chr16:57206706 G>A maps to NM_024946.2 Y69Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7489-01A-11D-2024-08 chr4:2696819 C>T maps to ENST00000324666 C789C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7006-01A-11D-2024-08 chr23:103411603 C>T did not map to a codon.
Sequencing variant TCGA-E1-A7YW-01A-11D-A34J-08 chr23:103411654 C>T did not map to a codon.
Sequencing variant TCGA-HT-A5RB-01A-11D-A289-08 chr23:103432818 C>A did not map to a codon.
Sequencing variant TCGA-VM-A8CF-01A-11D-A36O-08 chr3:68788282 C>G maps to NM_182522.3 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:195655 C>T maps to NM_020223.2 Y236Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U8-01A-21D-A33T-08 chr9:99694199 C>T maps to NM_001170741.1 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R8-01A-11D-A34J-08 chr10:124671155 A>G maps to NM_001029888.1 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WH-A86K-01A-11D-A36O-08 chr10:88950271 C>T maps to ENST00000298786 V849V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74L-01A-11D-A32B-08 chr1:245005360 G>C did not map to a codon.
Sequencing variant TCGA-DU-6400-01A-12D-1705-08 chr18:10677808 A>G maps to NM_022068.2 N2559N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr18:10671754 T>A maps to NM_022068.2 S2676S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr18:10691359 A>C maps to NM_022068.2 V2291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RV-01A-21D-A34A-08 chr18:10681657 G>A maps to NM_022068.2 T2480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:42729090 G>A maps to ENST00000398652 Q264Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RB-01A-11D-A289-08 chr21:42710401 C>T maps to ENST00000398652 Y126Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A840-01A-11D-A36O-08 chr21:42694892 C>G maps to ENST00000398652 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5140-01A-01D-1468-08 chr1:110581797 A>G maps to NM_033088.2 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:129096344 G>A maps to ENST00000450266 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:129103952 C>A maps to ENST00000450266 I599I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:129091499 C>A maps to ENST00000450266 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr3:194408802 T>C maps to NM_153690.4 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr1:118166434 C>T maps to NM_017709.3 N315N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:79699142 C>T did not map to a codon.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr23:34150159 G>A did not map to a codon.
Sequencing variant TCGA-DB-A64S-01A-11D-A29Q-08 chr23:34148779 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:34149818 C>T did not map to a codon.
Sequencing variant TCGA-DU-A6S8-01A-12D-A32B-08 chr23:34149548 G>A did not map to a codon.
Sequencing variant TCGA-E1-A7YK-01A-11D-A34A-08 chr23:34148668 C>T did not map to a codon.
Sequencing variant TCGA-HT-7479-01A-11D-2024-08 chr23:34149059 C>G did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr23:34149531 G>A did not map to a codon.
Sequencing variant TCGA-VM-A8CA-01A-11D-A36O-08 chr23:34149053 G>A did not map to a codon.
Sequencing variant TCGA-CS-6186-01A-12D-2024-08 chr23:34961314 G>T did not map to a codon.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr23:34962024 C>T did not map to a codon.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr23:34961869 C>T did not map to a codon.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr23:34962575 G>A did not map to a codon.
Sequencing variant TCGA-E1-A7YQ-01A-11D-A34J-08 chr23:34961675 G>A did not map to a codon.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr23:34962763 G>A did not map to a codon.
Sequencing variant TCGA-HT-A5R7-01A-11D-A289-08 chr23:34961354 A>G did not map to a codon.
Sequencing variant TCGA-TM-A84O-01A-11D-A36O-08 chr23:34962774 G>C did not map to a codon.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr23:37027823 G>T did not map to a codon.
Sequencing variant TCGA-DH-A66F-01A-11D-A29Q-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-DH-A66G-01A-21D-A31L-08 chr23:37029040 G>A did not map to a codon.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr23:37027910 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:37027306 C>A did not map to a codon.
Sequencing variant TCGA-DU-8165-01A-11D-2253-08 chr23:37027100 G>A did not map to a codon.
Sequencing variant TCGA-FG-7636-01A-11D-2086-08 chr23:37028133 C>T did not map to a codon.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-FG-8186-01A-11D-2253-08 chr23:37027155 C>G did not map to a codon.
Sequencing variant TCGA-HT-7470-01A-12D-2086-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-HT-7471-01A-11D-2253-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-HT-7480-01A-11D-2086-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-HT-7610-01A-21D-2086-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-HT-A5R7-01A-11D-A289-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-IK-8125-01A-11D-2253-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-P5-A731-01A-11D-A32B-08 chr23:37027113 C>T did not map to a codon.
Sequencing variant TCGA-QH-A6CS-01A-11D-A31L-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-RY-A845-01A-11D-A36O-08 chr23:37029163 C>T did not map to a codon.
Sequencing variant TCGA-S9-A6WE-01A-12D-A33T-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-S9-A7J3-01A-21D-A34J-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-S9-A7R2-01A-21D-A34J-08 chr23:37029460 T>C did not map to a codon.
Sequencing variant TCGA-VW-A8FI-01A-11D-A36O-08 chr23:37026704 C>T did not map to a codon.
Sequencing variant TCGA-WY-A859-01A-12D-A36O-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:37622073 C>T did not map to a codon.
Sequencing variant TCGA-DU-7302-01A-11D-2086-08 chr23:153678569 A>C did not map to a codon.
Sequencing variant TCGA-QH-A65R-01A-21D-A31L-08 chr6:3850194 G>T maps to NM_012135.1 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:126370556 G>A maps to NM_014661.3 N175N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:136565941 T>C maps to NM_138419.3 K43K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:641145 C>T maps to NM_024792.1 Y89Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5871-01A-12D-1705-08 chr23:152853847 T>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:152861627 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:29972986 C>A maps to ENST00000269209 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:29867590 G>A maps to ENST00000269209 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:67572649 C>T maps to NM_001193523.1 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:67579726 C>T maps to NM_001193523.1 L1137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8563-01A-11D-2395-08 chr16:67578713 G>A maps to NM_001193523.1 P970P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A72Z-01A-11D-A32B-08 chr16:67575591 T>G maps to NM_001193523.1 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5143-01A-01D-1468-08 chr6:24843452 G>A maps to NM_014722.2 C519C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr20:49225173 C>T maps to NM_080829.2 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A60K-01A-11D-A29Q-08 chr20:49224996 C>T maps to NM_080829.2 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5390-01A-02D-1468-08 chr23:119410864 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:119419069 C>A did not map to a codon.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr5:156589801 G>A maps to NM_130899.2 R492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8181-01A-11D-2253-08 chr5:156589826 T>C maps to NM_130899.2 K483K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr5:156590150 C>T maps to NM_130899.2 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr5:156593085 A>G maps to NM_130899.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RC-01A-11D-A289-08 chr12:100043169 G>A maps to NM_153364.2 E240E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:78272688 C>T maps to NM_198549.2 C180C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:131823541 G>A maps to NM_032809.2 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EW-01A-11D-A27K-08 chr9:43625419 A>G maps to NM_001145196.1 C1089C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66B-01A-11D-A29Q-08 chr9:90535985 G>A maps to NM_001145124.1 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8110-01A-11D-2395-08 chr9:90535985 G>A maps to NM_001145124.1 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CA-01A-11D-A36O-08 chr9:90535973 T>C maps to NM_001145124.1 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7490-01A-11D-2024-08 chr9:134136481 C>T maps to NM_033387.3 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr5:94749821 C>T maps to NM_152548.2 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F1-01A-11D-A289-08 chr5:94749872 A>G maps to NM_152548.2 K172K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:124219711 G>A maps to NM_032899.4 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YV-01A-11D-A34J-08 chr6:54805985 C>A maps to NM_001010872.1 S739S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8109-01A-11D-2395-08 chr6:54735128 C>T maps to NM_001010872.1 R29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6X8-01A-12D-A32B-08 chr6:54805862 G>A maps to NM_001010872.1 K698K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:37570621 C>T maps to NM_030919.2 D198D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:49104455 G>A maps to NM_017708.3 F449F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:40417585 C>T maps to NM_138435.2 Q358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:18881652 G>A maps to NM_001039999.2 S442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5963-01A-11D-1705-08 chr17:18874944 G>A maps to NM_001039999.2 N733N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7881-01A-11D-2395-08 chr8:12287927 T>C maps to NM_001137610.1 K91K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:231155730 C>A maps to NM_198552.2 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8187-01A-11D-2253-08 chr1:231155647 G>A maps to NM_198552.2 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr12:8376781 G>A maps to NM_018088.3 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:124792765 T>C maps to NM_144963.2 D229D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:33813497 G>A maps to ENST00000395190 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4X9-01A-11D-A26M-08 chr23:8993590 C>A did not map to a codon.
Sequencing variant TCGA-RY-A83X-01A-11D-A36O-08 chr23:13061058 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:14868628 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:14863290 T>G did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr23:14883270 C>T did not map to a codon.
Sequencing variant TCGA-IK-7675-01A-11D-2086-08 chr23:14863148 G>A did not map to a codon.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr3:10123118 G>A maps to NM_033084.3 L1065L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:10105595 G>T did not map to a codon.
Sequencing variant TCGA-P5-A5F4-01A-11D-A289-08 chr3:10107140 G>A maps to NM_033084.3 Q744Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:35076574 C>T maps to NM_004629.1 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:58388665 G>A maps to NM_001114636.1 C342C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:45645466 G>A maps to NM_020937.2 T1170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:45605530 C>T maps to NM_020937.2 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr14:45623199 A>G maps to NM_020937.2 Q376Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IY-01A-11D-A34A-08 chr10:127693464 G>A maps to ENST00000368692 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:99030087 C>T maps to NM_005766.2 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7877-01A-11D-2395-08 chr13:99076870 C>T maps to NM_005766.2 G624G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:242402850 C>T maps to NM_014808.2 F593F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr6:5431388 A>G maps to NM_006567.3 Q296Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7604-01A-11D-2086-08 chr1:172634804 C>A maps to NM_000639.1 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr1:172628550 C>A maps to NM_000639.1 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:80045216 C>T maps to NM_004104.4 L1069L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:80045227 G>A maps to NM_004104.4 L1066L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:80053283 G>A maps to NM_004104.4 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8012-01A-11D-2395-08 chr17:80051591 G>A maps to NM_004104.4 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UU-01A-12D-A34A-08 chr4:187630587 G>T maps to ENST00000260147 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:187539522 T>C maps to ENST00000260147 K2742K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:187524129 G>A maps to ENST00000260147 S3806S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7008-01A-11D-2024-08 chr4:187524636 A>G maps to ENST00000260147 V3684V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr4:187557900 C>T maps to ENST00000260147 P1270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YE-01A-11D-A34A-08 chr4:187542105 C>A maps to ENST00000260147 V1881V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IS-01A-11D-A34A-08 chr4:187540254 G>A maps to ENST00000260147 N2498N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6188-01A-11D-1893-08 chr5:150922416 G>A maps to NM_001447.2 H2757H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:150947376 A>G maps to NM_001447.2 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:150946497 T>C maps to NM_001447.2 E665E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:150947406 G>A maps to NM_001447.2 F362F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8165-01A-11D-2253-08 chr5:150943009 A>G maps to NM_001447.2 A1150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr5:150945297 C>T maps to NM_001447.2 G1065G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr5:150924338 G>A maps to NM_001447.2 R2117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A83Z-01A-11D-A36O-08 chr5:150885458 G>A maps to NM_001447.2 L4239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:92577644 G>A maps to ENST00000298047 A3704A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:92600233 C>T maps to ENST00000298047 L3996L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:92086201 T>G maps to ENST00000298047 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:92534101 C>T maps to ENST00000298047 S2641S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7489-01A-11D-2024-08 chr11:92600242 C>T maps to ENST00000298047 Q3999*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IS-01A-11D-A34A-08 chr11:92535040 C>T maps to ENST00000298047 S2954S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:126239716 C>T maps to NM_024582.4 D717D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:126336615 C>T maps to NM_024582.4 N2166N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6402-01A-11D-1705-08 chr4:126239158 C>T maps to NM_024582.4 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YE-01A-11D-A34A-08 chr4:126402776 C>T maps to NM_024582.4 R4234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8106-01A-11D-2395-08 chr4:126239281 C>G maps to NM_024582.4 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:73911095 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:40327308 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:40329704 C>T maps to NM_001436.3 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WM-01A-12D-A33T-08 chr19:40331066 C>T maps to NM_001436.3 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8163-01A-11D-2253-08 chr1:16101378 C>T maps to NM_001024215.1 C326C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr22:45914667 G>A did not map to a codon.
Sequencing variant TCGA-HT-A5R7-01A-11D-A289-08 chr3:13655524 C>T maps to NM_001165035.1 A530A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:92353549 G>A maps to ENST00000267620 G339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8109-01A-11D-2395-08 chr2:112944824 C>T maps to NM_153214.2 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5275-01A-01D-1468-08 chr15:48795984 T>C maps to NM_000138.4 S704S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5277-01A-01D-1468-08 chr15:48729543 G>T maps to NM_000138.4 I2118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:48829910 G>T maps to NM_000138.4 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:48707779 G>A maps to NM_000138.4 G2668G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:48714158 C>T maps to NM_000138.4 T2520T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr15:48764790 G>A maps to NM_000138.4 C1431C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6690-01A-11D-1893-08 chr15:48773870 T>C maps to NM_000138.4 K1315K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:127674748 G>A maps to NM_001999.3 I1116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:127641518 A>G maps to NM_001999.3 C1848C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EZ-01A-11D-A27K-08 chr5:127648341 G>A maps to NM_001999.3 C1621C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RS-01A-12D-A33T-08 chr5:127674744 C>A maps to NM_001999.3 E1118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:8159438 C>T maps to NM_032447.3 E1932E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:8151119 C>A maps to NM_032447.3 G2282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:8190851 G>A maps to NM_032447.3 C885C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:8139979 C>T maps to NM_032447.3 Q2559Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7006-01A-11D-2024-08 chr19:8152977 G>A maps to NM_032447.3 D2154D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr19:8188414 C>T maps to NM_032447.3 T1005T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RH-01A-12D-A34A-08 chr7:102604003 G>A maps to NM_145032.3 R234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:33418800 C>T maps to NM_012157.3 D275D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EW-01A-11D-A27K-08 chr8:145580131 G>A maps to NM_012162.1 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5144-01A-01D-1468-08 chr5:15937210 C>T maps to NM_012304.3 C464C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:37512651 G>T maps to NM_012166.2 P921P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6J1-01A-11D-A31L-08 chr18:71740935 C>T maps to NM_001142958.1 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A6YH-01A-21D-A32B-08 chr18:71740800 G>A maps to NM_001142958.1 H476H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:39433382 G>A maps to ENST00000448145 H69H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:100190524 C>A maps to NM_012172.4 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:100198335 C>T maps to NM_012172.4 C557C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8162-01A-21D-2253-08 chr7:100187921 G>A maps to NM_012172.4 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A858-01A-11D-A36O-08 chr7:100189398 T>C maps to NM_012172.4 D182D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:418713 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:381364 A>G maps to NM_183421.1 E53E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WO-01A-21D-A34A-08 chr19:39517587 G>A maps to NM_178820.3 D210D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R5-01A-11D-A289-08 chr6:146126347 A>G maps to NM_032145.4 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YJ-01A-11D-A34A-08 chr16:87377353 G>A maps to NM_024735.3 I169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YW-01A-11D-A34J-08 chr16:87367622 C>T maps to NM_024735.3 E422E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7855-01A-11D-2395-08 chr14:39870638 G>A maps to NM_203301.3 I379I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6670-01A-11D-1893-08 chr5:147803621 T>C maps to NM_205836.1 N560N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7301-01A-11D-2086-08 chr8:101146457 T>C maps to NM_001029860.3 G603G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:11718909 C>T maps to ENST00000376768 R193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:46215958 G>A maps to NM_001080469.1 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6405-01A-11D-1705-08 chr19:46216179 G>A maps to NM_001080469.1 R192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:37111186 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:37118181 C>T maps to NM_001008777.2 E100E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:11733670 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:32875190 C>T maps to NM_012179.3 Q116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:18682532 C>A maps to ENST00000395665 I1027I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:171303504 G>A maps to NM_012300.2 N314N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:139835905 G>A maps to NM_018998.2 Y418Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XD-01A-11D-A27K-08 chr12:117448195 G>A maps to NM_153348.2 T436T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:40419876 G>A maps to NM_003890.2 G1039G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:40412177 C>T maps to NM_003890.2 P1150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:40433185 C>T maps to NM_003890.2 V361V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YM-01A-11D-A34A-08 chr19:40408806 G>A maps to NM_003890.2 N1344N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7470-01A-12D-2086-08 chr19:40357727 G>A maps to NM_003890.2 S5195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:17888999 G>A maps to NM_015122.2 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7854-01A-11D-2253-08 chr19:17895688 G>A maps to NM_015122.2 V794V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R3-01A-11D-A34J-08 chr5:72383518 A>G maps to NM_138782.2 V783V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7694-01A-11D-2253-08 chr9:137804959 G>T maps to NM_002003.3 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6393-01A-11D-1705-08 chr1:157766908 C>T maps to NM_052938.4 G400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6400-01A-12D-1705-08 chr1:157667653 C>A maps to NM_052939.3 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7854-01A-11D-2253-08 chr1:157665875 G>A maps to NM_052939.3 N362N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UR-01A-11D-A33T-08 chr1:157545509 G>A maps to NM_031282.2 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6J3-01A-11D-A31L-08 chr1:157516957 G>A maps to NM_031281.2 Q28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A617-01A-11D-A29Q-08 chr1:157490930 C>T maps to NM_031281.2 S797S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr1:161681130 C>T maps to NM_001184866.1 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8164-01A-11D-2253-08 chr1:161681736 G>A maps to NM_001184866.1 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:111746476 T>C maps to NM_138378.1 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:114860792 G>A maps to NM_020177.2 R356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:97369333 G>A maps to NM_001113382.1 S1958S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:124987528 C>T maps to NM_001039112.2 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr8:125082818 C>T maps to NM_001039112.2 R1316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:6068528 G>A maps to NM_017671.4 G422G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TP-01A-11D-A289-08 chr15:91437241 C>T maps to NM_002005.3 P760P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:125359495 C>A maps to NM_005103.4 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8010-01A-11D-2395-08 chr19:35850685 G>A maps to NM_005304.3 W298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr4:155505773 G>A maps to NM_000508.3 D701D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YJ-01A-11D-A34A-08 chr4:155505467 A>G maps to NM_000508.3 Y803Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A89Z-01A-11D-A36O-08 chr4:155505788 G>A maps to NM_000508.3 F696F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:54472772 G>A did not map to a codon.
Sequencing variant TCGA-FG-A6J1-01A-11D-A31L-08 chr23:54497146 T>G did not map to a codon.
Sequencing variant TCGA-S9-A7IZ-01A-11D-A34A-08 chr23:54475672 G>A did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr6:36978765 C>T maps to NM_173558.3 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7008-01A-11D-2024-08 chr9:95795122 C>T maps to NM_033086.2 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr9:95738978 C>T maps to NM_033086.2 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5965-01B-11D-1893-08 chr12:32791722 C>G maps to NM_139241.2 A679A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:14862980 G>A maps to NM_152536.3 T801T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6405-01A-11D-1705-08 chr3:14862335 G>A maps to NM_152536.3 S586S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7677-01A-11D-2253-08 chr3:14862572 G>A maps to NM_152536.3 T665T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7483-01A-11D-2024-08 chr12:95604906 T>G maps to NM_018351.3 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:44305207 A>G maps to NM_004465.1 N172N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:137939698 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:137939757 C>T did not map to a codon.
Sequencing variant TCGA-DU-5874-01A-11D-1705-08 chr13:103053947 C>T maps to NM_175929.2 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:76711987 C>T did not map to a codon.
Sequencing variant TCGA-E1-A7YM-01A-11D-A34A-08 chr23:76711875 G>A did not map to a codon.
Sequencing variant TCGA-HT-7475-01A-11D-2024-08 chr8:16850595 T>C maps to NM_019851.2 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F0-01A-11D-A289-08 chr19:49261317 A>C maps to NM_019113.2 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YD-01A-11D-A34A-08 chr19:643471 C>T maps to NM_020637.1 Y127Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7304-01A-12D-2086-08 chr12:4479523 G>A maps to NM_020638.2 F247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7604-01A-11D-2086-08 chr11:69631174 C>T maps to NM_005247.2 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6J3-01A-11D-A31L-08 chr12:4543494 G>A maps to NM_020996.1 Y171Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:22275411 C>T maps to NM_002010.2 H155H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:38285862 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:1808272 C>T maps to NM_000142.4 V677V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7854-01A-11D-2253-08 chr5:176519744 C>T maps to NM_213647.1 I339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7875-01A-11D-2395-08 chr5:176520244 G>A maps to NM_213647.1 G388G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:1018774 C>T maps to NM_021923.3 A385A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4X9-01A-11D-A26M-08 chr7:76826041 G>A maps to NM_006682.2 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7606-01A-11D-2086-08 chr1:27943401 G>A maps to NM_005248.2 F216F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:153886115 G>A maps to NM_033393.2 Q363Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:153896905 C>A maps to NM_033393.2 S821S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A6MO-01A-11D-A33T-08 chr4:153864691 A>G maps to NM_033393.2 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:67272031 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:67272336 G>A maps to NM_013241.2 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:67264290 G>A maps to NM_013241.2 R993*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:34324062 G>A maps to NM_025135.2 S1141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:34092483 C>T maps to NM_025135.2 N163N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr9:133780651 C>T maps to NM_001145106.1 P365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:108913161 G>C maps to NM_007076.2 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7695-01A-11D-2253-08 chr23:15365419 A>G did not map to a codon.
Sequencing variant TCGA-HT-7606-01A-11D-2086-08 chr7:50513533 T>C maps to NM_022116.3 A484A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr6:76024623 C>T maps to NM_015687.2 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YI-01A-11D-A34A-08 chr4:54308817 A>C did not map to a codon.
Sequencing variant TCGA-S9-A6WN-01A-12D-A33T-08 chr14:24600894 A>G maps to NM_203402.2 E41E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:56103881 G>A maps to NM_032836.2 C475C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:30054473 A>G maps to NM_017946.2 H171H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:30058725 T>C maps to NM_017946.2 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:115932852 C>T maps to ENST00000446284 E930E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A87N-01A-11D-A36O-08 chr12:2909743 G>A did not map to a codon.
Sequencing variant TCGA-HT-7884-01B-11D-2395-08 chr12:2910515 G>A maps to NM_002014.3 E422E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr7:72754698 C>T maps to NM_003602.3 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6394-01A-11D-1705-08 chr19:18650227 C>T maps to NM_012181.3 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:33039867 C>T maps to NM_007270.3 G456G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A847-01A-11D-A36O-08 chr6:32097116 G>A maps to NM_022110.3 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:17120460 C>T maps to NM_144997.5 W366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr1:152275718 C>T maps to NM_002016.1 E3881E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr1:152280317 G>A maps to NM_002016.1 H2348H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:152282657 G>A maps to NM_002016.1 A1568A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:152279720 C>T maps to NM_002016.1 S2547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr1:152283913 G>T maps to NM_002016.1 R1150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr1:152282000 T>C maps to NM_002016.1 G1787G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KJ-01A-12D-A27K-08 chr1:152281298 G>A maps to NM_002016.1 G2021G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A89Z-01A-11D-A36O-08 chr1:152275640 G>A maps to NM_002016.1 R3907R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85E-01A-11D-A36O-08 chr1:152285645 T>G maps to NM_002016.1 R572R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:152326319 A>G maps to NM_001014342.2 T1314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RF-01A-11D-A33T-08 chr1:152324783 G>A maps to NM_001014342.2 H1826H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RM-01A-11D-A33T-08 chr1:152324114 G>A maps to NM_001014342.2 H2049H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:128680651 G>A maps to NM_002017.3 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:18156616 G>A maps to NM_002018.2 C337C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7902-01A-12D-2395-08 chr14:21552187 G>T maps to NM_018071.3 V1256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UU-01A-12D-A34A-08 chr9:84606221 C>A maps to NM_001001670.2 C279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5849-01A-11D-1705-08 chr9:84606295 T>A maps to NM_001001670.2 L304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84G-01A-11D-A36O-08 chr9:84609656 T>C maps to NM_001001670.2 D1424D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64Q-01A-11D-A29Q-08 chr23:153595806 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153596035 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153592533 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153582582 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153592949 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153581703 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153582629 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153587379 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153588192 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153583192 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153589696 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153587863 G>A did not map to a codon.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr23:153588483 C>T did not map to a codon.
Sequencing variant TCGA-DU-7302-01A-11D-2086-08 chr23:153593775 A>T did not map to a codon.
Sequencing variant TCGA-FG-7638-01B-11D-2086-08 chr23:153593613 G>A did not map to a codon.
Sequencing variant TCGA-FG-A70Z-01A-12D-A33T-08 chr23:153599590 G>A did not map to a codon.
Sequencing variant TCGA-FG-A713-01A-11D-A32B-08 chr23:153583248 C>T did not map to a codon.
Sequencing variant TCGA-TM-A7CF-01A-11D-A32B-08 chr23:153585625 G>T did not map to a codon.
Sequencing variant TCGA-VM-A8CF-01A-11D-A36O-08 chr23:153586583 G>A did not map to a codon.
Sequencing variant TCGA-DB-A64V-01A-11D-A29Q-08 chr3:58111407 C>T maps to NM_001164317.1 A1333A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:58080561 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:58132694 C>T maps to NM_001164317.1 G1932G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:58097996 C>T maps to NM_001164317.1 I899I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:58135652 C>A maps to NM_001164317.1 T2087T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7302-01A-11D-2086-08 chr3:58095049 G>C did not map to a codon.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr3:58080623 C>T maps to NM_001164317.1 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr3:58108830 C>T maps to NM_001164317.1 H1046H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-8125-01A-11D-2253-08 chr3:58097874 G>A did not map to a codon.
Sequencing variant TCGA-DB-A4XB-01A-11D-A26M-08 chr7:128482971 G>A maps to NM_001458.4 A838A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr7:128488740 G>A maps to NM_001458.4 A1569A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr7:128489529 C>T maps to NM_001458.4 D1699D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8186-01A-11D-2253-08 chr7:128480692 G>A maps to NM_001458.4 V547V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RM-01A-11D-A33T-08 chr7:128481608 G>A maps to NM_001458.4 K703K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RQ-01A-11D-A33T-08 chr7:128478759 C>T maps to NM_001458.4 C438C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RH-01A-12D-A34A-08 chr17:27207789 G>A maps to ENST00000394906 R452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:63884782 C>T maps to NM_013280.4 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:86088856 C>T maps to NM_013231.4 N333N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:86088011 C>T maps to NM_013231.4 R52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8182-01A-11D-2253-08 chr14:86089273 C>T maps to NM_013231.4 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7476-01A-11D-2024-08 chr20:14307456 C>T maps to NM_198391.2 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:28877366 G>A maps to NM_002019.4 I1318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:28908199 G>T maps to NM_002019.4 S852*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RP-01A-21D-A34A-08 chr13:29004259 C>A maps to NM_002019.4 E345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8109-01A-11D-2395-08 chr13:28611412 A>G maps to NM_004119.2 F406F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8109-01A-11D-2395-08 chr13:28609683 A>G maps to NM_004119.2 C515C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5871-01A-12D-1705-08 chr5:180046670 G>A maps to NM_182925.4 L881L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr5:180043381 G>A maps to NM_182925.4 Y1068Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7T6-01A-11D-A33T-08 chr5:180047674 G>C maps to NM_182925.4 V780V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr5:180046722 G>A maps to NM_182925.4 S863S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CV-01A-11D-A31L-08 chr5:180056399 G>A maps to NM_182925.4 R282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A89V-01A-11D-A36O-08 chr5:180038362 C>T maps to NM_182925.4 P1218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8161-01A-11D-2253-08 chr14:76101272 A>G maps to NM_017791.2 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F4-01A-11D-A289-08 chr16:2983272 G>A maps to ENST00000399667 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:33200737 G>A maps to NM_001103184.2 Y887Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7471-01A-11D-2253-08 chr1:240371420 C>T maps to ENST00000406993 P1246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7C5-01A-11D-A32B-08 chr1:240371405 T>A maps to ENST00000406993 P1241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:43322422 G>A maps to NM_005892.3 P892P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:43320642 G>T maps to NM_005892.3 R723R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr17:43314942 G>T maps to NM_005892.3 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6404-01A-11D-1705-08 chr2:153473699 C>T maps to NM_052905.3 V436V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7857-01A-11D-2395-08 chr12:50043068 A>G maps to NM_175736.4 Y786Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:171251410 C>T maps to NM_002021.1 P374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:171173167 C>T maps to NM_001460.2 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7882-01A-11D-2395-08 chr1:171079964 C>G maps to NM_006894.5 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr1:171300884 A>G maps to NM_002022.1 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5142-01A-01D-1468-08 chr1:203316987 G>A maps to NM_002023.3 H137H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:203316872 G>A maps to NM_002023.3 R176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr1:203311548 G>A maps to NM_002023.3 D351D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:147026456 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:147013975 A>G did not map to a codon.
Sequencing variant TCGA-FG-8188-01A-11D-2253-08 chr23:147010282 T>C did not map to a codon.
Sequencing variant TCGA-S9-A6WG-01A-11D-A33T-08 chr23:147014239 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:147084730 T>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:147088321 G>A did not map to a codon.
Sequencing variant TCGA-HT-7605-01A-11D-2086-08 chr23:147106437 A>G did not map to a codon.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr23:147084822 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:80684938 G>A maps to NM_024619.3 E274E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A614-01A-11D-A29Q-08 chr11:47753112 C>T maps to NM_015308.2 R607R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RU-01A-21D-A34A-08 chr11:47744590 A>T maps to NM_015308.2 P914P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CS-4941-01A-01D-1468-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr13:49772708 C>A maps to ENST00000497644 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:131008546 G>A maps to NM_133372.2 D530D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:159791563 C>T maps to ENST00000379346 T987T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:42927339 T>C maps to NM_002027.2 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr11:49207239 T>C maps to NM_004476.1 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:49207245 A>G maps to NM_004476.1 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6UA-01A-12D-A33T-08 chr11:71906439 G>A maps to NM_016729.2 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R1-01A-12D-A34J-08 chr11:71906325 G>A maps to NM_016729.2 W60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7T6-01A-11D-A33T-08 chr11:94038837 G>A maps to NM_001080486.1 W12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:46375613 G>A maps to NM_004497.2 K117K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr9:70177704 C>T maps to NM_001126334.1 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:100616504 C>T maps to NM_004473.3 H103H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5874-01A-11D-1705-08 chr16:86546528 A>G did not map to a codon.
Sequencing variant TCGA-HT-7684-01A-11D-2253-08 chr14:29237033 G>A maps to NM_005249.3 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RW-01A-11D-A33T-08 chr5:169533254 C>T maps to NM_012188.4 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5143-01A-01D-1468-08 chr12:8200511 G>A maps to NM_018416.2 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5143-01A-01D-1468-08 chr17:80544071 C>G maps to NM_004514.3 V524V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:80559224 G>A maps to NM_004514.3 S611S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:138664484 G>A maps to NM_023067.3 Y360Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7620-01A-11D-2253-08 chr12:2968214 C>T maps to NM_202002.1 T665T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:48602107 C>T maps to NM_002158.3 Y274Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:89628994 G>A maps to NM_001085471.1 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A733-01A-11D-A32B-08 chr23:70320667 C>T did not map to a codon.
Sequencing variant TCGA-S9-A7R8-01A-11D-A34J-08 chr23:70321219 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:71102875 G>A maps to NM_032682.4 Q111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5280-01A-01D-1468-08 chr7:114269948 A>G maps to NM_148898.3 Q187Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:114304485 G>A maps to NM_148898.3 P691P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IQ-01A-21D-A34A-08 chr7:114269972 A>G maps to NM_148898.3 Q195Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:55650154 A>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:55650713 G>A did not map to a codon.
Sequencing variant TCGA-HT-7691-01A-11D-2253-08 chr23:55650389 G>A did not map to a codon.
Sequencing variant TCGA-S9-A6WD-01A-12D-A33T-08 chr23:55651076 T>C did not map to a codon.
Sequencing variant TCGA-DH-A66F-01A-11D-A29Q-08 chr20:30432673 G>A maps to NM_004118.3 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:30433194 G>A maps to NM_004118.3 R51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A6S7-01A-21D-A32B-08 chr20:30433324 G>A maps to NM_004118.3 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A733-01A-11D-A32B-08 chr20:30432874 C>T maps to NM_004118.3 E157E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-8125-01A-11D-2253-08 chr9:130570868 C>G maps to NM_004957.4 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EY-01A-11D-A27K-08 chr19:52327321 C>A maps to NM_002030.3 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7US-01A-11D-A33T-08 chr4:79328943 A>G maps to NM_025074.6 V1419V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UU-01A-12D-A34A-08 chr4:79443926 A>G maps to NM_025074.6 P3591P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:79434659 C>T maps to NM_025074.6 H3376H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:79443852 T>C maps to NM_025074.6 L3567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:79443935 C>T maps to NM_025074.6 L3594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7637-01A-11D-2086-08 chr4:79204002 C>A maps to NM_025074.6 C379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A4DS-01A-11D-A26M-08 chr4:79387411 C>T maps to NM_025074.6 I2360I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:14748497 A>C maps to ENST00000380880 S1902S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:14819254 G>A maps to ENST00000380880 G844G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CF-01A-11D-A36O-08 chr9:14746436 C>T maps to ENST00000380880 G2059G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:39262269 C>T maps to NM_207361.4 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F6-A8O3-01A-11D-A36O-08 chr4:190864381 A>T maps to NM_004477.2 K30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WH-A86K-01A-11D-A36O-08 chr10:135440108 G>A maps to ENST00000443774 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:116277639 A>G maps to NM_002031.2 H311H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4942-01A-01D-1468-08 chr6:168479687 T>C maps to NM_024919.3 E29E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7469-01A-11D-2253-08 chr10:13825005 C>T maps to NM_018027.3 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7604-01A-11D-2086-08 chr10:13698930 G>A maps to NM_018027.3 G886G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RS-01A-12D-A33T-08 chr3:69230683 C>T maps to NM_015123.1 E739E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:52194542 C>T maps to ENST00000344768 F555F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A87N-01A-11D-A36O-08 chr14:52188775 G>A maps to ENST00000344768 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4942-01A-01D-1468-08 chr23:131216496 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:131228095 G>A did not map to a codon.
Sequencing variant TCGA-FG-8185-01A-11D-2253-08 chr23:131214291 C>G did not map to a codon.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr23:131212490 A>G did not map to a codon.
Sequencing variant TCGA-HW-7490-01A-11D-2024-08 chr23:131214036 T>C did not map to a codon.
Sequencing variant TCGA-S9-A6U1-01A-21D-A33T-08 chr23:131216553 C>A did not map to a codon.
Sequencing variant TCGA-S9-A6WI-01A-21D-A33T-08 chr10:49440275 G>A maps to NM_001018071.3 N350N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:12734903 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:12722502 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:12627866 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:12736535 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:12701656 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:12735194 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:12734612 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:12734711 G>A did not map to a codon.
Sequencing variant TCGA-DU-6394-01A-11D-1705-08 chr23:12701667 C>T did not map to a codon.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr23:12736403 C>T did not map to a codon.
Sequencing variant TCGA-E1-5319-01A-01D-1893-08 chr23:12735804 C>T did not map to a codon.
Sequencing variant TCGA-HT-7607-01A-11D-2086-08 chr23:12720060 C>T did not map to a codon.
Sequencing variant TCGA-HT-7884-01B-11D-2395-08 chr23:12736147 T>C did not map to a codon.
Sequencing variant TCGA-HW-7489-01A-11D-2024-08 chr23:12734263 C>T did not map to a codon.
Sequencing variant TCGA-QH-A65S-01A-11D-A29Q-08 chr23:12736537 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:100174573 C>T maps to NM_001013660.2 K587K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64Q-01A-11D-A29Q-08 chr6:41738832 G>A maps to NM_006653.3 Q335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:41738412 G>A maps to NM_006653.3 R475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5396-01A-02D-1468-08 chr13:32747574 A>C maps to NM_023037.2 V741V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:32826032 T>C maps to NM_023037.2 L2397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TB-01A-11D-A33T-08 chr13:32605976 A>G maps to NM_023037.2 K15K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7490-01A-11D-2024-08 chr13:32852685 G>C did not map to a codon.
Sequencing variant TCGA-HT-7477-01B-11D-A289-08 chr4:48536662 G>A maps to NM_015030.1 L2202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:183699581 G>A maps to NM_001463.3 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7481-01A-11D-2024-08 chr14:44975037 G>T maps to NM_032135.3 R385R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UV-01A-12D-A34A-08 chr7:127235773 T>C maps to NM_020369.2 D186D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64U-01A-11D-A29Q-08 chr19:4310576 A>G maps to NM_024333.2 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:49190102 G>T maps to NM_000145.3 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:49195865 G>A maps to NM_000145.3 C275C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr15:39910062 C>T maps to NM_152597.4 S524S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A83Z-01A-11D-A36O-08 chr2:186670583 A>G maps to NM_173651.2 K5606K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:52779373 C>T maps to NM_013409.1 C106C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:120121676 G>A maps to NM_007085.4 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R2-01A-21D-A34J-08 chr3:120123740 A>G maps to NM_007085.4 N180N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5874-01A-11D-1705-08 chr19:681420 G>A maps to NM_005860.2 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:132537632 G>A maps to NM_015082.1 N606N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5397-01A-01D-1893-08 chr4:162463804 T>C maps to NM_020116.3 R352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5318-01A-01D-1468-08 chr4:162577527 C>T maps to NM_020116.3 W282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7469-01A-11D-2253-08 chr4:162697148 G>A maps to NM_020116.3 Q163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:47570385 G>A maps to ENST00000397748 N230N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:31089584 C>T did not map to a codon.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr5:121187708 G>A maps to NM_177478.1 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7609-01A-11D-2086-08 chr5:121188110 C>T maps to NM_177478.1 D151D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8161-01A-11D-2253-08 chr23:48337055 A>G did not map to a codon.
Sequencing variant TCGA-IK-8125-01A-11D-2253-08 chr23:48339828 G>T did not map to a codon.
Sequencing variant TCGA-S9-A6WN-01A-12D-A33T-08 chr23:48337015 C>T did not map to a codon.
Sequencing variant TCGA-E1-A7Z3-01A-11D-A34J-08 chr16:71319562 C>T maps to NM_018348.5 E87E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:37429387 C>T maps to NM_015050.2 Q387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5390-01A-02D-1468-08 chr1:78430844 C>A maps to ENST00000436586 G203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5394-01A-01D-1468-08 chr1:78422351 C>T maps to ENST00000436586 W558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr1:78432435 C>T did not map to a codon.
Sequencing variant TCGA-DB-A64Q-01A-11D-A29Q-08 chr1:78429936 A>C did not map to a codon.
Sequencing variant TCGA-DB-A64V-01A-11D-A29Q-08 chr1:78430552 A>G did not map to a codon.
Sequencing variant TCGA-DH-5144-01A-01D-1468-08 chr1:78429847 C>T did not map to a codon.
Sequencing variant TCGA-DH-A7UR-01A-11D-A33T-08 chr1:78430643 C>A maps to ENST00000436586 G237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:78433849 G>A maps to ENST00000436586 D104D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YO-01A-11D-A34A-08 chr1:78430653 C>T did not map to a codon.
Sequencing variant TCGA-FG-A710-01A-12D-A33T-08 chr1:78429829 C>A maps to ENST00000436586 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7467-01A-11D-2024-08 chr1:78435639 A>C maps to ENST00000436586 Y60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7467-01A-11D-2024-08 chr1:78435642 A>C maps to ENST00000436586 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7471-01A-11D-2253-08 chr1:78430772 C>A maps to ENST00000436586 E227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7481-01A-11D-2024-08 chr1:78420961 C>T maps to ENST00000436586 W608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7620-01A-11D-2253-08 chr1:78429791 A>T maps to ENST00000436586 C353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CZ-01A-11D-A32B-08 chr1:78428498 G>A maps to ENST00000436586 Q455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A83Y-01A-11D-A36O-08 chr1:78429796 G>A maps to ENST00000436586 R352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7J3-01A-21D-A34J-08 chr1:78430432 C>T did not map to a codon.
Sequencing variant TCGA-TM-A84M-01A-11D-A36O-08 chr1:78432597 C>A maps to ENST00000436586 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A75K-01A-11D-A32B-08 chr6:143818528 T>G maps to NM_032020.4 T420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5964-01A-11D-1705-08 chr6:143823181 T>C maps to NM_032020.4 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:31199644 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:49254307 G>T maps to NM_000148.3 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:49253958 C>A maps to NM_000148.3 E194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7875-01A-11D-2395-08 chr11:94278273 C>T maps to NM_002033.3 D325D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:5832131 G>A maps to NM_001040701.1 D149D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XG-01A-11D-A27K-08 chr9:139925575 G>A maps to NM_004479.3 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr14:66028459 T>A maps to NM_178155.1 L60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:96651393 T>A maps to NM_006581.3 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:180685890 C>T maps to NM_005087.3 D417D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:180652994 A>G maps to NM_005087.3 E58E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:39126167 T>C maps to ENST00000263405 K668K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:39202951 G>A maps to ENST00000263405 N46N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr5:39202452 G>A maps to ENST00000263405 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6689-01A-11D-1893-08 chr5:39126187 A>G maps to ENST00000263405 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7858-01A-11D-2395-08 chr5:39203056 C>T maps to ENST00000263405 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:46008665 C>T maps to NM_024513.2 Q720Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5304-01A-01D-1468-08 chr3:46014620 C>T maps to NM_024513.2 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr3:46023169 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:130649217 G>A maps to NM_007197.3 S577S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:42636612 G>A maps to NM_001466.3 T519T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RU-01A-21D-A34A-08 chr11:86662453 T>C maps to NM_012193.2 A448A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr8:104337522 C>T maps to NM_003506.3 R397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:202900491 C>T maps to NM_003507.1 I374I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:35929970 C>T maps to NM_031866.2 W129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65Z-01A-11D-A29Q-08 chr1:209849304 C>T maps to NM_015714.3 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RK-01A-11D-A33T-08 chr14:31074771 A>T maps to NM_017769.3 K358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:151179872 A>G maps to NM_198395.1 E350E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:41052902 G>T maps to NM_000151.2 G4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153762599 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153774301 G>A did not map to a codon.
Sequencing variant TCGA-DU-6404-01A-11D-1705-08 chr23:153761825 C>T did not map to a codon.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr23:153760889 G>A did not map to a codon.
Sequencing variant TCGA-HT-7877-01A-11D-2395-08 chr23:153762633 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:78078630 C>T maps to NM_001079804.1 C82C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:78079615 G>A maps to NM_001079804.1 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YL-01A-11D-A34A-08 chr11:77961362 G>A maps to NM_080491.2 R154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A781-01A-11D-A32B-08 chr11:77937661 T>G maps to NM_080491.2 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153940893 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153940611 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153941610 G>T did not map to a codon.
Sequencing variant TCGA-HT-A5R5-01A-11D-A289-08 chr23:153906496 G>C did not map to a codon.
Sequencing variant TCGA-S9-A6TS-01A-12D-A33T-08 chr23:153940502 C>A did not map to a codon.
Sequencing variant TCGA-DB-A4XD-01A-11D-A27K-08 chr22:17444665 C>G maps to NM_001037814.1 P510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:29591180 T>C maps to NM_001470.2 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:101068591 G>A maps to NM_005458.7 N680N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RG-01A-11D-A33T-08 chr9:101068570 G>A maps to NM_005458.7 N687N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85E-01A-11D-A36O-08 chr9:101056065 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:50570878 G>A maps to NM_005254.5 Q380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:161317902 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:151424260 G>T did not map to a codon.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr23:151336929 A>T did not map to a codon.
Sequencing variant TCGA-HT-7607-01A-11D-2086-08 chr23:151532993 G>C did not map to a codon.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr23:151336861 C>T did not map to a codon.
Sequencing variant TCGA-DU-A7TJ-01A-11D-A34J-08 chr4:46967201 G>A maps to NM_000809.2 R307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WL-01A-21D-A33T-08 chr4:46967169 G>A maps to NM_000809.2 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:27193349 G>A maps to NM_000810.3 P453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XE-01A-11D-A27K-08 chr5:161119013 A>T maps to NM_000811.2 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5874-01A-11D-1705-08 chr23:151123360 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:151138182 C>A did not map to a codon.
Sequencing variant TCGA-DU-8162-01A-21D-2253-08 chr23:151123278 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:46043151 A>G maps to NM_173536.3 C417C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr4:46060561 A>G maps to NM_173536.3 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74O-01A-11D-A32B-08 chr4:46053575 C>T maps to NM_173536.3 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5397-01A-01D-1893-08 chr5:161580181 C>T maps to NM_198903.2 Y452Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:151806758 G>A did not map to a codon.
Sequencing variant TCGA-E1-A7YM-01A-11D-A34A-08 chr6:89888739 G>A maps to NM_002042.3 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:89977467 C>T maps to NM_002043.2 K247K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5396-01A-02D-1468-08 chr3:30885752 A>G maps to NM_207359.2 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:30842577 A>G maps to NM_207359.2 D351D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr23:49355892 C>G did not map to a codon.
Sequencing variant TCGA-S9-A6TV-01A-12D-A34J-08 chr23:49355892 C>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:68453073 C>T maps to NM_015973.3 R32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:30951065 G>A maps to NM_004861.1 I382I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6X5-01A-12D-A32B-08 chr14:88454497 C>A maps to NM_000153.2 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7299-01A-21D-2024-08 chr1:24124672 G>A maps to NM_001008216.1 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A60K-01A-11D-A29Q-08 chr2:38903111 C>T maps to NM_138801.2 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:88901651 G>A maps to NM_000512.4 N289N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TD-01A-12D-A34A-08 chr16:88889097 C>T maps to NM_000512.4 G421G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YE-01A-11D-A34A-08 chr18:33283592 G>T maps to NM_020474.3 E507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:153795488 C>T maps to NM_198321.3 R550R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:151807672 A>G maps to NM_022087.2 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R1-01A-12D-A34J-08 chr9:101608399 C>T maps to NM_024642.3 Q534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:155307044 C>T maps to NM_052917.2 N551N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:31133787 G>A maps to NM_024572.2 H546H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A711-01A-21D-A33T-08 chr2:31167746 G>A maps to NM_024572.2 R268R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:230372443 C>T maps to NM_004481.3 R194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:51759334 G>A maps to NM_007210.3 Y231Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:69787426 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:173269673 C>T maps to NM_001034845.2 N129N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CS-01A-11D-A31L-08 chr17:74071242 C>T maps to NM_003857.2 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr11:62400105 G>A maps to NM_198335.2 R331R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:57790693 C>T maps to NM_152687.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:128124974 C>T maps to NM_015635.2 Q1472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7472-01A-11D-2024-08 chr9:128124937 T>C maps to NM_015635.2 A1459A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8114-01A-11D-2395-08 chr13:114531663 C>T maps to ENST00000357389 A431A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6XC-01A-12D-A32B-08 chr17:9829984 G>A maps to NM_201433.1 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:39871717 C>A maps to NM_000805.3 I10I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr23:48650341 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:8115913 G>A maps to NM_001002295.1 T421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6407-01A-13D-1705-08 chr10:8100436 G>A maps to NM_001002295.1 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7604-01A-11D-2086-08 chr10:8100385 G>A maps to NM_001002295.1 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:19751404 G>A maps to NM_005257.3 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:153800487 C>T did not map to a codon.
Sequencing variant TCGA-DU-7302-01A-11D-2086-08 chr12:120894950 C>T maps to NM_176818.2 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr15:45658330 T>C maps to ENST00000432007 K350K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A61B-01A-11D-A29Q-08 chr9:35741040 T>C maps to NM_020944.2 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:104139344 A>G maps to NM_004193.2 R1570R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:104120793 C>T maps to NM_004193.2 R469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr10:104141972 C>T maps to NM_004193.2 G1820G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QW-01A-11D-A34A-08 chr9:136029209 C>T maps to NM_021996.4 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4943-01A-01D-1468-08 chr1:89520409 G>C maps to NM_002053.2 V540V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UU-01A-12D-A34A-08 chr1:89659074 C>T maps to NM_052941.4 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7695-01A-11D-2253-08 chr1:89730623 A>G maps to NM_052942.3 Y298Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:89848257 G>A maps to NM_198460.2 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:237074679 G>A maps to NM_001485.2 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:163215566 T>C maps to NM_012198.3 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:127224741 C>T maps to NM_024523.5 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:109103046 G>A maps to NM_181453.3 T1291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:109086934 G>T maps to NM_181453.3 E384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7470-01A-12D-2086-08 chr19:13006896 A>G maps to NM_000159.2 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:53370684 C>T maps to NM_001498.3 Q402Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:52993555 C>T maps to NM_003643.3 Q253Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:52993009 C>T maps to NM_003643.3 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7471-01A-11D-2253-08 chr6:52993189 G>A maps to NM_003643.3 Y375Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:10874353 G>A maps to NM_004752.3 H465H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:120613991 C>T maps to NM_006836.1 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr9:79117863 G>A maps to NM_001097636.1 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr6:10529179 G>A maps to NM_145649.4 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8163-01A-11D-2253-08 chr15:59911327 G>A maps to NM_004751.2 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:57924667 C>T maps to NM_001018090.3 R239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr15:57976626 G>C maps to NM_001018100.3 V444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5393-01A-01D-1468-08 chr1:118441727 C>A maps to NM_017686.3 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:56142562 C>T maps to NM_005811.3 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr12:7843232 G>A maps to NM_020634.1 N112N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:34021925 G>A maps to NM_000557.2 C429C. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DU-6392-01A-11D-1705-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:34022012 G>A maps to ENST00000374375 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr8:97156958 G>A maps to NM_001001557.2 H400H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TU-01A-12D-A32B-08 chr8:97157051 G>A maps to NM_001001557.2 D369D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:132197652 G>T maps to NM_005260.3 P331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:132198024 C>T maps to NM_005260.3 K207K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5144-01A-01D-1468-08 chr23:153668415 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153669465 C>T did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr23:153670770 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:69652786 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:69646846 C>T did not map to a codon.
Sequencing variant TCGA-DU-6404-01A-11D-1705-08 chr23:69652186 C>A did not map to a codon.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr23:69652494 A>T did not map to a codon.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr23:69652259 G>A did not map to a codon.
Sequencing variant TCGA-RY-A845-01A-11D-A36O-08 chr23:69645907 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:58009708 C>T maps to NM_001111270.1 R482R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:58007288 G>T maps to NM_001111270.1 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85C-01A-11D-A36O-08 chr8:95272440 A>G maps to NM_181702.2 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:649629 G>A maps to NM_015721.2 R551R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6666-01A-11D-1893-08 chr5:154307076 A>G maps to NM_015465.3 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:45593755 C>A maps to NM_024707.2 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr23:14027047 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:179743861 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:117884796 A>G maps to NM_005264.4 Y235Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A61C-01A-11D-A29Q-08 chr8:21608323 C>T maps to NM_001495.4 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65S-01A-11D-A29Q-08 chr22:38013018 G>A maps to ENST00000381756 E73E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr7:30538451 G>A maps to NM_024051.3 Y130Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84J-01A-11D-A36O-08 chr2:85780432 G>A maps to NM_000821.4 R359R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr19:38876365 G>A maps to NM_152657.3 S512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:24622177 G>A maps to NM_001099781.1 I365I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr17:4461801 G>A maps to ENST00000414312 S336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7294-01A-11D-2024-08 chr20:33439057 C>T maps to NM_178026.2 A567A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A733-01A-11D-A32B-08 chr20:33439993 C>T maps to NM_178026.2 W517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:31018825 C>T maps to NM_000823.3 R413R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:59604791 C>T maps to NM_005142.2 K242K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7300-01A-21D-2086-08 chr11:59611460 T>C maps to NM_005142.2 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A737-01A-11D-A32B-08 chr11:59612896 G>A maps to NM_005142.2 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7490-01A-11D-2024-08 chr7:100280313 G>A maps to NM_022574.4 G833G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:233710514 G>T maps to ENST00000373566 G1149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6405-01A-11D-1705-08 chr2:233674459 C>T maps to ENST00000373566 Q635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IY-01A-11D-A34A-08 chr2:233712218 C>T maps to ENST00000373566 Q1230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:150417358 C>T maps to NM_130759.3 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:150269742 C>T maps to ENST00000430830 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7605-01A-11D-2086-08 chr7:150439640 T>C maps to ENST00000447239 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:150327220 C>A maps to ENST00000438845 E4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6UA-01A-12D-A33T-08 chr7:150217541 C>T maps to NM_153236.3 C160C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8322-01A-11D-2395-08 chr19:14591416 G>A maps to NM_202470.1 Y154Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IX-01A-12D-A34A-08 chr17:27908354 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:110429452 C>T maps to NM_057169.3 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CX-01A-11D-A32B-08 chr6:90605137 T>C maps to NM_032602.1 N317N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XG-01A-11D-A27K-08 chr1:35260638 C>A maps to NM_002060.2 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:147380252 G>A maps to NM_005267.4 Q57Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:147380558 C>T maps to NM_005267.4 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:39340513 C>T maps to NM_030772.4 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7601-01A-11D-2086-08 chr13:20763147 G>A maps to NM_004004.5 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64V-01A-11D-A29Q-08 chr17:42882003 G>A maps to NM_001080383.1 V394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64W-01A-11D-A29Q-08 chr23:30739085 G>A did not map to a codon.
Sequencing variant TCGA-HT-7474-01A-11D-2024-08 chr4:80327818 A>G maps to NM_033214.2 G512G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RN-01A-11D-A33T-08 chr4:80329159 G>A maps to NM_033214.2 Y65Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:100662835 A>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:100662703 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:134239697 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:134179595 C>T maps to NM_001080407.2 N346N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F2-01A-11D-A289-08 chr11:134147258 C>T maps to NM_001080407.2 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:6540084 C>T maps to NM_000170.2 E877E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TB-01A-11D-A33T-08 chr15:51689742 C>T maps to NM_181789.2 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UU-01A-12D-A34A-08 chr2:121747053 G>T maps to NM_005270.4 P1188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5849-01A-11D-1705-08 chr2:121684943 G>A maps to NM_005270.4 Q52Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A6MO-01A-11D-A33T-08 chr2:121712959 C>A maps to NM_005270.4 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:42005517 C>T maps to NM_000168.5 R1051R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:42065983 G>A maps to NM_000168.5 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TA-01A-11D-A33T-08 chr7:42079654 A>T maps to NM_000168.5 L337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RC-01A-11D-A289-08 chr7:42006177 G>A maps to NM_000168.5 S831S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:75875738 C>T maps to NM_006851.2 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QZ-01A-12D-A34J-08 chr12:75741493 C>T maps to ENST00000378695 Y171Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:53980440 G>A maps to NM_147193.2 G405G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7882-01A-11D-2395-08 chr1:53995559 C>T maps to NM_147193.2 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7491-01A-11D-2024-08 chr16:4383345 A>G did not map to a codon.
Sequencing variant TCGA-DU-5851-01A-13D-1893-08 chr9:3828286 G>C maps to NM_001042413.1 V926V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7J0-01A-11D-A34A-08 chr9:4118145 G>T maps to NM_001042413.1 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RU-01A-21D-A34A-08 chr9:4118079 C>T maps to NM_001042413.1 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:679033 A>G maps to ENST00000397393 N332N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:674701 C>T did not map to a codon.
Sequencing variant TCGA-DU-7298-01A-11D-2024-08 chr17:685480 T>C maps to NM_016080.3 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:9729551 C>T maps to NM_004246.1 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6X5-01A-12D-A32B-08 chr23:14548193 A>G did not map to a codon.
Sequencing variant TCGA-QH-A6X8-01A-12D-A32B-08 chr23:14627179 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:175598270 C>T maps to NM_006529.2 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6542-01A-11D-1893-08 chr4:175565194 G>A maps to NM_006529.2 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VW-A7QS-01A-12D-A33T-08 chr4:175603979 G>A maps to NM_006529.2 R229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7474-01A-11D-2024-08 chr23:102962435 C>A did not map to a codon.
Sequencing variant TCGA-VM-A8CF-01A-11D-A36O-08 chr4:158059958 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:191818289 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:56867068 G>A maps to NM_013267.2 D464D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:129467472 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:17692075 C>T maps to NM_024656.2 D564D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7471-01A-11D-2253-08 chr19:17690295 G>A maps to NM_024656.2 V424V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VV-A829-01A-21D-A36O-08 chr19:17688022 G>A maps to NM_024656.2 E323E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8165-01A-11D-2253-08 chr1:183938502 C>T maps to NM_015101.2 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64Q-01A-11D-A29Q-08 chr9:138516116 C>T maps to NM_182974.2 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CV-01A-11D-A31L-08 chr19:48197799 C>T maps to NM_015711.3 S904S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R8-01A-11D-A34J-08 chr19:48248980 G>A maps to NM_015710.4 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85D-01A-11D-A36O-08 chr19:48248902 G>T maps to NM_015710.4 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:88811626 G>A maps to NM_005271.3 Q520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr23:120181765 C>T did not map to a codon.
Sequencing variant TCGA-DU-6401-01A-11D-1705-08 chr23:120182835 G>A did not map to a codon.
Sequencing variant TCGA-KT-A7W1-01A-11D-A34A-08 chr23:120181768 C>T did not map to a codon.
Sequencing variant TCGA-TM-A84R-01A-21D-A36O-08 chr23:120182971 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:58477641 C>T did not map to a codon.
Sequencing variant TCGA-WY-A85D-01A-11D-A36O-08 chr11:58480359 C>A did not map to a codon.
Sequencing variant TCGA-E1-A7YD-01A-11D-A34A-08 chr11:58711062 A>T maps to NM_080661.2 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TD-01A-12D-A34A-08 chr16:4882885 C>T maps to NM_032569.3 K61K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5276-01A-01D-1468-08 chr2:70092030 G>T did not map to a codon.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr6:1961059 C>T maps to NM_001500.2 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr19:19745857 T>G maps to NM_016573.2 I575I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:19740990 G>A maps to NM_016573.2 T898T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RO-01A-11D-A33T-08 chr8:143928000 C>T maps to NM_002066.2 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:49760893 G>A maps to NM_013334.2 D47D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RJ-01A-11D-A33T-08 chr6:16290834 A>G maps to NM_006877.3 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RR-01A-21D-A34A-08 chr14:24707596 C>T maps to ENST00000348719 G281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:50293707 G>A maps to NM_002070.2 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:50294241 C>A maps to NM_002070.2 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F6-01A-11D-A289-08 chr3:50290577 C>T maps to NM_002070.2 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8108-01A-11D-2395-08 chr18:11880998 G>A maps to NM_182978.2 T414T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:56388802 C>T maps to NM_020988.2 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7478-01A-11D-2024-08 chr16:56388961 C>G maps to NM_020988.2 Y354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TD-01A-12D-A34A-08 chr3:50229244 C>T maps to NM_000172.3 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YH-01A-11D-A34A-08 chr3:50230982 G>A maps to NM_000172.3 E112E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:23465440 C>T maps to NM_002073.2 Y297Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:1722019 G>A maps to NM_002074.2 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:100276321 C>T maps to NM_005273.3 V307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-8125-01A-11D-2253-08 chr9:36249250 G>A maps to NM_001128227.2 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8165-01A-11D-2253-08 chr3:52727061 G>A maps to NM_014366.4 Q348Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TS-01A-12D-A33T-08 chr23:54581026 T>C did not map to a codon.
Sequencing variant TCGA-VM-A8CF-01A-11D-A36O-08 chr23:54570717 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:102158792 G>A maps to NM_024312.4 D634D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:102158831 G>A maps to NM_024312.4 N621N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7Z4-01A-11D-A34J-08 chr12:102158786 C>T maps to NM_024312.4 R636R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7694-01A-11D-2253-08 chr4:68606312 C>T maps to NM_000406.2 W291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:127674200 G>A maps to NM_002077.3 H316H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6186-01A-12D-2024-08 chr9:131022429 C>T maps to NM_004486.4 S572S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:131022830 G>A maps to NM_004486.4 N530N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:133353255 G>A maps to NM_005895.3 G1314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YV-01A-11D-A34J-08 chr12:133358905 T>C maps to NM_005895.3 A1147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7676-01A-11D-2395-08 chr12:133353246 T>C maps to NM_005895.3 E1317E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WG-01A-11D-A33T-08 chr12:133353246 T>C maps to NM_005895.3 E1317E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A61B-01A-11D-A29Q-08 chr3:37396654 G>T maps to NM_001172713.1 E2229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:93303729 G>T did not map to a codon.
Sequencing variant TCGA-E1-A7YQ-01A-11D-A34J-08 chr15:75562494 G>T maps to NM_001164404.1 P679P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WN-01A-12D-A33T-08 chr15:75580620 C>T maps to NM_001145224.1 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:121415040 A>G maps to ENST00000393667 A1443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:121433773 C>T maps to ENST00000393667 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:32126329 C>T maps to NM_022130.3 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CX-01A-11D-A32B-08 chr1:204170870 C>T maps to NM_198447.1 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TJ-01A-11D-A34J-08 chr1:155721973 G>T maps to ENST00000368331 R2084R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84G-01A-11D-A36O-08 chr6:117892067 A>T maps to NM_020399.3 V289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:39142344 G>A maps to NM_031899.2 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:20337662 G>A maps to NM_001007240.1 R31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:145139717 C>T maps to NM_003801.3 F368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:113932025 A>G maps to NM_020918.4 Y236Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6188-01A-11D-1893-08 chr19:33608852 A>G maps to NM_018025.2 Q773Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RM-01A-11D-A33T-08 chr19:33581714 C>T maps to NM_018025.2 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:217793348 C>T maps to NM_018040.2 Q183Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:27223971 G>A maps to NM_022078.2 Y232Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr1:27224100 C>T maps to NM_022078.2 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:42477442 G>A maps to NM_001002909.2 R668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:42474971 A>G maps to NM_001002909.2 G1491G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A70Z-01A-12D-A33T-08 chr5:56542307 A>G maps to NM_001127236.2 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7604-01A-11D-2086-08 chr5:56546840 C>T maps to NM_001127236.2 R352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7018-01A-11D-2024-08 chr1:46120874 T>C maps to NM_021639.4 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RC-01A-11D-A289-08 chr1:46120390 G>A maps to NM_021639.4 R101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr23:132887605 C>A did not map to a codon.
Sequencing variant TCGA-DH-5144-01A-01D-1468-08 chr23:132887715 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:132887605 C>A did not map to a codon.
Sequencing variant TCGA-DU-7006-01A-11D-2024-08 chr23:133087086 C>T did not map to a codon.
Sequencing variant TCGA-DU-A7TJ-01A-11D-A34J-08 chr23:132888182 G>A did not map to a codon.
Sequencing variant TCGA-DB-A75L-01A-11D-A32B-08 chr23:132436967 C>G did not map to a codon.
Sequencing variant TCGA-FG-8188-01A-11D-2253-08 chr23:132458382 G>A did not map to a codon.
Sequencing variant TCGA-HT-A5R7-01A-11D-A289-08 chr23:132548971 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:92797192 C>T maps to NM_004466.4 C504C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TZ-01A-21D-A32B-08 chr13:93879732 G>T maps to NM_005708.3 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:5560709 A>C maps to NM_019593.3 Y139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A6S8-01A-12D-A32B-08 chr7:1131727 C>A maps to NM_001505.2 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5390-01A-02D-1468-08 chr14:67576891 G>A maps to NM_020806.4 R443R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:67382746 G>A maps to NM_020806.4 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:67579788 C>T maps to NM_020806.4 H509H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:34856218 G>A maps to NM_000175.3 W16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U0-01A-12D-A32B-08 chr8:144297320 C>T maps to NM_178172.3 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5965-01B-11D-1893-08 chr23:48972593 G>A did not map to a codon.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr23:13795536 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:136113611 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:136112327 G>A did not map to a codon.
Sequencing variant TCGA-TQ-A7RJ-01A-11D-A33T-08 chr23:136113494 C>G did not map to a codon.
Sequencing variant TCGA-TQ-A7RQ-01A-11D-A33T-08 chr23:136113802 C>T did not map to a codon.
Sequencing variant TCGA-KT-A74X-01A-11D-A32B-08 chr6:47647928 T>C maps to NM_153839.6 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64W-01A-11D-A29Q-08 chr23:135405391 C>T did not map to a codon.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr23:135405490 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:135405039 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:135427529 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:135405203 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:135429125 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:135430312 A>G did not map to a codon.
Sequencing variant TCGA-DU-6400-01A-12D-1705-08 chr23:135405537 G>A did not map to a codon.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr23:135430979 G>C did not map to a codon.
Sequencing variant TCGA-DU-A7T6-01A-11D-A33T-08 chr23:135439899 C>T did not map to a codon.
Sequencing variant TCGA-E1-A7YE-01A-11D-A34A-08 chr23:135405258 C>A did not map to a codon.
Sequencing variant TCGA-E1-A7YE-01A-11D-A34A-08 chr23:135485409 G>A did not map to a codon.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr23:135428468 G>C did not map to a codon.
Sequencing variant TCGA-HT-7485-01A-11D-2024-08 chr23:135432486 G>C did not map to a codon.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr23:135429889 C>A did not map to a codon.
Sequencing variant TCGA-R8-A73M-01A-11D-A32B-08 chr23:135431377 A>T did not map to a codon.
Sequencing variant TCGA-RY-A83Z-01A-11D-A36O-08 chr23:135426597 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:26532841 G>T maps to NM_001145168.1 S1070S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr6:47680158 C>T maps to NM_153838.3 R123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr6:46826759 C>T maps to NM_015234.4 R960R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6666-01A-11D-1893-08 chr6:46834707 T>C maps to NM_015234.4 G596G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:46826810 C>T maps to NM_015234.4 K943K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A73M-01A-11D-A32B-08 chr23:129519122 G>T did not map to a codon.
Sequencing variant TCGA-HT-7610-01A-21D-2086-08 chr8:37698690 C>T maps to NM_032777.9 C945C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74L-01A-11D-A32B-08 chr4:22390766 G>A maps to NM_145290.2 C889C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CY-01A-11D-A32B-08 chr4:22390724 C>T maps to NM_145290.2 R903R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A870-01A-11D-A36O-08 chr4:22438137 G>A maps to NM_145290.2 G404G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:131471763 C>T maps to NM_198827.3 N205N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7Z3-01A-11D-A34J-08 chr12:131620641 C>T maps to NM_198827.3 G776G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr1:236341828 C>T maps to NM_003272.3 R194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7007-01A-11D-2024-08 chr16:20043245 C>G maps to NM_001002911.2 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A83Z-01A-11D-A36O-08 chr16:20043305 G>A maps to NM_001002911.2 N271N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U1-01A-21D-A33T-08 chr7:37780774 C>T maps to NM_181791.1 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:9727378 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:9716628 T>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:9711661 C>A did not map to a codon.
Sequencing variant TCGA-FG-A6IZ-01A-11D-A31L-08 chr3:154056036 A>G maps to NM_001038705.1 I549I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:98251791 C>T maps to NM_005290.1 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:145894746 C>T maps to NM_194251.2 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:175301144 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:25877996 G>A maps to NM_020752.2 S605S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:169802422 C>A maps to NM_014373.2 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:168054972 G>A maps to NM_153832.1 Y462Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:6933543 C>T maps to NM_019858.1 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:6934735 C>T maps to NM_019858.1 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7605-01A-11D-2086-08 chr12:6933474 C>T maps to NM_019858.1 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F4-01A-11D-A289-08 chr12:6933810 C>A maps to NM_019858.1 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:150916563 G>A maps to NM_013308.3 R204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A615-01A-11D-A29Q-08 chr8:145584536 G>C maps to NM_024531.3 G400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CV-01A-11D-A31L-08 chr17:4937615 C>T maps to NM_017986.3 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A845-01A-11D-A36O-08 chr23:53105923 G>A did not map to a codon.
Sequencing variant TCGA-DU-A76R-01A-11D-A32B-08 chr23:78427139 G>A did not map to a codon.
Sequencing variant TCGA-FG-5965-01B-11D-1893-08 chr23:78427487 G>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:36490663 C>T maps to ENST00000398597 S570S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8166-01A-11D-2253-08 chr13:95275436 G>C maps to NM_180989.4 G323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7637-01A-11D-2086-08 chr13:95273350 A>G maps to NM_180989.4 Q252Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84I-01A-11D-A36O-08 chr9:125797417 C>T maps to NM_005294.1 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr10:125426408 G>A maps to NM_153442.3 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr3:71803790 G>T maps to NM_018971.1 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5853-01A-11D-1893-08 chr6:167570605 G>A maps to NM_005299.2 C238C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76K-01A-11D-A33T-08 chr19:51274417 C>T maps to NM_001506.1 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8011-01A-11D-2395-08 chr19:51274117 C>T maps to NM_001506.1 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:41554925 A>G did not map to a codon.
Sequencing variant TCGA-HT-A615-01A-11D-A29Q-08 chr23:41555136 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:124404175 G>A maps to NM_005302.2 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:133174974 C>T maps to NM_001508.2 Y120Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7490-01A-11D-2024-08 chr2:133175295 C>T maps to NM_001508.2 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr19:46094974 G>A maps to NM_005282.2 N50N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5273-01A-01D-1468-08 chr2:105858977 G>A maps to NM_007227.3 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:105858812 G>A maps to NM_007227.3 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5144-01A-01D-1468-08 chr23:150349209 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:150348631 G>A did not map to a codon.
Sequencing variant TCGA-DU-7300-01A-21D-2086-08 chr23:150349611 C>A did not map to a codon.
Sequencing variant TCGA-CS-6186-01A-12D-2024-08 chr2:231774732 C>T maps to NM_005683.3 T315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:57693390 C>T maps to NM_005682.5 D457D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8322-01A-11D-2395-08 chr6:110301178 C>T maps to ENST00000414000 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:110086835 C>T maps to NM_031936.4 R398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8321-01A-11D-2395-08 chr6:97246404 C>T maps to NM_030784.2 K401K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:19013147 G>T did not map to a codon.
Sequencing variant TCGA-DU-6396-01A-11D-1705-08 chr23:19027858 A>T did not map to a codon.
Sequencing variant TCGA-HT-A5RC-01A-11D-A289-08 chr23:19031905 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:88477670 C>T maps to NM_003608.3 C160C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7875-01A-11D-2395-08 chr14:91700785 C>T maps to ENST00000238699 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:54081848 C>T maps to NM_006794.2 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A736-01A-11D-A32B-08 chr2:54081032 T>C maps to NM_006794.2 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7677-01A-11D-2253-08 chr12:123214712 G>A maps to NM_032554.3 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:94126757 C>T maps to NM_016540.3 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6UB-01A-21D-A33T-08 chr11:94113632 C>T maps to NM_016540.3 K318K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:101005514 C>T maps to NM_022049.2 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:145765404 G>T maps to NM_001097612.1 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:90001395 G>T maps to NM_032119.3 G2856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:89988576 C>T maps to NM_032119.3 S2369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:89939702 G>T maps to NM_032119.3 T879T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr5:89933729 G>A maps to NM_032119.3 P735P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr5:90106490 C>T maps to NM_032119.3 P5138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7854-01A-11D-2253-08 chr5:90119412 G>A maps to NM_032119.3 K5456K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7882-01A-11D-2395-08 chr5:89979458 T>C maps to NM_032119.3 S1907S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A847-01A-11D-A36O-08 chr5:90079058 C>T maps to NM_032119.3 Y4450Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr23:101909473 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:101912596 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:101912338 T>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:101911927 G>A did not map to a codon.
Sequencing variant TCGA-DU-8162-01A-21D-2253-08 chr23:101912053 G>A did not map to a codon.
Sequencing variant TCGA-DU-A6S7-01A-21D-A32B-08 chr23:101911242 A>G did not map to a codon.
Sequencing variant TCGA-DU-A7T6-01A-11D-A33T-08 chr23:101909039 G>T did not map to a codon.
Sequencing variant TCGA-DU-A7T6-01A-11D-A33T-08 chr23:101909040 A>G did not map to a codon.
Sequencing variant TCGA-E1-A7YE-01A-11D-A34A-08 chr23:101912627 C>T did not map to a codon.
Sequencing variant TCGA-FG-6691-01A-11D-1893-08 chr23:101909850 G>C did not map to a codon.
Sequencing variant TCGA-FG-6691-01A-11D-1893-08 chr23:101910617 G>C did not map to a codon.
Sequencing variant TCGA-P5-A72U-01A-31D-A32B-08 chr23:101911739 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:101971014 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:101971331 G>A did not map to a codon.
Sequencing variant TCGA-HT-8563-01A-11D-2395-08 chr23:101970908 A>G did not map to a codon.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr23:101972001 G>C did not map to a codon.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr12:13061476 C>T maps to NM_003979.3 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7611-01A-11D-2395-08 chr16:19883180 G>C maps to NM_016235.1 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7611-01A-11D-2395-08 chr16:19883825 G>T maps to NM_016235.1 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr17:72436709 C>T maps to NM_022036.2 Y310Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:176026571 T>C maps to NM_052899.2 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TA-01A-11D-A33T-08 chr5:176026277 C>T maps to NM_052899.2 E186E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7638-01B-11D-2086-08 chr5:176026757 G>A maps to NM_052899.2 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr5:176025904 C>A maps to NM_052899.2 G311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:90170997 C>T maps to NM_198281.2 Q88Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RP-01A-21D-A34A-08 chr4:90171144 G>A maps to NM_198281.2 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7490-01A-11D-2024-08 chr14:65406295 C>T maps to NM_002083.2 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr6:28472104 G>A maps to NM_182701.1 D210D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:35510152 G>A maps to NM_020895.3 T424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F0-01A-11D-A289-08 chr19:35504507 C>T maps to NM_020895.3 D261D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:113655183 C>T maps to NM_017577.4 R510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A617-01A-11D-A29Q-08 chr3:113563351 G>T maps to NM_017577.4 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:18925334 C>T maps to NM_006613.3 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr17:18927575 G>A maps to NM_006613.3 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:52404839 C>T maps to NM_181711.2 H123H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr7:50686968 T>C maps to NM_005311.4 E225E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TU-01A-12D-A32B-08 chr17:37902418 C>T maps to ENST00000445327 C495C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RF-01A-11D-A33T-08 chr17:37902418 C>T maps to ENST00000445327 C495C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YS-01A-11D-A34A-08 chr2:11738848 G>A maps to NM_014668.3 K732K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A733-01A-11D-A32B-08 chr2:11716614 A>G maps to NM_014668.3 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A713-01A-11D-A32B-08 chr15:33023157 G>A maps to NM_013372.6 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr1:240656343 G>A maps to NM_022469.3 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R7-01A-11D-A289-08 chr8:102582592 T>G maps to NM_024915.3 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:24673117 C>T maps to NM_021180.3 G515G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:24657945 C>T maps to NM_021180.3 D21D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YK-01A-11D-A34A-08 chr1:24664501 C>T maps to NM_021180.3 F292F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr1:24671384 A>C did not map to a codon.
Sequencing variant TCGA-DU-6403-01A-11D-1705-08 chr5:153174270 C>T maps to NM_000827.3 C787C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr23:122561826 G>A did not map to a codon.
Sequencing variant TCGA-DH-A7UR-01A-11D-A33T-08 chr23:122536949 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:122536866 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:122538587 C>T did not map to a codon.
Sequencing variant TCGA-DU-7009-01A-11D-2024-08 chr23:122616847 T>A did not map to a codon.
Sequencing variant TCGA-FG-8186-01A-11D-2253-08 chr23:122598964 T>A did not map to a codon.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr23:122538739 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:94693537 T>C maps to NM_001510.2 N971N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:30909579 G>A maps to ENST00000327783 R941*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:37356572 G>T maps to NM_000831.3 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:37315909 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:120776144 C>T maps to NM_014619.2 Y473Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:9857311 G>A maps to NM_000833.3 S1363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6689-01A-11D-1893-08 chr16:9857956 C>T maps to NM_000833.3 P1148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R7-01A-11D-A289-08 chr16:10274070 G>A maps to NM_000833.3 D66D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr12:13764767 G>A maps to NM_000834.3 D557D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6393-01A-11D-1705-08 chr12:13716186 G>A maps to NM_000834.3 R1329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr12:13716622 C>T maps to NM_000834.3 T1183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4942-01A-01D-1468-08 chr9:104499940 C>T maps to NM_133445.2 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A4DS-01A-11D-A26M-08 chr19:1004801 C>T maps to NM_138690.1 D434D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:58001097 G>A maps to NM_015532.3 Q100Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:14555200 G>A maps to ENST00000507975 V635V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr23:48831680 C>G did not map to a codon.
Sequencing variant TCGA-HT-A615-01A-11D-A29Q-08 chr23:48830665 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:114325903 G>A maps to NM_002929.2 E306E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:121182769 C>A maps to NM_005308.2 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:121184564 T>C maps to NM_005308.2 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7489-01A-11D-2024-08 chr5:176857876 C>T maps to NM_002082.3 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5141-01A-01D-1468-08 chr6:146720658 G>C maps to NM_000838.3 G828G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A669-01A-12D-A31L-08 chr3:51751834 T>A did not map to a codon.
Sequencing variant TCGA-DU-A76R-01A-11D-A32B-08 chr7:86415888 C>T maps to NM_000840.2 R261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr7:86468866 G>A maps to NM_000840.2 R679R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6X9-01A-12D-A32B-08 chr6:34029797 C>T maps to NM_000841.1 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IX-01A-12D-A34A-08 chr6:34059819 G>A maps to NM_000841.1 Y192Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:88300405 G>T maps to NM_001143831.2 G815G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:88338067 G>T maps to NM_001143831.2 I404I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:88323888 G>A maps to NM_001143831.2 R524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:88242656 G>A maps to NM_001143831.2 S914S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5847-01A-11D-1705-08 chr5:178418950 C>T maps to NM_000843.3 W213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:7348184 G>A maps to NM_181874.2 K293K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8188-01A-11D-2253-08 chr3:7620371 T>C maps to NM_181874.2 I593I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:126173164 G>T maps to NM_001127323.1 I757I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr7:126173578 G>A maps to NM_001127323.1 R619R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CV-01A-11D-A31L-08 chr7:126173224 C>T maps to NM_001127323.1 R737R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TX-01A-21D-A32B-08 chr7:126079205 T>C maps to NM_000845.2 T898T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:16170512 C>T did not map to a codon.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr23:16168587 A>G did not map to a codon.
Sequencing variant TCGA-HT-A615-01A-11D-A29Q-08 chr23:16142350 C>T did not map to a codon.
Sequencing variant TCGA-IK-7675-01A-11D-2086-08 chr23:16170453 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:48956128 C>T maps to NM_031485.3 A396A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8110-01A-11D-2395-08 chr17:38073446 C>T maps to NM_001165958.1 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KK-01A-11D-A27K-08 chr8:144645067 C>A maps to NM_024736.6 P483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:13241673 G>A maps to ENST00000405543 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WD-01A-12D-A33T-08 chr16:27856320 G>A maps to NM_001109763.1 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7486-01A-11D-2024-08 chr3:119720904 G>A maps to NM_002093.3 D90D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TW-01A-12D-A32B-08 chr9:124080947 G>A maps to NM_000177.4 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:51488436 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:51486830 G>A did not map to a codon.
Sequencing variant TCGA-FG-5963-01A-11D-1705-08 chr23:51488254 T>A did not map to a codon.
Sequencing variant TCGA-HT-7606-01A-11D-2086-08 chr23:51488447 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:52657701 G>A maps to NM_145740.3 Y166Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A711-01A-21D-A33T-08 chr6:52616503 G>T maps to NM_000846.4 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7641-01B-11D-2253-08 chr6:52767169 G>A maps to NM_000847.4 Y82Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6X5-01A-12D-A32B-08 chr1:110217421 T>C maps to ENST00000369830 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U5-01A-12D-A33T-08 chr1:110210763 C>T maps to ENST00000369830 N9N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:110260003 C>T maps to ENST00000369812 R224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:24381722 G>A maps to NM_000853.2 D59D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:24376857 G>A maps to NM_000853.2 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:120469543 C>T maps to NM_005513.2 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:6389586 G>T maps to NM_002096.2 S65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RJ-01A-11D-A33T-08 chr19:6391945 T>C maps to NM_002096.2 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RW-01A-11D-A33T-08 chr12:124132660 C>T maps to NM_001516.3 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr7:74212377 T>C maps to NM_173537.2 K491K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:27510033 C>T maps to NM_001520.3 P694P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:27508991 G>A maps to NM_001520.3 G772G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:27518324 C>T maps to NM_001520.3 S465S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:27504542 A>G maps to NM_001520.3 I951I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:27480830 C>A maps to NM_001520.3 E1619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7638-01B-11D-2086-08 chr2:197657736 C>T maps to NM_012086.2 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr9:135546107 G>T maps to NM_012204.2 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:42355250 C>T maps to NM_176791.3 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7013-01A-11D-2024-08 chr6:42162501 C>T maps to NM_002098.5 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:156634623 C>T maps to NM_001130684.1 I487I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YI-01A-11D-A34A-08 chr4:156631928 C>T maps to NM_001130684.1 Y204Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:14805894 G>A maps to NM_004963.3 Y508Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TW-01A-12D-A32B-08 chr12:14804946 A>G maps to NM_004963.3 D517D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:108718909 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:108708436 G>T did not map to a codon.
Sequencing variant TCGA-DU-6405-01A-11D-1705-08 chr23:108719024 C>A did not map to a codon.
Sequencing variant TCGA-P5-A5F2-01A-11D-A289-08 chr23:108718946 C>A did not map to a codon.
Sequencing variant TCGA-P5-A77X-01A-11D-A32B-08 chr23:108719066 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:44682468 C>T maps to NM_021927.2 D59D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7636-01A-11D-2086-08 chr4:44693680 A>G did not map to a codon.
Sequencing variant TCGA-P5-A5EU-01A-11D-A27K-08 chr12:42512816 A>G maps to NM_173601.1 H157H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr23:2799185 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:2779760 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:2761276 C>T did not map to a codon.
Sequencing variant TCGA-S9-A89Z-01A-11D-A36O-08 chr12:21713427 T>C did not map to a codon.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr5:54329738 G>A maps to NM_002104.2 P260P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DU-6392-01A-11D-1705-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr23:103267992 G>T did not map to a codon.
Sequencing variant TCGA-QH-A65R-01A-21D-A31L-08 chr23:103267976 G>A did not map to a codon.
Sequencing variant TCGA-P5-A733-01A-11D-A32B-08 chr1:226252069 G>A maps to NM_002107.3 Q6Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:31944955 G>A maps to NM_001013699.2 R49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:9305382 C>T maps to NM_004285.3 H130H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:115341887 C>T maps to NM_004132.3 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XB-01A-11D-A26M-08 chr2:26437419 C>T maps to NM_000182.4 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:26424179 G>A maps to NM_000182.4 D410D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6IZ-01A-11D-A31L-08 chr2:26435459 G>A maps to NM_000182.4 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:26414364 C>T maps to NM_000182.4 P711P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R7-01A-11D-A289-08 chr1:119936433 C>T maps to ENST00000361035 R356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A83Y-01A-11D-A36O-08 chr1:119934801 C>T maps to ENST00000361035 R294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr5:82937338 G>A maps to NM_001884.3 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:46637622 C>T maps to NM_173811.3 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8161-01A-11D-2253-08 chr19:52220446 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:69143609 C>T maps to NM_005329.2 C104C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:69149136 G>T maps to NM_005329.2 E544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:172809431 C>A maps to NM_003642.3 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:172848173 G>T maps to NM_003642.3 E390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64V-01A-11D-A29Q-08 chr18:43700023 A>G maps to NM_138443.3 Q158Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-7675-01A-11D-2086-08 chr9:19093263 G>C maps to NM_017645.3 S114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7692-01A-12D-2253-08 chr5:156535949 C>T maps to NM_032782.3 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VV-A829-01A-21D-A36O-08 chr1:154246289 A>T maps to NM_006118.3 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YV-01A-11D-A34J-08 chr11:5274541 C>A maps to ENST00000399563 G142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YV-01A-11D-A34J-08 chr11:5274539 T>C maps to ENST00000399563 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7610-01A-21D-2086-08 chr16:202925 T>C maps to NM_005332.2 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5874-01A-11D-1705-08 chr23:11133052 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:11135462 C>T did not map to a codon.
Sequencing variant TCGA-HT-7684-01A-11D-2253-08 chr23:11135491 T>C did not map to a codon.
Sequencing variant TCGA-TM-A84T-01A-11D-A36O-08 chr23:11139865 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153223327 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153227080 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153215026 C>T did not map to a codon.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr23:153225449 G>C did not map to a codon.
Sequencing variant TCGA-HT-7607-01A-11D-2086-08 chr23:153228836 A>C did not map to a codon.
Sequencing variant TCGA-KT-A7W1-01A-11D-A34A-08 chr23:153217981 G>A did not map to a codon.
Sequencing variant TCGA-QH-A6CU-01A-11D-A31L-08 chr23:153222851 C>A did not map to a codon.
Sequencing variant TCGA-S9-A7QX-01A-11D-A34A-08 chr23:153222179 G>A did not map to a codon.
Sequencing variant TCGA-S9-A7R3-01A-11D-A34J-08 chr23:153236221 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:104490204 G>A maps to NM_013320.2 P578P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7882-01A-11D-2395-08 chr20:30667666 C>T maps to NM_002110.3 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EZ-01A-11D-A27K-08 chr20:30659554 C>T maps to NM_002110.3 Y51Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64S-01A-11D-A29Q-08 chr5:45262042 G>A maps to NM_021072.2 R885*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7686-01A-11D-2253-08 chr5:45262355 G>T maps to NM_021072.2 T780T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8319-01A-11D-2395-08 chr5:45262406 C>T maps to NM_021072.2 P763P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5302-01A-01D-1468-08 chr1:155257755 G>A maps to NM_020897.1 A609A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:73635839 C>T maps to NM_005477.2 S365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7691-01A-11D-2253-08 chr15:73615169 C>T maps to NM_005477.2 A1088A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A6MK-01A-11D-A32B-08 chr6:55113494 C>T maps to NM_001526.3 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:114279818 G>A maps to ENST00000398283 Q187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5872-01A-11D-1705-08 chr2:239976490 G>A maps to NM_006037.3 P1009P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:240029748 G>A maps to NM_006037.3 C698C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WI-01A-21D-A33T-08 chr2:240005916 G>A maps to NM_006037.3 S817S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:42168788 C>T maps to NM_001015053.1 T413T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:42168851 C>T maps to NM_001015053.1 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:48663860 G>A did not map to a codon.
Sequencing variant TCGA-DU-6401-01A-11D-1705-08 chr23:48682451 A>G did not map to a codon.
Sequencing variant TCGA-FG-5965-01B-11D-1893-08 chr23:48682403 G>T did not map to a codon.
Sequencing variant TCGA-DU-A76O-01A-11D-A32B-08 chr12:48188620 G>A maps to NM_015401.3 D460D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:50555542 C>T maps to NM_002112.3 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:22569977 G>A maps to NM_138574.2 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:4499513 C>T maps to ENST00000301284 D534D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QY-01A-11D-A34A-08 chr23:6995446 G>A did not map to a codon.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr2:242194884 G>A maps to NM_005336.3 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A4DV-01A-11D-A26M-08 chr2:242176035 A>C maps to NM_005336.3 A966A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5854-01A-11D-1705-08 chr23:83724442 A>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:83724244 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:83723697 G>A did not map to a codon.
Sequencing variant TCGA-DU-7294-01A-11D-2024-08 chr23:83616610 G>T did not map to a codon.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr23:83723853 A>G did not map to a codon.
Sequencing variant TCGA-HT-8114-01A-11D-2395-08 chr23:83724059 G>T did not map to a codon.
Sequencing variant TCGA-P5-A72U-01A-31D-A32B-08 chr23:83577003 G>T did not map to a codon.
Sequencing variant TCGA-DH-5142-01A-01D-1468-08 chr1:236724538 T>C maps to NM_018072.5 K1544K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:236737999 G>A maps to NM_018072.5 Y1096Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7637-01A-11D-2086-08 chr1:236738050 C>T maps to NM_018072.5 P1079P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:37297470 C>A maps to NM_019024.1 G277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:37297431 C>A maps to NM_019024.1 G290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A61C-01A-11D-A29Q-08 chr2:37289162 G>A maps to NM_019024.1 R539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A77W-01A-11D-A32B-08 chr2:37306395 G>A maps to NM_019024.1 R69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WE-01A-12D-A33T-08 chr2:37229590 C>T maps to NM_019024.1 R1725R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RV-01A-21D-A34A-08 chr2:37229590 C>T maps to NM_019024.1 R1725R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5144-01A-01D-1468-08 chr17:58133571 G>A maps to NM_022070.4 Y702Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:58121015 T>G maps to NM_022070.4 R1152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:145245826 C>T maps to NM_032450.2 R235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5397-01A-01D-1893-08 chr5:41055886 T>A maps to ENST00000296803 R330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6400-01A-12D-1705-08 chr5:41004890 G>A maps to ENST00000296803 S1333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr5:41058281 G>A maps to ENST00000296803 H213H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8189-01B-11D-A289-08 chr5:41065559 C>T maps to ENST00000296803 E78E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-7675-01A-11D-2086-08 chr5:41070935 C>A maps to ENST00000296803 E7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7609-01A-11D-2086-08 chr6:139487913 G>T maps to NM_016217.2 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:31641314 A>G maps to NM_015382.2 N390N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr14:31576336 G>A maps to NM_015382.2 F2247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UR-01A-11D-A33T-08 chr10:93247528 C>T maps to ENST00000446394 I399I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:93260257 G>T did not map to a codon.
Sequencing variant TCGA-DB-A64W-01A-11D-A29Q-08 chr7:43483865 G>A maps to NM_015052.3 Q365Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:43483895 C>T maps to NM_015052.3 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6403-01A-11D-1705-08 chr7:43581597 G>C did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr7:43484732 C>T maps to NM_015052.3 T654T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R2-01A-21D-A34J-08 chr7:43591855 C>T maps to NM_015052.3 A1477A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7858-01A-11D-2395-08 chr2:197183693 G>A maps to NM_020760.1 C640C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A87N-01A-11D-A36O-08 chr12:66703571 T>A maps to NM_033647.2 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:96333730 C>A maps to NM_018063.3 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-8125-01A-11D-2253-08 chr10:96352240 G>A maps to NM_018063.3 G647G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:65212052 T>C did not map to a codon.
Sequencing variant TCGA-DU-6407-01A-13D-1705-08 chr17:65105676 A>G maps to NM_014877.3 A1348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:124793760 C>T maps to NM_152722.4 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:65428013 C>T did not map to a codon.
Sequencing variant TCGA-HT-7695-01A-11D-2253-08 chr23:65427078 T>A did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr23:65427137 G>A did not map to a codon.
Sequencing variant TCGA-QH-A6CW-01A-11D-A32B-08 chr23:65486344 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:93837824 G>A maps to NM_001098672.1 W938*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RJ-01A-11D-A33T-08 chr11:93754554 T>A maps to NM_001098672.1 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RW-01A-11D-A33T-08 chr11:93797641 A>G maps to NM_001098672.1 K258K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:124789721 C>T maps to NM_001037558.2 Q26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:63948394 G>A maps to ENST00000261887 S3254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:63922784 C>T maps to ENST00000261887 P4282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:63944623 C>T maps to ENST00000261887 V3469V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:63904728 G>T maps to ENST00000261887 S4708S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8109-01A-11D-2395-08 chr15:63972936 C>T maps to ENST00000261887 T2088T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6XC-01A-12D-A32B-08 chr15:63970179 C>A maps to ENST00000261887 G2312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:28389915 G>A maps to NM_004667.4 R3681R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7Z3-01A-11D-A34J-08 chr15:28413708 C>A maps to NM_004667.4 P3419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RG-01A-11D-A33T-08 chr15:28375698 G>A maps to NM_004667.4 C4204C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:69714743 G>A maps to NM_022079.2 N731N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:89319297 C>T maps to NM_017912.3 F343F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8113-01A-11D-2395-08 chr7:35707096 T>C maps to NM_022373.4 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5143-01A-01D-1468-08 chr15:72668151 C>T maps to ENST00000457859 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:73985151 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:80393710 C>T maps to NM_173620.2 D198D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:26091279 C>T maps to NM_000410.3 H96H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7874-01A-11D-2395-08 chr6:26094420 C>T maps to NM_000410.3 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5273-01A-01D-1468-08 chr1:91818119 A>G maps to NM_001017975.3 F640F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:91731664 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:120352050 G>T maps to NM_000187.3 C377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr3:120360507 G>A maps to NM_000187.3 H269H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WO-01A-21D-A34A-08 chr3:120360528 C>T maps to NM_000187.3 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:81392042 T>C maps to NM_000601.4 K78K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6403-01A-11D-1705-08 chr7:81339499 G>A maps to NM_000601.4 R502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:3443841 C>T maps to ENST00000511533 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KL-01A-11D-A27K-08 chr4:3443796 C>G maps to ENST00000511533 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:79654061 C>T maps to NM_004712.4 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8320-01A-11D-2395-08 chr17:79653395 C>T maps to NM_004712.4 H59H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:43014187 G>A did not map to a codon.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr1:210761337 C>T maps to NM_001170580.1 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TW-01A-12D-A32B-08 chr1:210796934 G>A maps to NM_001170580.1 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:145635497 T>C maps to NM_022475.1 N515N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr4:145579960 G>A maps to NM_022475.1 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr1:222717480 C>T maps to NM_024746.3 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:62204913 A>G maps to ENST00000394997 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:102306287 G>T maps to ENST00000442724 E315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:123335812 C>T maps to NM_003959.1 Y182Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:139288933 A>G maps to NM_022740.4 L716L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:139285179 C>T maps to NM_022740.4 Q806Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr19:40895407 G>A maps to NM_144685.3 H134H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:19381927 G>A maps to NM_003325.3 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:19319034 G>A maps to NM_003325.3 I994I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:19385611 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:19365462 G>T maps to NM_003325.3 A514A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7CF-01A-11D-A32B-08 chr22:19381984 C>A maps to NM_003325.3 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:30004866 G>A maps to NM_003609.3 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8105-01A-11D-2395-08 chr6:26056629 G>C maps to NM_005319.3 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WO-01A-21D-A34A-08 chr6:26234905 T>A maps to NM_005320.2 K86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A669-01A-12D-A31L-08 chr6:26156725 T>A maps to NM_005321.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CH-01A-12D-A36O-08 chr6:25726458 G>A maps to NM_170745.3 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8189-01B-11D-A289-08 chr6:27833428 C>A maps to NM_003511.2 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8166-01A-11D-2253-08 chr6:26225732 C>T maps to NM_003532.2 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6666-01A-11D-1893-08 chr1:149785209 G>C maps to NM_001123375.2 R9R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IX-01A-12D-A34A-08 chr1:149784870 G>C maps to NM_001123375.2 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:12123222 C>A maps to NM_002114.2 G1065G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U2-01A-21D-A33T-08 chr6:12161697 C>T maps to NM_002114.2 R2172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6UB-01A-21D-A33T-08 chr6:12123516 G>A maps to NM_002114.2 Q1163Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:143081222 C>A maps to NM_006734.3 G2068*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr6:143089532 T>C maps to NM_006734.3 K1776K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8182-01A-11D-2253-08 chr6:143095692 T>C maps to NM_006734.3 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:41976859 G>T maps to NM_024503.3 L2161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:42045647 G>T maps to NM_024503.3 C1607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7300-01A-21D-2086-08 chr1:42048875 G>A maps to NM_024503.3 T531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7483-01A-11D-2024-08 chr1:42049198 G>A maps to NM_024503.3 R424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr1:42050150 C>T maps to NM_024503.3 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A614-01A-11D-A29Q-08 chr10:71160765 C>T maps to ENST00000439900 Q912*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:75107688 C>T maps to NM_000189.4 D521D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:37854499 C>T maps to NM_181786.2 H601H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7493-01A-11D-2024-08 chr19:37835618 C>G maps to NM_181786.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:31323154 C>T maps to ENST00000428231 E348E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6396-01A-11D-1705-08 chr6:32975238 G>C maps to NM_002119.3 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr6:32975226 C>T maps to NM_002119.3 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7884-01B-11D-2395-08 chr6:32975790 G>A maps to NM_002119.3 N110N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-7675-01A-11D-2086-08 chr6:32974942 A>G maps to NM_002119.3 C221C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YE-01A-11D-A34A-08 chr6:32782244 T>C maps to ENST00000452392 R772R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr6:33052886 C>A maps to NM_002121.4 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6J3-01A-11D-A31L-08 chr6:32410364 C>T maps to NM_019111.4 R75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:30459016 G>A maps to NM_005516.5 W238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6188-01A-11D-1893-08 chr6:29693048 C>T maps to NM_001098479.1 H284H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:38128858 G>A maps to NM_000411.5 R665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:38309234 G>A maps to NM_000411.5 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:53345265 G>A maps to NM_002126.4 E90E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:148750075 A>T maps to NM_003071.3 T987T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:148789434 C>A maps to NM_003071.3 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:148757855 C>A maps to NM_003071.3 E822*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8158-01A-11D-2253-08 chr3:148792095 A>C maps to NM_003071.3 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UU-01A-12D-A34A-08 chr8:28837638 G>A maps to ENST00000444075 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YL-01A-11D-A34A-08 chr8:28906543 C>T maps to ENST00000444075 D367D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UU-01A-12D-A34A-08 chr1:186057367 A>C maps to NM_031935.2 P3179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:186072760 T>G maps to NM_031935.2 T3577T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6542-01A-11D-1893-08 chr1:186045566 A>T maps to NM_031935.2 P2766P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8162-01A-21D-2253-08 chr1:186055384 A>T maps to NM_031935.2 P2964P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TS-01A-11D-A289-08 chr1:185969240 C>T maps to NM_031935.2 G1313G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A6S3-01A-12D-A32B-08 chr1:185987380 A>G maps to NM_031935.2 K1789K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A61A-01A-11D-A29Q-08 chr1:186084408 G>A maps to NM_031935.2 P3808P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8320-01A-11D-2395-08 chr1:186056427 C>T maps to NM_031935.2 G3042G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A77W-01A-11D-A32B-08 chr1:185988673 T>G maps to NM_031935.2 V1824V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6X9-01A-12D-A32B-08 chr1:186014931 A>G maps to NM_031935.2 K2139K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U6-01A-12D-A33T-08 chr1:186120453 A>T maps to NM_031935.2 K4911*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A89Z-01A-11D-A36O-08 chr1:185959533 T>C maps to NM_031935.2 T1112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7470-01A-12D-2086-08 chr12:66221788 C>T maps to NM_003483.4 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:174253296 T>C maps to NM_002129.3 E188E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UU-01A-12D-A34A-08 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:150154606 T>C did not map to a codon.
Sequencing variant TCGA-DU-A7TD-01A-12D-A34A-08 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-E1-A7YI-01A-11D-A34A-08 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-HT-7695-01A-11D-2253-08 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-QH-A6CY-01A-11D-A32B-08 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-S9-A6WP-01A-12D-A34A-08 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-TQ-A8XE-01A-11D-A36O-08 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:34330139 G>A maps to NM_145205.4 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:74650485 C>T maps to NM_000859.2 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7J2-01A-11D-A34A-08 chr1:120302571 A>T maps to NM_005518.3 Y200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WD-01A-12D-A33T-08 chr19:1080921 G>A maps to NM_012292.2 P683P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6407-01A-13D-1705-08 chr17:36059195 G>A maps to NM_000458.2 Y513Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5303-01A-01D-1468-08 chr17:36099518 C>T maps to NM_000458.2 Q152Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:76471093 C>T maps to NM_004133.4 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7482-01A-11D-2024-08 chr1:12908010 C>T maps to NM_001013631.1 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RP-01A-21D-A34A-08 chr1:12908037 C>T maps to NM_001013631.1 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A61B-01A-11D-A29Q-08 chr10:43882165 G>A maps to NM_001098204.1 Y389Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr5:179043154 G>A maps to NM_005520.2 Y424Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:100667625 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:100668320 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:100667952 G>T did not map to a codon.
Sequencing variant TCGA-DU-6407-01A-13D-1705-08 chr23:100667034 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:39328285 G>A maps to ENST00000221419 C521C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:39336648 G>A maps to ENST00000221419 Y156Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:245027150 G>A maps to NM_031844.2 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:41787068 C>T maps to NM_007040.3 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:62491094 G>A maps to NM_001079559.1 Y285Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:83347636 G>A maps to NM_031372.2 Q391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:38796364 G>A maps to NM_138394.3 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:60324162 C>T maps to NM_015888.4 Q436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:12883717 C>T maps to NM_013312.2 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:150679046 T>C maps to NM_032132.4 E262E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A70Z-01A-12D-A33T-08 chr1:150676783 C>T maps to NM_032132.4 Q280Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr7:27224589 G>A maps to NM_005523.5 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr7:27169088 G>A maps to NM_002141.4 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr7:27187207 G>T maps to NM_024014.2 S54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YS-01A-11D-A34A-08 chr17:46655327 C>T maps to NM_024015.4 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr17:46669798 C>G maps to NM_002147.3 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4943-01A-01D-1468-08 chr12:54338832 G>A maps to NM_017410.2 K262K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:54396214 C>T maps to NM_006897.1 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:177054164 G>A maps to ENST00000331462 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:176964816 G>A maps to NM_021193.3 E96E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8187-01A-11D-2253-08 chr2:177034189 A>G maps to NM_006898.4 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr2:177033895 G>A maps to NM_006898.4 Q18Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CD-01A-11D-A36O-08 chr2:177017668 A>G maps to NM_014621.2 *256W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:33354870 C>T maps to NM_002143.2 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A89Z-01A-11D-A36O-08 chr19:35556560 C>T maps to NM_182983.2 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4944-01A-01D-1468-08 chr16:72110679 C>T maps to ENST00000228226 Y286Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7636-01A-11D-2086-08 chr16:72110613 A>G maps to ENST00000228226 G264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A731-01A-11D-A32B-08 chr23:133627576 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:100202907 G>A maps to NM_000195.2 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6188-01A-11D-1893-08 chr3:148884978 G>A maps to NM_032383.3 P916P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:148880647 C>T maps to NM_032383.3 R822*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:103827247 C>T maps to NM_024747.4 L673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:100481451 A>G maps to NM_021828.4 I306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:6458288 G>A maps to NM_000613.2 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RO-01A-11D-A33T-08 chr11:6452913 C>T maps to NM_000613.2 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7469-01A-11D-2253-08 chr8:21982884 C>T maps to NM_005144.4 G563G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr19:49656970 G>A maps to NM_002152.2 G508G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A4DS-01A-11D-A26M-08 chr3:186383867 G>A maps to NM_000412.2 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:175111285 C>T maps to NM_001131055.1 V350V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr20:60793681 G>A maps to ENST00000317393 Y94Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6666-01A-11D-1893-08 chr1:152192978 G>A maps to NM_001009931.1 Q376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:152191230 T>C maps to NM_001009931.1 E958E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:152193228 C>T maps to NM_001009931.1 Q292Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6393-01A-11D-1705-08 chr1:152187066 A>T maps to NM_001009931.1 S2346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6403-01A-11D-1705-08 chr1:152192865 G>A maps to NM_001009931.1 R413R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YM-01A-11D-A34A-08 chr1:152187662 G>A maps to NM_001009931.1 R2148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5962-01B-11D-1893-08 chr1:152193267 C>T maps to NM_001009931.1 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TX-01A-21D-A32B-08 chr1:152188127 G>A maps to NM_001009931.1 R1993*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VV-A86M-01A-11D-A36O-08 chr1:152190972 G>A maps to NM_001009931.1 S1044S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RP-01A-21D-A34A-08 chr4:11401215 C>T maps to NM_005114.2 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5965-01B-11D-1893-08 chr16:26147049 T>A maps to NM_006040.2 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8011-01A-11D-2395-08 chr16:1962139 C>T maps to ENST00000454677 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7300-01A-21D-2086-08 chr23:132091352 C>T did not map to a codon.
Sequencing variant TCGA-DU-8165-01A-11D-2253-08 chr23:131762857 T>A did not map to a codon.
Sequencing variant TCGA-DU-A76O-01A-11D-A32B-08 chr23:131762929 T>C did not map to a codon.
Sequencing variant TCGA-VM-A8CB-01A-11D-A36O-08 chr13:97485205 C>T maps to NM_153456.2 N390N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr17:40705301 C>T maps to NM_000413.2 D86D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A70Z-01A-12D-A33T-08 chr4:88312102 C>A maps to NM_016245.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr16:82104637 C>T maps to NM_002153.2 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A845-01A-11D-A36O-08 chr16:82104724 C>T maps to NM_002153.2 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CW-01A-11D-A32B-08 chr9:99007647 G>A maps to NM_000197.1 Y195Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7008-01A-11D-2024-08 chr5:118867013 G>A maps to NM_000414.3 K636K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:120056730 C>T maps to ENST00000235547 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:84163650 C>T maps to NM_031463.4 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:56557566 G>T maps to NM_001080439.1 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85E-01A-11D-A36O-08 chr17:56565485 C>A maps to NM_001080439.1 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6X9-01A-12D-A32B-08 chr19:16268156 G>A maps to NM_032855.2 W204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:102552239 G>T maps to NM_001017963.2 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6666-01A-11D-1893-08 chr6:44220939 T>C maps to NM_007355.2 P630P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:104337580 C>T maps to NM_003299.1 Y652Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:118451867 G>T maps to NM_025015.2 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:118434330 C>T maps to NM_025015.2 S663S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8158-01A-11D-2253-08 chr21:15748039 G>A maps to NM_006948.4 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WD-01A-12D-A33T-08 chr21:15750616 T>C maps to NM_006948.4 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TS-01A-12D-A33T-08 chr10:14891774 G>A maps to NM_016299.2 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:31778006 C>T maps to NM_005527.3 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:65008247 C>T maps to NM_021979.3 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5394-01A-01D-1468-08 chr9:128001228 C>T maps to NM_005347.4 E329E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr5:137906679 G>A maps to NM_004134.6 R127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6405-01A-11D-1705-08 chr5:53751846 C>T maps to NM_006308.2 D76D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:122496625 C>T maps to NM_024610.4 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6666-01A-11D-1893-08 chr2:198361939 A>G maps to NM_199440.1 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:198358919 G>A maps to NM_199440.1 R221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7881-01A-11D-2395-08 chr2:198352635 A>T maps to NM_199440.1 A505A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr1:22211317 G>A maps to NM_005529.5 N483N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr1:22159013 G>A maps to NM_005529.5 G3727G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:22162126 G>A maps to NM_005529.5 I3453I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:22181425 C>T maps to NM_005529.5 T2016T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6407-01A-13D-1705-08 chr1:22174481 G>A maps to NM_005529.5 I2614I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr1:22166339 C>T maps to NM_005529.5 T3228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6X8-01A-12D-A32B-08 chr1:22172748 C>T did not map to a codon.
Sequencing variant TCGA-S9-A6U8-01A-21D-A33T-08 chr1:22176569 C>T maps to NM_005529.5 W2470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:31725127 G>A maps to NM_006644.2 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:135581813 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:135593700 C>A did not map to a codon.
Sequencing variant TCGA-E1-A7YE-01A-11D-A34A-08 chr23:135591289 G>C did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr1:23519884 G>A maps to NM_000864.4 H276H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr6:87725426 C>A maps to NM_000865.2 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:88040978 G>A maps to NM_000866.3 K360K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7008-01A-11D-2024-08 chr2:231973907 G>A maps to NM_000867.4 Q257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:113961364 C>T did not map to a codon.
Sequencing variant TCGA-FG-A87Q-01A-11D-A36O-08 chr23:114082600 G>A did not map to a codon.
Sequencing variant TCGA-S9-A6WI-01A-21D-A33T-08 chr23:114082754 C>T did not map to a codon.
Sequencing variant TCGA-HT-7470-01A-12D-2086-08 chr11:113803067 C>A maps to NM_006028.3 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:183774686 C>T maps to NM_130770.2 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6402-01A-11D-1705-08 chr3:183774717 C>T maps to NM_130770.2 R149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8109-01A-11D-2395-08 chr5:147889455 G>T maps to NM_001040173.2 Y213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WM-01A-12D-A33T-08 chr5:147830774 G>A maps to NM_001040169.2 D379D. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DU-A7T6-01A-11D-A33T-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-HT-8564-01A-11D-2395-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr7:154862917 C>T maps to NM_024012.2 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:38832616 G>A maps to NM_153692.3 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:3237091 C>T maps to NM_002111.6 D2846D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:3188446 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:3174045 G>T did not map to a codon.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr4:3225847 G>A maps to NM_002111.6 P2585P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:33371472 C>T maps to NM_014586.1 A707A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:656182 A>G maps to NM_148959.3 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:656868 G>A maps to NM_148959.3 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74K-01A-11D-A32B-08 chr6:656482 G>A maps to NM_148959.3 D154D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:53641541 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:53561479 A>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:53654812 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:53612073 G>A did not map to a codon.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr23:53654433 C>T did not map to a codon.
Sequencing variant TCGA-EZ-7264-01A-11D-2024-08 chr23:53618081 G>C did not map to a codon.
Sequencing variant TCGA-P5-A731-01A-11D-A32B-08 chr23:53579401 G>C did not map to a codon.
Sequencing variant TCGA-P5-A781-01A-11D-A32B-08 chr23:53576144 G>T did not map to a codon.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr23:53644040 C>A did not map to a codon.
Sequencing variant TCGA-TQ-A7RN-01A-11D-A33T-08 chr23:53613508 G>A did not map to a codon.
Sequencing variant TCGA-HT-7677-01A-11D-2253-08 chr12:111099097 G>C maps to NM_001040107.1 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TS-01A-12D-A33T-08 chr12:111099000 A>G maps to NM_001040107.1 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7641-01B-11D-2253-08 chr3:50332973 G>A maps to NM_003549.2 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5270-01A-02D-1468-08 chr16:71098694 C>G maps to NM_032821.2 G708G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:71061528 G>A maps to NM_032821.2 L1006L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:70972620 C>T maps to NM_032821.2 E2296E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7J1-01A-21D-A34J-08 chr16:70917931 G>A maps to NM_032821.2 D3289D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XF-01A-11D-A27K-08 chr11:118919445 C>T maps to NM_001130991.1 K715K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:95033828 C>A maps to ENST00000375660 G369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RW-01A-11D-A33T-08 chr9:95033877 G>A maps to ENST00000375660 C352C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A6S2-01A-21D-A32B-08 chr4:88731861 C>T maps to NM_004967.3 D117D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7Z2-01A-21D-A34J-08 chr4:88723846 C>T maps to NM_004967.3 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KT-A7W1-01A-11D-A34A-08 chr4:88732644 C>A maps to NM_004967.3 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:8167509 C>T maps to ENST00000422063 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:8178613 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:8261008 G>A maps to ENST00000422063 N92N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7855-01A-11D-2395-08 chr19:10445306 A>G maps to NM_002162.3 N363N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:10398512 C>T maps to NM_001544.3 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7309-01A-11D-2086-08 chr19:10402432 C>T maps to NM_003259.3 H207H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:45656873 G>A maps to ENST00000400379 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A6S8-01A-12D-A32B-08 chr21:45658329 C>T did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr21:45651220 G>A maps to ENST00000400379 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84G-01A-11D-A36O-08 chr21:45651186 G>A maps to ENST00000400379 R280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:23885872 G>A maps to NM_002167.3 C15C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:94214256 G>A maps to NM_004969.3 L1002L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr10:94266255 C>T maps to NM_004969.3 R423R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153055714 C>T did not map to a codon.
Sequencing variant TCGA-S9-A6U6-01A-12D-A33T-08 chr8:39840262 G>A maps to NM_194294.2 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XE-01A-11D-A27K-08 chr23:148568541 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:148585690 G>A did not map to a codon.
Sequencing variant TCGA-E1-5302-01A-01D-1468-08 chr6:30711943 C>T maps to NM_003897.3 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WM-01A-12D-A33T-08 chr6:30712190 G>A maps to NM_003897.3 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:79121165 C>A maps to NM_006417.4 I270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:163136556 G>A maps to NM_022168.2 N530N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:91066261 C>A maps to NM_001547.4 Y183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8110-01A-11D-2395-08 chr11:314977 C>T maps to ENST00000328221 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6408-01A-11D-1705-08 chr11:298551 C>T maps to NM_001025295.1 K116K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66G-01A-21D-A31L-08 chr9:21239547 C>T maps to NM_002172.2 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr9:21201903 G>A maps to NM_021057.2 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F2-01A-11D-A289-08 chr21:34717550 G>C did not map to a codon.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr21:34625022 G>A maps to NM_207585.1 K199K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:34804626 C>T maps to ENST00000381995 Y254Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:27524784 G>T maps to NM_020124.2 E151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr3:50326251 G>A maps to ENST00000336089 R500R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:1570039 A>G maps to NM_014714.3 I1294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:42232515 C>T maps to NM_016004.2 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CB-01A-11D-A36O-08 chr23:69370130 A>G did not map to a codon.
Sequencing variant TCGA-HT-7604-01A-11D-2086-08 chr15:65684523 C>T maps to NM_020962.1 V690V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:99467759 C>T maps to NM_000875.3 R877*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66D-01A-11D-A31L-08 chr17:47126778 T>C maps to NM_006546.3 S569S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TJ-01A-11D-A34J-08 chr17:47120866 G>A maps to NM_006546.3 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr3:185393094 G>A maps to NM_006548.4 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:185407363 A>G maps to NM_006548.4 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A83X-01A-11D-A36O-08 chr7:23381772 G>A maps to NM_006547.2 N371N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6670-01A-11D-1893-08 chr6:160497009 T>C maps to NM_000876.2 C1766C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:160468834 C>T maps to NM_000876.2 N747N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:160453617 C>T maps to NM_000876.2 C306C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:160496973 G>A maps to NM_000876.2 K1754K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RQ-01A-11D-A33T-08 chr7:45930165 C>T maps to NM_000596.2 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:46627141 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:201196085 G>A maps to NM_001164586.1 R3621R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:201183407 C>A maps to NM_001164586.1 T2944T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8164-01A-11D-2253-08 chr4:71527852 G>A maps to NM_144646.3 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:51828609 C>T maps to NM_001101372.1 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5140-01A-01D-1468-08 chr23:130416638 C>G did not map to a codon.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr23:130409140 C>T did not map to a codon.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr23:130413284 C>T did not map to a codon.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr23:130415781 T>G did not map to a codon.
Sequencing variant TCGA-HW-7495-01A-11D-2024-08 chr23:130412510 G>A did not map to a codon.
Sequencing variant TCGA-QH-A6X8-01A-12D-A32B-08 chr23:130412695 G>A did not map to a codon.
Sequencing variant TCGA-S9-A7IS-01A-11D-A34A-08 chr23:130409951 A>G did not map to a codon.
Sequencing variant TCGA-DU-5851-01A-13D-1893-08 chr3:151163026 G>T maps to NM_178822.4 S1581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:118624441 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:118649027 G>A maps to NM_152538.2 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:18741650 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:18735839 G>T maps to NM_173588.3 A594A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:18736139 G>A maps to NM_173588.3 S521S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:18735621 C>T maps to NM_173588.3 T624T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R5-01A-11D-A289-08 chr11:18739487 G>A maps to NM_173588.3 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:117150585 G>A maps to NM_001542.2 I400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6IZ-01A-11D-A31L-08 chr16:21655634 G>A maps to NM_005849.2 C170C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WD-01A-12D-A33T-08 chr16:21658502 C>T maps to NM_005849.2 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:159900179 C>T maps to NM_001135050.1 P621P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:159897170 C>T maps to NM_001135050.1 Q1168Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:133799567 A>C maps to NM_014987.1 V543V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:133789707 C>T maps to NM_014987.1 T1304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:140041218 G>A maps to NM_006083.3 G476G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:111651667 G>A maps to NM_003640.3 L1056L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:42163934 G>A maps to NM_001556.2 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6IZ-01A-11D-A31L-08 chr8:42147674 C>T maps to NM_001556.2 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U6-01A-12D-A33T-08 chr1:206650061 G>A maps to NM_014002.3 Q194Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A77X-01A-11D-A32B-08 chr23:153780225 G>A did not map to a codon.
Sequencing variant TCGA-DU-8161-01A-11D-2253-08 chr7:50459520 C>T maps to NM_006060.3 N270N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74H-01A-11D-A32B-08 chr7:50468069 C>T maps to NM_006060.3 Y435Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:37922060 G>A maps to NM_012481.3 H504H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr17:37947816 A>G maps to NM_012481.3 C148C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RQ-01A-11D-A33T-08 chr17:37922279 C>T maps to NM_012481.3 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:56428880 C>T maps to NM_022465.3 G508G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr10:124758012 C>T maps to NM_022466.5 Q43Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:206944380 C>T maps to NM_000572.2 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr11:117869740 G>T maps to NM_001558.3 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:34658655 G>A maps to NM_001142784.1 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5849-01A-11D-1705-08 chr19:18191675 C>T maps to NM_005535.1 K125K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7691-01A-11D-2253-08 chr19:18183117 C>T maps to NM_005535.1 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TS-01A-12D-A33T-08 chr1:67793918 A>G maps to NM_001559.2 Q172Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr23:117900528 A>G did not map to a codon.
Sequencing variant TCGA-S9-A6U9-01A-11D-A32B-08 chr23:117875041 A>G did not map to a codon.
Sequencing variant TCGA-TM-A84G-01A-11D-A36O-08 chr23:117895251 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:6001720 G>T maps to NM_002189.3 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7854-01A-11D-2253-08 chr15:81571958 C>T maps to NM_172217.3 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:88705693 C>T maps to NM_013278.3 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:17589305 C>T maps to NM_014339.5 A399A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:57132154 G>A maps to NM_017563.3 R526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6667-01A-12D-2024-08 chr22:50435798 G>A maps to NM_001001694.2 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7855-01A-11D-2395-08 chr2:102984510 T>A maps to NM_003855.2 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:103013336 C>T maps to NM_003855.2 S539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:103068625 G>A maps to NM_003853.2 Q595Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TD-01A-12D-A34A-08 chr2:103040544 C>T maps to NM_003853.2 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr2:113591146 G>A maps to NM_000576.2 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:113831904 G>A did not map to a codon.
Sequencing variant TCGA-HT-8108-01A-11D-2395-08 chr2:102641100 G>A maps to NM_004633.3 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7T6-01A-11D-A33T-08 chr23:29938150 T>C did not map to a codon.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr23:29972756 G>T did not map to a codon.
Sequencing variant TCGA-P5-A77X-01A-11D-A32B-08 chr23:29414469 A>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:104728340 C>T did not map to a codon.
Sequencing variant TCGA-DU-7290-01A-11D-2024-08 chr23:105011343 T>G did not map to a codon.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr23:104984621 A>G did not map to a codon.
Sequencing variant TCGA-E1-A7YN-01A-11D-A34A-08 chr23:104984674 C>T did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr23:104999269 T>A did not map to a codon.
Sequencing variant TCGA-TQ-A7RQ-01A-11D-A33T-08 chr23:104984644 A>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:102958728 A>G maps to NM_016232.4 Q219Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:102968194 G>A maps to NM_016232.4 A495A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr2:102957202 C>T maps to NM_016232.4 D175D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F2-01A-11D-A289-08 chr2:102968089 C>T maps to NM_016232.4 Y460Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U2-01A-21D-A33T-08 chr2:102964543 T>C maps to NM_016232.4 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8321-01A-11D-2395-08 chr2:102835530 A>G maps to NM_003854.2 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CA-01A-11D-A36O-08 chr2:102851426 G>A maps to NM_003854.2 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WM-01A-12D-A33T-08 chr4:123372927 G>A maps to NM_000586.3 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8161-01A-11D-2253-08 chr1:207039238 G>A maps to NM_018724.3 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:137338235 G>T maps to NM_014432.2 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:136699434 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:27460360 C>T maps to NM_181079.4 D480D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5319-01A-01D-1893-08 chr16:27448928 C>T maps to NM_181079.4 D113D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr16:27445713 G>A maps to NM_181079.4 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6290-01A-11D-1705-08 chr1:24447957 G>A maps to NM_021258.2 N354N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:24454688 G>A maps to NM_021258.2 C204C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TT-01A-11D-A289-08 chr1:24463672 C>T maps to NM_021258.2 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6XA-01A-12D-A32B-08 chr1:24447578 G>A maps to NM_021258.2 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:67724628 G>T maps to NM_144701.2 E570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:68619371 C>T maps to NM_018402.1 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XE-01A-11D-A27K-08 chr16:28510980 G>A maps to NM_145659.3 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8109-01A-11D-2395-08 chr19:14157293 G>A maps to NM_004843.2 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F2-01A-11D-A289-08 chr19:14157388 G>A maps to NM_004843.2 W367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WD-01A-12D-A33T-08 chr19:14157002 G>A maps to NM_004843.2 W269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7884-01B-11D-2395-08 chr19:39788647 G>A maps to NM_172140.1 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr10:6061421 C>T maps to NM_000417.2 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:55206492 G>A maps to NM_139017.4 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A83Z-01A-11D-A36O-08 chr5:55212674 C>T maps to NM_139017.4 C674C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:70694005 G>A maps to NM_152456.2 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:1484093 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:1464254 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:1471116 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:1475122 C>A did not map to a codon.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr19:50393076 C>T maps to NM_172374.1 E540E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr16:27372136 G>A did not map to a codon.
Sequencing variant TCGA-TQ-A7RQ-01A-11D-A33T-08 chr5:55237254 G>A maps to NM_002184.3 G804G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:35873727 T>A maps to NM_002185.2 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7018-01A-11D-2024-08 chr5:135231430 C>T maps to NM_000590.1 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr23:155239556 C>T did not map to a codon.
Sequencing variant TCGA-HT-8013-01A-11D-2395-08 chr23:155234152 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:121720627 C>A maps to ENST00000344209 G155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:10794425 G>T maps to NM_017620.2 G660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr19:10793938 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:86378641 A>G maps to NM_006839.2 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A845-01A-11D-A36O-08 chr2:86398454 C>T maps to NM_006839.2 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6405-01A-11D-1705-08 chr17:43922343 C>T maps to NM_175882.2 Y24Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TP-01A-11D-A289-08 chr17:43922532 G>T maps to NM_175882.2 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:22020581 G>T maps to NM_018439.3 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:128049494 C>A maps to NM_000883.3 E64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7856-01A-11D-2395-08 chr7:128040206 C>T maps to NM_000883.3 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr11:61912745 C>T maps to NM_001040694.1 D607D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:105179214 G>A maps to ENST00000252520 E887E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7607-01A-11D-2086-08 chr13:111372024 C>T maps to NM_005537.3 R339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:6761526 C>T maps to NM_001127582.1 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:242662452 C>A maps to NM_032329.4 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:57849417 A>G maps to NM_031479.3 K33K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:41372071 G>A maps to NM_017553.1 R320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:41347562 C>A did not map to a codon.
Sequencing variant TCGA-VM-A8C8-01A-11D-A36O-08 chr15:41308306 G>A maps to NM_017553.1 T1127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5390-01A-02D-1468-08 chr2:74682278 G>A maps to ENST00000452361 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:74683275 A>C maps to ENST00000452361 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5318-01A-01D-1468-08 chr2:74684816 G>A maps to ENST00000452361 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:99182578 G>A maps to NM_001134224.1 V794V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7875-01A-11D-2395-08 chr4:143094940 G>A maps to NM_003866.2 Y401Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A6MK-01A-11D-A32B-08 chr4:143094934 T>A maps to NM_003866.2 S403S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7474-01A-11D-2024-08 chr10:134521842 C>A maps to NM_005539.3 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WL-01A-21D-A33T-08 chr10:134523945 C>T maps to NM_005539.3 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TS-01A-12D-A33T-08 chr2:234113017 C>T maps to ENST00000359570 P1074P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RS-01A-12D-A33T-08 chr2:234112924 G>A maps to ENST00000359570 P1043P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A731-01A-11D-A32B-08 chr9:139326360 G>A maps to NM_019892.3 V488V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr22:31522442 C>T maps to ENST00000331075 D451D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WN-01A-12D-A33T-08 chr17:1401274 G>A maps to NM_016532.3 Y306Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr11:15222446 G>A maps to NM_001031853.3 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U0-01A-12D-A32B-08 chr2:118854302 C>T maps to NM_016133.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A73M-01A-11D-A32B-08 chr19:7132265 C>A maps to NM_000208.2 G915G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7301-01A-11D-2086-08 chr1:156814051 G>A maps to NM_014215.2 L920L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7680-01A-11D-2253-08 chr1:156823628 C>T maps to NM_014215.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7482-01A-11D-2024-08 chr7:1538969 C>A maps to ENST00000389470 E419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WO-01A-21D-A34A-08 chr7:1516293 C>G did not map to a codon.
Sequencing variant TCGA-DU-A7TA-01A-11D-A33T-08 chr8:19701702 C>T maps to NM_018142.2 C612C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6UA-01A-12D-A33T-08 chr8:19694645 G>A maps to NM_018142.2 S538S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr11:77672046 G>A maps to NM_033547.3 Y203Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5140-01A-01D-1468-08 chr11:77639507 A>T maps to NM_033547.3 V417V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:77635938 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:212141863 G>T maps to NM_015434.3 I667I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:95877900 G>A maps to NM_017864.2 T748T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:128626795 C>T maps to NM_015693.3 A539A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:103027135 T>C maps to NM_014425.2 N499N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:48732510 G>A maps to ENST00000443964 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:33693226 G>A maps to NM_054111.4 C252C. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-P5-A780-01A-12D-A32B-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:44423123 C>T maps to NM_014652.3 D481D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:44422630 G>A maps to NM_014652.3 E418E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:44415726 G>A maps to NM_014652.3 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R9-01A-11D-A289-08 chr14:24651579 G>A maps to ENST00000458132 H834H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:98645165 C>T maps to NM_002271.4 Y248Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:98654811 C>T maps to NM_002271.4 I418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:9455172 G>A maps to NM_006391.2 Q646Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:9451282 G>T maps to NM_006391.2 E552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7855-01A-11D-2395-08 chr1:201817720 A>G maps to NM_018085.4 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr2:237272425 G>A maps to ENST00000457693 F630F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QY-01A-11D-A34A-08 chr1:32671759 C>T maps to NM_001160042.1 C96C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5280-01A-01D-1468-08 chr3:51929061 G>A maps to NM_152397.2 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:51936999 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:67664559 G>T maps to NM_001031715.2 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr15:67629359 G>A maps to NM_001031715.2 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:91025200 C>A maps to NM_003870.3 P1113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7684-01A-11D-2253-08 chr15:91034588 C>T maps to NM_003870.3 Q1425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:75969776 T>C maps to NM_006633.2 P1070P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CY-01A-11D-A32B-08 chr5:75967775 G>T maps to NM_006633.2 V1012V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8110-01A-11D-2395-08 chr1:156499980 G>C maps to NM_178229.4 V1440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:12954951 G>T maps to ENST00000429247 I764I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:53285037 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:53277912 C>A did not map to a codon.
Sequencing variant TCGA-WY-A85E-01A-11D-A36O-08 chr23:53277941 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:266717 C>T maps to NM_001170738.1 P767P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:266832 C>T maps to NM_001170738.1 L806L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8162-01A-21D-2253-08 chr12:274928 C>T maps to NM_001170738.1 L948L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:123143078 T>C maps to NM_178827.4 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A6S8-01A-12D-A32B-08 chr23:153284092 G>A did not map to a codon.
Sequencing variant TCGA-S9-A7R3-01A-11D-A34J-08 chr23:153282061 G>A did not map to a codon.
Sequencing variant TCGA-QH-A86X-01A-11D-A36O-08 chr3:10255185 G>T maps to NM_001570.3 G248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:66638419 C>T maps to NM_007199.2 Q348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr15:78778045 G>A did not map to a codon.
Sequencing variant TCGA-E1-A7YK-01A-11D-A34A-08 chr5:131822745 C>A maps to NM_002198.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:46387583 G>A maps to NM_015649.1 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:50166498 G>A maps to NM_001571.5 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EY-01A-11D-A27K-08 chr19:50163009 C>T maps to NM_001571.5 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F2-01A-11D-A289-08 chr6:407543 C>T maps to NM_002460.3 I434I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A736-01A-11D-A32B-08 chr7:128587365 C>T maps to NM_001098629.1 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr16:85952326 C>T maps to NM_002163.2 N302N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:85936746 C>T maps to NM_002163.2 H42H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7604-01A-11D-2086-08 chr16:85952179 G>A maps to NM_002163.2 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CY-01A-11D-A32B-08 chr16:85954815 C>T maps to NM_002163.2 F403F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7C3-01A-11D-A32B-08 chr14:24634043 C>T maps to NM_006084.4 Q291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A75M-01A-11D-A32B-08 chr19:44223450 G>A maps to NM_019612.3 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr19:44222961 G>A maps to NM_019612.3 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:227662845 G>A maps to NM_005544.2 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FN-7833-01A-11D-2086-08 chr2:227662185 G>A maps to NM_005544.2 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EZ-01A-11D-A27K-08 chr2:227660232 C>T maps to NM_005544.2 R1074R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WD-01A-12D-A33T-08 chr2:227662548 T>G maps to NM_005544.2 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr23:107978514 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:107977625 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:107977145 G>T did not map to a codon.
Sequencing variant TCGA-DU-7300-01A-21D-2086-08 chr23:107978401 G>A did not map to a codon.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr23:107976810 C>T did not map to a codon.
Sequencing variant TCGA-HT-8108-01A-11D-2395-08 chr23:107979042 C>G did not map to a codon.
Sequencing variant TCGA-DU-5870-01A-11D-1705-08 chr5:2749841 G>A maps to NM_033267.4 Y103Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:54967550 G>A maps to NM_005853.5 A406A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A6MO-01A-11D-A33T-08 chr16:54967007 G>A maps to NM_005853.5 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8165-01A-11D-2253-08 chr16:55362678 G>A maps to NM_024335.2 E263E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr16:55361632 C>G maps to NM_024335.2 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R4-01A-12D-A34J-08 chr5:50683335 C>A maps to NM_002202.2 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:74425583 G>A maps to NM_001130137.1 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:74425649 C>T maps to NM_001130137.1 C185C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YN-01A-11D-A34A-08 chr15:74425298 C>T maps to NM_001130137.1 R68R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84G-01A-11D-A36O-08 chr20:13260456 C>T maps to NM_080826.1 D185D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:77942398 G>A maps to NM_199296.2 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr20:33068912 C>T maps to ENST00000262650 S706S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:2933325 G>A maps to NM_018463.3 Q437Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:2931988 C>T maps to NM_018463.3 C326C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:2930856 G>T did not map to a codon.
Sequencing variant TCGA-DB-A75O-01A-11D-A32B-08 chr16:312147 C>T maps to NM_032039.2 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr1:145534933 C>T maps to NM_003637.3 R613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:52379219 T>C maps to NM_002203.3 V1065V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85E-01A-11D-A36O-08 chr5:52355771 T>C maps to NM_002203.3 H414H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:48151343 G>A maps to NM_002204.2 K407K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr17:48157735 C>T maps to NM_002204.2 I939I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:182376436 A>G maps to NM_000885.4 A619A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TU-01A-12D-A32B-08 chr2:182359503 C>G maps to NM_000885.4 S435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:54795850 G>T maps to NM_002205.2 Y720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr12:56094109 G>A maps to ENST00000347027 Y246Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:15649768 G>T maps to NM_003638.1 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:37544691 A>G maps to NM_002207.2 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6401-01A-11D-1705-08 chr16:31419094 C>T maps to ENST00000444228 H305H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TP-01A-11D-A289-08 chr17:3656700 C>T maps to NM_002208.4 E517E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr16:30530024 C>T maps to NM_002209.2 N1071N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:30490413 C>A maps to NM_002209.2 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RF-01A-11D-A33T-08 chr16:30505560 G>A maps to NM_002209.2 R414R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr16:31308839 C>T maps to NM_001145808.1 G454G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84R-01A-21D-A36O-08 chr16:31332596 G>A maps to NM_001145808.1 Q582Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UT-01A-12D-A34A-08 chr2:187503007 T>C maps to NM_002210.3 F269F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:187501836 G>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:31367253 G>A maps to NM_000887.3 E26E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TT-01A-11D-A289-08 chr16:31391361 G>A maps to NM_000887.3 A1012A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YD-01A-11D-A34A-08 chr16:31391334 C>T maps to NM_000887.3 I1003I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A72U-01A-31D-A32B-08 chr16:31388577 G>A maps to NM_000887.3 V927V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U0-01A-12D-A32B-08 chr16:31374347 C>T maps to NM_000887.3 Y484Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WP-01A-12D-A34A-08 chr16:31371634 C>T maps to NM_000887.3 R238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:33218770 A>G maps to ENST00000374956 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:70523712 C>A did not map to a codon.
Sequencing variant TCGA-HT-7609-01A-11D-2086-08 chr23:70524874 G>A did not map to a codon.
Sequencing variant TCGA-DU-A5TT-01A-11D-A289-08 chr21:46320363 C>T maps to NM_000211.3 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YD-01A-11D-A34A-08 chr21:46321433 G>A maps to NM_000211.3 D238D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:45361951 C>T maps to NM_000212.2 R169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84S-01A-11D-A36O-08 chr17:45377876 A>G maps to NM_000212.2 G649G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A618-01A-11D-A29Q-08 chr17:73736511 C>T maps to NM_001005619.1 C840C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:160993948 G>A maps to NM_000888.3 C552C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr2:160982990 G>A maps to NM_000888.3 R594R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84S-01A-11D-A36O-08 chr2:161052118 C>T maps to NM_000888.3 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:20403299 C>A maps to NM_002214.2 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WD-01A-12D-A33T-08 chr13:102227853 C>T maps to NM_004791.1 D181D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:52811744 C>T maps to NM_002215.2 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7695-01A-11D-2253-08 chr3:52812972 C>T maps to NM_002215.2 N107N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RC-01A-11D-A289-08 chr3:52824843 C>T maps to NM_002215.2 R801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U9-01A-11D-A32B-08 chr3:52822009 C>T maps to NM_002215.2 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr10:7780698 G>A maps to NM_002216.2 T691T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A711-01A-21D-A33T-08 chr10:7774440 G>A did not map to a codon.
Sequencing variant TCGA-HT-7476-01A-11D-2024-08 chr3:52848084 G>A maps to ENST00000485816 Q882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr10:7618614 G>A maps to ENST00000256861 D593D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F0-01A-11D-A289-08 chr10:7679257 C>T maps to ENST00000256861 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VW-A7QS-01A-12D-A33T-08 chr10:7627945 T>C maps to ENST00000256861 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64Q-01A-11D-A29Q-08 chr23:54777672 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:54817512 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:54784181 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:54800550 T>C did not map to a codon.
Sequencing variant TCGA-DU-6400-01A-12D-1705-08 chr23:54777699 T>C did not map to a codon.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr23:54776461 C>T did not map to a codon.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr23:54785299 C>T did not map to a codon.
Sequencing variant TCGA-HT-8013-01A-11D-2395-08 chr23:54784548 A>G did not map to a codon.
Sequencing variant TCGA-HT-8563-01A-11D-2395-08 chr23:54784173 C>T did not map to a codon.
Sequencing variant TCGA-R8-A6ML-01A-11D-A32B-08 chr23:54783901 T>C did not map to a codon.
Sequencing variant TCGA-S9-A89V-01A-11D-A36O-08 chr23:54823432 G>T did not map to a codon.
Sequencing variant TCGA-TQ-A7RQ-01A-11D-A33T-08 chr23:54783459 G>A did not map to a codon.
Sequencing variant TCGA-WY-A85E-01A-11D-A36O-08 chr23:54783820 G>C did not map to a codon.
Sequencing variant TCGA-DU-6394-01A-11D-1705-08 chr1:160850420 G>A maps to NM_017625.2 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:78619023 C>A did not map to a codon.
Sequencing variant TCGA-TQ-A7RQ-01A-11D-A33T-08 chr14:93483147 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:226829633 G>A maps to NM_002221.3 I813I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:226822473 G>A maps to NM_002221.3 D913D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76R-01A-11D-A32B-08 chr1:226924703 C>T maps to NM_002221.3 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5280-01A-01D-1468-08 chr19:41223411 A>C maps to NM_025194.2 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:41235123 G>T maps to NM_025194.2 E425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:41224104 C>T maps to NM_025194.2 G355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:41223252 T>C maps to NM_025194.2 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6186-01A-12D-2024-08 chr3:4819012 C>A maps to ENST00000356617 I2078I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:4716020 G>A maps to ENST00000356617 T860T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr3:4725192 G>A maps to ENST00000356617 R1091R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A731-01A-11D-A32B-08 chr3:4829645 C>T maps to ENST00000356617 R2209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:26818922 G>A maps to NM_002223.2 Q491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr6:33626883 C>T maps to ENST00000374316 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:33632960 C>T maps to ENST00000374316 N460N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A72U-01A-31D-A32B-08 chr6:33643521 C>T maps to ENST00000374316 R1057R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84Q-01A-11D-A36O-08 chr6:33638465 C>T maps to ENST00000374316 N820N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RQ-01A-11D-A33T-08 chr6:33656146 C>T maps to ENST00000374316 S2169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TR-01A-11D-A289-08 chr10:106074372 G>A maps to NM_033397.2 I479I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:35186339 G>A maps to NM_003024.2 T897T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:35208936 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:35255924 C>A maps to NM_003024.2 I1542I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8114-01A-11D-2395-08 chr21:35183493 G>A maps to NM_003024.2 T845T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65Z-01A-11D-A29Q-08 chr21:35183493 G>A maps to NM_003024.2 T845T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:24494739 G>A maps to NM_006277.2 R718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:128260961 C>A did not map to a codon.
Sequencing variant TCGA-CS-6290-01A-11D-1705-08 chr20:10622191 C>T maps to NM_000214.2 V944V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:10625532 C>T maps to NM_000214.2 W774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:10639257 G>A maps to NM_000214.2 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:10628719 G>A maps to NM_000214.2 N536N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6IZ-01A-11D-A31L-08 chr20:10620232 C>T maps to NM_000214.2 P1190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr20:10624438 G>A maps to NM_000214.2 P815P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:105609256 C>T maps to NM_002226.3 A1164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:105615642 A>G maps to NM_002226.3 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6394-01A-11D-1705-08 chr14:105615618 G>A maps to NM_002226.3 N547N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74H-01A-11D-A32B-08 chr14:105622204 G>A maps to NM_002226.3 D199D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7009-01A-11D-2024-08 chr1:65303661 A>G maps to NM_002227.2 D1031D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr1:65323386 G>A maps to NM_002227.2 T470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr9:5090495 C>T maps to NM_004972.3 R938*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:6066609 G>A maps to NM_001099433.1 D476D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr4:6043921 G>A maps to NM_001099433.1 A687A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:133954007 C>T maps to NM_001105521.2 S466S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8106-01A-11D-2395-08 chr10:133967331 G>T did not map to a codon.
Sequencing variant TCGA-HT-7856-01A-11D-2395-08 chr11:134018706 C>T maps to NM_032801.3 D342D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YM-01A-11D-A34A-08 chr6:15501349 G>T maps to NM_004973.2 E720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8105-01A-11D-2395-08 chr7:27880481 G>A maps to NM_175061.3 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:139796537 C>A maps to NM_030647.1 E731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5394-01A-01D-1468-08 chr14:59970666 G>A maps to ENST00000356057 V285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:64967462 C>T maps to NM_032776.1 Q1322Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:42138144 C>T maps to NM_005090.3 I731I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:78610357 T>C maps to NM_152405.4 P781P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6XA-01A-12D-A32B-08 chr20:42788535 G>A maps to NM_020433.4 N297N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr16:87678020 C>T maps to NM_020655.2 D180D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5ET-01A-11D-A27K-08 chr16:87678404 G>A maps to NM_020655.2 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7298-01A-11D-2024-08 chr14:24040637 G>A maps to NM_032452.2 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:96125217 G>T maps to NM_003772.3 E469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4942-01A-01D-1468-08 chr23:8555922 T>C did not map to a codon.
Sequencing variant TCGA-DH-A7US-01A-11D-A33T-08 chr23:8502384 C>A did not map to a codon.
Sequencing variant TCGA-FG-7638-01B-11D-2086-08 chr23:8503843 G>T did not map to a codon.
Sequencing variant TCGA-DU-5854-01A-11D-1705-08 chr3:124393413 G>A maps to NM_001024660.3 A2382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U2-01A-21D-A33T-08 chr3:124418864 C>T maps to NM_001024660.3 R2661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WL-01A-21D-A33T-08 chr3:124418864 C>T maps to NM_001024660.3 R2661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VW-A7QS-01A-12D-A33T-08 chr3:124418864 C>T maps to NM_001024660.3 R2661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XD-01A-11D-A27K-08 chr9:713192 G>A maps to NM_015158.2 E809E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:711584 C>T maps to NM_015158.2 R273R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A736-01A-11D-A32B-08 chr9:742320 C>G maps to NM_015158.2 L1271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:11287387 G>A maps to NM_015493.6 A550A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:62740588 G>A maps to NM_181712.4 Q63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7880-01A-11D-2395-08 chr17:40269491 C>T maps to NM_021078.2 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:15361332 C>T maps to NM_201628.2 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:15382732 G>A maps to NM_201628.2 Q291Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WL-01A-21D-A33T-08 chr15:65369305 C>T maps to NM_001101362.2 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:42727514 C>T maps to NM_152393.2 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:41704781 G>A maps to NM_152903.4 C622C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:41767127 C>T maps to NM_032138.4 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KT-A74X-01A-11D-A32B-08 chr3:67054338 A>G maps to NM_032505.2 K316K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A733-01A-11D-A32B-08 chr3:67054665 C>T maps to NM_032505.2 C425C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr12:5021389 C>T maps to NM_000217.2 G282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:111060437 G>A maps to NM_005549.2 V324V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:111216891 G>A maps to NM_002232.3 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:5154305 C>T maps to NM_002234.2 C331C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TT-01A-11D-A289-08 chr3:155838414 G>T maps to NM_172160.2 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:6154463 C>T maps to NM_003636.3 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:7827317 G>A maps to NM_004732.2 R299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr8:73480217 C>T maps to NM_004770.2 N83N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:73849974 T>A maps to NM_004770.2 P795P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WD-01A-12D-A33T-08 chr8:73480199 C>T maps to NM_004770.2 C77C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7C4-01A-11D-A32B-08 chr8:73849509 A>G maps to NM_004770.2 T640T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RR-01A-21D-A34A-08 chr8:73848237 G>A maps to NM_004770.2 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:75441975 C>T maps to NM_139137.2 T579T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A70Z-01A-12D-A33T-08 chr12:75601451 G>A maps to NM_139137.2 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6667-01A-12D-2024-08 chr23:48826089 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:48819928 G>A did not map to a codon.
Sequencing variant TCGA-HT-7616-01A-11D-2253-08 chr7:119914853 G>A maps to NM_012281.2 Q56Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TZ-01A-21D-A32B-08 chr7:119915147 C>T maps to NM_012281.2 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:11053346 C>A maps to NM_002236.4 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7480-01A-11D-2086-08 chr20:49626812 G>A maps to NM_002237.3 D21D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CV-01A-11D-A31L-08 chr20:49626566 G>A maps to NM_002237.3 N103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6668-01A-11D-1893-08 chr18:77624218 G>A maps to NM_012283.1 V184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6396-01A-11D-1705-08 chr18:77659302 C>G maps to NM_012283.1 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KT-A7W1-01A-11D-A34A-08 chr1:211307259 G>A maps to NM_172362.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:49950230 A>G maps to NM_012284.1 E849E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:49950197 G>A maps to NM_012284.1 K838K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr12:49937974 G>T maps to NM_012284.1 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:61601539 C>T maps to NM_030779.2 C39C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YJ-01A-11D-A34A-08 chr17:61613106 C>T maps to NM_030779.2 Y393Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:163291759 A>T maps to NM_033272.2 S634S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:163374645 G>A maps to NM_033272.2 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:163291735 G>T maps to NM_033272.2 I642I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4943-01A-01D-1468-08 chr3:19575086 C>T maps to NM_144633.2 G940G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:19498416 C>T maps to NM_144633.2 F661F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8011-01A-11D-2395-08 chr3:19575086 C>T maps to NM_144633.2 G940G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr17:21319340 C>T maps to NM_021012.4 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A72W-01A-11D-A32B-08 chr2:155555775 C>G maps to NM_002239.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:38823261 G>A maps to NM_152868.1 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:128781758 G>A maps to NM_000890.3 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TS-01A-12D-A33T-08 chr11:128781869 C>A maps to NM_000890.3 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:39087048 G>A maps to NM_002240.2 N137N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RW-01A-11D-A33T-08 chr12:21919154 A>T maps to NM_004982.2 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:88729674 G>A maps to NM_138318.2 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr14:88652406 G>A maps to NM_138318.2 H368H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr14:90650848 G>A maps to NM_022054.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:39284630 G>A maps to NM_032115.3 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:118960676 A>G maps to NM_181840.1 E77E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YD-01A-11D-A34A-08 chr10:118969302 A>C maps to NM_181840.1 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7608-01A-11D-2086-08 chr10:118957047 C>T maps to NM_181840.1 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85B-01A-11D-A36O-08 chr1:215368302 C>T maps to NM_001017425.2 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:178960735 G>A maps to NM_171828.1 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6410-01A-11D-1893-08 chr1:154842347 C>T maps to NM_002249.4 Q31Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:44273957 C>A maps to NM_002250.2 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:133152420 G>A maps to NM_004519.2 A490A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6J3-01A-11D-A31L-08 chr8:133198388 C>A maps to NM_004519.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A710-01A-12D-A33T-08 chr8:133141583 G>A maps to NM_004519.2 S848S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A89V-01A-11D-A36O-08 chr8:133142021 C>T maps to NM_004519.2 V702V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6186-01A-12D-2024-08 chr2:18113039 G>A maps to NM_002252.3 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:138671300 T>C maps to ENST00000298480 L942L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:138662883 C>T maps to ENST00000298480 Q651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr9:138669221 C>T maps to ENST00000298480 Y796Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YW-01A-11D-A34J-08 chr9:138642848 G>A maps to ENST00000298480 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RB-01A-11D-A289-08 chr9:138676391 G>A maps to ENST00000298480 K985K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:196451509 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:196288612 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:196367747 A>G maps to NM_198503.2 C413C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8018-01A-11D-2395-08 chr1:196274363 C>T maps to NM_198503.2 K865K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6667-01A-12D-2024-08 chr8:36694321 A>G maps to NM_001031836.2 P459P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7605-01A-11D-2086-08 chr8:36642080 T>C maps to NM_001031836.2 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7610-01A-21D-2086-08 chr8:36721927 C>A maps to NM_001031836.2 S633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A617-01A-11D-A29Q-08 chr8:36671861 G>T maps to NM_001031836.2 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr8:36793053 C>T maps to NM_001031836.2 A1022A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:7256632 C>T maps to NM_001002914.2 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:77734237 G>A maps to NM_023930.3 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr16:67327472 C>T maps to NM_001100915.1 W731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:77885171 G>A maps to NM_001029859.1 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:77885144 G>T maps to NM_001029859.1 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RJ-01A-11D-A33T-08 chr11:77885165 G>A maps to NM_001029859.1 N145N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:215793455 G>A maps to NM_016121.3 R648R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:6505921 G>A maps to NM_006854.3 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6X8-01A-12D-A32B-08 chr7:6505723 G>A maps to NM_006854.3 F194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr1:23405540 C>T maps to NM_001009999.2 C642C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:137721802 G>A maps to NM_016604.3 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:137717215 C>T maps to NM_016604.3 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr19:5131426 G>A maps to NM_015015.2 E552E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64R-01A-11D-A29Q-08 chr9:6805636 T>G maps to NM_015061.3 Y61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:6990510 G>T maps to NM_015061.3 A591A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr9:6990510 G>A maps to NM_015061.3 A591A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8107-01A-13D-2395-08 chr11:94731684 G>A maps to NM_018039.2 R383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:416168 A>G maps to NM_001042603.1 D1339D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QX-01A-11D-A34A-08 chr12:442739 G>C maps to NM_001042603.1 A522A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64P-01A-11D-A29Q-08 chr1:202719899 G>A maps to ENST00000367264 R606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7882-01A-11D-2395-08 chr1:202702738 C>T maps to ENST00000367264 L1269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84Q-01A-11D-A36O-08 chr1:202727566 C>A maps to ENST00000367264 G419G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:53239947 T>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:53241016 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:53222209 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:53240001 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:53230838 C>T did not map to a codon.
Sequencing variant TCGA-P5-A72Z-01A-11D-A32B-08 chr23:53226062 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:44919320 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:44920632 A>G did not map to a codon.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr23:44949045 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:7752260 C>T maps to NM_001080424.1 G885G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5847-01A-11D-1705-08 chr4:55956203 C>T maps to NM_002253.2 S1037S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YK-01A-11D-A34A-08 chr4:55962465 G>C maps to NM_002253.2 L886L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr4:55961109 G>A maps to NM_002253.2 R944*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A77X-01A-11D-A32B-08 chr4:55984888 G>A maps to NM_002253.2 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:10600039 G>A maps to NM_203500.1 V512V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TA-01A-11D-A33T-08 chr19:10602359 G>A maps to NM_203500.1 C406C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A87Q-01A-11D-A36O-08 chr7:142651435 G>T maps to NM_000420.2 Y253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EX-01A-12D-A289-08 chr7:142638439 G>A maps to NM_000420.2 R700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr12:91449806 T>C maps to NM_007035.3 E84E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr6:62611198 G>A maps to NM_152688.2 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RG-01A-11D-A33T-08 chr14:24901558 G>A maps to NM_015299.2 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr19:6416894 T>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:2828697 C>T maps to NM_014878.4 Q311Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:19550000 G>T maps to NM_015047.1 T755T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8011-01A-11D-2395-08 chr1:19563720 C>T maps to NM_015047.1 Q408Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:26962483 C>T maps to NM_014680.2 E707E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TP-01A-11D-A289-08 chr17:26961607 A>G maps to NM_014680.2 P999P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8189-01B-11D-A289-08 chr17:26961607 A>G maps to NM_014680.2 P999P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:64658212 G>T maps to NM_001029989.1 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:48320492 C>T maps to NM_001080394.1 Q283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5847-01A-11D-1705-08 chr16:71958717 T>C maps to NM_014761.2 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:71949615 T>C maps to NM_014761.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WP-01A-12D-A34A-08 chr16:85704655 G>A maps to NM_014615.2 R1157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:73492413 C>T maps to ENST00000375248 G1041G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:126044598 C>T maps to ENST00000377985 W1078*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7601-01A-11D-2086-08 chr8:126075803 G>C maps to ENST00000377985 V461V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:197402329 G>T maps to NM_014687.1 I901I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:197444952 A>C maps to NM_014687.1 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7605-01A-11D-2086-08 chr3:197408182 G>A maps to NM_014687.1 C749C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:6864925 C>A maps to NM_014743.2 T939T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:42832679 G>A maps to NM_015349.1 V912V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:105353629 G>A maps to ENST00000453495 T1019T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UR-01A-11D-A33T-08 chr14:75134269 G>A maps to NM_001039479.1 Q648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A6S8-01A-12D-A32B-08 chr6:24559319 C>T maps to NM_014809.3 V885V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:35921615 G>A maps to NM_024874.4 Q552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IY-01A-11D-A34A-08 chr1:35944786 A>G maps to NM_024874.4 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5397-01A-01D-1893-08 chr9:114246645 A>C maps to NM_001080398.1 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6668-01A-11D-1893-08 chr9:114170942 G>A maps to NM_001080398.1 R1032*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:114190320 C>T did not map to a codon.
Sequencing variant TCGA-DH-A7UT-01A-12D-A34A-08 chr6:127771347 C>T maps to NM_014702.4 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr7:4824641 C>T maps to ENST00000450194 F1009F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A669-01A-12D-A31L-08 chr1:43897194 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:3662290 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:3662559 A>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:85100901 C>T maps to NM_014732.2 N75N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:27751588 C>T maps to NM_015202.2 L657L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8188-01A-11D-2253-08 chr16:27786308 G>A maps to NM_015202.2 V1451V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7855-01A-11D-2395-08 chr16:27640071 T>C maps to NM_015202.2 N77N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6290-01A-11D-1705-08 chr1:3740069 G>A maps to NM_014704.3 D807D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:42440106 G>A maps to NM_015058.1 S426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:42161671 G>A maps to NM_015058.1 F1749F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UR-01A-11D-A33T-08 chr9:138378890 G>A maps to NM_014811.3 L845L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:138379301 C>T maps to NM_014811.3 S982S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:138378992 G>A maps to NM_014811.3 R879R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7873-01B-11D-2395-08 chr9:138379181 C>T maps to NM_014811.3 T942T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CZ-01A-11D-A32B-08 chr9:138377993 G>A maps to NM_014811.3 A546A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7C4-01A-11D-A32B-08 chr9:138378947 C>T maps to NM_014811.3 T864T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7480-01A-11D-2086-08 chr11:46671756 G>A maps to NM_001142673.1 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7603-01A-21D-2086-08 chr17:2605306 G>A maps to NM_015229.3 R136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:55356409 A>G maps to NM_001098815.1 H424H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84J-01A-11D-A36O-08 chr12:55357559 C>T maps to NM_001098815.1 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:6515457 C>T maps to NM_014804.2 Q442Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KK-01A-11D-A27K-08 chr1:39876725 A>G maps to NM_015038.1 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6UA-01A-12D-A33T-08 chr1:39878106 C>T maps to NM_015038.1 L724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:8826085 C>T maps to ENST00000456698 L1845L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7478-01A-11D-2024-08 chr19:19456111 G>A did not map to a codon.
Sequencing variant TCGA-HT-A74O-01A-11D-A32B-08 chr16:67210812 G>A maps to NM_001040715.1 H439H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7Z3-01A-11D-A34J-08 chr1:155895454 T>C maps to NM_014949.2 R287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:75561189 C>T maps to NM_015037.2 N1814N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:75550023 C>T maps to NM_015037.2 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:154557571 G>A maps to NM_001131007.1 S1559S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6670-01A-11D-1893-08 chr5:5466480 C>G maps to NM_015325.1 S1976*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:5464589 C>T maps to NM_015325.1 Q1715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R2-01A-21D-A34J-08 chr5:5463793 T>A maps to NM_015325.1 P1449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7676-01A-11D-2395-08 chr6:84896079 T>C maps to NM_014895.2 S457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EX-01A-12D-A289-08 chr15:79749238 C>T maps to NM_015206.2 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64P-01A-11D-A29Q-08 chr4:123166208 C>T maps to NM_015312.3 R1651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:123109180 G>A maps to NM_015312.3 K253K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:123252486 G>A maps to NM_015312.3 T3752T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr4:123140535 A>G maps to NM_015312.3 E763E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:141385375 G>A maps to NM_001080392.1 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:34372161 C>T maps to NM_020702.3 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr9:34372001 G>A maps to NM_020702.3 R314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:175774999 T>C maps to NM_020444.3 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:81234671 C>T maps to NM_018689.1 Y1231Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:81212432 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:118227692 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:118242364 A>G did not map to a codon.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr23:118284500 G>A did not map to a codon.
Sequencing variant TCGA-HT-7481-01A-11D-2024-08 chr23:118222474 C>A did not map to a codon.
Sequencing variant TCGA-HW-7493-01A-11D-2024-08 chr23:118242328 C>A did not map to a codon.
Sequencing variant TCGA-TQ-A7RH-01A-12D-A34A-08 chr23:118222262 G>A did not map to a codon.
Sequencing variant TCGA-WY-A85E-01A-11D-A36O-08 chr23:118223154 G>T did not map to a codon.
Sequencing variant TCGA-DU-7019-01A-11D-2024-08 chr4:57182124 G>A maps to NM_020722.1 S819S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7476-01A-11D-2024-08 chr4:57193876 G>A maps to NM_020722.1 P1203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:24835129 C>T maps to NM_019590.3 S1903S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:24822048 T>A maps to NM_019590.3 Y1099*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7T8-01A-21D-A34J-08 chr10:24813329 C>T maps to NM_019590.3 A845A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F6-A8O3-01A-11D-A36O-08 chr10:24669988 A>G maps to NM_019590.3 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5964-01A-11D-1705-08 chr10:24833959 C>T maps to NM_019590.3 A1754A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6J3-01A-11D-A31L-08 chr10:24508621 C>T maps to NM_019590.3 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-8125-01A-11D-2253-08 chr10:24832987 A>T maps to NM_019590.3 K1597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:138584260 G>A maps to NM_020340.4 T547T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A70Y-01A-12D-A34J-08 chr6:138618037 G>A maps to NM_020340.4 R1198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:72324205 C>A maps to NM_014431.2 L783L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:109714635 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:109740232 C>A maps to NM_020775.3 A753A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7471-01A-11D-2253-08 chr1:109707133 C>T maps to NM_020775.3 N96N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:34415333 G>T maps to NM_020776.1 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr18:34414310 C>T maps to NM_020776.1 Y29Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:52901016 T>C maps to NM_019600.2 K698K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:52901466 G>T maps to NM_019600.2 S548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:101829097 G>A did not map to a codon.
Sequencing variant TCGA-FG-5962-01B-11D-1893-08 chr1:232941482 C>T maps to NM_019090.2 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:113684176 C>T maps to NM_020817.1 W879*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5304-01A-01D-1468-08 chr3:113761685 C>T maps to NM_020817.1 E93E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RI-01A-11D-A33T-08 chr3:113684007 G>A maps to NM_020817.1 N935N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:94121729 C>T maps to ENST00000393153 L2206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YY-01A-11D-A34J-08 chr14:94160679 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:5765700 C>T maps to ENST00000414202 R1014*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:30316835 G>T maps to NM_020848.2 A747A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8161-01A-11D-2253-08 chr10:30315251 G>A maps to NM_020848.2 S1275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8113-01A-11D-2395-08 chr10:30318650 G>A maps to NM_020848.2 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:108285441 G>T maps to NM_020890.2 I439I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:100085190 G>A maps to ENST00000375206 V595V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:7682810 G>A maps to NM_001080429.2 S1233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:138602433 C>T maps to NM_001164665.1 A646A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TT-01A-11D-A289-08 chr6:56918472 T>C maps to NM_020931.2 A392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:118700087 G>A maps to NM_001127211.1 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr16:84516257 C>T maps to NM_020947.3 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5142-01A-01D-1468-08 chr1:180904727 G>A maps to NM_020950.1 Q561Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TZ-01A-21D-A32B-08 chr1:180885463 A>G maps to NM_020950.1 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr18:43496144 G>A maps to NM_020964.2 P1137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5871-01A-12D-1705-08 chr18:43447536 T>C maps to NM_020964.2 V2134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:18378151 C>T maps to NM_001145304.1 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A6S7-01A-21D-A32B-08 chr4:175224898 C>T maps to NM_001145314.1 Q95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:36846681 G>T maps to NM_001029864.1 A881A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U8-01A-21D-A33T-08 chr20:36874468 G>A maps to NM_001029864.1 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr9:20866926 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:233518141 A>G maps to NM_032435.2 S932S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RP-01A-21D-A34A-08 chr1:233518414 C>T maps to NM_032435.2 S1023S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5277-01A-01D-1468-08 chr2:61315600 A>C maps to NM_001129993.1 I362I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:115422291 C>T maps to NM_133465.2 T698T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:115337334 G>A maps to NM_133465.2 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:139701207 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:139697114 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:11983088 C>T maps to ENST00000376576 V497V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:113379796 G>A maps to NM_001009899.2 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:113377543 G>T maps to NM_001009899.2 T995T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr23:73963360 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:73959987 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:73962650 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:73960017 T>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:73960266 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:73960954 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:73960022 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:73960347 A>G did not map to a codon.
Sequencing variant TCGA-S9-A7IX-01A-12D-A34A-08 chr23:73964002 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:8957801 C>T maps to NM_020738.2 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5963-01A-11D-1705-08 chr2:8958893 G>A maps to NM_020738.2 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:17788043 G>A maps to NM_022113.4 Y1108Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:17771431 C>T maps to NM_022113.4 Q1498Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:44893798 C>T maps to NM_020242.2 R1358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A83Y-01A-11D-A36O-08 chr3:44879795 T>C maps to NM_020242.2 H1067H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:16486691 A>G maps to NM_024704.4 T281T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DU-6392-01A-11D-1705-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FG-A60L-01A-12D-A31L-08 chr20:16359696 C>A maps to NM_024704.4 E984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:21016708 C>T maps to NM_020816.2 T451T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr1:20992722 G>A maps to NM_020816.2 D965D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6X8-01A-12D-A32B-08 chr17:43003540 A>G maps to ENST00000438933 S834S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:72339247 C>T maps to NM_153209.3 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:241722502 C>T maps to ENST00000373308 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:241680732 G>A maps to ENST00000373308 Y1234Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6J1-01A-11D-A31L-08 chr1:10386357 C>G maps to ENST00000377086 L955L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:91484804 T>C maps to ENST00000416354 L631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6XC-01A-12D-A32B-08 chr10:91486210 A>G maps to ENST00000416354 K721K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:39763652 C>A maps to ENST00000395670 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:39725523 G>A maps to ENST00000395670 L1041L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:200948843 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:200943315 G>A maps to NM_017596.2 C1594C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:200956012 C>T maps to NM_017596.2 P1216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7309-01A-11D-2086-08 chr16:29808400 C>T maps to NM_007317.1 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:69732274 T>C maps to NM_138555.1 Y582Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:168445636 G>A maps to NM_030615.2 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6394-01A-11D-1705-08 chr14:104643665 C>A maps to NM_015656.1 S1514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U2-01A-21D-A33T-08 chr14:104643171 G>A maps to NM_015656.1 K1349K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YQ-01A-11D-A34J-08 chr1:245849236 C>T maps to NM_018012.3 S984S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7637-01A-11D-2086-08 chr1:245530296 C>T maps to NM_018012.3 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7Z4-01A-11D-A34J-08 chr9:86518657 C>A maps to NM_017576.1 E259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:132034984 G>T maps to ENST00000403231 P670P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:30904662 G>A maps to NM_004798.3 R578R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:69637829 G>T did not map to a codon.
Sequencing variant TCGA-E1-A7YH-01A-11D-A34A-08 chr23:69572506 G>A did not map to a codon.
Sequencing variant TCGA-P5-A5EX-01A-12D-A289-08 chr23:69615590 T>G did not map to a codon.
Sequencing variant TCGA-FG-A70Z-01A-12D-A33T-08 chr5:154397003 G>A maps to NM_001099293.1 S1195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CV-01A-11D-A31L-08 chr5:154395582 C>T maps to NM_001099293.1 R722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66G-01A-21D-A31L-08 chr12:57960997 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:57969502 C>T maps to NM_004984.2 D662D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:32306235 G>A maps to NM_004521.2 R866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6UB-01A-21D-A33T-08 chr2:149679716 A>G maps to NM_004522.1 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:39507778 C>A maps to NM_145027.4 G549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:47307307 C>T maps to NM_182902.3 E276E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5305-01A-01D-1893-08 chr3:47284701 A>G maps to NM_182902.3 P516P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A858-01A-11D-A36O-08 chr3:47307319 G>C maps to NM_182902.3 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5275-01A-01D-1468-08 chr1:170003638 T>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:33371557 C>A maps to NM_002263.3 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UU-01A-12D-A34A-08 chr16:57803768 G>T maps to NM_005550.3 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CF-01A-11D-A36O-08 chr19:55284914 C>T maps to ENST00000291633 N67N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76K-01A-11D-A33T-08 chr19:55325145 T>C maps to ENST00000396289 D293D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:55331357 C>T maps to ENST00000355608 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A669-01A-12D-A31L-08 chr1:158061182 G>A maps to ENST00000368173 G452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:126301386 G>A maps to NM_032531.3 A541A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr13:33591132 G>C maps to NM_004795.3 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5304-01A-01D-1468-08 chr2:10188339 G>T maps to NM_003597.4 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6393-01A-11D-1705-08 chr7:130418290 A>G maps to NM_138693.2 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TS-01A-12D-A33T-08 chr1:44595584 G>A maps to NM_173484.3 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EZ-01A-11D-A27K-08 chr4:38690342 G>A maps to NM_016531.5 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:73636831 C>A maps to NM_001730.3 P365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U0-01A-12D-A32B-08 chr13:73649879 C>T maps to NM_001730.3 C410C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:56291820 C>A did not map to a codon.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr7:129710590 T>G maps to NM_014997.3 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:27933541 C>T maps to NM_020782.1 D93D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr1:18808236 C>T maps to NM_152375.2 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7873-01B-11D-2395-08 chr1:18809172 G>A maps to NM_152375.2 T566T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:49210219 C>T maps to NM_173546.2 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W9-A837-01A-11D-A36O-08 chr3:49210375 A>G maps to NM_173546.2 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A733-01A-11D-A32B-08 chr1:161069999 C>T maps to NM_152366.4 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:40010059 G>A maps to NM_018143.1 Q687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:117033090 G>A did not map to a codon.
Sequencing variant TCGA-DU-6404-01A-11D-1705-08 chr23:117043974 C>T did not map to a codon.
Sequencing variant TCGA-HT-7601-01A-11D-2086-08 chr23:117032911 T>G did not map to a codon.
Multiple mappings detected for codon TCGA-DU-5855-01A-11D-1705-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr18:30349843 C>T maps to ENST00000426194 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:30260221 G>A maps to NM_020805.1 R500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8191-01A-11D-2253-08 chr18:30322012 C>A did not map to a codon.
Multiple mappings detected for codon TCGA-HT-7473-01A-11D-2024-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HT-7473-01A-11D-2024-08 chr18:30349852 C>T maps to ENST00000426194 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6X4-01A-51D-A32B-08 chr18:30275429 C>T maps to NM_020805.1 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:24007069 A>G did not map to a codon.
Sequencing variant TCGA-DU-7302-01A-11D-2086-08 chr23:24006739 T>C did not map to a codon.
Sequencing variant TCGA-QH-A6X5-01A-12D-A32B-08 chr23:24024161 T>C did not map to a codon.
Sequencing variant TCGA-E1-5302-01A-01D-1468-08 chr3:47361234 C>T maps to NM_025010.4 C74C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:173721015 C>A maps to NM_014458.3 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:173744788 T>A maps to NM_014458.3 P482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:6653595 G>A maps to NM_014851.2 S541S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:183381372 G>T maps to NM_017644.3 E350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7608-01A-11D-2086-08 chr15:86312651 G>A maps to NM_022480.3 H130H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EZ-7264-01A-11D-2024-08 chr19:18779268 G>A maps to NM_018316.1 T354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr14:45403685 T>C maps to ENST00000355081 G339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:239057696 G>A maps to NM_198582.3 S463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7636-01A-11D-2086-08 chr2:239050039 G>A maps to NM_198582.3 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:21675839 G>A did not map to a codon.
Sequencing variant TCGA-TQ-A7RJ-01A-11D-A33T-08 chr23:21675337 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:75133659 G>A maps to NM_001039548.2 H572H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:84695192 C>T maps to NM_024731.2 Y435Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr8:124664239 G>A maps to NM_001081675.2 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A72W-01A-11D-A32B-08 chr8:124664296 G>A maps to NM_001081675.2 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:86890606 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:183209810 G>A maps to NM_130446.2 C590C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:23205475 C>T maps to NM_001031710.2 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:21334318 G>A maps to NM_018847.2 N180N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4938-01B-11D-1893-08 chr19:51518741 G>A maps to NM_001077500.1 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IS-01A-11D-A34A-08 chr19:51535255 C>A maps to NM_019598.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:51559996 T>C maps to NM_015596.1 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr19:51330970 G>A maps to NM_017509.2 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr19:51330299 G>A maps to NM_017509.2 N105N. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-E1-5318-01A-01D-1468-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-QH-A6XC-01A-12D-A32B-08 chr19:51453166 G>A maps to NM_012427.4 C93C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6405-01A-11D-1705-08 chr19:51466621 C>T maps to NM_001012964.1 L127L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-TQ-A7RV-01A-21D-A34A-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-W9-A837-01A-11D-A36O-08 chr12:10601987 C>A did not map to a codon.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr12:9995005 G>A maps to NM_016523.1 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr1:241749982 C>G maps to NM_003679.3 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A843-01A-11D-A36O-08 chr10:135003171 C>T maps to ENST00000368572 N504N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:186457160 G>A maps to NM_001102416.2 E361E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7636-01A-11D-2086-08 chr3:186450324 C>T maps to NM_001102416.2 C264C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:123067322 G>A maps to NM_014708.4 Q1018Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U8-01A-21D-A33T-08 chr12:123071290 C>T maps to NM_014708.4 C1239C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:122168491 T>G maps to NM_002264.3 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:122170391 C>A maps to NM_002264.3 E248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:47986472 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:25398279 G>A maps to NM_033360.2 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:10675644 G>A maps to NM_023008.3 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EW-01A-11D-A27K-08 chr19:10668900 G>A maps to NM_023008.3 D409D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:91830632 T>C maps to NM_194456.1 V710V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:91852279 G>A maps to NM_194456.1 R423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F6-01A-11D-A289-08 chr7:91865758 T>C maps to NM_194456.1 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F4-01A-11D-A289-08 chr17:39673185 G>A maps to NM_002275.3 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:53344641 C>T maps to NM_000224.2 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KT-A7W1-01A-11D-A34A-08 chr17:39680189 C>T maps to NM_002276.4 A336A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TC-01A-21D-A34J-08 chr12:53045434 G>A maps to NM_000423.2 N164N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RO-01A-11D-A33T-08 chr17:39041251 G>A maps to NM_019010.2 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr17:38812820 G>A maps to NM_152349.2 R241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr17:38857427 G>A maps to NM_019016.2 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:38906729 G>A maps to NM_181534.3 T359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6410-01A-11D-1893-08 chr17:38906789 C>T maps to NM_181534.3 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6J1-01A-11D-A31L-08 chr17:38906789 C>T maps to NM_181534.3 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A6ML-01A-11D-A32B-08 chr17:38906798 C>T maps to NM_181534.3 A336A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WM-01A-12D-A33T-08 chr17:38907515 G>A maps to NM_181534.3 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A89V-01A-11D-A36O-08 chr17:38905573 G>T maps to NM_181534.3 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:38922876 G>A maps to NM_181539.4 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:38927951 G>A maps to NM_181539.4 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:38926513 A>G maps to NM_181539.4 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7609-01A-11D-2086-08 chr17:38926338 G>A maps to NM_181539.4 N239N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:38938541 G>T maps to NM_181537.3 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7610-01A-21D-2086-08 chr17:38936092 G>A maps to NM_181537.3 C235C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74H-01A-11D-A32B-08 chr17:38933307 A>C maps to NM_181537.3 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr17:38954584 G>A maps to NM_181535.3 R198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:38953512 G>A maps to NM_181535.3 C237C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr17:39553719 G>C maps to ENST00000393998 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CV-01A-11D-A31L-08 chr17:39506827 G>A maps to NM_004138.2 N64N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:39521182 C>T maps to ENST00000394004 Q316Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:39522798 G>A maps to ENST00000394004 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:39521688 C>A maps to ENST00000394004 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F6-A8O3-01A-11D-A36O-08 chr17:39521492 C>T maps to ENST00000394004 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4X9-01A-11D-A26M-08 chr17:39535941 G>A maps to NM_021013.3 N252N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CF-01A-11D-A36O-08 chr17:39535344 G>A maps to NM_021013.3 N362N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7479-01A-11D-2024-08 chr17:39596990 G>A maps to NM_006771.3 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr17:39595475 G>C maps to NM_006771.3 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A72U-01A-31D-A32B-08 chr17:39135152 G>A maps to NM_182497.3 R367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr12:52913801 G>A maps to NM_000424.3 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YJ-01A-11D-A34A-08 chr12:52910608 G>A maps to NM_000424.3 A417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:52943137 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:53005047 G>A maps to NM_175068.2 I350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:52824342 C>T maps to ENST00000252245 E393E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A86X-01A-11D-A36O-08 chr12:52822481 G>A maps to ENST00000252245 R415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A83Y-01A-11D-A36O-08 chr12:52826916 C>T maps to ENST00000252245 E260E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5393-01A-01D-1468-08 chr12:53088517 G>A maps to NM_175078.2 D324D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:53224076 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:52566079 C>T maps to NM_182507.2 A360A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:52682228 G>A maps to NM_002281.3 C217C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8188-01A-11D-2253-08 chr12:52680929 G>A maps to NM_002281.3 I401I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:52789940 G>A maps to NM_033033.3 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:52779069 G>A maps to NM_033045.3 D100D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:52775246 G>A maps to NM_033045.3 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7490-01A-11D-2024-08 chr12:52777393 G>A maps to NM_033045.3 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:52758804 G>A maps to NM_002283.3 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F6-A8O3-01A-11D-A36O-08 chr12:52760835 G>A maps to NM_002283.3 C118C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6393-01A-11D-1705-08 chr21:46057414 C>T maps to NM_181688.1 C27C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5302-01A-01D-1468-08 chr21:46066416 C>T maps to NM_198692.2 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8188-01A-11D-2253-08 chr21:46117133 C>T maps to NM_198699.1 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:45970948 A>G maps to NM_198693.2 C131C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RH-01A-12D-A34A-08 chr21:45993835 C>T maps to NM_198687.1 C67C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XF-01A-11D-A27K-08 chr21:46011885 G>A maps to NM_198688.2 C160C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7854-01A-11D-2253-08 chr21:46011552 A>G maps to NM_198688.2 C271C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr21:46032409 C>T maps to NM_198695.2 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr21:46086743 G>A maps to NM_181684.2 C20C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr21:31798185 G>A maps to NM_181622.1 H15H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:31852399 C>T maps to NM_181607.1 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WL-01A-21D-A33T-08 chr21:31859628 G>A maps to NM_181608.1 C13C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A710-01A-12D-A33T-08 chr21:32410672 G>A maps to NM_001099219.1 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A711-01A-21D-A33T-08 chr21:32119421 G>A maps to NM_181617.1 Y33Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr17:39274306 G>T maps to NM_033059.3 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr17:39274237 A>G maps to NM_033059.3 C110C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:39305719 G>A maps to NM_033188.3 C100C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IX-01A-12D-A34A-08 chr17:39240559 T>C maps to ENST00000377731 C34C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5273-01A-01D-1468-08 chr17:39261777 A>G maps to NM_001146041.1 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R7-01A-11D-A289-08 chr17:39261777 A>G maps to NM_001146041.1 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:1605654 C>T maps to NM_001005922.1 Q275Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr11:1606185 A>G maps to NM_001005922.1 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8105-01A-11D-2395-08 chr11:1606209 G>A maps to NM_001005922.1 G90G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DU-6392-01A-11D-1705-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-HT-7880-01A-11D-2395-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:1643314 G>T maps to ENST00000359229 C3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8320-01A-11D-2395-08 chr11:1642984 G>A maps to ENST00000359229 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:1651249 C>G maps to NM_001001480.2 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr11:1718510 C>T maps to NM_001012416.1 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:71260185 C>A maps to NM_005553.3 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:39406016 G>A maps to ENST00000431129 R15R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:39406253 C>T maps to NM_033191.2 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:39394563 G>C maps to NM_031963.2 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4942-01A-01D-1468-08 chr2:27665527 C>T maps to NM_001168364.1 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:27666107 G>A maps to NM_001168364.1 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7018-01A-11D-2024-08 chr2:27666915 G>A maps to NM_001168364.1 W239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A859-01A-12D-A36O-08 chr19:35979706 G>T maps to NM_207392.1 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TZ-01A-21D-A32B-08 chr17:25937179 G>A maps to ENST00000268763 E716E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:117962775 G>A maps to ENST00000339824 N700N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8321-01A-11D-2395-08 chr3:119204195 G>A maps to NM_152305.2 W200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TV-01A-12D-A34J-08 chr3:119187878 G>A maps to NM_152305.2 W4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85C-01A-11D-A36O-08 chr3:119196232 C>T maps to NM_152305.2 R132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85E-01A-11D-A36O-08 chr3:119187878 G>A maps to NM_152305.2 W4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F2-01A-11D-A289-08 chr1:52499412 G>A maps to NM_138417.2 C7C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76R-01A-11D-A32B-08 chr14:56084853 T>C did not map to a codon.
Sequencing variant TCGA-VM-A8CH-01A-12D-A36O-08 chr3:134323110 C>T maps to NM_178554.4 T432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr23:153130306 G>T did not map to a codon.
Sequencing variant TCGA-DH-A7UR-01A-11D-A33T-08 chr23:153135291 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153130423 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153128321 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153138121 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153134066 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153132842 G>A did not map to a codon.
Sequencing variant TCGA-DU-6403-01A-11D-1705-08 chr23:153133299 G>A did not map to a codon.
Sequencing variant TCGA-FG-A711-01A-21D-A33T-08 chr23:153128220 G>A did not map to a codon.
Sequencing variant TCGA-P5-A735-01A-11D-A32B-08 chr23:153133834 G>A did not map to a codon.
Sequencing variant TCGA-S9-A6WG-01A-11D-A33T-08 chr23:153133890 C>T did not map to a codon.
Sequencing variant TCGA-TQ-A7RG-01A-11D-A33T-08 chr23:153130846 G>A did not map to a codon.
Sequencing variant TCGA-TM-A84F-01A-11D-A36O-08 chr1:62676146 T>C maps to NM_019079.4 D567D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:130372422 A>C maps to NM_032438.2 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7US-01A-11D-A33T-08 chr6:108841009 C>T maps to NM_145315.3 S438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:6886955 G>T did not map to a codon.
Sequencing variant TCGA-QH-A6X9-01A-12D-A32B-08 chr23:153707093 C>A did not map to a codon.
Sequencing variant TCGA-DH-A7UT-01A-12D-A34A-08 chr19:55019287 A>C maps to NM_002288.3 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5962-01B-11D-1893-08 chr18:7036072 G>A maps to NM_005559.2 G584G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8185-01A-11D-2253-08 chr18:7023259 C>A maps to NM_005559.2 G868G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WH-A86K-01A-11D-A36O-08 chr18:7033054 G>A maps to NM_005559.2 A697A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:129724974 T>C maps to NM_000426.3 D1912D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:129601265 C>T maps to NM_000426.3 V837V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6401-01A-11D-1705-08 chr6:129419502 T>C maps to NM_000426.3 D194D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7686-01A-11D-2253-08 chr6:129468138 G>T maps to NM_000426.3 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RH-01A-12D-A34A-08 chr6:129419487 G>A maps to NM_000426.3 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5872-01A-11D-1705-08 chr18:21425085 T>G maps to ENST00000416669 L1241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:21492724 G>A maps to ENST00000416669 L2405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:112499371 G>A maps to NM_001105206.1 H380H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:60887094 G>T maps to NM_005560.3 C3172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65Z-01A-11D-A29Q-08 chr20:60888746 G>A maps to NM_005560.3 D2872D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4942-01A-01D-1468-08 chr3:49159714 G>A maps to NM_002292.3 H1554H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A669-01A-12D-A31L-08 chr3:49161201 G>A maps to NM_002292.3 A1252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:49159016 G>A maps to NM_002292.3 R1703R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:107696369 G>A maps to NM_007356.2 S1154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:107763605 G>A maps to NM_007356.2 Q2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:107707028 A>T maps to NM_007356.2 P821P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5140-01A-01D-1468-08 chr1:183091038 C>T maps to NM_002293.3 C724C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:183072601 C>T maps to NM_002293.3 Y186Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7610-01A-21D-2086-08 chr1:183087213 T>C maps to NM_002293.3 P641P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:183204708 G>A did not map to a codon.
Sequencing variant TCGA-FG-A6J3-01A-11D-A31L-08 chr1:183192354 T>A maps to NM_005562.2 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7301-01A-11D-2086-08 chr9:133942443 C>T maps to ENST00000355048 N815N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A843-01A-11D-A36O-08 chr9:133948657 G>A maps to ENST00000355048 Q1148Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5318-01A-01D-1468-08 chr23:119581703 G>A did not map to a codon.
Sequencing variant TCGA-HW-7490-01A-11D-2024-08 chr23:119573052 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:37515054 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:34046550 G>A maps to NM_133642.3 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F4-01A-11D-A289-08 chr22:33670457 G>A maps to NM_133642.3 Y742Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:129012277 C>T maps to NM_018078.2 R161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:50829387 A>G maps to ENST00000429001 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:875495 A>G maps to NM_015155.1 F318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:71125302 G>T maps to NM_018357.2 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:45441825 C>T maps to NM_015340.3 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:64743530 G>T did not map to a codon.
Sequencing variant TCGA-DU-8161-01A-11D-2253-08 chr23:64752491 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:8326598 C>T maps to NM_024552.2 S292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:28997062 T>C did not map to a codon.
Sequencing variant TCGA-WY-A85D-01A-11D-A36O-08 chr6:150005420 C>T maps to NM_004690.2 W268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr13:21563345 G>A maps to NM_014572.2 Y191Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7480-01A-11D-2086-08 chr13:21549239 G>A maps to NM_014572.2 N1012N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6403-01A-11D-1705-08 chr2:30457269 G>T did not map to a codon.
Sequencing variant TCGA-E1-5305-01A-01D-1893-08 chr20:36983810 T>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:80196728 G>A maps to NM_181714.3 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RM-01A-11D-A33T-08 chr1:152777783 C>T maps to NM_178351.3 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr1:152671571 C>T maps to NM_178428.3 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr1:152671461 C>T maps to NM_178428.3 R29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:25175975 C>T maps to ENST00000380963 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RW-01A-11D-A33T-08 chr9:130912581 G>A maps to ENST00000373013 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EZ-01A-11D-A27K-08 chr9:139640325 G>A maps to NM_198946.2 R91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66G-01A-21D-A31L-08 chr10:98715303 C>T maps to NM_001170765.1 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RQ-01A-11D-A33T-08 chr13:46718595 G>A maps to NM_002298.4 R412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:169689859 C>T maps to NM_005565.3 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:136555612 G>T maps to NM_002299.2 G1654G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W9-A837-01A-11D-A36O-08 chr2:136594246 G>A maps to NM_002299.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:66845561 C>T maps to NM_207338.2 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:103870644 C>T maps to NM_001113407.1 E111E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:88446978 C>T maps to NM_001171610.1 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:88485984 G>A maps to NM_001171610.1 W695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:36250938 G>T maps to NM_174902.2 E344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A780-01A-12D-A32B-08 chr23:140271195 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:44892749 C>T maps to NM_032287.2 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:53277789 C>T maps to NM_007015.2 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A713-01A-11D-A32B-08 chr13:53298164 G>A maps to NM_007015.2 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76K-01A-11D-A33T-08 chr5:135288603 G>A maps to NM_002302.2 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5270-01A-02D-1468-08 chr4:109000757 A>G maps to NM_016269.4 H245H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:109084771 G>A maps to NM_016269.4 N122N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WO-01A-21D-A34A-08 chr4:108985489 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:226125266 G>T maps to NM_003240.3 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RK-01A-11D-A33T-08 chr3:156745896 T>C maps to NM_001004316.2 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:65639940 G>T did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr12:65637237 T>C maps to NM_014319.4 F792F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:54969111 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:54963828 G>A did not map to a codon.
Sequencing variant TCGA-DU-A7T6-01A-11D-A33T-08 chr19:54963362 G>A maps to ENST00000431846 Q44Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YL-01A-11D-A34A-08 chr19:54974076 C>A maps to NM_198988.1 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CF-01A-11D-A36O-08 chr19:54974124 C>T maps to NM_198988.1 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:52242104 G>A maps to NM_138792.2 S566S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8110-01A-11D-2395-08 chr7:127892091 C>T maps to NM_000230.2 C7C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr4:1824792 C>T maps to NM_012318.2 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr8:38250440 C>T maps to ENST00000379957 D143D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr8:38261999 G>A maps to ENST00000379957 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:51447580 G>A maps to ENST00000448283 K150K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RP-01A-21D-A34A-08 chr19:40095887 C>T maps to NM_013268.2 R55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EU-01A-11D-A27K-08 chr22:37966743 T>C did not map to a codon.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr17:76967756 C>T maps to NM_005567.3 S553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr19:39299581 G>A maps to NM_006149.3 F47F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U6-01A-12D-A33T-08 chr19:39299488 C>T maps to NM_006149.3 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:236702295 A>G maps to NM_201545.1 E84E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A858-01A-11D-A36O-08 chr1:236700804 G>A maps to NM_201545.1 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5847-01A-11D-1705-08 chr17:18396172 G>A maps to NM_001040078.2 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:25013963 G>A maps to NM_018176.3 N271N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:22011707 G>A maps to NM_139278.2 D123D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CV-01A-11D-A31L-08 chr8:22006353 G>A maps to NM_139278.2 D322D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7301-01A-11D-2086-08 chr12:71978153 C>G maps to NM_003667.2 S788S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:202245466 G>A maps to NM_001017403.1 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65R-01A-21D-A31L-08 chr1:202288164 C>T maps to NM_001017403.1 L912L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:63990678 G>T maps to NM_016571.2 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:48936112 G>A maps to NM_000233.3 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:111914519 G>T did not map to a codon.
Sequencing variant TCGA-FG-A6IZ-01A-11D-A31L-08 chr23:111914412 C>T did not map to a codon.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr23:111914406 G>C did not map to a codon.
Sequencing variant TCGA-IK-8125-01A-11D-2253-08 chr23:111914413 G>A did not map to a codon.
Sequencing variant TCGA-S9-A6TS-01A-12D-A33T-08 chr23:111914413 G>A did not map to a codon.
Sequencing variant TCGA-E1-A7Z2-01A-21D-A34J-08 chr17:35300250 G>A maps to NM_005568.3 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A6S2-01A-21D-A32B-08 chr9:126777628 C>T maps to NM_004789.3 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:75622579 G>A maps to NM_001001933.1 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr13:108861246 T>C maps to NM_001098268.1 E790E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8182-01A-11D-2253-08 chr19:55112236 C>T maps to NM_006863.1 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr19:55086780 G>A maps to NM_001130917.1 E238E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr19:54849685 G>A maps to NM_012276.3 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IS-01A-11D-A34A-08 chr19:54849447 G>A maps to NM_012276.3 N138N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:54742903 G>T maps to NM_024318.2 V457V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr19:54746594 C>T maps to ENST00000407860 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YS-01A-11D-A34A-08 chr19:55147059 G>A maps to ENST00000427581 R600R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8011-01A-11D-2395-08 chr19:54778557 G>A maps to ENST00000391747 Y608Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8011-01A-11D-2395-08 chr19:54780126 C>A maps to ENST00000391747 E546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5871-01A-12D-1705-08 chr19:55178178 C>T maps to ENST00000391733 D341D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A83Z-01A-11D-A36O-08 chr19:54758865 C>T maps to NM_001081442.1 Q329Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7637-01A-11D-2086-08 chr12:50598435 G>A maps to NM_001113546.1 R255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5322-01A-01D-1468-08 chr4:41646514 A>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:45714234 C>A maps to NM_014240.2 I565I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:45636937 G>A maps to NM_014240.2 K189K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:61776414 G>A maps to NM_030576.3 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:31654372 C>T maps to NM_001031801.1 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EZ-01A-11D-A27K-08 chr22:31663037 G>A maps to NM_001031801.1 Q349Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4943-01A-01D-1468-08 chr2:128399629 G>A maps to NM_017980.4 H242H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr1:26751933 G>A maps to NM_024674.4 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:83891527 T>C maps to NM_194282.2 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:77906436 T>C maps to NM_032808.5 A604A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:77906904 G>A maps to NM_032808.5 A448A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:27949355 C>T maps to NM_152570.1 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6405-01A-11D-1705-08 chr1:151774673 T>C maps to NM_001004432.2 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:90984985 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:42906779 G>A maps to NM_005357.2 S982S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7601-01A-11D-2086-08 chr19:42930578 A>T maps to NM_005357.2 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr19:42912408 G>A maps to NM_005357.2 H495H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:185251377 T>C maps to NM_139248.2 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:185236960 G>A maps to NM_139248.2 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:96443186 G>A maps to NM_153234.4 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:18140193 C>T maps to NM_004140.3 Q518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7601-01A-11D-2086-08 chr17:73567817 G>A maps to NM_001031803.1 V749V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CD-01A-11D-A36O-08 chr17:73566102 C>T maps to NM_001031803.1 A547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:156555832 A>G maps to ENST00000354505 C196C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RV-01A-21D-A34A-08 chr5:36141228 C>T maps to NM_001007527.1 W116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:8590438 C>T maps to NM_014583.2 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6407-01A-13D-1705-08 chr3:8590438 C>T maps to NM_014583.2 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:921308 G>A maps to ENST00000262301 F310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:50943311 G>A maps to NM_033200.2 Y452Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr3:197707306 C>T maps to NM_001136049.2 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A86X-01A-11D-A36O-08 chr1:156105906 G>A maps to NM_170707.2 E384E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:76427473 G>A maps to ENST00000357063 P1467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:76287326 G>T maps to NM_005358.5 E79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5854-01A-11D-1705-08 chr9:129453249 C>T maps to NM_001174147.1 D154D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:19257607 C>A maps to ENST00000410050 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6J1-01A-11D-A31L-08 chr19:19260142 G>A maps to ENST00000410050 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:5700880 G>A maps to NM_004793.2 N475N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:118147044 T>G did not map to a codon.
Sequencing variant TCGA-P5-A5EW-01A-11D-A27K-08 chr23:118123489 C>A did not map to a codon.
Sequencing variant TCGA-QH-A6X8-01A-12D-A32B-08 chr23:118151571 C>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:23177528 G>A maps to NM_002318.2 R447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8186-01A-11D-2253-08 chr10:100012143 G>A maps to NM_032211.6 A639A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8109-01A-11D-2395-08 chr10:100013488 C>T maps to NM_032211.6 P552P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A75K-01A-11D-A32B-08 chr6:161026076 C>T did not map to a codon.
Sequencing variant TCGA-DU-5854-01A-11D-1705-08 chr6:161006127 C>T maps to NM_005577.2 S1413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:160999635 G>A maps to NM_005577.2 R1464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr6:161027641 A>G maps to NM_005577.2 P884P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:85331179 C>T maps to NM_012152.2 R208R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UR-01A-11D-A33T-08 chr23:78011461 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:78010458 C>T did not map to a codon.
Sequencing variant TCGA-DU-6401-01A-11D-1705-08 chr23:78010567 A>G did not map to a codon.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr19:14271031 G>A maps to NM_001008701.2 D569D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RS-01A-12D-A33T-08 chr19:14266956 C>A maps to NM_001008701.2 V1035V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5140-01A-01D-1468-08 chr1:82456735 T>C maps to ENST00000370717 N1444N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:82451004 A>G maps to ENST00000370717 S1169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:82417648 C>T maps to ENST00000370717 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr1:82372828 G>A maps to ENST00000370717 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IZ-01A-11D-A34A-08 chr1:82456564 T>C maps to ENST00000370717 Y1387Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:62758587 C>T maps to ENST00000506720 S565S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:2921601 G>A maps to NM_014646.2 L791L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:2940710 C>A did not map to a codon.
Sequencing variant TCGA-DU-A7TJ-01A-11D-A34J-08 chr18:2951270 T>C maps to NM_014646.2 K124K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr1:99753519 G>C did not map to a codon.
Sequencing variant TCGA-S9-A6WQ-01A-12D-A34A-08 chr1:99753612 C>T maps to NM_014839.4 D105D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CS-01A-11D-A31L-08 chr1:99380374 T>C maps to NM_001037317.1 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:155670275 G>A maps to NM_004744.3 W227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:151791758 C>A did not map to a codon.
Sequencing variant TCGA-TQ-A7RQ-01A-11D-A33T-08 chr4:151792589 G>A maps to NM_006726.3 V758V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:47262040 C>T maps to NM_001164211.1 Q293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A87N-01A-11D-A36O-08 chr13:47266678 C>T maps to NM_001164211.1 D341D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6396-01A-11D-1705-08 chr19:39798914 G>C maps to NM_020862.1 R558R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:40400645 G>A maps to NM_020737.1 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:66625625 G>T maps to NM_024036.4 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:42356640 C>T maps to NM_152447.3 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:133881835 C>T maps to NM_144648.1 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:66465423 C>T maps to NM_015541.2 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:66502058 T>C did not map to a codon.
Sequencing variant TCGA-WY-A85D-01A-11D-A36O-08 chr1:113657235 C>T maps to NM_014813.1 A756A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5319-01A-01D-1893-08 chr12:59272813 A>C maps to NM_153377.3 A625A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5322-01A-01D-1468-08 chr12:59271320 C>T maps to NM_153377.3 S799S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8182-01A-11D-2253-08 chr12:59276786 G>A maps to NM_153377.3 C448C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A83X-01A-11D-A36O-08 chr12:59274456 G>A maps to NM_153377.3 R569R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RB-01A-11D-A289-08 chr10:86001153 C>T maps to NM_015613.2 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:57599407 C>A maps to NM_002332.2 L3846L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:57532251 T>G maps to NM_002332.2 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:57574961 C>T maps to NM_002332.2 C1850C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:57599398 C>T maps to NM_002332.2 G3843G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84I-01A-11D-A36O-08 chr12:57552233 C>T maps to NM_002332.2 I537I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RM-01A-11D-A33T-08 chr12:57575036 C>T maps to NM_002332.2 A1875A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:141072546 G>A maps to NM_018557.2 S4254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:141072506 G>A maps to NM_018557.2 L4268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:142004837 G>A maps to NM_018557.2 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:141298622 A>G maps to NM_018557.2 L2478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:141232863 G>A maps to NM_018557.2 G3156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7299-01A-21D-2024-08 chr2:141128327 A>G maps to NM_018557.2 D3653D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8191-01A-11D-2253-08 chr2:141607788 G>A maps to NM_018557.2 D1607D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:141816538 G>A maps to NM_018557.2 R441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TU-01A-12D-A32B-08 chr2:141986793 A>G maps to NM_018557.2 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6666-01A-11D-1893-08 chr2:170048451 G>A maps to NM_004525.2 G2974G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XG-01A-11D-A27K-08 chr2:170112637 C>T maps to NM_004525.2 P916P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:170177287 G>A maps to NM_004525.2 C62C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:170012829 G>T maps to NM_004525.2 G4035G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:170013929 G>T maps to NM_004525.2 S3990S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YK-01A-11D-A34A-08 chr2:170068529 A>G maps to NM_004525.2 F2076F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YN-01A-11D-A34A-08 chr2:170050322 G>A maps to NM_004525.2 D2926D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7684-01A-11D-2253-08 chr2:170038747 C>T maps to NM_004525.2 Q3309Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:170060606 G>A maps to NM_004525.2 T2630T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A72U-01A-31D-A32B-08 chr2:170038124 G>T maps to NM_004525.2 Y3334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A77X-01A-11D-A32B-08 chr2:170027172 G>A maps to NM_004525.2 P3756P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84I-01A-11D-A36O-08 chr2:170101386 T>C maps to NM_004525.2 A1082A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QY-01A-11D-A34A-08 chr4:186295494 G>A maps to ENST00000362004 R153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:46921052 G>A maps to ENST00000256991 D189D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:46920467 G>A maps to ENST00000256991 D266D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7470-01A-12D-2086-08 chr11:46893135 G>A maps to ENST00000256991 L1589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:25750680 G>A maps to NM_001135772.1 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TC-01A-21D-A34J-08 chr12:12291283 T>C maps to NM_002336.2 V1194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U9-01A-11D-A32B-08 chr1:53736989 G>A maps to NM_004631.3 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:53762157 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:25280062 G>T maps to NM_017640.5 E14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RJ-01A-11D-A33T-08 chr6:25610404 G>A maps to NM_017640.5 Q1325Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:24528896 T>C maps to NM_138360.3 N608N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:26995812 A>G maps to NM_022901.2 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:18502921 C>A maps to NM_145256.2 E265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7471-01A-11D-2253-08 chr21:45876869 C>T maps to NM_030891.3 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:169574502 C>T maps to NM_024727.2 G215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:169574163 T>C maps to NM_024727.2 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7304-01A-12D-2086-08 chr3:169572754 C>T maps to NM_024727.2 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8105-01A-11D-2395-08 chr3:169558000 G>A maps to NM_024727.2 N476N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5281-01A-01D-1468-08 chr11:76371898 G>C maps to NM_001128922.1 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EW-01A-11D-A27K-08 chr11:76371009 G>A maps to NM_001128922.1 L543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VW-A8FI-01A-11D-A36O-08 chr3:196387650 C>T maps to NM_198565.1 T379T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:169525278 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:67401010 G>A maps to NM_018296.5 K282K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YO-01A-11D-A34A-08 chr17:62892256 G>A maps to NM_199340.2 V373V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:100620646 G>A maps to NM_144620.2 Q258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RM-01A-11D-A33T-08 chr1:100621828 G>A maps to NM_144620.2 N186N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66F-01A-11D-A29Q-08 chr7:127670471 G>A maps to NM_022143.4 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7477-01B-11D-A289-08 chr7:127668929 G>C maps to NM_022143.4 S588S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CU-01A-11D-A31L-08 chr1:46752045 G>A maps to ENST00000254454 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8108-01A-11D-2395-08 chr12:122684843 G>A maps to NM_001098519.1 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IQ-01A-21D-A34A-08 chr12:122674760 C>T maps to NM_001098519.1 H249H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A710-01A-12D-A33T-08 chr17:79988539 T>C maps to NM_144999.2 S624S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:3703679 G>A maps to NM_020710.2 G270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:71188216 G>A maps to NM_017691.3 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:51021412 G>A maps to NM_001080457.1 D519D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:40135960 G>A maps to NM_020929.1 R628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8189-01B-11D-A289-08 chr11:40137056 G>C maps to NM_020929.1 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:84188401 C>A maps to NM_178452.4 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85C-01A-11D-A36O-08 chr1:165532815 C>T maps to NM_001005214.3 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:56949378 C>T maps to NM_001005210.2 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:550079 C>T maps to NM_198075.3 Y144Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:554167 C>T maps to NM_198075.3 R507R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr1:70504173 G>A maps to NM_020794.2 P851P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YE-01A-11D-A34A-08 chr1:70509662 T>G maps to NM_020794.2 V1294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6400-01A-12D-1705-08 chr1:90048482 C>T maps to NM_015350.2 R92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7606-01A-11D-2086-08 chr1:90400075 C>T maps to NM_001134479.1 P483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6396-01A-11D-1705-08 chr19:7960544 G>T maps to NM_025061.3 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:86044045 C>A maps to NM_033402.4 A606A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WM-01A-12D-A33T-08 chr3:37107433 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:85450907 C>A maps to NM_001079910.1 P779P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:85546113 A>G maps to NM_001079910.1 T1462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:85450484 A>G maps to NM_001079910.1 K638K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:85638664 C>T maps to NM_001079910.1 H1705H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8563-01A-11D-2395-08 chr12:85518291 A>G maps to NM_001079910.1 E1334E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RK-01A-11D-A33T-08 chr12:85623367 C>T maps to NM_001079910.1 Y1632Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr1:74507114 T>C maps to NM_001105659.1 R500R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:169540251 C>T maps to NM_001080460.1 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:169540228 C>T maps to NM_001080460.1 R174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7T6-01A-11D-A33T-08 chr3:169540296 C>T maps to NM_001080460.1 D196D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr3:169540470 C>T maps to NM_001080460.1 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:101528953 C>T maps to NM_024652.3 Y183Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7606-01A-11D-2086-08 chr15:101588787 A>G maps to NM_024652.3 T1075T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A840-01A-11D-A36O-08 chr15:101528896 G>A maps to NM_024652.3 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84G-01A-11D-A36O-08 chr15:101589863 C>T maps to NM_024652.3 D1105D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:40722195 C>A maps to NM_198578.3 A1897A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:40688679 C>T maps to NM_198578.3 R948*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:3888473 T>C maps to NM_020873.5 *717Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:3887497 C>T maps to NM_020873.5 F391F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:3888445 C>T maps to NM_020873.5 V707V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:6022759 G>T maps to NM_152611.3 C377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:6022180 G>A maps to NM_152611.3 C570C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:6031519 C>T maps to NM_152611.3 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7J3-01A-21D-A34J-08 chr11:62455806 C>T maps to NM_203422.2 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr2:77746148 C>T maps to NM_001134745.1 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:130259536 C>T maps to NM_001005374.2 G612G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:115561377 G>A maps to NM_002338.3 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:42113578 G>C maps to ENST00000411445 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:34710692 A>G maps to NM_001114093.1 G349G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:47626622 C>T maps to NM_002340.5 G509G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5142-01A-01D-1468-08 chr12:21205041 A>C maps to ENST00000381541 V422V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6666-01A-11D-1893-08 chr6:31541358 C>T maps to NM_000595.2 H169H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R8-01A-11D-A34J-08 chr14:24785429 G>T maps to NM_181657.3 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:33623536 G>A maps to ENST00000354476 V1698V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YO-01A-11D-A34A-08 chr2:33477780 T>C maps to ENST00000354476 C679C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R2-01A-21D-A34J-08 chr2:33412099 C>G maps to ENST00000354476 S460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr14:74969479 G>A maps to NM_000428.2 P1682P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:65319441 C>T did not map to a codon.
Sequencing variant TCGA-FG-A713-01A-11D-A32B-08 chr11:65320905 G>A maps to NM_001130144.2 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:41120227 C>T maps to ENST00000308370 D963D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7694-01A-11D-2253-08 chr19:41125345 G>T maps to ENST00000308370 P1121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YO-01A-11D-A34A-08 chr15:41801322 G>A maps to NM_002344.5 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7884-01B-11D-2395-08 chr15:41796599 G>A maps to NM_002344.5 H762H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr6:144171326 A>C maps to NM_032860.3 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74H-01A-11D-A32B-08 chr6:144167302 C>A maps to NM_032860.3 S84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84M-01A-11D-A36O-08 chr7:139083361 A>G maps to NM_016019.2 E58E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:23420598 A>G maps to NM_001142546.1 I52I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RC-01A-11D-A289-08 chr1:23418834 C>T maps to NM_001142546.1 P640P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8158-01A-11D-2253-08 chr23:114541267 G>A did not map to a codon.
Sequencing variant TCGA-TQ-A7RO-01A-11D-A33T-08 chr23:114541284 T>G did not map to a codon.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr6:31644772 G>A maps to NM_025262.3 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5851-01A-13D-1893-08 chr1:160783601 C>T maps to ENST00000263285 R211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7684-01A-11D-2253-08 chr19:42341279 T>G maps to NM_173506.4 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:54963655 C>T maps to ENST00000419058 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:235973132 G>A maps to NM_000081.2 R329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:235972443 C>T maps to NM_000081.2 L558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:235827838 G>A maps to NM_000081.2 S3707S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:235929517 T>C maps to NM_000081.2 K1994K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:235969486 C>T maps to NM_000081.2 R983R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:45870073 C>A maps to NM_020347.2 E212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A72U-01A-31D-A32B-08 chr22:21349016 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:20110343 G>A maps to NM_021020.2 Y366Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:20110544 C>T maps to NM_021020.2 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:151504912 C>T maps to NM_006439.4 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr7:20198441 G>T maps to NM_182762.3 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:39835839 G>A maps to ENST00000361689 K2297K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:39763311 G>A maps to ENST00000361689 E797E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8162-01A-21D-2253-08 chr1:39900288 A>G maps to ENST00000361689 Q3861Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:15948228 C>T maps to ENST00000310348 G313G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TW-01A-12D-A32B-08 chr7:2255587 G>A maps to NM_003550.2 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A858-01A-11D-A36O-08 chr19:498502 G>A maps to NM_130760.2 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A72U-01A-31D-A32B-08 chr11:47311779 C>T maps to NM_003682.3 H1028H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:1316185 G>A maps to ENST00000505177 E158E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:1332392 C>T maps to ENST00000505177 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:166958630 C>T maps to NM_032858.1 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr19:35802841 C>T maps to NM_002361.3 P546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74H-01A-11D-A32B-08 chr23:151303922 G>A did not map to a codon.
Sequencing variant TCGA-TM-A7C3-01A-11D-A32B-08 chr23:151304072 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:148798333 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:148797685 C>A did not map to a codon.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr23:148798318 C>T did not map to a codon.
Sequencing variant TCGA-S9-A6TZ-01A-21D-A32B-08 chr23:148797889 G>C did not map to a codon.
Sequencing variant TCGA-DB-A4XE-01A-11D-A27K-08 chr23:151900224 G>T did not map to a codon.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr23:151900376 T>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:151935889 C>A did not map to a codon.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr23:151935720 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:151092393 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:151092965 G>T did not map to a codon.
Sequencing variant TCGA-RY-A83Z-01A-11D-A36O-08 chr23:151092298 C>T did not map to a codon.
Sequencing variant TCGA-RY-A83Z-01A-11D-A36O-08 chr23:151092271 C>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:151870015 G>T did not map to a codon.
Sequencing variant TCGA-DU-6405-01A-11D-1705-08 chr23:151870193 G>A did not map to a codon.
Sequencing variant TCGA-P5-A5F2-01A-11D-A289-08 chr23:151870085 G>A did not map to a codon.
Sequencing variant TCGA-R8-A6MO-01A-11D-A33T-08 chr23:151870086 G>T did not map to a codon.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr23:149013641 C>A did not map to a codon.
Sequencing variant TCGA-QH-A6X8-01A-12D-A32B-08 chr23:149013733 G>C did not map to a codon.
Sequencing variant TCGA-WY-A858-01A-11D-A36O-08 chr23:149013817 T>A did not map to a codon.
Sequencing variant TCGA-P5-A5EX-01A-12D-A289-08 chr23:30269582 C>T did not map to a codon.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr23:27840124 C>T did not map to a codon.
Sequencing variant TCGA-CS-6186-01A-12D-2024-08 chr23:35820490 A>T did not map to a codon.
Sequencing variant TCGA-DU-A5TT-01A-11D-A289-08 chr23:35820626 C>T did not map to a codon.
Sequencing variant TCGA-HT-8011-01A-11D-2395-08 chr23:35821246 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:26158033 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:30237281 C>A did not map to a codon.
Sequencing variant TCGA-E1-5318-01A-01D-1468-08 chr23:30237370 A>T did not map to a codon.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr23:30237646 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:30254596 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:30255065 G>A did not map to a codon.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr23:30260294 C>T did not map to a codon.
Sequencing variant TCGA-P5-A72U-01A-31D-A32B-08 chr23:30261032 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:26213142 G>A did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr23:26212349 C>T did not map to a codon.
Sequencing variant TCGA-QH-A6X8-01A-12D-A32B-08 chr23:26212015 C>T did not map to a codon.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr23:26212565 G>A did not map to a codon.
Sequencing variant TCGA-TM-A84G-01A-11D-A36O-08 chr23:26212855 A>T did not map to a codon.
Sequencing variant TCGA-VW-A8FI-01A-11D-A36O-08 chr23:26212101 G>A did not map to a codon.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr23:140996035 T>C did not map to a codon.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr23:140995928 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:140994995 G>T did not map to a codon.
Sequencing variant TCGA-DU-6401-01A-11D-1705-08 chr23:140995654 C>T did not map to a codon.
Sequencing variant TCGA-DU-7006-01A-11D-2024-08 chr23:140996472 G>A did not map to a codon.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr23:140994959 G>A did not map to a codon.
Sequencing variant TCGA-HT-7874-01A-11D-2395-08 chr23:140994427 C>A did not map to a codon.
Sequencing variant TCGA-HT-8563-01A-11D-2395-08 chr23:140995061 T>C did not map to a codon.
Sequencing variant TCGA-QH-A6X9-01A-12D-A32B-08 chr23:140993966 T>A did not map to a codon.
Sequencing variant TCGA-TQ-A7RJ-01A-11D-A33T-08 chr23:140995746 A>G did not map to a codon.
Sequencing variant TCGA-TQ-A8XE-01A-11D-A36O-08 chr23:140994959 G>A did not map to a codon.
Sequencing variant TCGA-WY-A858-01A-11D-A36O-08 chr23:140996486 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:141291665 C>A did not map to a codon.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr23:141290651 T>A did not map to a codon.
Sequencing variant TCGA-FG-A4MY-01A-11D-A26M-08 chr23:141291733 T>C did not map to a codon.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr23:140969495 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:140969285 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:140984680 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:140983166 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:51640311 G>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:51641415 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:51640975 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:75648781 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:75651069 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:75649429 G>A did not map to a codon.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr23:75649857 T>C did not map to a codon.
Sequencing variant TCGA-DU-A7T6-01A-11D-A33T-08 chr23:75651162 G>T did not map to a codon.
Sequencing variant TCGA-HT-A74H-01A-11D-A32B-08 chr23:75649649 G>A did not map to a codon.
Sequencing variant TCGA-S9-A6WM-01A-12D-A33T-08 chr23:75648838 G>A did not map to a codon.
Sequencing variant TCGA-WY-A858-01A-11D-A36O-08 chr23:75649950 T>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:75003401 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:75004710 G>T did not map to a codon.
Sequencing variant TCGA-DU-7294-01A-11D-2024-08 chr23:75004653 C>T did not map to a codon.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr23:75003754 A>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:55478844 C>T did not map to a codon.
Sequencing variant TCGA-DB-5275-01A-01D-1468-08 chr15:23890477 A>G maps to NM_019066.4 F804F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IX-01A-12D-A34A-08 chr3:65342559 G>A maps to NM_001033057.1 C1294C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7294-01A-11D-2024-08 chr7:77998516 G>C maps to NM_012301.3 G353G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5396-01A-02D-1468-08 chr1:114225639 A>G maps to NM_001142782.1 E1150E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:114196467 C>T maps to NM_001142782.1 D819D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U6-01A-12D-A33T-08 chr1:114215353 G>A maps to NM_001142782.1 R1012R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5319-01A-01D-1893-08 chr23:49022445 G>A did not map to a codon.
Sequencing variant TCGA-S9-A6TS-01A-12D-A33T-08 chr1:53692716 C>T maps to NM_002370.2 *147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CU-01A-11D-A31L-08 chr12:10763279 C>A did not map to a codon.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr8:33356081 C>A maps to NM_032509.3 R280R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A730-01A-11D-A32B-08 chr8:33346580 C>T maps to NM_032509.3 R106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QX-01A-11D-A34A-08 chr8:120233831 C>T maps to ENST00000276681 F46F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:56376781 A>G maps to NM_006785.2 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6186-01A-12D-2024-08 chr9:72724720 G>A did not map to a codon.
Sequencing variant TCGA-DB-5281-01A-01D-1468-08 chr11:95826018 G>A maps to NM_032427.1 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:140810708 G>T maps to ENST00000509479 P627P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:140641268 G>A maps to ENST00000509479 S875S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A6S3-01A-12D-A32B-08 chr4:140811116 C>T maps to ENST00000509479 Q491Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A83X-01A-11D-A36O-08 chr4:140811107 C>T maps to ENST00000509479 Q494Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:149671606 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:149639225 G>A did not map to a codon.
Sequencing variant TCGA-HT-7680-01A-11D-2253-08 chr23:149639634 A>T did not map to a codon.
Sequencing variant TCGA-HT-7877-01A-11D-2395-08 chr23:149638920 C>G did not map to a codon.
Sequencing variant TCGA-HT-8013-01A-11D-2395-08 chr23:149638128 T>A did not map to a codon.
Sequencing variant TCGA-HT-A5R9-01A-11D-A289-08 chr23:149639634 A>T did not map to a codon.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr23:149638771 G>A did not map to a codon.
Sequencing variant TCGA-P5-A780-01A-12D-A32B-08 chr23:149639253 A>G did not map to a codon.
Sequencing variant TCGA-RY-A83Y-01A-11D-A36O-08 chr6:119510997 G>A maps to NM_005907.2 I459I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:117945000 G>T maps to NM_006699.3 G166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8106-01A-11D-2395-08 chr9:139996093 C>T maps to NM_016219.3 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:12760166 C>T maps to NM_000528.3 R781R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:12762981 C>T maps to NM_000528.3 Q677Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr19:12768301 G>A maps to NM_000528.3 N459N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:6596379 C>T maps to NM_015274.1 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:6610848 G>A maps to NM_015274.1 T610T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:6595013 C>A maps to NM_015274.1 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YW-01A-11D-A34J-08 chr4:6578363 C>T maps to NM_015274.1 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7881-01A-11D-2395-08 chr4:6599986 G>A maps to NM_015274.1 T437T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7490-01A-11D-2024-08 chr4:6612959 C>T maps to NM_015274.1 L840L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5143-01A-01D-1468-08 chr12:12483293 C>T maps to NM_018050.2 P321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:43542815 A>C did not map to a codon.
Sequencing variant TCGA-E1-A7YV-01A-11D-A34J-08 chr23:43590512 G>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:43820240 C>A maps to ENST00000382031 P2428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7C5-01A-11D-A32B-08 chr15:43819304 G>A maps to ENST00000382031 W2116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:71491725 C>T maps to NM_005909.3 V848V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:71482481 C>T maps to NM_005909.3 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:71492952 G>A maps to NM_005909.3 P1257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74O-01A-11D-A32B-08 chr2:172945091 G>A maps to NM_199227.1 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:33147674 C>T maps to NM_181509.1 Y117Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MX-01A-11D-A26M-08 chr19:17845206 C>T maps to NM_018174.4 D1050D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7011-01A-11D-2024-08 chr2:210560052 T>C maps to NM_002374.3 F1053F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:4110572 C>T maps to NM_030662.3 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:67537833 C>A maps to NM_002758.3 T315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CB-01A-11D-A36O-08 chr17:67501927 G>A maps to NM_002758.3 K8K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TY-01A-12D-A32B-08 chr19:7975887 G>A maps to ENST00000425613 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:40715067 C>T maps to NM_002446.3 S498S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:53878922 G>T maps to NM_001193511.1 I352I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-8125-01A-11D-2253-08 chr12:53877508 T>A did not map to a codon.
Sequencing variant TCGA-DU-7008-01A-11D-2024-08 chr3:185161415 A>G maps to NM_004721.3 K281K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:43343969 G>A maps to ENST00000344686 R837*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:19389623 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:19389496 T>C did not map to a codon.
Sequencing variant TCGA-RY-A83Z-01A-11D-A36O-08 chr23:19378945 C>A did not map to a codon.
Sequencing variant TCGA-S9-A6WL-01A-21D-A33T-08 chr23:19443788 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:128072387 C>T maps to NM_006609.3 Q466Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr17:61765934 C>T maps to NM_203351.1 D284D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:161508877 G>A maps to NM_005922.2 K905K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A83Z-01A-11D-A36O-08 chr6:161469729 G>A maps to NM_005922.2 Q142Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CE-01A-11D-A36O-08 chr6:161530824 G>A maps to NM_005922.2 G1425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84O-01A-11D-A36O-08 chr6:136882673 G>A maps to NM_005923.3 S1328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:91263200 G>T maps to NM_145331.1 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:30747035 C>T maps to NM_005204.2 I299I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:39108526 G>A maps to NM_001042600.1 V3V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:39499677 G>A maps to NM_003618.2 F600F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R7-01A-11D-A34J-08 chr11:75298871 A>T maps to NM_033063.1 S558S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8114-01A-11D-2395-08 chr6:136682202 C>T maps to NM_001198609.1 Q577Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KK-01A-11D-A27K-08 chr6:136710580 T>A maps to NM_001198609.1 K129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A736-01A-11D-A32B-08 chr6:136686876 G>A maps to NM_001198609.1 G453G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5397-01A-01D-1893-08 chr23:20044026 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:20034271 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:20060731 G>A did not map to a codon.
Sequencing variant TCGA-TM-A7C3-01A-11D-A32B-08 chr23:20033362 T>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:135303000 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:135314089 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:135326875 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:135314192 T>C did not map to a codon.
Sequencing variant TCGA-DU-8162-01A-21D-2253-08 chr23:135313711 G>A did not map to a codon.
Sequencing variant TCGA-E1-5322-01A-01D-1468-08 chr23:135323364 T>A did not map to a codon.
Sequencing variant TCGA-E1-A7YE-01A-11D-A34A-08 chr23:135310867 T>C did not map to a codon.
Sequencing variant TCGA-FG-A70Y-01A-12D-A34J-08 chr23:135312999 A>G did not map to a codon.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr23:135313708 A>G did not map to a codon.
Sequencing variant TCGA-TM-A84G-01A-11D-A36O-08 chr23:135312699 G>A did not map to a codon.
Sequencing variant TCGA-TM-A84B-01A-11D-A36O-08 chr22:50705841 C>T maps to NM_002751.5 E125E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:36103601 C>T maps to NM_002754.3 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R8-01A-11D-A34J-08 chr8:144802970 T>G maps to NM_139021.2 L293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:30128549 G>A maps to NM_002746.2 R278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7854-01A-11D-2253-08 chr16:30134371 G>A maps to NM_002746.2 Y53Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:19283923 C>T maps to NM_139034.2 Y134Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:45926109 C>T maps to NM_005456.2 Q591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:128305419 A>G maps to NM_001006617.1 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R9-01A-11D-A289-08 chr1:206904036 A>C maps to NM_032960.2 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:50677822 G>A maps to NM_004635.3 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:42113211 A>G maps to NM_001128608.1 P894P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A83Y-01A-11D-A36O-08 chr15:42107937 G>A maps to NM_001128608.1 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6408-01A-11D-1705-08 chr17:44068857 G>A maps to NM_001123066.3 P471P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7487-01A-11D-2024-08 chr4:164450154 G>C maps to ENST00000514618 A461A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:60879032 G>A maps to NM_152598.2 Q22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:60813929 G>T maps to NM_152598.2 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7690-01A-11D-2253-08 chr17:60879009 A>G maps to NM_152598.2 Y29Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U9-01A-11D-A32B-08 chr17:60802386 G>A maps to NM_152598.2 P672P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:94109578 A>G maps to NM_017824.4 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:10387154 G>A maps to NM_005885.2 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr12:58152526 G>A maps to NM_138396.4 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr1:220831177 T>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:220804429 G>A maps to NM_018650.3 K321K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5319-01A-01D-1893-08 chr1:220791710 T>C maps to NM_018650.3 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6410-01A-11D-1893-08 chr11:63667347 A>G maps to NM_001039469.2 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YI-01A-11D-A34A-08 chr14:103915253 A>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:45781871 T>C maps to NM_031417.3 I335I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:68728779 C>T maps to NM_001038603.2 R455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:68715760 C>A maps to NM_001038603.2 Y183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6668-01A-11D-1893-08 chr16:71668567 C>T maps to NM_052858.3 F356F. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DU-6392-01A-11D-1705-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-HT-8564-01A-11D-2395-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-QH-A65X-01A-11D-A32B-08 chr16:71668159 C>A maps to NM_052858.3 Y220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7641-01B-11D-2253-08 chr6:29454623 G>A maps to NM_052967.1 I352I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:186943253 G>A maps to NM_001879.5 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:186953537 G>A maps to NM_139125.3 Y707Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:12963038 C>A maps to NM_014975.2 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7T8-01A-21D-A34J-08 chr19:12976206 T>C maps to NM_014975.2 A572A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RV-01A-21D-A34A-08 chr19:12969473 C>T maps to NM_014975.2 A429A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:46295223 C>T maps to NM_015112.2 Q147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7695-01A-11D-2253-08 chr1:46497239 C>A maps to NM_015112.2 S1057*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IX-01A-12D-A34A-08 chr1:46295174 G>A maps to NM_015112.2 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7856-01A-11D-2395-08 chr19:18248096 G>A maps to NM_015016.1 W645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:66430418 C>T maps to NM_001164664.1 D765D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5302-01A-01D-1468-08 chr5:66448609 G>A maps to NM_001164664.1 S1147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A89Z-01A-11D-A36O-08 chr5:66458524 A>G maps to NM_001164664.1 S1292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:27459939 G>A maps to NM_001172303.1 S684S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:3779616 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:3845044 C>A maps to NM_020746.3 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KJ-01A-12D-A27K-08 chr20:3841976 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:1578392 G>A maps to NM_003926.5 D274D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr12:57919680 G>A maps to NM_052897.3 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:131540344 G>A did not map to a codon.
Sequencing variant TCGA-DU-7309-01A-11D-2086-08 chr23:131524901 C>G did not map to a codon.
Sequencing variant TCGA-FG-A4MY-01A-11D-A26M-08 chr23:131520819 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:8998832 C>T maps to NM_138799.2 S513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66D-01A-11D-A31L-08 chr23:21886591 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:21900675 A>G did not map to a codon.
Sequencing variant TCGA-DU-A6S6-01A-21D-A32B-08 chr23:21871589 G>A did not map to a codon.
Sequencing variant TCGA-S9-A6U2-01A-21D-A33T-08 chr23:21896658 T>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:13884764 G>A maps to NM_000529.2 C251C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74H-01A-11D-A32B-08 chr18:13884770 G>T maps to NM_000529.2 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A6MK-01A-11D-A32B-08 chr18:13884743 G>A maps to NM_000529.2 F258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A75K-01A-11D-A32B-08 chr18:13826399 G>A maps to NM_005913.2 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74H-01A-11D-A32B-08 chr18:13826282 C>T maps to NM_005913.2 C173C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:103349435 G>A did not map to a codon.
Sequencing variant TCGA-DU-6403-01A-11D-1705-08 chr23:103349185 C>A did not map to a codon.
Sequencing variant TCGA-DU-7008-01A-11D-2024-08 chr23:103349503 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:43529483 C>T maps to NM_173467.4 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr22:43529108 G>A maps to NM_173467.4 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:112406885 G>T maps to NM_001085377.1 T610T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:112418618 G>A maps to NM_001085377.1 H574H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6397-01A-11D-1705-08 chr5:112439957 G>T maps to NM_001085377.1 S374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr3:182759529 T>C maps to NM_020166.3 A364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:70945894 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:31496808 C>A maps to NM_001011700.2 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:138670584 C>A did not map to a codon.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr23:138678851 T>C did not map to a codon.
Sequencing variant TCGA-DU-8166-01A-11D-2253-08 chr23:138689853 T>G did not map to a codon.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr23:138711937 T>A did not map to a codon.
Sequencing variant TCGA-TQ-A7RF-01A-11D-A33T-08 chr23:138697039 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:113743998 C>T maps to NM_001112732.1 Y1027Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:113729439 G>A maps to NM_001112732.1 A472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RW-01A-11D-A33T-08 chr13:113742082 C>T maps to NM_001112732.1 Y943Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:182910808 G>T maps to NM_015078.2 A998A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:41077580 C>A maps to NM_005297.3 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TT-01A-11D-A289-08 chr6:100390943 G>A maps to NM_032503.2 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:13228228 C>A maps to NM_182751.2 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:13214454 C>T maps to NM_182751.2 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:13246220 C>T maps to NM_182751.2 C786C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4943-01A-01D-1468-08 chr3:127337889 C>T maps to NM_004526.2 F678F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7006-01A-11D-2024-08 chr21:47700423 G>A maps to NM_003906.3 H503H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WP-01A-12D-A34A-08 chr21:47704303 G>A maps to NM_003906.3 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:48883348 C>A maps to NM_182746.1 C571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr22:35811940 C>T maps to NM_006739.3 V441V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TJ-01A-11D-A34J-08 chr2:136622581 C>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:99695276 G>A maps to NM_005916.3 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:99690593 C>T maps to NM_005916.3 W707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7J3-01A-21D-A34J-08 chr7:99697241 T>C maps to NM_005916.3 Q82Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:5974202 C>A maps to NM_032485.4 S764S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:5948474 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:119232881 G>A maps to ENST00000316316 F361F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:6312715 C>A maps to NM_024596.3 G626G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YQ-01A-11D-A34J-08 chr12:49959389 A>G maps to NM_001012300.1 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7469-01A-11D-2253-08 chr5:94248539 G>T maps to NM_024717.4 R498R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RO-01A-11D-A33T-08 chr5:94248549 G>A maps to NM_024717.4 Y494Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:94942269 G>A maps to NM_018349.3 E623E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr23:119739937 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:30680173 G>T maps to NM_014641.2 A515A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6689-01A-11D-1893-08 chr6:30679447 C>T maps to NM_014641.2 L708L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RF-01A-11D-A33T-08 chr6:30668316 C>A maps to NM_014641.2 L2065L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:41621129 C>T maps to NM_005586.3 C186C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:37620021 C>A maps to ENST00000297153 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr14:47311141 G>T maps to NM_001113498.2 R1024R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:47530557 G>A maps to NM_001113498.2 I473I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:69210695 C>T maps to NM_002392.3 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85C-01A-11D-A36O-08 chr12:69210668 A>C maps to NM_002392.3 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:90513144 G>A maps to NM_014611.1 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76L-01A-11D-A32B-08 chr6:90472239 C>T maps to NM_014611.1 P718P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:24683346 G>A maps to NM_138476.3 C138C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:83938601 C>A maps to NM_002395.4 E359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RW-01A-11D-A33T-08 chr6:84025054 G>A maps to NM_002395.4 D226D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:86158193 G>T maps to NM_001014811.1 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:168849256 G>A maps to NM_004991.3 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CW-01A-11D-A32B-08 chr3:168812873 C>T maps to NM_004991.3 G1003G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153296282 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153363098 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153296255 G>A did not map to a codon.
Sequencing variant TCGA-DU-7304-01A-12D-2086-08 chr23:153297773 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:37563933 G>A maps to NM_004774.3 R1514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:37566108 C>A maps to NM_004774.3 E789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7875-01A-11D-2395-08 chr17:37565971 T>A maps to NM_004774.3 P834P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66D-01A-11D-A31L-08 chr23:70357060 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:70347222 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:70349264 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:70354680 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:70349569 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:70344031 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:70352362 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:70339946 T>C did not map to a codon.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr23:70345936 C>A did not map to a codon.
Sequencing variant TCGA-DU-7290-01A-11D-2024-08 chr23:70351407 C>A did not map to a codon.
Sequencing variant TCGA-E1-A7YE-01A-11D-A34A-08 chr23:70339253 G>C did not map to a codon.
Sequencing variant TCGA-FG-A4MY-01A-11D-A26M-08 chr23:70341256 G>T did not map to a codon.
Sequencing variant TCGA-FG-A60K-01A-11D-A29Q-08 chr23:70346298 C>G did not map to a codon.
Sequencing variant TCGA-TM-A7C3-01A-11D-A32B-08 chr23:70352985 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:150877650 G>A maps to NM_053002.4 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65X-01A-11D-A32B-08 chr3:151129235 G>A maps to NM_053002.4 P1992P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:60060018 C>T maps to NM_005121.2 T1115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:60108946 G>A maps to NM_005121.2 D289D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RC-01A-11D-A289-08 chr17:60111220 C>T maps to NM_005121.2 K247K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:116675278 G>A maps to NM_015335.4 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:116403925 C>T maps to NM_015335.4 S2116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5394-01A-01D-1468-08 chr23:40572232 T>C did not map to a codon.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr23:40518770 T>C did not map to a codon.
Sequencing variant TCGA-HW-8321-01A-11D-2395-08 chr23:40534572 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:885907 G>A maps to NM_005481.2 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr6:131917228 A>G maps to ENST00000403834 Y957Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R7-01A-11D-A289-08 chr6:131913581 T>C maps to ENST00000403834 R1145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:38185089 C>A maps to NM_014815.3 R466R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:16688337 G>A maps to NM_004831.3 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr19:16687578 C>T maps to NM_004831.3 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:48653988 T>G maps to NM_014166.2 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:156565836 T>C maps to NM_004270.4 E202E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:17394697 C>T maps to NM_018019.2 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A73M-01A-11D-A32B-08 chr16:3293587 C>T maps to NM_000243.2 P633P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7CA-01A-21D-A33T-08 chr16:3293587 C>T maps to NM_000243.2 P633P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:126676322 G>A did not map to a codon.
Sequencing variant TCGA-VM-A8CH-01A-12D-A36O-08 chr15:66210373 G>A maps to NM_032445.2 N672N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:42866663 C>T maps to ENST00000251268 C1991C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:42840957 G>T did not map to a codon.
Sequencing variant TCGA-DU-7301-01A-11D-2086-08 chr19:42857650 G>A maps to ENST00000251268 R1195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WH-A86K-01A-11D-A36O-08 chr19:42873082 C>T maps to ENST00000251268 N2190N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:66664996 G>A maps to ENST00000407092 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TJ-01A-11D-A34J-08 chr15:37186972 C>T maps to NM_170677.2 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:47920150 G>A maps to NM_020160.1 D85D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:64575410 G>A maps to NM_130804.2 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R4-01A-12D-A34J-08 chr11:64571945 G>A maps to NM_130804.2 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr7:15652020 C>T maps to NM_005924.4 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:46806764 C>T maps to NM_005588.2 A711A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8164-01A-11D-2253-08 chr6:46801255 G>A maps to NM_005588.2 S530S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr6:46803178 C>T maps to NM_005588.2 G659G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:29793157 C>T maps to NM_005925.2 R405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:112686865 C>T maps to NM_006343.2 N77N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:116435788 T>C maps to NM_001127500.1 T1311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7482-01A-11D-2024-08 chr7:116381016 C>T maps to NM_001127500.1 R547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A61C-01A-11D-A29Q-08 chr7:116412044 T>A did not map to a codon.
Sequencing variant TCGA-TQ-A7RS-01A-12D-A33T-08 chr7:116414968 C>T maps to NM_001127500.1 C1039C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:95887832 C>T maps to NM_006838.3 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:2323635 G>A maps to NM_024086.3 G439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8158-01A-11D-2253-08 chr17:2324129 G>A maps to NM_024086.3 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:21463326 C>T maps to NM_001029991.1 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr14:21458173 C>T maps to NM_001029991.1 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QY-01A-11D-A34A-08 chr1:171765757 G>A maps to NM_015935.4 L654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:60504003 C>T maps to NM_181725.3 R183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:128119555 C>T maps to NM_018396.2 R183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr14:21971989 G>A maps to NM_019852.3 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:21968794 G>A maps to NM_019852.3 D382D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TR-01A-11D-A289-08 chr19:1556791 C>T maps to NM_001174118.1 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:17303390 C>A did not map to a codon.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr15:89453059 C>T maps to NM_005928.2 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:8748216 C>T maps to NM_004225.2 Q784Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:196751282 G>A maps to NM_005929.5 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr1:12071582 C>T maps to NM_014874.3 L745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8010-01A-11D-2395-08 chr22:37882151 G>A maps to NM_002405.3 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:40432322 C>A maps to NM_001136493.1 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:24239759 G>A maps to ENST00000338315 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UR-01A-11D-A33T-08 chr12:53647527 C>T maps to NM_001170790.1 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:8702264 G>A maps to NM_152599.3 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:41989148 G>A maps to ENST00000219905 G647G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WQ-01A-12D-A34A-08 chr15:41961362 C>T maps to ENST00000219905 R91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A89V-01A-11D-A36O-08 chr15:42019567 A>G maps to ENST00000219905 K1207K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:141727475 G>T maps to ENST00000475668 G388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr7:141708342 G>A maps to ENST00000475668 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:39884758 G>A maps to NM_001098270.1 Q469Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5142-01A-01D-1468-08 chr2:99279631 G>A maps to NM_012214.2 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84S-01A-11D-A36O-08 chr5:179228988 C>T maps to NM_054013.3 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A736-01A-11D-A32B-08 chr12:86373299 G>A maps to ENST00000393205 Q431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:88423596 G>A maps to NM_152706.2 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:88424199 A>T maps to NM_152706.2 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7637-01A-11D-2086-08 chr10:103577686 C>A maps to NM_012215.3 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:131506228 C>T maps to NM_002412.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:15035206 C>A maps to NM_001190839.1 E85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7604-01A-11D-2086-08 chr16:4732910 C>T maps to NM_015246.2 G482G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TT-01A-11D-A289-08 chr14:39722039 G>A maps to NM_054024.3 S552S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:222802499 C>T maps to NM_198551.2 D646D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8185-01A-11D-2253-08 chr1:222803483 C>G maps to NM_198551.2 V974V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr1:222835661 C>T maps to NM_198551.2 L1750L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:1560485 C>T maps to NM_080875.2 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:1563490 C>T maps to NM_080875.2 I706I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5302-01A-01D-1468-08 chr1:1563187 C>T maps to NM_080875.2 R668R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7Z4-01A-11D-A34J-08 chr6:31378927 C>T maps to NM_000247.1 Y135Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8019-01A-21D-2395-08 chr6:31378386 T>C maps to NM_000247.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WH-A86K-01A-11D-A36O-08 chr6:31379099 C>T maps to NM_000247.1 R193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:109775384 G>T maps to NM_022765.3 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:109769589 G>T maps to NM_022765.3 P557P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A6MO-01A-11D-A33T-08 chr6:109766000 C>T maps to NM_022765.3 T994T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A87Q-01A-11D-A36O-08 chr11:12281412 C>T maps to NM_014632.2 A1101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:18347659 G>A maps to NM_001136004.1 S994S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:18385395 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:18368816 C>A maps to NM_015241.2 E690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:18300808 G>A maps to NM_015241.2 Q1540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr22:18301253 C>T maps to NM_015241.2 L1391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:12316327 C>A maps to NM_032867.2 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8163-01A-11D-2253-08 chr11:12315445 A>G maps to NM_032867.2 K156K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr22:38323451 G>A maps to NM_033386.2 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr6:31473998 C>T maps to NM_005931.3 Y135Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A4DS-01A-11D-A26M-08 chr6:31473466 G>A maps to NM_005931.3 E48E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RG-01A-11D-A33T-08 chr6:31474145 G>A maps to NM_005931.3 Q184Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:10535404 A>G did not map to a codon.
Sequencing variant TCGA-HT-A5R9-01A-11D-A289-08 chr23:10417628 T>C did not map to a codon.
Sequencing variant TCGA-HT-A5RC-01A-11D-A289-08 chr23:10534971 C>T did not map to a codon.
Sequencing variant TCGA-P5-A780-01A-12D-A32B-08 chr23:10442674 C>G did not map to a codon.
Sequencing variant TCGA-QH-A65V-01A-11D-A29Q-08 chr23:38664317 A>T did not map to a codon.
Sequencing variant TCGA-WY-A859-01A-12D-A36O-08 chr23:38664285 C>G did not map to a codon.
Sequencing variant TCGA-DH-5143-01A-01D-1468-08 chr23:107084364 G>A did not map to a codon.
Sequencing variant TCGA-TM-A7C5-01A-11D-A32B-08 chr23:107084061 G>A did not map to a codon.
Sequencing variant TCGA-WH-A86K-01A-11D-A36O-08 chr23:107084268 C>G did not map to a codon.
Sequencing variant TCGA-HT-7677-01A-11D-2253-08 chr19:1255052 C>T maps to NM_177401.4 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:97668831 T>G maps to NM_153182.2 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr17:4797497 T>C maps to NM_153827.4 H900H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WL-01A-21D-A33T-08 chr10:89311946 G>A maps to NM_004897.4 A392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:129903286 C>A maps to NM_002417.4 G2273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:129906299 T>C maps to NM_002417.4 R1268R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:40825628 G>A maps to NM_020831.3 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:14307466 C>T maps to NM_014048.3 H114H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:14341009 C>T maps to NM_014048.3 H631H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:14342791 C>T maps to NM_014048.3 Q703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6668-01A-11D-1893-08 chr7:131128403 T>C maps to NM_013255.4 C446C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:47030790 G>T maps to NM_003684.4 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7469-01A-11D-2253-08 chr19:2039674 C>T maps to NM_199054.2 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr19:2043518 G>A maps to NM_199054.2 Y134Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6XC-01A-12D-A32B-08 chr7:140154463 G>A maps to NM_013446.3 N434N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A858-01A-11D-A36O-08 chr17:56294062 C>T maps to NM_017777.3 E75E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:27964175 C>T maps to NM_173576.2 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr10:28023586 G>A maps to NM_173576.2 Y212Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:50502618 G>A maps to NM_015166.3 Y301Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr3:158314691 G>C maps to NM_001195432.1 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr4:185650177 T>C maps to NM_024629.3 Q36Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:37056035 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:74719481 C>A did not map to a codon.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr16:74725173 C>T did not map to a codon.
Sequencing variant TCGA-QH-A6CX-01A-11D-A32B-08 chr16:74712847 G>A maps to NM_152649.2 H329H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5853-01A-11D-1893-08 chr11:118344300 T>A maps to NM_001197104.1 S809S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:118342983 C>A maps to NM_001197104.1 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:118352682 G>A maps to NM_001197104.1 K1296K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7479-01A-11D-2024-08 chr11:118367048 G>A maps to NM_001197104.1 A1877A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RK-01A-11D-A33T-08 chr11:118373221 C>G maps to NM_001197104.1 P2205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7475-01A-11D-2024-08 chr12:49446389 T>C maps to NM_003482.3 Q405Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7681-01A-11D-2395-08 chr12:49416132 G>A maps to NM_003482.3 R5448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr12:49445920 C>T maps to NM_003482.3 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:151962265 G>A maps to ENST00000355193 C347C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7T8-01A-21D-A34J-08 chr7:151945154 A>T maps to ENST00000355193 S788S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TG-01A-21D-A34J-08 chr7:151864269 A>G maps to ENST00000355193 V3237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7J3-01A-21D-A34J-08 chr7:151845754 T>C maps to ENST00000355193 L4476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RM-01A-11D-A33T-08 chr7:151935818 A>G maps to ENST00000355193 P875P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:36214651 G>A maps to NM_014727.1 T1026T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:104742433 G>A maps to NM_182931.2 Q663Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:104752552 T>G maps to NM_182931.2 P1450P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr7:104753521 G>A maps to NM_182931.2 P1773P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RO-01A-11D-A33T-08 chr9:20414312 G>A maps to NM_004529.2 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:168352038 G>A maps to ENST00000400822 S1327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:36873733 G>A maps to NM_005937.3 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7014-01A-11D-2024-08 chr13:49796305 C>T maps to NM_001507.1 F344F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr2:238449503 C>T maps to NM_024101.5 D450D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:2258453 C>T maps to NM_022372.4 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TP-01A-11D-A289-08 chr16:2258823 C>T maps to NM_022372.4 G309G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:83948757 C>T maps to NM_012213.2 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:83948952 C>A maps to NM_012213.2 S447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:45974725 C>T maps to NM_015506.2 R230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:154802022 C>T maps to NM_007289.2 R23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:2522445 G>A maps to NM_033467.3 R775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7294-01A-11D-2024-08 chr1:2529662 G>A maps to NM_033467.3 R419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr1:2524271 G>A maps to NM_033467.3 N667N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr1:2541235 C>T maps to NM_033467.3 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr23:135047267 G>A did not map to a codon.
Sequencing variant TCGA-E1-A7YD-01A-11D-A34A-08 chr11:102666017 A>T maps to NM_002421.3 R262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7490-01A-11D-2024-08 chr11:102666336 C>T maps to NM_002421.3 E209E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F6-A8O4-01A-11D-A36O-08 chr11:102647463 G>T maps to NM_002425.2 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F0-01A-11D-A289-08 chr11:102649941 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:89053796 G>T maps to NM_005941.4 I572I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5872-01A-11D-1705-08 chr12:132329881 G>T maps to NM_016155.4 V364V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:56231368 C>T maps to NM_002429.4 W386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:102477309 G>A maps to NM_004771.3 D303D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8185-01A-11D-2253-08 chr11:102465487 C>G maps to NM_004771.3 R318R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8185-01A-11D-2253-08 chr20:33862231 C>T maps to NM_006690.3 D586D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:102713309 C>T maps to NM_002422.3 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr4:90833187 A>G maps to NM_007351.2 K279K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:90833184 G>A maps to NM_007351.2 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:28192904 G>A maps to NM_002430.2 S1209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:28193519 C>T maps to NM_002430.2 A1004A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:28193732 C>T maps to NM_002430.2 K933K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:154318426 G>A maps to NM_032117.2 Q136Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7C3-01A-11D-A32B-08 chr15:56721343 G>A maps to NM_018365.2 F481F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7690-01A-11D-2253-08 chr19:2076842 G>A maps to NM_130807.2 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:39881124 G>A maps to ENST00000425303 D231D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UU-01A-12D-A34A-08 chr20:49575489 A>G maps to NM_014484.3 E37E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F6-A8O3-01A-11D-A36O-08 chr6:29638124 C>T maps to NM_002433.4 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:223554129 T>C maps to NM_058165.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:75439996 T>C maps to NM_025098.2 F271F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:100843728 G>T maps to NM_178176.2 Y59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:100839253 G>A maps to NM_178176.2 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TA-01A-11D-A33T-08 chr7:100839295 C>A maps to NM_178176.2 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:74689079 C>T maps to NM_006302.2 T612T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr3:108773664 T>A maps to NM_014429.3 K414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RF-01A-11D-A33T-08 chr3:108773716 G>A maps to NM_014429.3 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66B-01A-11D-A29Q-08 chr22:31330833 A>C maps to ENST00000397641 V709V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6J1-01A-11D-A31L-08 chr22:31328608 T>C maps to ENST00000397641 E890E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4X9-01A-11D-A26M-08 chr23:106185948 T>A did not map to a codon.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr23:106224615 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:106185815 G>T did not map to a codon.
Sequencing variant TCGA-E1-A7Z6-01A-11D-A34J-08 chr23:106229294 A>G did not map to a codon.
Sequencing variant TCGA-WY-A85E-01A-11D-A36O-08 chr23:106185254 T>A did not map to a codon.
Sequencing variant TCGA-HT-7681-01A-11D-2395-08 chr23:102931855 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:2318950 G>A maps to NM_024848.1 Q89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:122097204 G>A maps to NM_173855.4 D65D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr12:122091088 G>A maps to NM_173855.4 H180H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6668-01A-11D-1893-08 chr9:124932033 A>G maps to NM_198469.2 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:124936901 C>T maps to NM_198469.2 N145N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7603-01A-21D-2086-08 chr1:220936308 T>C maps to NM_017898.3 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:134033181 A>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:50558969 T>C maps to NM_018995.2 Y498Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:7490862 G>A maps to NM_004870.3 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr9:13206052 C>A maps to ENST00000319217 E446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:58979411 C>T maps to NM_001039396.1 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YU-01A-11D-A34J-08 chr16:133121 G>T maps to NM_002434.2 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WD-01A-12D-A33T-08 chr16:135640 G>A maps to NM_002434.2 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85B-01A-11D-A36O-08 chr16:133193 G>A maps to NM_002434.2 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7300-01A-21D-2086-08 chr13:20221184 C>T maps to ENST00000414242 T324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A72Z-01A-11D-A32B-08 chr12:123687256 G>T maps to NM_022782.2 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:75190062 C>T maps to NM_002435.1 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:75188493 G>A maps to NM_002435.1 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:43804211 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:4352925 G>A maps to ENST00000262967 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:56355247 G>A maps to ENST00000340482 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:56350916 G>A maps to ENST00000340482 V525V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7475-01A-11D-2024-08 chr17:56357984 G>A maps to ENST00000340482 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F2-01A-11D-A289-08 chr17:56355275 G>A maps to ENST00000340482 N404N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:154020422 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:41975704 G>T maps to NM_005374.3 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:41903201 G>A maps to ENST00000398393 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:24727058 C>T maps to ENST00000409253 D525D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VW-A8FI-01A-11D-A36O-08 chr7:24720069 G>A maps to ENST00000409253 P501P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:28358722 C>T maps to NM_173496.3 Q394Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8563-01A-11D-2395-08 chr10:28414005 C>T maps to NM_173496.3 K154K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8319-01A-11D-2395-08 chr10:28345528 T>C maps to NM_173496.3 L477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7Z2-01A-21D-A34J-08 chr22:43821098 G>A maps to NM_001044370.1 R36R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:37425476 C>T maps to NM_021126.4 Y292Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A86X-01A-11D-A36O-08 chr16:15501854 C>G maps to NM_001128423.1 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EU-01A-11D-A27K-08 chr1:161275671 C>T maps to ENST00000360451 K257K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:167757091 C>T maps to NM_003953.5 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:167757088 C>T maps to NM_003953.5 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A6ML-01A-11D-A32B-08 chr11:118133773 G>T maps to NM_144765.2 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7873-01B-11D-2395-08 chr6:84799070 G>A maps to NM_138409.2 K163K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WL-01A-21D-A33T-08 chr10:17949594 G>A maps to NM_002438.2 W1320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:60749357 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:60765892 C>A maps to NM_006039.3 T1031T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TZ-01A-21D-A32B-08 chr11:68747596 G>A maps to NM_198923.2 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr11:19077574 G>A maps to NM_054030.2 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RM-01A-11D-A33T-08 chr11:19076983 C>T maps to NM_054030.2 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74K-01A-11D-A32B-08 chr11:18158871 G>A maps to NM_054031.3 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WM-01A-12D-A33T-08 chr11:18159393 C>T maps to NM_054031.3 Y215Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4938-01B-11D-1893-08 chr11:18195378 T>C maps to NM_054032.3 C192C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:66204827 C>A maps to NM_016050.3 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A669-01A-12D-A31L-08 chr8:55060053 C>G maps to NM_014175.3 Y222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:55055239 G>A maps to NM_014175.3 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:75879387 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:156708197 C>T maps to NM_145729.2 K72K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6397-01A-11D-1705-08 chr3:131190116 A>C maps to ENST00000425847 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:54681863 G>A maps to NM_016491.3 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:26978877 G>A maps to NM_080794.3 Q55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:10369090 C>T maps to NM_146387.1 D185D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:140446581 C>T maps to NM_032477.2 R17*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DU-6392-01A-11D-1705-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:84379554 A>C maps to NM_016067.2 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:41323301 T>C maps to NM_005830.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RG-01A-11D-A33T-08 chr13:41303681 C>T maps to NM_005830.3 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:105713699 G>A maps to NM_182640.2 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:10597986 A>G maps to NM_001098579.1 S868S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:60230539 G>T maps to NM_152866.2 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7684-01A-11D-2253-08 chr11:60183352 T>C maps to NM_032597.3 F304F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8108-01A-11D-2395-08 chr11:59830059 G>A maps to NM_006138.4 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A87Q-01A-11D-A36O-08 chr11:60064761 C>T maps to NM_148975.1 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr11:60068529 G>C maps to NM_148975.1 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R4-01A-12D-A34J-08 chr11:60059748 A>G maps to NM_148975.1 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RP-01A-21D-A34A-08 chr11:60064770 C>T maps to NM_148975.1 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CX-01A-11D-A32B-08 chr11:60197173 G>A maps to NM_023945.2 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:59940568 G>A maps to NM_152852.1 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YN-01A-11D-A34A-08 chr11:59949074 G>A maps to NM_152852.1 H42H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7C3-01A-11D-A32B-08 chr11:59949074 G>A maps to NM_152852.1 H42H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6402-01A-11D-1705-08 chr11:60107364 T>A maps to NM_139249.2 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5277-01A-01D-1468-08 chr11:60150652 C>T maps to NM_206939.1 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr11:60152679 T>C maps to NM_206939.1 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WL-01A-21D-A33T-08 chr8:72756361 G>A maps to NM_005098.3 Q18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RJ-01A-11D-A33T-08 chr6:31726365 C>T maps to ENST00000375742 V412V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:48027089 C>A maps to NM_000179.2 P656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:11783815 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:11783770 G>T did not map to a codon.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr23:11783853 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:234775681 T>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:234775380 G>A did not map to a codon.
Sequencing variant TCGA-DU-A7TC-01A-21D-A34J-08 chr2:234775675 C>T did not map to a codon.
Sequencing variant TCGA-QH-A6CX-01A-11D-A32B-08 chr2:234775386 G>A did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr16:814960 G>A maps to NM_013404.4 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr16:830601 C>T maps to NM_001025190.1 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A780-01A-12D-A32B-08 chr23:64947732 A>G did not map to a codon.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr8:16026363 C>T maps to ENST00000445506 W96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A780-01A-12D-A32B-08 chr8:9912034 G>C maps to NM_012331.3 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84O-01A-11D-A36O-08 chr12:65847523 C>T maps to NM_001031679.2 H103H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R5-01A-11D-A289-08 chr3:49723303 C>T maps to NM_020998.3 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:49940859 G>A maps to NM_002447.2 Y61Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr23:131208174 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:190924925 C>T maps to NM_005259.2 W203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:56686498 C>T maps to NM_005947.2 C15C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A87N-01A-11D-A36O-08 chr16:56602774 G>A maps to NM_032935.2 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:105930810 C>T maps to NM_004689.3 C417C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:121463487 C>T maps to NM_022045.3 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84C-01A-11D-A36O-08 chr8:121468834 A>G maps to NM_022045.3 V224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:36949364 G>A maps to ENST00000373627 Y135Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:47640455 C>A maps to NM_014342.3 G281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5854-01A-11D-1705-08 chr23:154293906 T>C did not map to a codon.
Sequencing variant TCGA-TQ-A7RR-01A-21D-A34A-08 chr8:97270777 T>G maps to NM_015942.3 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:93594928 G>T maps to NM_007358.3 E362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:93602427 G>A maps to NM_007358.3 E542E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr15:65312541 C>T maps to NM_139242.3 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:64920512 C>T maps to NM_005956.3 I833I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:64916228 C>T maps to NM_005956.3 A782A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:74432915 C>A maps to NM_006636.3 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:11863019 G>A maps to ENST00000376585 R93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:86575409 C>A maps to NM_001159377.1 E192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:28009964 T>C maps to NM_152912.4 Q228Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:68514825 G>T maps to NM_004923.3 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:149809826 C>T did not map to a codon.
Sequencing variant TCGA-S9-A6TS-01A-12D-A33T-08 chr23:149828188 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:149905194 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:149905114 C>T did not map to a codon.
Sequencing variant TCGA-DU-A76K-01A-11D-A33T-08 chr23:149898641 A>G did not map to a codon.
Sequencing variant TCGA-FG-A710-01A-12D-A33T-08 chr23:149924317 A>G did not map to a codon.
Sequencing variant TCGA-S9-A7QW-01A-11D-A34A-08 chr23:149905113 A>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:9719031 G>T maps to NM_001077525.2 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:9714434 G>A maps to NM_001077525.2 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A73M-01A-11D-A32B-08 chr3:9695405 G>A maps to NM_001077525.2 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:30416680 C>T maps to NM_021090.3 S1011S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7858-01A-11D-2395-08 chr22:30416521 C>T maps to NM_021090.3 C958C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:63569915 G>T did not map to a codon.
Sequencing variant TCGA-E1-A7Z6-01A-11D-A34J-08 chr23:63563594 C>G did not map to a codon.
Sequencing variant TCGA-P5-A736-01A-11D-A32B-08 chr23:63579298 G>A did not map to a codon.
Sequencing variant TCGA-FG-8191-01A-11D-2253-08 chr11:92714796 T>C maps to NM_005959.3 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5965-01B-11D-1893-08 chr6:74183325 G>A maps to NM_001123226.1 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7478-01A-11D-2024-08 chr1:11184640 C>T maps to NM_004958.3 L2192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:30611539 G>T maps to ENST00000358107 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr10:30602555 T>C maps to ENST00000358107 T707T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:237057784 C>T maps to NM_000254.2 S1111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:237023144 G>T maps to NM_000254.2 G656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:237001796 C>T maps to NM_000254.2 S471S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:237044081 G>A maps to NM_000254.2 P874P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:237025634 G>T maps to NM_000254.2 E766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:41814543 T>C maps to NM_004294.2 R241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:7878149 C>T maps to NM_024010.2 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CV-01A-11D-A31L-08 chr5:7900164 G>A maps to NM_024010.2 W724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:125575090 C>A maps to NM_014751.4 G323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U6-01A-12D-A33T-08 chr8:125603404 T>G maps to NM_014751.4 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:100543914 A>G maps to ENST00000511045 G892G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:17611315 C>T maps to NM_001001924.2 K667K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr8:17581235 T>G maps to NM_001001924.2 G798G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:29608053 T>A maps to NM_001033602.2 C756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TJ-01A-11D-A34J-08 chr13:29600874 C>T maps to NM_001033602.2 H690H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YN-01A-11D-A34A-08 chr11:26584678 G>A maps to NM_001135091.1 D303D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5275-01A-01D-1468-08 chr19:9069715 A>C maps to NM_024690.2 T5910T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64P-01A-11D-A29Q-08 chr19:9082769 A>G maps to NM_024690.2 T3015T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr19:9089903 G>A maps to NM_024690.2 S637S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5853-01A-11D-1893-08 chr19:9046746 T>A maps to NM_024690.2 P11628P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:9086384 T>C maps to NM_024690.2 K1810K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:9021061 G>A maps to NM_024690.2 Q12421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr19:9070399 G>A maps to NM_024690.2 P5682P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr19:9090830 A>G maps to NM_024690.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7636-01A-11D-2086-08 chr19:9068569 T>A maps to NM_024690.2 T6292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7638-01B-11D-2086-08 chr19:9090830 A>G maps to NM_024690.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8182-01A-11D-2253-08 chr19:8987332 G>A maps to NM_024690.2 T13918T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7471-01A-11D-2253-08 chr19:9090830 A>G maps to NM_024690.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr19:9087884 A>G maps to NM_024690.2 P1310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr19:9089321 C>T maps to NM_024690.2 S831S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8106-01A-11D-2395-08 chr19:9069934 G>T maps to NM_024690.2 P5837P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RB-01A-11D-A289-08 chr19:9088745 T>C maps to NM_024690.2 T1023T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74H-01A-11D-A32B-08 chr19:9075891 T>G maps to NM_024690.2 R3852R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EZ-01A-11D-A27K-08 chr19:9075049 T>A maps to NM_024690.2 S4132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6X8-01A-12D-A32B-08 chr19:9058489 G>A maps to NM_024690.2 P9652P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7J0-01A-11D-A34A-08 chr19:8973983 G>A maps to NM_024690.2 D14229D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84M-01A-11D-A36O-08 chr19:9049227 C>T maps to NM_024690.2 A10801A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RP-01A-21D-A34A-08 chr19:9006761 G>A maps to NM_024690.2 T13162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr7:100677936 T>C maps to NM_001040105.1 S1080S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:100684836 T>A maps to NM_001040105.1 S3380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:100680858 G>A maps to NM_001040105.1 T2054T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:100674975 G>A maps to NM_001040105.1 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:100675686 T>G maps to NM_001040105.1 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:100686240 C>A maps to NM_001040105.1 T3848T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7309-01A-11D-2086-08 chr7:100696422 G>C maps to NM_001040105.1 V4420V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr7:100681272 G>T maps to NM_001040105.1 V2192V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YD-01A-11D-A34A-08 chr7:100679148 T>C maps to NM_001040105.1 S1484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr7:100679592 A>G maps to NM_001040105.1 L1632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7854-01A-11D-2253-08 chr7:100676699 C>A maps to NM_001040105.1 S668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7902-01A-12D-2395-08 chr7:100677106 G>T maps to NM_001040105.1 G804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R2-01A-21D-A34J-08 chr7:100678560 G>T maps to NM_001040105.1 T1288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RM-01A-11D-A33T-08 chr7:100679418 A>G maps to NM_001040105.1 P1574P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:1099268 G>A maps to ENST00000441003 T2416T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YM-01A-11D-A34A-08 chr11:1081706 G>A maps to ENST00000441003 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr11:1102175 C>T maps to ENST00000441003 H2604H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr11:1080293 C>T maps to ENST00000441003 D338D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A73M-01A-11D-A32B-08 chr11:1093739 G>C maps to ENST00000441003 P1853P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7J1-01A-21D-A34J-08 chr11:1095755 G>T maps to ENST00000441003 P2089P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:195453067 G>T maps to ENST00000447234 E532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:195480102 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:195474115 G>T maps to NM_018406.5 V5390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:195487872 G>T maps to NM_018406.5 I4910I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:195538616 A>G maps to NM_018406.5 H24H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr3:195488979 C>T maps to NM_018406.5 Q4830Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr11:1268696 C>T maps to ENST00000447027 T3532T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:1256407 C>T maps to ENST00000447027 G911G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:1279401 G>A maps to ENST00000447027 E5511E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:1271360 C>A maps to ENST00000447027 T4420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A70Z-01A-12D-A33T-08 chr11:1267409 G>A maps to ENST00000447027 P3103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A710-01A-12D-A33T-08 chr11:1269134 G>A maps to ENST00000447027 P3678P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr11:1265831 C>G maps to ENST00000447027 V2577V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A72W-01A-11D-A32B-08 chr11:1272725 A>T maps to ENST00000447027 G4875G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A6ML-01A-11D-A32B-08 chr11:1268735 A>G maps to ENST00000447027 T3545T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6UB-01A-21D-A33T-08 chr11:1247989 C>T maps to ENST00000447027 N115N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WM-01A-12D-A33T-08 chr11:1248557 C>T maps to ENST00000447027 Y199Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84H-01A-11D-A36O-08 chr11:1269641 C>A maps to ENST00000447027 T3847T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8C8-01A-11D-A36O-08 chr11:1267979 C>A maps to ENST00000447027 T3293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:1024852 G>A maps to NM_005961.2 C1072C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr11:1025337 G>A maps to NM_005961.2 N943N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A70Z-01A-12D-A33T-08 chr4:71347069 A>G maps to NM_152291.2 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:105450703 G>A did not map to a codon.
Sequencing variant TCGA-DU-6402-01A-11D-1705-08 chr23:105449890 G>A did not map to a codon.
Sequencing variant TCGA-P5-A5F4-01A-11D-A289-08 chr23:105449980 T>C did not map to a codon.
Sequencing variant TCGA-S9-A7QW-01A-11D-A34A-08 chr23:105450234 T>C did not map to a codon.
Sequencing variant TCGA-VV-A86M-01A-11D-A36O-08 chr23:105450653 T>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:88721164 G>A maps to NM_002461.1 D316D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:42821136 G>A maps to NM_001144925.1 V449V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7469-01A-11D-2253-08 chr21:42774041 C>T maps to NM_002463.1 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7616-01A-11D-2253-08 chr21:42749751 A>T maps to NM_002463.1 K96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A72U-01A-31D-A32B-08 chr21:42774000 C>T maps to NM_002463.1 Q507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:2252324 G>A maps to NM_006454.2 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr23:3228181 C>T did not map to a codon.
Sequencing variant TCGA-DU-5851-01A-13D-1893-08 chr23:3240115 C>T did not map to a codon.
Sequencing variant TCGA-DU-5854-01A-11D-1705-08 chr23:3228241 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:3235910 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:3248418 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:3241891 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:3229610 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:3229643 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:3238347 G>A did not map to a codon.
Sequencing variant TCGA-DU-7019-01A-11D-2024-08 chr23:3239836 T>C did not map to a codon.
Sequencing variant TCGA-DU-7290-01A-11D-2024-08 chr23:3229517 C>T did not map to a codon.
Sequencing variant TCGA-DU-A7T8-01A-21D-A34J-08 chr23:3228565 T>C did not map to a codon.
Sequencing variant TCGA-E1-A7YE-01A-11D-A34A-08 chr23:3248146 C>T did not map to a codon.
Sequencing variant TCGA-HT-7471-01A-11D-2253-08 chr23:3238336 C>T did not map to a codon.
Sequencing variant TCGA-HT-7616-01A-11D-2253-08 chr23:3241680 C>T did not map to a codon.
Sequencing variant TCGA-S9-A6WN-01A-12D-A33T-08 chr23:3240985 T>C did not map to a codon.
Sequencing variant TCGA-TQ-A7RK-01A-11D-A33T-08 chr23:3235705 C>T did not map to a codon.
Sequencing variant TCGA-TQ-A7RP-01A-21D-A34A-08 chr23:3240936 A>T did not map to a codon.
Sequencing variant TCGA-TQ-A8XE-01A-11D-A36O-08 chr23:3241757 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:135518457 G>A maps to NM_001130173.1 S521S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr6:135522781 A>G maps to NM_001130173.1 E652E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IZ-01A-11D-A34A-08 chr8:67485729 T>C maps to NM_001080416.2 T494T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:102020662 C>A maps to NM_002465.2 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:50939872 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:50964890 C>T maps to NM_004533.3 T1008T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VW-A8FI-01A-11D-A36O-08 chr19:50939060 T>C maps to NM_004533.3 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:77631173 G>A maps to NM_015057.4 R4462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:77632511 C>T maps to NM_015057.4 T4390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7684-01A-11D-2253-08 chr13:77807396 G>C maps to NM_015057.4 G877G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VW-A7QS-01A-12D-A33T-08 chr13:77667376 C>T maps to NM_015057.4 P3430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7694-01A-11D-2253-08 chr3:38180394 G>A maps to NM_001172567.1 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:81110944 C>T maps to NM_005593.2 R35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr12:81111279 T>C maps to NM_005593.2 Y146Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:81101659 C>T maps to NM_002469.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:10402091 A>G maps to NM_005963.3 C1344C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:10397682 T>C maps to NM_005963.3 Q1885Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:10398331 C>T maps to NM_005963.3 V1794V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A858-01A-11D-A36O-08 chr17:10411265 G>A maps to NM_005963.3 G635G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DB-A4XF-01A-11D-A27K-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HT-7485-01A-11D-2024-08 chr17:8424574 G>A maps to ENST00000360416 V662V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr17:8379259 A>C maps to ENST00000360416 G1962G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:15814827 G>A maps to NM_001040114.1 D1560D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:10210258 C>T maps to NM_003802.2 T1764T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr17:10223517 G>A maps to NM_003802.2 D1100D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6186-01A-12D-2024-08 chr19:50750372 G>A maps to NM_001145809.1 K441K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:10428205 A>G maps to NM_017534.5 S1613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:10451165 G>A maps to NM_017534.5 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UR-01A-11D-A33T-08 chr17:10547673 G>A maps to NM_002470.2 I468I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A614-01A-11D-A29Q-08 chr17:10370010 G>A maps to NM_017533.2 R18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84M-01A-11D-A36O-08 chr17:10366487 G>A maps to NM_017533.2 R275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CF-01A-11D-A36O-08 chr17:10348673 G>C maps to NM_017533.2 T1725T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:23871974 G>A maps to NM_002471.3 Y311Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7013-01A-11D-2024-08 chr14:23855274 G>A maps to NM_002471.3 I1675I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr14:23884932 A>G maps to NM_000257.2 L1688L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5874-01A-11D-1705-08 chr14:23887504 A>C maps to NM_000257.2 L1361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:23893175 G>A maps to NM_000257.2 I954I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:23893259 C>T maps to NM_000257.2 L926L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr14:23887504 A>C maps to NM_000257.2 L1361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TG-01A-21D-A34J-08 chr14:23897870 G>A maps to NM_000257.2 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WO-01A-21D-A34A-08 chr14:23886515 C>T maps to NM_000257.2 E1455E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:33575076 C>T maps to NM_020884.3 A420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8185-01A-11D-2253-08 chr20:33567543 G>A maps to NM_020884.3 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84F-01A-11D-A36O-08 chr20:33586195 G>A maps to NM_020884.3 T1324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr17:10297736 C>T maps to NM_002472.2 R1665R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7605-01A-11D-2086-08 chr17:10303715 G>A maps to NM_002472.2 S1242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7608-01A-11D-2086-08 chr17:10299696 G>A maps to NM_002472.2 Q1535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr17:10299868 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:36697594 C>T maps to NM_002473.4 E872E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:36684351 G>A maps to NM_002473.4 I1626I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:36716361 A>G maps to NM_002473.4 N305N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6J3-01A-11D-A31L-08 chr22:36681963 G>A maps to NM_002473.4 A1699A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:111352091 G>A maps to NM_000432.3 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A6S7-01A-21D-A32B-08 chr20:35173451 C>T maps to NM_006097.3 H55H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7879-01A-11D-2395-08 chr20:35177630 C>T maps to NM_006097.3 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:16145385 C>T maps to NM_013262.3 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:16145220 T>C maps to NM_013262.3 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A70Y-01A-12D-A34J-08 chr3:123375991 C>T maps to NM_053025.3 T1423T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7487-01A-11D-2024-08 chr3:123419710 G>A maps to NM_053025.3 D868D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:46744667 T>G maps to NM_182493.2 T716T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:46771764 C>A maps to NM_182493.2 G287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IZ-01A-11D-A34A-08 chr6:2678590 C>T maps to NM_001012418.3 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:16763612 C>A maps to NM_012334.2 E491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:18023070 G>A maps to ENST00000205890 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TT-01A-11D-A289-08 chr17:18023394 C>T maps to ENST00000205890 H427H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7T6-01A-11D-A33T-08 chr13:109777628 G>C maps to NM_015011.1 R1213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:26422935 C>T maps to ENST00000407587 D2334D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6J1-01A-11D-A31L-08 chr22:26423238 C>T maps to ENST00000407587 Y2435Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:57432320 G>T maps to NM_005379.2 S545S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7877-01A-11D-2395-08 chr12:57423553 G>A maps to NM_005379.2 A898A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7493-01A-11D-2024-08 chr2:192234305 C>G maps to NM_001130158.1 Y357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CV-01A-11D-A31L-08 chr2:192251948 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:1380797 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:1380818 C>T maps to NM_001080779.1 K518K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U5-01A-12D-A33T-08 chr17:1375271 C>T maps to NM_001080779.1 G650G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QZ-01A-12D-A34J-08 chr17:1384089 G>T maps to NM_001080779.1 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:30986140 A>G maps to NM_015194.1 I779I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:45005866 G>T maps to NM_033054.2 T654T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:109879448 C>A maps to NM_001101421.3 I840I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IY-01A-11D-A34A-08 chr12:109826585 G>A maps to NM_001101421.3 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr10:26500780 G>A maps to NM_017433.4 A1580A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:26443733 G>A maps to NM_017433.4 T925T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6407-01A-13D-1705-08 chr10:26359113 T>C maps to NM_017433.4 Y415Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8191-01A-11D-2253-08 chr10:26432480 A>G maps to NM_017433.4 L789L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A83Z-01A-11D-A36O-08 chr10:26463167 T>A maps to NM_017433.4 R1325R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TX-01A-21D-A32B-08 chr10:26377302 C>T maps to NM_017433.4 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84J-01A-11D-A36O-08 chr10:26482182 C>T maps to NM_017433.4 P1496P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74L-01A-11D-A32B-08 chr2:171259405 C>T maps to NM_138995.3 F726F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6186-01A-12D-2024-08 chr15:52622645 G>A maps to ENST00000358212 R1487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:52613634 C>T maps to ENST00000358212 R1624R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:52605915 G>A maps to ENST00000358212 L1874L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84O-01A-11D-A36O-08 chr15:52668650 G>A maps to ENST00000358212 I771I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:47431074 G>T maps to NM_001080467.2 T846T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:47479644 G>A maps to NM_001080467.2 I579I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:47389691 C>T maps to NM_001080467.2 P1283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr18:47383223 T>G maps to NM_001080467.2 G1327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R3-01A-11D-A34J-08 chr18:47367797 C>T maps to NM_001080467.2 T1546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VW-A7QS-01A-12D-A33T-08 chr18:47369673 G>A maps to NM_001080467.2 N1516N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7638-01B-11D-2086-08 chr15:52537631 G>A maps to NM_018728.3 Y699Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr15:52534267 G>A maps to NM_018728.3 L845L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R2-01A-21D-A34J-08 chr15:52532037 G>A maps to NM_018728.3 Y865Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5141-01A-01D-1468-08 chr11:76922333 G>A maps to NM_000260.3 L2063L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:76869429 G>A maps to NM_000260.3 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76L-01A-11D-A32B-08 chr11:76903157 C>T maps to NM_000260.3 Y1329Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TJ-01A-11D-A34J-08 chr2:128341726 C>T maps to ENST00000389524 N458N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5874-01A-11D-1705-08 chr15:72122613 T>C maps to ENST00000424560 P2363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:72338702 C>A maps to ENST00000424560 E68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YM-01A-11D-A34A-08 chr15:72338853 T>C maps to ENST00000424560 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7873-01B-11D-2395-08 chr15:72172771 G>A maps to ENST00000424560 N1913N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8109-01A-11D-2395-08 chr15:72190410 A>T maps to ENST00000424560 L1478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:17298835 C>T maps to NM_004145.3 S890S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:17322803 G>A maps to NM_004145.3 T2053T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:171605811 C>T maps to NM_000261.1 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6J1-01A-11D-A31L-08 chr1:171605166 A>T maps to NM_000261.1 Y471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:12655754 C>T maps to NM_001146312.1 R384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8106-01A-11D-2395-08 chr17:12655918 T>A maps to NM_001146312.1 S438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr17:12655843 G>A maps to NM_001146312.1 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YM-01A-11D-A34A-08 chr10:95082848 G>A maps to NM_013451.3 D1814D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7874-01A-11D-2395-08 chr10:95072806 G>A maps to NM_013451.3 Y1953Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr10:95095761 G>A maps to NM_013451.3 G1493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IX-01A-12D-A34A-08 chr10:95072806 G>A maps to NM_013451.3 Y1953Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R4-01A-12D-A34J-08 chr10:95191197 G>T maps to NM_013451.3 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr18:3135614 G>A maps to NM_003803.3 R713R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7309-01A-11D-2086-08 chr8:2040225 G>A maps to NM_003970.2 S627S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8162-01A-21D-2253-08 chr8:2027639 G>A did not map to a codon.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr8:2048768 C>T maps to NM_003970.2 F848F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A6S8-01A-12D-A32B-08 chr8:2037955 G>A maps to NM_003970.2 R590R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A4DV-01A-11D-A26M-08 chr5:150050052 G>A maps to NM_133371.3 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:69966568 G>A maps to NM_032578.2 Q1234Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7604-01A-11D-2086-08 chr19:46394510 C>T maps to NM_001012643.2 Q190Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:40192658 G>A maps to NM_015460.2 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:31141658 C>T maps to NM_182958.2 Y328Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7477-01B-11D-A289-08 chr8:41790658 T>G maps to NM_006766.3 P1693P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8015-01B-11D-A289-08 chr8:41790658 T>G maps to NM_006766.3 P1693P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8111-01A-11D-2395-08 chr8:41790658 T>G maps to NM_006766.3 P1693P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R5-01A-11D-A289-08 chr8:41790658 T>G maps to NM_006766.3 P1693P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr8:41790658 T>G maps to NM_006766.3 P1693P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74K-01A-11D-A32B-08 chr8:41798680 T>C maps to NM_006766.3 S906S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F0-01A-11D-A289-08 chr8:41790658 T>G maps to NM_006766.3 P1693P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F1-01A-11D-A289-08 chr8:41790658 T>G maps to NM_006766.3 P1693P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F2-01A-11D-A289-08 chr8:41790658 T>G maps to NM_006766.3 P1693P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F4-01A-11D-A289-08 chr8:41790658 T>G maps to NM_006766.3 P1693P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F6-01A-11D-A289-08 chr8:41790658 T>G maps to NM_006766.3 P1693P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:76729776 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:76789240 C>T maps to NM_012330.2 S1553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:62854706 C>T maps to NM_004535.2 D841D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:62854527 T>C did not map to a codon.
Sequencing variant TCGA-DU-7299-01A-21D-2024-08 chr20:62839581 G>T maps to NM_004535.2 E345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8018-01A-11D-2395-08 chr20:62839767 C>T maps to NM_004535.2 Q407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:1795746 G>A maps to ENST00000399161 Y1151Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:1982977 G>A maps to ENST00000399161 D37D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7013-01A-11D-2024-08 chr2:1843078 G>A maps to ENST00000399161 S974S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7479-01A-11D-2024-08 chr2:1906993 C>T maps to ENST00000399161 P630P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr2:1926214 C>T maps to ENST00000399161 T442T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:48596355 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:48596021 A>G maps to NM_153029.3 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UR-01A-11D-A33T-08 chr13:33111031 T>A maps to ENST00000505213 R45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr13:33017398 C>T maps to NM_033111.3 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6400-01A-12D-1705-08 chr5:177547252 G>A maps to NM_015111.1 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr23:153195615 T>C did not map to a codon.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr23:153195524 T>C did not map to a codon.
Sequencing variant TCGA-E1-A7Z2-01A-21D-A34J-08 chr4:80246704 C>A maps to NM_032693.2 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7857-01A-11D-2395-08 chr4:140262068 G>A maps to NM_057175.3 W83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:41936258 C>T maps to NM_024561.4 Y501Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:41897202 C>T maps to NM_024561.4 Y138Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:112518932 G>A maps to NM_024953.3 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:112509780 G>A maps to NM_024953.3 R318R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr11:63721926 G>C maps to NM_024771.2 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:64824953 G>T maps to ENST00000340252 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:175165104 G>A maps to NM_207015.2 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7616-01A-11D-2253-08 chr12:57487217 G>A maps to NM_005967.3 P435P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8105-01A-11D-2395-08 chr12:57487286 A>G maps to NM_005967.3 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5281-01A-01D-1468-08 chr12:57110585 G>A maps to NM_001113203.1 S1576S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:57115004 T>C maps to NM_001113203.1 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7606-01A-11D-2086-08 chr12:57111704 G>A maps to NM_001113203.1 P1203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7854-01A-11D-2253-08 chr12:57111704 G>A maps to NM_001113203.1 P1203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr12:57111731 G>T maps to NM_001113203.1 A1194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr12:57112307 A>G maps to NM_001113203.1 T1002T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RC-01A-11D-A289-08 chr12:57112307 A>G maps to NM_001113203.1 T1002T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F2-01A-11D-A289-08 chr12:57112307 A>G maps to NM_001113203.1 T1002T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr1:1686108 C>T maps to ENST00000344463 R384R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:71209550 C>T maps to NM_018161.4 Q683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TB-01A-11D-A33T-08 chr4:164050410 G>A maps to NM_138386.2 R375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8105-01A-11D-2395-08 chr17:40695938 G>T maps to NM_000263.3 E639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:5078080 G>A maps to NM_016256.3 D342D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr16:5081776 T>C maps to NM_016256.3 Q217Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QW-01A-11D-A34A-08 chr5:70308493 G>A maps to NM_004536.2 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:101735164 G>A maps to NM_052867.2 L1254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:46417657 A>G maps to NM_001029861.2 C98C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:100843120 C>T maps to NM_018946.3 D209D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5277-01A-01D-1468-08 chr12:76453622 C>T maps to NM_139207.2 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UR-01A-11D-A33T-08 chr23:72433892 G>A did not map to a codon.
Sequencing variant TCGA-FG-A710-01A-12D-A33T-08 chr23:72433963 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:92927766 A>G did not map to a codon.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr23:92927162 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:102760493 C>T maps to ENST00000455523 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:10540397 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:50864364 G>A maps to NM_004851.1 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:55283208 T>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:78277318 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:34160751 A>G maps to NM_024662.2 G742G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr4:2065802 C>G maps to ENST00000423729 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:20122652 C>T maps to ENST00000396087 R2177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:20124898 C>T maps to ENST00000396087 H2231H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KK-01A-11D-A27K-08 chr11:19970368 C>T maps to ENST00000396087 D819D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr12:78513089 T>G maps to NM_014903.4 P1038P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7694-01A-11D-2253-08 chr2:15523365 T>C maps to NM_015909.2 T1111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr13:35923242 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:36241641 C>T maps to ENST00000400445 R2845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7014-01A-11D-2024-08 chr13:36242524 C>T maps to ENST00000400445 D2873D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6J1-01A-11D-A31L-08 chr2:204001497 G>A did not map to a codon.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr1:19981873 A>C maps to NM_182744.2 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:90993000 G>A maps to NM_002485.4 C147C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:16901707 G>A maps to NM_017940.3 D712D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6X5-01A-12D-A32B-08 chr1:145368515 G>A maps to NM_001039703.4 P3498P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66G-01A-21D-A31L-08 chr1:21795208 C>T maps to NM_032264.2 N54N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6J1-01A-11D-A31L-08 chr17:41352481 A>G maps to NM_005899.3 E775E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6690-01A-11D-1893-08 chr11:113076287 G>A maps to ENST00000316851 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6X4-01A-51D-A32B-08 chr21:22710760 A>G maps to NM_004540.2 Q317Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5302-01A-01D-1468-08 chr19:19337661 G>A maps to NM_004386.2 R480R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:6638998 C>T maps to NM_014865.3 R1238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EZ-01A-11D-A27K-08 chr12:6635635 C>G maps to NM_014865.3 L863L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6X8-01A-12D-A32B-08 chr11:134054558 T>C maps to NM_015261.2 A808A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84J-01A-11D-A36O-08 chr11:134080161 A>C did not map to a codon.
Multiple mappings detected for codon TCGA-DU-6392-01A-11D-1705-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FG-5964-01A-11D-1705-08 chr22:50956004 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:100407397 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:196663926 G>A maps to NM_007362.3 Y142Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:36028225 C>T maps to NM_001014839.1 D459D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:74191611 G>T did not map to a codon.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr7:74203028 G>A maps to NM_000265.4 Q344Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr1:183543622 C>T maps to NM_001127651.2 W167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CV-01A-11D-A31L-08 chr22:37266497 C>T maps to NM_013416.3 D128D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:136665136 G>A maps to NM_006153.4 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr3:136646966 C>T maps to NM_006153.4 R42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7609-01A-11D-2086-08 chr2:183829475 T>C maps to NM_205842.1 S569S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66G-01A-21D-A31L-08 chr12:54925285 G>T maps to NM_005337.4 V872V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:54917614 C>T maps to NM_005337.4 D677D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr12:54917242 G>A maps to NM_005337.4 R648R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7014-01A-11D-2024-08 chr2:133540756 G>T maps to NM_207363.2 T1209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A70Z-01A-12D-A33T-08 chr2:133541328 G>A maps to NM_207363.2 R1019*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7605-01A-11D-2086-08 chr2:133721291 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:50191177 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:50190544 C>T maps to NM_001037806.3 A366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A77W-01A-11D-A32B-08 chr12:50189044 G>A maps to NM_001037806.3 G866G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UR-01A-11D-A33T-08 chr2:24952521 G>A maps to NM_003743.4 R1013R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:71075084 C>T maps to NM_006540.2 K279K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TJ-01A-11D-A34J-08 chr20:46279832 G>A maps to NM_181659.2 Q1253Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7Z2-01A-21D-A34J-08 chr20:46262894 A>T maps to NM_181659.2 V356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7472-01A-11D-2024-08 chr20:46267763 C>G maps to NM_181659.2 S842*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WP-01A-12D-A34A-08 chr20:46279862 G>A maps to NM_181659.2 Q1263Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VV-A829-01A-21D-A36O-08 chr20:46279832 G>A maps to NM_181659.2 Q1253Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:33337720 C>T maps to NM_014071.2 T759T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6IZ-01A-11D-A31L-08 chr20:33345722 C>T maps to NM_014071.2 Q276Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:15973652 G>T maps to ENST00000395857 R1463R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:15942849 A>G maps to ENST00000395857 V2299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:15942968 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:16021242 G>A maps to ENST00000395857 R672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A87N-01A-11D-A36O-08 chr17:15971337 C>T maps to ENST00000395857 G1553G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7694-01A-11D-2253-08 chr17:15978995 C>T maps to ENST00000395857 Q1190Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:124950730 G>A maps to NM_006312.4 Y231Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:124870299 C>T maps to NM_006312.4 K670K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:124816897 G>A maps to NM_006312.4 L2298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr12:124826570 C>T maps to NM_006312.4 P1669P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A614-01A-11D-A29Q-08 chr12:124810103 G>A maps to NM_006312.4 P2470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CD-01A-11D-A36O-08 chr6:31556918 C>T maps to NM_147130.2 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:2578943 C>T maps to NM_006101.2 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr16:15758700 G>A maps to NM_001143979.1 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5302-01A-01D-1468-08 chr9:140110622 A>G maps to NM_001144026.1 A553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84B-01A-11D-A36O-08 chr9:140110109 G>A did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr14:21486615 C>T maps to NM_201537.1 K287K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IY-01A-11D-A34A-08 chr20:35293690 C>A maps to ENST00000373803 E236*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DU-6392-01A-11D-1705-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:149927814 G>A maps to NM_001543.4 K727K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr5:149927940 C>T maps to NM_001543.4 H769H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:240944660 G>A maps to ENST00000404554 Q286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:8376448 C>T maps to NM_005001.2 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:4791406 C>T maps to NM_005002.4 Y279Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:41688735 G>A maps to NM_016013.2 D174D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TR-01A-11D-A289-08 chr5:60241192 G>A maps to NM_174889.4 Q37Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:49059859 G>A maps to NM_199069.1 E53E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:47002074 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:207006689 G>A maps to ENST00000455934 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YM-01A-11D-A34A-08 chr2:207009617 G>T maps to ENST00000455934 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:161179309 C>T maps to NM_004550.4 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:1390943 C>T maps to NM_024407.4 Y101Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:67379589 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:67376949 C>T maps to NM_007103.3 D118D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5273-01A-01D-1468-08 chr2:152406212 A>G maps to NM_001164507.1 Y6662Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5142-01A-01D-1468-08 chr2:152342396 C>T maps to NM_001164507.1 V8485V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:152534195 G>A maps to NM_001164507.1 A1219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8111-01A-11D-2395-08 chr2:152534213 G>A maps to NM_001164507.1 V1213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5ET-01A-11D-A27K-08 chr2:152409935 C>T maps to NM_001164507.1 K6569K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RN-01A-11D-A33T-08 chr2:152420363 G>A maps to NM_001164507.1 A6184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5304-01A-01D-1468-08 chr10:21097514 G>A maps to ENST00000430741 D897D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A87N-01A-11D-A36O-08 chr10:21098828 T>C maps to ENST00000377187 E840E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VW-A8FI-01A-11D-A36O-08 chr10:21462708 G>A maps to NM_213569.2 V18V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:16782361 C>A maps to NM_018090.4 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:16770222 G>A maps to NM_018090.4 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:56134235 A>G maps to ENST00000508342 D997D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A840-01A-11D-A36O-08 chr14:24687633 G>A maps to NM_006156.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YN-01A-11D-A34A-08 chr8:24771449 G>C maps to NM_005382.2 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr1:72163700 A>G maps to NM_173808.2 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A859-01A-12D-A36O-08 chr15:75641377 C>G maps to NM_024608.2 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr4:170428877 G>A maps to ENST00000507142 I633I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RU-01A-21D-A34A-08 chr4:170428868 C>A maps to ENST00000507142 L636L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7006-01A-11D-2024-08 chr3:27352498 G>A maps to ENST00000396636 Q193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7Z2-01A-21D-A34J-08 chr9:127074825 G>A maps to NM_001166171.1 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5281-01A-01D-1468-08 chr17:27068157 C>T maps to NM_178170.2 R599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:27064984 C>T maps to NM_178170.2 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:27061883 G>A maps to NM_178170.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5322-01A-01D-1468-08 chr17:27065005 C>T maps to NM_178170.2 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WI-01A-21D-A33T-08 chr17:27061087 G>A maps to NM_178170.2 R45R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7006-01A-11D-2024-08 chr14:75574124 C>T maps to NM_033116.4 Q416Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RW-01A-11D-A33T-08 chr14:75553846 C>T maps to NM_033116.4 V897V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:45108471 G>T maps to NM_001145107.1 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7616-01A-11D-2253-08 chr12:45000950 C>T did not map to a codon.
Sequencing variant TCGA-DB-5270-01A-02D-1468-08 chr15:73581487 G>A maps to NM_002499.3 G1217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr15:73541989 C>T maps to NM_002499.3 R608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7692-01A-12D-2253-08 chr1:156642350 T>C maps to NM_006617.1 K543K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A6ML-01A-11D-A32B-08 chr10:5498929 T>C maps to NM_001047160.1 G588G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:70417388 C>T maps to NM_153181.2 S482S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YV-01A-11D-A34J-08 chr11:74717143 T>A maps to NM_006656.5 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TS-01A-12D-A33T-08 chr11:74716639 C>G maps to NM_006656.5 Y163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:242757435 C>T maps to NM_001167599.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr2:242755716 C>T maps to NM_001167599.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:105349996 G>A maps to NM_004210.4 T531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8C9-01A-11D-A36O-08 chr20:44517456 C>T maps to NM_080749.2 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:7224922 G>A maps to NM_032442.2 Q1019*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A845-01A-11D-A36O-08 chr17:7226075 C>T maps to NM_032442.2 K901K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7884-01B-11D-2395-08 chr4:113436145 C>T maps to NM_024019.2 W162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:78383378 C>T maps to NM_144573.3 D52D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:78392296 G>A did not map to a codon.
Sequencing variant TCGA-CS-5397-01A-01D-1893-08 chr17:29563006 G>A maps to NM_001042492.2 W1314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64O-01A-11D-A29Q-08 chr17:29552215 T>A maps to NM_001042492.2 L650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A75K-01A-11D-A32B-08 chr17:29684325 C>T maps to NM_001042492.2 R2637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5847-01A-11D-1705-08 chr17:29497015 G>A did not map to a codon.
Sequencing variant TCGA-DU-5847-01A-11D-1705-08 chr17:29677226 C>T maps to NM_001042492.2 R2450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:29554596 T>C maps to NM_001042492.2 Y794Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:29508477 C>T maps to NM_001042492.2 Q209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6394-01A-11D-1705-08 chr17:29670154 T>A did not map to a codon.
Sequencing variant TCGA-DU-6394-01A-11D-1705-08 chr17:29553696 C>A maps to NM_001042492.2 S749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6397-01A-11D-1705-08 chr17:29663349 G>C did not map to a codon.
Sequencing variant TCGA-DU-6402-01A-11D-1705-08 chr17:29663746 T>G maps to NM_001042492.2 L2081*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5963-01A-11D-1705-08 chr17:29677226 C>T maps to NM_001042492.2 R2450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A87N-01A-11D-A36O-08 chr17:29654515 G>C did not map to a codon.
Sequencing variant TCGA-HT-7857-01A-11D-2395-08 chr17:29576000 G>A did not map to a codon.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr17:29664445 T>A maps to NM_001042492.2 L2163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6UA-01A-12D-A33T-08 chr17:29684021 A>T maps to NM_001042492.2 K2595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WP-01A-12D-A34A-08 chr17:29556221 T>A maps to NM_001042492.2 Y863*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A89V-01A-11D-A36O-08 chr17:29665040 A>T maps to ENST00000444181 R28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84C-01A-11D-A36O-08 chr17:29665156 G>A maps to NM_001042492.2 K2273K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RI-01A-11D-A33T-08 chr17:29553520 C>G maps to NM_001042492.2 A690A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RI-01A-11D-A33T-08 chr17:29654674 G>A maps to NM_001042492.2 P1809P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:204943841 C>T maps to ENST00000367172 N483N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TT-01A-11D-A289-08 chr1:204946827 T>A maps to ENST00000367172 T617T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8011-01A-11D-2395-08 chr16:69689702 G>A did not map to a codon.
Sequencing variant TCGA-HT-7604-01A-11D-2086-08 chr18:77227574 C>T maps to NM_172387.1 P682P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr20:50091993 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:24842969 C>T maps to NM_001136022.1 I606I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:24839158 C>T maps to NM_001136022.1 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TI-01A-11D-A33T-08 chr12:54687024 G>A maps to NM_001136023.1 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YE-01A-11D-A34A-08 chr2:178097222 G>C maps to NM_006164.3 S164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4938-01B-11D-1893-08 chr7:26224961 T>C maps to NM_004289.6 P548P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:14307195 G>A maps to ENST00000397581 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:13184287 G>A maps to ENST00000397661 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:13184822 C>A maps to ENST00000397661 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:103537624 C>T maps to NM_003998.3 S928S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:103528834 C>T maps to NM_003998.3 Y718Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr14:35872894 C>T did not map to a codon.
Sequencing variant TCGA-E1-A7YV-01A-11D-A34J-08 chr8:145665835 A>T maps to NM_013432.4 I396I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VW-A8FI-01A-11D-A36O-08 chr8:145667764 G>A maps to NM_013432.4 R203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:101572668 C>T maps to NM_031419.3 S433S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:33295379 C>T maps to NM_002504.4 R330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:47857180 C>T did not map to a codon.
Sequencing variant TCGA-HT-A617-01A-11D-A29Q-08 chr4:47850314 A>T maps to NM_152995.4 R867R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr12:104517156 C>T maps to NM_006166.3 E92E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr14:23940134 A>G maps to NM_001042635.1 Q31Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:25773920 A>G maps to NM_018297.3 I438I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7US-01A-11D-A33T-08 chr4:103870459 T>C maps to NM_139173.3 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7690-01A-11D-2253-08 chr4:103822447 G>A maps to NM_139173.3 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:116380609 A>T maps to NM_005599.3 Y128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RG-01A-11D-A33T-08 chr10:115639378 T>C maps to NM_198514.3 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr23:17394315 G>A did not map to a codon.
Sequencing variant TCGA-DB-A64W-01A-11D-A29Q-08 chr23:17744929 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:17744596 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:17710489 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:17745135 G>A did not map to a codon.
Sequencing variant TCGA-FG-A6J3-01A-11D-A31L-08 chr23:17739568 C>A did not map to a codon.
Sequencing variant TCGA-HT-8018-01A-11D-2395-08 chr23:17743967 G>T did not map to a codon.
Sequencing variant TCGA-TM-A7C4-01A-11D-A32B-08 chr23:17750477 T>C did not map to a codon.
Sequencing variant TCGA-WY-A859-01A-12D-A36O-08 chr23:17750114 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:71359882 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:49462402 G>A maps to NM_032316.3 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:236143156 G>A maps to NM_002508.2 S1158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:52535643 C>T maps to NM_007361.3 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6690-01A-11D-1893-08 chr14:52520996 G>A maps to NM_007361.3 I270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6XC-01A-12D-A32B-08 chr14:52535571 G>C maps to NM_007361.3 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:201756935 C>A maps to NM_001136039.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr12:674454 G>A maps to NM_016533.4 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:25470564 C>T maps to NM_025176.4 S514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7474-01A-11D-2024-08 chr20:25436317 C>T maps to NM_025176.4 L1316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7474-01A-11D-2024-08 chr20:25436401 C>T maps to NM_025176.4 L1288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VW-A7QS-01A-12D-A33T-08 chr20:25507064 G>T maps to NM_025176.4 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:23006490 C>T maps to NM_030922.6 W271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7877-01A-11D-2395-08 chr4:48037777 G>T maps to NM_207330.1 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7Z4-01A-11D-A34J-08 chr5:156899688 C>A maps to NM_001099287.1 I374I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5141-01A-01D-1468-08 chr5:37008731 C>G maps to NM_133433.3 S1443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:37008825 G>T did not map to a codon.
Sequencing variant TCGA-DU-7009-01A-11D-2024-08 chr5:36961656 C>T maps to NM_133433.3 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr5:36985703 C>T maps to NM_133433.3 R808*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A730-01A-11D-A32B-08 chr5:36961652 T>A maps to NM_133433.3 Y142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IY-01A-11D-A34A-08 chr5:37026329 G>A did not map to a codon.
Sequencing variant TCGA-TQ-A7RG-01A-11D-A33T-08 chr5:36976455 G>T maps to NM_133433.3 E483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W9-A837-01A-11D-A36O-08 chr5:36972045 G>A did not map to a codon.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr9:107513271 C>T maps to NM_015469.1 Y32Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:107528736 C>A maps to NM_018376.2 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A617-01A-11D-A29Q-08 chr3:52489674 C>T maps to NM_007184.3 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84J-01A-11D-A36O-08 chr3:52525404 G>T maps to NM_007184.3 R1260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:100057991 C>T maps to NM_020202.4 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr23:119077533 C>A did not map to a codon.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr23:119070600 C>A did not map to a codon.
Sequencing variant TCGA-DB-A64V-01A-11D-A29Q-08 chr6:28228313 C>T maps to NM_001007531.1 R389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7018-01A-11D-2024-08 chr6:28228258 A>G maps to NM_001007531.1 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:118724033 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:118723314 T>A did not map to a codon.
Sequencing variant TCGA-FG-A711-01A-21D-A33T-08 chr23:118725077 A>T did not map to a codon.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr23:118724015 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:42674294 A>G maps to NM_005385.3 K251K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr14:36987092 G>T maps to NM_001079668.2 S199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:36988463 G>A maps to NM_001079668.2 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66D-01A-11D-A31L-08 chr20:21492937 G>A maps to NM_002509.2 Q149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr14:37051528 C>T maps to NM_014360.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8106-01A-11D-2395-08 chr4:13543757 G>C maps to NM_001189.3 R287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:7311771 C>T maps to NM_020795.2 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:7319303 G>A maps to NM_020795.2 L504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XE-01A-11D-A27K-08 chr23:70367669 T>A did not map to a codon.
Sequencing variant TCGA-DB-A75L-01A-11D-A32B-08 chr23:70386885 A>G did not map to a codon.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr23:70389236 C>T did not map to a codon.
Sequencing variant TCGA-E1-5318-01A-01D-1468-08 chr23:70387551 G>T did not map to a codon.
Sequencing variant TCGA-TQ-A7RJ-01A-11D-A33T-08 chr23:70367806 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:5821214 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:5821134 C>T did not map to a codon.
Sequencing variant TCGA-HT-7607-01A-11D-2086-08 chr23:5811259 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:26518100 C>T maps to NM_016231.4 R431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RM-01A-11D-A33T-08 chr16:3614463 G>A maps to ENST00000448023 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66B-01A-11D-A29Q-08 chr2:32449595 A>G maps to NM_021209.4 F1007F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:32474691 C>T maps to NM_021209.4 Q747Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:32449720 G>A maps to NM_021209.4 Q966*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7013-01A-11D-2024-08 chr2:32476670 C>T did not map to a codon.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr2:32461394 G>A maps to NM_021209.4 H845H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A6MO-01A-11D-A33T-08 chr2:32476398 C>A maps to NM_021209.4 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:57092916 C>A maps to NM_032206.3 A1288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RG-01A-11D-A33T-08 chr16:57110787 G>A maps to NM_032206.3 R1603R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VW-A8FI-01A-11D-A36O-08 chr16:57054710 C>T maps to NM_032206.3 N29N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:5461657 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:5487181 C>T maps to NM_033004.3 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74H-01A-11D-A32B-08 chr19:56307588 G>A maps to NM_145007.3 S733S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr19:54299147 C>G maps to ENST00000391773 R1022R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A6S6-01A-21D-A32B-08 chr19:54314477 C>T maps to ENST00000391773 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A72U-01A-31D-A32B-08 chr19:54314081 C>T maps to ENST00000391773 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TS-01A-11D-A289-08 chr19:56421927 C>T did not map to a codon.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr11:7061016 G>A did not map to a codon.
Sequencing variant TCGA-TM-A84B-01A-11D-A36O-08 chr19:55494751 C>T maps to NM_017852.3 N562N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5277-01A-01D-1468-08 chr1:247582221 G>A maps to NM_004895.4 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr1:247608069 C>G maps to NM_004895.4 V986V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5870-01A-11D-1705-08 chr19:56369919 C>T maps to NM_134444.4 G387G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:56363644 C>T maps to NM_134444.4 Q67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:56572786 C>T maps to NM_153447.4 Q1166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:56544906 G>T did not map to a codon.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr19:56539140 C>T maps to NM_153447.4 G514G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr19:56539530 C>T maps to NM_153447.4 D644D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A615-01A-11D-A29Q-08 chr19:56515294 C>T maps to NM_153447.4 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84Q-01A-11D-A36O-08 chr19:56515393 G>A maps to NM_153447.4 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RR-01A-21D-A34A-08 chr19:56539875 G>A did not map to a codon.
Sequencing variant TCGA-WY-A85D-01A-11D-A36O-08 chr19:56538684 C>T maps to NM_153447.4 D362D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WQ-01A-12D-A34A-08 chr11:284540 C>T maps to NM_138329.1 A813A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74H-01A-11D-A32B-08 chr19:55451247 C>T maps to ENST00000446217 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7487-01A-11D-2024-08 chr19:56249566 C>A maps to NM_176820.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TX-01A-21D-A32B-08 chr19:56223199 A>G maps to NM_176820.2 L937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:119053928 G>A maps to NM_024618.2 G903G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A713-01A-11D-A32B-08 chr2:101097608 C>T maps to NM_001011717.1 R132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:43180479 C>T maps to NM_021079.3 F385F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:15170446 G>A maps to ENST00000378143 R332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:232393707 G>T maps to NM_006056.4 C8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:36151086 C>T maps to NM_005386.2 Q58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr5:43613178 A>G maps to NM_182977.2 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6403-01A-11D-1705-08 chr7:144096875 G>A maps to ENST00000467773 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr7:144096158 G>A maps to ENST00000467773 A451A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:892505 C>T maps to NM_015658.3 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:96109021 G>A maps to NM_022451.9 Y414Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:50750879 A>G maps to NM_022162.1 A875A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WQ-01A-12D-A34A-08 chr22:38084872 G>C maps to NM_024313.2 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:31685088 C>T maps to NM_003787.4 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:31684025 G>A maps to NM_003787.4 N208N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7475-01A-11D-2024-08 chr18:31709957 T>C maps to NM_003787.4 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7CF-01A-11D-A32B-08 chr18:31709984 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:33468870 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:103916957 C>T maps to ENST00000405356 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R8-01A-11D-A34J-08 chr16:18554944 A>C maps to NM_001004060.1 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:70519875 C>T did not map to a codon.
Sequencing variant TCGA-S9-A6WQ-01A-12D-A34A-08 chr23:70514289 T>C did not map to a codon.
Sequencing variant TCGA-CS-5397-01A-01D-1893-08 chr12:117705871 A>G maps to ENST00000338101 N639N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5275-01A-01D-1468-08 chr12:117768409 G>A maps to ENST00000338101 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:117655918 G>A maps to ENST00000338101 Y1441Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:117768385 G>A maps to ENST00000338101 Y163Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6394-01A-11D-1705-08 chr12:117669889 G>A maps to ENST00000338101 T1128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7013-01A-11D-2024-08 chr12:117723944 C>T maps to ENST00000338101 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74L-01A-11D-A32B-08 chr12:117701761 C>T maps to ENST00000338101 T718T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:162326910 A>G maps to NM_014697.2 Q308Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:162337148 C>T maps to NM_014697.2 D471D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:26110132 C>A did not map to a codon.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr17:26116670 G>A maps to NM_000625.4 Q52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VW-A8FI-01A-11D-A36O-08 chr17:26084289 C>T maps to NM_000625.4 L1148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:150706121 C>A maps to NM_000603.4 A739A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:50062188 G>A maps to NM_015953.3 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5390-01A-02D-1468-08 chr9:139412202 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:139396308 C>T maps to NM_017617.3 W1843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:139397729 G>A maps to NM_017617.3 Q1691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:139393413 G>A maps to NM_017617.3 N2039N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:139395021 G>A maps to NM_017617.3 D1972D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr9:139401405 G>A maps to NM_017617.3 N1221N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8322-01A-11D-2395-08 chr9:139395300 T>G did not map to a codon.
Sequencing variant TCGA-CS-6188-01A-11D-1893-08 chr1:120502126 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:15303017 G>A maps to NM_000435.2 C144C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:15291939 G>A maps to NM_000435.2 G942G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-8125-01A-11D-2253-08 chr19:15299836 G>A maps to NM_000435.2 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7C4-01A-11D-A32B-08 chr19:15284919 G>A maps to NM_000435.2 S1565S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5270-01A-02D-1468-08 chr6:32178696 G>T maps to NM_004557.3 S899S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:32163318 A>T maps to NM_004557.3 P1969P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7636-01A-11D-2086-08 chr6:32188017 G>T maps to NM_004557.3 C401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-8125-01A-11D-2253-08 chr6:32166812 G>A maps to NM_004557.3 R1475R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-8125-01A-11D-2253-08 chr6:32190324 C>T maps to NM_004557.3 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:79916836 G>A maps to NM_178493.5 N169N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:100105196 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:100104858 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:100117424 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:155761124 G>A maps to NM_015718.2 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:69329519 C>T maps to NM_024505.3 C447C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr15:69348972 G>A maps to NM_024505.3 L745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:101591353 G>A maps to NM_002518.3 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6394-01A-11D-1705-08 chr14:34263251 T>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:108068109 C>T maps to NM_002519.2 Q25Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:108059857 G>A maps to NM_002519.2 H177H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr11:108059893 T>C maps to NM_002519.2 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7Z6-01A-11D-A34J-08 chr11:108043103 A>G maps to NM_002519.2 A869A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6690-01A-11D-1893-08 chr11:108043928 A>G maps to NM_002519.2 N594N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:53853033 G>A maps to NM_005285.3 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr8:53852886 C>T maps to NM_005285.3 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr18:21114451 G>A maps to NM_000271.4 R1183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A75K-01A-11D-A32B-08 chr7:44579884 G>A maps to NM_013389.2 D37D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:44579467 G>A maps to NM_013389.2 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:44575998 C>A maps to NM_013389.2 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7637-01A-11D-2086-08 chr7:44579719 G>A maps to NM_013389.2 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6X5-01A-12D-A32B-08 chr9:139934449 C>T maps to ENST00000371600 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:72897731 G>A maps to NM_004885.2 Q38Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7875-01A-11D-2395-08 chr4:72994631 A>T maps to NM_004885.2 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:110907761 G>T maps to NM_000272.3 P441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:132408039 C>A maps to ENST00000393156 E921*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr19:36340182 G>A maps to NM_004646.3 C265C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:170827848 C>T maps to NM_002520.6 R197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F1-01A-11D-A289-08 chr1:11918782 C>T maps to NM_002521.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7480-01A-11D-2086-08 chr1:153655964 C>T maps to NM_000906.3 N459N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7609-01A-11D-2086-08 chr1:153654205 C>T maps to NM_000906.3 H354H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:35792410 G>A maps to NM_003995.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74L-01A-11D-A32B-08 chr9:35801064 A>G did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr5:32739000 C>T maps to ENST00000265074 H308H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:50385823 G>T maps to NM_006545.4 C246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:34698113 G>T maps to NM_207172.1 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7677-01A-11D-2253-08 chr7:34724168 G>A maps to NM_207172.1 E51E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:78445555 G>A maps to NM_002522.3 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A87Q-01A-11D-A36O-08 chr7:98254435 C>T maps to NM_002523.2 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A780-01A-12D-A32B-08 chr7:98256571 C>T maps to NM_002523.2 D328D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr7:24329162 G>A maps to NM_000905.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6394-01A-11D-1705-08 chr4:164247118 G>A maps to NM_000909.4 Y196Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RI-01A-11D-A33T-08 chr4:156135534 G>A maps to NM_000910.2 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr4:164271442 C>T maps to NM_006174.2 D6D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A72U-01A-31D-A32B-08 chr4:164272198 T>A maps to NM_006174.2 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:3019873 G>A maps to NM_000904.3 W227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:30327012 C>A did not map to a codon.
Sequencing variant TCGA-DU-A6S8-01A-12D-A32B-08 chr23:30327410 G>A did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr3:15065636 T>A maps to NM_003298.3 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RJ-01A-11D-A33T-08 chr6:108492764 C>T maps to ENST00000368983 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:142780044 C>T maps to NM_001024094.1 K120K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7477-01B-11D-A289-08 chr4:149075975 T>G maps to ENST00000511528 P701P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8012-01A-11D-2395-08 chr4:149075975 T>G maps to ENST00000511528 P701P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F1-01A-11D-A289-08 chr4:149075975 T>G maps to ENST00000511528 P701P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F2-01A-11D-A289-08 chr4:149075975 T>G maps to ENST00000511528 P701P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:27663749 C>T maps to ENST00000379863 V432V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:52289366 A>C maps to NM_002525.2 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:52343975 G>A maps to NM_002525.2 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YL-01A-11D-A34A-08 chr1:52260508 C>A maps to NM_002525.2 L942L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:129357078 G>A maps to ENST00000393231 T362T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:32585587 C>T maps to NM_013956.3 Y208Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:32474381 G>T maps to NM_013956.3 E161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A6ML-01A-11D-A32B-08 chr10:84733605 C>T maps to ENST00000404547 V449V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A75L-01A-11D-A32B-08 chr11:124615508 G>A maps to NM_001126181.1 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:16338403 C>A maps to NM_003489.3 E704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XE-01A-11D-A27K-08 chr23:105178374 T>A did not map to a codon.
Sequencing variant TCGA-DB-A4XF-01A-11D-A27K-08 chr23:105167229 A>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:105193585 C>A did not map to a codon.
Sequencing variant TCGA-DU-7298-01A-11D-2024-08 chr23:105167162 C>T did not map to a codon.
Sequencing variant TCGA-TQ-A7RF-01A-11D-A33T-08 chr10:33619799 G>A maps to NM_003873.5 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6X9-01A-12D-A32B-08 chr2:206628527 C>G maps to NM_201266.1 G725G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8113-01A-11D-2395-08 chr2:50723229 G>C maps to ENST00000404971 Y1001*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:79933702 C>T maps to NM_004796.4 I761I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:79746879 C>T maps to ENST00000440563 H82H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U9-01A-11D-A32B-08 chr14:79433548 A>G did not map to a codon.
Sequencing variant TCGA-DU-7299-01A-21D-2024-08 chr23:152034374 G>A did not map to a codon.
Sequencing variant TCGA-IK-8125-01A-11D-2253-08 chr23:152037636 C>T did not map to a codon.
Sequencing variant TCGA-VM-A8C8-01A-11D-A36O-08 chr23:152034433 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:44806224 C>T maps to NM_006178.2 Y611Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7469-01A-11D-2253-08 chr20:1445044 G>A maps to ENST00000476071 D44D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:59498524 G>A maps to NM_001144772.1 G858G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:27268843 C>T maps to NM_145080.3 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:72717607 G>A maps to NM_148956.2 V425V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TB-01A-11D-A33T-08 chr1:40131319 A>T maps to NM_032526.1 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:18766031 G>T maps to ENST00000455492 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:18764134 G>A maps to ENST00000455492 Y417Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:39992197 C>A maps to NM_052935.4 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5874-01A-11D-1705-08 chr12:5603653 C>T maps to NM_001102654.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7854-01A-11D-2253-08 chr12:5603796 C>T maps to NM_001102654.1 Y152Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:2093649 G>A maps to NM_002528.5 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr16:2522816 C>T maps to NM_006181.1 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8012-01A-11D-2395-08 chr1:156841488 G>A maps to NM_002529.3 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:87342788 C>T maps to NM_006180.3 D358D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:87635122 C>T maps to NM_006180.3 V725V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:88678611 C>T maps to NM_001012338.1 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5142-01A-01D-1468-08 chr2:11798781 A>T maps to NM_012344.3 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:151065933 C>T maps to ENST00000355851 N403N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:49422351 G>A maps to NM_006184.5 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R5-01A-11D-A289-08 chr19:49422369 G>T maps to NM_006184.5 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:17317742 C>T maps to ENST00000458064 D79D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:17323299 C>T maps to ENST00000458064 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6400-01A-12D-1705-08 chr23:51075879 G>A did not map to a codon.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr23:51076023 G>A did not map to a codon.
Sequencing variant TCGA-P5-A5EW-01A-11D-A27K-08 chr23:51076023 G>A did not map to a codon.
Sequencing variant TCGA-DH-A7UR-01A-11D-A33T-08 chr23:51239215 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:51239030 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:102894604 A>G maps to NM_031438.2 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:105643108 C>A did not map to a codon.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr8:21965731 C>T maps to NM_024815.3 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:33200137 T>C maps to NM_001105570.1 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:163310176 C>A maps to NM_145697.2 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:45533617 T>G maps to NM_012345.2 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:71729309 G>A maps to ENST00000393695 C305C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr11:71725527 C>T maps to ENST00000393695 A1013A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr11:71726289 T>C maps to ENST00000393695 E759E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:73750786 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:69135687 C>T maps to NM_020401.2 H866H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7Z6-01A-11D-A34J-08 chr12:69085758 G>C maps to NM_020401.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:229623231 T>C maps to NM_018230.2 K441K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:229596378 A>G maps to NM_018230.2 I941I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:17629744 C>T maps to ENST00000430136 S926S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:17706522 C>T maps to ENST00000430136 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr6:17629744 C>T maps to ENST00000430136 S926S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:37350343 T>C maps to NM_153485.1 Q249Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:37294508 G>A maps to NM_153485.1 F1284F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:47819385 G>A maps to NM_015231.1 H1078H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:47858489 G>T maps to NM_015231.1 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:131760482 C>T maps to NM_015354.1 D1135D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A614-01A-11D-A29Q-08 chr9:131768628 G>A maps to NM_015354.1 Q1685Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:135304413 C>T maps to NM_015135.2 L1403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6J1-01A-11D-A31L-08 chr7:135272652 A>G maps to NM_015135.2 E462E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr7:135298929 C>T maps to NM_015135.2 C1073C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:13381786 C>T maps to NM_024923.2 P1080P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:13373854 A>G maps to NM_024923.2 P1291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4X9-01A-11D-A26M-08 chr1:153995730 G>A maps to NM_207308.2 L1389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:154125287 A>G maps to NM_207308.2 C88C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:154127367 C>T maps to NM_207308.2 E51E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8164-01A-11D-2253-08 chr1:154062057 G>A maps to NM_207308.2 R734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4943-01A-01D-1468-08 chr9:134073212 A>G maps to ENST00000451030 Q1445Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:134021674 C>A maps to ENST00000451030 V643V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:183995272 G>A maps to NM_138285.3 Q113Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7641-01B-11D-2253-08 chr17:5312117 T>A maps to NM_002532.3 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:3697535 G>A maps to NM_016320.4 S1752S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:25914214 A>G maps to NM_014089.3 G581G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:224477368 G>A maps to NM_002533.2 H464H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7019-01A-11D-2024-08 chr19:16860739 C>T maps to ENST00000438489 F429F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7495-01A-11D-2024-08 chr19:16874670 G>A maps to ENST00000438489 T722T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8C8-01A-11D-A36O-08 chr19:16905359 C>T maps to ENST00000438489 A1100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5849-01A-11D-1705-08 chr23:102338547 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:102334162 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:102338620 C>A did not map to a codon.
Sequencing variant TCGA-TM-A84I-01A-11D-A36O-08 chr23:102339303 G>A did not map to a codon.
Sequencing variant TCGA-E1-A7YI-01A-11D-A34A-08 chr23:101092591 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:57619493 C>T maps to NM_007224.3 D297D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A6S8-01A-12D-A32B-08 chr23:108780166 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:24884335 C>T maps to NM_025081.2 D1127D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8162-01A-21D-2253-08 chr14:24884569 G>A maps to NM_025081.2 G1205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:41333678 G>T did not map to a codon.
Sequencing variant TCGA-QH-A6X9-01A-12D-A32B-08 chr23:41333726 G>A did not map to a codon.
Sequencing variant TCGA-S9-A7QY-01A-11D-A34A-08 chr23:41333635 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:120099604 G>A maps to NM_178507.2 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:121461852 G>A maps to NM_003733.2 C329C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:228524810 G>A maps to NM_001098623.1 S5548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:228402554 C>T maps to NM_001098623.1 S528S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:228543885 C>T maps to NM_052843.2 T6232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7Z2-01A-21D-A34J-08 chr1:228471426 C>T maps to NM_001098623.1 C2987C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5964-01A-11D-1705-08 chr1:228529313 G>A maps to NM_001098623.1 W6011*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6J1-01A-11D-A31L-08 chr1:228557666 C>T maps to NM_001098623.1 A6664A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RC-01A-11D-A289-08 chr1:228548162 C>T maps to NM_052843.2 R6524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A72W-01A-11D-A32B-08 chr1:228465549 C>T maps to NM_001098623.1 R2284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65R-01A-21D-A31L-08 chr1:228437882 C>T maps to NM_001098623.1 T1417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CV-01A-11D-A31L-08 chr1:228437712 C>T maps to NM_001098623.1 Q1361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84B-01A-11D-A36O-08 chr1:228564857 C>T maps to NM_001098623.1 R7715R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W9-A837-01A-11D-A36O-08 chr1:228481237 C>T maps to NM_001098623.1 R3684R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85E-01A-11D-A36O-08 chr1:228476494 C>T maps to NM_001098623.1 C3415C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:220422966 G>A maps to NM_015311.2 D1147D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F2-01A-11D-A289-08 chr2:220432494 G>A maps to NM_015311.2 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr8:133044198 C>T maps to ENST00000262283 P532P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5393-01A-01D-1468-08 chr15:28235790 G>A maps to NM_000275.2 I349I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:28273045 C>T maps to NM_000275.2 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A737-01A-11D-A32B-08 chr15:28202828 C>T maps to NM_000275.2 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CV-01A-11D-A31L-08 chr15:28259948 C>T maps to NM_000275.2 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IS-01A-11D-A34A-08 chr15:28263614 C>T maps to NM_000275.2 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:48834662 C>T maps to NM_001168254.1 R13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:68805039 G>A maps to NM_002538.2 Q41Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr23:128692668 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:128723881 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:128724231 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:128692973 T>C did not map to a codon.
Sequencing variant TCGA-HT-7609-01A-11D-2086-08 chr23:128710472 C>G did not map to a codon.
Sequencing variant TCGA-RY-A843-01A-11D-A36O-08 chr23:128703311 A>G did not map to a codon.
Sequencing variant TCGA-QH-A6X5-01A-12D-A32B-08 chr4:71063663 A>G maps to NM_017855.3 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:10582300 C>A did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:10582005 G>A maps to NM_002539.1 G321G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YJ-01A-11D-A34A-08 chr15:76018477 G>A maps to NM_175881.3 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5395-01A-01D-1468-08 chr23:123654450 C>T did not map to a codon.
Sequencing variant TCGA-CS-5396-01A-02D-1468-08 chr23:123680891 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:123517893 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:123554643 T>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:124097528 C>T did not map to a codon.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr23:123525988 A>G did not map to a codon.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr23:123785902 C>T did not map to a codon.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr23:123785887 G>A did not map to a codon.
Sequencing variant TCGA-HT-7606-01A-11D-2086-08 chr23:123525931 C>T did not map to a codon.
Sequencing variant TCGA-HT-7609-01A-11D-2086-08 chr23:123519790 C>A did not map to a codon.
Sequencing variant TCGA-HT-7902-01A-12D-2395-08 chr23:123517775 G>A did not map to a codon.
Sequencing variant TCGA-HT-8108-01A-11D-2395-08 chr23:123518057 C>T did not map to a codon.
Sequencing variant TCGA-P5-A5EX-01A-12D-A289-08 chr23:123519690 G>C did not map to a codon.
Sequencing variant TCGA-QH-A65R-01A-21D-A31L-08 chr23:123517992 C>T did not map to a codon.
Sequencing variant TCGA-QH-A870-01A-11D-A36O-08 chr23:123518248 G>A did not map to a codon.
Sequencing variant TCGA-QH-A870-01A-11D-A36O-08 chr23:123663834 T>A did not map to a codon.
Sequencing variant TCGA-S9-A6TS-01A-12D-A33T-08 chr23:123615605 C>G did not map to a codon.
Sequencing variant TCGA-S9-A6WM-01A-12D-A33T-08 chr23:123516545 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:167675249 C>T maps to NM_001122679.1 R2427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84J-01A-11D-A36O-08 chr5:167675299 G>A maps to NM_001122679.1 P2443P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:183721440 C>T maps to NM_001080477.1 P2679P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8188-01A-11D-2253-08 chr4:183609325 T>C maps to NM_001080477.1 C681C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TV-01A-12D-A34J-08 chr4:183710373 G>A maps to NM_001080477.1 L1811L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RN-01A-11D-A33T-08 chr4:183714761 C>T maps to NM_001080477.1 L2313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:78383350 A>G maps to NM_001098816.2 S1840S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:78423725 T>C maps to NM_001098816.2 T1285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:78387400 G>A maps to NM_001098816.2 A1764A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:78369120 G>A maps to NM_001098816.2 S2764S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr11:78369774 T>C maps to NM_001098816.2 T2546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:13775825 C>T did not map to a codon.
Sequencing variant TCGA-HT-7607-01A-11D-2086-08 chr23:13786332 C>T did not map to a codon.
Sequencing variant TCGA-WY-A858-01A-11D-A36O-08 chr23:13767611 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:44747185 G>A maps to ENST00000444676 S949S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:44737296 C>T maps to ENST00000444676 I773I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:44746902 C>T maps to ENST00000444676 C919C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:44739828 C>T maps to ENST00000444676 H855H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:44737281 G>A maps to ENST00000444676 T768T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr6:72011296 C>T maps to NM_024576.3 Q301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:95155415 G>A maps to NM_033014.2 R127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:70783180 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:70787570 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:70757809 G>A did not map to a codon.
Sequencing variant TCGA-DU-7006-01A-11D-2024-08 chr23:70784540 G>T did not map to a codon.
Sequencing variant TCGA-DU-7009-01A-11D-2024-08 chr23:70793626 G>A did not map to a codon.
Sequencing variant TCGA-DU-A6S7-01A-21D-A32B-08 chr23:70783245 C>T did not map to a codon.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr23:70776955 G>T did not map to a codon.
Sequencing variant TCGA-HT-7879-01A-11D-2395-08 chr23:70767812 T>G did not map to a codon.
Sequencing variant TCGA-DU-7304-01A-12D-2086-08 chr10:74673064 G>C did not map to a codon.
Sequencing variant TCGA-DB-A75L-01A-11D-A32B-08 chr19:9968435 C>A maps to NM_058164.2 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6408-01A-11D-1705-08 chr19:9965170 C>T maps to NM_058164.2 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr13:53624245 G>A maps to NM_006418.3 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YD-01A-11D-A34A-08 chr9:127563859 C>T maps to NM_182487.2 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7CA-01A-21D-A33T-08 chr1:161967951 C>T maps to ENST00000451379 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A870-01A-11D-A36O-08 chr12:10312558 G>A maps to NM_002543.3 R248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:59004855 G>A maps to NM_145243.3 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:29622719 A>G maps to NM_002544.4 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:55103709 C>T maps to NM_004852.2 H254H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:193363414 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:193333518 G>A maps to NM_130837.2 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6667-01A-12D-2024-08 chr11:132527045 C>T maps to NM_002545.3 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5847-01A-11D-1705-08 chr23:67283789 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:67417059 G>T did not map to a codon.
Sequencing variant TCGA-FG-A6J3-01A-11D-A31L-08 chr23:67273589 G>T did not map to a codon.
Sequencing variant TCGA-HT-8108-01A-11D-2395-08 chr23:67414333 G>C did not map to a codon.
Sequencing variant TCGA-P5-A5EW-01A-11D-A27K-08 chr23:67413795 T>C did not map to a codon.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr23:153416329 C>T did not map to a codon.
Sequencing variant TCGA-DU-A6S8-01A-12D-A32B-08 chr23:153418563 C>T did not map to a codon.
Sequencing variant TCGA-E1-A7YN-01A-11D-A34A-08 chr23:153421854 C>G did not map to a codon.
Sequencing variant TCGA-P5-A733-01A-11D-A32B-08 chr23:153496080 T>G did not map to a codon.
Sequencing variant TCGA-S9-A7QY-01A-11D-A34A-08 chr23:153459014 C>T did not map to a codon.
Sequencing variant TCGA-TQ-A8XE-01A-11D-A36O-08 chr23:153496072 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:241757989 G>A maps to NM_014322.2 R317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:88414582 C>T maps to NM_001030015.2 Q15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8162-01A-21D-2253-08 chr10:88418310 C>T maps to NM_001030015.2 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65S-01A-11D-A29Q-08 chr10:88418274 T>C maps to NM_001030015.2 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6405-01A-11D-1705-08 chr6:47754300 C>T maps to ENST00000489301 R61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:29185540 G>A maps to NM_000911.3 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KT-A7W1-01A-11D-A34A-08 chr8:54142150 G>A maps to NM_000912.3 F283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A89Z-01A-11D-A36O-08 chr6:154412153 T>A maps to NM_001145279.1 C330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:203472683 C>T maps to NM_014359.3 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7638-01B-11D-2086-08 chr11:123886808 C>T maps to NM_001004462.1 Y176Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr11:123886715 C>T maps to NM_001004462.1 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4X9-01A-11D-A26M-08 chr11:123909444 G>C maps to NM_001004463.1 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr11:123909048 G>A maps to NM_001004463.1 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7692-01A-12D-2253-08 chr11:123901192 C>T maps to ENST00000375021 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:123894465 C>T maps to NM_001001953.1 C249C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr19:15918655 G>A maps to NM_013940.2 C64C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QZ-01A-12D-A34J-08 chr19:15918424 G>A maps to NM_013940.2 C141C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YV-01A-11D-A34J-08 chr19:15905374 G>T maps to NM_001004466.1 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A83X-01A-11D-A36O-08 chr19:15905217 C>T maps to NM_001004466.1 Y120Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5854-01A-11D-1705-08 chr1:159283477 C>T maps to NM_001004467.1 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TS-01A-12D-A33T-08 chr1:159284143 G>T maps to NM_001004467.1 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7Z4-01A-11D-A34J-08 chr1:159504969 C>T maps to NM_001004469.1 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:57995807 G>A maps to NM_001004471.2 N180N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TT-01A-11D-A289-08 chr1:158449813 A>G maps to NM_001004472.1 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85D-01A-11D-A36O-08 chr1:158450563 G>A maps to NM_001004472.1 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:59480454 G>T maps to NM_001005324.1 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VW-A7QS-01A-12D-A33T-08 chr1:158549194 G>A maps to NM_001004477.1 C165C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5874-01A-11D-1705-08 chr14:20666310 A>T maps to NM_001005503.1 R273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:20692851 C>T maps to NM_001004480.1 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TU-01A-12D-A32B-08 chr1:248004292 T>C maps to NM_001001959.1 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7676-01A-11D-2395-08 chr10:45799360 G>A maps to NM_001004297.2 C170C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:107367203 G>A maps to NM_001004481.1 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8011-01A-11D-2395-08 chr9:107298218 C>T maps to NM_001001961.1 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A737-01A-11D-A32B-08 chr9:107361001 C>T maps to NM_001004482.1 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TT-01A-11D-A289-08 chr9:107331777 G>A maps to NM_001004483.1 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76R-01A-11D-A32B-08 chr9:107332224 C>T maps to NM_001004483.1 Y259Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6UB-01A-21D-A33T-08 chr9:107266929 C>T maps to NM_001004485.1 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:247836049 G>T maps to NM_001005487.1 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7882-01A-11D-2395-08 chr1:247835491 C>T maps to NM_001005487.1 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8109-01A-11D-2395-08 chr1:247835569 G>T maps to NM_001005487.1 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QY-01A-11D-A34A-08 chr9:35869708 C>T maps to NM_001004487.1 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:248845563 C>T maps to NM_001004734.1 E14E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6668-01A-11D-1893-08 chr17:3119075 C>T maps to NM_014565.2 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64R-01A-11D-A29Q-08 chr17:3119150 T>C maps to NM_014565.2 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7018-01A-11D-2024-08 chr17:3119138 G>A maps to NM_014565.2 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8013-01A-11D-2395-08 chr17:3100859 A>G maps to NM_012352.1 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6X9-01A-12D-A32B-08 chr17:3101423 C>T maps to NM_012352.1 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WL-01A-21D-A33T-08 chr17:3101420 C>T maps to NM_012352.1 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:3336706 G>A maps to NM_003554.1 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6394-01A-11D-1705-08 chr9:125273991 C>A maps to NM_054107.1 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A6S7-01A-21D-A32B-08 chr9:125486747 C>T maps to NM_001005235.1 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:9204426 C>T maps to ENST00000305465 C172C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:9204456 C>T maps to ENST00000305465 C182C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr19:9204447 C>T maps to ENST00000305465 H179H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6UA-01A-12D-A33T-08 chr19:9204099 C>A maps to ENST00000305465 Y63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:125289053 A>G maps to ENST00000359439 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:125315825 C>T maps to NM_001004457.1 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:125377138 C>T maps to NM_012364.1 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A72Z-01A-11D-A32B-08 chr7:143826708 C>T maps to NM_001001659.1 C168C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A780-01A-12D-A32B-08 chr7:143771699 C>T maps to NM_001004488.1 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7Z2-01A-21D-A34J-08 chr7:143748418 A>C maps to NM_012365.1 R309R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A72Z-01A-11D-A32B-08 chr7:143748006 C>T maps to NM_012365.1 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RH-01A-12D-A34A-08 chr7:143956628 G>A maps to NM_001005328.1 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QW-01A-11D-A34A-08 chr7:99474197 G>A maps to NM_001005276.1 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6666-01A-11D-1893-08 chr11:6806339 T>C maps to NM_001004489.2 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7606-01A-11D-2086-08 chr11:6789588 G>A maps to NM_001004490.1 Y200Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TS-01A-12D-A33T-08 chr11:6789588 G>A maps to NM_001004490.1 Y200Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:27880069 G>A maps to NM_033057.2 Q10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6290-01A-11D-1705-08 chr6:27925798 C>T maps to NM_012367.1 Q261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:247695567 G>A maps to NM_198074.4 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84T-01A-11D-A36O-08 chr1:247695156 G>A maps to NM_198074.4 Y219Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5847-01A-11D-1705-08 chr11:6913293 T>C maps to NM_003700.1 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:6913226 G>A maps to NM_003700.1 R169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:143657788 C>A maps to NM_012369.2 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr1:247769423 C>T maps to NM_001001914.1 C179C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7637-01A-11D-2086-08 chr1:248685219 C>T maps to NM_001013355.1 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr1:248685543 C>T maps to NM_001013355.1 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6397-01A-11D-1705-08 chr6:29556083 C>T maps to NM_007160.3 Y121Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:29079846 A>T maps to NM_001005216.2 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:29079849 A>C maps to NM_001005216.2 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6X9-01A-12D-A32B-08 chr1:248224012 T>C maps to NM_001004687.1 D10D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6188-01A-11D-1893-08 chr1:248112251 T>C maps to NM_001001963.1 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A77X-01A-11D-A32B-08 chr1:248366668 A>G maps to NM_001004689.1 Q100Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:248308746 C>T maps to NM_001004690.1 Q100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr1:248309135 A>T maps to NM_001004690.1 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8319-01A-11D-2395-08 chr1:248570029 C>T maps to NM_030904.1 Y245Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:248756343 G>T maps to NM_001004693.1 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:248756982 C>T maps to NM_001004693.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:248789940 G>A maps to NM_001001964.1 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7008-01A-11D-2024-08 chr1:248789592 C>T maps to NM_001001964.1 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A730-01A-11D-A32B-08 chr1:248789592 C>T maps to NM_001001964.1 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8163-01A-11D-2253-08 chr1:248458715 C>T maps to NM_001004692.1 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YL-01A-11D-A34A-08 chr1:248458220 G>A maps to NM_001004692.1 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4X9-01A-11D-A26M-08 chr1:248616319 C>T maps to NM_001004136.1 Y74Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84J-01A-11D-A36O-08 chr1:248813321 G>C maps to NM_001001824.1 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr1:248637421 C>T maps to NM_001005495.1 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74K-01A-11D-A32B-08 chr1:248637376 C>T maps to NM_001005495.1 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr1:248637145 C>T maps to NM_001005495.1 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr1:248737287 G>A maps to NM_001001821.1 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EY-01A-11D-A27K-08 chr1:248801911 C>G maps to NM_001001827.1 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7C3-01A-11D-A32B-08 chr1:248525694 C>A maps to NM_001004696.1 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A711-01A-21D-A33T-08 chr1:248651993 C>A maps to NM_001004697.1 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6188-01A-11D-1893-08 chr1:248084418 T>C maps to NM_001005522.1 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8163-01A-11D-2253-08 chr1:248084483 G>A maps to NM_001005522.1 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8186-01A-11D-2253-08 chr5:180166656 G>T maps to NM_001001657.1 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr19:8841994 C>A maps to NM_001004699.1 S202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7019-01A-11D-2024-08 chr17:3181605 G>A maps to NM_002551.3 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YM-01A-11D-A34A-08 chr17:3324352 C>T maps to NM_012373.2 N164N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A618-01A-11D-A29Q-08 chr11:55136012 C>A maps to NM_001005275.1 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr11:55110939 C>T maps to NM_001005274.1 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6J1-01A-11D-A31L-08 chr11:55111416 C>T maps to NM_001005274.1 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A847-01A-11D-A36O-08 chr11:48510451 C>A maps to NM_001005512.2 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7634-01A-11D-2086-08 chr11:51411930 C>T maps to NM_001005272.3 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TS-01A-12D-A33T-08 chr11:55371228 A>G maps to NM_001004700.1 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YM-01A-11D-A34A-08 chr11:50003755 C>T maps to NM_001005270.2 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EU-01A-11D-A27K-08 chr11:49974105 G>T maps to NM_001001955.2 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84O-01A-11D-A36O-08 chr11:49974111 C>T maps to NM_001001955.2 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RF-01A-11D-A33T-08 chr11:49974720 T>C maps to NM_001001955.2 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7902-01A-12D-2395-08 chr11:55339752 C>T maps to NM_001004701.2 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CZ-01A-11D-A32B-08 chr11:55339920 C>A maps to NM_001004701.2 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R7-01A-11D-A34J-08 chr11:51515454 C>A maps to NM_001004703.1 Y58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74H-01A-11D-A32B-08 chr11:55433100 C>T maps to NM_001004704.1 H153H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R2-01A-21D-A34J-08 chr11:55433373 G>T maps to NM_001004704.1 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:59245180 C>A maps to NM_001004705.1 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QY-01A-11D-A34A-08 chr11:123811090 C>T maps to NM_001001965.1 Y256Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7475-01A-11D-2024-08 chr11:59224534 G>T maps to NM_001004708.1 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IX-01A-12D-A34A-08 chr11:59282741 G>A maps to NM_001004711.1 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84Q-01A-11D-A36O-08 chr14:20404019 T>C maps to NM_001004063.2 N65N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:20443742 A>G maps to NM_001005486.1 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:20344653 C>T maps to NM_001005501.1 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7480-01A-11D-2086-08 chr14:20345253 C>A maps to NM_001005501.1 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:20389535 C>A maps to NM_001005483.1 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A75L-01A-11D-A32B-08 chr14:20248552 A>G maps to NM_001005500.1 Q24Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:20249131 C>A maps to NM_001005500.1 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:20248801 T>G maps to NM_001005500.1 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7882-01A-11D-2395-08 chr11:55406510 C>A maps to NM_001004124.1 Y226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QY-01A-11D-A34A-08 chr11:48328583 C>T maps to NM_001004725.1 I270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr11:48286041 C>T maps to NM_001004726.1 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr11:48266711 C>T maps to NM_001004727.1 C19C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7470-01A-12D-2086-08 chr11:48266882 T>C maps to NM_001004727.1 D76D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A669-01A-12D-A31L-08 chr11:5364388 A>T maps to NM_001005567.1 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YM-01A-11D-A34A-08 chr11:4703776 G>A maps to NM_030774.3 H55H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YN-01A-11D-A34A-08 chr11:4842971 C>T maps to NM_001004753.1 H119H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FN-7833-01A-11D-2086-08 chr11:4842845 C>T maps to NM_001004753.1 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr11:4944909 G>A maps to NM_001005237.1 Y220Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RM-01A-11D-A33T-08 chr11:5462402 T>A maps to NM_001005288.2 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr11:5020871 T>C maps to NM_001004755.1 Y220Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8319-01A-11D-2395-08 chr11:5021018 T>C maps to NM_001004755.1 H269H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:5410780 C>A maps to NM_001004756.2 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RH-01A-12D-A34A-08 chr11:4869859 A>T maps to NM_001004758.1 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr11:4903764 C>T maps to NM_001004759.1 D239D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85B-01A-11D-A36O-08 chr11:4903764 C>T maps to NM_001004759.1 D239D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64W-01A-11D-A29Q-08 chr11:4388940 T>C maps to NM_001005161.3 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:5080058 G>A maps to NM_001005164.2 R267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CV-01A-11D-A31L-08 chr11:5080740 G>A maps to NM_001005164.2 I39I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:5906256 T>C maps to NM_001005165.1 H245H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8161-01A-11D-2253-08 chr11:5906224 C>T maps to NM_001005165.1 R235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84H-01A-11D-A36O-08 chr11:5906364 T>C maps to NM_001005165.1 Y281Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TI-01A-11D-A33T-08 chr11:5878092 T>A maps to NM_001005168.1 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7470-01A-12D-2086-08 chr11:5878263 A>C maps to NM_001005168.1 Y223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr11:4615306 T>C maps to ENST00000450052 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6IZ-01A-11D-A31L-08 chr11:4510366 G>A maps to NM_001005171.2 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:6221304 C>T maps to NM_001005178.1 N284N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A61C-01A-11D-A29Q-08 chr11:6023640 G>A maps to NM_001005179.2 D246D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CF-01A-11D-A36O-08 chr11:59210796 C>T maps to NM_001004728.1 I52I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74K-01A-11D-A32B-08 chr3:97806630 T>A maps to NM_054106.1 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8563-01A-11D-2395-08 chr11:59132062 C>T maps to NM_001004729.1 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U9-01A-11D-A32B-08 chr11:56409456 G>C maps to NM_001002925.1 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VV-A829-01A-21D-A36O-08 chr11:55797923 T>C maps to NM_001001921.1 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A711-01A-21D-A33T-08 chr11:58207288 G>C maps to NM_001004733.2 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:58190026 C>T maps to NM_001005566.2 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YS-01A-11D-A34A-08 chr11:58190260 A>G maps to NM_001005566.2 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TJ-01A-11D-A34J-08 chr9:125551963 C>T maps to NM_001001923.1 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:55541188 A>G maps to NM_001001967.1 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:55541338 C>A maps to NM_001001967.1 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:55541584 C>T maps to NM_001001967.1 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr11:55563531 G>T maps to NM_001004735.1 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6X3-01A-21D-A32B-08 chr11:55563198 A>G maps to NM_001004735.1 K56K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr11:55587485 T>A maps to ENST00000395203 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A87Q-01A-11D-A36O-08 chr11:55587764 G>A maps to ENST00000395203 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F4-01A-11D-A289-08 chr11:55587451 T>G maps to ENST00000395203 L118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:55761474 C>T maps to NM_003697.1 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:55762080 G>T maps to NM_003697.1 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7US-01A-11D-A33T-08 chr3:97868351 G>A maps to NM_001005514.1 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CX-01A-11D-A32B-08 chr3:97868981 C>A maps to NM_001005514.1 Y251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:97888394 G>A maps to NM_001005515.1 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7469-01A-11D-2253-08 chr3:97887872 A>T maps to NM_001005515.1 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5322-01A-01D-1468-08 chr3:97983514 T>C maps to NM_001005479.1 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:98188701 C>A maps to NM_001004736.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TS-01A-11D-A289-08 chr3:98188704 T>C maps to NM_001004736.2 Y95Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7475-01A-11D-2024-08 chr11:56237958 G>A maps to NM_001004742.1 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WO-01A-21D-A34A-08 chr11:56237367 G>C maps to NM_001004742.1 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5273-01A-01D-1468-08 chr11:56258828 C>T maps to NM_001005282.1 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:56258290 G>A maps to NM_001005282.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7CA-01A-21D-A33T-08 chr11:56258357 G>T maps to NM_001005282.1 Y163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CF-01A-11D-A36O-08 chr11:56230094 G>C maps to NM_001004743.1 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr11:56185614 A>G maps to NM_001004744.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RK-01A-11D-A33T-08 chr11:56043713 T>C maps to NM_001004745.1 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:29323528 G>T maps to NM_030876.5 C148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:55715120 C>A maps to NM_001005182.1 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7858-01A-11D-2395-08 chr12:55846752 C>T maps to NM_054105.1 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:55725687 C>A maps to NM_054104.1 I68I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A858-01A-11D-A36O-08 chr12:55725990 C>T maps to NM_054104.1 N169N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:55641850 C>A maps to NM_001005490.1 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MT-01A-11D-A26M-08 chr1:247875305 C>T maps to NM_001005286.1 W251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:158687329 C>T maps to ENST00000368146 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr11:123676271 G>A maps to NM_001005325.1 N262N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7491-01A-11D-2024-08 chr11:57798999 G>A maps to NM_001005186.2 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6X9-01A-12D-A32B-08 chr14:21109289 C>A maps to NM_001001968.1 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:123813654 C>T maps to NM_001005187.1 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:142749946 C>T maps to NM_001001667.1 D170D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:14952326 G>A maps to NM_001005190.1 D121D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8105-01A-11D-2395-08 chr19:14938183 A>G maps to NM_017506.1 Y290Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr19:15052350 C>T maps to NM_012377.1 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:9297233 C>T maps to NM_175883.2 H259H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7692-01A-12D-2253-08 chr19:9296886 C>T maps to NM_175883.2 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CW-01A-11D-A32B-08 chr11:124190081 T>G maps to NM_001002918.1 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A83Z-01A-11D-A36O-08 chr11:56058376 C>T maps to NM_001005199.1 Q54Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6X9-01A-12D-A32B-08 chr11:55890586 G>T maps to NM_001005201.1 G247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6542-01A-11D-1893-08 chr11:55861307 T>C maps to NM_001003750.1 H175H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7472-01A-11D-2024-08 chr11:55861580 G>A maps to NM_001003750.1 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RC-01A-11D-A289-08 chr11:55904471 G>A maps to NM_001004064.1 C241C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EZ-7264-01A-11D-2024-08 chr11:56086682 C>T maps to NM_001005202.1 R301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7008-01A-11D-2024-08 chr7:142723664 G>A maps to NM_001001658.1 C185C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76K-01A-11D-A33T-08 chr7:142723327 G>A maps to NM_001001658.1 R298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:141618740 A>G maps to NM_001001656.1 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-7675-01A-11D-2086-08 chr11:56468237 C>T maps to NM_001013358.1 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WP-01A-12D-A34A-08 chr11:56468108 G>C maps to NM_001013358.1 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr11:56511044 C>G maps to NM_001005284.1 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8319-01A-11D-2395-08 chr11:56510828 G>A maps to NM_001005284.1 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RO-01A-11D-A33T-08 chr11:57947746 C>T maps to NM_001005212.3 Y277Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64R-01A-11D-A29Q-08 chr7:102087147 G>A maps to NM_032831.2 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:102087138 C>T maps to NM_032831.2 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:52861729 G>A maps to NM_004153.3 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:88331703 G>A maps to NM_181837.2 A386A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YE-01A-11D-A34A-08 chr6:88374459 G>C did not map to a codon.
Sequencing variant TCGA-DU-7015-01A-11D-2024-08 chr2:148716408 G>A maps to NM_181742.3 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:103828794 A>T maps to NM_002553.3 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:59344073 C>T maps to NM_002556.2 W800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:31289152 G>A maps to NM_030758.3 K638K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:31286929 C>T maps to NM_030758.3 D613D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:31302205 G>A maps to NM_030758.3 T877T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:60859100 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:24839810 G>A maps to NM_015550.2 V885V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RQ-01A-11D-A33T-08 chr11:3128639 C>T maps to NM_020896.3 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:179247886 C>A maps to ENST00000392505 V611V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:45890676 G>A maps to NM_145798.2 Y564Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:45886547 G>A maps to NM_145798.2 G688G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A710-01A-12D-A33T-08 chr12:76881290 G>T maps to NM_020841.4 S14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74H-01A-11D-A32B-08 chr1:52252271 C>T maps to ENST00000428468 N661N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QW-01A-11D-A34A-08 chr19:54600416 C>T maps to NM_130771.3 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr5:38923282 C>T maps to NM_003999.2 F599F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5874-01A-11D-1705-08 chr8:99962882 G>A did not map to a codon.
Sequencing variant TCGA-TM-A84O-01A-11D-A36O-08 chr8:99961350 G>A maps to ENST00000457907 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5965-01B-11D-1893-08 chr9:77752521 T>G maps to NM_012383.4 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:26688592 G>A maps to NM_194248.2 N1582N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YJ-01A-11D-A34A-08 chr2:26700045 C>T maps to NM_194248.2 A839A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:26700617 C>T maps to NM_194322.2 Q48Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7290-01A-11D-2024-08 chr4:4214702 G>A maps to NM_177998.1 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EU-01A-11D-A27K-08 chr2:241079505 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:146067418 G>A maps to ENST00000447906 S474S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr4:146058890 A>C maps to ENST00000447906 V1012V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:48780952 C>A did not map to a codon.
Sequencing variant TCGA-DU-7018-01A-11D-2024-08 chr23:48791844 G>A did not map to a codon.
Sequencing variant TCGA-S9-A6U2-01A-21D-A33T-08 chr23:48792063 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:69282891 G>A did not map to a codon.
Sequencing variant TCGA-P5-A733-01A-11D-A32B-08 chr23:69282577 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:92090720 G>A maps to NM_016023.3 Q181Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:31862286 G>A maps to ENST00000382902 R89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RM-01A-11D-A33T-08 chr1:149919214 G>A maps to NM_020205.2 V420V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RG-01A-11D-A33T-08 chr2:63283168 G>A maps to NM_014562.3 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr17:1946241 G>A maps to NM_080822.2 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:42991052 C>T maps to NM_148962.4 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:107722881 C>T maps to NM_001198533.1 R553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A731-01A-11D-A32B-08 chr8:107704966 C>T maps to NM_001198533.1 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TP-01A-11D-A289-08 chr3:25833093 C>T maps to NM_017897.2 R195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:121605289 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:151056189 G>T maps to NM_022788.3 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:72945749 C>A maps to NM_176071.1 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6405-01A-11D-1705-08 chr11:72945404 G>A maps to NM_176071.1 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:69479339 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:69478905 C>T did not map to a codon.
Sequencing variant TCGA-S9-A6WM-01A-12D-A33T-08 chr23:69478763 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:73007688 G>A maps to NM_004154.3 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:1585027 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:1584700 C>T did not map to a codon.
Sequencing variant TCGA-QH-A6X5-01A-12D-A32B-08 chr23:1584768 C>G did not map to a codon.
Sequencing variant TCGA-S9-A7IS-01A-11D-A34A-08 chr23:1585385 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:131554262 C>T maps to NM_001142599.1 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:79803049 G>A maps to NM_000918.3 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5874-01A-11D-1705-08 chr12:56504239 C>T maps to NM_006191.2 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7309-01A-11D-2086-08 chr12:56501318 A>G maps to NM_006191.2 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TP-01A-11D-A289-08 chr12:56504344 C>T maps to NM_006191.2 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr20:43560999 A>G maps to NM_001124756.1 A419A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:90691272 G>T did not map to a codon.
Sequencing variant TCGA-TQ-A7RM-01A-11D-A33T-08 chr23:90691182 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:23793492 C>A maps to NM_004643.3 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:163510400 C>T maps to NM_152410.2 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr4:20715161 C>T maps to ENST00000503585 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr6:34498364 G>A did not map to a codon.
Sequencing variant TCGA-HW-8320-01A-11D-2395-08 chr11:47202191 C>T maps to NM_016223.4 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:17413087 G>A maps to NM_007365.2 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F2-01A-11D-A289-08 chr1:17418909 G>A maps to NM_007365.2 Y216Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:39880394 G>A maps to NM_019088.2 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A75O-01A-11D-A32B-08 chr8:81897058 C>T maps to NM_018440.3 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr23:49455851 C>T did not map to a codon.
Sequencing variant TCGA-R8-A73M-01A-11D-A32B-08 chr23:49459348 A>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:103310896 C>T maps to NM_000277.1 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:77090937 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:110388119 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:110406217 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:110391029 G>T did not map to a codon.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr23:110385377 A>G did not map to a codon.
Sequencing variant TCGA-FG-A4MY-01A-11D-A26M-08 chr23:110385327 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:40564516 C>A maps to NM_020168.4 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6IZ-01A-11D-A31L-08 chr15:40564819 C>T maps to NM_020168.4 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:23641563 G>T maps to NM_024675.3 P637P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8109-01A-11D-2395-08 chr16:23646264 A>G maps to NM_024675.3 S534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:169432879 C>A maps to NM_001166108.1 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:746642 C>T maps to NM_002579.2 I331I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WI-01A-21D-A33T-08 chr9:112686116 G>A maps to NM_007203.4 K120K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CV-01A-11D-A31L-08 chr11:35463134 G>A maps to NM_015430.2 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:56716230 G>A maps to NM_001127460.2 D895D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:3888789 G>A maps to NM_153638.2 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:50617666 C>T maps to NM_052839.3 F665F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:50257162 C>T maps to NM_001040284.2 R401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:73721703 G>A maps to ENST00000427855 T535T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:97002274 G>A maps to NM_032632.3 Q323Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:96994340 G>T maps to NM_032632.3 E165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr9:118949844 C>T maps to NM_002581.3 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr9:119097281 C>A maps to NM_002581.3 S1180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr1:176525626 C>T maps to NM_020318.2 R57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6IZ-01A-11D-A31L-08 chr1:176525559 G>A maps to NM_020318.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:3021867 C>T maps to NM_152341.3 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:26189403 C>T maps to NM_178422.5 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:26190159 G>A maps to NM_178422.5 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:26189631 C>T maps to NM_178422.5 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QW-01A-11D-A34A-08 chr6:52268805 C>T maps to ENST00000361841 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:142681701 C>T maps to NM_198504.2 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:34688289 G>A maps to NM_019619.3 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7J0-01A-11D-A34A-08 chr20:49366586 C>T maps to NM_032521.2 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:77918259 G>A maps to NM_032510.3 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8012-01A-11D-2395-08 chr6:161781237 C>T did not map to a codon.
Sequencing variant TCGA-DH-A7UR-01A-11D-A33T-08 chr1:8037766 C>T maps to NM_001123377.1 H126H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:183585820 G>A maps to NM_018622.5 C51C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr3:183580580 C>T maps to NM_018622.5 K157K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:226552831 G>A maps to NM_001618.3 G843G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr8:145058233 G>A maps to NM_032789.3 N573N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:122351053 C>T maps to NM_001113523.1 Y520Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5275-01A-01D-1468-08 chr14:20818732 G>T maps to NM_005484.3 E138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:51979068 C>T maps to NM_001003931.2 F237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VW-A7QS-01A-12D-A33T-08 chr3:51979051 C>T maps to NM_001003931.2 Q232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:25009093 G>A maps to NM_006437.3 P1395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:25029233 C>T maps to NM_006437.3 L893L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:50123878 C>A maps to ENST00000505697 T693T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8C9-01A-11D-A36O-08 chr3:122274171 C>T maps to NM_031458.2 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-8125-01A-11D-2253-08 chr22:44489820 G>A maps to NM_001003828.1 Q75Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RG-01A-11D-A33T-08 chr22:44583735 G>A maps to NM_001137606.1 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R9-01A-11D-A289-08 chr23:150793998 T>C did not map to a codon.
Sequencing variant TCGA-RY-A845-01A-11D-A36O-08 chr23:150842517 A>G did not map to a codon.
Sequencing variant TCGA-S9-A6WQ-01A-12D-A34A-08 chr23:150790021 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:242075445 A>C maps to ENST00000358649 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:242066234 G>A maps to ENST00000358649 L699L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:59420448 G>A maps to NM_152716.2 H388H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:127252040 C>T maps to NM_006193.2 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8163-01A-11D-2253-08 chr11:31816307 T>C maps to NM_001604.4 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:27668568 G>A maps to NM_018492.2 D226D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:27680706 C>T maps to NM_018492.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5394-01A-01D-1468-08 chr3:52621371 G>C maps to ENST00000296302 V1040V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A669-01A-12D-A31L-08 chr3:52643672 C>T maps to ENST00000296302 P741P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5849-01A-11D-1705-08 chr3:52643531 T>A maps to ENST00000296302 S788S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:52637554 G>A maps to ENST00000296302 R921*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8158-01A-11D-2253-08 chr3:52597304 G>A maps to ENST00000296302 P1360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7604-01A-11D-2086-08 chr6:32157563 C>A maps to NM_002586.4 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8187-01A-11D-2253-08 chr19:19672910 G>A maps to NM_025245.1 Q350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:66617326 G>A maps to NM_022172.2 L968L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:72644920 G>A maps to NM_000281.2 N68N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:53865486 G>A maps to NM_005016.5 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:53861625 G>A maps to NM_005016.5 W279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:101182404 C>T maps to NM_000282.3 L724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CE-01A-11D-A36O-08 chr4:134072584 C>A maps to NM_032961.1 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr23:91090534 C>T did not map to a codon.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr23:91133711 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:91134163 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:91132649 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:91873474 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:91090697 A>G did not map to a codon.
Sequencing variant TCGA-DU-6400-01A-12D-1705-08 chr23:91090709 C>T did not map to a codon.
Sequencing variant TCGA-E1-A7YV-01A-11D-A34J-08 chr23:91642840 C>T did not map to a codon.
Sequencing variant TCGA-HT-7882-01A-11D-2395-08 chr23:91133910 C>A did not map to a codon.
Sequencing variant TCGA-HT-8018-01A-11D-2395-08 chr23:91134294 C>A did not map to a codon.
Sequencing variant TCGA-HT-8110-01A-11D-2395-08 chr23:91133711 G>A did not map to a codon.
Sequencing variant TCGA-CS-4943-01A-01D-1468-08 chr24:5369104 G>T did not map to a codon.
Sequencing variant TCGA-DU-6393-01A-11D-1705-08 chr24:5605957 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:55663125 A>G maps to NM_001142763.1 N1131N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:138442722 C>T maps to NM_019035.3 T956T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:99551660 C>A did not map to a codon.
Sequencing variant TCGA-DU-6403-01A-11D-1705-08 chr23:99662057 C>A did not map to a codon.
Sequencing variant TCGA-E1-5319-01A-01D-1893-08 chr23:99662275 G>A did not map to a codon.
Sequencing variant TCGA-E1-A7YQ-01A-11D-A34J-08 chr23:99661864 T>C did not map to a codon.
Sequencing variant TCGA-FG-A4MX-01A-11D-A26M-08 chr23:99551564 G>A did not map to a codon.
Sequencing variant TCGA-HT-7476-01A-11D-2024-08 chr23:99662027 T>C did not map to a codon.
Sequencing variant TCGA-HT-7609-01A-11D-2086-08 chr23:99661765 G>A did not map to a codon.
Sequencing variant TCGA-HT-7874-01A-11D-2395-08 chr23:99662609 T>C did not map to a codon.
Sequencing variant TCGA-QH-A65S-01A-11D-A29Q-08 chr23:99662600 A>G did not map to a codon.
Sequencing variant TCGA-R8-A73M-01A-11D-A32B-08 chr23:99662866 G>A did not map to a codon.
Sequencing variant TCGA-S9-A6U1-01A-21D-A33T-08 chr23:99662843 G>A did not map to a codon.
Sequencing variant TCGA-HT-7469-01A-11D-2253-08 chr13:61986932 G>A maps to NM_022843.3 N433N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr4:30723436 C>G maps to NM_001173523.1 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A83Y-01A-11D-A36O-08 chr4:30921803 G>A maps to NM_001173523.1 V1068V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7CA-01A-21D-A33T-08 chr4:31144317 G>T maps to NM_001173523.1 L1205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7634-01A-11D-2086-08 chr13:67800157 T>C maps to NM_203487.2 Q805Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:140167236 G>A maps to NM_018900.2 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:140167107 C>T maps to NM_018900.2 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RG-01A-11D-A33T-08 chr5:140166993 C>T maps to NM_018900.2 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:140236493 G>A maps to NM_018901.2 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:140235800 G>A maps to NM_018901.2 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YM-01A-11D-A34A-08 chr5:140237072 C>T maps to NM_018901.2 D480D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8113-01A-11D-2395-08 chr5:140237336 C>G maps to NM_018901.2 P568P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5870-01A-11D-1705-08 chr5:140249977 T>C maps to NM_018902.3 G430G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:140249194 C>A maps to NM_018902.3 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:140250149 C>T maps to NM_018902.3 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:140250250 G>A maps to NM_018902.3 P521P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7695-01A-11D-2253-08 chr5:140263553 G>A maps to NM_018904.2 T567T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6402-01A-11D-1705-08 chr5:140176069 C>T maps to NM_018905.2 Y507Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A61B-01A-11D-A29Q-08 chr5:140176510 C>T maps to NM_018905.2 H654H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:140182353 C>T maps to NM_018906.2 D524D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:140182644 G>A maps to NM_018906.2 P621P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7299-01A-21D-2024-08 chr5:140181906 C>T maps to NM_018906.2 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr5:140182209 G>T maps to NM_018906.2 T476T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A710-01A-12D-A33T-08 chr5:140182635 G>A maps to NM_018906.2 A618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8106-01A-11D-2395-08 chr5:140181051 A>C maps to NM_018906.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr5:140182695 C>T maps to NM_018906.2 D638D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:140203006 G>A maps to NM_018908.2 T549T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VW-A8FI-01A-11D-A36O-08 chr5:140203423 C>T maps to NM_018908.2 P688P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YU-01A-11D-A34J-08 chr5:140207759 C>T maps to NM_018909.2 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:140214408 G>A maps to NM_018910.2 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8165-01A-11D-2253-08 chr5:140214297 G>T maps to NM_018910.2 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CS-01A-11D-A31L-08 chr5:140215320 C>T maps to NM_018910.2 N451N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:140222792 C>T maps to NM_018911.2 G629G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RW-01A-11D-A33T-08 chr5:140230179 G>C maps to NM_031857.1 L700L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:140307658 C>A maps to NM_018898.3 Y394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:140347584 C>T maps to NM_018899.5 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:140347265 G>A maps to NM_018899.5 R305R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:140431570 G>A maps to NM_013340.2 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:140574227 G>A maps to NM_018930.3 S701S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:140589846 C>T maps to NM_018932.3 Y456Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:140590515 C>T maps to NM_018932.3 A679A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:140604399 C>T maps to NM_018934.2 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:140627341 T>C maps to NM_018935.2 F732F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A60L-01A-12D-A31L-08 chr5:140626621 G>A maps to NM_018935.2 P492P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:140562775 G>A maps to NM_020957.1 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5849-01A-11D-1705-08 chr5:140474487 C>T maps to NM_018936.2 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:140474605 C>T maps to NM_018936.2 Q78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:140475744 C>A maps to NM_018936.2 S457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6402-01A-11D-1705-08 chr5:140475879 C>T maps to NM_018936.2 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66B-01A-11D-A29Q-08 chr5:140502917 C>T maps to NM_018938.2 N446N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A870-01A-11D-A36O-08 chr5:140503913 C>G maps to NM_018938.2 T778T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:140516911 C>T maps to NM_015669.2 R632R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:140553825 C>T maps to NM_018940.2 I470I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:140554317 C>T maps to NM_018940.2 D634D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:140554239 G>A maps to NM_018940.2 K608K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:140552832 C>A maps to NM_018940.2 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XC-01A-11D-A26M-08 chr5:140710808 C>T maps to NM_018912.2 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YJ-01A-11D-A34A-08 chr5:140712440 C>T maps to NM_018912.2 G730G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EW-01A-11D-A27K-08 chr5:140711255 C>A maps to NM_018912.2 I335I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:140793482 C>A maps to NM_018913.2 T247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7018-01A-11D-2024-08 chr5:140801468 C>T maps to NM_018914.2 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:140811663 C>T maps to NM_003735.2 N446N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:140720328 C>T maps to NM_018915.2 D597D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7616-01A-11D-2253-08 chr5:140718978 G>T maps to NM_018915.2 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7C3-01A-11D-A32B-08 chr5:140719293 G>A maps to NM_018915.2 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:140725816 C>T maps to NM_018916.3 H739H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5311-01A-01D-1468-08 chr5:140724037 G>A maps to NM_018916.3 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VW-A7QS-01A-12D-A33T-08 chr5:140723836 G>A maps to NM_018916.3 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr5:140736509 C>T maps to NM_018917.2 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:140745792 G>A maps to NM_018918.2 L632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6408-01A-11D-1705-08 chr5:140746017 C>T maps to NM_018918.2 F707F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr5:140755692 C>T maps to NM_018919.2 S681S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TW-01A-12D-A32B-08 chr5:140754996 G>A maps to NM_018919.2 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YL-01A-11D-A34A-08 chr5:140763941 C>T maps to NM_018920.2 A492A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EZ-01A-11D-A27K-08 chr5:140762774 G>A maps to NM_018920.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U2-01A-21D-A33T-08 chr5:140762582 G>A maps to NM_018920.2 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:140773750 C>A maps to NM_032088.1 Y457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:140774314 C>A maps to NM_032088.1 A645A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:140773876 G>A maps to NM_032088.1 A499A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:140783913 C>T maps to NM_018921.2 N465N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76L-01A-11D-A32B-08 chr5:140751397 C>T maps to NM_018924.2 P479P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WP-01A-12D-A34A-08 chr5:140768347 T>C maps to NM_003736.2 I299I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:140788767 A>G maps to NM_018926.2 V333V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85A-01A-21D-A36O-08 chr5:140799048 G>A maps to NM_018927.2 A541A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A70Z-01A-12D-A33T-08 chr5:140857254 C>T maps to NM_002588.2 P524P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:140864799 C>T maps to NM_018928.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5964-01A-11D-1705-08 chr5:140866539 A>G maps to NM_018928.2 S600S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr5:140865843 G>A maps to NM_018928.2 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CZ-01A-11D-A32B-08 chr5:140869682 C>T maps to NM_018929.2 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IS-01A-11D-A34A-08 chr11:82877729 G>A maps to NM_015885.3 W597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:93008277 G>T maps to NM_032373.3 E76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:93008307 C>T maps to NM_032373.3 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:44576321 G>A maps to NM_022104.3 S681S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7007-01A-11D-2024-08 chr20:44567655 C>T maps to NM_022104.3 H6H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QY-01A-11D-A34A-08 chr20:44569127 G>T maps to NM_022104.3 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:56137899 C>T maps to NM_002591.3 G185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:24569429 C>T maps to NM_001018073.1 C414C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6403-01A-11D-1705-08 chr7:82785656 C>T maps to NM_033026.5 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7011-01A-11D-2024-08 chr7:82584493 T>C maps to NM_033026.5 T1925T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7294-01A-11D-2024-08 chr7:82583260 G>A maps to NM_033026.5 S2336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TD-01A-12D-A34A-08 chr7:82532024 G>A maps to NM_033026.5 Y4490Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A618-01A-11D-A29Q-08 chr7:82583284 G>A maps to NM_033026.5 A2328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A72U-01A-31D-A32B-08 chr7:82581400 C>T maps to NM_033026.5 Q2956Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7884-01B-11D-2395-08 chr8:17794713 T>C maps to NM_006197.3 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6542-01A-11D-1893-08 chr8:52733123 A>T maps to NM_052937.2 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RP-01A-21D-A34A-08 chr8:52746175 G>A maps to NM_052937.2 R162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:47851603 G>A maps to NM_006031.5 E2742E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:47851751 C>T maps to NM_006031.5 Q2792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:47836173 C>T maps to NM_006031.5 S2114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr21:47845845 C>T maps to NM_006031.5 D2427D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A618-01A-11D-A29Q-08 chr14:71443879 A>T maps to NM_014982.2 K276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5143-01A-01D-1468-08 chr1:233150466 G>C maps to NM_014801.3 A1632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:233394056 C>T maps to NM_014801.3 S517S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:233353845 G>T maps to NM_014801.3 G863G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr1:233150465 G>A maps to NM_014801.3 L1633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CV-01A-11D-A31L-08 chr1:233160995 G>A maps to NM_014801.3 Q1501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:65396305 C>T maps to NM_032223.2 F1276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5270-01A-02D-1468-08 chr20:17462657 G>A maps to NM_002594.2 E620E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5141-01A-01D-1468-08 chr20:17434532 C>T maps to NM_002594.2 D344D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:17434412 C>T maps to NM_002594.2 Y304Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A711-01A-21D-A33T-08 chr20:17437094 T>A did not map to a codon.
Sequencing variant TCGA-HT-7467-01A-11D-2024-08 chr20:17339013 C>T maps to NM_002594.2 R109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7681-01A-11D-2395-08 chr20:17462591 G>A maps to NM_002594.2 P598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U0-01A-12D-A32B-08 chr20:17462501 G>A maps to NM_002594.2 W568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:1487016 G>A maps to NM_017573.3 G301G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:78638727 A>C maps to NM_001190482.1 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:78710933 C>T maps to NM_001190482.1 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr9:78686646 C>T maps to NM_001190482.1 R243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr15:101971659 G>A maps to NM_002570.3 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:117094830 G>A maps to NM_004716.2 Y339Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6290-01A-11D-1705-08 chr1:55523125 C>T maps to NM_174936.3 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8188-01A-11D-2253-08 chr2:70504433 C>T maps to NM_016297.3 N476N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:24690691 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:105160227 C>T maps to NM_014976.1 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:105176258 T>C maps to NM_014976.1 C510C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr10:105184817 G>A maps to NM_014976.1 T947T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:5534952 C>T maps to NM_025239.3 H88H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:170889155 T>C maps to NM_002598.3 K232K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:112645009 G>T did not map to a codon.
Sequencing variant TCGA-WY-A85E-01A-11D-A36O-08 chr15:65425255 C>T maps to NM_005707.1 K288K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:56428577 C>T maps to NM_152401.2 K188K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74J-01A-12D-A32B-08 chr6:165863790 C>G maps to NM_001130690.1 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7013-01A-11D-2024-08 chr2:178682595 G>A maps to NM_016953.3 R545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:57542582 C>T maps to NM_177966.5 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5302-01A-01D-1468-08 chr2:183095780 A>C maps to NM_005019.3 Y181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:31877482 C>T did not map to a codon.
Sequencing variant TCGA-CS-6186-01A-12D-2024-08 chr11:72289380 C>T maps to NM_002599.3 E837E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66G-01A-21D-A31L-08 chr12:20801758 C>T maps to NM_000921.3 V901V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A6S8-01A-12D-A32B-08 chr12:20783010 T>C maps to NM_000921.3 S570S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R3-01A-11D-A34J-08 chr12:20769225 C>A maps to NM_000921.3 T444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:14852271 A>G maps to NM_000922.3 E612E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:66831426 C>T maps to NM_001037341.1 S454S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:18324237 C>T maps to NM_000923.3 E516E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:18331254 C>T maps to NM_000923.3 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6395-01A-12D-1705-08 chr19:18329191 G>A maps to NM_000923.3 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:144865845 G>A maps to NM_014644.4 R1912*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:144904623 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:144918897 G>A maps to NM_014644.4 R430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MY-01A-11D-A26M-08 chr1:144856851 C>T maps to NM_014644.4 A2211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5397-01A-01D-1893-08 chr4:619540 G>A maps to NM_000283.3 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64U-01A-11D-A29Q-08 chr4:663880 C>A maps to NM_000283.3 T850T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:619546 C>T maps to NM_000283.3 C44C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:656909 G>A maps to NM_000283.3 K618K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:651255 C>T maps to NM_000283.3 C458C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:652778 C>T maps to NM_000283.3 C480C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5322-01A-01D-1468-08 chr4:659048 A>G maps to NM_000283.3 A733A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:95418726 A>G maps to NM_006204.3 K702K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:95422399 G>A maps to NM_006204.3 K789K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7301-01A-11D-2086-08 chr10:95385364 G>T maps to NM_006204.3 E300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84L-01A-11D-A36O-08 chr17:79620302 C>G maps to ENST00000331056 R61R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76L-01A-11D-A32B-08 chr15:85656621 C>T maps to NM_002605.2 R377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr5:76649191 G>A maps to NM_003719.3 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7CA-01A-21D-A33T-08 chr5:76715663 A>G maps to NM_003719.3 E734E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:44189184 C>T maps to NM_002606.2 R504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:157688927 G>A maps to NM_016205.2 H306H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:103870924 G>A maps to NM_025208.4 N61N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:103870878 G>A maps to NM_025208.4 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5962-01B-11D-1893-08 chr11:103870851 G>A maps to NM_025208.4 Q86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5854-01A-11D-1705-08 chr4:55139757 C>T maps to NM_006206.4 I473I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:55156517 C>T maps to ENST00000507166 D733D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:55161378 C>T maps to ENST00000507166 I830I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YI-01A-11D-A34A-08 chr4:55136820 G>C maps to NM_006206.4 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7479-01A-11D-2024-08 chr4:55152039 C>T maps to ENST00000507166 V584V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:149501461 G>A maps to NM_002609.3 Y775Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr23:19368153 C>T did not map to a codon.
Sequencing variant TCGA-DU-5854-01A-11D-1705-08 chr23:19369426 G>A did not map to a codon.
Sequencing variant TCGA-E1-5318-01A-01D-1468-08 chr23:19368117 G>C did not map to a codon.
Sequencing variant TCGA-E1-5322-01A-01D-1468-08 chr23:19369426 G>A did not map to a codon.
Sequencing variant TCGA-QH-A6X5-01A-12D-A32B-08 chr23:19373475 T>A did not map to a codon.
Sequencing variant TCGA-S9-A7IQ-01A-21D-A34A-08 chr23:19377662 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:96761688 C>T maps to NM_005390.4 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YI-01A-11D-A34A-08 chr4:96761795 C>T maps to NM_005390.4 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7884-01B-11D-2395-08 chr4:96761528 A>G maps to NM_005390.4 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IY-01A-11D-A34A-08 chr7:148709067 G>A maps to NM_004911.4 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6402-01A-11D-1705-08 chr2:10929976 G>A maps to ENST00000381611 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64W-01A-11D-A29Q-08 chr16:20387484 G>A maps to NM_174924.1 R150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76L-01A-11D-A32B-08 chr16:20396138 C>T maps to NM_174924.1 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:24512863 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:24552110 G>T did not map to a codon.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr23:24545691 A>T did not map to a codon.
Sequencing variant TCGA-QH-A6X8-01A-12D-A32B-08 chr23:24552176 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:97028546 G>T maps to NM_020992.2 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XE-01A-11D-A27K-08 chr5:176918074 C>T maps to NM_005451.3 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr16:66919575 C>T maps to NM_020786.2 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7694-01A-11D-2253-08 chr16:66919404 C>T maps to NM_020786.2 F406F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:70180085 C>A maps to NM_017990.3 S639S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:70187440 G>T maps to NM_017990.3 E734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:39878616 G>A maps to NM_001100399.1 R717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CZ-01A-11D-A32B-08 chr4:39922019 C>G did not map to a codon.
Sequencing variant TCGA-S9-A6WE-01A-12D-A33T-08 chr4:39911876 C>T maps to NM_001100399.1 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:26998655 G>A maps to NM_014317.3 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:45165990 C>T maps to NM_003681.4 D121D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:32059378 C>T maps to NM_178140.2 C745C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153069202 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153069212 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153069755 G>A did not map to a codon.
Sequencing variant TCGA-DU-7008-01A-11D-2024-08 chr23:153069773 G>T did not map to a codon.
Sequencing variant TCGA-DU-A76K-01A-11D-A33T-08 chr23:153069950 G>A did not map to a codon.
Sequencing variant TCGA-HT-8018-01A-11D-2395-08 chr23:153069211 C>T did not map to a codon.
Sequencing variant TCGA-KT-A7W1-01A-11D-A34A-08 chr23:153069355 C>T did not map to a codon.
Sequencing variant TCGA-P5-A72Z-01A-11D-A32B-08 chr23:153068981 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:41966492 C>T maps to NM_001164595.1 R638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A617-01A-11D-A29Q-08 chr1:160181385 G>T maps to ENST00000368075 E39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:22584730 G>A maps to NM_144962.2 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7480-01A-11D-2086-08 chr1:32101081 C>T maps to NM_012392.3 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:94293535 T>C maps to NM_001172437.1 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:66241284 G>A maps to NM_145065.2 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr11:66243520 C>A maps to NM_145065.2 A431A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6X9-01A-12D-A32B-08 chr11:66243322 C>T maps to NM_145065.2 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WQ-01A-12D-A34A-08 chr11:66243443 C>T maps to NM_145065.2 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76O-01A-11D-A32B-08 chr5:52097256 C>T maps to NM_015946.4 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5277-01A-01D-1468-08 chr17:4578456 C>G maps to ENST00000301396 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:239180111 G>A maps to NM_022817.2 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:7902733 C>A maps to ENST00000377532 A1184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:7886618 C>T maps to ENST00000377532 H679H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:7887364 C>A maps to ENST00000377532 T792T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:92126079 T>C maps to NM_000466.2 L910L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:2340117 G>A maps to NM_153818.1 R125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:7550888 G>A maps to NM_080662.2 C28C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:61258830 G>T maps to NM_002618.3 E124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:7362698 G>A maps to NM_001131023.1 S615S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F4-01A-11D-A289-08 chr12:7362770 C>T maps to NM_001131023.1 D639D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:42936094 G>A maps to NM_000287.3 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:54975617 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:54985338 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:54960306 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:54984795 C>A did not map to a codon.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr1:207252342 G>A maps to NM_001018053.1 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr10:6257193 C>G maps to NM_004566.3 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84C-01A-11D-A36O-08 chr3:48594201 G>A maps to NM_004567.2 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TJ-01A-11D-A34J-08 chr21:45732144 G>A maps to NM_002626.4 W132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84H-01A-11D-A36O-08 chr10:3175463 C>T maps to NM_002627.3 G660G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:77224500 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:197708652 T>C maps to NM_024989.3 L828L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KK-01A-11D-A27K-08 chr2:197708796 A>G maps to NM_024989.3 N780N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:28268752 G>A maps to NM_032507.3 Q374Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:28268878 G>A maps to NM_032507.3 K416K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TS-01A-12D-A33T-08 chr1:10479684 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:75416191 G>A maps to ENST00000405431 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:114573600 C>A maps to NM_005023.3 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A75L-01A-11D-A32B-08 chr23:77369612 C>A did not map to a codon.
Sequencing variant TCGA-HT-8013-01A-11D-2395-08 chr23:77380494 C>T did not map to a codon.
Sequencing variant TCGA-HT-7477-01B-11D-A289-08 chr6:49754105 G>A maps to NM_138733.4 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6670-01A-11D-1893-08 chr19:46526066 G>A maps to NM_005091.2 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr19:46522886 G>A maps to NM_005091.2 D102D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TT-01A-11D-A289-08 chr19:15586703 C>T maps to NM_052890.3 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7309-01A-11D-2086-08 chr1:153315566 T>C maps to NM_020393.2 K157K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5853-01A-11D-1893-08 chr1:64100509 G>A maps to NM_002633.2 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A711-01A-21D-A33T-08 chr4:37857281 A>G maps to NM_018290.3 G552G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A61C-01A-11D-A29Q-08 chr11:74085468 C>T maps to NM_173582.3 Q90Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:71114240 C>T maps to NM_021965.3 Y526Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr9:70993120 C>T maps to NM_021965.3 R90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr11:100998772 C>A maps to NM_000926.4 R343R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5318-01A-01D-1468-08 chr23:118370560 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:144093463 T>G maps to NM_001100164.1 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6402-01A-11D-1705-08 chr20:58349321 G>A maps to NM_080672.3 G317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr1:28793238 T>C maps to NM_023923.3 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:9089801 G>A maps to ENST00000433083 R931R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr1:33837952 G>A maps to ENST00000419414 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:169820405 G>A maps to NM_024947.3 S898S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:169863240 C>T maps to NM_024947.3 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:169863246 C>T maps to NM_024947.3 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr3:169835094 A>G maps to NM_024947.3 P704P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr3:169815125 T>C maps to NM_024947.3 G960G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5396-01A-02D-1468-08 chr23:22095666 T>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:22115093 C>T did not map to a codon.
Sequencing variant TCGA-RY-A83Z-01A-11D-A36O-08 chr23:22245634 A>T did not map to a codon.
Sequencing variant TCGA-S9-A6U2-01A-21D-A33T-08 chr23:22231074 G>T did not map to a codon.
Sequencing variant TCGA-S9-A7QY-01A-11D-A34A-08 chr23:22094542 C>T did not map to a codon.
Sequencing variant TCGA-TQ-A7RP-01A-21D-A34A-08 chr23:22095782 C>A did not map to a codon.
Sequencing variant TCGA-DB-5277-01A-01D-1468-08 chr6:33383709 C>A maps to NM_024165.2 P513P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A87Q-01A-11D-A36O-08 chr6:33382303 T>G maps to NM_024165.2 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:6681483 G>A maps to NM_153812.2 W230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7607-01A-11D-2086-08 chr1:6681633 C>G maps to NM_153812.2 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:11075410 C>T maps to ENST00000303905 Q534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:11091394 G>A maps to ENST00000303905 P823P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5874-01A-11D-1705-08 chr5:133914910 C>T maps to ENST00000448712 S819S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8010-01A-11D-2395-08 chr23:46884201 A>G did not map to a codon.
Sequencing variant TCGA-P5-A5F2-01A-11D-A289-08 chr23:46887418 G>A did not map to a codon.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr4:129782914 C>T maps to NM_199320.2 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:96339132 C>T maps to NM_005392.3 C26C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74O-01A-11D-A32B-08 chr20:34451081 C>T maps to NM_016436.4 R190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:133854924 A>G maps to ENST00000395386 K852K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:45309845 G>A maps to NM_138415.3 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7490-01A-11D-2024-08 chr17:7139546 T>C maps to NM_024297.2 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:64401710 C>T maps to NM_015153.2 G758G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8186-01A-11D-2253-08 chr6:64394226 C>T maps to NM_015153.2 R202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65Z-01A-11D-A29Q-08 chr6:64423123 C>G maps to NM_015153.2 G1880G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7607-01A-11D-2086-08 chr23:133527973 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:54011401 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:54012202 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:53965632 G>A did not map to a codon.
Sequencing variant TCGA-FG-A6IZ-01A-11D-A31L-08 chr23:53966855 G>C did not map to a codon.
Sequencing variant TCGA-QH-A6CW-01A-11D-A32B-08 chr23:53965657 A>G did not map to a codon.
Sequencing variant TCGA-CS-5390-01A-02D-1468-08 chr6:79650980 G>C maps to NM_017934.5 S1632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:79650990 C>A maps to NM_017934.5 G1629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:71876092 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:71846866 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:71886143 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:18926164 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:18966862 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:18954255 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:18912468 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:18938251 G>A did not map to a codon.
Sequencing variant TCGA-DU-6403-01A-11D-1705-08 chr23:18912470 G>C did not map to a codon.
Sequencing variant TCGA-HT-A4DV-01A-11D-A26M-08 chr23:18924630 G>A did not map to a codon.
Sequencing variant TCGA-HT-A74J-01A-12D-A32B-08 chr23:18913285 A>T did not map to a codon.
Sequencing variant TCGA-P5-A77W-01A-11D-A32B-08 chr23:18936875 C>T did not map to a codon.
Sequencing variant TCGA-DU-A5TT-01A-11D-A289-08 chr16:47694708 C>T maps to NM_000293.2 H725H. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-S9-A7IZ-01A-11D-A34A-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:111632215 G>A maps to NM_001134438.1 K462K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:60645922 C>T maps to NM_194449.2 S1471S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:71683148 G>A maps to NM_015020.2 R1206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:71692148 G>A maps to NM_015020.2 L756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7015-01A-11D-2024-08 chr11:608554 G>A maps to ENST00000264555 A1033A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6UB-01A-21D-A33T-08 chr11:587409 G>A maps to ENST00000264555 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:114246747 C>A maps to NM_006608.2 S615S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:114248604 A>G maps to NM_006608.2 I526I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:77579011 G>A maps to ENST00000427986 E659E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:77569879 A>C maps to ENST00000427986 T592T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:22085843 G>A maps to NM_014759.3 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:21083710 G>A maps to NM_058004.2 S1466S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr22:21083937 C>T maps to NM_058004.2 T1432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:151288717 C>A maps to NM_002651.2 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:68468893 C>T maps to NM_016166.1 D461D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:73401953 C>A maps to NM_006346.2 R333R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5965-01B-11D-1893-08 chr13:73505356 A>G maps to NM_006346.2 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:85693046 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:15350017 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:15349837 T>C did not map to a codon.
Sequencing variant TCGA-RY-A845-01A-11D-A36O-08 chr23:15342871 G>C did not map to a codon.
Sequencing variant TCGA-DU-8162-01A-21D-2253-08 chr4:527752 G>A maps to NM_001127178.1 L906L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7480-01A-11D-2086-08 chr9:35093983 G>A maps to NM_032634.2 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr16:633561 C>T maps to NM_148920.1 S737S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YW-01A-11D-A34J-08 chr1:207112704 C>T maps to NM_002644.3 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr17:26890905 G>A maps to NM_033198.3 C102C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8189-01B-11D-A289-08 chr3:196674804 G>A maps to NM_025163.2 N321N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6290-01A-11D-1705-08 chr19:49954794 C>A maps to NM_017916.2 E13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:49951092 G>A maps to NM_017916.2 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:111941222 A>G maps to NM_138789.3 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:17190991 T>C maps to NM_002645.2 E99E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:17190741 C>A maps to NM_002645.2 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:17158124 G>T maps to NM_002645.2 I584I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6X8-01A-12D-A32B-08 chr11:17156656 C>T did not map to a codon.
Sequencing variant TCGA-E1-A7YN-01A-11D-A34A-08 chr1:204438816 G>A maps to NM_002646.3 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YN-01A-11D-A34A-08 chr1:204438639 G>A maps to NM_002646.3 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:18691179 A>G maps to NM_004570.4 E1097E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:18435200 C>A maps to NM_004570.4 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:9783239 A>G maps to ENST00000361110 V852V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:67592151 C>A maps to ENST00000396611 C664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YE-01A-11D-A34A-08 chr5:67591246 G>C did not map to a codon.
Sequencing variant TCGA-FG-8188-01A-11D-2253-08 chr5:67569269 G>A maps to ENST00000396611 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CS-01A-11D-A31L-08 chr5:67591286 C>T maps to ENST00000396611 N595N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7475-01A-11D-2024-08 chr19:18272832 C>T maps to NM_005027.2 H291H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:8792128 C>T maps to NM_001142633.1 E325E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8110-01A-11D-2395-08 chr17:8794081 G>A maps to NM_001142633.1 D210D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RC-01A-11D-A289-08 chr17:8741185 C>T maps to NM_001010855.2 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:37139064 A>G maps to ENST00000373507 E226E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:48772383 G>T did not map to a codon.
Sequencing variant TCGA-S9-A6WQ-01A-12D-A34A-08 chr23:48772534 A>T did not map to a codon.
Sequencing variant TCGA-S9-A6WQ-01A-12D-A34A-08 chr23:48772457 C>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:10623372 G>T maps to NM_017884.4 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:22830766 C>T maps to NM_005028.4 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr12:57989813 G>A maps to NM_024779.4 Q171Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:151196879 T>C maps to NM_001135638.1 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:67267734 G>A maps to NM_004910.2 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:67261828 G>A maps to NM_004910.2 N915N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7601-01A-11D-2086-08 chr11:67269772 C>T maps to NM_004910.2 Q135Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr12:123473363 G>A maps to NM_020845.2 D929D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YN-01A-11D-A34A-08 chr17:6380416 C>T maps to NM_031220.3 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr17:6381926 T>A maps to NM_031220.3 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F1-01A-11D-A289-08 chr10:3190473 G>A maps to ENST00000380989 C627C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5874-01A-11D-1705-08 chr5:134364858 G>A maps to NM_002653.4 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85E-01A-11D-A36O-08 chr4:111539466 C>A maps to NM_153426.1 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:130846068 C>T maps to NM_004764.4 I631I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:130855858 C>T maps to NM_004764.4 Y820Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:25147374 G>T maps to NM_001008496.2 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R5-01A-11D-A289-08 chr22:25119190 G>A maps to NM_001008496.2 R764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5311-01A-01D-1468-08 chr11:94328553 G>A maps to NM_152431.2 R410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7CA-01A-21D-A33T-08 chr11:94328503 C>T maps to NM_152431.2 Q394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr16:2164290 C>A maps to NM_001009944.2 V911V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5874-01A-11D-1705-08 chr16:2161834 G>A maps to NM_001009944.2 F1111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7T6-01A-11D-A33T-08 chr16:2159761 C>G maps to NM_001009944.2 V1802V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5302-01A-01D-1468-08 chr16:2147948 G>A maps to NM_001009944.2 Q3363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5311-01A-01D-1468-08 chr16:2155891 A>G maps to NM_001009944.2 L2613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7881-01A-11D-2395-08 chr16:2139949 G>A maps to NM_001009944.2 N4230N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:47894785 G>A maps to NM_138295.3 P1556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:47847886 G>A maps to NM_138295.3 C2595C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7300-01A-21D-2086-08 chr7:47840378 G>A maps to NM_138295.3 P2687P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:81232504 G>T maps to NM_052892.3 T435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A89V-01A-11D-A36O-08 chr16:81183424 G>A maps to NM_052892.3 R1541R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:102054793 G>A maps to NM_016112.2 A481A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr10:102057296 G>A maps to NM_016112.2 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:137241999 C>A maps to ENST00000230643 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:46655313 G>A maps to NM_006071.1 N1302N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:46652820 G>T maps to NM_006071.1 V2133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A77W-01A-11D-A32B-08 chr22:46652876 C>A maps to NM_006071.1 E2115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:51484202 C>T maps to NM_138694.3 V3967V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:51524156 C>T maps to NM_138694.3 Q3589Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:51748013 A>G maps to NM_138694.3 S2409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:51695674 G>A maps to NM_138694.3 D2762D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6402-01A-11D-1705-08 chr6:51882308 C>T maps to NM_138694.3 S1833S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7636-01A-11D-2086-08 chr6:51799070 G>A maps to NM_138694.3 H1986H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U9-01A-11D-A32B-08 chr6:51484034 G>A maps to NM_138694.3 D4023D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:110456103 C>A maps to ENST00000426474 G1588G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:110464460 G>A maps to ENST00000426474 G2153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6J3-01A-11D-A31L-08 chr8:110418624 T>A maps to ENST00000426474 S577S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A617-01A-11D-A29Q-08 chr8:110468611 A>G maps to ENST00000426474 T2332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A83X-01A-11D-A36O-08 chr8:110530474 G>A maps to ENST00000426474 L3924L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TS-01A-12D-A33T-08 chr8:110477388 C>T maps to ENST00000426474 D2776D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:14581098 C>T maps to NM_213560.1 Y812Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:89251811 C>T maps to NM_006256.2 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7880-01A-11D-2395-08 chr9:131475881 G>C maps to NM_013355.3 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6668-01A-11D-1893-08 chr1:201282316 G>A maps to NM_000299.3 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A86X-01A-11D-A36O-08 chr1:201291188 G>A maps to NM_000299.3 E498E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5397-01A-01D-1893-08 chr12:32974415 G>A maps to NM_004572.3 G673G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:396683 C>A maps to NM_007183.2 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TS-01A-11D-A289-08 chr2:159537146 T>C maps to NM_003628.3 Y1179Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A89V-01A-11D-A36O-08 chr2:159459580 G>A did not map to a codon.
Sequencing variant TCGA-QH-A6CZ-01A-11D-A32B-08 chr3:119336992 G>A maps to NM_015900.2 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76K-01A-11D-A33T-08 chr10:74701026 G>A maps to NM_032562.2 C122C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66G-01A-21D-A31L-08 chr16:68288857 T>C maps to NM_012320.3 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:120762743 G>T maps to NM_000928.2 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:48556296 C>A maps to NM_003706.2 E513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:48565308 C>T maps to NM_003706.2 T401T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6188-01A-11D-1893-08 chr15:42371770 C>G maps to NM_178034.3 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:42360977 G>A maps to NM_178034.3 Q798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84M-01A-11D-A36O-08 chr15:42363708 G>A maps to NM_178034.3 A538A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr15:42434837 G>A maps to ENST00000397272 D741D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr15:42438415 G>A maps to ENST00000397272 D483D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr2:160832716 A>G maps to NM_007366.4 Y819Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr23:133700589 G>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:145464108 C>T maps to NM_001029869.1 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7477-01B-11D-A289-08 chr10:81901856 T>A maps to NM_001012973.1 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7013-01A-11D-2024-08 chr8:57079206 G>A maps to NM_002655.2 G366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:75672799 C>A maps to NM_002658.3 Y104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr10:75675024 G>A maps to NM_002658.3 P329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:28847957 C>T maps to NM_153021.4 R1188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:28785935 C>T maps to NM_153021.4 N392N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr12:113824840 C>T maps to NM_173542.3 F462F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6689-01A-11D-1893-08 chr20:8665705 G>A maps to NM_015192.2 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A72U-01A-31D-A32B-08 chr20:8862381 C>T maps to NM_015192.2 H1179H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YV-01A-11D-A34J-08 chr15:40594678 G>A maps to NM_004573.2 N121N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:64032852 C>T maps to NM_000932.2 R972*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:9319617 C>T maps to NM_001172646.1 C101C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:9424887 A>T maps to NM_001172646.1 K960*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:38049631 C>T maps to NM_001130964.1 T707T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:43190526 G>A maps to NM_133373.3 D697D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EZ-01A-11D-A27K-08 chr2:219500984 G>C maps to ENST00000432688 G716G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5142-01A-01D-1468-08 chr10:95790841 T>C maps to ENST00000371380 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:96005762 C>T maps to ENST00000371380 Y827Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:39793913 C>T maps to NM_002660.2 Y472Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:39794926 C>T maps to NM_002660.2 S631S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:39796514 T>C maps to NM_002660.2 Y775Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TD-01A-12D-A34A-08 chr16:81957131 C>T maps to NM_002661.2 R784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr16:81925183 G>A maps to NM_002661.2 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7472-01A-11D-2024-08 chr16:81927340 C>T maps to NM_002661.2 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WN-01A-12D-A33T-08 chr16:81990346 G>A maps to NM_002661.2 R1206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:155210520 G>A maps to ENST00000340059 G756G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:155215115 C>A maps to ENST00000340059 V617V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7007-01A-11D-2024-08 chr3:155198969 G>A maps to ENST00000340059 T1623T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8105-01A-11D-2395-08 chr3:155200025 C>T maps to ENST00000340059 T1271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U5-01A-12D-A33T-08 chr2:198950469 G>A maps to NM_006226.3 G743G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6IZ-01A-11D-A31L-08 chr23:205504 G>A did not map to a codon.
Sequencing variant TCGA-QH-A6XC-01A-12D-A32B-08 chr23:209793 G>A did not map to a codon.
Sequencing variant TCGA-DU-5851-01A-13D-1893-08 chr5:41381989 G>T maps to NM_001005473.2 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:41382285 T>A maps to NM_001005473.2 K152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:171330139 A>G maps to NM_002662.3 V937V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:171426564 C>T maps to NM_002662.3 E375E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:171417542 G>A maps to NM_002662.3 R407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:4725990 C>T maps to NM_002663.3 Y878Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A858-01A-11D-A36O-08 chr17:4718862 G>A maps to NM_002663.3 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:40872795 C>T maps to NM_012268.2 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5302-01A-01D-1468-08 chr19:40883896 C>G maps to NM_012268.2 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WI-01A-21D-A33T-08 chr19:40872762 C>T maps to NM_012268.2 Y62Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7881-01A-11D-2395-08 chr14:105399117 G>A maps to NM_138790.2 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7T6-01A-11D-A33T-08 chr8:144997376 C>G maps to NM_201380.2 L2377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr8:144995969 C>T maps to NM_201380.2 A2810A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:68609736 C>T maps to NM_002664.2 D148D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-7675-01A-11D-2086-08 chr12:19475546 T>C maps to ENST00000429027 D798D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U1-01A-21D-A33T-08 chr1:204214033 C>A maps to ENST00000367191 V730V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:16838748 G>A maps to ENST00000448080 P488P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5393-01A-01D-1468-08 chr7:30092390 C>T maps to ENST00000440706 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:65207965 C>T maps to ENST00000394691 S577S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:65209907 C>T maps to ENST00000394691 D1049D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:67322136 G>A maps to NM_001129729.1 S1096S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:67314867 G>T maps to NM_001129729.1 E227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:67318662 G>A maps to NM_001129729.1 E580E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:163453 T>C maps to NM_052909.3 P733P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7611-01A-11D-2395-08 chr5:161917 A>G maps to NM_052909.3 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:6532585 C>T did not map to a codon.
Sequencing variant TCGA-S9-A6WI-01A-21D-A33T-08 chr1:6530294 C>T did not map to a codon.
Sequencing variant TCGA-RY-A83Y-01A-11D-A36O-08 chr12:6425455 C>T maps to NM_001144856.1 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:68042712 G>A maps to NM_020715.2 K781K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:43927113 G>A maps to NM_172069.3 E339E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:16059186 G>A maps to ENST00000420314 L1065L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6J3-01A-11D-A31L-08 chr1:16060353 G>A maps to ENST00000420314 L1098L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:208866153 G>C maps to NM_001080475.2 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7636-01A-11D-2086-08 chr1:907740 C>T maps to ENST00000379409 R365R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VW-A8FI-01A-11D-A36O-08 chr1:905680 C>T maps to ENST00000379409 R70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:150128390 C>T maps to ENST00000443480 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:150131487 C>T maps to ENST00000443480 R365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XB-01A-11D-A26M-08 chr6:161173246 C>T maps to NM_000301.3 T742T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:161137784 C>A maps to NM_000301.3 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A6MK-01A-11D-A32B-08 chr6:161143572 G>A maps to NM_000301.3 Q410Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7634-01A-11D-2086-08 chr9:19116569 G>A maps to NM_001122.2 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5140-01A-01D-1468-08 chr19:4511094 G>A maps to NM_001080400.1 G945G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:4510833 G>A maps to NM_001080400.1 H1032H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6400-01A-12D-1705-08 chr19:4511136 G>A maps to NM_001080400.1 T931T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66G-01A-21D-A31L-08 chr5:57751225 G>A maps to NM_006622.2 Y547Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:57751886 T>C maps to NM_006622.2 R450R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VV-A86M-01A-11D-A36O-08 chr5:57753313 C>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:12025565 C>T maps to ENST00000376369 H547H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr1:12024321 C>T maps to ENST00000376369 S478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:145794588 G>A maps to NM_182943.2 Q553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:103040567 C>T did not map to a codon.
Sequencing variant TCGA-DU-6405-01A-11D-1705-08 chr23:103043373 C>T did not map to a codon.
Sequencing variant TCGA-HT-A74L-01A-11D-A32B-08 chr23:103045488 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:49030696 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:155463419 C>T maps to NM_002669.2 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7680-01A-11D-2253-08 chr4:155459181 G>A maps to NM_002669.2 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:114883750 A>G did not map to a codon.
Sequencing variant TCGA-HW-8319-01A-11D-2395-08 chr23:114882252 T>G did not map to a codon.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr23:114880829 G>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:44531096 C>T maps to NM_006227.2 Q363Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:37264439 C>T maps to NM_020405.4 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6X8-01A-12D-A32B-08 chr3:126708284 G>A maps to NM_032242.3 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:208315691 G>A maps to NM_025179.3 Y496Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:208215501 G>T maps to NM_025179.3 L1409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:208217961 G>A maps to NM_025179.3 I1255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:208215489 G>A maps to NM_025179.3 I1413I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5396-01A-02D-1468-08 chr23:153695647 G>T did not map to a codon.
Sequencing variant TCGA-DU-5872-01A-11D-1705-08 chr23:153688766 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153696662 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153699860 C>A did not map to a codon.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr23:153698492 C>T did not map to a codon.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr23:153693429 C>T did not map to a codon.
Sequencing variant TCGA-P5-A5F6-01A-11D-A289-08 chr23:153688924 G>A did not map to a codon.
Sequencing variant TCGA-P5-A737-01A-11D-A32B-08 chr23:153697252 G>A did not map to a codon.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr7:131848963 G>A maps to NM_020911.1 G1479G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:132192524 G>A maps to NM_020911.1 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:131831448 G>A maps to NM_020911.1 I1625I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TP-01A-11D-A289-08 chr7:131848942 G>A maps to NM_020911.1 S1486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KT-A7W1-01A-11D-A34A-08 chr7:131844256 C>T maps to NM_020911.1 R1545R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:50722624 G>A maps to NM_012401.2 N733N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153040343 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153034401 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153037428 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153035556 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153037029 G>A did not map to a codon.
Sequencing variant TCGA-E1-A7Z2-01A-21D-A34J-08 chr23:153033030 G>A did not map to a codon.
Sequencing variant TCGA-HT-A4DV-01A-11D-A26M-08 chr23:153043474 T>C did not map to a codon.
Sequencing variant TCGA-HW-A5KL-01A-11D-A27K-08 chr23:153039466 C>A did not map to a codon.
Sequencing variant TCGA-S9-A7QW-01A-11D-A34A-08 chr23:153032990 G>C did not map to a codon.
Sequencing variant TCGA-TM-A7C3-01A-11D-A32B-08 chr23:153036312 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:94645257 G>A maps to NM_005761.1 W945*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A713-01A-11D-A32B-08 chr3:129305067 C>G maps to NM_015103.2 G556G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WL-01A-21D-A33T-08 chr3:129291459 C>T maps to NM_015103.2 T1023T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5963-01A-11D-1705-08 chr1:205814451 C>G did not map to a codon.
Sequencing variant TCGA-HT-A5R9-01A-11D-A289-08 chr15:74290532 C>T maps to NM_033238.2 N106N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CB-01A-11D-A36O-08 chr15:74328198 T>C maps to NM_033239.2 P799P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:82359585 G>T maps to NM_002677.3 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A87N-01A-11D-A36O-08 chr7:102952300 T>C maps to NM_004279.2 Y429Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:154898881 G>A maps to NM_006556.3 R130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:152938139 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:152936197 C>A did not map to a codon.
Sequencing variant TCGA-R8-A6MO-01A-11D-A33T-08 chr23:152938702 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:118321148 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:118359628 C>T maps to NM_006229.2 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr23:152226070 T>C did not map to a codon.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr23:152226307 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:152226234 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:152226089 C>A did not map to a codon.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr23:152226633 C>T did not map to a codon.
Sequencing variant TCGA-E1-A7YE-01A-11D-A34A-08 chr23:152225468 G>T did not map to a codon.
Sequencing variant TCGA-E1-A7YN-01A-11D-A34A-08 chr23:152226590 A>T did not map to a codon.
Sequencing variant TCGA-DU-5854-01A-11D-1705-08 chr23:152159962 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:152159086 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:152159205 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:152159755 G>A did not map to a codon.
Sequencing variant TCGA-HT-A5RC-01A-11D-A289-08 chr23:152159279 C>T did not map to a codon.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr23:152159710 G>A did not map to a codon.
Sequencing variant TCGA-DH-A7US-01A-11D-A33T-08 chr19:46998530 G>A maps to NM_020709.1 A64A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-FG-8186-01A-11D-2253-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FG-8186-01A-11D-2253-08 chr19:46998155 G>A maps to ENST00000377652 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:39650605 C>T maps to NM_002687.3 R565*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DU-A5TS-01A-11D-A289-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:20944541 G>T did not map to a codon.
Sequencing variant TCGA-DU-A5TS-01A-11D-A289-08 chr14:20940626 C>T maps to NM_000270.3 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:36262001 C>A maps to ENST00000457797 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-8125-01A-11D-2253-08 chr6:36262064 C>A maps to ENST00000457797 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:7868853 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:7889874 G>A did not map to a codon.
Sequencing variant TCGA-E1-A7YV-01A-11D-A34J-08 chr19:7614923 C>A maps to NM_001166111.1 G589G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr19:7619473 C>T maps to NM_001166111.1 A843A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr9:140409906 C>T maps to NM_001098537.1 A383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WL-01A-21D-A33T-08 chr9:140356487 C>T maps to NM_001098537.1 V1217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:53544531 T>C maps to NM_153703.4 P498P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:53542951 G>A maps to NM_153703.4 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:127390344 C>T maps to NM_015720.2 Y498Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XG-01A-11D-A27K-08 chr23:84586011 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:84614634 C>A did not map to a codon.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr23:84600915 G>A did not map to a codon.
Sequencing variant TCGA-FG-A6J1-01A-11D-A31L-08 chr23:84614571 C>A did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr23:84563164 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:151395885 G>T maps to NM_015100.3 P555P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr23:24830875 G>A did not map to a codon.
Sequencing variant TCGA-CS-6667-01A-12D-2024-08 chr23:24753560 T>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:24859934 C>A did not map to a codon.
Sequencing variant TCGA-DU-6396-01A-11D-1705-08 chr23:24735545 G>C did not map to a codon.
Sequencing variant TCGA-S9-A6U2-01A-21D-A33T-08 chr11:65055247 G>A maps to NM_002689.2 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:50918727 C>T maps to ENST00000391817 D892D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76K-01A-11D-A33T-08 chr19:50906760 C>T maps to ENST00000391817 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WQ-01A-12D-A34A-08 chr19:50910397 G>A maps to ENST00000391817 Q551Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:74340268 C>T maps to NM_006591.1 R303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:133201532 G>A maps to ENST00000455752 Y2238Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:133241014 G>A maps to ENST00000455752 I837I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:133202894 G>A maps to ENST00000455752 S2116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr12:133250238 G>A maps to ENST00000455752 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr12:133254166 G>A maps to ENST00000455752 H239H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:50122473 C>T maps to NM_002692.3 E281E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6668-01A-11D-1893-08 chr15:89864981 G>A maps to NM_002693.2 T861T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:89871700 C>T maps to NM_002693.2 P412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:74889812 G>A maps to NM_016218.2 K489K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:74892159 G>T maps to NM_016218.2 E548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7605-01A-11D-2086-08 chr10:103343336 G>A maps to NM_013274.3 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64Q-01A-11D-A29Q-08 chr3:121186387 T>A maps to ENST00000393672 R2451R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CD-01A-11D-A36O-08 chr3:121154998 G>T maps to ENST00000393672 R2641R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4942-01A-01D-1468-08 chr2:86316950 G>A maps to NM_015425.3 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:86315722 G>A maps to NM_015425.3 H232H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:86258710 G>A maps to NM_015425.3 N1440N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:86297352 G>A maps to NM_015425.3 R552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:113326459 C>T maps to NM_019014.4 N685N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:113322006 C>T maps to NM_019014.4 D559D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:43484912 C>T maps to NM_203290.1 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr17:7406571 G>A maps to NM_000937.4 R963R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:57504907 C>A maps to NM_032940.2 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr16:57504026 C>T maps to NM_032940.2 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7013-01A-11D-2024-08 chr19:1090942 C>T maps to NM_002695.3 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr10:79785905 G>A maps to NM_007055.3 Y42Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:106903273 C>T maps to NM_018082.5 L1117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:106903276 C>T maps to NM_018082.5 Q1118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:22337274 G>A maps to NM_018119.2 A514A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7472-01A-11D-2024-08 chr22:41936718 G>A maps to NM_138338.3 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:72416128 C>T maps to ENST00000434423 T1178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:53103888 G>T maps to NM_182595.3 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:29242704 G>T maps to NM_015932.5 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:134385313 G>A maps to NM_007171.3 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TZ-01A-21D-A32B-08 chr14:77765886 G>A maps to NM_013382.5 H278H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7006-01A-11D-2024-08 chr7:94947700 G>A maps to NM_000446.5 R27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TP-01A-11D-A289-08 chr7:94940782 G>T maps to NM_000446.5 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:99168367 G>A maps to NM_015029.2 E716E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7294-01A-11D-2024-08 chr8:99169862 G>A maps to NM_015029.2 K813K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:75608863 A>G maps to NM_000941.2 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7469-01A-11D-2253-08 chr7:75601766 G>A maps to NM_000941.2 K75K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:48369777 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:48372937 A>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:48368272 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:48370737 A>T did not map to a codon.
Sequencing variant TCGA-VM-A8C8-01A-11D-A36O-08 chr23:48369766 G>T did not map to a codon.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr13:38153416 A>G maps to NM_006475.2 G580G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A615-01A-11D-A29Q-08 chr13:38171319 C>T did not map to a codon.
Sequencing variant TCGA-S9-A6WP-01A-12D-A34A-08 chr8:43173618 G>A maps to NM_001005365.2 K347K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A6S8-01A-12D-A32B-08 chr18:14542920 G>A maps to ENST00000444806 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YU-01A-11D-A34J-08 chr18:14542920 G>A maps to ENST00000444806 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7608-01A-11D-2086-08 chr18:14543091 G>A maps to ENST00000444806 F18F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TV-01A-12D-A34J-08 chr2:132021796 C>T maps to NM_001083538.1 F923F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5847-01A-11D-1705-08 chr2:130832725 G>A maps to NM_001099771.2 H773H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7018-01A-11D-2024-08 chr14:19553817 C>T maps to NM_001005356.2 H134H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5964-01A-11D-1705-08 chr14:19553811 G>A maps to NM_001005356.2 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A70Y-01A-12D-A34J-08 chr14:19553673 C>T maps to NM_001005356.2 H86H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5390-01A-02D-1468-08 chr22:16287513 G>A maps to NM_001136213.1 D124D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A70Y-01A-12D-A34J-08 chr14:20019962 G>A maps to ENST00000439503 H86H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WH-A86K-01A-11D-A36O-08 chr14:20019848 G>A maps to ENST00000439503 D124D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:82763426 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:82763475 C>T did not map to a codon.
Sequencing variant TCGA-FG-A6IZ-01A-11D-A31L-08 chr7:39125629 C>T maps to NM_007252.3 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:38124794 T>C maps to NM_001102559.1 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5396-01A-02D-1468-08 chr9:134165666 C>A maps to NM_032728.3 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr3:12458612 C>T maps to NM_015869.4 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:23814672 A>G maps to NM_013261.3 R623R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:23803419 G>A maps to NM_013261.3 N742N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:23815350 C>T maps to NM_013261.3 R585R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8563-01A-11D-2395-08 chr4:23815629 T>C maps to NM_013261.3 E492E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:149212523 C>A maps to NM_133263.3 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:18768030 G>A did not map to a codon.
Sequencing variant TCGA-DU-A7TI-01A-11D-A33T-08 chr23:18822065 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:70172384 A>G maps to NM_003626.2 E208E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5311-01A-01D-1468-08 chr11:70208263 G>A maps to NM_003626.2 T882T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:81676814 C>A maps to NM_003625.2 E998*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84B-01A-11D-A36O-08 chr12:81746922 A>G maps to NM_003625.2 L657L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CV-01A-11D-A31L-08 chr19:49636259 G>A maps to NM_003660.2 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:203045490 A>G maps to ENST00000367238 G1178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:203029424 G>A maps to ENST00000367238 S867S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CF-01A-11D-A36O-08 chr11:7662770 G>A maps to NM_003621.2 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:42840047 T>C maps to NM_016488.6 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:42778745 C>T maps to NM_016488.6 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:42729719 C>T maps to NM_016488.6 R6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7008-01A-11D-2024-08 chr12:42835163 G>A maps to NM_016488.6 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:122365004 C>A maps to NM_000943.4 G76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WE-01A-12D-A33T-08 chr5:122361499 A>G maps to NM_000943.4 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5851-01A-13D-1893-08 chr10:81113477 T>C maps to NM_005729.3 H168H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:22039066 G>A maps to NM_148175.2 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:102522048 C>A maps to ENST00000451606 T1081T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QY-01A-11D-A34A-08 chr5:102519069 T>C maps to ENST00000451606 L1035L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:4934268 G>A maps to NM_002705.4 R1463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TW-01A-12D-A32B-08 chr16:4934533 G>A maps to NM_002705.4 S1374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6UB-01A-21D-A33T-08 chr16:4934296 C>T maps to NM_002705.4 P1453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8C8-01A-11D-A36O-08 chr16:4945353 G>A maps to NM_002705.4 R384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7677-01A-11D-2253-08 chr2:44457549 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:58734075 A>G maps to NM_003620.3 E378E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R7-01A-11D-A289-08 chr1:113257683 C>T maps to NM_005167.5 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A615-01A-11D-A29Q-08 chr3:160786804 C>T maps to NM_139245.2 R315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YN-01A-11D-A34A-08 chr19:46002330 C>A maps to NM_001080401.1 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:30571786 C>T maps to NM_002714.2 E502E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:104205228 G>T maps to NM_015316.2 I908I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr19:45885826 C>T maps to NM_001142502.1 A802A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:64012291 G>T maps to NM_138689.2 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:41107958 C>T maps to NM_001130143.1 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7008-01A-11D-2024-08 chr20:37536525 C>T maps to NM_015568.2 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:113522167 C>A maps to NM_002711.3 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:113519732 C>A maps to NM_002711.3 G472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7018-01A-11D-2024-08 chr7:113517990 A>G maps to NM_002711.3 T1052T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A70Y-01A-12D-A34J-08 chr7:113518983 A>G maps to NM_002711.3 I721I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A780-01A-12D-A32B-08 chr7:113558562 T>C maps to NM_002711.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7CA-01A-21D-A33T-08 chr7:113519702 A>G maps to NM_002711.3 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RJ-01A-11D-A33T-08 chr7:113518830 C>T maps to NM_002711.3 A772A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr23:49126931 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:49143181 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:49143231 G>T did not map to a codon.
Sequencing variant TCGA-HT-7884-01B-11D-2395-08 chr23:49142308 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:242122066 C>T maps to NM_002712.1 N304N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:242102713 C>T maps to NM_002712.1 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:26227730 G>A maps to NM_001177591.1 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:146070693 C>T maps to ENST00000394414 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:6473899 G>A maps to NM_020416.3 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr4:6380247 G>A maps to NM_181876.2 Q74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:35576556 C>A maps to NM_017917.2 G176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:63862002 C>T maps to ENST00000422769 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TB-01A-11D-A33T-08 chr4:101947177 G>A maps to NM_000944.4 F470F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:22368597 G>T did not map to a codon.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr2:68413614 A>G maps to ENST00000406334 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RC-01A-11D-A289-08 chr9:104356876 G>A maps to NM_147180.2 N112N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:30096137 G>A maps to NM_002720.1 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5874-01A-11D-1705-08 chr18:9549243 G>A maps to NM_001042388.1 N880N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:73096444 C>T maps to NM_174907.2 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MT-01A-11D-A26M-08 chr10:103899572 G>A maps to NM_015062.3 P436P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:32125412 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:47087292 C>A maps to NM_005972.4 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:47086887 G>A maps to NM_005972.4 Q35Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7Z4-01A-11D-A34J-08 chr10:47086810 C>T maps to NM_005972.4 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:12856087 C>A maps to NM_023013.2 P456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:12853430 A>T maps to NM_023013.2 R19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8C9-01A-11D-A36O-08 chr1:12854385 C>T maps to NM_023013.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7008-01A-11D-2024-08 chr1:12884886 G>T maps to NM_001146344.1 P408P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F6-A8O4-01A-11D-A36O-08 chr1:12887676 A>G maps to NM_001146344.1 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8161-01A-11D-2253-08 chr1:12837724 C>T maps to NM_001080830.1 Q479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6J3-01A-11D-A31L-08 chr1:12837336 C>A maps to NM_001080830.1 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr1:12943050 C>T maps to NM_001009611.2 K55K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YE-01A-11D-A34A-08 chr12:11507488 C>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:106554793 C>T maps to NM_001198.3 H637H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F4-01A-11D-A289-08 chr6:106553786 C>T maps to NM_001198.3 F584F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5393-01A-01D-1468-08 chr11:129784708 G>A maps to NM_020228.2 R915*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:129772398 A>G maps to NM_020228.2 L1098L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:129827805 C>A did not map to a codon.
Sequencing variant TCGA-HW-7495-01A-11D-2024-08 chr11:129817094 C>T maps to NM_020228.2 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:70964425 G>A maps to NM_024504.2 S534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7018-01A-11D-2024-08 chr8:70978497 C>T maps to NM_024504.2 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7482-01A-11D-2024-08 chr8:70981759 C>T maps to NM_024504.2 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:43242387 G>A maps to NM_022115.3 I955I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:43222907 G>A maps to NM_022115.3 G1335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A60L-01A-12D-A31L-08 chr21:43274912 G>A maps to NM_022115.3 D466D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:3322123 C>T maps to NM_022114.3 H366H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6395-01A-12D-1705-08 chr1:14143063 A>G maps to NM_001135610.1 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7298-01A-11D-2024-08 chr4:121631493 C>T maps to NM_018699.2 T566T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr16:90124771 G>A maps to NM_001098173.1 S468S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5281-01A-01D-1468-08 chr5:23527686 G>A maps to NM_020227.2 K830K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YE-01A-11D-A34A-08 chr5:23526453 A>G maps to NM_020227.2 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YJ-01A-11D-A34A-08 chr5:23522419 G>A maps to NM_020227.2 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QW-01A-11D-A34A-08 chr5:23526936 T>G maps to NM_020227.2 Y580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:45981479 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:45977086 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:23685738 C>T did not map to a codon.
Sequencing variant TCGA-S9-A7IQ-01A-21D-A34A-08 chr2:27356047 G>A maps to NM_013388.4 C161C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:105800934 G>T maps to NM_002726.4 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr20:47266678 C>T maps to NM_020820.3 P961P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:69069573 G>T maps to NM_024870.2 G1417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8C8-01A-11D-A36O-08 chr8:68956772 T>C maps to NM_024870.2 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64W-01A-11D-A29Q-08 chr10:72358831 A>C maps to NM_005041.4 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F6-A8O4-01A-11D-A36O-08 chr1:186276098 C>T maps to NM_005807.3 T416T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8182-01A-11D-2253-08 chr1:186276305 T>C maps to NM_005807.3 T485T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UR-01A-11D-A33T-08 chr20:62196934 G>A maps to NM_001037335.2 D1080D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:62190667 G>A maps to NM_001037335.2 C2627C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:62198523 G>A maps to NM_001037335.2 H729H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7006-01A-11D-2024-08 chr20:62193042 A>G maps to NM_001037335.2 A2249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr20:62195518 C>T maps to NM_001037335.2 L1552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85E-01A-11D-A36O-08 chr20:62195644 C>T maps to NM_001037335.2 P1510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5872-01A-11D-1705-08 chr12:42858962 A>G maps to NM_153026.2 C291C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:42860068 G>A maps to NM_153026.2 D234D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7875-01A-11D-2395-08 chr12:42860092 T>A maps to NM_153026.2 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RM-01A-11D-A33T-08 chr12:42854057 G>A maps to NM_153026.2 S683S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:64184477 C>T maps to NM_198859.3 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:64145735 G>A maps to NM_198859.3 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:64184561 G>A maps to NM_198859.3 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8110-01A-11D-2395-08 chr6:41753226 C>T maps to NM_013397.5 C177C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7019-01A-11D-2024-08 chr6:57185253 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:40764714 G>A maps to NM_206907.3 R461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:120106186 C>A maps to NM_006253.4 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:14218162 A>T maps to NM_002730.3 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:84668409 C>A maps to NM_182948.2 I276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:219692320 C>T maps to NM_017431.2 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7299-01A-21D-2024-08 chr7:751124 G>C maps to NM_002735.2 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:64683230 C>T maps to NM_002737.2 R178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:64684447 C>T maps to NM_002737.2 R239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7290-01A-11D-2024-08 chr17:64785021 G>A maps to NM_002737.2 E593E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7J2-01A-11D-A34A-08 chr16:23848693 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:6340467 C>T maps to NM_145040.2 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:46386776 C>T maps to NM_005400.2 G651G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6UA-01A-12D-A33T-08 chr19:54403578 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:61997174 C>T maps to NM_006255.3 G541G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UR-01A-11D-A33T-08 chr3:169998191 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:169977799 C>A maps to NM_002740.5 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:6557046 G>A maps to NM_006257.2 C17C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:6549436 G>A maps to NM_006257.2 R114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7469-01A-11D-2253-08 chr10:6527129 C>T maps to NM_006257.2 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RU-01A-21D-A34A-08 chr10:6553001 C>T maps to NM_006257.2 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7687-01A-11D-2253-08 chr14:30105554 G>A maps to NM_002742.2 N377N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:48749832 G>A maps to NM_006904.6 S2566S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:48715995 C>A maps to NM_006904.6 E3264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:48771460 C>T maps to NM_006904.6 T2097T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:48826495 C>A maps to NM_006904.6 E916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WD-01A-12D-A33T-08 chr8:48715930 G>A maps to NM_006904.6 C3285C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr8:48790317 A>T maps to NM_006904.6 L1776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74L-01A-11D-A32B-08 chr10:53893605 T>C maps to NM_001098512.1 D299D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr4:82026997 G>A maps to NM_006259.1 R678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4942-01A-01D-1468-08 chr2:179314990 G>T maps to NM_003690.4 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:22294742 G>A maps to ENST00000397199 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr5:35065589 C>T maps to NM_000949.4 T490T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:148579096 A>T maps to NM_138364.2 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7019-01A-11D-2024-08 chr4:148594114 G>T maps to NM_138364.2 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7C3-01A-11D-A32B-08 chr4:148605023 G>A maps to NM_138364.2 Q39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:20515714 C>T maps to NM_005788.3 V467V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:20417379 A>G maps to NM_005788.3 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:23390199 C>T maps to NM_006109.3 K609K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76K-01A-11D-A33T-08 chr1:107599765 A>G maps to NM_018137.2 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr20:4705631 C>T maps to NM_012409.2 C145C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:128183682 C>A maps to ENST00000409048 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:18918707 G>A maps to NM_016335.4 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5318-01A-01D-1468-08 chr19:36302866 C>T maps to NM_021232.1 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr19:36293162 G>T maps to NM_021232.1 G452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:95950733 G>A maps to NM_144707.2 R582R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:95953981 C>T maps to NM_144707.2 C756C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TY-01A-12D-A32B-08 chr2:95940489 C>T maps to NM_144707.2 R53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YJ-01A-11D-A34A-08 chr11:60658694 G>A maps to NM_014502.4 H486H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A77X-01A-11D-A32B-08 chr11:60665316 C>G did not map to a codon.
Sequencing variant TCGA-S9-A7QW-01A-11D-A34A-08 chr19:54628007 C>T maps to NM_015629.3 H276H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:109241946 C>T maps to NM_018061.2 R316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr14:45583421 G>A maps to NM_017922.3 L598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7608-01A-11D-2086-08 chr12:50036430 C>G maps to NM_001031698.1 L675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:4050045 C>T maps to NM_003913.4 R703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:1578971 G>T maps to NM_006445.3 P938P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7290-01A-11D-2024-08 chr17:1585130 C>T maps to NM_006445.3 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FN-7833-01A-11D-2086-08 chr17:1557306 C>T maps to NM_006445.3 V1997V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6401-01A-11D-1705-08 chr6:42690066 C>T maps to NM_000322.4 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8189-01B-11D-A289-08 chr23:106890920 G>A did not map to a codon.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr23:12838860 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:12828158 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:12828248 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:12837721 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:74344662 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:50099341 G>T maps to NM_020719.1 G584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr19:50123628 C>T maps to NM_020719.1 L1840L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65Z-01A-11D-A29Q-08 chr19:50100108 A>C maps to NM_020719.1 P839P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R5-01A-11D-A289-08 chr16:30666112 A>C maps to NM_024031.2 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65V-01A-11D-A29Q-08 chr16:30664040 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:42813972 C>T maps to NM_199285.2 H79H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr19:42814702 G>A maps to NM_199285.2 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr19:42813897 G>T maps to NM_199285.2 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YV-01A-11D-A34J-08 chr19:5783641 G>A maps to NM_001134316.1 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:138763114 G>A maps to NM_001134657.1 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr16:855738 G>A maps to NM_001013638.1 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:45110539 C>T maps to ENST00000352766 N68N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:36472880 G>A maps to NM_001160167.1 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:119203985 C>A maps to NM_003619.3 G774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7875-01A-11D-2395-08 chr7:142481315 T>C maps to ENST00000311757 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R5-01A-11D-A289-08 chr7:142480059 C>T maps to ENST00000311757 C78C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TU-01A-12D-A32B-08 chr7:142481345 T>C maps to ENST00000311757 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7470-01A-12D-2086-08 chr16:2906138 G>A maps to NM_022119.3 C75C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7882-01A-11D-2395-08 chr6:84233952 C>T maps to NM_153362.2 R265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R5-01A-11D-A289-08 chr6:84233253 A>T maps to NM_153362.2 R32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr3:46755846 G>A maps to NM_013270.4 N205N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5275-01A-01D-1468-08 chr16:58324918 G>A maps to NM_001080492.1 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6XC-01A-12D-A32B-08 chr8:10388837 C>T maps to NM_198464.3 N127N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TA-01A-11D-A33T-08 chr16:31143812 C>T maps to NM_002773.3 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A737-01A-11D-A32B-08 chr15:55916584 T>C maps to NM_173814.4 E1016E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7009-01A-11D-2024-08 chr9:79324330 G>A maps to NM_015225.2 N953N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:80921248 C>A maps to ENST00000421149 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:104176345 C>T maps to NM_002779.3 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:139216471 C>T maps to NM_032289.2 R494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5397-01A-01D-1893-08 chr8:18725327 G>C maps to ENST00000440756 S497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7477-01B-11D-A289-08 chr8:18729530 T>A maps to ENST00000440756 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr8:18490300 T>C maps to ENST00000440756 K746K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UR-01A-11D-A33T-08 chr2:113940278 C>T maps to NM_012455.2 D82D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UR-01A-11D-A33T-08 chr2:113958748 G>A maps to NM_012455.2 E976E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:227071419 C>T maps to ENST00000391872 N85N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85E-01A-11D-A36O-08 chr19:43382063 C>T did not map to a codon.
Sequencing variant TCGA-DU-8165-01A-11D-2253-08 chr19:43519343 A>G maps to ENST00000306308 N302N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:43708104 G>T maps to NM_002780.3 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6XC-01A-12D-A32B-08 chr19:43433783 A>G maps to NM_002783.2 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7290-01A-11D-2024-08 chr19:43766010 C>T did not map to a codon.
Sequencing variant TCGA-E1-A7YO-01A-11D-A34A-08 chr19:43763053 G>A maps to NM_002784.3 R315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:15479597 G>A maps to NM_001128217.1 R182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:67943503 C>T maps to NM_006742.2 G284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:87076753 C>A maps to ENST00000276616 E98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:60718344 G>A maps to NM_002792.2 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UV-01A-12D-A34A-08 chr16:67968567 G>A maps to NM_002801.2 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WQ-01A-12D-A34A-08 chr16:67970345 A>T maps to NM_002801.2 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:23511604 C>T maps to NM_001099780.1 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:103008237 C>T maps to NM_002803.2 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:231941834 C>T maps to NM_002807.3 R344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5872-01A-11D-1705-08 chr17:65341916 T>A maps to NM_002816.3 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:38146434 C>T maps to NM_002809.2 V322V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YD-01A-11D-A34A-08 chr14:24606639 G>A maps to NM_176783.1 E82E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65V-01A-11D-A29Q-08 chr17:40990762 C>T maps to NM_176863.1 Q154*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DB-A75O-01A-11D-A32B-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:109823527 G>A maps to ENST00000409138 R289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6395-01A-12D-1705-08 chr1:97278638 T>A maps to ENST00000370197 T486T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:99026724 C>A did not map to a codon.
Sequencing variant TCGA-DU-6401-01A-11D-1705-08 chr7:99026818 G>A maps to NM_001198879.1 I323I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RM-01A-11D-A33T-08 chr5:71616215 C>T maps to NM_024754.3 R3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr1:45291948 G>A maps to NM_003738.4 G1029G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr1:45294291 G>A maps to NM_003738.4 G492G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr23:23353201 T>G did not map to a codon.
Sequencing variant TCGA-DH-A7UR-01A-11D-A33T-08 chr23:23398282 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:23398058 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:23398313 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:23353125 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:23411053 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:23411709 A>G did not map to a codon.
Sequencing variant TCGA-DU-A6S2-01A-21D-A32B-08 chr23:23411555 G>A did not map to a codon.
Sequencing variant TCGA-FG-A87Q-01A-11D-A36O-08 chr23:23397846 G>A did not map to a codon.
Sequencing variant TCGA-QH-A6X9-01A-12D-A32B-08 chr23:23410782 T>C did not map to a codon.
Sequencing variant TCGA-S9-A7R1-01A-12D-A34J-08 chr23:23398113 C>T did not map to a codon.
Sequencing variant TCGA-S9-A7R4-01A-12D-A34J-08 chr10:27702369 G>A maps to NM_001034842.3 Y270Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84G-01A-11D-A36O-08 chr10:27688134 A>G maps to NM_001034842.3 S464S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TD-01A-12D-A34A-08 chr10:89720874 G>A maps to NM_000314.4 K342K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CX-01A-11D-A32B-08 chr10:89720851 C>T maps to NM_000314.4 R335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TW-01A-12D-A32B-08 chr10:89717660 C>G maps to NM_000314.4 S229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RP-01A-21D-A34A-08 chr10:89717740 G>T maps to NM_000314.4 E256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7641-01B-11D-2253-08 chr10:16526577 T>C maps to NM_030664.3 Y65Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:139873513 T>C maps to ENST00000224167 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:52781700 G>A maps to NM_000956.3 Q145Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:71512567 G>T maps to ENST00000354608 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:40681275 C>T maps to NM_000958.2 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85E-01A-11D-A36O-08 chr5:40681652 C>T maps to NM_000958.2 Y186Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5874-01A-11D-1705-08 chr9:130885211 C>T maps to ENST00000492057 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:117492099 C>T maps to NM_020440.2 C373C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:117509947 C>A maps to NM_020440.2 T685T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:117529444 C>A maps to NM_020440.2 P832P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TJ-01A-11D-A34J-08 chr1:117487661 G>A maps to NM_020440.2 Q260Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:48140672 G>A maps to NM_000961.3 Y259Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TA-01A-11D-A33T-08 chr1:186645671 G>A maps to NM_000963.2 C299C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7477-01B-11D-A289-08 chr1:186643727 A>G maps to NM_000963.2 V524V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr2:209309553 C>A maps to NM_005048.2 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:141711022 A>G maps to NM_005607.4 D844D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:27287913 G>A maps to NM_004103.3 K216K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:27288418 G>A maps to NM_004103.3 Q232Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8012-01A-11D-2395-08 chr8:27310643 G>A maps to NM_004103.3 G854G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr8:27279864 G>A maps to NM_004103.3 E172E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:62162170 G>A maps to NM_005975.2 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:62168628 A>C maps to NM_005975.2 Y13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:43106884 C>T maps to NM_002821.3 F458F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:142435203 C>T maps to NM_032611.1 D54D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RP-01A-21D-A34A-08 chr9:96859861 C>T maps to ENST00000434261 H338H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8C8-01A-11D-A36O-08 chr9:96859723 G>A maps to ENST00000434261 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YE-01A-11D-A34A-08 chr15:65847276 C>T maps to NM_016395.2 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:21015895 C>T did not map to a codon.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr20:49195081 G>A maps to NM_002827.2 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:112926975 G>A maps to ENST00000392596 E536E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:112919927 C>T maps to ENST00000392596 G381G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6670-01A-11D-1893-08 chr4:87643479 T>C maps to NM_080685.2 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:214576227 G>A maps to NM_005401.4 H193H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:131116869 C>T maps to NM_014369.3 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:88967683 G>A maps to NM_007039.3 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7637-01A-11D-2086-08 chr3:47447436 C>A maps to NM_015466.2 C149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:112170620 T>G maps to NM_002829.3 R539R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr9:112166751 G>A maps to NM_002829.3 S643S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr2:120709679 A>G maps to NM_002830.2 E596E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TD-01A-12D-A34A-08 chr11:18765711 G>A maps to NM_032781.3 D44D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7J3-01A-21D-A34J-08 chr1:202124737 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:3002824 C>A maps to NM_002836.3 A429A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:70989892 A>G maps to NM_001109754.1 N398N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6410-01A-11D-1893-08 chr12:70980858 G>A maps to NM_001109754.1 R747*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8185-01A-11D-2253-08 chr12:71002870 C>T maps to NM_001109754.1 E319E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F4-01A-11D-A289-08 chr12:70949899 G>A maps to NM_001109754.1 C1581C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TA-01A-11D-A33T-08 chr1:198703523 C>A maps to ENST00000271610 V749V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr1:198687262 A>T maps to ENST00000271610 S497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KT-A7W1-01A-11D-A34A-08 chr1:198676001 A>G maps to ENST00000271610 E275E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:67203584 G>T maps to NM_005608.2 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XB-01A-11D-A26M-08 chr9:8633422 G>A maps to NM_002839.3 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6542-01A-11D-1893-08 chr9:8376663 C>T maps to NM_002839.3 T1483T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7Z6-01A-11D-A34J-08 chr9:8341764 C>T maps to NM_002839.3 L1625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr1:44056970 C>T maps to NM_002840.3 S426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R9-01A-11D-A289-08 chr1:44019523 G>A maps to NM_002840.3 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:62063839 C>T maps to NM_002841.3 Q175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7902-01A-12D-2395-08 chr3:62248552 C>G maps to NM_002841.3 Y880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:55702873 G>T maps to NM_002842.3 V793V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7467-01A-11D-2024-08 chr19:55693460 G>A maps to NM_002842.3 Q1041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WD-01A-12D-A33T-08 chr11:48146662 C>A maps to NM_002843.3 R340R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TA-01A-11D-A33T-08 chr6:128312441 G>A maps to ENST00000368210 G1010G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A669-01A-12D-A31L-08 chr18:7888161 C>A maps to NM_001105244.1 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:8069838 C>T maps to NM_001105244.1 R430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76L-01A-11D-A32B-08 chr18:7949213 C>T maps to NM_001105244.1 I233I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7475-01A-11D-2024-08 chr18:7949177 G>A did not map to a codon.
Sequencing variant TCGA-TQ-A7RJ-01A-11D-A33T-08 chr18:8370964 A>G maps to NM_001105244.1 L1044L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CD-01A-11D-A36O-08 chr18:8394605 C>G maps to NM_001105244.1 L1447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:157370802 G>A maps to NM_002847.3 I842I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:157370772 G>A maps to NM_002847.3 G852G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8164-01A-11D-2253-08 chr12:15654566 T>C maps to NM_030667.1 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr12:71094988 G>A maps to NM_002849.2 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr12:71094999 G>A maps to NM_002849.2 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:5240338 C>T maps to NM_002850.3 P525P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7014-01A-11D-2024-08 chr20:40735470 G>A maps to ENST00000373198 C1137C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:29606578 G>A maps to NM_005704.4 P598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:29585239 G>A maps to NM_005704.4 W143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:29644279 G>A maps to NM_005704.4 P1188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7605-01A-11D-2086-08 chr1:29585122 C>A maps to NM_005704.4 Y104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr1:29611339 C>T maps to NM_005704.4 L759L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66B-01A-11D-A29Q-08 chr7:121693972 C>T maps to NM_002851.2 Q2088*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:121651949 G>A maps to NM_002851.2 V950V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:121650942 G>T maps to NM_002851.2 E615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:121652219 G>A maps to NM_002851.2 A1040A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:159849770 G>C maps to NM_004219.2 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A75M-01A-11D-A32B-08 chr3:157154852 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:1537617 G>A maps to NM_001013658.1 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84G-01A-11D-A36O-08 chr16:1536428 G>A maps to NM_001013658.1 Y311Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:144898850 C>A maps to NM_078480.1 E507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6J1-01A-11D-A31L-08 chr7:44924341 G>A maps to NM_033224.3 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CV-01A-11D-A31L-08 chr8:30854162 A>T maps to NM_001015508.1 C305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:61198656 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:105148911 C>A maps to NM_019042.3 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KT-A74X-01A-11D-A32B-08 chr7:105148878 A>G maps to NM_019042.3 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4938-01B-11D-1893-08 chr12:44149036 A>G maps to NM_031292.3 D4D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:108102954 C>A maps to NM_007062.1 I412I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:45544499 C>T maps to NM_005049.2 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:159545951 G>A maps to NM_001130864.1 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A61B-01A-11D-A29Q-08 chr10:134219371 G>A maps to NM_138499.3 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:1684082 C>T maps to NM_012293.1 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr8:52233388 G>A maps to NM_144651.4 A1405A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7884-01B-11D-2395-08 chr12:133277885 G>A maps to NM_018663.1 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TJ-01A-11D-A34J-08 chr20:32308004 G>C maps to NM_007238.4 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:144689167 G>T maps to NM_023078.3 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:25259040 G>A maps to NM_002862.3 S314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:25255256 C>T maps to NM_002862.3 Y186Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:25228966 C>T maps to NM_002862.3 D51D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5851-01A-13D-1893-08 chr14:51378915 G>A maps to NM_002863.4 R576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A83Y-01A-11D-A36O-08 chr14:51382684 C>T maps to NM_002863.4 W366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:64527345 C>A maps to NM_005609.2 E9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:158943459 A>G maps to NM_152501.3 A461A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5393-01A-01D-1468-08 chr12:21593339 A>G maps to NM_024854.3 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr12:21615671 A>G did not map to a codon.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr10:100143598 G>A maps to NM_032709.2 R568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5143-01A-01D-1468-08 chr12:9317914 G>A maps to NM_002864.2 T769T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7471-01A-11D-2253-08 chr12:9309930 G>A maps to NM_002864.2 A1130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:17492297 C>A maps to NM_000320.2 E206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QY-01A-11D-A34A-08 chr3:49083857 C>T maps to NM_198880.1 K557K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YD-01A-11D-A34A-08 chr17:74287132 G>A maps to NM_032134.1 T1059T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:107113855 C>A maps to NM_018292.4 A522A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:32954222 C>T maps to NM_001076786.1 Y344Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8113-01A-11D-2395-08 chr9:139118661 G>A maps to NM_181701.3 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TC-01A-21D-A34J-08 chr2:136389572 T>A did not map to a codon.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr12:57674221 C>T maps to ENST00000438036 Q439Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6188-01A-11D-1893-08 chr8:37729418 C>T maps to NM_001002814.2 S967S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:37730080 C>A maps to NM_001002814.2 G747*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7637-01A-11D-2086-08 chr8:37730000 G>A maps to NM_001002814.2 P773P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A711-01A-21D-A33T-08 chr8:37732634 C>T maps to NM_001002814.2 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7481-01A-11D-2024-08 chr8:37734855 G>A maps to NM_001002814.2 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr8:37734843 C>T maps to NM_001002814.2 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:119799880 C>T maps to ENST00000369199 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:560782 C>T maps to NM_014700.3 I541I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:570583 C>T maps to NM_014700.3 S714S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:73316021 G>A maps to NM_015470.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:123949284 A>G maps to NM_016322.3 Y99Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:123952956 G>A maps to NM_016322.3 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:123943690 C>A maps to NM_016322.3 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr2:238483769 G>A maps to NM_022449.3 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:27822775 C>T maps to NM_021252.3 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:66039662 C>T maps to NM_030981.2 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:111176380 C>T maps to NM_017817.1 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:129318395 C>A did not map to a codon.
Sequencing variant TCGA-HT-7877-01A-11D-2395-08 chr23:129306041 G>A did not map to a codon.
Sequencing variant TCGA-HT-8563-01A-11D-2395-08 chr23:129318701 C>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:27043036 C>T maps to NM_001144943.1 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YJ-01A-11D-A34A-08 chr22:23503696 G>T maps to NM_004914.2 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6UA-01A-12D-A33T-08 chr22:23487581 T>A maps to NM_004914.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A847-01A-11D-A36O-08 chr2:135926348 T>G maps to NM_001172435.1 *989G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RR-01A-21D-A34A-08 chr1:220345392 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:70149247 G>A maps to NM_175623.2 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RW-01A-11D-A33T-08 chr12:70194026 G>A maps to NM_175623.2 K325K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:102754929 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:102192954 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:102192393 G>A did not map to a codon.
Sequencing variant TCGA-F6-A8O4-01A-11D-A36O-08 chr16:677516 C>T maps to NM_021168.4 A247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:13727015 G>A did not map to a codon.
Sequencing variant TCGA-IK-7675-01A-11D-2086-08 chr17:5257697 A>G maps to NM_004703.4 K336K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:28925766 G>A maps to NM_024816.2 C228C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:28925757 G>A maps to NM_024816.2 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:127990303 C>T maps to NM_005833.3 D214D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:125748527 C>T maps to NM_012197.3 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:24737352 G>T maps to NM_182836.1 S370S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr14:24737795 G>A maps to NM_182836.1 N310N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:114399651 A>G maps to ENST00000409875 E221E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:100959651 G>A maps to NM_022777.2 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:50400276 A>G maps to NM_013277.3 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:68687667 C>T maps to NM_133339.1 N350N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:13063630 C>A maps to NM_005053.2 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:131953825 C>T maps to NM_005732.3 R1077*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7298-01A-11D-2024-08 chr5:131930713 T>A maps to NM_005732.3 I649I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YM-01A-11D-A34A-08 chr2:17698257 C>T maps to NM_001099218.2 T475T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84L-01A-11D-A36O-08 chr2:17697555 C>T maps to NM_001099218.2 Q709Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VV-A829-01A-21D-A36O-08 chr2:17698689 G>A maps to NM_001099218.2 Y331Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:68301879 G>A maps to NM_133509.3 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64P-01A-11D-A29Q-08 chr12:1023181 A>T maps to NM_134424.2 L358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KT-A74X-01A-11D-A32B-08 chr8:95403998 G>A maps to NM_012415.2 C549C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:51667723 C>T maps to NM_015106.2 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UR-01A-11D-A33T-08 chr7:4874837 C>T maps to NM_018059.4 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5851-01A-13D-1893-08 chr7:4855892 G>A maps to NM_018059.4 S644S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:4855922 C>T maps to NM_018059.4 S634S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A713-01A-11D-A32B-08 chr7:4917590 C>T maps to NM_018059.4 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:150342235 G>A maps to NM_130900.2 Q146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7694-01A-11D-2253-08 chr3:12653551 G>A maps to ENST00000415519 R73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr11:36596674 C>T maps to NM_000448.2 D607D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:155110753 C>A maps to NM_018845.3 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6667-01A-12D-2024-08 chr11:36614245 G>A maps to NM_000536.3 P491P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:17696879 T>C maps to ENST00000395776 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:34803817 A>G maps to NM_001145521.1 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:34808725 C>T maps to NM_001145521.1 C139C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:17819071 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:17818659 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:17818947 G>T did not map to a codon.
Sequencing variant TCGA-E1-A7YQ-01A-11D-A34J-08 chr23:17819634 G>C did not map to a codon.
Sequencing variant TCGA-HT-7605-01A-11D-2086-08 chr7:39726380 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:9522279 G>T maps to NM_006788.3 E276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:36219825 G>T maps to NM_194301.2 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:36217957 C>A maps to NM_194301.2 E362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7014-01A-11D-2024-08 chr14:36226109 T>C maps to NM_194301.2 Q184Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R2-01A-21D-A34J-08 chr14:36147302 C>A maps to NM_194301.2 E987*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85A-01A-21D-A36O-08 chr20:20484147 C>T maps to NM_020343.3 V1685V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:135974141 C>T maps to NM_006266.2 K859K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:178875980 C>T maps to NM_152663.3 A567A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8188-01A-11D-2253-08 chr7:45222923 C>T maps to NM_005856.2 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:170395323 G>A maps to NM_022897.3 W551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:109382973 C>T maps to NM_006267.4 S1993S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RW-01A-11D-A33T-08 chr2:109368335 C>T maps to NM_006267.4 N547N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A70Z-01A-12D-A33T-08 chr5:36301464 G>T maps to NM_001161429.1 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:6012453 C>A maps to NM_012416.2 E1052*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:13657461 C>T maps to NM_005493.2 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:21938055 G>A maps to NM_001145658.1 D308D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:21937986 G>A maps to NM_001145658.1 H331H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8188-01A-11D-2253-08 chr17:2909298 C>T maps to NM_015085.4 N441N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:131351030 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:131348448 A>G did not map to a codon.
Sequencing variant TCGA-HT-7603-01A-21D-2086-08 chr23:131351244 C>T did not map to a codon.
Sequencing variant TCGA-S9-A6TS-01A-12D-A33T-08 chr23:131351246 G>T did not map to a codon.
Sequencing variant TCGA-S9-A6TZ-01A-21D-A32B-08 chr23:131348313 G>A did not map to a codon.
Sequencing variant TCGA-S9-A7QY-01A-11D-A34A-08 chr23:131348281 G>T did not map to a codon.
Sequencing variant TCGA-TM-A7CF-01A-11D-A32B-08 chr23:131351119 T>C did not map to a codon.
Sequencing variant TCGA-DU-7304-01A-12D-2086-08 chr9:134501729 G>A maps to NM_198679.1 N428N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5393-01A-01D-1468-08 chr4:160277113 G>A maps to NM_014247.2 P1426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:160277279 C>T maps to NM_014247.2 Q1482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:173825906 C>T maps to NM_007023.3 R217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:130815252 C>T maps to ENST00000514667 K728K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84B-01A-11D-A36O-08 chr11:47469621 G>A maps to NM_005055.3 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:25636122 A>G maps to NM_000965.3 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KK-01A-11D-A27K-08 chr3:25470377 A>G maps to NM_000965.3 Q52Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5281-01A-01D-1468-08 chr12:53609146 G>A maps to NM_000966.4 N135N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6667-01A-12D-2024-08 chr7:150037191 A>G maps to NM_002889.3 N92N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:88251664 G>A maps to NM_020320.3 Q195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:114757975 G>A maps to ENST00000389544 L751L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:178433520 C>T maps to ENST00000263528 L1110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R8-01A-11D-A34J-08 chr1:178427189 G>A maps to ENST00000263528 S910S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:17398696 C>T maps to NM_016084.3 K196K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7608-01A-11D-2086-08 chr22:35947955 C>T maps to NM_014310.3 D226D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:82369300 T>C maps to NM_152545.1 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7US-01A-11D-A33T-08 chr15:79296447 C>T maps to NM_002891.4 P731P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:79382708 G>A maps to NM_002891.4 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:79324527 G>A maps to NM_002891.4 Y363Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:79317729 G>A maps to NM_002891.4 R490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:79350823 C>T did not map to a codon.
Sequencing variant TCGA-DU-8161-01A-11D-2253-08 chr15:79277480 G>A maps to NM_002891.4 I1110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr15:79296192 G>A maps to NM_002891.4 G816G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CV-01A-11D-A31L-08 chr15:79310180 C>T maps to NM_002891.4 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr5:80366345 A>G maps to NM_006909.1 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R7-01A-11D-A289-08 chr2:33745640 T>G maps to NM_170672.2 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RJ-01A-11D-A33T-08 chr19:38912755 G>A maps to ENST00000405332 R21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7019-01A-11D-2024-08 chr22:29709886 G>A maps to NM_006477.3 Y103Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TW-01A-12D-A32B-08 chr3:50368773 C>T maps to NM_170714.1 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:4776462 C>T maps to NM_014737.2 Q95Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TV-01A-12D-A34J-08 chr20:4771249 C>T maps to NM_014737.2 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:206760237 G>A maps to NM_182663.2 V395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr1:206711606 C>T maps to NM_182663.2 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TS-01A-11D-A289-08 chr12:86199244 A>G maps to NM_005447.3 D181D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KJ-01A-12D-A27K-08 chr12:86199469 C>T maps to NM_005447.3 E106E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RP-01A-21D-A34A-08 chr12:86198644 T>C maps to NM_005447.3 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:65234398 C>T maps to ENST00000294428 R104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5847-01A-11D-1705-08 chr13:48953727 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:53570291 C>T maps to NM_014781.4 T699T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:5104163 T>C maps to NM_021163.3 H359H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:33145305 G>T maps to NM_005610.2 *426Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:24578498 C>A maps to NM_006910.4 S542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:16870700 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:16863951 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:35672548 G>A maps to NM_002895.2 H570H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UU-01A-12D-A34A-08 chr16:53495679 T>C maps to NM_005611.3 A458A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:47045958 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:47039291 C>T did not map to a codon.
Sequencing variant TCGA-S9-A7R8-01A-11D-A34J-08 chr23:47044861 G>A did not map to a codon.
Sequencing variant TCGA-S9-A6U9-01A-11D-A32B-08 chr20:34240877 A>G maps to NM_001198838.1 P789P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:94746081 C>A maps to NM_203390.2 E853*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr8:94747711 C>G maps to NM_203390.2 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5390-01A-02D-1468-08 chr6:155143449 G>T maps to NM_014892.3 T611T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:6152027 C>T maps to NM_001145547.1 Y214Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7018-01A-11D-2024-08 chr5:150073654 C>T maps to NM_018047.2 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:73578419 G>A maps to NM_021239.2 K734K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KT-A7W1-01A-11D-A34A-08 chr14:73577738 C>T maps to NM_021239.2 G631G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A870-01A-11D-A36O-08 chr14:73572993 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:79911337 G>T maps to ENST00000438737 R879R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:127965878 C>A maps to NM_018077.2 E399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5143-01A-01D-1468-08 chr7:155530751 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:106310866 T>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:106310817 A>G did not map to a codon.
Sequencing variant TCGA-HT-7482-01A-11D-2024-08 chr23:106310756 C>A did not map to a codon.
Sequencing variant TCGA-DU-7006-01A-11D-2024-08 chr4:155719189 C>T maps to NM_144979.3 R127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YK-01A-11D-A34A-08 chr4:40434727 G>A maps to NM_001098634.1 A494A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr3:50099411 C>T maps to NM_005777.2 P819P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:50005100 G>A maps to NM_005777.2 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:161159997 G>A maps to NM_016836.3 Q135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:56980710 G>T did not map to a codon.
Sequencing variant TCGA-E1-A7YM-01A-11D-A34A-08 chr3:30029662 G>A maps to NM_001003793.2 G376G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr3:29977602 C>T maps to NM_001003793.2 D322D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8018-01A-11D-2395-08 chr3:29323192 G>A maps to NM_001003793.2 Q7Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:135957741 G>A did not map to a codon.
Sequencing variant TCGA-FG-A710-01A-12D-A33T-08 chr23:135957424 T>C did not map to a codon.
Sequencing variant TCGA-HT-7469-01A-11D-2253-08 chr23:135956318 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:129546779 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:129546421 G>T did not map to a codon.
Sequencing variant TCGA-P5-A72U-01A-31D-A32B-08 chr11:7111073 C>T maps to NM_014469.4 R241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr3:139237307 C>T maps to NM_002899.3 E165E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5276-01A-01D-1468-08 chr10:48390166 G>A maps to NM_002900.2 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6410-01A-11D-1893-08 chr4:26422325 C>T maps to NM_005349.2 Q172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8106-01A-11D-2395-08 chr20:43945325 G>A maps to NM_014276.2 R427R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A843-01A-11D-A36O-08 chr8:30335337 G>A maps to NM_001008712.1 K56K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:125618094 C>T maps to NM_001100588.1 W839*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A89Z-01A-11D-A36O-08 chr9:125652609 T>A maps to NM_001100588.1 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:35890510 G>A maps to NM_004414.5 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A72U-01A-31D-A32B-08 chr13:50123696 C>T maps to NM_018191.3 R314R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6UA-01A-12D-A33T-08 chr13:49075984 T>C maps to NM_001268.2 T379T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A870-01A-11D-A36O-08 chr1:17735687 G>A maps to NM_018715.2 V489V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:76434491 G>A maps to NM_015436.2 D35D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TZ-01A-21D-A32B-08 chr19:50031917 A>G maps to NM_020650.2 E63E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85D-01A-11D-A36O-08 chr19:50031743 A>G maps to NM_020650.2 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:9801417 G>A maps to NM_002903.2 N199N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66B-01A-11D-A29Q-08 chr1:211652455 G>A maps to NM_183059.2 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:31922670 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:31922130 A>G maps to ENST00000375425 R284R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TY-01A-12D-A32B-08 chr14:68192801 G>A maps to NM_152443.2 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:55556516 C>A maps to NM_001145971.1 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:110124680 G>A maps to ENST00000405097 Q317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5962-01B-11D-1893-08 chr11:110134884 A>C maps to ENST00000405097 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:24649282 G>A maps to NM_005132.2 P541P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5854-01A-11D-1705-08 chr9:36102222 C>A maps to NM_021111.2 Y477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:36109990 T>C maps to NM_021111.2 C601C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:145739846 T>C maps to ENST00000428558 Q561Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:145741145 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:73627597 G>T maps to NM_004259.5 P460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RV-01A-21D-A34A-08 chr2:86509291 C>T did not map to a codon.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr19:1495533 C>T maps to ENST00000395479 Y92Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CH-01A-12D-A36O-08 chr2:79349250 G>A maps to NM_002909.4 K107K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:120337241 T>C maps to NM_032044.3 *159W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr11:65429216 T>C maps to NM_021975.3 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:65429437 T>C maps to NM_021975.3 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6188-01A-11D-1893-08 chr7:103338476 C>T maps to ENST00000428762 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:103293191 A>G maps to ENST00000428762 V523V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:103202384 C>A maps to ENST00000428762 R1742R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7014-01A-11D-2024-08 chr7:103216082 T>C maps to ENST00000428762 G1405G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A83Z-01A-11D-A36O-08 chr7:103234845 C>T maps to ENST00000428762 Q1211Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QZ-01A-12D-A34J-08 chr7:103216049 G>A maps to ENST00000428762 C1416C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:73101670 G>A did not map to a codon.
Sequencing variant TCGA-E1-5319-01A-01D-1893-08 chr11:73102212 C>T maps to NM_152222.1 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A72Z-01A-11D-A32B-08 chr11:73105560 G>A maps to NM_152222.1 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YI-01A-11D-A34A-08 chr20:30064293 C>T maps to NM_014012.4 R16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7467-01A-11D-2024-08 chr14:23354153 G>A maps to NM_173527.2 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84M-01A-11D-A36O-08 chr14:23354538 C>A maps to NM_173527.2 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64R-01A-11D-A29Q-08 chr23:153209005 G>A did not map to a codon.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr23:153208401 G>T did not map to a codon.
Sequencing variant TCGA-HT-8108-01A-11D-2395-08 chr23:153208517 T>G did not map to a codon.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr23:17073014 C>T did not map to a codon.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr23:17065568 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:17065503 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:2328569 C>T maps to NM_007033.4 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:8418646 C>T maps to NM_012102.3 E1316E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:15262091 C>T maps to NM_032918.2 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:18234204 C>A maps to NM_024730.2 E180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RN-01A-11D-A33T-08 chr4:57796226 G>A maps to NM_005612.4 K401K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CF-01A-11D-A36O-08 chr4:57796250 A>G maps to NM_005612.4 K409K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5322-01A-01D-1468-08 chr10:43609022 A>G maps to NM_020975.4 G593G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7616-01A-11D-2253-08 chr10:43622042 G>A maps to NM_020975.4 A1020A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A77X-01A-11D-A32B-08 chr10:43619142 G>A maps to NM_020975.4 W942*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IS-01A-11D-A34A-08 chr10:43604536 G>A maps to NM_020975.4 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:7735144 C>T maps to NM_020415.3 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6397-01A-11D-1705-08 chr3:108475915 G>T maps to NM_032579.2 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:85573179 G>T maps to NM_017750.3 I345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:85573131 T>C maps to NM_017750.3 E361E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5142-01A-01D-1468-08 chr6:111726681 T>G maps to NM_002912.3 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:111695588 A>T maps to NM_002912.3 V1323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RU-01A-21D-A34A-08 chr6:111710362 G>A maps to NM_002912.3 Q270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:1821568 C>T maps to NM_020695.3 K781K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:114320643 G>T maps to NM_015523.3 E221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr4:39306545 C>T maps to ENST00000381897 E667E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:186522415 G>A maps to NM_181573.2 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TD-01A-12D-A34A-08 chr22:32587157 G>A maps to NM_001098527.2 D246D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7694-01A-11D-2253-08 chr3:53126462 C>T maps to NM_052859.3 R460R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-TQ-A7RN-01A-11D-A33T-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DU-6406-01A-11D-1705-08 chr1:176132078 G>A maps to NM_022457.5 Q230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8164-01A-11D-2253-08 chr19:14083695 G>C maps to NM_002918.4 G391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:6004262 G>A maps to NM_000635.3 G483G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:5994950 G>A maps to NM_000635.3 G689G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A618-01A-11D-A29Q-08 chr19:6013016 C>T maps to NM_000635.3 Q293Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WM-01A-12D-A33T-08 chr9:3257178 G>A maps to NM_134428.1 C542C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7US-01A-11D-A33T-08 chr12:107144430 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:107033140 G>A maps to ENST00000357881 K63K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QY-01A-11D-A34A-08 chr12:107083126 A>G maps to ENST00000357881 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr6:117198500 C>T maps to NM_173560.3 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr6:117245847 T>C maps to NM_173560.3 I524I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:117246730 C>A maps to NM_173560.3 T598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7605-01A-11D-2086-08 chr15:56387425 G>A maps to NM_022841.5 Q834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr23:109695333 A>T did not map to a codon.
Sequencing variant TCGA-CS-5393-01A-01D-1468-08 chr23:109694415 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:109694909 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:109695588 G>A did not map to a codon.
Sequencing variant TCGA-DU-6400-01A-12D-1705-08 chr23:109696414 G>A did not map to a codon.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr23:109698483 G>T did not map to a codon.
Sequencing variant TCGA-E1-5322-01A-01D-1468-08 chr23:109695812 G>A did not map to a codon.
Sequencing variant TCGA-FG-A70Y-01A-12D-A34J-08 chr23:109696776 C>T did not map to a codon.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr23:109694049 C>G did not map to a codon.
Sequencing variant TCGA-S9-A6TS-01A-12D-A33T-08 chr23:109694100 G>C did not map to a codon.
Sequencing variant TCGA-S9-A7J3-01A-21D-A34J-08 chr23:109695423 C>A did not map to a codon.
Sequencing variant TCGA-VW-A7QS-01A-12D-A33T-08 chr23:109694735 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:71350055 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:71350536 C>T did not map to a codon.
Sequencing variant TCGA-E1-A7Z6-01A-11D-A34J-08 chr23:71350456 G>A did not map to a codon.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr23:71350422 C>T did not map to a codon.
Sequencing variant TCGA-HT-8108-01A-11D-2395-08 chr23:71350843 C>T did not map to a codon.
Sequencing variant TCGA-S9-A6WI-01A-21D-A33T-08 chr23:71351176 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:33259950 C>T maps to NM_004761.3 P754P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:33261843 C>A did not map to a codon.
Sequencing variant TCGA-DU-7014-01A-11D-2024-08 chr6:33264225 T>C maps to NM_004761.3 E145E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:93595312 G>A maps to NM_020211.2 G185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5395-01A-01D-1468-08 chr23:46943842 C>T did not map to a codon.
Sequencing variant TCGA-E1-A7YE-01A-11D-A34A-08 chr23:46949263 T>C did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr23:46951572 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:73161800 G>A maps to NM_001080479.2 E705E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:107073522 C>T maps to ENST00000304514 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8013-01A-11D-2395-08 chr2:107041182 C>T maps to ENST00000304514 R1080R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RF-01A-11D-A33T-08 chr2:107040252 A>G maps to ENST00000304514 N1390N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6X8-01A-12D-A32B-08 chr2:108487633 A>G maps to NM_182588.2 K1058K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84B-01A-11D-A36O-08 chr2:108455410 T>C maps to NM_182588.2 Y132Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:121259696 G>A maps to NM_001005339.1 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr16:321438 C>T maps to NM_183337.1 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:3344776 T>C maps to NM_198229.2 L665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7309-01A-11D-2086-08 chr5:176792986 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:62705619 G>A maps to NM_005873.2 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:62705658 T>C maps to NM_005873.2 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YE-01A-11D-A34A-08 chr20:62705640 C>T maps to NM_005873.2 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R2-01A-21D-A34J-08 chr8:100990159 G>A maps to NM_015668.3 D1168D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A75L-01A-11D-A32B-08 chr9:116357879 C>T maps to NM_144488.4 Y1082Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:116267768 C>T maps to NM_144488.4 C315C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:116346482 C>T maps to NM_144488.4 L931L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr9:116356591 C>T maps to NM_144489.2 N131N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr14:72976873 C>T maps to NM_004296.4 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6UB-01A-21D-A33T-08 chr14:72431531 A>G maps to NM_004296.4 Q8Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IZ-01A-11D-A34A-08 chr14:72976894 G>A maps to NM_004296.4 W333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5142-01A-01D-1468-08 chr6:49604489 C>A maps to NM_000324.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A87Q-01A-11D-A36O-08 chr7:75511477 C>T maps to NM_001040456.1 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A669-01A-12D-A31L-08 chr16:109806 G>A maps to NM_022450.3 S580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:108626 G>T maps to NM_022450.3 T760T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7470-01A-12D-2086-08 chr16:111433 G>A maps to NM_022450.3 Y448Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:727826 G>A maps to NM_003961.1 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YW-01A-11D-A34J-08 chr1:25718593 G>A maps to NM_020485.4 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:25611235 C>A maps to ENST00000357542 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:129252542 C>T maps to NM_000539.3 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TR-01A-11D-A289-08 chr3:129251554 G>A maps to NM_000539.3 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:49399937 C>T maps to NM_001664.2 K133K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5871-01A-12D-1705-08 chr10:62648195 A>G maps to NM_014836.4 P410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5962-01B-11D-1893-08 chr5:95119547 C>T maps to NM_014899.3 Q502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:113244176 G>A maps to NM_175744.4 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:63747714 C>A maps to NM_020663.3 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:30521075 A>G maps to NM_001033568.1 R273R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8C8-01A-11D-A36O-08 chr8:144462858 G>C maps to ENST00000422773 V463V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7857-01A-11D-2395-08 chr23:53455597 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:12823148 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:152292041 G>A maps to NM_018151.4 S381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7300-01A-21D-2086-08 chr2:152319417 C>T maps to NM_018151.4 D1128D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:123900467 C>A maps to NM_145058.1 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:130912848 C>A maps to NM_015347.4 E746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7603-01A-21D-2086-08 chr12:130898839 G>A maps to NM_015347.4 R828*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CV-01A-11D-A31L-08 chr12:130919311 G>A maps to NM_015347.4 D723D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WM-01A-12D-A33T-08 chr12:130963554 G>A maps to NM_015347.4 R2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84I-01A-11D-A36O-08 chr12:130919377 G>A maps to NM_015347.4 Y701Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:42875794 C>T maps to NM_173642.3 Q208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr1:42880614 C>T maps to NM_173642.3 N382N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:8902617 C>T maps to NM_020734.2 C112C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YV-01A-11D-A34J-08 chr6:72889333 G>C maps to NM_014989.4 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7C3-01A-11D-A32B-08 chr6:72889436 C>T maps to NM_014989.4 R211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:104955038 G>A maps to NM_001100117.2 E862E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YW-01A-11D-A34J-08 chr8:105263255 G>A maps to NM_001100117.2 P1232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:66102522 C>G maps to NM_004292.2 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr20:19945626 C>T maps to ENST00000255006 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:93118182 G>A maps to NM_024832.3 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7304-01A-12D-2086-08 chr14:93043730 C>T maps to NM_024832.3 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr7:105187663 G>A maps to NM_021930.4 W241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:7401280 G>T maps to NM_031480.2 E191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:21054956 G>A maps to NM_003831.3 K353K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:3111145 G>A maps to NM_003804.3 T562T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5854-01A-11D-1705-08 chr21:43161993 G>A maps to ENST00000352483 C501C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:43161660 G>A maps to ENST00000352483 S612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7608-01A-11D-2086-08 chr21:43161858 G>A maps to ENST00000352483 N546N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr21:43161011 G>A maps to ENST00000352483 R829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5964-01A-11D-1705-08 chr6:84567020 G>A maps to NM_001009994.1 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr23:73812348 G>A did not map to a codon.
Sequencing variant TCGA-DU-5851-01A-13D-1893-08 chr23:73811937 G>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:73815756 C>T did not map to a codon.
Sequencing variant TCGA-FG-A70Z-01A-12D-A33T-08 chr23:73811937 G>C did not map to a codon.
Sequencing variant TCGA-HT-7478-01A-11D-2024-08 chr23:73811937 G>C did not map to a codon.
Sequencing variant TCGA-TQ-A7RN-01A-11D-A33T-08 chr9:5304439 G>A maps to NM_134441.1 C47C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:67682845 C>T maps to NM_001013838.1 G520G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7695-01A-11D-2253-08 chr16:67688718 A>G maps to NM_001013838.1 P1207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr16:67690170 G>A maps to NM_001013838.1 S1261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:151766609 G>A maps to NM_017909.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:177571011 G>A maps to NM_022762.3 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:21359857 C>T maps to NM_002935.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:41180610 C>T maps to NM_005440.4 R200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7884-01B-11D-2395-08 chr2:151328167 G>A maps to NM_005168.3 H152H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6668-01A-11D-1893-08 chr2:86831208 T>C maps to NM_005667.3 E605E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:86831490 G>A maps to NM_005667.3 N511N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IS-01A-11D-A34A-08 chr23:119004588 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:98828638 G>A maps to NM_178861.4 F284F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:71671879 G>A maps to NM_018320.4 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr18:29648290 C>T maps to NM_017831.3 R215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:648906 G>A maps to ENST00000340092 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:106016253 A>T did not map to a codon.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr23:105937388 G>A did not map to a codon.
Sequencing variant TCGA-S9-A6WM-01A-12D-A33T-08 chr23:105937248 G>T did not map to a codon.
Sequencing variant TCGA-E1-5302-01A-01D-1468-08 chr7:122338204 G>A maps to NM_139175.1 C256C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:29324278 G>A maps to NM_032322.3 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RQ-01A-11D-A33T-08 chr17:29325785 G>A maps to NM_032322.3 W292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:141357957 G>T maps to NM_183399.1 E133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:18427915 G>A maps to NM_182757.3 E90E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:141832499 G>A maps to NM_020724.1 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64V-01A-11D-A29Q-08 chr21:30342875 A>C maps to NM_015565.2 A437A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CA-01A-11D-A36O-08 chr21:30318164 C>T maps to NM_015565.2 W1290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KT-A7W1-01A-11D-A34A-08 chr17:4848110 G>T maps to NM_015528.1 E285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8186-01A-11D-2253-08 chr13:25428133 G>A maps to ENST00000381927 Q1203Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:78317076 G>A maps to NM_020914.4 A2094A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6410-01A-11D-1893-08 chr17:78320933 G>A maps to NM_020914.4 A2982A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:117109761 C>T maps to NM_207343.2 R185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:5692114 G>A maps to NM_207111.2 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:3925865 C>A did not map to a codon.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr14:24619440 A>T maps to NM_017999.4 R327R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:24620579 C>T maps to NM_017999.4 R577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:156468553 G>A maps to NM_001184997.1 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76L-01A-11D-A32B-08 chr7:156437434 G>A maps to NM_001184997.1 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7690-01A-11D-2253-08 chr17:56435581 G>A maps to NM_017763.4 R519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66D-01A-11D-A31L-08 chr5:175956357 C>T maps to NM_014901.4 A389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:499118 C>T maps to NM_203389.1 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8166-01A-11D-2253-08 chr1:201972431 G>T maps to NM_020216.3 G498G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7681-01A-11D-2395-08 chr1:201966605 C>T maps to NM_020216.3 N338N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:241516171 G>A maps to NM_018226.3 P346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XE-01A-11D-A27K-08 chr3:77617552 C>T maps to ENST00000332191 L647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6403-01A-11D-1705-08 chr3:77614191 C>T maps to ENST00000332191 I590I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U1-01A-21D-A33T-08 chr3:77526571 A>G maps to ENST00000332191 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:18546977 C>T maps to NM_005406.2 E1084E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A6YH-01A-21D-A32B-08 chr18:18550344 T>C maps to NM_005406.2 R928R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:114997177 C>A did not map to a codon.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr11:62381889 C>T maps to NM_000327.3 Q251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:125694465 C>T maps to NM_001012337.1 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8108-01A-11D-2395-08 chr5:10461351 C>T maps to NM_031916.3 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5273-01A-01D-1468-08 chr1:64515591 C>T maps to NM_005012.2 C131C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YE-01A-11D-A34A-08 chr9:94486330 C>T maps to NM_004560.2 P815P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr9:77257631 C>T maps to ENST00000396204 Q191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R5-01A-11D-A289-08 chr9:77277522 G>T did not map to a codon.
Sequencing variant TCGA-VM-A8CA-01A-11D-A36O-08 chr9:77280503 A>G maps to ENST00000396204 K342K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4943-01A-01D-1468-08 chr6:117609711 A>G maps to NM_002944.2 P2329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UV-01A-12D-A34A-08 chr6:117717387 T>C maps to NM_002944.2 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TB-01A-11D-A33T-08 chr6:117700220 C>A did not map to a codon.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr6:117686237 G>A maps to NM_002944.2 R1035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TA-01A-11D-A33T-08 chr8:55534813 C>G maps to NM_006269.1 Y251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A711-01A-21D-A33T-08 chr8:55537674 A>G maps to NM_006269.1 Q411Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:10470314 G>A maps to NM_178857.5 H431H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A4DS-01A-11D-A26M-08 chr8:10470653 G>A maps to NM_178857.5 D318D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VW-A8FI-01A-11D-A36O-08 chr8:10469465 C>T maps to NM_178857.5 Q714Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:46713007 G>A did not map to a codon.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr17:1798389 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:1747292 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:92789214 C>T maps to NM_024813.2 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5277-01A-01D-1468-08 chr12:48096530 C>T maps to NM_024604.2 W31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CD-01A-11D-A36O-08 chr12:48063933 T>C maps to NM_024604.2 A494A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:21793077 G>A maps to NM_020366.3 S688S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr16:53679915 C>T did not map to a codon.
Sequencing variant TCGA-QH-A65S-01A-11D-A29Q-08 chr2:89037525 C>T maps to NM_144563.2 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153627881 T>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153627701 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153628931 C>T did not map to a codon.
Sequencing variant TCGA-DU-6402-01A-11D-1705-08 chr14:47120402 G>A maps to NM_080746.2 D179D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:52028025 C>T maps to NM_000992.2 K73K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr9:136217155 C>T maps to NM_000972.2 H159H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:35812581 G>T did not map to a codon.
Sequencing variant TCGA-FG-8181-01A-11D-2253-08 chr20:35812667 C>T maps to NM_002951.3 D33D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:30313001 C>A maps to ENST00000428040 Y18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5303-01A-01D-1468-08 chr15:75248607 C>T maps to NM_017793.2 W106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:150444345 T>G maps to NM_015203.3 L974L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WQ-01A-12D-A34A-08 chr16:2012754 G>A maps to NM_002952.3 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:71494902 C>A did not map to a codon.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr23:71493767 G>T did not map to a codon.
Sequencing variant TCGA-HW-7490-01A-11D-2024-08 chr24:22930743 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:26900688 G>A maps to NM_001006665.1 L744L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:166831721 G>A maps to ENST00000510118 D668D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:20190904 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:20185730 G>A did not map to a codon.
Sequencing variant TCGA-DU-7300-01A-21D-2086-08 chr23:20205953 C>A did not map to a codon.
Sequencing variant TCGA-FG-A87Q-01A-11D-A36O-08 chr23:20227404 C>A did not map to a codon.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr11:64137196 C>T maps to NM_003942.2 P543P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:91386578 T>A maps to NM_004755.2 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TT-01A-11D-A289-08 chr23:83319381 A>G did not map to a codon.
Sequencing variant TCGA-FG-5965-01B-11D-1893-08 chr23:83403056 A>G did not map to a codon.
Sequencing variant TCGA-S9-A7J0-01A-11D-A34A-08 chr23:83352827 G>A did not map to a codon.
Sequencing variant TCGA-TM-A7C4-01A-11D-A32B-08 chr23:83442861 C>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:58024065 C>T maps to NM_003161.2 R499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:213277797 C>T maps to NM_012424.3 R89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7472-01A-11D-2024-08 chr1:213414639 T>C maps to NM_012424.3 D607D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UR-01A-11D-A33T-08 chr1:152129199 G>A maps to NM_001122965.1 H125H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8165-01A-11D-2253-08 chr1:152129013 T>C maps to NM_001122965.1 R187R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr16:837404 G>A maps to NM_058192.2 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:66956203 C>T maps to NM_004165.2 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:55757806 T>G did not map to a codon.
Sequencing variant TCGA-FG-A711-01A-21D-A33T-08 chr23:55782314 T>C did not map to a codon.
Sequencing variant TCGA-DU-5854-01A-11D-1705-08 chr11:14303173 A>C maps to NM_012250.5 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R2-01A-21D-A34J-08 chr20:17602583 C>T maps to ENST00000377813 S1052S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:7231481 G>A maps to NM_001003699.3 P1050P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:7230521 C>T maps to NM_001003699.3 I730I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YO-01A-11D-A34A-08 chr6:7229726 C>T maps to NM_001003699.3 I465I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7479-01A-11D-2024-08 chr6:7229936 G>T maps to NM_001003699.3 P535P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RC-01A-11D-A289-08 chr6:7229900 G>C maps to NM_001003699.3 T523T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EX-01A-12D-A289-08 chr6:7229900 G>C maps to NM_001003699.3 T523T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:4123241 C>T maps to NM_001033.3 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A72U-01A-31D-A32B-08 chr11:4144499 C>T maps to NM_001033.3 T402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76O-01A-11D-A32B-08 chr2:10263518 T>C maps to NM_001165931.1 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RM-01A-11D-A33T-08 chr8:103226347 G>C maps to NM_015713.4 Y241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:99131922 T>C maps to NM_015179.3 R750R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:42910711 C>T maps to NM_015703.4 E178E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr23:18660176 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:18665340 T>C did not map to a codon.
Sequencing variant TCGA-HT-7616-01A-11D-2253-08 chr23:18665416 C>G did not map to a codon.
Sequencing variant TCGA-TQ-A7RM-01A-11D-A33T-08 chr23:18660258 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:7018120 G>T maps to NM_080657.4 E64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr2:7027290 G>A maps to NM_080657.4 W245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EU-01A-11D-A27K-08 chr1:114308979 G>A maps to NM_018364.3 F677F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:77383089 C>A maps to NM_016578.3 E1250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:77412656 A>G maps to NM_016578.3 T539T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:43913093 G>A maps to NM_080860.2 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8189-01B-11D-A289-08 chr6:159403543 C>T maps to NM_031924.4 E365E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5390-01A-02D-1468-08 chr6:116938226 A>G maps to NM_001010892.2 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:116949301 G>T maps to NM_001010892.2 G478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5281-01A-01D-1468-08 chr6:43612864 G>A maps to NM_152732.4 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:127471637 C>A maps to ENST00000368317 Y119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CV-01A-11D-A31L-08 chr16:57238590 C>T maps to NM_133368.1 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:157841750 G>A maps to NM_016625.2 Q97Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:158261970 G>A did not map to a codon.
Sequencing variant TCGA-DU-A76K-01A-11D-A33T-08 chr19:12936717 G>T maps to NM_031429.1 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A843-01A-11D-A36O-08 chr22:23406093 C>T maps to NM_014433.2 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:101350843 G>A maps to NM_001134888.2 D94D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:63487003 C>T maps to ENST00000377819 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:63488067 C>A maps to ENST00000377819 S698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5270-01A-02D-1468-08 chr22:20229581 C>T maps to ENST00000425986 A443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:57235239 C>T maps to NM_178570.1 R64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr18:67695980 A>C maps to NM_173630.3 L1934L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CV-01A-11D-A31L-08 chr18:67817252 C>T maps to NM_173630.3 W709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5273-01A-01D-1468-08 chr5:179016594 C>T maps to NM_025158.3 Q359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A61B-01A-11D-A29Q-08 chr5:178996302 C>T maps to NM_025158.3 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84M-01A-11D-A36O-08 chr5:179028900 G>A maps to NM_025158.3 R590R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:71650589 A>G maps to NM_001037442.2 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:42392183 C>T maps to NM_001144825.1 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:36259225 G>A maps to NM_001754.4 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XC-01A-11D-A26M-08 chr6:45390465 A>G maps to ENST00000359524 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8163-01A-11D-2253-08 chr6:45390465 A>G maps to ENST00000359524 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8163-01A-11D-2253-08 chr6:45390462 G>A maps to ENST00000359524 Q132Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A70Y-01A-12D-A34J-08 chr6:45390462 G>A maps to ENST00000359524 Q132Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7884-01B-11D-2395-08 chr6:45390465 A>G maps to ENST00000359524 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KL-01A-11D-A27K-08 chr6:45390465 A>G maps to ENST00000359524 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65V-01A-11D-A29Q-08 chr6:45390462 G>A maps to ENST00000359524 Q132Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U2-01A-21D-A33T-08 chr6:45390465 A>G maps to ENST00000359524 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RN-01A-11D-A33T-08 chr6:45390462 G>A maps to ENST00000359524 Q132Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5847-01A-11D-1705-08 chr4:159526261 C>T maps to ENST00000440678 C172C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5871-01A-12D-1705-08 chr4:159533493 A>C maps to ENST00000440678 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CV-01A-11D-A31L-08 chr4:159566102 T>G maps to ENST00000440678 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:33937966 C>T maps to NM_016568.3 S374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr9:137293637 G>A maps to NM_002957.4 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A70Z-01A-12D-A33T-08 chr9:137309088 G>A maps to NM_002957.4 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8110-01A-11D-2395-08 chr1:165389158 G>A maps to NM_006917.4 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr3:133878163 G>A maps to ENST00000296084 Y544Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:133896787 T>C maps to ENST00000296084 P435P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:38946360 C>T maps to NM_000540.2 S587S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr19:38976394 G>T maps to NM_000540.2 A1700A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr19:38942435 C>T maps to NM_000540.2 D385D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7469-01A-11D-2253-08 chr19:39039014 C>T maps to NM_000540.2 Y4079Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:237777566 C>A maps to NM_001035.2 S1713S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:237632392 G>A maps to NM_001035.2 A538A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:237619940 C>T maps to NM_001035.2 H506H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YK-01A-11D-A34A-08 chr1:237660041 T>C maps to NM_001035.2 H731H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65Z-01A-11D-A29Q-08 chr1:237957282 C>T maps to NM_001035.2 L4633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:34078052 G>A maps to NM_001036.3 L3153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:33955766 C>T maps to NM_001036.3 D1816D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:33893741 C>T maps to NM_001036.3 N637N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:34130615 C>A maps to NM_001036.3 A4145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7T6-01A-11D-A33T-08 chr15:33955886 G>A maps to NM_001036.3 A1856A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8188-01A-11D-2253-08 chr15:33893720 C>G maps to NM_001036.3 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6J3-01A-11D-A31L-08 chr15:33955019 G>A maps to NM_001036.3 E1763E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:33292323 T>C maps to NM_022753.2 N208N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7490-01A-11D-2024-08 chr1:101705574 C>T maps to NM_001400.4 I345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr19:10334890 G>A maps to NM_004230.3 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:23906958 G>A maps to NM_014363.4 Q3686*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:23912409 C>A maps to NM_014363.4 E1869*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:23914981 C>T maps to NM_014363.4 Q1011Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:5590371 G>A maps to NM_014649.2 H814H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5851-01A-13D-1893-08 chr23:134988649 C>T did not map to a codon.
Sequencing variant TCGA-DU-5854-01A-11D-1705-08 chr23:134994994 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:134989493 C>A did not map to a codon.
Sequencing variant TCGA-E1-5319-01A-01D-1893-08 chr23:134992596 C>T did not map to a codon.
Sequencing variant TCGA-E1-A7YS-01A-11D-A34A-08 chr23:134991046 G>A did not map to a codon.
Sequencing variant TCGA-FG-A710-01A-12D-A33T-08 chr23:134988633 C>T did not map to a codon.
Sequencing variant TCGA-HT-7609-01A-11D-2086-08 chr23:134988659 G>A did not map to a codon.
Sequencing variant TCGA-S9-A6WM-01A-12D-A33T-08 chr23:134989500 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:21993528 G>T maps to NM_005407.1 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:76754540 C>T maps to NM_171999.2 I850I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:50407071 G>A maps to NM_020436.3 G650G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:50401031 G>A maps to NM_020436.3 G978G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:50406791 G>A maps to NM_020436.3 Q744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TR-01A-11D-A289-08 chr20:50407509 G>A maps to NM_020436.3 P504P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:55034669 C>T maps to NM_015589.4 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:169644877 C>T maps to NM_182610.2 D276D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:76924435 G>A maps to ENST00000372690 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76R-01A-11D-A32B-08 chr7:92733349 G>A maps to NM_017654.3 G687G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:92762299 G>A maps to NM_152703.2 Y995Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7301-01A-11D-2086-08 chr21:15893492 G>T maps to ENST00000285670 S104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QW-01A-11D-A34A-08 chr2:128747139 G>C maps to NM_001145928.1 S619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CE-01A-11D-A36O-08 chr2:128744414 G>C maps to NM_001145928.1 P660P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:73702561 C>T maps to NM_013260.6 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7304-01A-12D-2086-08 chr22:50875936 C>A maps to ENST00000216061 A562A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr22:50882543 C>T maps to ENST00000216061 D950D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7692-01A-12D-2253-08 chr11:68337356 T>C maps to NM_001164160.1 L424L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DU-6392-01A-11D-1705-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:136531991 G>A maps to NM_007101.3 D832D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A4DV-01A-11D-A26M-08 chr9:136578199 C>T maps to NM_007101.3 E399E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:109778672 A>T maps to ENST00000369923 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:39421199 G>A maps to NM_017827.3 D59D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr11:65733981 A>G maps to NM_005146.4 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:65745327 C>T maps to NM_005146.4 I710I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:65733942 C>A maps to NM_005146.4 I368I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YS-01A-11D-A34A-08 chr11:65729298 G>T maps to NM_005146.4 T16T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4X9-01A-11D-A26M-08 chr23:128926407 G>A did not map to a codon.
Sequencing variant TCGA-DU-7018-01A-11D-2024-08 chr23:128914083 G>A did not map to a codon.
Sequencing variant TCGA-DU-6396-01A-11D-1705-08 chr23:23801977 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:18457581 G>A maps to ENST00000332610 Y146Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:18462279 C>T maps to ENST00000332610 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr3:18428051 G>A maps to ENST00000332610 Q422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5390-01A-02D-1468-08 chr23:84363188 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:84363607 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:84349940 G>A did not map to a codon.
Sequencing variant TCGA-KT-A74X-01A-11D-A32B-08 chr23:84362996 C>T did not map to a codon.
Sequencing variant TCGA-QH-A6CU-01A-11D-A31L-08 chr23:84362659 G>A did not map to a codon.
Sequencing variant TCGA-TM-A84I-01A-11D-A36O-08 chr23:84362923 G>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:66458362 T>C maps to NM_016038.2 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:50898013 G>A maps to ENST00000337034 R1201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7881-01A-11D-2395-08 chr22:50898007 G>A maps to ENST00000337034 P1203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:28328852 C>T maps to NM_001024401.2 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8165-01A-11D-2253-08 chr16:28331419 G>C maps to NM_001024401.2 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr16:28331452 G>C maps to NM_001024401.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr19:56041300 C>T maps to NM_001101401.2 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:123812038 G>T maps to NM_001167856.1 T542T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr12:123834922 G>A maps to NM_001167856.1 D22D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr19:50156699 A>C maps to NM_021228.2 R1018R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A614-01A-11D-A29Q-08 chr19:50154596 C>T maps to NM_021228.2 D317D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WL-01A-21D-A33T-08 chr19:50157636 C>A maps to NM_021228.2 A1116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:1918986 G>A maps to NM_079834.2 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YK-01A-11D-A34A-08 chr6:28540056 A>G maps to NM_052923.1 N1203N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YN-01A-11D-A34A-08 chr6:28539969 G>A maps to NM_052923.1 T1232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7620-01A-11D-2253-08 chr6:28540668 G>A maps to NM_052923.1 C999C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:47459174 C>T maps to NM_012235.2 P863P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:47460251 G>A maps to NM_012235.2 D674D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:47460852 C>T maps to NM_012235.2 T635T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:76726651 C>A did not map to a codon.
Sequencing variant TCGA-HT-8110-01A-11D-2395-08 chr15:77064286 C>T maps to ENST00000324767 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:27516826 C>T maps to NM_016240.2 D380D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:125302181 G>A maps to NM_005505.4 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:125270965 G>A maps to NM_005505.4 Y446Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A6S2-01A-21D-A32B-08 chr4:77100702 G>T maps to NM_005506.2 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85D-01A-11D-A36O-08 chr22:20783911 G>A maps to NM_153334.4 G445G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:246923290 C>T maps to NM_016002.2 G282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7309-01A-11D-2086-08 chr10:102112183 C>T maps to NM_005063.4 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:83557906 T>C maps to NM_001037582.2 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:53740161 G>A maps to NM_152540.3 R677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:51975414 G>T did not map to a codon.
Sequencing variant TCGA-HT-7855-01A-11D-2395-08 chr11:62037738 C>T maps to NM_002411.2 Y17Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:147261007 G>T did not map to a codon.
Sequencing variant TCGA-HT-A5R9-01A-11D-A289-08 chr3:159482638 C>A maps to NM_001197113.1 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:12680115 C>T maps to NM_001112706.2 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr1:41579186 C>T maps to NM_001031694.2 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:41579056 G>A maps to NM_001031694.2 R205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:18264932 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:18276361 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:38739838 G>A maps to NM_006514.2 F1624F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7491-01A-11D-2024-08 chr3:38739793 G>A maps to NM_006514.2 D1639D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-7675-01A-11D-2086-08 chr3:38768258 T>C maps to NM_006514.2 Q975Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A845-01A-11D-A36O-08 chr3:38812789 A>G maps to NM_006514.2 D193D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:38908883 G>T maps to ENST00000302328 I1293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VW-A7QS-01A-12D-A33T-08 chr3:38888490 G>A maps to ENST00000302328 T1690T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:166847987 G>A maps to NM_001165963.1 R1933*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8165-01A-11D-2253-08 chr2:166901576 T>C maps to NM_001165963.1 E546E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TS-01A-11D-A289-08 chr19:35524707 G>A maps to NM_199037.3 W171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A6S3-01A-12D-A32B-08 chr2:166165900 G>A maps to NM_001040142.1 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A70Z-01A-12D-A33T-08 chr2:166246282 C>T maps to NM_001040142.1 D1989D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:165986518 A>G maps to NM_006922.3 C951C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:165986695 G>A maps to NM_006922.3 I892I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:165947769 G>A maps to NM_006922.3 I1631I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7677-01A-11D-2253-08 chr2:165948830 G>C maps to NM_006922.3 L1580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:62036795 G>T maps to NM_000334.4 V616V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:62020441 G>A maps to NM_000334.4 G1344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7695-01A-11D-2253-08 chr17:62043902 C>T maps to NM_000334.4 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QZ-01A-12D-A34J-08 chr17:62045569 C>T maps to NM_000334.4 W283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:167168077 A>G maps to ENST00000303354 Y63Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UV-01A-12D-A34A-08 chr12:6483847 T>C maps to NM_001159576.1 E93E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84I-01A-11D-A36O-08 chr12:6457371 G>A maps to NM_001159576.1 F618F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr16:23392079 G>A maps to ENST00000307331 P672P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RV-01A-21D-A34A-08 chr8:144895056 G>T maps to NM_182706.3 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5302-01A-01D-1468-08 chr7:29963704 G>A maps to NM_001145514.1 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U5-01A-12D-A33T-08 chr8:145556984 G>A maps to NM_031309.4 H303H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:644557 C>T maps to NM_033129.3 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:43606934 G>A maps to NM_173050.2 H792H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:43654255 G>A maps to NM_173050.2 Y232Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7477-01B-11D-A289-08 chr22:43606073 G>A maps to NM_173050.2 G852G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:9068912 T>C maps to ENST00000457346 E664E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:9077442 G>T maps to ENST00000457346 C368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:50295878 C>T maps to NM_004713.3 W375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr14:50269392 A>C maps to NM_004713.3 L656L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5851-01A-13D-1893-08 chr7:4259753 G>T maps to NM_152744.3 V1851V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:4260952 C>T maps to NM_152744.3 G1928G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr7:4026874 C>T maps to NM_152744.3 H684H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A89Z-01A-11D-A36O-08 chr7:4091418 C>T maps to NM_152744.3 D956D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:71381993 G>A maps to NM_001144952.1 R1521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:71384090 G>A maps to NM_001144952.1 S1426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6402-01A-11D-1705-08 chr17:71410869 G>A maps to NM_001144952.1 H799H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr2:192711354 C>T maps to NM_004657.5 K99K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A6S7-01A-21D-A32B-08 chr16:82033699 T>C maps to NM_145168.2 K66K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:57323239 G>A maps to NM_148897.2 R220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64W-01A-11D-A29Q-08 chr12:113830760 A>G maps to NM_006843.2 N324N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:85230934 G>A maps to NM_014300.2 R78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr18:56816767 C>T maps to NM_033280.2 F37F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:10353768 G>A maps to ENST00000343726 C156C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64U-01A-11D-A29Q-08 chr17:75190802 A>G maps to NM_001039573.2 E173E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:75208174 C>A maps to NM_001039573.2 T585T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:75208276 C>T maps to NM_001039573.2 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr17:75208129 G>A maps to NM_001039573.2 S570S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr17:75205559 T>C did not map to a codon.
Sequencing variant TCGA-TM-A84I-01A-11D-A36O-08 chr22:30890139 G>A maps to NM_174977.3 R193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:5046881 G>A maps to NM_014692.1 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A713-01A-11D-A32B-08 chr16:5053534 C>T maps to NM_014692.1 I421I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:139341772 C>T maps to NM_014866.1 G2201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KT-A7W1-01A-11D-A34A-08 chr9:139371998 G>A maps to NM_014866.1 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F0-01A-11D-A289-08 chr1:177936855 G>A maps to NM_033127.2 D87D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84M-01A-11D-A36O-08 chr1:145109583 G>A maps to NM_004892.4 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5874-01A-11D-1705-08 chr14:39502454 G>A maps to NM_006364.2 S762S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6186-01A-12D-2024-08 chr20:18516371 G>T maps to NM_001172745.1 E464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7US-01A-11D-A33T-08 chr20:18529341 G>A maps to NM_001172745.1 R611R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U1-01A-21D-A33T-08 chr10:121663644 C>T maps to NM_007190.2 Y319Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U2-01A-21D-A33T-08 chr4:110459713 A>G maps to NM_006323.2 R1218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr4:119649798 G>A maps to ENST00000379735 L960L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:119754818 C>T maps to ENST00000379735 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R7-01A-11D-A289-08 chr4:83742200 T>G maps to ENST00000505472 R1189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:102265249 G>T maps to NM_015490.3 I349I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr3:127786280 C>T maps to ENST00000464451 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6UA-01A-12D-A33T-08 chr3:127783858 T>C maps to ENST00000464451 F258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr6:108214764 A>T maps to NM_007214.4 L532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VV-A86M-01A-11D-A36O-08 chr6:108202454 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:91940431 C>A maps to NM_024077.3 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:91964706 C>T maps to NM_024077.3 D585D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:49309098 G>A maps to NM_001193489.1 A455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7634-01A-11D-2086-08 chr18:12955478 A>G maps to NM_001013437.1 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:81946081 A>G maps to NM_005065.4 D683D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr20:13912351 T>G maps to NM_025229.1 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IS-01A-11D-A34A-08 chr20:13856731 C>T maps to NM_025229.1 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:25819871 G>A maps to NM_015187.3 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RG-01A-11D-A33T-08 chr4:25849363 G>A maps to NM_015187.3 N95N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr1:169699642 C>A maps to NM_000450.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7902-01A-12D-2395-08 chr1:151338897 G>A maps to ENST00000435071 D274D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:169565262 A>C maps to NM_003005.3 T667T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:83592531 G>A maps to NM_006080.2 R617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A73M-01A-11D-A32B-08 chr7:83739851 C>T maps to NM_006080.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74O-01A-11D-A32B-08 chr7:80457915 A>G maps to NM_006379.2 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5395-01A-01D-1468-08 chr3:50225346 C>T maps to NM_004186.3 G719G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:52476299 C>T maps to NM_020163.1 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A6ML-01A-11D-A32B-08 chr3:52474395 G>A maps to NM_020163.1 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WH-A86K-01A-11D-A36O-08 chr1:156131198 G>T maps to NM_022367.3 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8166-01A-11D-2253-08 chr9:91994101 C>T maps to NM_006378.3 A702A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr9:91993633 G>A maps to NM_006378.3 D858D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A6YH-01A-21D-A32B-08 chr9:91994296 T>C maps to NM_006378.3 Q637Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:9052039 G>A maps to NM_003966.2 C930C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:122641111 G>T maps to NM_001031702.2 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:115837949 G>A maps to ENST00000257414 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F0-01A-11D-A289-08 chr5:115813738 G>A maps to ENST00000257414 G513G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WM-01A-12D-A33T-08 chr5:115818155 G>A maps to ENST00000257414 R360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UR-01A-11D-A33T-08 chr19:4544494 C>T maps to NM_032108.3 S595S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A710-01A-12D-A33T-08 chr19:4550874 G>A maps to NM_032108.3 R353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:151105841 G>A maps to NM_001178061.1 G669G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr15:48052513 T>A maps to NM_153618.1 Y41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:185318631 G>C maps to ENST00000427465 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:185304248 C>T maps to ENST00000427465 C91C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7610-01A-21D-2086-08 chr17:7474040 C>T maps to ENST00000321337 R508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:76412675 G>A maps to NM_015571.2 A868A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:76412579 A>G maps to NM_015571.2 V836V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr1:87369112 C>A maps to NM_004261.3 E35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:30455950 G>T maps to ENST00000478753 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A70Z-01A-12D-A33T-08 chr7:55902219 C>T maps to NM_207366.2 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8162-01A-21D-2253-08 chr23:118774682 C>T did not map to a codon.
Sequencing variant TCGA-E1-A7YH-01A-11D-A34A-08 chr23:118774725 C>T did not map to a codon.
Sequencing variant TCGA-HT-7680-01A-11D-2253-08 chr23:118771067 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:132099457 C>T maps to NM_001098811.1 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:158569912 C>T maps to NM_032861.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UR-01A-11D-A33T-08 chr11:17981079 G>A maps to NM_012139.2 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7T6-01A-11D-A33T-08 chr14:94849109 C>T maps to NM_001127707.1 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:94914892 G>T maps to NM_001080451.1 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:94964254 G>A maps to NM_173850.2 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr14:94964686 C>A maps to NM_173850.2 T16T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7Z3-01A-11D-A34J-08 chr14:95053929 C>T maps to NM_000624.4 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr23:105280486 A>C did not map to a codon.
Sequencing variant TCGA-HT-7884-01B-11D-2395-08 chr23:105280576 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:2836161 G>A maps to NM_030666.2 Y221Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:61597397 G>T maps to NM_005024.1 E204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YS-01A-11D-A34A-08 chr18:61600314 A>T maps to NM_005024.1 K223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7011-01A-11D-2024-08 chr18:61377582 G>A maps to NM_080475.2 E52E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr18:61570517 C>T maps to NM_001143818.1 F409F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YJ-01A-11D-A34A-08 chr18:61558847 T>A did not map to a codon.
Sequencing variant TCGA-CS-5397-01A-01D-1893-08 chr18:61326674 G>A maps to NM_006919.2 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:61305126 A>G maps to NM_002974.2 F333F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RS-01A-12D-A33T-08 chr18:61306945 G>A maps to NM_002974.2 N178N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:61459677 G>A did not map to a codon.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr18:61465876 C>A maps to NM_001040147.1 S165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A780-01A-12D-A32B-08 chr18:61468116 C>T maps to NM_001040147.1 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A89V-01A-11D-A36O-08 chr18:61449740 C>T maps to NM_001040147.1 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr6:2890402 C>T maps to NM_004155.4 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CX-01A-11D-A32B-08 chr22:21133989 C>T maps to NM_000185.3 N130N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8322-01A-11D-2395-08 chr7:100779017 G>A maps to NM_000602.3 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A6MO-01A-11D-A33T-08 chr7:100779026 G>A maps to NM_000602.3 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:51915232 G>A maps to NM_001101320.1 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YM-01A-11D-A34A-08 chr11:57373886 G>A maps to ENST00000403558 W342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XD-01A-11D-A27K-08 chr11:75282972 C>T maps to NM_001235.2 Q368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5849-01A-11D-1705-08 chr3:167508322 T>C maps to NM_005025.4 H138H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WP-01A-12D-A34A-08 chr3:167189538 T>C maps to NM_006217.3 E28E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:64863789 G>T maps to NM_014755.2 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:28599171 G>A maps to NM_031459.3 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5322-01A-01D-1468-08 chr1:28598955 C>T maps to NM_031459.3 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:94918425 G>A maps to NM_144665.2 N252N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:131456918 G>T did not map to a codon.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr18:42531833 C>T maps to NM_015559.2 C843C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:42643158 C>T maps to NM_015559.2 H1429H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:42532229 C>A maps to NM_015559.2 T975T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:30977388 G>A maps to NM_014712.1 P729P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:47161784 G>T maps to NM_014159.6 P1447P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:47098652 C>T maps to NM_014159.6 Q2207Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr3:47098399 G>A maps to NM_014159.6 Q2292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7684-01A-11D-2253-08 chr3:47103766 G>C maps to NM_014159.6 S2060*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr14:99865138 G>A maps to NM_032233.2 N554N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A75M-01A-11D-A32B-08 chr14:99865291 T>C maps to NM_032233.2 E503E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:99865306 C>T maps to NM_032233.2 P498P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TS-01A-11D-A289-08 chr12:123889486 G>A maps to NM_020382.3 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:150936217 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:50050629 A>G maps to NM_031915.2 E120E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr3:4354790 C>T maps to NM_006515.3 C122C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65S-01A-11D-A29Q-08 chr3:4355171 C>G maps to NM_006515.3 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:135204623 G>T maps to ENST00000372169 I787I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6396-01A-11D-1705-08 chr17:27286488 G>A maps to NM_178860.4 A591A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr16:29900011 C>T maps to NM_201575.2 P296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr11:64532974 G>A maps to NM_201995.2 G601G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XD-01A-11D-A27K-08 chr19:2247980 A>C maps to NM_007165.4 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8188-01A-11D-2253-08 chr1:38435136 C>A did not map to a codon.
Sequencing variant TCGA-CS-5397-01A-01D-1893-08 chr2:198273240 A>G maps to NM_012433.2 I323I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RW-01A-11D-A33T-08 chr2:198267532 A>C maps to NM_012433.2 T608T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:144416568 G>A maps to NM_031287.2 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:31976256 G>A did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr22:31976292 C>A maps to NM_001007467.1 T397T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:52968828 G>A maps to NM_016329.3 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:7409761 C>T maps to NM_001018039.1 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YJ-01A-11D-A34A-08 chr4:154702728 G>A maps to NM_003013.2 N254N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WI-01A-21D-A33T-08 chr4:154709561 G>A maps to NM_003013.2 C142C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr7:37955896 G>A maps to ENST00000223214 Y103Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:65473449 G>A maps to NM_001077199.1 G563G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:33063197 A>G maps to NM_020706.2 V599V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:1712676 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:1712573 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:1713083 C>T did not map to a codon.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr23:1720260 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:99850490 G>A maps to NM_032870.2 R418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:46326921 T>C maps to NM_004719.2 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RJ-01A-11D-A33T-08 chr12:46316742 G>A maps to NM_004719.2 S1367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5305-01A-01D-1893-08 chr6:36569523 T>C maps to NM_003017.4 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:29475268 G>A maps to NM_005626.4 R380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:132212923 C>T maps to NM_004592.2 N344N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76R-01A-11D-A32B-08 chr12:132262623 G>A maps to NM_004592.2 T719T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6394-01A-11D-1705-08 chr12:120903591 T>A did not map to a codon.
Sequencing variant TCGA-IK-7675-01A-11D-2086-08 chr1:168205988 C>T maps to NM_199344.2 Q132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7634-01A-11D-2086-08 chr14:36946256 G>A maps to NM_001101341.1 C60C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr10:81373778 G>A maps to NM_001093770.2 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7603-01A-21D-2086-08 chr10:81706232 G>A maps to NM_003019.4 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:73249649 C>A did not map to a codon.
Sequencing variant TCGA-QH-A65X-01A-11D-A32B-08 chr2:73188271 C>T maps to NM_144579.2 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:52895890 C>A maps to NM_000232.4 G128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:94229022 G>A maps to NM_001099401.1 N350N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7Z6-01A-11D-A34J-08 chr8:14181680 C>T maps to NM_139167.2 K89K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A781-01A-11D-A32B-08 chr8:13959902 C>T maps to NM_139167.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:67185055 C>T maps to ENST00000237247 V601V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76R-01A-11D-A32B-08 chr6:134491420 C>T maps to NM_001143676.1 T522T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:42977491 G>A maps to NM_032237.3 W175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:8175939 G>A maps to NM_001080826.1 G1315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RH-01A-12D-A34A-08 chr8:8185588 G>A maps to NM_001080826.1 G901G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A780-01A-12D-A32B-08 chr3:20215786 T>A maps to NM_001012410.3 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84T-01A-11D-A36O-08 chr2:201437990 T>C maps to NM_152524.5 D974D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:72631634 T>C maps to NM_003901.3 C317C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr17:78184760 G>A maps to NM_000199.3 Y333Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XE-01A-11D-A27K-08 chr17:2282480 C>A maps to NM_014853.2 I1017I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:2265507 G>T maps to NM_014853.2 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:2274583 C>A maps to NM_014853.2 G484G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:40802148 C>A maps to NM_015705.4 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr22:40803286 C>T maps to NM_015705.4 R441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WO-01A-21D-A34A-08 chr7:101960849 G>A maps to ENST00000306803 W482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr23:123504070 C>G did not map to a codon.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr23:123480555 G>T did not map to a codon.
Sequencing variant TCGA-R8-A6MO-01A-11D-A33T-08 chr1:156784872 C>T maps to NM_001161441.1 Q88Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:6755084 C>T maps to NM_005490.2 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:6754117 C>T maps to NM_005490.2 A443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:6760692 G>A maps to NM_005490.2 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:15298411 G>A maps to NM_004844.3 G366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7605-01A-11D-2086-08 chr1:249107312 G>A maps to NM_030645.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:152070713 C>A did not map to a codon.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr9:17747098 C>T maps to NM_003026.2 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:19713849 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:19626116 C>T did not map to a codon.
Sequencing variant TCGA-FG-A710-01A-12D-A33T-08 chr23:19713789 C>T did not map to a codon.
Sequencing variant TCGA-HW-7495-01A-11D-2024-08 chr23:19764443 T>A did not map to a codon.
Sequencing variant TCGA-VW-A7QS-01A-12D-A33T-08 chr23:19713825 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:105361941 G>A maps to ENST00000369774 G1011G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:105377024 G>A maps to ENST00000369774 D283D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:105362349 G>A maps to ENST00000369774 S875S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:170038809 G>A maps to NM_020870.3 G547G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:145317697 C>T maps to NM_152550.3 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8165-01A-11D-2253-08 chr5:145393443 G>A maps to NM_152550.3 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:110015263 G>A maps to NM_001099289.1 T388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:110065842 C>A maps to NM_001099289.1 A682A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:8233805 C>T maps to NM_018986.3 C1018C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A72U-01A-31D-A32B-08 chr4:8229064 G>A maps to NM_018986.3 G548G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RP-01A-21D-A34A-08 chr4:8218825 G>A maps to NM_018986.3 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5277-01A-01D-1468-08 chr5:148407827 G>A maps to NM_024577.3 F489F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:51190043 C>T maps to ENST00000391814 V813V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:70332437 G>A maps to ENST00000338508 D1314D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:70333217 C>T maps to ENST00000338508 P1054P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YL-01A-11D-A34A-08 chr11:70331642 C>T maps to ENST00000338508 P1579P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:51160847 G>A maps to NM_001080420.1 S1545S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:51117810 C>T maps to NM_001080420.1 N280N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:145154070 G>A maps to NM_030974.3 D320D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:145153816 G>T maps to NM_030974.3 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:38068630 C>T maps to NM_003028.2 W4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:7533525 G>A maps to NM_001040.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7692-01A-12D-2253-08 chr17:7535329 T>C maps to NM_001040.3 D283D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:422273 C>A maps to NM_012435.2 E498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7Z2-01A-21D-A34J-08 chr16:46655217 C>T maps to NM_024745.4 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8110-01A-11D-2395-08 chr19:4284901 G>A did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr19:4290593 G>A maps to NM_020209.3 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:154459138 G>A maps to NM_001010846.2 R349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7470-01A-12D-2086-08 chr15:45470423 T>C maps to ENST00000437903 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:41086792 C>T maps to NM_138392.3 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:57627031 C>T maps to NM_005412.5 Y309Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:3513957 G>A maps to NM_013276.2 Q445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6395-01A-12D-1705-08 chr6:146215309 T>C maps to ENST00000367503 Q1561Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7616-01A-11D-2253-08 chr6:146271525 G>A maps to ENST00000367503 Q286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr23:9900278 G>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:9905179 G>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:9900703 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:9912766 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:9900465 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:9864182 G>A did not map to a codon.
Sequencing variant TCGA-HT-7695-01A-11D-2253-08 chr23:9905236 G>A did not map to a codon.
Sequencing variant TCGA-HT-A617-01A-11D-A29Q-08 chr23:9900905 A>G did not map to a codon.
Sequencing variant TCGA-S9-A6TZ-01A-21D-A32B-08 chr23:9863273 C>A did not map to a codon.
Sequencing variant TCGA-VW-A7QS-01A-12D-A33T-08 chr23:9907312 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:77700011 C>A maps to NM_020859.3 A1891A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:77660255 C>T maps to NM_020859.3 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:50350482 C>A did not map to a codon.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr23:50378310 C>A did not map to a codon.
Sequencing variant TCGA-P5-A77X-01A-11D-A32B-08 chr23:50377746 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:164750399 C>T maps to NM_001041.3 G882G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76L-01A-11D-A32B-08 chr3:164757759 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:124509616 C>T maps to NM_170601.3 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:48396192 T>C maps to NM_001006610.1 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7T6-01A-11D-A33T-08 chr16:48399313 C>T maps to NM_001006610.1 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TS-01A-12D-A33T-08 chr16:48396114 G>T maps to NM_001006610.1 C106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:408206 C>A did not map to a codon.
Sequencing variant TCGA-DU-A5TT-01A-11D-A289-08 chr11:406532 A>G maps to NM_021805.2 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A70Y-01A-12D-A34J-08 chr11:408720 G>A maps to NM_021805.2 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr20:3670828 G>A maps to NM_023068.3 S1558S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:3684576 G>A maps to NM_023068.3 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7014-01A-11D-2024-08 chr20:3677340 G>A maps to NM_023068.3 L859L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A845-01A-11D-A36O-08 chr19:52130493 C>T maps to ENST00000222107 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:51955821 G>T maps to NM_014442.2 P437P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:51628932 C>A maps to NM_014441.2 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7CA-01A-21D-A33T-08 chr9:34635805 C>T maps to NM_005866.2 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:116798085 C>A maps to ENST00000445177 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7474-01A-11D-2024-08 chr11:116719847 G>A maps to ENST00000445177 S1262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr12:56348102 T>C maps to NM_006928.3 V627V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:56351339 G>T maps to NM_006928.3 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7879-01A-11D-2395-08 chr12:56350745 C>T maps to NM_006928.3 T447T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr6:100841630 G>A maps to ENST00000262901 C434C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XG-01A-11D-A27K-08 chr6:100868814 G>A maps to ENST00000262901 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8108-01A-11D-2395-08 chr6:100911317 C>T maps to ENST00000262901 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr6:100868815 C>A maps to ENST00000262901 G339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7489-01A-11D-2024-08 chr21:38098526 G>A maps to NM_005069.3 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7856-01A-11D-2395-08 chr15:75688838 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:16957836 G>A maps to NM_015260.1 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8166-01A-11D-2253-08 chr19:16973237 C>T maps to NM_015260.1 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YK-01A-11D-A34A-08 chr19:16973732 C>T maps to NM_015260.1 D435D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:65409021 G>A maps to NM_153253.29 E210E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A618-01A-11D-A29Q-08 chr11:65408859 G>A maps to NM_153253.29 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5396-01A-02D-1468-08 chr14:72055665 C>T maps to NM_015556.1 T359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:72139291 G>A maps to NM_015556.1 T1019T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:72165698 C>T maps to NM_015556.1 L1126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R2-01A-21D-A34J-08 chr14:72055539 A>G maps to NM_015556.1 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5874-01A-11D-1705-08 chr1:232626741 G>A maps to NM_020808.3 R562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:232551264 G>A maps to NM_020808.3 L1579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:232649690 C>T maps to NM_020808.3 Q465Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5964-01A-11D-1705-08 chr1:232607259 C>T maps to NM_020808.3 R700R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr19:38643515 T>C maps to NM_015073.1 D1190D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:1559044 C>A maps to NM_006065.3 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8105-01A-11D-2395-08 chr20:1517873 C>T maps to ENST00000381621 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TY-01A-12D-A32B-08 chr10:69669182 A>G maps to NM_012238.4 P447P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85E-01A-11D-A36O-08 chr19:39369941 C>T maps to NM_012237.3 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CA-01A-11D-A36O-08 chr6:13612076 G>T maps to NM_012241.3 E305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84J-01A-11D-A36O-08 chr17:79872256 C>T maps to NM_016538.2 G243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R5-01A-11D-A289-08 chr5:54720584 C>T maps to NM_015360.4 A1038A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr8:134050854 G>A maps to NM_006748.3 R289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:35262912 C>T maps to NM_032214.2 E57E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr1:160604538 G>T maps to NM_003037.2 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:160461052 C>A maps to NM_001184714.1 G170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr1:160719611 G>A maps to NM_021181.3 E126E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:103710635 G>A maps to NM_000452.2 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153716010 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153717056 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:82606127 C>G maps to NM_001010893.2 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:87769929 G>A maps to NM_197965.2 N113N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6400-01A-12D-1705-08 chr2:219258871 G>A maps to NM_000578.3 T448T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76L-01A-11D-A32B-08 chr2:219259396 C>T maps to NM_000578.3 C477C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A735-01A-11D-A32B-08 chr2:219251431 G>A maps to NM_000578.3 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64O-01A-11D-A29Q-08 chr5:127448570 G>A maps to NM_001046.2 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:127503457 T>C maps to NM_001046.2 A874A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A75M-01A-11D-A32B-08 chr16:56906652 G>A maps to NM_000339.2 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66G-01A-21D-A31L-08 chr16:56913500 C>A maps to NM_000339.2 I461I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr16:56928467 C>T maps to NM_000339.2 L858L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:56913135 C>T maps to NM_000339.2 Y444Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F2-01A-11D-A289-08 chr16:56921898 G>A maps to NM_000339.2 Q747Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:67983746 G>A maps to NM_005072.4 G568G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:67980443 G>T maps to NM_005072.4 I778I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:67991893 G>T maps to NM_005072.4 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:44665967 C>T maps to NM_001134771.1 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F4-01A-11D-A289-08 chr20:44672350 C>T maps to NM_001134771.1 I462I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6IZ-01A-11D-A31L-08 chr15:34528986 G>A maps to NM_133647.1 Y988Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr5:1081824 C>T maps to NM_006598.2 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:1065544 G>A maps to NM_006598.2 L764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:1083923 G>T maps to NM_006598.2 Y355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:1064314 G>A maps to NM_006598.2 N830N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:124906140 G>T maps to NM_001195483.1 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:100457590 G>A maps to NM_020246.2 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7468-01A-11D-2024-08 chr7:122768984 C>T maps to NM_022444.3 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RC-01A-11D-A289-08 chr7:122759133 C>T did not map to a codon.
Sequencing variant TCGA-S9-A7R7-01A-11D-A34J-08 chr7:122763177 A>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:26818458 T>C maps to NM_001145975.1 N242N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:26820648 C>T maps to NM_001145975.1 C362C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:135391026 G>T maps to NM_012450.2 C129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RG-01A-11D-A33T-08 chr17:6599238 G>A maps to NM_177550.3 C287C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:43217041 G>A maps to NM_007163.3 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr18:43219721 C>T maps to NM_007163.3 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A89V-01A-11D-A36O-08 chr13:99337170 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:121634111 G>A maps to NM_021082.3 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:113460589 G>T maps to NM_003051.3 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5871-01A-12D-1705-08 chr10:91192820 T>C maps to NM_213606.3 *517W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr2:230923894 G>A maps to NM_152527.4 N58N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:73740956 G>A did not map to a codon.
Sequencing variant TCGA-RY-A83Z-01A-11D-A36O-08 chr23:73740893 G>A did not map to a codon.
Sequencing variant TCGA-DU-7013-01A-11D-2024-08 chr17:80195560 C>T maps to NM_001042423.1 N305N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6UB-01A-21D-A33T-08 chr17:80195353 G>A maps to NM_001042423.1 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:110921952 G>A maps to NM_004696.1 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:73089919 C>A maps to ENST00000450736 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:61413993 C>A maps to NM_194298.2 E264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A735-01A-11D-A32B-08 chr6:25921306 T>A maps to NM_005835.2 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QY-01A-11D-A34A-08 chr6:25913552 G>A maps to NM_005835.2 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr6:25779394 G>A maps to NM_005495.2 E491E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:74304811 T>C maps to NM_012434.4 G492G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7015-01A-11D-2024-08 chr11:22363145 C>T maps to NM_020346.2 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr19:49933844 C>T maps to NM_020309.3 P538P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YJ-01A-11D-A34A-08 chr19:49934334 G>A maps to NM_020309.3 N442N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A6S8-01A-12D-A32B-08 chr20:61594020 C>T maps to NM_022082.3 Y181Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:119015148 G>A maps to NM_003054.4 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YI-01A-11D-A34A-08 chr10:119012954 T>C maps to NM_003054.4 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:46945843 C>A maps to NM_194255.1 E394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:46951792 G>A maps to NM_194255.1 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr21:46951524 G>T maps to NM_194255.1 R243R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:35339031 G>A maps to NM_004171.3 R17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:65228623 G>A maps to NM_003038.4 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RV-01A-21D-A34A-08 chr2:65245297 C>T maps to NM_003038.4 T376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5281-01A-01D-1468-08 chr19:15073100 G>A maps to NM_005071.1 N216N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QZ-01A-12D-A34J-08 chr2:113418739 A>G maps to NM_005415.3 A605A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:42329845 G>T maps to NM_006749.3 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7604-01A-11D-2086-08 chr8:42297082 C>T maps to NM_006749.3 E273E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:160543248 C>T maps to NM_003057.2 D94D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr11:63064781 C>T maps to NM_001039752.3 R172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5872-01A-11D-1705-08 chr11:64323647 G>A maps to NM_018484.2 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr11:64360336 C>T maps to NM_144585.2 C163C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:38347804 C>A maps to NM_004803.3 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:116563483 C>T maps to NM_018420.2 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8162-01A-21D-2253-08 chr6:110778135 G>A maps to NM_033125.2 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7Z3-01A-11D-A34J-08 chr6:110778051 G>A maps to NM_033125.2 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:23818479 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:62911080 G>A maps to NM_001136506.1 D57D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:160829797 A>G maps to ENST00000392145 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:131671562 C>A maps to NM_003059.2 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7C4-01A-11D-A32B-08 chr5:131714134 G>A maps to ENST00000435065 V177V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8320-01A-11D-2395-08 chr11:62749447 G>A maps to NM_004790.3 C221C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U1-01A-21D-A33T-08 chr11:62744651 C>T maps to NM_004790.3 W523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:62768253 G>A maps to ENST00000430500 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:62782136 G>T maps to ENST00000430500 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7014-01A-11D-2024-08 chr11:62762131 A>G maps to ENST00000430500 D366D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:63176243 C>A maps to NM_080866.2 P498P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:63141202 T>C maps to NM_080866.2 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:19665994 C>T maps to NM_020689.3 F438F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:129480617 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:129499619 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:129492621 G>A did not map to a codon.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr23:129498600 G>A did not map to a codon.
Sequencing variant TCGA-S9-A6TS-01A-12D-A33T-08 chr23:129480617 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:70248234 C>T maps to NM_152707.2 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6404-01A-11D-1705-08 chr17:73282426 G>A maps to NM_021734.4 H82H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:140683315 C>T maps to NM_031947.2 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TS-01A-11D-A289-08 chr11:792433 G>T maps to NM_001191061.1 Y204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:6442162 G>A maps to NM_024103.2 I410I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TU-01A-12D-A32B-08 chr6:46637947 C>A maps to NM_004277.3 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:100759258 C>T maps to NM_001039355.1 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:128688326 C>T maps to NM_031291.2 G195G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr4:128651876 C>T maps to NM_031291.2 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:9627404 A>G maps to NM_032315.2 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7Z2-01A-21D-A34J-08 chr17:42400906 G>A maps to NM_001143780.1 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5140-01A-01D-1468-08 chr7:87466057 G>A maps to NM_018843.3 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:87476300 G>A maps to NM_018843.3 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:87476282 A>G maps to NM_018843.3 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr23:118540572 A>T did not map to a codon.
Sequencing variant TCGA-E1-A7Z6-01A-11D-A34J-08 chr23:118603878 G>A did not map to a codon.
Sequencing variant TCGA-FG-A711-01A-21D-A33T-08 chr23:118602490 G>A did not map to a codon.
Sequencing variant TCGA-FG-A713-01A-11D-A32B-08 chr23:118603878 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:1508333 G>A did not map to a codon.
Sequencing variant TCGA-DB-A64R-01A-11D-A29Q-08 chr12:58014089 C>T maps to NM_133489.2 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7US-01A-11D-A33T-08 chr5:149359992 G>A maps to NM_000112.3 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:107427950 G>A maps to NM_000111.2 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:107330591 C>T maps to NM_000441.1 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65Z-01A-11D-A29Q-08 chr7:107314666 C>T maps to NM_000441.1 D158D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7J0-01A-11D-A34A-08 chr7:107312616 C>T maps to NM_000441.1 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:103015034 T>C maps to ENST00000354356 Q684Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:92352737 G>T maps to NM_134266.1 G329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:35912038 G>A maps to NM_052961.3 Q851*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:205904888 G>A maps to NM_134325.2 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7480-01A-11D-2086-08 chr1:205897098 G>A maps to NM_134325.2 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:17615405 C>T maps to NM_198580.1 G642G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:17597671 G>A maps to NM_198580.1 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:128365297 T>C maps to NM_001017372.1 S527S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CX-01A-11D-A32B-08 chr15:85476482 G>A maps to NM_004213.3 E397E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76O-01A-11D-A32B-08 chr15:45559991 T>C maps to NM_004212.3 R399R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A858-01A-11D-A36O-08 chr15:45554260 C>T maps to NM_004212.3 H73H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A70Z-01A-12D-A33T-08 chr9:86903094 T>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:66136898 C>T maps to NM_001532.2 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:43396877 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:24220039 C>T maps to NM_030807.3 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:24210756 C>T maps to NM_030807.3 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R1-01A-12D-A34J-08 chr22:24217411 C>T maps to NM_030807.3 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:40158578 T>C maps to NM_052885.3 A509A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QY-01A-11D-A34A-08 chr12:7984360 C>T did not map to a codon.
Sequencing variant TCGA-DH-A669-01A-12D-A31L-08 chr20:62372749 C>T maps to NM_020062.3 D103D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:62374306 C>T maps to NM_020062.3 C376C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:9083026 G>A maps to NM_207420.2 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5275-01A-01D-1468-08 chr15:45777516 T>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:68417567 C>A maps to NM_022902.2 A539A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A781-01A-11D-A32B-08 chr8:118183315 T>A maps to NM_173851.2 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:176815129 C>T maps to NM_003052.4 G260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8C8-01A-11D-A36O-08 chr5:176824065 C>T maps to NM_003052.4 S469S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:25676130 C>T maps to NM_006424.2 I446I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:25678250 G>A maps to NM_006424.2 A651A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7608-01A-11D-2086-08 chr4:25677956 G>A maps to NM_006424.2 R553R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7609-01A-11D-2086-08 chr4:25677848 G>A maps to NM_006424.2 G517G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7694-01A-11D-2253-08 chr6:88187185 C>G maps to NM_006416.4 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64R-01A-11D-A29Q-08 chr23:48763801 A>T did not map to a codon.
Sequencing variant TCGA-E1-A7YS-01A-11D-A34A-08 chr1:100483314 G>A maps to ENST00000370153 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:8428252 G>T maps to NM_001142540.1 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:45827636 C>T maps to NM_018389.4 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:44983844 G>A maps to NM_173179.2 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:67513001 G>A maps to NM_015139.2 N194N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:67470070 C>T maps to NM_015139.2 Q340Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:137245551 G>A maps to NM_001008783.1 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6405-01A-11D-1705-08 chr6:137245386 G>T maps to NM_001008783.1 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:16664711 G>A maps to NM_024881.4 Y337Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:107677490 C>A maps to NM_017515.4 G176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8161-01A-11D-2253-08 chr1:234454540 C>T maps to NM_173508.2 A333A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A70Z-01A-12D-A33T-08 chr1:234367196 G>A maps to NM_173508.2 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:58056154 C>T maps to NM_001080455.1 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:58063576 G>T maps to NM_001080455.1 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7T6-01A-11D-A33T-08 chr2:114508046 C>T maps to NM_025181.2 W124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6J3-01A-11D-A31L-08 chr5:150714963 A>G maps to NM_181776.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:43963668 C>T maps to NM_018964.3 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:124947385 C>T maps to NM_198277.2 N92N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7491-01A-11D-2024-08 chr7:140058507 G>A maps to NM_207113.1 N151N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr17:79256072 C>T maps to NM_001037984.1 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5ET-01A-11D-A27K-08 chr17:79219798 G>A maps to NM_001037984.1 Q973*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A737-01A-11D-A32B-08 chr12:46758435 A>G maps to NM_018976.4 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr14:61451519 A>G maps to NM_001172702.1 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:84075743 C>A maps to NM_001080442.1 G7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TB-01A-11D-A33T-08 chr16:84050238 C>T maps to NM_001080442.1 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RH-01A-12D-A34A-08 chr2:196582985 C>T maps to NM_001127257.1 F692F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CU-01A-11D-A31L-08 chr8:22273316 G>A maps to NM_001135153.1 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr8:145639356 C>G maps to NM_130849.2 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:56629382 G>T maps to NM_001135195.1 E282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:33169640 C>A maps to NM_006979.2 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VV-A86M-01A-11D-A36O-08 chr6:33169243 A>G maps to NM_006979.2 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:69908876 C>T maps to NM_018375.3 H99H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:62655900 G>A maps to NM_001012661.1 A574A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:190428486 G>A maps to NM_014585.5 R409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:205767836 C>T maps to NM_173854.4 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:125741742 G>A maps to NM_001008485.1 R211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7467-01A-11D-2024-08 chr17:1516557 G>A maps to ENST00000382147 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A72W-01A-11D-A32B-08 chr11:57193591 C>T maps to ENST00000428603 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:108120688 G>A maps to NM_080546.3 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:108126891 C>T maps to NM_080546.3 Q382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YS-01A-11D-A34A-08 chr1:75684272 G>A maps to NM_152697.4 C477C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:8386013 G>A maps to ENST00000377479 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CS-01A-11D-A31L-08 chr1:8399631 C>A maps to ENST00000377479 T652T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:33984676 G>A maps to NM_016180.3 N4N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84S-01A-11D-A36O-08 chr5:33951713 G>A maps to NM_016180.3 V367V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:205628646 C>T maps to NM_033102.2 A459A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:205628523 C>T maps to NM_033102.2 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr8:142228889 G>A maps to NM_001080431.1 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6405-01A-11D-1705-08 chr9:115648894 T>G maps to NM_033051.3 G405G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:19480754 C>T maps to ENST00000395585 G534G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:3212182 C>T maps to NM_001174090.1 K290K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:3209229 G>A maps to NM_001174090.1 F815F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76K-01A-11D-A33T-08 chr20:3210079 G>A maps to NM_001174090.1 C630C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7692-01A-12D-2253-08 chr20:3209829 G>A maps to NM_001174090.1 S686S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:27887224 G>A maps to NM_018158.2 E202E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CA-01A-11D-A36O-08 chr7:150767817 C>T maps to NM_003040.3 C523C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:220493263 C>T maps to NM_201574.2 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:220498004 C>T maps to NM_201574.2 N456N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5851-01A-13D-1893-08 chr4:72121037 A>C maps to NM_001098484.2 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7J0-01A-11D-A34A-08 chr5:139740528 C>T maps to ENST00000507527 C145C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4938-01B-11D-1893-08 chr22:32498214 G>A maps to NM_000343.3 P552P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr22:32487647 C>T maps to NM_000343.3 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CV-01A-11D-A31L-08 chr22:32479070 G>A maps to NM_000343.3 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CB-01A-11D-A36O-08 chr22:32487698 C>T maps to NM_000343.3 Y410Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6IZ-01A-11D-A31L-08 chr16:24883541 T>G did not map to a codon.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr11:26734220 G>C maps to NM_178498.3 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:35468351 G>A maps to NM_006933.4 R285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7692-01A-12D-2253-08 chr21:35468231 A>G maps to NM_006933.4 K245K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TD-01A-12D-A34A-08 chr22:32614590 C>T maps to NM_014227.2 T630T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr2:108604712 C>T maps to NM_021815.2 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:101587497 T>C maps to NM_145913.3 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:101588871 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:101598313 A>G maps to NM_145913.3 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8C8-01A-11D-A36O-08 chr3:11068037 G>A maps to NM_003042.3 A357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:301736 G>A maps to NM_003044.3 Y536Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:318998 C>A maps to NM_003044.3 E52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:115573908 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:115569064 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:85257247 A>T maps to NM_182767.4 P596P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7482-01A-11D-2024-08 chr12:85255482 A>G maps to NM_182767.4 A707A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85E-01A-11D-A36O-08 chr12:85257322 A>T maps to NM_182767.4 Y571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A70Z-01A-12D-A33T-08 chr19:49793873 C>T maps to NM_014037.2 W643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:110717533 G>A maps to NM_001010898.2 W235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7Z2-01A-21D-A34J-08 chr1:110741026 C>T maps to NM_001010898.2 S715S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F6-A8O4-01A-11D-A36O-08 chr5:1221295 C>A maps to NM_001003841.2 G523G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:55732427 C>A maps to NM_001043.3 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A6S3-01A-12D-A32B-08 chr3:45804411 G>A maps to NM_020208.3 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:1403054 C>T maps to NM_001044.4 L583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7471-01A-11D-2253-08 chr5:1409835 G>A maps to NM_001044.4 N466N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85E-01A-11D-A36O-08 chr5:1414806 G>A maps to NM_001044.4 D385D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:28544282 C>T maps to ENST00000394821 Q288Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:28530323 G>A maps to ENST00000394821 Q604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EY-01A-11D-A27K-08 chr17:28548856 G>A maps to ENST00000394821 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:20658806 C>A maps to NM_004211.3 C609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A70Z-01A-12D-A33T-08 chr23:152960345 T>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:44476506 T>C maps to NM_201649.2 K99K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:30097548 G>A maps to NM_003045.4 Y301Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:139140511 C>T maps to ENST00000280612 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XE-01A-11D-A27K-08 chr8:17409357 C>A maps to NM_001164771.1 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4944-01A-01D-1468-08 chr23:70148833 C>A did not map to a codon.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr23:70148063 C>T did not map to a codon.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr14:23282565 C>T maps to NM_001126106.1 E14E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:40342395 G>A maps to NM_021097.2 F973F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:47940749 C>T maps to NM_015063.2 E693E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:47960707 C>T maps to NM_015063.2 E273E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr19:47935601 G>A maps to NM_015063.2 F737F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7J0-01A-11D-A34A-08 chr19:47944424 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:27426800 C>T maps to NM_003047.3 Q815Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:27426980 G>A maps to NM_003047.3 D755D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7873-01B-11D-2395-08 chr1:27440679 G>A maps to NM_003047.3 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6IZ-01A-11D-A31L-08 chr1:173526562 C>T maps to NM_178527.3 W377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IS-01A-11D-A34A-08 chr1:173526625 C>G maps to NM_178527.3 V356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr2:103281659 G>A maps to NM_003048.3 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4X9-01A-11D-A26M-08 chr5:491956 G>A maps to NM_004174.2 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7C3-01A-11D-A32B-08 chr5:488442 G>A maps to NM_004174.2 D221D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:2087921 A>G maps to ENST00000191922 R352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:103119908 C>T maps to NM_001011552.3 V241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A711-01A-21D-A33T-08 chr2:103120020 T>C maps to NM_001011552.3 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:67292253 G>A maps to NM_004594.2 Q510Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8166-01A-11D-2253-08 chr16:67304912 C>T maps to NM_004594.2 L831L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr23:135112295 G>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:135067916 C>A did not map to a codon.
Sequencing variant TCGA-DU-7009-01A-11D-2024-08 chr23:135106544 C>T did not map to a codon.
Sequencing variant TCGA-DB-A64O-01A-11D-A29Q-08 chr23:46510651 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:46472780 C>T did not map to a codon.
Sequencing variant TCGA-KT-A7W1-01A-11D-A34A-08 chr23:46466457 G>T did not map to a codon.
Sequencing variant TCGA-TQ-A7RM-01A-11D-A33T-08 chr23:46531995 A>G did not map to a codon.
Sequencing variant TCGA-DU-7304-01A-12D-2086-08 chr12:21422505 A>G maps to NM_134431.3 D663D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7489-01A-11D-2024-08 chr12:21392092 T>C maps to NM_006446.4 S682S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A75L-01A-11D-A32B-08 chr12:21033839 A>C maps to NM_019844.2 S461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr12:21030808 C>T maps to NM_019844.2 Y358Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F4-01A-11D-A289-08 chr12:21028268 T>C maps to NM_019844.2 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7855-01A-11D-2395-08 chr3:133654660 G>A maps to NM_005630.2 R591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:61291875 C>T maps to NM_016354.3 Q334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr20:61288351 G>A maps to NM_016354.3 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5871-01A-12D-1705-08 chr5:101585437 C>T maps to NM_180991.4 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:101592826 T>C maps to NM_180991.4 S487S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:101585410 T>C maps to NM_180991.4 G517G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7006-01A-11D-2024-08 chr5:101583041 C>T maps to NM_180991.4 A575A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7882-01A-11D-2395-08 chr5:101582954 C>A did not map to a codon.
Sequencing variant TCGA-P5-A77W-01A-11D-A32B-08 chr5:101627179 T>C maps to NM_180991.4 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RM-01A-11D-A33T-08 chr5:101575024 A>G maps to NM_180991.4 N648N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7634-01A-11D-2086-08 chr17:33679773 C>T maps to NM_152270.3 W769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EZ-7264-01A-11D-2024-08 chr17:33738551 C>T maps to NM_018042.3 S514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EU-01A-11D-A27K-08 chr17:33738558 A>C maps to NM_018042.3 L512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KJ-01A-12D-A27K-08 chr10:98797513 G>A maps to NM_003061.2 D769D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:20512132 C>T maps to ENST00000273739 N314N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8165-01A-11D-2253-08 chr4:20597370 C>T maps to ENST00000273739 D1091D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5322-01A-01D-1468-08 chr4:20597442 C>T maps to ENST00000273739 C1115C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A615-01A-11D-A29Q-08 chr4:20618725 G>A maps to ENST00000273739 Q1360Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:168201247 G>A maps to NM_003062.2 I429I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:168149936 C>T did not map to a codon.
Sequencing variant TCGA-HW-A5KJ-01A-12D-A27K-08 chr5:168093479 G>A maps to NM_003062.2 C1517C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66G-01A-21D-A31L-08 chr23:144905824 G>T did not map to a codon.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr23:144904328 C>A did not map to a codon.
Sequencing variant TCGA-VM-A8C8-01A-11D-A36O-08 chr23:144904069 A>G did not map to a codon.
Sequencing variant TCGA-DU-A76R-01A-11D-A32B-08 chr3:164907772 G>T maps to NM_014926.2 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr23:142717274 G>A did not map to a codon.
Sequencing variant TCGA-DB-A75K-01A-11D-A32B-08 chr23:142716808 C>T did not map to a codon.
Sequencing variant TCGA-DU-A5TT-01A-11D-A289-08 chr23:142717375 G>T did not map to a codon.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr23:142716491 A>G did not map to a codon.
Sequencing variant TCGA-S9-A6WM-01A-12D-A33T-08 chr23:142717978 C>T did not map to a codon.
Sequencing variant TCGA-HT-8105-01A-11D-2395-08 chr13:88329499 A>G maps to NM_015567.1 V619V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7J1-01A-21D-A34J-08 chr13:88327978 A>T maps to NM_015567.1 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:86369281 G>A maps to NM_032229.2 T454T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:86369035 G>A maps to NM_032229.2 S536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:86368645 A>T maps to NM_032229.2 T666T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RW-01A-11D-A33T-08 chr10:105780332 C>T maps to NM_014720.2 Q1137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:57894827 C>A maps to ENST00000428312 A533A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IQ-01A-21D-A34A-08 chr3:57847744 T>C maps to ENST00000428312 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:59182556 C>A maps to NM_024755.2 E668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:37446849 G>A maps to NM_001127217.2 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:37439704 C>T maps to NM_001127217.2 T324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:40881993 G>A maps to NM_022733.2 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr23:128632025 C>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:128630768 C>A did not map to a codon.
Sequencing variant TCGA-DU-A7T6-01A-11D-A33T-08 chr23:128631956 G>C did not map to a codon.
Sequencing variant TCGA-HT-7902-01A-12D-2395-08 chr23:128633715 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:11145687 C>T maps to NM_001128849.1 D1350D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:11135026 C>T maps to NM_001128849.1 C998C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:11098591 C>T maps to NM_001128849.1 R370R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:11134246 G>A maps to NM_001128849.1 V971V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7C3-01A-11D-A32B-08 chr19:11170532 G>A maps to NM_001128849.1 E1612E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:144465100 A>T maps to NM_003601.2 G716G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:144457706 T>C maps to NM_003601.2 C457C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YS-01A-11D-A34A-08 chr4:95147294 A>G maps to NM_001128429.1 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:47823104 C>T maps to NM_003074.3 K61K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:47663812 C>A maps to NM_003074.3 E889*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr12:56568510 G>A maps to NM_003075.3 R474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IZ-01A-11D-A34A-08 chr12:56558273 C>T maps to NM_003075.3 P1127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:50490634 C>T maps to NM_003076.4 I424I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:38786990 G>A maps to NM_003079.4 D334D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7601-01A-11D-2086-08 chr17:38792703 C>T maps to NM_003079.4 W104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:53423220 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:53426540 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:53440255 C>T did not map to a codon.
Sequencing variant TCGA-E1-A7YO-01A-11D-A34A-08 chr23:53432802 G>A did not map to a codon.
Sequencing variant TCGA-R8-A6ML-01A-11D-A32B-08 chr23:53432431 C>A did not map to a codon.
Sequencing variant TCGA-TM-A84M-01A-11D-A36O-08 chr23:53440234 G>A did not map to a codon.
Sequencing variant TCGA-TQ-A7RU-01A-21D-A34A-08 chr23:53440218 G>A did not map to a codon.
Sequencing variant TCGA-DH-5144-01A-01D-1468-08 chr22:45768072 C>A maps to NM_148674.3 E720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:45768172 C>A did not map to a codon.
Sequencing variant TCGA-HT-8106-01A-11D-2395-08 chr22:45779409 G>A maps to NM_148674.3 C665C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:106887380 C>T maps to NM_001042550.1 Q816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7CA-01A-21D-A33T-08 chr9:106877085 C>A maps to NM_001042550.1 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:112362339 G>T maps to NM_005445.3 E1072*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74L-01A-11D-A32B-08 chr3:160149453 T>A maps to NM_005496.3 P1046P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:72897423 G>A maps to NM_015110.3 G302G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:17888592 A>G maps to ENST00000381272 C659C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr2:17884528 C>T maps to ENST00000381272 T705T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TS-01A-11D-A289-08 chr1:152857173 G>A maps to NM_030663.2 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6408-01A-11D-1705-08 chr17:18219588 G>A maps to NM_144775.2 Q162Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:91947961 A>C maps to ENST00000417249 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WH-A86K-01A-11D-A36O-08 chr1:28285339 C>T maps to NM_014474.2 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:21990048 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:21985377 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:88387389 G>A maps to NM_198274.3 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7018-01A-11D-2024-08 chr2:88393053 C>G maps to NM_198274.3 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:88387389 G>A maps to NM_198274.3 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:1703451 G>A maps to NM_052928.2 C412C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6J3-01A-11D-A31L-08 chr17:1715302 C>A maps to NM_052928.2 E81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:73446051 C>T maps to NM_006062.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr8:49833788 G>A maps to NM_003068.3 N12N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:10273854 C>T maps to NM_130811.1 D70D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7611-01A-11D-2395-08 chr1:153633755 C>T maps to NM_012437.4 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:242021116 C>T maps to NM_001080437.1 N1314N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:11770175 C>T maps to NM_003498.5 H87H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:43389475 C>T maps to NM_017719.4 G575G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8162-01A-21D-2253-08 chr2:96970468 C>T maps to NM_014014.3 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:49593546 G>T did not map to a codon.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr19:41268828 G>A maps to NM_004596.4 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RJ-01A-11D-A33T-08 chr8:121823846 C>A maps to NM_021021.3 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:75890977 G>A maps to ENST00000371091 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64U-01A-11D-A29Q-08 chr6:86237977 A>G did not map to a codon.
Sequencing variant TCGA-DU-5871-01A-12D-1705-08 chr11:64803112 C>T maps to NM_013306.4 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:64799949 C>T maps to NM_013306.4 D61D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:130785539 C>A maps to NM_014758.2 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7470-01A-12D-2086-08 chr11:130750570 G>A maps to NM_014758.2 Q902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:44463099 A>G maps to NM_033421.2 E94E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:186283233 G>A maps to NM_031953.2 Q772Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85C-01A-11D-A36O-08 chr4:186263215 G>A maps to NM_031953.2 W547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:151664939 C>A maps to ENST00000458013 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:151630869 C>T maps to ENST00000458013 R235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WD-01A-12D-A33T-08 chr16:12662398 G>A maps to NM_001080530.2 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:75942138 C>A maps to NM_153271.1 C232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:35062308 A>C maps to NM_152233.2 Y232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W9-A837-01A-11D-A36O-08 chr14:35074872 T>C maps to NM_152233.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:158323017 C>T maps to NM_016224.3 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7018-01A-11D-2024-08 chr1:179320473 T>C maps to NM_003101.4 N491N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A710-01A-12D-A33T-08 chr1:179314135 T>C maps to NM_003101.4 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr1:179310291 C>G maps to NM_003101.4 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8185-01A-11D-2253-08 chr16:11349038 G>T maps to NM_003745.1 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:55510640 C>T maps to NM_199421.1 Y294Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr2:46985883 C>A maps to NM_144949.2 S72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:67992735 G>T maps to NM_004232.3 E278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TT-01A-11D-A289-08 chr9:138590204 G>A maps to NM_001101677.1 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5855-01A-11D-1705-08 chr13:36776074 A>G maps to ENST00000511166 V145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr13:36764135 G>A maps to ENST00000511166 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A711-01A-21D-A33T-08 chr13:36743176 C>T maps to ENST00000511166 A501A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8191-01A-11D-2253-08 chr16:598067 C>T maps to NM_005632.2 P410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5280-01A-01D-1468-08 chr21:34927009 C>T maps to NM_138927.1 R1825*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:97096670 C>T maps to NM_001034954.1 T1082T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:186536047 G>A maps to ENST00000355634 I1040I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:186544815 G>A maps to ENST00000355634 S685S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:108337254 G>A maps to NM_052918.3 R1144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A70Z-01A-12D-A33T-08 chr10:108357141 G>A maps to NM_001013031.1 R1078*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:7725422 G>T did not map to a codon.
Sequencing variant TCGA-P5-A77X-01A-11D-A32B-08 chr4:7533274 G>A maps to NM_020777.2 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A6MO-01A-11D-A33T-08 chr4:7668882 C>A maps to NM_020777.2 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:106937889 C>T maps to NM_014978.1 D656D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U8-01A-21D-A33T-08 chr15:45357561 A>G maps to NM_003104.5 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:121461725 C>A maps to NM_003105.5 P1410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr11:121429380 G>C maps to NM_003105.5 L915L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8113-01A-11D-2395-08 chr11:121358799 T>A maps to NM_003105.5 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KM-01A-11D-A27K-08 chr11:121428039 C>T maps to NM_003105.5 G863G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:39224151 C>A maps to NM_005633.3 G998*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KJ-01A-12D-A27K-08 chr22:38379482 G>A maps to NM_006941.3 H103H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr8:55370801 C>A maps to NM_022454.3 S35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr8:55370803 C>T maps to NM_022454.3 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:181430972 C>T maps to NM_003106.2 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:139586631 C>T did not map to a codon.
Sequencing variant TCGA-DU-7302-01A-11D-2086-08 chr23:139586762 G>A did not map to a codon.
Sequencing variant TCGA-E1-A7Z3-01A-11D-A34J-08 chr23:139586562 A>G did not map to a codon.
Sequencing variant TCGA-DU-A76K-01A-11D-A33T-08 chr6:21596084 C>T maps to NM_003107.2 S440S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:23687227 G>A maps to NM_006940.4 Y739Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:16340159 G>A maps to NM_001145819.1 R106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:10583853 G>A maps to ENST00000354846 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:10583613 G>A maps to ENST00000354846 G319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr8:10587871 C>T maps to NM_031439.2 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr2:231367784 A>G maps to NM_001080391.1 R575R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TX-01A-21D-A32B-08 chr2:231249984 G>A maps to NM_138402.4 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:21469478 A>G maps to NM_003112.3 Q232Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:21470441 T>C maps to NM_003112.3 V553V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:20824832 G>A maps to NM_182700.4 H201H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TA-01A-11D-A33T-08 chr19:49110579 G>T maps to NM_133498.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:118642421 G>A maps to NM_206996.2 D212D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr1:118516182 T>C maps to NM_206996.2 E2002E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QY-01A-11D-A34A-08 chr1:118657952 G>A maps to NM_206996.2 R143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8320-01A-11D-2395-08 chr9:35811424 G>A maps to NM_001039592.1 D206D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A780-01A-12D-A32B-08 chr23:140335726 G>A did not map to a codon.
Sequencing variant TCGA-TQ-A7RM-01A-11D-A33T-08 chr23:140336552 C>G did not map to a codon.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr23:140785690 G>T did not map to a codon.
Sequencing variant TCGA-FG-5964-01A-11D-1705-08 chr23:140785766 A>G did not map to a codon.
Sequencing variant TCGA-FG-A4MT-01A-11D-A26M-08 chr23:140785681 G>T did not map to a codon.
Sequencing variant TCGA-HT-7873-01B-11D-2395-08 chr23:140785748 C>T did not map to a codon.
Sequencing variant TCGA-HW-A5KL-01A-11D-A27K-08 chr23:140785838 G>A did not map to a codon.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr23:144337222 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:144337284 G>T did not map to a codon.
Sequencing variant TCGA-CS-6186-01A-12D-2024-08 chr23:142795436 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:57107736 T>A maps to NM_181727.1 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:24860368 C>T maps to ENST00000424834 N810N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6IZ-01A-11D-A31L-08 chr13:24823638 C>T maps to ENST00000424834 R597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5872-01A-11D-1705-08 chr3:172631477 A>G maps to NM_031955.5 N520N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:217975156 C>T maps to NM_138796.2 R324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6X8-01A-12D-A32B-08 chr1:217915373 C>T maps to NM_138796.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:16731548 G>A maps to NM_198546.1 Q242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:89764614 G>A maps to NM_152339.3 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:123978365 C>A maps to NM_145207.2 T712T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:124177313 C>T maps to NM_145207.2 T828T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7695-01A-11D-2253-08 chr15:45713341 C>T maps to NM_024063.2 C732C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74H-01A-11D-A32B-08 chr8:145094825 G>A maps to NM_198572.2 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85E-01A-11D-A36O-08 chr2:201303980 A>T maps to ENST00000409151 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:169745978 C>T maps to NM_020675.3 W17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr6:34508916 G>A maps to NM_012391.1 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8191-01A-11D-2253-08 chr11:64939961 A>G maps to NM_001008778.1 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:44044818 C>T maps to NM_175064.2 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:35654815 C>T maps to NM_024867.3 H322H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:35641673 C>T maps to NM_024867.3 Y101Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr5:35697830 T>C maps to NM_024867.3 L693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:220309640 G>A maps to NM_005876.4 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8107-01A-13D-2395-08 chr2:220344808 T>C maps to NM_005876.4 F1763F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WG-01A-11D-A33T-08 chr2:220342457 C>T maps to NM_005876.4 R1593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:16245446 A>T maps to NM_015001.2 G474G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:16254738 C>T maps to NM_015001.2 Y668Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:16260840 G>A maps to NM_015001.2 G2702G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TJ-01A-11D-A34J-08 chr1:16261677 G>A maps to NM_015001.2 T2981T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YN-01A-11D-A34A-08 chr15:69238118 C>T maps to NM_145658.3 D82D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6IZ-01A-11D-A31L-08 chr13:36888511 A>G maps to NM_001142294.1 T445T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:89598877 C>T maps to NM_003119.2 G386G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A61B-01A-11D-A29Q-08 chr16:89620235 C>T maps to NM_003119.2 I657I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6402-01A-11D-1705-08 chr2:228890205 G>A maps to NM_001142644.1 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7470-01A-12D-2086-08 chr2:228846501 G>A maps to NM_001142644.1 Y1678Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr19:50926143 G>A maps to NM_003121.3 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:91083494 C>T maps to NM_006717.2 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WM-01A-12D-A33T-08 chr23:62570230 G>A did not map to a codon.
Sequencing variant TCGA-E1-A7YS-01A-11D-A34A-08 chr15:41136874 C>T maps to NM_181642.2 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:44351047 C>A maps to NM_178455.1 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:29676224 C>T maps to NM_003123.3 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:28995228 C>T maps to NM_032038.2 T481T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WG-01A-11D-A33T-08 chr17:4352553 C>T maps to NM_182538.4 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr2:139308481 G>A maps to NM_001001664.2 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6X4-01A-51D-A32B-08 chr2:234959501 C>T maps to NM_006944.2 Y24Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6XA-01A-12D-A32B-08 chr12:121221496 T>C maps to NM_139015.3 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:38643406 C>T maps to NM_152594.2 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TV-01A-12D-A34J-08 chr1:153012732 C>T maps to NM_006945.4 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr1:153085128 A>G maps to NM_001014450.1 C27C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:124323306 C>T maps to NM_199327.1 C187C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66B-01A-11D-A29Q-08 chr13:80911692 G>A maps to NM_005842.2 R50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr23:155004314 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:141694442 C>T maps to NM_030964.3 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr5:141693968 C>T maps to NM_030964.3 W258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5872-01A-11D-1705-08 chr11:55655603 C>T maps to NM_032681.3 R202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6402-01A-11D-1705-08 chr11:55653033 C>T maps to NM_032681.3 Q44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A4DS-01A-11D-A26M-08 chr11:55653245 G>A maps to NM_032681.3 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:158612618 G>A maps to NM_003126.2 D1530D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:158637678 C>T maps to NM_003126.2 W669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:158641243 C>A did not map to a codon.
Sequencing variant TCGA-R8-A6MK-01A-11D-A32B-08 chr1:158596677 A>G maps to NM_003126.2 Y1928Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5142-01A-01D-1468-08 chr9:131337004 C>T maps to NM_001130438.2 R139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:65263286 G>A maps to ENST00000389723 R447R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7013-01A-11D-2024-08 chr14:65258513 G>A maps to ENST00000389723 L913L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YK-01A-11D-A34A-08 chr14:65236306 C>T did not map to a codon.
Sequencing variant TCGA-CS-5393-01A-01D-1468-08 chr2:54880942 C>G maps to NM_003128.2 L1925L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:54885014 C>T maps to NM_003128.2 D2025D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:54886385 C>T maps to NM_003128.2 A2113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:54858297 C>T maps to NM_003128.2 A1038A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:66472097 G>A maps to NM_006946.2 R883R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5847-01A-11D-1705-08 chr19:40998961 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:41040139 C>T maps to NM_020971.2 Q1417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6396-01A-11D-1705-08 chr19:41063164 C>T maps to NM_020971.2 D1842D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VV-A829-01A-21D-A36O-08 chr19:41012264 C>T maps to NM_020971.2 A596A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5140-01A-01D-1468-08 chr15:42172440 A>G maps to ENST00000320955 L910L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YN-01A-11D-A34A-08 chr15:42166141 G>A maps to ENST00000320955 I1597I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:94842324 C>A maps to NM_006415.2 G134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:94874735 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:79616243 C>T maps to NM_032567.3 N70N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:79617029 G>A maps to NM_032567.3 Q332Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:45981347 G>T maps to NM_021199.2 E410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr15:45974845 C>T maps to NM_021199.2 T345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:142731108 C>T maps to NM_001080415.1 R46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WL-01A-21D-A33T-08 chr3:142741379 A>C maps to NM_001080415.1 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr2:45616591 G>A maps to NM_018079.4 R949*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8110-01A-11D-2395-08 chr2:45620174 C>T maps to NM_018079.4 E869E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr16:30734515 C>G maps to NM_006662.2 L1375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:76024570 G>A maps to NM_080744.1 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YV-01A-11D-A34J-08 chr7:76033639 A>T maps to NM_080744.1 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:206632040 C>T maps to ENST00000414359 S783S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:206619486 G>A maps to ENST00000414359 S570S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:206634617 G>A maps to ENST00000414359 R946R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TS-01A-12D-A33T-08 chr1:206634404 G>A maps to ENST00000414359 S875S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7482-01A-11D-2024-08 chr16:4242360 G>A maps to ENST00000330063 F843F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:62172559 G>T maps to NM_080823.2 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7636-01A-11D-2086-08 chr20:62178603 A>G maps to NM_080823.2 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8189-01B-11D-A289-08 chr17:74068494 A>C maps to NM_014230.2 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:57344543 G>T did not map to a codon.
Sequencing variant TCGA-HT-7477-01B-11D-A289-08 chr4:57340269 C>T maps to NM_006947.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7470-01A-12D-2086-08 chr7:104782647 T>C maps to ENST00000336613 P481P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:99901317 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:2222126 T>C maps to NM_021947.1 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8185-01A-11D-2253-08 chr1:24995839 T>C maps to NM_005839.3 L656L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr16:2820395 C>A maps to NM_016333.3 R2689R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7474-01A-11D-2024-08 chr2:170667376 C>T maps to NM_003142.3 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:182780676 C>A maps to NM_001130445.1 S770S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:27959345 C>A maps to NM_033389.2 E929*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5311-01A-01D-1468-08 chr17:27994186 G>A maps to NM_033389.2 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8105-01A-11D-2395-08 chr17:27975226 C>T maps to NM_033389.2 T427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CV-01A-11D-A31L-08 chr17:27959166 C>T maps to NM_033389.2 R988R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:26383930 A>G maps to NM_005086.4 K218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:149500074 C>T maps to NM_198455.2 C2568C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:149523190 C>T maps to NM_198455.2 C4764C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:149491915 T>C maps to NM_198455.2 P2040P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:149481157 C>T maps to NM_198455.2 C880C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr7:149474866 G>A maps to NM_198455.2 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7299-01A-21D-2024-08 chr7:149489166 G>A maps to NM_198455.2 Q1805Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5319-01A-01D-1893-08 chr7:149486392 C>T maps to NM_198455.2 L1458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RH-01A-12D-A34A-08 chr7:149489292 G>A maps to NM_198455.2 P1847P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RO-01A-11D-A33T-08 chr7:149485857 A>G maps to NM_198455.2 Q1360Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:156266707 C>T maps to ENST00000467789 K115K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:187386858 G>T maps to NM_001048.3 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6188-01A-11D-1893-08 chr14:38679007 G>C maps to NM_001049.2 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U1-01A-21D-A33T-08 chr14:38679187 C>G maps to NM_001049.2 T198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TD-01A-12D-A34A-08 chr22:37603623 C>T maps to NM_001051.2 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:48125806 G>A did not map to a codon.
Sequencing variant TCGA-DU-7008-01A-11D-2024-08 chr23:48116710 G>T did not map to a codon.
Sequencing variant TCGA-HT-7476-01A-11D-2024-08 chr23:48125815 C>T did not map to a codon.
Sequencing variant TCGA-FG-8186-01A-11D-2253-08 chr23:48053621 G>A did not map to a codon.
Sequencing variant TCGA-HW-7493-01A-11D-2024-08 chr23:48053570 T>A did not map to a codon.
Sequencing variant TCGA-S9-A6UB-01A-21D-A33T-08 chr23:48053615 C>T did not map to a codon.
Sequencing variant TCGA-S9-A7R1-01A-12D-A34J-08 chr23:48053652 C>T did not map to a codon.
Sequencing variant TCGA-S9-A6TS-01A-12D-A33T-08 chr23:52681397 C>G did not map to a codon.
Sequencing variant TCGA-S9-A6TY-01A-12D-A32B-08 chr22:41223195 T>C maps to NM_003932.3 G295G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4943-01A-01D-1468-08 chr11:130069891 C>T maps to NM_021978.3 G618G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:130068296 C>T maps to NM_021978.3 S518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TZ-01A-21D-A32B-08 chr11:130079711 G>A maps to NM_021978.3 G854G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:53084706 A>G maps to NM_014682.2 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8106-01A-11D-2395-08 chr8:53079463 C>T maps to NM_014682.2 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:70416788 G>A maps to NM_006927.3 H266H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:44290429 T>G maps to NM_174963.2 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RU-01A-21D-A34A-08 chr2:86073607 G>A maps to NM_003896.3 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:186760526 C>A maps to NM_003032.2 C12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7309-01A-11D-2086-08 chr2:107460055 C>T maps to NM_001142351.1 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7638-01B-11D-2086-08 chr9:130672315 G>C maps to NM_175039.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:130653133 G>A maps to NM_013443.3 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5311-01A-01D-1468-08 chr12:22408290 G>A maps to NM_003034.3 C138C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:93007443 G>A maps to NM_006011.3 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:93007422 C>T maps to NM_006011.3 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WD-01A-12D-A33T-08 chr5:100222197 G>A maps to NM_005668.4 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7US-01A-11D-A33T-08 chr3:52546659 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:52556110 G>A maps to NM_015136.2 Q2110Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TS-01A-11D-A289-08 chr3:52539709 C>T maps to NM_015136.2 D536D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7471-01A-11D-2253-08 chr3:52552601 C>T maps to NM_015136.2 H1620H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RG-01A-11D-A33T-08 chr3:52538883 C>T maps to NM_015136.2 Q457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XD-01A-11D-A27K-08 chr12:104033986 G>A maps to NM_017564.9 P331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5302-01A-01D-1468-08 chr12:104138999 C>A maps to NM_017564.9 S2027S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5302-01A-01D-1468-08 chr12:104049283 C>T maps to NM_017564.9 Y553Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CZ-01A-11D-A32B-08 chr12:104140465 C>T maps to NM_017564.9 D2076D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CY-01A-11D-A32B-08 chr3:136240171 G>A maps to NM_005862.2 R187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:123185183 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:123185163 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:123179217 G>T did not map to a codon.
Sequencing variant TCGA-HT-7610-01A-21D-2086-08 chr23:123196966 A>T did not map to a codon.
Sequencing variant TCGA-HT-8011-01A-11D-2395-08 chr23:123179196 C>T did not map to a codon.
Sequencing variant TCGA-TM-A7C3-01A-11D-A32B-08 chr23:123227872 G>A did not map to a codon.
Sequencing variant TCGA-TM-A7C3-01A-11D-A32B-08 chr23:123179120 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:99800140 G>A maps to NM_012447.2 G876G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:153000471 T>C maps to NM_005843.4 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:152988659 T>C maps to NM_005843.4 P331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7879-01A-11D-2395-08 chr2:153003684 T>C maps to NM_005843.4 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:68436815 C>T maps to NM_012108.2 Y45Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:4332027 C>T maps to ENST00000314714 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CD-01A-11D-A36O-08 chr8:38006210 G>A maps to NM_000349.2 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:33684068 G>T maps to NM_178007.2 I988I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:33703427 G>A maps to NM_178007.2 V454V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8185-01A-11D-2253-08 chr18:51858175 G>A maps to NM_139171.1 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:96858171 C>A maps to NM_020151.3 E260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:67939136 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:67937776 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:191862733 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:191874730 C>A did not map to a codon.
Sequencing variant TCGA-TM-A84B-01A-11D-A36O-08 chr2:191865865 G>A maps to NM_007315.3 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6J3-01A-11D-A31L-08 chr17:40369406 G>A maps to NM_012448.3 H415H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QX-01A-11D-A34A-08 chr17:40354365 G>A maps to NM_012448.3 Y743Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7470-01A-12D-2086-08 chr4:70866653 A>G maps to NM_003154.2 Q59Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:47734472 C>A maps to NM_017453.2 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5319-01A-01D-1893-08 chr20:47732386 T>C maps to NM_017453.2 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CX-01A-11D-A32B-08 chr7:89791295 G>A maps to ENST00000433102 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:47745933 C>T maps to NM_001048166.1 Q732Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:63960581 C>T maps to ENST00000358794 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:1220377 C>T maps to NM_000455.4 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:99127179 G>A maps to NM_003576.3 G176G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DU-6392-01A-11D-1705-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:242437036 G>A maps to NM_006374.3 F366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:23810622 G>T did not map to a codon.
Sequencing variant TCGA-HT-7855-01A-11D-2395-08 chr7:23871942 T>A maps to NM_031414.3 C1006*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8563-01A-11D-2395-08 chr4:5461891 C>G maps to NM_018401.1 Y282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:36464530 T>C maps to NM_007271.2 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A61B-01A-11D-A29Q-08 chr12:27467497 C>T maps to NM_015000.3 Y193Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:26227578 C>A did not map to a codon.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr20:62272735 G>A maps to NM_015894.2 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr15:74281474 G>A maps to NM_004809.3 R122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7611-01A-11D-2395-08 chr13:39564827 G>A maps to NM_145286.2 Q11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:48808410 G>A maps to NM_172311.2 E213E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:70645582 C>T maps to NM_001130161.2 G677G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QX-01A-11D-A34A-08 chr10:70645060 A>G maps to NM_001130161.2 R503R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:184930404 C>T maps to NM_020225.1 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:202344894 C>T maps to NM_018571.5 F418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RH-01A-12D-A34A-08 chr2:202323544 C>A maps to NM_018571.5 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R5-01A-11D-A289-08 chr12:16050899 C>T maps to ENST00000025399 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:47228076 G>T maps to NM_001039877.1 P534P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:125488334 G>A maps to NM_152713.3 E614E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EU-01A-11D-A27K-08 chr6:144508399 C>T maps to NM_003764.3 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U2-01A-21D-A33T-08 chr6:144508015 C>T maps to NM_003764.3 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7007-01A-11D-2024-08 chr3:93733521 A>G maps to NM_001001850.1 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:131291535 G>A maps to NM_194356.1 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A840-01A-11D-A36O-08 chr11:59564806 T>C maps to NM_004177.4 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:31049323 C>T maps to NM_004604.3 N152N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:147703944 G>A maps to NM_001127715.1 R1075R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:75634662 G>A maps to NM_016086.2 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TS-01A-11D-A289-08 chr10:104353822 G>T did not map to a codon.
Sequencing variant TCGA-CS-5394-01A-01D-1468-08 chr20:46305255 C>A maps to NM_001161841.1 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TS-01A-12D-A33T-08 chr20:46291957 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:28604832 G>A maps to NM_001054.3 Y143Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr16:28606982 C>T maps to NM_001054.3 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R4-01A-12D-A34J-08 chr16:28606752 G>A maps to NM_001054.3 R103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:70599225 C>A did not map to a codon.
Sequencing variant TCGA-S9-A6U0-01A-12D-A32B-08 chr4:70620860 T>C maps to NM_014465.3 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YJ-01A-11D-A34A-08 chr4:70709894 C>T maps to NM_005420.2 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr4:70709894 C>T maps to NM_005420.2 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:37414559 T>A maps to NM_001032377.1 K46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr3:4491009 G>A maps to NM_182760.3 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:56140720 G>T maps to ENST00000395437 E108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:56145874 C>T maps to ENST00000395437 N246N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7302-01A-11D-2086-08 chr7:56145815 A>T maps to ENST00000395437 K227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7019-01A-11D-2024-08 chr17:73177150 C>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:46233926 C>T maps to ENST00000411651 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A859-01A-12D-A36O-08 chr7:893043 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:44971422 G>A maps to NM_181356.1 D168D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U2-01A-21D-A33T-08 chr6:45073682 C>T maps to NM_181356.1 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:27027529 C>T maps to NM_003170.3 H1602H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:27020845 C>T maps to NM_003170.3 R1256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:70968442 C>T maps to NM_003171.3 H671H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:114860831 C>T maps to NM_022486.3 T464T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:223441961 A>G maps to NM_017982.3 H139H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:223402632 G>A maps to NM_017982.3 C274C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A845-01A-11D-A36O-08 chr1:223536658 G>A maps to NM_017982.3 Q37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:48559101 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:48557419 C>T did not map to a codon.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr23:48559032 G>C did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr11:67925271 G>A maps to NM_017635.3 D847D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr17:30303571 C>T maps to NM_015355.2 R286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:75427913 G>A maps to NM_014979.1 K113K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:113234559 G>A maps to ENST00000374463 Y881Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:113212496 T>G maps to ENST00000374463 P1315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:113170043 G>A maps to ENST00000374463 D2615D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:113312384 C>A did not map to a codon.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr9:113170751 A>G maps to ENST00000374463 C2379C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8185-01A-11D-2253-08 chr9:113139602 G>C maps to ENST00000374463 R3487R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-7675-01A-11D-2086-08 chr9:113275227 G>A maps to ENST00000374463 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TY-01A-12D-A32B-08 chr9:113171072 C>T maps to ENST00000374463 P2272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7C5-01A-11D-A32B-08 chr9:113238565 G>A maps to ENST00000374463 D839D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:29801768 G>A maps to NM_021738.2 S1137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6400-01A-12D-1705-08 chr10:29820186 G>A maps to NM_021738.2 V680V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:9735164 A>G maps to NM_015055.2 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7681-01A-11D-2395-08 chr23:16774793 C>A did not map to a codon.
Sequencing variant TCGA-TM-A84G-01A-11D-A36O-08 chr23:16773204 T>A did not map to a codon.
Sequencing variant TCGA-DU-6408-01A-11D-1705-08 chr1:115401332 G>A did not map to a codon.
Sequencing variant TCGA-HT-7469-01A-11D-2253-08 chr1:115401229 A>G maps to NM_003176.2 K118K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A870-01A-11D-A36O-08 chr1:115488992 A>G maps to NM_003176.2 R746R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A6YH-01A-21D-A32B-08 chr20:58467638 T>C maps to NM_014258.2 G637G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:25549894 C>T maps to NM_015484.4 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr9:93606245 G>A maps to NM_003177.5 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:46331148 C>T maps to NM_004819.2 A671A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YQ-01A-11D-A34J-08 chr22:32923908 C>T maps to NM_003490.3 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YU-01A-11D-A34J-08 chr6:86324824 A>G maps to NM_006372.4 A507A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XD-01A-11D-A27K-08 chr6:152763233 C>A maps to NM_182961.2 R1328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:152728207 C>A maps to NM_182961.2 E2222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:152771911 G>A maps to NM_182961.2 I1081I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:152589209 C>A maps to NM_182961.2 E6266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:152647663 G>A maps to NM_182961.2 G5020G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:152792773 G>A maps to NM_182961.2 Y530Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:152557333 T>C maps to NM_182961.2 Q6768Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:152718082 G>A maps to NM_182961.2 S2461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7290-01A-11D-2024-08 chr6:152783986 T>C maps to NM_182961.2 E712E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KK-01A-11D-A27K-08 chr6:152651647 C>T maps to NM_182961.2 A4724A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A72Z-01A-11D-A32B-08 chr6:152647525 G>A maps to NM_182961.2 T5066T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CX-01A-11D-A32B-08 chr6:152722322 A>G maps to NM_182961.2 L2327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:64596582 A>G maps to NM_182914.2 L4701L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:64469557 A>T maps to NM_182914.2 K1303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:64591873 C>A maps to NM_182914.2 T4500T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:64497762 T>C maps to NM_182914.2 D2303D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85D-01A-11D-A36O-08 chr14:64656883 A>T maps to NM_182914.2 A5989A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66F-01A-11D-A29Q-08 chr21:34038342 G>A maps to NM_003895.3 F724F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:34045775 G>A maps to NM_003895.3 R573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TS-01A-12D-A33T-08 chr21:34053877 T>A maps to NM_003895.3 S466S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:158516906 G>A maps to NM_003898.3 P1334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:158464355 C>T maps to NM_003898.3 Y240Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:70842479 G>T maps to NM_018373.2 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:99673043 G>A maps to ENST00000336292 A1492A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:99672812 C>T maps to ENST00000336292 H1415H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:99670343 G>A maps to ENST00000336292 P592P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:63466614 G>A maps to NM_001130003.1 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:35900586 A>G maps to NM_007247.4 S1087S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:35896176 G>T maps to NM_007247.4 A1190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:35900532 G>A maps to NM_007247.4 P1105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr12:33529815 A>G maps to NM_198992.3 S507S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:210273718 G>T maps to NM_001146261.1 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:46961978 C>T maps to NM_031912.3 T419T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:19195192 G>A maps to NM_016524.2 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WH-A86K-01A-11D-A36O-08 chr19:51132649 C>T maps to NM_001160329.1 R394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:114640390 T>C maps to ENST00000369545 A491A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A8XE-01A-11D-A36O-08 chr11:7439281 C>T maps to NM_175733.3 N420N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:27675608 T>C maps to NM_001193308.1 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A70Z-01A-12D-A33T-08 chr1:27675626 G>A maps to NM_001193308.1 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:85445198 C>T maps to NM_001162953.1 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:85422206 C>T maps to ENST00000359152 P1439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5319-01A-01D-1893-08 chr11:85420399 C>T maps to ENST00000359152 A1504A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:99941131 G>T did not map to a codon.
Sequencing variant TCGA-DU-8165-01A-11D-2253-08 chr23:99931047 C>A did not map to a codon.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr23:99956504 C>T did not map to a codon.
Sequencing variant TCGA-FG-A4MY-01A-11D-A26M-08 chr23:99931058 C>T did not map to a codon.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr23:99934380 C>A did not map to a codon.
Sequencing variant TCGA-HT-A4DV-01A-11D-A26M-08 chr23:37969645 C>T did not map to a codon.
Sequencing variant TCGA-DU-A7TI-01A-11D-A33T-08 chr11:64900458 A>C maps to NM_172230.2 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7J0-01A-11D-A34A-08 chr6:132938560 T>A maps to NM_001033080.1 K262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:132910360 G>T maps to NM_003967.2 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CV-01A-11D-A31L-08 chr6:132874646 G>A maps to NM_053278.1 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7856-01A-11D-2395-08 chr22:39814842 G>A maps to NM_006116.2 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4942-01A-01D-1468-08 chr6:149699802 C>A maps to NM_015093.4 S251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:30872593 T>C did not map to a codon.
Sequencing variant TCGA-P5-A72U-01A-31D-A32B-08 chr23:30873303 G>T did not map to a codon.
Sequencing variant TCGA-FG-A713-01A-11D-A32B-08 chr12:57409568 G>A maps to NM_013251.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85E-01A-11D-A36O-08 chr8:38646270 C>T maps to ENST00000379931 R71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6186-01A-12D-2024-08 chr10:123844063 C>T maps to NM_206862.2 P683P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:123846232 A>C maps to NM_206862.2 P1406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:123846832 C>T maps to NM_206862.2 C1606C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YE-01A-11D-A34A-08 chr10:123846262 C>T maps to NM_206862.2 F1416F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:1729692 C>A maps to NM_006342.1 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:71175704 G>A maps to NM_001057.2 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A75K-01A-11D-A32B-08 chr23:70607289 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:70627486 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:70627448 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:70586308 G>A did not map to a codon.
Sequencing variant TCGA-HT-7605-01A-11D-2086-08 chr23:70626501 G>T did not map to a codon.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr23:70618474 G>A did not map to a codon.
Sequencing variant TCGA-HT-7854-01A-11D-2253-08 chr23:70621405 G>T did not map to a codon.
Sequencing variant TCGA-HT-8012-01A-11D-2395-08 chr23:70679528 G>T did not map to a codon.
Sequencing variant TCGA-S9-A7QY-01A-11D-A34A-08 chr23:70612781 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:34172000 C>T maps to NM_139215.1 Y566Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8113-01A-11D-2395-08 chr16:84213254 G>A maps to NM_005679.2 A634A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:32630509 A>G maps to NM_153809.2 L1690L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6393-01A-11D-1705-08 chr9:32630689 A>G maps to NM_153809.2 L1630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YN-01A-11D-A34A-08 chr9:32632118 C>T maps to NM_153809.2 L1153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7691-01A-11D-2253-08 chr10:105145229 C>T maps to NM_006951.3 G604G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:229745873 G>A maps to NM_014409.3 R76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:229738319 G>A maps to NM_014409.3 D198D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:99710502 G>A maps to ENST00000472509 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6666-01A-11D-1893-08 chr23:100530267 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:100537367 A>G did not map to a codon.
Sequencing variant TCGA-S9-A6WG-01A-11D-A33T-08 chr5:68660799 A>G maps to NM_001015892.1 D255D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RS-01A-12D-A33T-08 chr5:68660799 A>G maps to NM_001015892.1 D255D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5390-01A-02D-1468-08 chr23:77394338 C>T did not map to a codon.
Sequencing variant TCGA-DH-A7UV-01A-12D-A34A-08 chr6:159457332 G>A maps to NM_054114.3 H574H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:111732373 C>T maps to NM_001008272.1 Y192Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:47689769 G>A maps to ENST00000371883 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:160055500 C>T maps to NM_033394.2 L1061L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:160027191 C>T maps to NM_033394.2 G409G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr2:160053204 T>C maps to NM_033394.2 T1022T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84J-01A-11D-A36O-08 chr17:61483615 C>T maps to ENST00000389520 T1115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr17:27849513 C>T maps to NM_020791.2 R709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:29998655 C>A maps to NM_016151.2 A1021A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YY-01A-11D-A34J-08 chr16:29994403 C>G maps to NM_016151.2 P337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:118636870 G>A maps to NM_016281.3 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7603-01A-21D-2086-08 chr12:118693345 T>C maps to NM_016281.3 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:32805575 G>T maps to ENST00000452392 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6410-01A-11D-1893-08 chr5:33445452 A>G maps to ENST00000455217 Q27Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A713-01A-11D-A32B-08 chr1:6639508 G>T maps to NM_138697.3 L797L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr1:19168268 G>A maps to NM_152232.2 F515F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5872-01A-11D-1705-08 chr1:19166819 G>T maps to NM_152232.2 S598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7882-01A-11D-2395-08 chr1:19181132 G>A maps to NM_152232.2 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:10978289 A>G maps to NM_023921.1 C193C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7875-01A-11D-2395-08 chr12:11061882 C>T maps to NM_023920.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7C3-01A-11D-A32B-08 chr12:11183916 G>A maps to NM_176885.2 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:141672739 G>T maps to NM_176817.4 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RN-01A-11D-A33T-08 chr7:143140841 G>A maps to NM_177437.1 Q99Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr12:10959420 G>A maps to NM_023918.1 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:10962215 C>T maps to NM_023917.2 W153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IX-01A-12D-A34A-08 chr12:10962395 A>G maps to NM_023917.2 N93N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:13514788 C>T did not map to a codon.
Sequencing variant TCGA-DU-6407-01A-13D-1705-08 chr16:71610261 G>A maps to NM_000353.2 D19D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:27831735 C>T maps to ENST00000409980 R384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153648574 G>A did not map to a codon.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr23:153640434 A>T did not map to a codon.
Sequencing variant TCGA-S9-A7QY-01A-11D-A34A-08 chr23:153641817 G>T did not map to a codon.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr4:38091701 C>T maps to NM_015173.2 L734L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:30688801 G>A maps to ENST00000403477 R370R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:67176495 G>A maps to NM_198517.2 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:96234513 T>C maps to NM_015188.1 T395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:7026799 C>T maps to NM_001113361.1 R609R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5270-01A-02D-1468-08 chr12:72315225 A>T maps to NM_022771.4 K616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:72278786 T>C maps to NM_022771.4 Y180Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:77921464 G>A maps to NM_019020.2 D569D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:50386139 C>A maps to NM_024682.2 I306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:26640403 A>G maps to NM_018317.2 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8320-01A-11D-2395-08 chr4:26640407 C>T maps to NM_018317.2 Q129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CV-01A-11D-A31L-08 chr9:100963793 C>A maps to NM_018421.3 R808R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6407-01A-13D-1705-08 chr15:74178444 C>T maps to NM_153356.1 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr3:99979909 C>T maps to ENST00000394144 D16D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:100015050 G>T maps to ENST00000394144 E270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr23:48418190 C>T did not map to a codon.
Sequencing variant TCGA-DU-7006-01A-11D-2024-08 chr23:48418953 C>G did not map to a codon.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr23:48418055 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:78317660 C>T maps to NM_144572.1 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KM-01A-11D-A27K-08 chr17:34499226 G>A maps to NM_001001417.5 R162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:75898491 G>T maps to ENST00000431480 S693S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7605-01A-11D-2086-08 chr13:75861014 G>A maps to ENST00000431480 P1271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:101648804 C>A maps to NM_001102426.1 E606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:101654023 C>T maps to NM_001102426.1 Q459Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr23:106109196 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:106108806 G>T did not map to a codon.
Sequencing variant TCGA-DU-A5TP-01A-11D-A289-08 chr23:106083909 T>C did not map to a codon.
Sequencing variant TCGA-HT-8018-01A-11D-2395-08 chr23:106061969 C>G did not map to a codon.
Sequencing variant TCGA-S9-A6WI-01A-21D-A33T-08 chr23:106082570 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:77004140 C>A maps to NM_004607.2 E29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84B-01A-11D-A36O-08 chr1:235543459 G>C maps to NM_003193.3 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:176752028 C>A maps to NM_024665.4 G403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr24:6911097 C>T did not map to a codon.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr6:170871042 G>A maps to NM_003194.4 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7881-01A-11D-2395-08 chr6:170871093 G>A maps to NM_003194.4 Q90Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8106-01A-11D-2395-08 chr6:170871039 A>G maps to NM_003194.4 Q72Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A618-01A-11D-A29Q-08 chr6:170871039 A>G maps to NM_003194.4 Q72Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A618-01A-11D-A29Q-08 chr6:170871045 A>G maps to NM_003194.4 Q74Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7J0-01A-11D-A34A-08 chr6:170871042 G>A maps to NM_003194.4 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RV-01A-21D-A34A-08 chr6:170871042 G>A maps to NM_003194.4 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A6MK-01A-11D-A32B-08 chr2:162275515 C>T maps to NM_006593.2 F361F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5143-01A-01D-1468-08 chr7:45148518 C>T maps to ENST00000404564 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:19751789 C>T maps to NM_080647.1 Q209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:19752590 C>T maps to NM_080647.1 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6396-01A-11D-1705-08 chr22:19751680 C>T maps to NM_080647.1 Y172Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7473-01A-11D-2024-08 chr6:85448224 A>T maps to NM_001080508.1 I363I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IX-01A-12D-A34A-08 chr1:168282170 G>A maps to NM_005149.2 S426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr7:35280565 C>T maps to NM_001077653.2 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5276-01A-01D-1468-08 chr23:79279562 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:79282314 T>G did not map to a codon.
Sequencing variant TCGA-WY-A85C-01A-11D-A36O-08 chr23:79286145 G>A did not map to a codon.
Sequencing variant TCGA-E1-A7YH-01A-11D-A34A-08 chr17:59560651 T>C maps to ENST00000393853 F472F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U5-01A-12D-A33T-08 chr17:59560288 C>T maps to ENST00000393853 C351C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6396-01A-11D-1705-08 chr12:114793417 G>A maps to NM_000192.3 G492G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8107-01A-13D-2395-08 chr19:3600464 A>C maps to NM_201636.2 G56G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:139661746 G>T maps to NM_001166253.1 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8186-01A-11D-2253-08 chr7:139529239 G>A maps to NM_001166253.1 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A75M-01A-11D-A32B-08 chr23:102885052 A>G did not map to a codon.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr23:102864216 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:101396114 C>A did not map to a codon.
Sequencing variant TCGA-FG-6690-01A-11D-1893-08 chr23:101395951 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:13681172 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:13680767 T>C did not map to a codon.
Sequencing variant TCGA-HT-7601-01A-11D-2086-08 chr8:74858990 C>T maps to NM_005648.2 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5273-01A-01D-1468-08 chr18:44561500 C>T maps to NM_016427.2 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:44559559 G>A maps to NM_016427.2 G692G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:44560996 G>A maps to NM_016427.2 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8185-01A-11D-2253-08 chr18:44561110 T>G maps to NM_016427.2 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CW-01A-11D-A32B-08 chr18:44560213 G>A maps to NM_016427.2 Y474Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EZ-01A-11D-A27K-08 chr18:44549185 C>T maps to NM_145653.3 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr15:57543546 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:31129329 G>A maps to NM_007109.2 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:42610432 C>T maps to NM_005650.1 Q293Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:134210780 C>T maps to NM_003206.3 N82N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr2:85531437 C>T maps to NM_031283.2 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:152082938 G>A maps to NM_007113.2 R918R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:152085220 G>A maps to NM_007113.2 Q158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:152080721 G>A maps to NM_007113.2 R1657R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:152059176 G>A maps to NM_001008536.1 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5ET-01A-11D-A27K-08 chr11:67816586 G>T maps to NM_006019.3 L571L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76K-01A-11D-A33T-08 chr11:59620691 G>A maps to NM_001062.3 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr11:59623423 G>A maps to NM_001062.3 N285N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:149759186 G>T maps to ENST00000451292 G917G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5962-01B-11D-1893-08 chr5:149755649 A>G maps to ENST00000451292 K633K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U9-01A-11D-A32B-08 chr6:167796319 G>A maps to NM_004610.3 D14D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7J2-01A-11D-A34A-08 chr6:167796319 G>A maps to NM_004610.3 D14D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CH-01A-12D-A36O-08 chr6:167585685 G>A maps to NM_001145121.1 E18E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:35089994 G>T maps to NM_001093728.1 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6186-01A-12D-2024-08 chr6:170144256 C>T maps to NM_174910.1 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:196043049 G>A maps to NM_152773.3 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:124179473 T>C maps to NM_024809.3 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:124171498 T>C maps to NM_024809.3 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A4DS-01A-11D-A26M-08 chr12:104374740 G>T did not map to a codon.
Sequencing variant TCGA-DB-A4XE-01A-11D-A27K-08 chr14:90455298 C>T maps to NM_018319.3 V394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6IZ-01A-11D-A31L-08 chr14:90509459 G>A maps to NM_018319.3 T600T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A87N-01A-11D-A36O-08 chr10:115964539 T>C maps to NM_198795.1 C395C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:61083898 T>C maps to NM_001146070.1 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:46657578 C>T maps to NM_001010870.2 R572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr6:46655894 G>A maps to NM_001010870.2 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr6:46656281 C>T maps to NM_001010870.2 C139C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:100193222 C>T maps to NM_014290.2 C72C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R3-01A-11D-A34J-08 chr9:100190780 C>T maps to NM_014290.2 R12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:151752493 G>A maps to NM_001083965.1 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64Q-01A-11D-A29Q-08 chr11:12901385 G>A maps to NM_021961.5 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:12923602 C>A maps to NM_021961.5 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:12904599 C>T maps to NM_021961.5 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:12904596 T>C maps to NM_021961.5 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7882-01A-11D-2395-08 chr6:35445109 C>T maps to ENST00000357281 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7478-01A-11D-2024-08 chr12:3129911 C>T maps to NM_003213.3 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:97874289 C>T maps to ENST00000379795 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:102912196 C>A maps to NM_014844.3 L996L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6IZ-01A-11D-A31L-08 chr4:65274898 C>T maps to NM_001010874.4 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:120980053 C>T maps to NM_005422.2 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:121033014 C>A maps to NM_005422.2 A1736A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:121032924 G>A maps to NM_005422.2 G1706G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RQ-01A-11D-A33T-08 chr10:114057886 C>T maps to NM_058222.1 F244F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr22:41783619 A>G maps to ENST00000417325 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8011-01A-11D-2395-08 chr22:41791867 C>T maps to ENST00000417325 N277N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YJ-01A-11D-A34A-08 chr9:27169601 G>A maps to NM_000459.3 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TG-01A-21D-A34J-08 chr17:6704169 C>T maps to NM_053285.1 T315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:53448968 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:20850091 G>A maps to NM_007110.4 C1468C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:20854313 G>A maps to NM_007110.4 L968L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R5-01A-11D-A289-08 chr5:1264586 G>A maps to NM_198253.2 H925H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YH-01A-11D-A34A-08 chr10:70332827 C>T maps to NM_030625.2 Q245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7636-01A-11D-2086-08 chr10:70451204 C>T maps to NM_030625.2 H2015H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84O-01A-11D-A36O-08 chr4:106157154 A>T maps to ENST00000513237 R707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:74274916 C>T maps to ENST00000409262 R532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:74275218 C>T maps to ENST00000409262 P632P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5319-01A-01D-1893-08 chr2:74300736 C>T maps to ENST00000409262 V759V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7309-01A-11D-2086-08 chr23:70073156 C>A did not map to a codon.
Sequencing variant TCGA-DU-A7TI-01A-11D-A33T-08 chr23:69871333 G>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:104465050 C>T did not map to a codon.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr23:104464685 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:107225147 G>A did not map to a codon.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr8:30694847 T>G maps to NM_031271.3 I2601I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:30701742 G>A maps to NM_031271.3 Y1597Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:62270985 T>C maps to NM_018469.3 R703R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A733-01A-11D-A32B-08 chr3:133495948 G>A maps to NM_001063.3 S643S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XC-01A-11D-A26M-08 chr6:50811002 C>G maps to ENST00000263046 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TS-01A-12D-A33T-08 chr6:50810825 G>T maps to ENST00000263046 T377T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65X-01A-11D-A32B-08 chr20:55211766 C>T maps to NM_003222.3 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:50719022 T>C maps to NM_172238.3 H375H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6396-01A-11D-1705-08 chr6:50683277 G>T maps to NM_172238.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A73M-01A-11D-A32B-08 chr6:50740355 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:4322671 C>A maps to NM_003223.2 G26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:121995413 C>T maps to NM_014553.2 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7609-01A-11D-2086-08 chr2:121991691 G>A maps to NM_014553.2 D391D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8012-01A-11D-2395-08 chr2:122005805 G>A maps to NM_014553.2 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:114290929 C>T maps to NM_007111.4 C307C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5280-01A-01D-1468-08 chr23:132351779 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:132351435 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:132351786 G>T did not map to a codon.
Sequencing variant TCGA-DU-6403-01A-11D-1705-08 chr23:132351925 G>A did not map to a codon.
Sequencing variant TCGA-DU-7300-01A-21D-2086-08 chr23:48887869 G>T did not map to a codon.
Sequencing variant TCGA-DU-8163-01A-11D-2253-08 chr6:41658429 G>A maps to ENST00000343317 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr7:115590970 G>A maps to NM_012252.2 R158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:100455465 C>T maps to NM_001007565.2 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:100432640 C>T maps to NM_001007565.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:100447623 C>T maps to NM_001007565.2 R113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:26895171 G>A maps to NM_012143.2 D409D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5962-01B-11D-1893-08 chr2:188332561 G>A maps to NM_006287.4 C242C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5270-01A-02D-1468-08 chr7:100229561 G>A maps to NM_003227.3 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:100238478 G>A maps to NM_003227.3 Y101Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:100228539 G>A maps to NM_003227.3 F414F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:133935688 C>T maps to NM_003235.4 D1545D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:133900547 C>T maps to NM_003235.4 V832V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr8:133912510 G>A maps to NM_003235.4 S1120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:101894963 G>T maps to NM_004612.2 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:105924278 G>A maps to NM_004257.4 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:105889456 G>A maps to NM_004257.4 H609H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr23:89177200 T>A did not map to a codon.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr23:89177101 C>T did not map to a codon.
Sequencing variant TCGA-RY-A847-01A-11D-A36O-08 chr24:3447661 C>T did not map to a codon.
Sequencing variant TCGA-E1-A7YS-01A-11D-A34A-08 chr20:36768009 G>A maps to NM_004613.2 G382G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:44951681 G>A maps to NM_003241.3 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7902-01A-12D-2395-08 chr15:43545092 C>T maps to NM_201631.3 W242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:2411125 G>A maps to NM_198994.2 K571K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:2413264 C>T maps to NM_198994.2 I699I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6XC-01A-12D-A32B-08 chr20:2375140 C>T maps to NM_198994.2 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8110-01A-11D-2395-08 chr15:43574757 G>A maps to NM_052955.2 N355N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WD-01A-12D-A33T-08 chr2:85554632 C>T maps to ENST00000409015 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RM-01A-11D-A33T-08 chr2:85554506 C>T maps to ENST00000409015 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A77W-01A-11D-A32B-08 chr8:56699383 A>T maps to NM_024831.6 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:57568586 C>T maps to NM_198976.1 D485D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:43800056 G>A maps to ENST00000330266 R602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4X9-01A-11D-A26M-08 chr16:67876786 G>A maps to NM_020457.2 Q110Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:108205180 A>G maps to NM_001130475.1 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:76452330 T>C maps to NM_144721.4 D192D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5393-01A-01D-1468-08 chr15:39883402 A>G maps to NM_003246.2 P755P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5870-01A-11D-1705-08 chr15:39882076 G>A maps to NM_003246.2 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:39874934 C>T maps to NM_003246.2 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr15:39884879 C>T maps to NM_003246.2 Q882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:169641931 C>T maps to NM_003247.2 E272E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CZ-01A-11D-A32B-08 chr6:169634880 G>A maps to NM_003247.2 C533C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YW-01A-11D-A34J-08 chr5:79355294 A>C maps to NM_003248.4 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CX-01A-11D-A32B-08 chr1:151823572 C>T maps to NM_182578.3 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6394-01A-11D-1705-08 chr6:128135073 G>A maps to NM_001164685.1 R238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EZ-7264-01A-11D-2024-08 chr6:128134186 T>C maps to NM_001164685.1 E533E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66D-01A-11D-A31L-08 chr23:122755190 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:122837342 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:122757748 A>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:122765687 C>T did not map to a codon.
Sequencing variant TCGA-DU-7006-01A-11D-2024-08 chr23:122747328 G>C did not map to a codon.
Sequencing variant TCGA-FN-7833-01A-11D-2086-08 chr23:122758004 C>T did not map to a codon.
Sequencing variant TCGA-R8-A73M-01A-11D-A32B-08 chr23:122757970 A>G did not map to a codon.
Sequencing variant TCGA-TQ-A7RM-01A-11D-A33T-08 chr16:3075923 G>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:36752439 G>A maps to NM_005119.3 E203E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:36769413 C>T maps to NM_005119.3 G888G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:24164437 G>A maps to NM_001128177.1 H441H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TS-01A-12D-A33T-08 chr11:77775097 C>T maps to NM_003251.2 Y57Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A618-01A-11D-A29Q-08 chr15:72040863 G>A maps to NM_024817.2 P782P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8321-01A-11D-2395-08 chr15:71535119 C>T maps to NM_024817.2 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:11676124 C>T maps to ENST00000423059 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:138400109 G>A maps to ENST00000272643 R1287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:138376001 T>C maps to ENST00000272643 G1205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:137814101 C>T maps to ENST00000272643 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-8125-01A-11D-2253-08 chr2:137814592 G>A maps to ENST00000272643 W248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:70454955 T>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:155451106 C>T maps to ENST00000456144 Y250Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:155451208 C>T maps to ENST00000456144 G284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:43770804 G>A maps to NM_005424.2 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:43777686 G>A maps to NM_005424.2 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr1:43779638 G>A maps to NM_005424.2 S803S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7487-01A-11D-2024-08 chr5:134785347 C>T maps to NM_001099221.1 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:153691370 G>A maps to NM_145720.2 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7T6-01A-11D-A33T-08 chr4:153691334 C>T maps to NM_145720.2 E274E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8165-01A-11D-2253-08 chr5:149375644 G>T maps to NM_030953.2 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7608-01A-11D-2086-08 chr3:114026860 A>G maps to ENST00000481065 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KM-01A-11D-A27K-08 chr3:114014404 C>G maps to ENST00000481065 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7689-01A-11D-2253-08 chr5:156378736 G>A maps to NM_138379.2 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:56826251 G>A maps to NM_003920.3 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U1-01A-21D-A33T-08 chr12:56815191 C>T maps to NM_003920.3 V937V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:57296338 C>A maps to NM_012456.2 E42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:4393217 C>T maps to NM_016069.8 Q26Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A8XE-01A-11D-A36O-08 chr23:47442889 T>A did not map to a codon.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr17:76851868 C>T maps to NM_003255.4 K181K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr6:54173455 T>C maps to NM_014464.3 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:54214694 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:54208055 G>A maps to NM_014464.3 E219E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8106-01A-11D-2395-08 chr6:54254704 G>A maps to NM_014464.3 T471T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:30024970 G>A maps to NM_003257.3 G595G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8163-01A-11D-2253-08 chr15:30001003 G>A maps to NM_003257.3 R1537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr15:30003071 C>T maps to NM_003257.3 A1445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:71869244 C>T maps to NM_004817.3 R1176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R8-01A-11D-A34J-08 chr9:71861645 C>T maps to NM_004817.3 G869G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:53262327 A>G maps to ENST00000423516 Y489Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8013-01A-11D-2395-08 chr3:53276167 C>T maps to ENST00000423516 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R8-01A-11D-A34J-08 chr3:53264613 C>T maps to ENST00000423516 G330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YY-01A-11D-A34J-08 chr4:164393860 C>A maps to NM_032136.4 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KT-A7W1-01A-11D-A34A-08 chr4:164394264 C>A maps to NM_032136.4 E208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:3013774 G>A maps to NM_003260.4 C255C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6670-01A-11D-1893-08 chr15:70366871 C>T maps to NM_005078.2 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:70350627 G>A maps to NM_005078.2 N307N. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-E1-A7YV-01A-11D-A34J-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:166963177 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:166964540 C>T maps to ENST00000507499 Y498Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IZ-01A-11D-A34A-08 chr4:166924713 C>A maps to ENST00000507499 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:98165091 C>A did not map to a codon.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr10:98129890 G>A maps to NM_012465.3 Y948Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RO-01A-11D-A33T-08 chr9:35720835 G>A maps to NM_006289.3 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:63055878 C>T maps to NM_015059.2 D1693D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:63017290 T>C maps to NM_015059.2 L1081L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:62939550 C>T maps to NM_015059.2 N14N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7309-01A-11D-2086-08 chr15:63127958 T>C maps to NM_015059.2 A2384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr15:63032968 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:38799507 C>T maps to NM_003263.3 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7469-01A-11D-2253-08 chr4:38799738 C>T maps to NM_003263.3 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7486-01A-11D-2024-08 chr4:38799738 C>T maps to NM_003263.3 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:154625597 G>A maps to NM_003264.3 T513T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:187004231 C>A maps to NM_003265.2 S464S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WL-01A-21D-A33T-08 chr4:187004789 G>A maps to NM_003265.2 T650T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7013-01A-11D-2024-08 chr9:120475557 C>A maps to NM_138554.3 G384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8182-01A-11D-2253-08 chr9:120475608 A>G maps to NM_138554.3 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:223285839 G>T maps to NM_003268.5 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VW-A7QS-01A-12D-A33T-08 chr1:223285749 C>T maps to NM_003268.5 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr23:12906719 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:12904192 G>A did not map to a codon.
Sequencing variant TCGA-DU-7294-01A-11D-2024-08 chr23:12904192 G>C did not map to a codon.
Sequencing variant TCGA-E1-A7YQ-01A-11D-A34J-08 chr23:12905053 G>C did not map to a codon.
Sequencing variant TCGA-P5-A733-01A-11D-A32B-08 chr23:12904512 C>T did not map to a codon.
Sequencing variant TCGA-S9-A7QY-01A-11D-A34A-08 chr23:12905354 T>C did not map to a codon.
Sequencing variant TCGA-TM-A84T-01A-11D-A36O-08 chr23:12905883 G>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:12937545 G>A did not map to a codon.
Sequencing variant TCGA-DU-8165-01A-11D-2253-08 chr23:12938643 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:62190777 C>T maps to ENST00000371180 W67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:64880800 C>A maps to NM_003273.2 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YL-01A-11D-A34A-08 chr8:105367370 G>A maps to NM_030788.2 P432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:100193920 G>A maps to NM_004800.1 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8161-01A-11D-2253-08 chr20:30723917 A>G maps to NM_014742.3 E57E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WG-01A-11D-A33T-08 chr9:75355080 G>T maps to NM_138691.2 G137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:2592910 C>T maps to NM_080751.2 N556N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:2592934 G>A maps to NM_080751.2 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A731-01A-11D-A32B-08 chr15:81627191 T>C maps to ENST00000454937 S779S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7641-01B-11D-2253-08 chr17:76109645 C>T maps to NM_007267.6 E779E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7471-01A-11D-2253-08 chr17:76130032 G>A maps to NM_152468.4 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:129389444 A>G maps to NM_001017395.3 S413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:129389912 G>A maps to NM_001017395.3 D257D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr3:129389498 T>C maps to NM_001017395.3 E395E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:205240996 G>A maps to NM_014858.3 Q625Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr12:94975588 G>A maps to NM_020698.2 N268N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:94976227 C>T maps to NM_020698.2 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:114149982 G>A maps to NM_017905.4 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:20097880 C>A maps to NM_181719.4 G92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7298-01A-11D-2024-08 chr1:20073704 C>T maps to NM_181719.4 K188K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YD-01A-11D-A34A-08 chr1:20072023 C>T did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr5:140021556 G>A maps to ENST00000252100 E139E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:42090508 C>T maps to NM_032376.2 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:44781980 A>G maps to NM_032256.1 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:108985994 C>T maps to NM_181724.2 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:98375499 G>A maps to NM_015348.1 L1741L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7294-01A-11D-2024-08 chr2:98377069 G>A maps to NM_015348.1 S1698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr2:98388788 C>T maps to NM_015348.1 K1473K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RK-01A-11D-A33T-08 chr2:98409856 C>G did not map to a codon.
Sequencing variant TCGA-DB-5281-01A-01D-1468-08 chr11:60703700 A>T maps to NM_017870.3 A799A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:126128632 C>T maps to NM_052907.2 N478N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:130185166 G>A maps to NM_133448.2 H52H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr12:130185195 G>A maps to NM_133448.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76L-01A-11D-A32B-08 chr12:130184842 G>A maps to NM_133448.2 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr12:129566504 G>A maps to NM_133448.2 H574H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KT-A7W1-01A-11D-A34A-08 chr12:130184802 G>A maps to NM_133448.2 R174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:48848499 G>A maps to NM_018273.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KT-A7W1-01A-11D-A34A-08 chr19:48863391 C>T maps to NM_018273.2 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:5778488 C>T maps to NM_152784.3 I733I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:5754219 G>A maps to NM_152784.3 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:5778416 C>A maps to NM_152784.3 I709I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A87Q-01A-11D-A36O-08 chr19:5772948 C>T maps to NM_152784.3 F638F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7694-01A-11D-2253-08 chr3:152058573 A>G maps to NM_001123228.1 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A736-01A-11D-A32B-08 chr3:152058330 T>C maps to NM_001123228.1 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:83406870 G>A maps to NM_001080506.1 Y181Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:122681479 G>T maps to NM_152399.2 S121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:19243997 C>T maps to NM_017814.1 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A615-01A-11D-A29Q-08 chr23:109416565 A>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:56290770 G>T maps to NM_018475.3 G287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65S-01A-11D-A29Q-08 chr2:62729686 T>C did not map to a codon.
Sequencing variant TCGA-CS-5395-01A-01D-1468-08 chr16:75481521 T>G maps to NM_145254.1 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A72U-01A-31D-A32B-08 chr5:72419283 C>T maps to NM_173490.6 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7294-01A-11D-2024-08 chr7:150500856 C>A maps to NM_018487.2 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6186-01A-12D-2024-08 chr10:104233396 C>T maps to NM_024789.3 Y332Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:103378808 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:38617603 G>A maps to NM_012264.4 Q366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:148555494 T>C maps to NM_018241.2 T409T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A75L-01A-11D-A32B-08 chr23:148690456 A>G did not map to a codon.
Sequencing variant TCGA-E1-A7YV-01A-11D-A34J-08 chr23:148690438 G>T did not map to a codon.
Sequencing variant TCGA-FG-A4MY-01A-11D-A26M-08 chr23:153247935 G>C did not map to a codon.
Sequencing variant TCGA-HT-7467-01A-11D-2024-08 chr20:48700713 T>C maps to NM_199203.2 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7638-01B-11D-2086-08 chr12:72091159 C>T maps to NM_018279.3 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:15599896 C>A did not map to a codon.
Sequencing variant TCGA-DH-A7UU-01A-12D-A34A-08 chr9:74347284 G>T maps to NM_013390.2 T515T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:74300190 G>A maps to NM_013390.2 D1358D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YN-01A-11D-A34A-08 chr1:9661230 C>A maps to NM_001130924.2 C225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr1:9661303 C>T maps to NM_001130924.2 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:1584371 C>T maps to NM_024600.4 C32C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A87Q-01A-11D-A36O-08 chr9:32784297 C>T maps to NM_212558.2 N39N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr11:61161356 T>G maps to NM_001173991.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R9-01A-11D-A289-08 chr11:61161356 T>G maps to NM_001173991.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F4-01A-11D-A289-08 chr11:61161356 T>G maps to NM_001173991.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:136574385 C>T maps to NM_025246.2 Q362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:123754809 G>T maps to NM_001013743.1 Y145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5397-01A-01D-1893-08 chr23:15682842 G>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:16791392 G>T did not map to a codon.
Sequencing variant TCGA-HW-8321-01A-11D-2395-08 chr3:12779641 T>G maps to ENST00000431022 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:185212549 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:34657421 G>T did not map to a codon.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr23:34648525 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:54266449 G>A maps to NM_018087.4 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr17:57842390 C>T maps to NM_030938.3 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:54518690 G>T maps to ENST00000371338 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:77423537 G>A maps to NM_032936.3 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:55452038 G>A maps to NM_182532.1 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr6:44116116 C>T maps to NM_018426.1 T372T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:77719719 G>A did not map to a codon.
Sequencing variant TCGA-HT-A61C-01A-11D-A29Q-08 chr8:94828613 C>T maps to NM_153704.5 I974I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8010-01A-11D-2395-08 chr8:56663636 G>A maps to ENST00000434581 H191H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr8:133764098 G>A maps to ENST00000395406 C82C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WD-01A-12D-A33T-08 chr10:45430278 C>G maps to NM_001123376.1 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7486-01A-11D-2024-08 chr15:34517775 C>G maps to NM_016454.2 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr11:18723159 G>A maps to NM_153347.1 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:426670 G>A maps to NM_021259.2 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:422016 G>A maps to NM_021259.2 N762N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7302-01A-11D-2086-08 chr16:427458 G>A maps to NM_021259.2 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:24523831 C>T maps to NM_024893.1 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:48356667 G>A maps to NM_153229.2 *160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7477-01B-11D-A289-08 chr17:48356659 G>A maps to NM_153229.2 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8011-01A-11D-2395-08 chr17:38991039 T>A maps to NM_001195386.1 L91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:154754130 G>A did not map to a codon.
Sequencing variant TCGA-TQ-A8XE-01A-11D-A36O-08 chr23:154736768 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:52060586 C>T maps to NM_014548.3 D85D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YM-01A-11D-A34A-08 chr15:52074949 A>G maps to NM_014548.3 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5277-01A-01D-1468-08 chr1:151146888 C>G maps to NM_013353.2 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85D-01A-11D-A36O-08 chr12:98927084 A>G maps to NM_003276.2 Q350Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:33135231 G>A maps to NM_001039770.2 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:33134501 G>A maps to NM_001039770.2 Q396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A710-01A-12D-A33T-08 chr4:69097009 C>T maps to NM_182502.3 Q199Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A89V-01A-11D-A36O-08 chr4:69344612 C>T maps to NM_014058.3 D338D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TZ-01A-21D-A32B-08 chr4:68938110 C>T maps to NM_207407.2 K148K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:19653380 G>A maps to NM_002772.2 L882L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6666-01A-11D-1893-08 chr21:42845268 G>A maps to NM_001135099.1 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:43808546 G>A maps to ENST00000380399 Y221Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:43795968 G>A maps to ENST00000380399 S485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:37499318 G>A maps to ENST00000381792 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7006-01A-11D-2024-08 chr22:37462867 G>A maps to ENST00000381792 Q772*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RC-01A-11D-A289-08 chr22:37471259 G>A maps to ENST00000381792 A419A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:111782477 C>T maps to ENST00000443106 C506C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:111766664 G>A maps to ENST00000443106 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:2405513 G>A maps to NM_182973.1 W237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A70Z-01A-12D-A33T-08 chr12:29904596 A>C did not map to a codon.
Sequencing variant TCGA-E1-A7YK-01A-11D-A34A-08 chr13:101257375 C>A maps to NM_032813.2 G719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8105-01A-11D-2395-08 chr13:101294548 C>T maps to NM_032813.2 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RP-01A-21D-A34A-08 chr7:150779521 C>T maps to NM_031434.3 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:42266536 C>T maps to NM_001076674.1 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:57505439 A>G maps to NM_015959.3 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr11:57480128 G>A maps to NM_015959.3 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:117840387 G>T maps to NM_002160.2 T836T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:117819615 G>A maps to NM_002160.2 F1465F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr9:117849481 G>A maps to NM_002160.2 C176C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U2-01A-21D-A33T-08 chr9:117826998 C>T maps to NM_002160.2 T1138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A61A-01A-11D-A29Q-08 chr6:138201286 C>T maps to NM_006290.2 C662C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A840-01A-11D-A36O-08 chr5:118728916 C>T maps to NM_014350.2 H146H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:22900720 G>A maps to NM_003842.4 D60D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:23003219 G>T maps to NM_003840.3 R233R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr18:60052047 C>T maps to NM_003839.2 G544G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A75K-01A-11D-A32B-08 chr8:119941084 T>A maps to NM_002546.3 K162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:119941091 G>T maps to NM_002546.3 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:119936678 C>T maps to NM_002546.3 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6393-01A-11D-1705-08 chr8:119945443 G>A maps to NM_002546.3 D42D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7493-01A-11D-2024-08 chr13:24234627 C>T maps to NM_018647.2 C245C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7475-01A-11D-2024-08 chr12:6438609 C>T maps to NM_001065.3 P412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:12248850 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:1148384 G>A maps to NM_003327.3 Y119Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:62329813 G>A maps to NM_003823.2 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:7460101 C>T maps to NM_172089.3 D127D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QZ-01A-12D-A34J-08 chr19:6665023 C>T maps to NM_003807.3 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7C3-01A-11D-A32B-08 chr19:6664983 G>A maps to NM_003807.3 R226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:170819284 G>A maps to NM_015028.2 S848S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:150444601 C>A maps to NM_006058.3 G19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XF-01A-11D-A27K-08 chr8:9609162 G>A maps to NM_003747.2 E959E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RB-01A-11D-A289-08 chr8:9588458 C>T maps to NM_003747.2 P687P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:57076179 C>A maps to NM_033396.2 R1335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:57077835 C>A maps to NM_033396.2 G783G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:93619381 C>T maps to NM_025235.3 D1086D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A843-01A-11D-A36O-08 chr10:93590771 G>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:99848937 A>G did not map to a codon.
Sequencing variant TCGA-DU-6542-01A-11D-1893-08 chr1:175046808 C>A maps to NM_022093.1 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7474-01A-11D-2024-08 chr1:175048763 C>T maps to NM_022093.1 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr1:201384345 G>A maps to ENST00000367312 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:72171522 C>T maps to NM_002270.3 R254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:128641246 C>T maps to ENST00000471166 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:175360538 G>A maps to NM_003285.2 S464S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:5399144 T>G maps to NM_001080495.2 R1573R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U8-01A-21D-A33T-08 chr7:5360234 G>C maps to NM_001080495.2 Y2188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5281-01A-01D-1468-08 chr16:24802980 A>C maps to NM_014494.2 S1006S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr16:24802266 T>C maps to NM_014494.2 D768D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7603-01A-21D-2086-08 chr16:24788378 C>T maps to NM_014494.2 Q97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F1-01A-11D-A289-08 chr16:24800570 C>G maps to NM_014494.2 S203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr17:76094487 G>T maps to NM_001142640.1 L1493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66B-01A-11D-A29Q-08 chr7:47407971 G>A maps to NM_022748.11 T757T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:38645060 G>A maps to NM_032865.5 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F1-01A-11D-A289-08 chr17:38645117 A>G maps to NM_032865.5 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IS-01A-11D-A34A-08 chr17:38635966 T>C maps to NM_032865.5 K623K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7C3-01A-11D-A32B-08 chr17:38645138 C>T maps to NM_032865.5 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:32063390 C>A maps to ENST00000375244 E747*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8321-01A-11D-2395-08 chr6:32018081 G>A maps to ENST00000375244 A3044A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:35726440 C>T maps to ENST00000451197 D298D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:52992098 G>T maps to NM_005486.2 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:17770234 G>A maps to NM_001082968.1 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:17751068 G>T maps to NM_001082968.1 A468A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:58869411 G>A maps to NM_207377.2 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:144400186 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:25686850 T>C maps to ENST00000264331 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr3:25675376 T>C maps to ENST00000264331 K327K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TA-01A-11D-A33T-08 chr3:25646357 G>C maps to ENST00000264331 S1461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RP-01A-21D-A34A-08 chr3:25670392 G>A maps to ENST00000264331 D617D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:18194248 G>A maps to NM_004618.3 I458I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7608-01A-11D-2086-08 chr22:22322989 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:132584874 G>A maps to ENST00000437532 N175N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:179887079 A>G maps to ENST00000398836 A487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4X9-01A-11D-A26M-08 chr1:179819994 G>A maps to NM_145034.4 R180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:132571243 G>A maps to NM_014506.1 K234K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:179057218 T>C maps to NM_022371.3 F271F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7C5-01A-11D-A32B-08 chr8:59750658 A>C maps to NM_014729.2 L302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4X9-01A-11D-A26M-08 chr17:7577142 C>T maps to NM_001126112.1 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XC-01A-11D-A26M-08 chr17:7579405 G>C maps to NM_001126112.1 S94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5140-01A-01D-1468-08 chr17:7574034 T>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:7579311 C>A maps to NM_001126112.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6395-01A-12D-1705-08 chr17:7579362 A>C maps to NM_001126112.1 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7007-01A-11D-2024-08 chr17:7579310 C>G did not map to a codon.
Sequencing variant TCGA-DU-7298-01A-11D-2024-08 chr17:7578176 C>T maps to NM_001126112.1 E224E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr17:7574033 C>G did not map to a codon.
Sequencing variant TCGA-E1-A7YD-01A-11D-A34A-08 chr17:7578523 G>A maps to NM_001126112.1 Q136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YI-01A-11D-A34A-08 chr17:7577021 G>A maps to NM_001126112.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6690-01A-11D-1893-08 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8182-01A-11D-2253-08 chr17:7579310 C>T did not map to a codon.
Sequencing variant TCGA-FG-8182-01A-11D-2253-08 chr17:7574011 C>A maps to NM_001126112.1 E339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr17:7577156 T>G did not map to a codon.
Sequencing variant TCGA-HT-7602-01A-21D-2086-08 chr17:7578491 C>T maps to NM_001126112.1 W146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7602-01A-21D-2086-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7604-01A-11D-2086-08 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8018-01A-11D-2395-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8106-01A-11D-2395-08 chr17:7577021 G>A maps to NM_001126112.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8114-01A-11D-2395-08 chr17:7578290 T>C did not map to a codon.
Sequencing variant TCGA-HT-A74J-01A-12D-A32B-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8319-01A-11D-2395-08 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F1-01A-11D-A289-08 chr17:7578491 C>T maps to NM_001126112.1 W146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A735-01A-11D-A32B-08 chr17:7579698 C>T did not map to a codon.
Sequencing variant TCGA-S9-A6WG-01A-11D-A33T-08 chr17:7576854 G>A maps to NM_001126112.1 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WO-01A-21D-A34A-08 chr17:7579414 C>T maps to NM_001126112.1 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QX-01A-11D-A34A-08 chr17:7577609 T>C did not map to a codon.
Sequencing variant TCGA-S9-A7R4-01A-12D-A34J-08 chr17:7579311 C>T maps to NM_001126112.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7CA-01A-21D-A33T-08 chr17:7574002 G>A maps to NM_001126112.1 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RJ-01A-11D-A33T-08 chr17:7577021 G>A maps to NM_001126112.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A8XE-01A-11D-A36O-08 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A858-01A-11D-A36O-08 chr17:7576896 G>A maps to NM_001126112.1 Q317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5397-01A-01D-1893-08 chr15:43714317 C>A maps to NM_001141980.1 E1279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:189587134 T>C maps to NM_003722.4 G384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U0-01A-12D-A32B-08 chr3:189586470 G>A maps to NM_003722.4 S365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5277-01A-01D-1468-08 chr6:83075655 G>A maps to NM_006670.4 P326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:68822720 C>T maps to NM_139075.3 D110D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:68855399 G>A maps to NM_139075.3 P746P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:125584089 G>A maps to NM_003287.2 E199E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WQ-01A-12D-A34A-08 chr20:62500709 C>T maps to NM_199360.1 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:144288548 G>A maps to NM_022445.3 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5849-01A-11D-1705-08 chr15:63354773 G>A did not map to a codon.
Sequencing variant TCGA-TQ-A7RU-01A-21D-A34A-08 chr19:16178535 C>T maps to NM_001145160.1 D34D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:1491743 C>T maps to NM_000547.5 G583G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:6640145 C>T maps to ENST00000453338 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:6640079 G>A maps to ENST00000453338 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:103268765 C>A maps to ENST00000376052 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:103287938 C>T maps to ENST00000376052 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr13:103287940 G>A maps to ENST00000376052 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7013-01A-11D-2024-08 chr5:665357 C>A maps to NM_007030.2 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:186329452 A>G maps to NM_003292.2 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A6S3-01A-12D-A32B-08 chr19:48305250 A>G maps to NM_198479.2 D339D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FN-7833-01A-11D-2086-08 chr16:1291160 C>T maps to ENST00000461509 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr16:1292147 C>T maps to ENST00000461509 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:65817503 G>T maps to NM_003596.3 E353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R8-01A-11D-A34J-08 chr7:65705882 T>A maps to NM_003596.3 C157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr22:26937281 G>A maps to NM_003595.3 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:10934118 A>G maps to NM_199261.2 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7475-01A-11D-2024-08 chr21:10970031 G>A maps to NM_199261.2 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7877-01A-11D-2395-08 chr21:10906910 G>A maps to NM_199261.2 S550S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WI-01A-21D-A33T-08 chr21:10942731 G>A maps to NM_199261.2 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WQ-01A-12D-A34A-08 chr21:10921984 T>C maps to NM_199261.2 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr20:30388771 G>C did not map to a codon.
Sequencing variant TCGA-TQ-A7RJ-01A-11D-A33T-08 chr20:30363724 C>T maps to ENST00000340513 Q222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:23545427 G>A maps to NM_013293.3 R259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6UB-01A-21D-A33T-08 chr3:185637271 T>A maps to NM_004593.2 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QW-01A-11D-A34A-08 chr22:50636344 C>T maps to NM_025204.2 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A61C-01A-11D-A29Q-08 chr9:139815578 C>T maps to ENST00000359662 Y402Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85D-01A-11D-A36O-08 chr6:111912848 C>T maps to ENST00000340026 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:27075048 C>A maps to NM_004295.3 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:36511762 C>T maps to NM_145803.1 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:36512080 G>A maps to NM_145803.1 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UR-01A-11D-A33T-08 chr16:2225553 C>T maps to NM_032271.2 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WI-01A-21D-A33T-08 chr3:49869464 C>T maps to NM_005879.2 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XF-01A-11D-A27K-08 chr3:36873435 A>G maps to NM_014831.2 D2502D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:36879870 G>A maps to NM_014831.2 L1793L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:36896951 G>A maps to NM_014831.2 L1377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8106-01A-11D-2395-08 chr3:36875228 A>G maps to NM_014831.2 L1905L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84R-01A-21D-A36O-08 chr21:45502894 G>A maps to NM_003274.4 T650T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:7747354 C>T maps to NM_001042461.1 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:7747555 C>T maps to NM_001042461.1 C139C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YN-01A-11D-A34A-08 chr8:141407832 C>T maps to NM_031466.5 A438A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6XC-01A-12D-A32B-08 chr3:108549620 C>T maps to NM_016388.2 R38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TC-01A-21D-A34J-08 chr10:17204165 T>A maps to NM_004412.5 R108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr6:123687318 G>A maps to NM_006073.2 R428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YI-01A-11D-A34A-08 chr6:41129256 C>T maps to NM_018965.2 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7694-01A-11D-2253-08 chr6:41165997 G>A maps to ENST00000373108 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:42224501 A>T maps to NM_033502.2 A848A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84L-01A-11D-A36O-08 chr6:42210984 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:152710593 G>A did not map to a codon.
Sequencing variant TCGA-DU-8163-01A-11D-2253-08 chr3:129695839 G>A maps to NM_007117.3 E170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5965-01B-11D-1893-08 chr3:129695935 C>T maps to NM_007117.3 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr12:72893327 C>T maps to NM_013381.2 D500D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:110131386 G>A maps to NM_003301.4 W300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R5-01A-11D-A289-08 chr8:110100139 C>G maps to NM_003301.4 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:126445614 G>A maps to NM_025195.2 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76O-01A-11D-A32B-08 chr1:228588829 T>A maps to NM_145214.2 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7489-01A-11D-2024-08 chr13:50586069 G>A did not map to a codon.
Sequencing variant TCGA-DU-A7TJ-01A-11D-A34J-08 chr6:30136148 C>T maps to NM_033229.2 R184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:15532147 G>A maps to NM_006470.3 F492F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr17:15532458 G>A maps to ENST00000455584 Q403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:228602719 G>T maps to NM_016102.3 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:5719630 G>A maps to NM_006074.4 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84Q-01A-11D-A36O-08 chr11:5719735 C>G maps to NM_006074.4 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85E-01A-11D-A36O-08 chr11:5729463 C>T maps to NM_006074.4 R279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:64887631 C>T maps to NM_001656.3 R563R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YS-01A-11D-A34A-08 chr7:138252323 C>T maps to NM_015905.2 N543N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A840-01A-11D-A36O-08 chr7:138263956 T>C maps to NM_015905.2 Y755Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A6S3-01A-12D-A32B-08 chr6:28872362 G>T maps to NM_006510.4 Y342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:59057240 G>A maps to NM_005762.2 K188K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:27151644 G>A maps to NM_171982.3 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7478-01A-11D-2024-08 chr8:27145294 C>T maps to NM_171982.3 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YD-01A-11D-A34A-08 chr5:114469803 A>G maps to NM_018700.3 V429V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:57093035 A>T maps to NM_015294.3 A837A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:140409859 C>T maps to NM_152616.4 F637F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:140419809 C>T maps to NM_152616.4 H722H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:140407029 C>T maps to NM_152616.4 D502D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr3:140401984 C>T maps to NM_152616.4 I341I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6542-01A-11D-1893-08 chr11:55035823 A>G did not map to a codon.
Sequencing variant TCGA-DH-A7UU-01A-12D-A34A-08 chr7:100732731 A>G maps to NM_030961.1 G713G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A89Z-01A-11D-A36O-08 chr7:100730604 C>T maps to NM_030961.1 H4H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr4:165962268 C>T maps to NM_152620.2 R349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:33646763 C>T maps to NM_018207.2 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5854-01A-11D-1705-08 chr15:45050859 T>C maps to NM_182985.3 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:45059498 C>T maps to NM_182985.3 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr3:32932669 C>T maps to NM_001039111.1 G658G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:104416969 G>A maps to NM_030912.2 P505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr14:51446209 T>C maps to ENST00000338969 R736R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64X-01A-11D-A29Q-08 chr4:189065195 G>A maps to NM_178556.3 E255E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:189060810 C>T maps to NM_178556.3 H33H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KT-A7W1-01A-11D-A34A-08 chr4:189068384 C>T maps to NM_178556.3 N422N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6X3-01A-21D-A32B-08 chr4:189060900 G>A maps to NM_178556.3 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:14462919 G>T maps to NM_007118.2 G1851G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A83Z-01A-11D-A36O-08 chr22:38121460 C>T maps to NM_001039141.2 G966G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7Z3-01A-11D-A34J-08 chr14:92466344 T>C maps to NM_004239.3 Q1555Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7610-01A-21D-2086-08 chr2:230668910 G>A maps to ENST00000389044 R868*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6290-01A-11D-1705-08 chr15:64716293 A>T maps to NM_016213.4 K475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7477-01B-11D-A289-08 chr7:100465833 G>A maps to NM_003302.2 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:40309782 G>A maps to ENST00000316891 R408R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YL-01A-11D-A34A-08 chr1:40315878 A>G maps to ENST00000316891 R205R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DU-6392-01A-11D-1705-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:100276144 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:100274324 C>A did not map to a codon.
Sequencing variant TCGA-E1-A7YH-01A-11D-A34A-08 chr23:100277043 A>G did not map to a codon.
Sequencing variant TCGA-E1-A7YS-01A-11D-A34A-08 chr23:100278579 G>A did not map to a codon.
Sequencing variant TCGA-TQ-A8XE-01A-11D-A36O-08 chr23:100275474 C>A did not map to a codon.
Sequencing variant TCGA-R8-A6MO-01A-11D-A33T-08 chr20:5927166 G>A maps to NM_015939.3 F47F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:103996557 G>A maps to ENST00000299201 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:29084148 A>G maps to NM_017910.3 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A780-01A-12D-A32B-08 chr2:29074042 C>A maps to NM_017910.3 G403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64W-01A-11D-A29Q-08 chr23:54957390 A>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:54955238 C>T did not map to a codon.
Sequencing variant TCGA-DU-6396-01A-11D-1705-08 chr23:54955788 G>A did not map to a codon.
Sequencing variant TCGA-DU-6404-01A-11D-1705-08 chr23:54953050 C>T did not map to a codon.
Sequencing variant TCGA-DU-7014-01A-11D-2024-08 chr23:54952876 G>A did not map to a codon.
Sequencing variant TCGA-DH-A7UU-01A-12D-A34A-08 chr8:72948520 A>G did not map to a codon.
Sequencing variant TCGA-HT-8111-01A-11D-2395-08 chr8:72969168 G>A maps to NM_007332.2 R393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85E-01A-11D-A36O-08 chr8:72970012 A>G maps to NM_007332.2 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IX-01A-12D-A34A-08 chr13:38225433 T>A maps to NM_003306.1 R683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:33637790 C>A maps to NM_015638.2 G179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:33632377 C>T maps to NM_015638.2 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:111195532 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:111195636 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:111090400 G>A did not map to a codon.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr23:111024434 C>T did not map to a codon.
Sequencing variant TCGA-S9-A6TS-01A-12D-A33T-08 chr23:111097326 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:101341916 G>A maps to NM_004621.5 N802N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7294-01A-11D-2024-08 chr11:101323745 A>G maps to NM_004621.5 L912L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85A-01A-21D-A36O-08 chr11:101375498 C>T maps to NM_004621.5 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:31318474 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:31295068 C>T maps to NM_002420.4 T1256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A70Z-01A-12D-A33T-08 chr21:45861582 C>T maps to ENST00000397932 H1515H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R9-01A-11D-A289-08 chr21:45774547 G>A maps to ENST00000397932 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:73426149 C>T maps to ENST00000419692 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YK-01A-11D-A34A-08 chr9:73235248 T>C maps to ENST00000419692 T578T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A87Q-01A-11D-A36O-08 chr11:2444188 G>A maps to ENST00000452833 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5142-01A-01D-1468-08 chr9:77435279 A>G maps to NM_017662.4 S358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr9:77435240 C>T maps to NM_017662.4 E371E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr9:77390826 G>A maps to NM_017662.4 H1125H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6XC-01A-12D-A32B-08 chr9:77415325 C>T maps to NM_017662.4 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:50950005 C>A maps to NM_017672.4 G32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76R-01A-11D-A32B-08 chr15:50905957 C>T maps to NM_017672.4 K572K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:234878919 C>T maps to NM_024080.4 F735F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U2-01A-21D-A33T-08 chr2:234905160 G>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:3493175 C>T maps to ENST00000399756 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A711-01A-21D-A33T-08 chr17:3470221 G>A maps to ENST00000399756 R814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84J-01A-11D-A36O-08 chr17:3491592 G>A maps to ENST00000399756 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66F-01A-11D-A29Q-08 chr17:16321162 C>T maps to NM_016113.4 R61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5849-01A-11D-1705-08 chr17:16336964 C>T maps to NM_016113.4 T689T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:16335328 C>T maps to NM_016113.4 G568G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr17:3458039 G>A maps to ENST00000381913 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:110224597 G>A maps to NM_021625.4 F751F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr12:110234443 G>A maps to NM_021625.4 F406F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6542-01A-11D-1893-08 chr7:142609710 G>A maps to NM_019841.4 I575I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YN-01A-11D-A34A-08 chr7:142606687 G>A maps to NM_019841.4 C621C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5854-01A-11D-1705-08 chr7:142573226 T>C maps to NM_018646.2 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:142569692 G>A maps to NM_018646.2 Q649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:98564773 C>T maps to ENST00000359863 N2422N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:98527691 G>T maps to ENST00000359863 G1086*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:98562282 C>T maps to ENST00000359863 S2280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:98515136 G>A maps to ENST00000359863 S819S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:98506446 G>A maps to ENST00000359863 K404K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TC-01A-21D-A34J-08 chr7:98575904 T>A maps to ENST00000359863 A2812A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7638-01B-11D-2086-08 chr7:98576478 C>T maps to ENST00000359863 C2855C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6J1-01A-11D-A31L-08 chr7:98547851 C>T maps to ENST00000359863 N1760N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:141952369 G>A maps to NM_001001317.2 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:2125815 G>A maps to NM_000548.3 P854P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:45008932 A>G maps to NM_183422.2 N1017N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:107018361 C>A did not map to a codon.
Sequencing variant TCGA-DU-5871-01A-12D-1705-08 chr7:100064707 C>A maps to NM_030935.3 R354R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7694-01A-11D-2253-08 chr7:100064671 G>T maps to NM_030935.3 R366R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U6-01A-12D-A33T-08 chr3:12544758 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:54695427 C>A maps to NM_001077446.2 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr11:18503251 G>A maps to NM_006292.2 N336N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TD-01A-12D-A34A-08 chr11:65726677 C>T maps to NM_152762.2 T480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:81422107 C>A maps to NM_000369.2 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8185-01A-11D-2253-08 chr18:72999932 G>A maps to NM_005786.4 T812T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A780-01A-12D-A32B-08 chr18:72999830 C>T maps to NM_005786.4 S778S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7Z2-01A-21D-A34J-08 chr19:31769600 G>A maps to NM_020856.2 Y366Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A870-01A-11D-A36O-08 chr19:31767581 A>G maps to NM_020856.2 T1039T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RW-01A-11D-A33T-08 chr19:31770236 A>G maps to NM_020856.2 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr19:50249905 G>A maps to NM_021733.1 N271N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr19:50265269 C>T maps to NM_021733.1 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QX-01A-11D-A34A-08 chr19:50243410 G>A maps to NM_021733.1 H509H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:143310940 C>A did not map to a codon.
Sequencing variant TCGA-DU-7006-01A-11D-2024-08 chr8:143427184 G>A maps to ENST00000445818 Q53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:67858678 C>T maps to ENST00000339830 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7602-01A-21D-2086-08 chr10:82264512 G>A maps to NM_030927.2 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr10:71258151 G>A maps to NM_012339.3 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6691-01A-11D-1893-08 chr19:11417341 G>A maps to NM_012466.2 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:176078861 C>T maps to NM_012171.2 C82C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:176084698 G>T maps to NM_012171.2 *333Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6405-01A-11D-1705-08 chr11:44948235 G>C maps to ENST00000425677 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A859-01A-12D-A36O-08 chr7:128804400 C>T maps to NM_178562.3 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:99887564 C>A did not map to a codon.
Sequencing variant TCGA-VM-A8C8-01A-11D-A36O-08 chr23:38546914 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:53114478 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:53117081 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:98289178 G>A maps to NM_033512.2 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr23:54470610 G>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:19118977 C>A maps to NM_053006.4 S22S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DU-6392-01A-11D-1705-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:19119139 C>T maps to NM_053006.4 Y76Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:19625987 G>A maps to NM_032037.2 N83N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr19:19625702 C>T maps to NM_032037.2 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:43251564 G>A maps to NM_032538.1 P1029P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:43223590 C>T maps to NM_032538.1 Y286Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-8125-01A-11D-2253-08 chr6:43251408 G>A maps to NM_032538.1 A977A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:43067671 C>A maps to ENST00000263802 V958V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:113233176 G>T maps to NM_017868.3 E557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:113211390 G>T maps to NM_017868.3 E278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr11:113233184 G>A maps to NM_017868.3 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:3428405 C>A maps to NM_016030.5 Y463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:3469441 C>T maps to NM_016030.5 S584S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:43423044 C>T maps to NM_018259.5 C423C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:166775890 G>T maps to NM_024753.3 P523P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CX-01A-11D-A32B-08 chr1:55251699 G>A maps to NM_001114108.1 R326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:99762036 G>A maps to NM_022905.4 C71C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A737-01A-11D-A32B-08 chr15:99678296 G>C maps to NM_022905.4 S421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:33012101 C>T maps to NM_017735.4 H628H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:38569869 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:38560896 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:46684452 G>A maps to NM_017931.2 Q350Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:46677494 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:47184093 G>A maps to ENST00000394850 E155E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:91155894 G>A maps to NM_001010854.1 Y313Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QZ-01A-12D-A34J-08 chr9:135251349 G>A maps to NM_007344.2 H890H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:80744845 C>T maps to NM_003318.4 R587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:43471559 G>A maps to NM_012263.4 I11I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:9870916 G>A maps to NM_001025930.3 Q607Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:219602860 T>C maps to NM_014640.4 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7C3-01A-11D-A32B-08 chr2:219602959 G>A maps to NM_014640.4 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5277-01A-01D-1468-08 chr14:76241855 A>G maps to NM_015072.4 A722A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TS-01A-12D-A33T-08 chr17:46846533 G>T maps to NM_001130918.1 L831L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4938-01B-11D-1893-08 chr1:84356050 T>C maps to NM_024686.4 L774L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:84417648 T>C maps to NM_024686.4 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A77W-01A-11D-A32B-08 chr22:50484309 G>A maps to NM_001080447.1 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CV-01A-11D-A31L-08 chr22:50480123 C>T maps to NM_001080447.1 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6186-01A-12D-2024-08 chr2:179453436 C>T maps to NM_133378.4 K18437K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6670-01A-11D-1893-08 chr2:179589233 C>T maps to NM_133378.4 P5712P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr2:179645980 C>T maps to NM_133378.4 V1130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5275-01A-01D-1468-08 chr2:179422825 A>G maps to NM_133378.4 L26517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:179427754 G>A maps to NM_133378.4 R25134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:179494084 G>A maps to NM_133378.4 Y12221Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:179587192 G>A maps to NM_133378.4 R6197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:179606115 G>T maps to NM_133437.3 R3777R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:179592327 C>T maps to NM_133378.4 T5415T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:179576704 T>C maps to NM_133378.4 G8040G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:179553505 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:179614544 T>C maps to ENST00000375038 Q4196Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:179398129 G>T maps to NM_133378.4 S31836S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:179414087 G>A maps to NM_133378.4 I28187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:179588274 G>A maps to NM_133378.4 N5940N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:179476841 G>A maps to NM_133378.4 R14198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:179500810 G>A maps to NM_133378.4 G11261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:179584371 G>T maps to NM_133378.4 P6705P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:179453592 T>C maps to NM_133378.4 K18385K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:179424590 A>G maps to NM_133378.4 I26188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:179446358 T>C maps to NM_133378.4 L19644L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:179435366 G>A maps to NM_133378.4 D22596D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:179429821 G>A maps to NM_133378.4 R24445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7014-01A-11D-2024-08 chr2:179579722 G>A maps to NM_133378.4 I7486I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr2:179495025 C>T maps to NM_133378.4 T12173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TB-01A-11D-A33T-08 chr2:179445325 C>T maps to NM_133378.4 E19692E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TC-01A-21D-A34J-08 chr2:179426429 A>T maps to NM_133378.4 S25575S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TJ-01A-11D-A34J-08 chr2:179453325 A>G maps to NM_133378.4 N18474N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5303-01A-01D-1468-08 chr2:179456088 G>A maps to NM_133378.4 T17553T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YJ-01A-11D-A34A-08 chr2:179500729 G>A maps to NM_133378.4 N11288N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YL-01A-11D-A34A-08 chr2:179591949 G>T maps to NM_133378.4 Y5470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr2:179396155 A>G maps to NM_133378.4 Y32494Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr2:179498030 C>T maps to NM_133378.4 K11755K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7468-01A-11D-2024-08 chr2:179434376 G>A maps to NM_133378.4 D22926D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7611-01A-11D-2395-08 chr2:179417787 G>A maps to NM_133378.4 R27379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7616-01A-11D-2253-08 chr2:179455635 C>T maps to NM_133378.4 P17704P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr2:179463963 G>A maps to NM_133378.4 G16284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr2:179431331 A>G maps to NM_133378.4 G23941G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr2:179577500 G>T maps to NM_133378.4 S7840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8563-01A-11D-2395-08 chr2:179413637 G>A maps to NM_133378.4 G28337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr2:179579893 G>A maps to NM_133378.4 H7429H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr2:179453925 A>G maps to NM_133378.4 Y18274Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A618-01A-11D-A29Q-08 chr2:179430062 A>T maps to NM_133378.4 A24364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr2:179456395 T>C maps to NM_133378.4 V17482V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7486-01A-11D-2024-08 chr2:179611496 T>C maps to ENST00000375038 P5212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EX-01A-12D-A289-08 chr2:179410160 A>G maps to NM_133378.4 S29324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CS-01A-11D-A31L-08 chr2:179477175 G>A maps to NM_133378.4 D14124D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A83Z-01A-11D-A36O-08 chr2:179437478 C>G maps to NM_133378.4 V21892V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TU-01A-12D-A32B-08 chr2:179466814 G>A maps to NM_133378.4 Q15827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WM-01A-12D-A33T-08 chr2:179650718 G>A maps to NM_133378.4 S742S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QW-01A-11D-A34A-08 chr2:179598482 G>A maps to NM_133378.4 D3967D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7C4-01A-11D-A32B-08 chr2:179474645 C>T maps to NM_133378.4 W14600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84F-01A-11D-A36O-08 chr2:179438183 C>T maps to NM_133378.4 P21657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RU-01A-21D-A34A-08 chr2:179569117 C>T maps to NM_133378.4 R8749R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VW-A8FI-01A-11D-A36O-08 chr2:179489453 G>A maps to NM_133378.4 P12283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7007-01A-11D-2024-08 chr17:72246148 C>T maps to NM_032646.5 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7479-01A-11D-2024-08 chr17:72233512 C>T maps to NM_032646.5 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7684-01A-11D-2253-08 chr17:72249348 G>A maps to NM_032646.5 Q463Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7473-01A-11D-2024-08 chr7:2696108 C>G maps to NM_025250.2 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5963-01A-11D-1705-08 chr12:49523048 A>G maps to NM_006082.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XE-01A-11D-A27K-08 chr13:19752463 C>T maps to NM_006001.1 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:19748044 C>A maps to NM_006001.1 V437V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5871-01A-12D-1705-08 chr2:220115526 A>G maps to NM_006000.1 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:30691216 C>T maps to NM_178014.2 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr20:57597952 C>T maps to NM_030773.3 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:140137260 C>T maps to NM_006088.5 D197D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7478-01A-11D-2024-08 chr9:140136261 G>A maps to NM_006088.5 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YD-01A-11D-A34A-08 chr16:90001620 C>T maps to ENST00000304984 A601A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YD-01A-11D-A34A-08 chr18:12311032 G>T maps to NM_032525.1 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr17:40766566 G>A maps to NM_001070.4 P350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7477-01B-11D-A289-08 chr13:113181322 A>C maps to NM_006322.4 V496V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84R-01A-21D-A36O-08 chr15:22861860 G>A maps to NM_052903.4 K627K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8166-01A-11D-2253-08 chr22:50659211 A>G maps to NM_020461.3 S1192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5311-01A-01D-1468-08 chr22:50658941 G>C maps to NM_020461.3 L1282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7636-01A-11D-2086-08 chr22:50659211 A>G maps to NM_020461.3 S1192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7854-01A-11D-2253-08 chr22:50659211 A>G maps to NM_020461.3 S1192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-7675-01A-11D-2086-08 chr22:50659211 A>G maps to NM_020461.3 S1192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64O-01A-11D-A29Q-08 chr6:35474050 C>T maps to NM_003322.3 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R7-01A-11D-A34J-08 chr6:35466202 C>T maps to NM_003322.3 A510A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:3039510 C>T maps to NM_001160408.1 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:3047392 C>T maps to NM_001160408.1 F379F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:158923089 C>T maps to NM_020245.3 Q799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:158850910 G>A maps to NM_020245.3 W175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7470-01A-12D-2086-08 chr6:158850781 G>A maps to NM_020245.3 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7477-01B-11D-A289-08 chr6:158923247 G>C maps to NM_020245.3 P851P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr6:158923247 G>C maps to NM_020245.3 P851P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RW-01A-11D-A33T-08 chr6:158870155 G>T maps to NM_020245.3 V224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6690-01A-11D-1893-08 chr7:19738082 G>A maps to NM_001002926.1 D291D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:48081961 A>C maps to NM_003328.2 Y380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6394-01A-11D-1705-08 chr4:48114403 A>G maps to NM_003328.2 N100N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A616-01A-11D-A29Q-08 chr22:36872904 T>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:11785170 C>T maps to ENST00000356957 K652K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QW-01A-11D-A34A-08 chr1:52507234 T>C maps to NM_015913.2 E44E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-5963-01A-11D-1705-08 chr14:52922040 C>T did not map to a codon.
Sequencing variant TCGA-WY-A85E-01A-11D-A36O-08 chr7:37889883 C>T maps to NM_016616.4 R6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UU-01A-12D-A34A-08 chr6:7888997 C>G maps to NM_030810.3 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:12695728 C>T maps to NM_000550.2 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:66548516 C>T maps to NM_018264.2 Q459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RS-01A-12D-A33T-08 chr7:66479412 T>C maps to NM_018264.2 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:72081662 G>A maps to NM_001145440.1 H593H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:72209576 G>A maps to NM_001145440.1 V322V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr7:72281139 G>A maps to NM_001145440.1 R117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:70960100 G>A maps to NM_018003.2 L974L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:70969449 G>A maps to NM_018003.2 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr15:70991906 C>T maps to NM_018003.2 K57K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U1-01A-21D-A33T-08 chr15:70961405 G>A maps to NM_018003.2 T539T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7475-01A-11D-2024-08 chr1:162557441 C>T maps to ENST00000367925 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7603-01A-21D-2086-08 chr19:34929584 G>A maps to NM_005499.2 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:69120749 G>A maps to NM_003968.3 Q95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:68543397 G>A maps to NM_018227.5 Y132Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:49847822 G>A maps to NM_003335.2 G502G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:49850777 G>A maps to NM_003335.2 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:49849916 T>A maps to NM_003335.2 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:49847551 G>A maps to NM_003335.2 G566G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:33926986 C>T maps to NM_018449.2 P821P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A780-01A-12D-A32B-08 chr9:33933501 G>A maps to NM_018449.2 L698L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64V-01A-11D-A29Q-08 chr21:43833167 G>A maps to NM_018961.2 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:43829701 C>T maps to NM_018961.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8185-01A-11D-2253-08 chr17:16285490 C>T maps to NM_018955.2 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F4-01A-11D-A289-08 chr17:16285559 T>C maps to NM_018955.2 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A83X-01A-11D-A36O-08 chr12:125397210 G>A maps to NM_021009.5 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TV-01A-12D-A34J-08 chr12:125397651 T>C maps to NM_021009.5 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WN-01A-12D-A33T-08 chr12:125397662 A>G maps to NM_021009.5 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MT-01A-11D-A26M-08 chr6:29523935 G>T maps to NM_006398.3 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7294-01A-11D-2024-08 chr5:133725923 G>T maps to NM_003337.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:23848870 C>T maps to NM_003341.3 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84J-01A-11D-A36O-08 chr2:238925256 C>T maps to NM_080678.1 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:129474839 G>A maps to NM_003344.2 D163D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76K-01A-11D-A33T-08 chr7:129474884 G>A maps to NM_003344.2 Y148Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YM-01A-11D-A34A-08 chr6:90039673 G>A maps to NM_016021.2 Y227Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:1192380 C>T maps to NM_194315.1 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:57322033 C>T maps to NM_004223.3 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YV-01A-11D-A34J-08 chr23:142967237 C>A did not map to a codon.
Sequencing variant TCGA-TQ-A7RK-01A-11D-A33T-08 chr23:142967508 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:74394561 G>A maps to NM_022066.3 D629D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:74392625 G>A maps to NM_022066.3 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:25601966 A>G maps to NM_000462.2 T613T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:25616696 G>T maps to NM_000462.2 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:156994432 C>A maps to NM_014671.2 A450A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7019-01A-11D-2024-08 chr11:118239406 C>T maps to NM_004788.2 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:10195194 G>A maps to NM_001105562.2 T725T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:23570942 G>A maps to ENST00000219638 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:11333833 G>A maps to NM_013319.2 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:153714146 G>A did not map to a codon.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr15:74751067 A>G maps to NM_201265.1 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr16:4927425 G>A maps to NM_016936.3 A1102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:33453087 G>T maps to NM_001128161.1 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:86297962 A>G maps to NM_013438.4 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:56590892 C>T did not map to a codon.
Sequencing variant TCGA-HW-A5KL-01A-11D-A27K-08 chr23:56590704 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:5537068 C>T maps to NM_145053.4 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U6-01A-12D-A33T-08 chr6:42620361 G>A maps to NM_015255.2 W916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84R-01A-21D-A36O-08 chr2:170863699 A>G maps to ENST00000442603 P1410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:19403374 C>A maps to ENST00000375267 E5137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:19415396 G>T maps to ENST00000375267 T4762T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:19464553 G>A maps to ENST00000375267 G2951G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7304-01A-12D-2086-08 chr1:19510669 C>T did not map to a codon.
Sequencing variant TCGA-FG-A87N-01A-11D-A36O-08 chr1:19439193 G>A maps to ENST00000375267 C3875C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WH-01A-12D-A33T-08 chr1:19523633 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:103266625 G>A maps to NM_015902.4 C2768C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:103341315 A>G did not map to a codon.
Sequencing variant TCGA-DU-6395-01A-12D-1705-08 chr8:103359283 T>C maps to NM_015902.4 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7857-01A-11D-2395-08 chr8:103266679 G>A maps to NM_015902.4 P2750P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TV-01A-12D-A34J-08 chr8:103269901 C>T maps to NM_015902.4 W2715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84L-01A-11D-A36O-08 chr1:26629320 C>T maps to NM_183008.2 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:4452489 C>A did not map to a codon.
Sequencing variant TCGA-S9-A7QY-01A-11D-A34A-08 chr19:4446150 G>A maps to NM_025241.2 F365F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:134404363 G>A maps to NM_031432.2 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:62577806 G>A maps to NM_017859.3 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A6S7-01A-21D-A32B-08 chr20:62571548 C>T maps to NM_017859.3 A507A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:13276237 G>A maps to NM_145314.1 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7469-01A-11D-2253-08 chr2:27530454 C>T maps to NM_003353.2 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5853-01A-11D-1893-08 chr11:73714924 G>A maps to NM_003356.3 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr7:100486856 C>T maps to NM_001015072.3 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:128900741 G>A maps to NM_020120.3 P598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5390-01A-02D-1468-08 chr13:96489362 G>A maps to NM_020121.3 Q1460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr13:96592231 A>G maps to NM_020121.3 S597S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:234669694 G>A maps to NM_000463.2 W254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6542-01A-11D-1893-08 chr2:234602345 C>T maps to NM_001072.3 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MU-01B-11D-A289-08 chr2:234590756 C>T maps to NM_019077.2 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:234526718 G>A maps to NM_019076.4 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:70512792 A>C maps to ENST00000514019 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84B-01A-11D-A36O-08 chr4:70465098 C>T maps to ENST00000514019 T453T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7309-01A-11D-2086-08 chr4:70080095 G>A maps to NM_001073.1 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6402-01A-11D-1705-08 chr4:69434169 C>T maps to NM_001076.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QZ-01A-12D-A34J-08 chr4:69403356 T>A maps to NM_001076.2 K527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7608-01A-11D-2086-08 chr4:70146856 C>T maps to NM_053039.1 N213N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:70361048 G>A maps to NM_021139.2 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:70361516 C>T maps to NM_021139.2 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A83Z-01A-11D-A36O-08 chr4:69962276 A>G maps to NM_001074.2 Q13Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TZ-01A-21D-A32B-08 chr4:69962318 G>T maps to NM_001074.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7604-01A-11D-2086-08 chr6:34827129 G>A maps to NM_017754.3 E999E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:100452366 A>G maps to NM_015054.1 D896D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:100452846 C>T maps to NM_015054.1 E736E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7641-01B-11D-2253-08 chr12:100502163 C>T maps to NM_015054.1 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:150267535 T>C maps to NM_025217.2 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:150387290 G>A maps to NM_024518.1 H32H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6670-01A-11D-1893-08 chr3:41795899 A>G maps to NM_017886.2 Y758Y. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DU-6392-01A-11D-1705-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DU-7309-01A-11D-2086-08 chr21:43519273 G>A maps to NM_173568.3 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7487-01A-11D-2024-08 chr21:43519135 C>T maps to NM_173568.3 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:26874427 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:121154476 C>T maps to NM_001080533.1 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7469-01A-11D-2253-08 chr19:17743589 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:35386235 A>G maps to ENST00000396787 T943T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:35403966 C>T maps to ENST00000396787 D1602D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7469-01A-11D-2253-08 chr9:35381620 C>T maps to ENST00000396787 D783D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:54307634 T>C maps to ENST00000260323 S845S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7478-01A-11D-2024-08 chr15:54306801 C>T maps to ENST00000260323 Q568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6290-01A-11D-1705-08 chr17:33475299 G>A maps to NM_173167.2 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5142-01A-01D-1468-08 chr17:33482400 C>T maps to NM_173167.2 C242C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76K-01A-11D-A33T-08 chr17:33486481 G>A maps to NM_173167.2 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WH-A86K-01A-11D-A36O-08 chr17:33495211 A>T maps to NM_173167.2 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:176297467 C>T maps to NM_133369.2 N273N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A845-01A-11D-A36O-08 chr4:96124100 G>A maps to NM_003728.3 V639V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:40996204 C>T maps to NM_173561.2 Q488Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:41000827 C>T maps to NM_173561.2 Q248Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr6:41002807 G>A maps to NM_173561.2 C2C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U2-01A-21D-A33T-08 chr6:40996228 C>T maps to NM_173561.2 R480R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:35579905 C>T maps to ENST00000416672 V437V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:35541168 C>T maps to ENST00000416672 D225D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:35616914 C>A maps to ENST00000416672 T752T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7301-01A-11D-2086-08 chr8:35583682 C>T maps to ENST00000416672 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr8:35406822 C>T maps to ENST00000416672 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5853-01A-11D-1893-08 chr6:167717404 A>G did not map to a codon.
Sequencing variant TCGA-FG-8182-01A-11D-2253-08 chr6:167728855 C>T maps to NM_018974.3 C430C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:73808616 G>A maps to NM_001080419.1 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VW-A7QS-01A-12D-A33T-08 chr16:1451674 C>T maps to ENST00000508903 Q164Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:18965816 G>A maps to ENST00000418384 A476A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:18966763 C>T maps to ENST00000418384 I536I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A89V-01A-11D-A36O-08 chr19:18968241 G>A maps to ENST00000418384 R705R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65R-01A-21D-A31L-08 chr23:118979240 A>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:74513319 G>T did not map to a codon.
Sequencing variant TCGA-EZ-7264-01A-11D-2024-08 chr23:74519577 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:229779331 C>A maps to NM_014777.2 A1229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:229794980 C>T maps to NM_014777.2 L1504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:229794944 G>A maps to NM_014777.2 S1492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:43917188 C>A maps to NM_001077663.1 E625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VW-A8FI-01A-11D-A36O-08 chr7:43916838 C>T maps to NM_001077663.1 Q741Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:126224681 G>A maps to NM_001165974.1 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:161011485 G>A maps to NM_007122.3 Q143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:17544784 G>A maps to NM_153676.3 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TT-01A-11D-A289-08 chr11:17531091 C>T maps to NM_153676.3 P608P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr11:17531253 G>A maps to NM_153676.3 P554P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:72916249 G>A maps to NM_173477.2 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6186-01A-12D-2024-08 chr1:216251646 G>A maps to ENST00000366943 Q1786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:216419933 A>G maps to ENST00000366943 C934C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:216166437 G>A maps to ENST00000366943 G2243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:216052353 A>G maps to ENST00000366943 N2770N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7298-01A-11D-2024-08 chr1:216496988 A>C maps to ENST00000366943 P459P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7490-01A-11D-2024-08 chr1:215914868 T>C maps to ENST00000366943 G3853G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8320-01A-11D-2395-08 chr1:216062130 G>A maps to ENST00000366943 L2620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:76708249 T>C maps to NM_003715.2 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:84779109 C>A maps to NM_005153.2 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:47098480 G>T did not map to a codon.
Sequencing variant TCGA-DU-7008-01A-11D-2024-08 chr23:47101044 G>A did not map to a codon.
Sequencing variant TCGA-FG-7638-01B-11D-2086-08 chr23:47104793 G>A did not map to a codon.
Sequencing variant TCGA-FG-A6J1-01A-11D-A31L-08 chr23:47107221 C>T did not map to a codon.
Sequencing variant TCGA-HT-7475-01A-11D-2024-08 chr23:47092454 G>A did not map to a codon.
Sequencing variant TCGA-HT-8010-01A-11D-2395-08 chr23:47101901 C>T did not map to a codon.
Sequencing variant TCGA-TQ-A7RQ-01A-11D-A33T-08 chr23:47099837 G>A did not map to a codon.
Sequencing variant TCGA-HW-8321-01A-11D-2395-08 chr13:27680003 C>T maps to NM_182488.3 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7480-01A-11D-2086-08 chr18:202879 C>T maps to NM_005151.3 R293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:62783718 C>T maps to ENST00000280377 R599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr12:62715344 T>C maps to ENST00000280377 N192N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:30426426 C>T maps to NM_006447.2 S797S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7884-01B-11D-2395-08 chr21:30419418 T>C maps to NM_006447.2 N596N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:132630507 G>A maps to NM_001008563.3 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QW-01A-11D-A34A-08 chr9:132620333 C>T maps to NM_001008563.3 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:20922430 C>T maps to ENST00000455117 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5395-01A-01D-1468-08 chr1:55638163 C>T maps to NM_015306.2 W196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A75O-01A-11D-A32B-08 chr1:55598322 C>A maps to NM_015306.2 L1144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:55560967 G>A maps to NM_015306.2 R2055*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VW-A8FI-01A-11D-A36O-08 chr1:55563342 C>T maps to NM_015306.2 L1881L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:17246799 A>G maps to ENST00000285681 G950G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:17246838 T>C maps to ENST00000285681 C963C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr21:17250116 A>G maps to ENST00000285681 K966K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TU-01A-12D-A32B-08 chr21:17199373 A>G maps to ENST00000285681 R515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64W-01A-11D-A29Q-08 chr23:132159578 T>C did not map to a codon.
Sequencing variant TCGA-DH-A66G-01A-21D-A31L-08 chr23:132160725 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:132161315 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:132161016 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:132160550 T>C did not map to a codon.
Sequencing variant TCGA-P5-A780-01A-12D-A32B-08 chr23:132160181 A>G did not map to a codon.
Sequencing variant TCGA-QH-A6CV-01A-11D-A31L-08 chr23:132162097 G>A did not map to a codon.
Sequencing variant TCGA-VM-A8CB-01A-11D-A36O-08 chr23:132160494 C>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:113673878 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:113683094 G>T maps to NM_020886.2 S625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:57641353 T>A maps to NM_020903.2 I437I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6XC-01A-12D-A32B-08 chr19:57642571 C>T maps to NM_020903.2 S843S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:63880965 C>T maps to NM_006537.2 Y427Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7620-01A-11D-2253-08 chr12:109519736 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:58260798 G>A maps to NM_032582.3 R1284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:58275769 C>T maps to NM_032582.3 K1095K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr17:58259032 C>T maps to NM_032582.3 R1400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5852-01A-11D-1705-08 chr2:61468709 C>T maps to NM_014709.3 S2254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:61441452 G>T maps to NM_014709.3 V2808V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:77921495 C>A maps to NM_020798.2 C865*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TJ-01A-11D-A34J-08 chr17:76803535 G>A maps to NM_025090.3 D530D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7CF-01A-11D-A32B-08 chr2:219418377 G>A maps to NM_020935.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:85868166 C>A maps to NM_006590.2 I451I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:85848691 G>A maps to NM_006590.2 K141K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65R-01A-21D-A31L-08 chr3:49323549 T>A maps to NM_003363.3 G727G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TS-01A-11D-A289-08 chr2:234408534 A>G maps to NM_018218.2 S891S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:95927507 C>T maps to NM_032147.2 K175K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A618-01A-11D-A29Q-08 chr12:95914958 G>A maps to NM_032147.2 R585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:11961974 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:22047589 A>G maps to NM_032236.5 D611D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U1-01A-21D-A33T-08 chr1:22030797 C>T maps to NM_032236.5 V824V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:41773650 G>T maps to ENST00000373009 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:41773746 G>A maps to ENST00000373009 C325C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4942-01A-01D-1468-08 chr23:55514657 A>G did not map to a codon.
Sequencing variant TCGA-CS-6665-01A-11D-1893-08 chr23:55514134 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:55514741 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:55515232 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:120181735 C>A maps to NM_019050.2 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U5-01A-12D-A33T-08 chr10:75331187 G>A maps to NM_152586.3 C77C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6UA-01A-12D-A33T-08 chr10:75331187 G>A maps to NM_152586.3 C77C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr17:5072169 C>T maps to NM_004505.2 R1113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A735-01A-11D-A32B-08 chr17:5066178 A>G maps to NM_004505.2 R972R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7J3-01A-21D-A34J-08 chr17:5039170 C>T maps to NM_004505.2 D204D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:11535182 T>C maps to NM_001080491.2 Q160Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:8988699 G>A maps to NM_003470.2 R1018*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6410-01A-11D-1893-08 chr16:9000423 C>T maps to NM_003470.2 E429E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TY-01A-12D-A32B-08 chr16:8988965 C>T maps to NM_003470.2 E987E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F0-01A-11D-A289-08 chr15:50769065 G>C maps to NM_005154.3 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XD-01A-11D-A27K-08 chr23:41084137 A>G did not map to a codon.
Sequencing variant TCGA-DB-A64L-01A-11D-A29Q-08 chr23:41075259 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:41027338 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:41048718 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:41075234 A>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:41073891 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:41048649 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:41043671 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:41025362 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:41029754 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:41091709 G>A did not map to a codon.
Sequencing variant TCGA-DU-6410-01A-11D-1893-08 chr23:41057787 T>C did not map to a codon.
Sequencing variant TCGA-S9-A7QW-01A-11D-A34A-08 chr23:41069806 A>C did not map to a codon.
Sequencing variant TCGA-VM-A8CF-01A-11D-A36O-08 chr23:41057975 A>G did not map to a codon.
Sequencing variant TCGA-FG-8188-01A-11D-2253-08 chr6:149340327 A>G maps to NM_005715.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YI-01A-11D-A34A-08 chr23:129060300 G>A did not map to a codon.
Sequencing variant TCGA-KT-A7W1-01A-11D-A34A-08 chr23:129060250 A>T did not map to a codon.
Sequencing variant TCGA-S9-A6U2-01A-21D-A33T-08 chr23:129042646 C>T did not map to a codon.
Sequencing variant TCGA-TQ-A7RI-01A-11D-A33T-08 chr23:129042693 C>T did not map to a codon.
Sequencing variant TCGA-HW-7491-01A-11D-2024-08 chr13:52605153 C>G maps to NM_021645.5 Y738*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W9-A837-01A-11D-A36O-08 chr5:72866465 C>G maps to NM_032175.2 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:49365521 C>A maps to NM_016001.2 I487I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A75K-01A-11D-A32B-08 chr12:101720954 C>T maps to NM_014503.2 A1046A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A870-01A-11D-A36O-08 chr4:71555329 C>A maps to NM_020368.2 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:144803407 T>C maps to NM_007124.2 L1191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:144747451 G>A maps to NM_007124.2 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr6:145149991 G>C did not map to a codon.
Sequencing variant TCGA-TM-A7C3-01A-11D-A32B-08 chr6:145156984 G>A maps to NM_007124.2 P3245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7603-01A-21D-2086-08 chr24:15410958 A>G did not map to a codon.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr24:15522900 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:70765432 C>A maps to NM_018052.3 R542R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:70814780 G>A maps to NM_018052.3 D336D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:31752243 G>T maps to NM_006295.2 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7636-01A-11D-2086-08 chr6:31747884 G>A maps to NM_006295.2 L991L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MY-01A-11D-A26M-08 chr9:136641199 C>T maps to NM_001134398.1 P656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:108299951 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:108319904 C>A maps to NM_006113.4 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:154456690 G>A did not map to a codon.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr1:101198154 A>G maps to NM_001078.3 T569T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:82835796 G>A maps to NM_004385.4 G2325G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6UB-01A-21D-A33T-08 chr10:75877842 G>A maps to NM_014000.2 R1107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:35066786 G>A maps to NM_007126.3 Y110Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WL-01A-21D-A33T-08 chr9:35060872 T>G maps to NM_007126.3 V469V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:7811789 C>T did not map to a codon.
Sequencing variant TCGA-DU-A7T6-01A-11D-A33T-08 chr23:8138192 C>G did not map to a codon.
Sequencing variant TCGA-HT-A74H-01A-11D-A32B-08 chr23:6451821 A>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:8433556 C>A did not map to a codon.
Sequencing variant TCGA-HW-8322-01A-11D-2395-08 chr23:8434345 G>A did not map to a codon.
Sequencing variant TCGA-HT-7694-01A-11D-2253-08 chr10:76980617 G>A maps to NM_001184783.1 E173E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:64003357 G>A maps to NM_003377.3 E59E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr3:156978934 G>A maps to NM_001167912.1 T830T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U9-01A-11D-A32B-08 chr6:117591790 C>T maps to NM_182645.2 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7875-01A-11D-2395-08 chr3:87018079 A>G maps to NM_016206.2 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8185-01A-11D-2253-08 chr3:10191621 C>T maps to NM_000551.2 R205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5396-01A-02D-1468-08 chr1:156268965 C>T maps to NM_001004319.2 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:156268734 C>T maps to NM_001004319.2 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7606-01A-11D-2086-08 chr2:219295518 C>T maps to NM_007127.2 A340A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R7-01A-11D-A289-08 chr2:219293032 G>A maps to NM_007127.2 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5277-01A-01D-1468-08 chr2:37035631 C>T maps to NM_053276.3 N469N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:37035649 C>T maps to NM_053276.3 H475H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:36986259 C>T maps to NM_001177972.1 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:37041324 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:2645694 T>C maps to NM_003383.3 I478I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:2643436 C>T maps to NM_003383.3 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr9:2648301 G>A maps to NM_003383.3 K639K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:150572152 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:53761867 C>T maps to NM_173856.2 H80H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6IZ-01A-11D-A31L-08 chr19:53762632 C>T maps to NM_173856.2 Y335Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:118944659 C>T maps to NM_021729.4 R412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:118948751 C>T maps to NM_021729.4 S578S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:79955197 A>G maps to ENST00000376646 Q2293Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A710-01A-12D-A33T-08 chr9:79853106 A>C maps to ENST00000376646 A595A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:100396496 G>A maps to NM_017890.3 T962T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:100830942 T>C maps to NM_017890.3 I2841I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:100866173 G>A maps to NM_017890.3 L3544L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:62165443 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:62277143 C>A maps to NM_020821.2 E545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:62201255 A>G maps to NM_020821.2 H2971H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:12353761 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:12368698 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:12418628 A>G maps to NM_015378.2 G3371G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8188-01A-11D-2253-08 chr1:12461734 T>C maps to NM_015378.2 F3953F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QW-01A-11D-A34A-08 chr1:12557679 C>T maps to NM_015378.2 D4263D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:2843289 C>T maps to NM_022575.2 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:41192695 A>G maps to NM_020857.2 A560A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8166-01A-11D-2253-08 chr15:41193043 G>A maps to NM_020857.2 P676P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A619-01A-11D-A29Q-08 chr15:41193148 C>T maps to NM_020857.2 R711R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:40928261 G>T did not map to a codon.
Sequencing variant TCGA-HT-7877-01A-11D-2395-08 chr17:40926664 A>G maps to NM_032353.2 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:122716792 C>A maps to NM_022916.4 *597Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:91551162 C>T maps to NM_018668.3 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:53008986 G>A maps to NM_016075.2 Q128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CB-01A-11D-A36O-08 chr13:52991269 A>T maps to NM_016075.2 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7482-01A-11D-2024-08 chr7:38796518 G>A maps to NM_014396.3 D538D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84H-01A-11D-A36O-08 chr7:38805188 T>C maps to NM_014396.3 G440G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:150048338 C>T maps to NM_007259.3 D106D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:150040754 C>T maps to NM_007259.3 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:150082691 T>C maps to NM_007259.3 T525T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5144-01A-01D-1468-08 chr6:33235063 G>A maps to NM_022553.4 N342N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TD-01A-12D-A34A-08 chr2:64193064 G>T maps to NM_016516.2 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:151149422 G>T maps to ENST00000354473 T275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7299-01A-21D-2024-08 chr1:151158054 C>T maps to ENST00000354473 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5849-01A-11D-1705-08 chr2:58311263 A>G maps to NM_001130480.2 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5142-01A-01D-1468-08 chr23:107310284 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:107310333 A>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:107301374 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:107288393 C>T did not map to a codon.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr23:107316039 C>T did not map to a codon.
Sequencing variant TCGA-QH-A65X-01A-11D-A32B-08 chr23:107288368 C>T did not map to a codon.
Sequencing variant TCGA-CS-6668-01A-11D-1893-08 chr23:65247364 G>A did not map to a codon.
Sequencing variant TCGA-DB-A4XF-01A-11D-A27K-08 chr23:65253351 C>T did not map to a codon.
Sequencing variant TCGA-DB-A75K-01A-11D-A32B-08 chr23:65247906 T>C did not map to a codon.
Sequencing variant TCGA-FG-8182-01A-11D-2253-08 chr23:65253474 G>A did not map to a codon.
Sequencing variant TCGA-HT-8018-01A-11D-2395-08 chr23:65253438 A>G did not map to a codon.
Sequencing variant TCGA-P5-A72X-01A-11D-A32B-08 chr23:65252308 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:54612358 C>T maps to ENST00000404951 Q42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6186-01A-12D-2024-08 chr20:25057043 A>C maps to NM_014588.4 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7009-01A-11D-2024-08 chr20:25059380 A>T maps to NM_199425.1 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:142491539 T>C maps to NM_016485.3 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TD-01A-12D-A34A-08 chr6:142519681 T>C maps to NM_016485.3 Y209Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:114575090 C>T maps to NM_145206.2 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:68118191 T>C maps to NM_006370.2 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr1:1374626 G>A maps to NM_022834.4 T266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74L-01A-11D-A32B-08 chr10:116049183 C>T maps to NM_198496.1 I686I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U9-01A-11D-A32B-08 chr10:116038487 C>G maps to NM_198496.1 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5281-01A-01D-1468-08 chr2:98928737 C>T maps to NM_144992.4 R1271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7902-01A-12D-2395-08 chr2:98744703 T>C maps to NM_144992.4 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:123988404 C>T maps to NM_014622.4 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8011-01A-11D-2395-08 chr7:49842317 C>T maps to NM_198570.3 C236C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:6173433 G>A maps to NM_000552.3 D470D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:88218789 G>A maps to ENST00000342368 Y956Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:100801231 G>A maps to NM_173701.1 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr1:119576826 G>A maps to NM_015836.3 H175H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6400-01A-12D-1705-08 chr23:48542339 A>G did not map to a codon.
Sequencing variant TCGA-DU-8167-01A-11D-2253-08 chr23:48545244 A>T did not map to a codon.
Sequencing variant TCGA-HT-8105-01A-11D-2395-08 chr7:74486565 G>A maps to NM_030798.3 C114C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6403-01A-11D-1705-08 chr7:70597850 C>T maps to NM_022479.1 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:73108320 G>T did not map to a codon.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr7:73280002 C>T maps to NM_182504.3 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:224759040 C>T maps to NM_020830.3 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:10079511 C>T maps to NM_017491.3 T478T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr4:10077031 G>A maps to NM_017491.3 A597A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:203760928 G>A maps to NM_018256.3 C156C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WL-01A-21D-A33T-08 chr4:177067235 G>A maps to NM_170710.4 G564G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4942-01A-01D-1468-08 chr19:991973 C>T maps to NM_024100.3 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TA-01A-11D-A33T-08 chr4:39271707 T>A maps to NM_025132.3 Y1157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:737584 G>A maps to ENST00000248142 C342C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7495-01A-11D-2024-08 chr1:224619389 C>T maps to NM_025160.6 W172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:170064352 G>A maps to NM_182552.3 H271H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A6ML-01A-11D-A32B-08 chr6:170013707 G>A maps to NM_182552.3 F756F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:118488741 T>C maps to NM_006784.2 C454C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:118501574 A>G maps to NM_006784.2 P875P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:20130199 C>T maps to NM_001006657.1 Q1037Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:20160375 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:110428060 C>T maps to NM_139281.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:110461364 C>T maps to NM_139281.2 R860*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RS-01A-12D-A33T-08 chr10:1149738 C>T maps to ENST00000416775 Y309Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:117528035 C>T did not map to a codon.
Sequencing variant TCGA-HW-7495-01A-11D-2024-08 chr23:117527111 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:48933404 G>A did not map to a codon.
Sequencing variant TCGA-CS-6670-01A-11D-1893-08 chr3:167246908 A>G maps to NM_178824.3 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RR-01A-21D-A34A-08 chr3:113082075 C>T maps to NM_001164496.1 E950E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A614-01A-11D-A29Q-08 chr2:74652339 G>A maps to NM_032118.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:158716266 G>A maps to NM_018051.4 T700T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:36594734 C>T maps to NM_001083961.1 S1335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:85592237 C>A maps to NM_145172.3 T719T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6396-01A-11D-1705-08 chr12:122399966 C>T maps to NM_144668.4 T797T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:124117637 T>C maps to NM_145647.3 S381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:228755969 G>T did not map to a codon.
Sequencing variant TCGA-HT-A5R7-01A-11D-A289-08 chr2:228770990 C>T maps to NM_178821.1 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr18:54446753 C>T maps to NM_015285.2 R1014*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:54424106 T>C maps to NM_015285.2 D761D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:54424344 G>T maps to NM_015285.2 G841*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TY-01A-11D-A289-08 chr18:54423953 G>A maps to NM_015285.2 P710P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr18:54424325 G>A maps to NM_015285.2 S834S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:37721296 C>T maps to NM_018034.2 Y499Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:37392109 G>T maps to NM_018034.2 E62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:53957929 G>A maps to NM_182758.2 R601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A83Z-01A-11D-A36O-08 chr15:53907716 G>A maps to NM_182758.2 R896*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4944-01A-01D-1468-08 chr2:190313122 T>C maps to NM_032168.1 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QW-01A-11D-A34A-08 chr1:67292588 G>A maps to NM_024763.4 Y751Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:1634378 C>A maps to NM_001163809.1 A1328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-7675-01A-11D-2086-08 chr17:1637325 C>T maps to NM_001163809.1 S1665S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8CH-01A-12D-A36O-08 chr17:1633761 G>A maps to NM_001163809.1 L1252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:33666396 C>T maps to NM_173479.3 G446G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YM-01A-11D-A34A-08 chr16:705312 G>A maps to NM_145294.4 A521A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A86X-01A-11D-A36O-08 chr16:705147 G>A did not map to a codon.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr15:90265287 T>C maps to NM_020212.1 D266D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U0-01A-12D-A32B-08 chr15:90246287 G>A maps to NM_020212.1 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7294-01A-11D-2024-08 chr20:44237303 G>A maps to NM_147198.2 N79N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:48918031 C>T maps to NM_175575.5 S461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:6304140 C>T maps to NM_006005.3 G873G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:6303630 C>A maps to NM_006005.3 R703R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr4:6304059 C>T maps to NM_006005.3 S846S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:1932477 C>T maps to NM_133335.3 V512V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YN-01A-11D-A34A-08 chr8:38187123 G>A maps to NM_023034.1 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7292-01A-11D-2024-08 chr12:65460501 G>A maps to NM_007191.4 R217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:29915573 C>T maps to NM_001080529.1 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YE-01A-11D-A34A-08 chr17:66446946 C>G maps to NM_017983.5 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:5232790 C>T maps to NM_015610.3 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XG-01A-11D-A27K-08 chr8:134225312 C>T maps to NM_003882.2 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8011-01A-11D-2395-08 chr20:43344045 G>A maps to NM_003881.2 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YJ-01A-11D-A34A-08 chr12:977318 A>G maps to NM_001184985.1 V809V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64W-01A-11D-A29Q-08 chr9:96018612 C>T maps to ENST00000297954 P689P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:54319603 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:54321077 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:54359997 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:54224903 T>C did not map to a codon.
Sequencing variant TCGA-DU-A6S7-01A-21D-A32B-08 chr23:54321051 C>A did not map to a codon.
Sequencing variant TCGA-FG-A710-01A-12D-A33T-08 chr23:54259291 C>T did not map to a codon.
Sequencing variant TCGA-HT-8113-01A-11D-2395-08 chr23:54335535 C>A did not map to a codon.
Sequencing variant TCGA-TM-A84G-01A-11D-A36O-08 chr23:54275529 G>T did not map to a codon.
Sequencing variant TCGA-TQ-A7RQ-01A-11D-A33T-08 chr23:54324777 C>A did not map to a codon.
Sequencing variant TCGA-S9-A7IX-01A-12D-A34A-08 chr17:40940793 G>A maps to NM_032387.4 P712P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:219754748 C>T maps to NM_025216.2 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8191-01A-11D-2253-08 chr7:116937825 G>A maps to NM_003391.2 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:44845838 G>A maps to NM_030753.3 H305H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6393-01A-11D-1705-08 chr17:44845703 G>A maps to NM_030753.3 D350D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85E-01A-11D-A36O-08 chr17:44851145 G>C maps to NM_030753.3 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A736-01A-11D-A32B-08 chr3:13916573 G>A maps to NM_004625.3 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr21:40765206 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:30973986 C>T maps to NM_000553.4 G797G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr8:30938763 G>A maps to NM_000553.4 Q407Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:25639314 C>T maps to NM_015626.8 R396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IZ-01A-11D-A34A-08 chr12:108589875 C>T maps to ENST00000261400 Y89Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:160176189 C>A maps to NM_004906.3 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6667-01A-12D-2024-08 chr23:10106878 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:10098023 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:10096200 G>T did not map to a codon.
Sequencing variant TCGA-DU-7015-01A-11D-2024-08 chr23:10085415 G>T did not map to a codon.
Sequencing variant TCGA-DU-7300-01A-21D-2086-08 chr23:10085534 C>T did not map to a codon.
Sequencing variant TCGA-DU-8166-01A-11D-2253-08 chr23:10090692 G>T did not map to a codon.
Sequencing variant TCGA-P5-A780-01A-12D-A32B-08 chr23:10107546 G>A did not map to a codon.
Sequencing variant TCGA-HT-8012-01A-11D-2395-08 chr16:78458904 C>T maps to NM_016373.1 C248C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7873-01B-11D-2395-08 chr8:87443689 A>C maps to NM_007013.3 T481T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U2-01A-21D-A33T-08 chr16:69874116 G>A maps to NM_007014.3 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84B-01A-11D-A36O-08 chr16:69971125 C>T maps to NM_007014.3 D741D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:7685534 C>T maps to NM_020196.2 A664A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:7684866 C>T maps to NM_020196.2 Q787Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:52844173 C>T did not map to a codon.
Sequencing variant TCGA-HT-7875-01A-11D-2395-08 chr1:168510201 G>A maps to NM_003175.3 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A737-01A-11D-A32B-08 chr1:168510201 G>A maps to NM_003175.3 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RW-01A-11D-A33T-08 chr1:168510201 G>A maps to NM_003175.3 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7298-01A-11D-2024-08 chr2:31588393 G>A maps to NM_000379.3 R825*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YD-01A-11D-A34A-08 chr2:31589807 G>A maps to NM_000379.3 T750T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:2729408 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:2729414 G>A did not map to a codon.
Sequencing variant TCGA-HT-A5R7-01A-11D-A289-08 chr23:2729412 C>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:123019850 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:123025088 T>C did not map to a codon.
Sequencing variant TCGA-FG-5965-01B-11D-1893-08 chr23:123020095 G>C did not map to a codon.
Sequencing variant TCGA-HT-7604-01A-11D-2086-08 chr23:123034426 A>G did not map to a codon.
Sequencing variant TCGA-TQ-A7RJ-01A-11D-A33T-08 chr23:123019611 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:39229154 G>T maps to NM_194293.2 I594I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7J1-01A-21D-A34J-08 chr3:39225410 G>A maps to NM_194293.2 A1842A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:168102965 C>T maps to NM_152381.5 N1688N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:168114996 C>T maps to ENST00000420519 D680D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7008-01A-11D-2024-08 chr23:37587095 T>A did not map to a codon.
Sequencing variant TCGA-DU-7010-01A-11D-2024-08 chr23:37553612 G>A did not map to a codon.
Sequencing variant TCGA-DU-A7T6-01A-11D-A33T-08 chr8:56015368 C>G maps to NM_052898.1 Y107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U6-01A-12D-A33T-08 chr8:10756202 G>A maps to NM_173683.3 C395C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:100183176 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:100169499 T>A did not map to a codon.
Sequencing variant TCGA-DU-7008-01A-11D-2024-08 chr23:100169557 T>A did not map to a codon.
Sequencing variant TCGA-CS-4943-01A-01D-1468-08 chr9:100459508 G>A maps to NM_000380.3 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A86X-01A-11D-A36O-08 chr9:100459556 C>T maps to NM_000380.3 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:111642354 C>T maps to NM_020383.3 E292E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:111637816 C>A did not map to a codon.
Sequencing variant TCGA-QH-A65Z-01A-11D-A29Q-08 chr23:128879231 A>T did not map to a codon.
Sequencing variant TCGA-TQ-A7RM-01A-11D-A33T-08 chr23:128879232 G>T did not map to a codon.
Sequencing variant TCGA-S9-A6UA-01A-12D-A33T-08 chr13:21361631 C>T maps to NM_022459.4 R1051R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VM-A8C9-01A-11D-A36O-08 chr13:21361631 C>T maps to NM_022459.4 R1051R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:21833991 C>T maps to ENST00000434536 D250D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr12:64811870 G>A maps to NM_007235.3 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:152346194 G>A maps to NM_005431.1 H125H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-7486-01A-11D-2024-08 chr2:216983867 T>C maps to NM_021141.3 C157C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:42046724 A>G did not map to a codon.
Sequencing variant TCGA-DB-A64Q-01A-11D-A29Q-08 chr3:142136034 C>T maps to NM_019001.3 Q461Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:21327051 G>T did not map to a codon.
Sequencing variant TCGA-DU-6393-01A-11D-1705-08 chr20:21328890 G>A maps to NM_012255.3 P591P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XF-01A-11D-A27K-08 chr16:17235123 G>A maps to NM_022166.3 G491G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A83Z-01A-11D-A36O-08 chr17:48432927 C>T maps to NM_022167.2 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7CA-01A-21D-A33T-08 chr11:102076696 A>G maps to NM_001130145.2 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6IZ-01A-11D-A31L-08 chr3:183495361 G>A maps to NM_018023.4 Q870Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:54348856 C>A maps to NM_018982.4 G42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U9-01A-11D-A32B-08 chr6:43480226 G>A maps to ENST00000506469 H291H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A75K-01A-11D-A32B-08 chr23:67751799 T>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:67741283 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:67731766 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:75265632 T>C maps to NM_019589.2 A1211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YE-01A-11D-A34A-08 chr14:75266313 T>G maps to NM_019589.2 S1438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:27431369 G>A maps to NM_139312.1 R183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:57465708 C>T maps to NM_001005404.3 R47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85E-01A-11D-A36O-08 chr17:57465702 C>T maps to NM_001005404.3 Q45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5395-01A-01D-1468-08 chr2:135745372 G>A maps to NM_025052.3 R357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:135745328 C>T maps to NM_025052.3 K371K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A89V-01A-11D-A36O-08 chr2:135744236 C>T maps to NM_025052.3 E735E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A614-01A-11D-A29Q-08 chr4:69189858 G>A maps to NM_001031732.2 Q478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:112927862 C>T maps to NM_022828.3 S1400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:75958908 G>A maps to NM_012479.3 G243G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DU-6392-01A-11D-1705-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:155649257 C>A maps to ENST00000368339 E161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64R-01A-11D-A29Q-08 chr23:21875532 T>C did not map to a codon.
Sequencing variant TCGA-DB-A75L-01A-11D-A32B-08 chr23:21875030 A>G did not map to a codon.
Sequencing variant TCGA-DH-A669-01A-12D-A31L-08 chr23:21875400 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:72913975 A>G maps to NM_175907.4 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UT-01A-12D-A34A-08 chr7:100365617 G>A maps to ENST00000349350 Q1675Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr7:100377161 C>T maps to ENST00000349350 R2137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R2-01A-21D-A34J-08 chr7:100349692 C>T maps to ENST00000349350 T655T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7007-01A-11D-2024-08 chr3:166960402 G>T maps to ENST00000307529 T761T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:2407351 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:2406828 C>A did not map to a codon.
Sequencing variant TCGA-DU-6400-01A-12D-1705-08 chr23:2407264 T>A did not map to a codon.
Sequencing variant TCGA-P5-A5ET-01A-11D-A27K-08 chr23:2406763 T>C did not map to a codon.
Sequencing variant TCGA-DB-A64W-01A-11D-A29Q-08 chr3:101373566 G>A maps to NM_014415.3 R764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:101378785 C>T maps to NM_014415.3 S629S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:101383380 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:101383908 G>A maps to NM_014415.3 R508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5270-01A-02D-1468-08 chr6:31868386 A>G maps to NM_181842.2 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:151694679 G>A maps to NM_020861.1 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A845-01A-11D-A36O-08 chr6:151687323 G>A maps to NM_020861.1 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6393-01A-11D-1705-08 chr3:114069361 G>A maps to NM_001164342.1 P521P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A60K-01A-11D-A29Q-08 chr3:114070288 C>T maps to NM_001164342.1 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8563-01A-11D-2395-08 chr3:114070215 G>A maps to NM_001164342.1 Q237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QX-01A-11D-A34A-08 chr3:114058160 G>A maps to NM_001164342.1 C639C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5144-01A-01D-1468-08 chr6:109802896 A>T maps to NM_014797.2 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6J3-01A-11D-A31L-08 chr6:109787071 A>T maps to NM_014797.2 L692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:62519915 G>A maps to NM_024784.3 Y457Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:119387917 G>T did not map to a codon.
Sequencing variant TCGA-S9-A6WL-01A-21D-A33T-08 chr23:119388486 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:141161790 A>G maps to NM_001080412.2 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QW-01A-11D-A34A-08 chr3:141161850 C>T maps to NM_001080412.2 D207D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MW-01A-11D-A26M-08 chr1:22852747 G>A maps to NM_014870.3 E1193E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:197169498 G>T maps to NM_194314.2 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:129596168 C>T maps to NM_014007.3 Q461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:59028725 G>A maps to NM_032792.2 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A6S2-01A-21D-A32B-08 chr19:59028509 C>T maps to NM_032792.2 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:62378405 G>A maps to NM_025224.2 G549G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:62421633 C>T maps to NM_025224.2 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IZ-01A-11D-A34A-08 chr20:62422011 G>T maps to NM_025224.2 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:42701049 G>A maps to NM_145166.3 G401G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:4303754 T>C maps to NM_145291.3 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7636-01A-11D-2086-08 chr4:4304567 G>A maps to NM_145291.3 K335K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:37442056 G>A maps to NM_014872.2 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WG-01A-11D-A33T-08 chr9:125674071 C>A maps to NM_006626.4 E94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:4054045 G>A maps to NM_015898.2 G395G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:154988694 G>T did not map to a codon.
Sequencing variant TCGA-HT-7602-01A-21D-2086-08 chr1:154988752 C>T maps to ENST00000417934 C438C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:45566686 G>A maps to NM_001039360.2 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:45566386 C>T maps to NM_001039360.2 Q364Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:45556203 G>A maps to NM_001039360.2 F429F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A710-01A-12D-A33T-08 chr6:33423476 A>C maps to NM_152735.3 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7695-01A-11D-2253-08 chr6:33423521 G>A maps to NM_152735.3 E215E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A781-01A-11D-A32B-08 chr6:33423521 G>A maps to NM_152735.3 E215E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:56515434 G>A maps to NM_032786.1 T363T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:203819730 C>T maps to NM_014827.4 H676H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr23:64721963 C>A did not map to a codon.
Sequencing variant TCGA-DU-5851-01A-13D-1893-08 chr23:64719803 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:64708942 C>T did not map to a codon.
Sequencing variant TCGA-DU-6400-01A-12D-1705-08 chr23:64721754 C>T did not map to a codon.
Sequencing variant TCGA-TQ-A7RM-01A-11D-A33T-08 chr23:64722739 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:110030071 C>T maps to NM_033390.1 D335D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A65V-01A-11D-A29Q-08 chr13:46619597 A>G maps to ENST00000242848 T15T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:89039185 G>A maps to NM_024824.4 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:89038557 C>T maps to NM_024824.4 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:144621218 C>T maps to NM_015117.2 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:47572364 G>A maps to NM_015168.1 D794D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7019-01A-11D-2024-08 chr19:47575122 G>A maps to NM_015168.1 P686P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7604-01A-11D-2086-08 chr19:47593320 G>A maps to NM_015168.1 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8319-01A-11D-2395-08 chr19:47570839 G>A maps to NM_015168.1 A895A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:113089839 G>A maps to NM_198581.2 A1115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EX-01A-12D-A289-08 chr2:113089665 A>G maps to NM_198581.2 S1057S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5277-01A-01D-1468-08 chr16:11857361 C>G maps to NM_014153.3 L658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:11861425 A>G maps to NM_014153.3 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5RB-01A-11D-A289-08 chr22:41739417 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:138793933 G>A maps to ENST00000464606 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A615-01A-11D-A29Q-08 chr23:64139084 C>A did not map to a codon.
Sequencing variant TCGA-DB-5280-01A-01D-1468-08 chr1:52889612 C>T maps to NM_001009881.2 S1644S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TB-01A-11D-A33T-08 chr1:52902558 G>A maps to NM_001009881.2 R1344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YK-01A-11D-A34A-08 chr1:52891126 A>G maps to NM_001009881.2 R1588R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QY-01A-11D-A34A-08 chr1:52940851 G>A maps to NM_001009881.2 H793H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XF-01A-11D-A27K-08 chr23:117959413 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:117959636 A>G did not map to a codon.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr23:117959417 G>A did not map to a codon.
Sequencing variant TCGA-FG-5962-01B-11D-1893-08 chr23:117959417 G>A did not map to a codon.
Sequencing variant TCGA-HT-7695-01A-11D-2253-08 chr23:117959417 G>A did not map to a codon.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr23:117960228 G>A did not map to a codon.
Sequencing variant TCGA-S9-A6U0-01A-12D-A32B-08 chr23:117960275 A>G did not map to a codon.
Sequencing variant TCGA-S9-A7IZ-01A-11D-A34A-08 chr23:117959360 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:73524565 G>A did not map to a codon.
Sequencing variant TCGA-E1-A7Z6-01A-11D-A34J-08 chr23:111698668 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:103358834 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:103359094 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:103359492 C>T did not map to a codon.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr4:25351254 C>T maps to NM_024936.2 Q301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:77913580 C>A did not map to a codon.
Sequencing variant TCGA-FG-A87Q-01A-11D-A36O-08 chr23:77913358 G>A did not map to a codon.
Sequencing variant TCGA-HT-7606-01A-11D-2086-08 chr23:77912923 G>T did not map to a codon.
Sequencing variant TCGA-HT-7874-01A-11D-2395-08 chr23:77913194 A>T did not map to a codon.
Sequencing variant TCGA-S9-A6WN-01A-12D-A33T-08 chr23:77913569 C>T did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr9:88967853 G>A maps to NM_024617.3 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:37304255 C>A maps to NM_032226.2 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:122958463 C>T maps to NM_017612.2 P568P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr5:80604489 C>T maps to NM_032280.2 H165H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:100006187 G>T maps to NM_017984.3 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A75O-01A-11D-A32B-08 chr2:207171519 G>A maps to NM_020923.1 P756P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5143-01A-01D-1468-08 chr2:207169635 G>A maps to NM_020923.1 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8187-01A-11D-2253-08 chr2:207175935 G>A maps to NM_020923.1 S2228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U0-01A-12D-A32B-08 chr2:207169614 T>A maps to NM_020923.1 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VW-A8FI-01A-11D-A36O-08 chr2:207170472 T>C maps to NM_020923.1 S407S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:131484063 G>A maps to ENST00000372667 C130C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:19173708 G>T maps to NM_019028.2 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:19167743 C>T maps to NM_019028.2 R64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EZ-01A-11D-A27K-08 chr6:158066843 C>T maps to NM_024630.2 I276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:99213590 G>A maps to NM_198046.1 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:77220686 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:27177722 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:77605799 G>A maps to NM_174976.2 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr3:113677374 C>T maps to NM_173570.3 I402I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RI-01A-11D-A33T-08 chr11:66307296 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:45000729 G>A maps to NM_016598.2 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:6621737 C>T maps to NM_018106.3 Q76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6399-01A-12D-1705-08 chr7:6624734 C>T maps to NM_018106.3 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:31791291 C>T maps to NM_001174096.1 C113C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:145147064 C>A maps to NM_014795.3 E1200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:145158777 G>A maps to NM_014795.3 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr2:145156356 A>G maps to NM_014795.3 S799S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7604-01A-11D-2086-08 chr2:145147368 T>C maps to NM_014795.3 K1098K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:82615064 G>T maps to NM_024699.2 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6U0-01A-12D-A32B-08 chr6:38120149 G>A maps to NM_021943.2 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7638-01B-11D-2086-08 chr9:74970964 G>A maps to ENST00000437241 D234D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:135524754 C>T maps to NM_020863.3 V1108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:135649809 G>A maps to NM_020863.3 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7693-01A-11D-2253-08 chr8:135649704 T>C maps to NM_020863.3 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5275-01A-01D-1468-08 chr16:72821212 C>A maps to NM_006885.3 S3654S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:72828426 C>T maps to NM_006885.3 A2718A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6410-01A-11D-1893-08 chr16:72827286 T>C maps to NM_006885.3 Q3098Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5EV-01A-11D-A27K-08 chr16:72991938 G>C maps to NM_006885.3 V702V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A86X-01A-11D-A36O-08 chr16:72831384 T>C maps to NM_006885.3 Q1732Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:42740425 G>T maps to NM_022473.1 S970S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:44840820 T>A maps to ENST00000412927 K76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:36831671 G>A maps to NM_020917.2 C352C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:5291621 G>A maps to NM_003409.3 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6410-01A-11D-1893-08 chr18:5291660 G>A maps to NM_003409.3 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:178358811 C>A maps to NM_030613.2 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:4995470 C>A maps to NM_153018.2 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A7C5-01A-11D-A32B-08 chr14:69256927 G>A maps to NM_004926.2 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:115806438 G>A maps to NM_003408.1 D153D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7606-01A-11D-2086-08 chr9:115811699 T>C maps to NM_003408.1 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr8:144332525 C>T maps to NM_173832.3 Y171Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:188924380 G>A maps to NM_174900.3 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:188924293 C>T maps to NM_174900.3 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:50769212 G>A maps to NM_018197.2 P506P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7306-01A-11D-2086-08 chr20:50701275 G>A maps to NM_199427.2 G586G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CY-01A-11D-A32B-08 chr20:50701173 G>A maps to NM_199427.2 S620S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RW-01A-11D-A33T-08 chr20:50701716 C>T maps to NM_199427.2 E439E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:36884445 G>A maps to NM_133466.2 R266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:88598605 C>T maps to NM_153813.2 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TV-01A-12D-A34J-08 chr5:32407028 A>T maps to NM_016107.3 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7QY-01A-11D-A34A-08 chr5:32407028 A>T maps to NM_016107.3 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:3825225 A>G did not map to a codon.
Sequencing variant TCGA-DU-A76K-01A-11D-A33T-08 chr19:3825252 G>A maps to NM_015174.1 P396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:24197583 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:24197418 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:24228931 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:24227139 C>T did not map to a codon.
Sequencing variant TCGA-E1-5303-01A-01D-1468-08 chr23:24229262 C>T did not map to a codon.
Sequencing variant TCGA-TM-A84H-01A-11D-A36O-08 chr23:24197759 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:73441589 A>G maps to NM_021260.2 C628C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:79746289 G>A maps to NM_014733.3 L1089L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TY-01A-12D-A32B-08 chr15:41105572 C>T maps to NM_001077268.1 D356D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr14:104194141 G>A maps to ENST00000216602 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WE-01A-12D-A33T-08 chr14:68274235 C>T maps to NM_015346.3 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:99509275 G>A maps to NM_001002261.3 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr4:2306941 C>T maps to NM_020972.2 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TS-01A-11D-A289-08 chr16:2881940 C>A maps to NM_145252.2 Y136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:123964115 C>T maps to NM_014943.3 Y122Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YH-01A-11D-A34A-08 chr20:39831588 A>T maps to NM_015035.3 I656I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7602-01A-21D-2086-08 chr13:100637725 G>T maps to NM_007129.2 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A75K-01A-11D-A32B-08 chr23:136649635 C>T did not map to a codon.
Sequencing variant TCGA-QH-A65R-01A-21D-A31L-08 chr23:136651128 A>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:147113650 G>A maps to NM_001168379.1 R264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8185-01A-11D-2253-08 chr3:147108851 G>C maps to NM_001168379.1 R328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F4-01A-11D-A289-08 chr7:99631510 T>C maps to NM_003439.1 Y461Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:25263242 G>A maps to NM_001012981.4 N264N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7019-01A-11D-2024-08 chr16:25251835 G>A maps to NM_001012981.4 A735A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:28331479 A>G maps to NM_024493.2 K215K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WO-01A-21D-A34A-08 chr23:101138845 T>C did not map to a codon.
Sequencing variant TCGA-TQ-A7RN-01A-11D-A33T-08 chr23:101138797 T>C did not map to a codon.
Sequencing variant TCGA-E1-5303-01A-01D-1468-08 chr3:178748787 C>G did not map to a codon.
Sequencing variant TCGA-DU-8168-01A-11D-2253-08 chr7:44799775 C>T maps to NM_031449.3 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MX-01A-11D-A26M-08 chr13:20656934 C>T maps to NM_001190965.1 R1195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:70460820 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:70469914 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:70465907 C>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:70463818 G>A did not map to a codon.
Sequencing variant TCGA-FG-A60K-01A-11D-A29Q-08 chr23:70463797 C>T did not map to a codon.
Sequencing variant TCGA-HT-8104-01A-11D-2395-08 chr23:70464670 G>C did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr23:70464209 C>A did not map to a codon.
Sequencing variant TCGA-S9-A6WN-01A-12D-A33T-08 chr23:70469911 G>A did not map to a codon.
Sequencing variant TCGA-S9-A7QW-01A-11D-A34A-08 chr23:70469385 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:35857930 G>T maps to NM_005095.2 V902V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:35847202 C>T maps to NM_005095.2 C471C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr13:20398891 A>G maps to NM_001142684.1 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5144-01A-01D-1468-08 chr10:285430 A>G maps to NM_006624.4 Q221Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WM-01A-12D-A33T-08 chr9:140477530 C>G maps to NM_138462.2 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:21910279 T>C maps to NM_173531.3 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:64441792 C>T maps to NM_015852.3 K2K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RN-01A-11D-A33T-08 chr7:64439186 G>A maps to NM_015852.3 C254C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:6732107 A>G maps to ENST00000330442 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YO-01A-11D-A34A-08 chr5:43161368 T>C maps to ENST00000509156 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TY-01A-12D-A32B-08 chr19:58948510 T>C maps to NM_003433.3 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:58131537 T>C maps to NM_003435.3 H17H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:12297984 G>A maps to NM_003437.3 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:12298440 A>G maps to NM_003437.3 G416G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:19822990 G>A maps to NM_021030.2 R367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:133682648 A>T maps to NM_003440.2 R262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr11:9522710 C>T maps to NM_003442.5 H347H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6UA-01A-12D-A33T-08 chr11:9534058 C>T maps to NM_003442.5 D480D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:44495783 C>T maps to NM_003445.2 R34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6667-01A-12D-2024-08 chr23:47272248 A>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:47272856 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:47272258 A>C did not map to a codon.
Sequencing variant TCGA-DU-7294-01A-11D-2024-08 chr23:47269680 G>A did not map to a codon.
Sequencing variant TCGA-E1-A7YQ-01A-11D-A34J-08 chr23:47270080 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:146157521 G>T maps to NM_006958.2 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:53571785 A>G maps to NM_001102603.1 H667H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:53573044 G>A maps to NM_001102603.1 R248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8187-01A-11D-2253-08 chr6:28053479 C>T maps to NM_003447.3 C74C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:44611870 C>A maps to NM_018651.2 T423T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:52091536 G>A maps to NM_007147.2 S651S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:52091116 C>A maps to NM_007147.2 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CW-01A-11D-A32B-08 chr19:44982040 T>C maps to NM_013256.3 K219K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:47835671 T>G did not map to a codon.
Sequencing variant TCGA-HT-8010-01A-11D-2395-08 chr23:47836605 C>T did not map to a codon.
Sequencing variant TCGA-CS-4938-01B-11D-1893-08 chr23:152083047 T>C did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:152135743 G>T did not map to a codon.
Sequencing variant TCGA-TM-A7C3-01A-11D-A32B-08 chr6:28121481 C>A maps to NM_006298.2 S475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8161-01A-11D-2253-08 chr11:3380677 C>T maps to NM_001130520.1 K520K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5874-01A-11D-1705-08 chr3:44683422 G>A maps to NM_006991.3 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:3273915 G>T maps to NM_198088.2 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8165-01A-11D-2253-08 chr16:3282874 C>T maps to NM_198088.2 K99K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-5397-01A-01D-1893-08 chr11:123601197 C>A maps to NM_003455.2 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr11:123596989 C>T maps to NM_003455.2 A554A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr16:3169668 C>T maps to NM_001042428.1 Y336Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7688-01A-11D-2253-08 chr17:30696690 G>A maps to ENST00000394679 P469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6397-01A-11D-1705-08 chr19:22155222 T>C maps to NM_007153.3 K871K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CV-01A-11D-A31L-08 chr19:22171639 C>T maps to NM_007153.3 Q25Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:148947528 C>T maps to NM_012256.3 Q102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:3190966 G>A maps to NM_001134655.1 A333A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:7021899 G>A maps to NM_013249.2 D338D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:52198660 G>A maps to NM_006526.2 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A5TW-01A-11D-A289-08 chr19:44536348 G>A maps to NM_001129996.1 K214K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:44679882 C>T maps to NM_001032372.1 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IZ-01A-11D-A34A-08 chr19:44660573 G>A maps to NM_006630.2 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:74631730 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:74637347 C>T maps to NM_007345.3 R1287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:244218515 C>T maps to NM_205768.2 C480C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WY-A85D-01A-11D-A36O-08 chr1:244218426 C>T maps to NM_205768.2 Q451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:32919924 G>A maps to NM_006965.2 R146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:38241495 T>C maps to NM_145011.2 G310G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:145947655 G>A maps to NM_138367.1 C463C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:24310259 A>T maps to NM_203282.2 G486G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RF-01A-11D-A33T-08 chr19:24309233 G>A maps to NM_203282.2 Q144Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RQ-01A-11D-A33T-08 chr19:24310730 G>A maps to NM_203282.2 S643S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7873-01B-11D-2395-08 chr19:58453809 T>C maps to NM_005773.2 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:116652882 C>T maps to NM_003904.3 K390K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F1-01A-11D-A289-08 chr19:37005408 T>C maps to NM_001166038.1 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:9523992 T>C maps to NM_006631.2 R536R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:152612496 G>A did not map to a codon.
Sequencing variant TCGA-HW-8319-01A-11D-2395-08 chr23:152612568 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:89795645 C>T maps to NM_001113525.1 D363D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:111958313 A>G maps to NM_021994.2 E181E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-A5KJ-01A-12D-A27K-08 chr22:22869693 C>T maps to NM_080740.3 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7012-01A-11D-2024-08 chr22:22843525 C>T maps to NM_080764.2 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr23:129354411 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:129370552 G>T did not map to a codon.
Sequencing variant TCGA-HT-A5R7-01A-11D-A289-08 chr23:129354400 C>G did not map to a codon.
Sequencing variant TCGA-S9-A7R3-01A-11D-A34J-08 chr23:129370583 G>A did not map to a codon.
Sequencing variant TCGA-TQ-A7RJ-01A-11D-A33T-08 chr23:129370526 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:56923982 G>A maps to NM_017661.2 R885*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:16455235 G>T maps to NM_020653.2 T740T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:87943142 G>A maps to NM_015021.1 K213K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:87966301 T>G maps to NM_015021.1 G985G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8187-01A-11D-2253-08 chr21:43411482 G>A maps to NM_020727.4 L908L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YM-01A-11D-A34A-08 chr6:28963223 T>G maps to NM_001010877.2 R519R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:9271664 C>T maps to NM_020933.4 C448C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:9270911 C>T maps to NM_020933.4 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:43322514 G>A maps to NM_014345.2 R853*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:43316060 C>T did not map to a codon.
Sequencing variant TCGA-HT-7884-01B-11D-2395-08 chr16:58030900 C>T maps to NM_020807.1 A423A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:58640738 C>T maps to NM_024620.3 E44E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:54080794 C>T maps to NM_001079907.1 H327H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:45130707 G>A maps to NM_018102.3 R424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:44581338 G>A maps to NM_022095.3 P904P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84T-01A-11D-A36O-08 chr20:44577645 T>C maps to NM_022095.3 Q1325Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:25655667 T>C maps to NM_015655.2 *752W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64P-01A-11D-A29Q-08 chr10:43089023 T>C maps to NM_006955.1 V458V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6690-01A-11D-1893-08 chr10:43089128 G>A maps to NM_006955.1 Y423Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HW-8320-01A-11D-2395-08 chr10:43088768 A>G maps to NM_006955.1 H543H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:32379025 C>T maps to ENST00000375200 C756C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:37368418 T>G maps to NM_003419.3 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:53643863 G>A maps to NM_001172674.1 C740C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7634-01A-11D-2086-08 chr19:53652554 G>A maps to NM_001172674.1 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WQ-01A-12D-A34A-08 chr19:53644839 G>T maps to NM_001172674.1 S415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:44701409 C>T maps to NM_003420.3 R519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84O-01A-11D-A36O-08 chr19:52468456 G>A maps to ENST00000391795 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:178140503 A>C maps to NM_005649.2 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:178310184 T>C maps to NM_058230.2 C244C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CV-01A-11D-A31L-08 chr19:7585111 C>T maps to NM_018083.4 F328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr5:71739618 C>T maps to NM_152625.1 R733R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6UB-01A-21D-A33T-08 chr5:71756108 C>T maps to NM_152625.1 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:37733453 G>T maps to NM_152604.1 G106*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DH-A7UT-01A-12D-A34A-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:21462708 G>A maps to NM_024697.2 Y395Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A5R5-01A-11D-A289-08 chr7:99091496 G>A maps to NM_032164.2 C447C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:148876568 C>T maps to NM_170686.2 G535G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4942-01A-01D-1468-08 chr23:47307252 T>G did not map to a codon.
Sequencing variant TCGA-CS-5397-01A-01D-1893-08 chr23:47308565 G>T did not map to a codon.
Sequencing variant TCGA-DB-5274-01A-01D-1468-08 chr23:47307605 T>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:47307379 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:47308163 G>T did not map to a codon.
Sequencing variant TCGA-DU-8166-01A-11D-2253-08 chr23:47315319 C>A did not map to a codon.
Sequencing variant TCGA-FG-A70Z-01A-12D-A33T-08 chr23:47308232 G>T did not map to a codon.
Sequencing variant TCGA-HT-A5RA-01A-11D-A289-08 chr23:47307145 G>A did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr19:58084869 C>T maps to NM_017879.1 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:9639634 C>T maps to NM_024106.1 K362K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:21720456 G>A maps to NM_001001415.2 E534E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YV-01A-11D-A34J-08 chr19:21991521 T>A maps to NM_003423.2 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A5F4-01A-11D-A289-08 chr19:21216299 T>C maps to NM_025189.3 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:21366677 C>A maps to NM_133473.2 S524S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A845-01A-11D-A36O-08 chr19:12126625 G>A maps to NM_001080411.1 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:31137484 G>A maps to NM_182755.2 R617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:12383809 G>T maps to NM_001164276.1 P468P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:12383464 C>T maps to NM_001164276.1 K583K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:11892633 C>T maps to NM_152355.2 H665H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr19:11890885 G>T maps to NM_152355.2 G83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:12460634 T>C maps to NM_030824.2 R588R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A736-01A-11D-A32B-08 chr19:12460799 G>A maps to NM_030824.2 V533V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:12542574 T>C maps to NM_005815.4 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64V-01A-11D-A29Q-08 chr3:44496822 C>T maps to NM_181489.5 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:44489263 G>T maps to NM_181489.5 T633T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:44488738 A>G maps to NM_181489.5 H808H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:134494385 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:44419005 A>G maps to NM_003425.3 C194C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7015-01A-11D-2024-08 chr19:44417943 C>T maps to NM_003425.3 R548R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5872-01A-11D-1705-08 chr6:57012700 G>A maps to NM_001031623.2 W606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RR-01A-21D-A34A-08 chr5:178373364 G>A maps to NM_182594.2 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:109690566 A>G maps to NM_021224.4 L1458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-5307-01A-01D-1893-08 chr9:109689382 C>T maps to NM_021224.4 Q1064*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:57089729 G>T maps to NM_001001668.3 G645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:30409125 C>A maps to ENST00000495929 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:30409536 G>A maps to ENST00000495929 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:114289833 G>A maps to NM_133464.2 Q53Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7006-01A-11D-2024-08 chr19:11917409 G>A maps to NM_152356.3 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:247492712 G>A maps to NM_032752.1 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:44776048 G>T maps to NM_145044.2 G46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A4MT-01A-11D-A26M-08 chr10:77159073 C>T maps to NM_032772.4 A458A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:32844566 C>A maps to NM_014910.4 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:32844171 C>T maps to NM_014910.4 Q146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:32844254 C>T maps to NM_014910.4 H173H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:99521448 G>A maps to NM_014930.1 R555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:62591492 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:74091872 G>A maps to ENST00000443185 L733L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:10445300 A>C maps to NM_053042.2 L884L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7290-01A-11D-2024-08 chr18:14106370 C>T maps to NM_145287.3 E56E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:22805396 G>A maps to NM_015461.2 R829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:52909766 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:37038280 G>T maps to NM_001145649.1 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:56586802 C>T maps to NM_018181.4 V428V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr18:56586415 G>A maps to NM_018181.4 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-4941-01A-01D-1468-08 chr19:31038958 G>A maps to NM_014717.1 P811P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5847-01A-11D-1705-08 chr19:30935047 C>T maps to NM_014717.1 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:30935399 C>T maps to NM_014717.1 Q311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6692-01A-11D-1893-08 chr19:31040140 C>T maps to NM_014717.1 G1205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7882-01A-11D-2395-08 chr19:31040080 C>T maps to NM_014717.1 T1185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A4DS-01A-11D-A26M-08 chr19:31040263 G>A maps to NM_014717.1 A1246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A74O-01A-11D-A32B-08 chr19:30935437 C>T maps to NM_014717.1 H323H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:38103578 C>A maps to NM_152606.3 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:57888580 C>A maps to NM_173631.2 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:57888884 G>T maps to NM_173631.2 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CS-6188-01A-11D-1893-08 chr19:2852902 C>T maps to NM_152791.4 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YQ-01A-11D-A34J-08 chr19:7083502 C>G maps to NM_024341.2 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr19:9453654 C>T maps to NM_032497.1 R510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8011-01A-11D-2395-08 chr19:9578275 T>A maps to NM_152476.2 G449G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:12638452 G>A maps to NM_144976.3 R157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RY-A843-01A-11D-A36O-08 chr19:36674608 G>A maps to ENST00000355114 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:36940118 G>A maps to NM_001145343.1 Y340Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:37211221 C>A maps to ENST00000423498 P531P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A731-01A-11D-A32B-08 chr19:37903534 C>T maps to NM_152484.2 S675S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:125989976 T>C maps to NM_152412.2 I489I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:38230583 A>G maps to NM_001172690.1 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:42584572 C>A maps to ENST00000222339 Y695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A76R-01A-11D-A32B-08 chr19:42584407 C>G maps to ENST00000222339 P640P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5276-01A-01D-1468-08 chr19:56901870 C>T did not map to a codon.
Sequencing variant TCGA-DH-5141-01A-01D-1468-08 chr19:56895639 G>C maps to NM_144690.1 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:37644026 C>T maps to ENST00000356958 K258K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5279-01A-01D-1468-08 chr15:85326611 C>T maps to NM_014630.2 R236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:2051687 G>A maps to ENST00000431526 G303G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:2048277 G>A maps to ENST00000431526 D890D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:53270474 C>T maps to NM_198457.2 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:38190629 T>C maps to NM_032689.4 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:38190098 G>A maps to NM_032689.4 C311C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:53209368 T>C maps to NM_001161500.1 K313K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr9:116750642 C>T maps to ENST00000374126 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr9:116811426 C>T maps to ENST00000374126 Y615Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6405-01A-11D-1705-08 chr17:16527451 C>A maps to NM_020787.3 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:20808169 T>C maps to NM_001076675.2 K171K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:55994998 G>A maps to NM_033113.2 Q809Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7300-01A-21D-2086-08 chr23:47918327 A>C did not map to a codon.
Sequencing variant TCGA-FG-5963-01A-11D-1705-08 chr23:47920206 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr12:48741013 G>A maps to NM_001172682.1 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A66B-01A-11D-A29Q-08 chr1:91405998 G>T maps to NM_201269.1 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr1:91382482 G>A maps to NM_201269.1 R1286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7874-01A-11D-2395-08 chr23:22291313 G>A did not map to a codon.
Sequencing variant TCGA-HT-A615-01A-11D-A29Q-08 chr23:22291549 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:31088178 A>G maps to NM_014699.3 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6UA-01A-12D-A33T-08 chr16:31090149 C>T maps to NM_014699.3 G835G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:11597973 C>A did not map to a codon.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr9:40774425 G>A maps to NM_033160.5 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:53668764 G>T maps to NM_024733.3 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:53668593 G>A maps to NM_024733.3 F383F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:56953757 G>A maps to ENST00000342634 C330C. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DU-6392-01A-11D-1705-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:58232808 A>G maps to ENST00000335820 N215N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:58232136 G>A maps to ENST00000335820 H439H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TM-A84J-01A-11D-A36O-08 chr19:58232670 G>A maps to ENST00000335820 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:46322660 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:46360571 C>A did not map to a codon.
Sequencing variant TCGA-DH-A66B-01A-11D-A29Q-08 chr19:22363762 G>A maps to NM_001001411.2 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RM-01A-11D-A33T-08 chr19:22363969 G>T maps to NM_001001411.2 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:53740686 G>A maps to NM_182609.2 H431H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6WG-01A-11D-A33T-08 chr19:53747060 G>A maps to NM_182609.2 D35D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A780-01A-12D-A32B-08 chr19:23927679 T>C maps to NM_138286.2 K224K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:151261877 C>T maps to NM_020832.1 C832C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7T6-01A-11D-A33T-08 chr1:151262419 G>C maps to NM_020832.1 L967L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7681-01A-11D-2395-08 chr1:151258916 A>G maps to NM_020832.1 E50E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr1:151261050 C>T maps to NM_020832.1 S721S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KT-A7W1-01A-11D-A34A-08 chr19:12059660 G>A maps to NM_144566.1 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:37556059 C>A maps to NM_025069.1 P547P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:37555576 C>T maps to NM_025069.1 H386H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7676-01A-11D-2395-08 chr8:81577127 C>T maps to NM_001033723.2 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:144776282 C>T maps to NM_173831.3 C233C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr8:144775880 T>C maps to NM_173831.3 H99H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:21477089 A>G maps to NM_021269.2 C226C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RR-01A-21D-A34A-08 chr19:21492111 G>C maps to NM_021269.2 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:57133186 C>A maps to NM_021216.4 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6410-01A-11D-1893-08 chr19:57133635 G>A maps to NM_021216.4 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:90611595 C>T maps to NM_198526.2 C409C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr15:90610755 C>T maps to NM_198526.2 D129D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A6YH-01A-21D-A32B-08 chr15:90611148 T>G maps to NM_198526.2 G260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:84520138 T>A did not map to a codon.
Sequencing variant TCGA-DU-A5TU-01A-11D-A289-08 chr23:84525046 A>G did not map to a codon.
Sequencing variant TCGA-DH-5142-01A-01D-1468-08 chr7:56006945 A>C maps to NM_182633.1 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RG-01A-11D-A33T-08 chr7:57528832 T>C maps to NM_001159279.1 F222F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:437870 C>A maps to NM_133474.2 G129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:437124 A>G maps to NM_133474.2 N377N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5277-01A-01D-1468-08 chr17:80789718 G>C maps to NM_024702.2 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr17:80788323 G>A maps to NM_024702.2 C622C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:134421642 G>T did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:134424993 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:134421741 G>T did not map to a codon.
Sequencing variant TCGA-E1-5302-01A-01D-1468-08 chr6:35255506 C>A maps to NM_003427.3 S106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-8191-01A-11D-2253-08 chr19:53958930 C>G maps to NM_001008401.3 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6X9-01A-12D-A32B-08 chr19:53958523 C>T maps to NM_001008401.3 R255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6408-01A-11D-1705-08 chr19:53911500 G>A maps to NM_001040185.1 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-6688-01A-11D-1893-08 chr15:35274298 G>C maps to NM_014106.3 S446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:57988040 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:57987133 G>A maps to NM_001024596.2 D31D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:150094417 C>T maps to NM_173680.3 C283C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:58264657 G>T maps to ENST00000431353 *59Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:149129625 G>A maps to ENST00000440594 C580C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr7:149152972 A>G maps to ENST00000440594 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QH-A6CY-01A-11D-A32B-08 chr16:89293577 C>T maps to NM_182531.2 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:40581100 T>C maps to NM_001142577.1 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YK-01A-11D-A34A-08 chr19:37314665 T>G maps to NM_206894.2 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:12738654 C>A maps to NM_153358.2 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:12740022 C>A maps to NM_153358.2 A560A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:12735513 C>T maps to NM_153358.2 R61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-7008-01A-11D-2024-08 chr19:12739848 G>T maps to NM_153358.2 G502G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:12503016 A>G maps to NM_001080821.2 C65C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:12501582 C>T maps to NM_001080821.2 W543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:57755400 G>A maps to NM_001023563.3 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UU-01A-12D-A34A-08 chr23:47774901 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:47774562 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:47775286 C>T did not map to a codon.
Sequencing variant TCGA-FG-A60J-01A-11D-A289-08 chr23:47774743 T>C did not map to a codon.
Sequencing variant TCGA-DH-A66G-01A-21D-A31L-08 chr4:146823888 G>A maps to ENST00000508784 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr4:146824125 C>A maps to ENST00000508784 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7R4-01A-12D-A34J-08 chr13:115090945 A>G maps to NM_032436.2 P543P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:37383200 G>T maps to NM_001171979.1 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-8163-01A-11D-2253-08 chr19:53116800 G>A maps to NM_018300.3 H339H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7US-01A-11D-A33T-08 chr20:57782004 T>C maps to NM_178457.1 S1307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:57768128 C>T maps to NM_178457.1 S685S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr20:57766793 C>T maps to NM_178457.1 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P5-A72W-01A-11D-A32B-08 chr20:57768515 G>A maps to NM_178457.1 G814G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr19:57176020 C>T maps to NM_001005850.1 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:52569223 G>T maps to NM_001136499.1 Y637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:53856300 A>G maps to NM_138374.1 A791A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RW-01A-11D-A33T-08 chr19:9874045 G>A maps to NM_001077624.1 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:21131626 A>C maps to NM_003429.4 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:21131859 C>T maps to NM_003429.4 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R8-A6MK-01A-11D-A32B-08 chr3:32031029 T>C maps to NM_001137674.1 D153D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IK-8125-01A-11D-2253-08 chr19:12154972 G>A maps to NM_001080404.1 R462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:23544667 A>G maps to NM_003430.2 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7480-01A-11D-2086-08 chr19:22574656 T>C maps to NM_001098626.1 K460K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A6S8-01A-12D-A32B-08 chr19:22941744 A>G maps to ENST00000397104 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:64884243 C>T maps to NM_014205.2 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:86172137 G>A maps to NM_017953.3 R237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr22:29446490 C>T maps to NM_032173.2 Y674Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6IZ-01A-11D-A31L-08 chr19:5456173 C>T maps to NM_181710.3 V224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:60641121 C>T maps to NM_207341.2 G482G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr11:60638463 C>T maps to NM_207341.2 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-A7UU-01A-12D-A34A-08 chr16:21212760 G>T maps to NM_003460.1 V541V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A6J3-01A-11D-A31L-08 chr16:21218254 G>A maps to NM_003460.1 H129H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A6TS-01A-12D-A33T-08 chr16:21209104 C>A maps to NM_003460.1 E693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A4XH-01A-11D-A27K-08 chr1:238048464 C>T maps to NM_021186.3 P437P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7T6-01A-11D-A33T-08 chr1:238049137 G>A maps to NM_021186.3 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7474-01A-11D-2024-08 chr7:49977165 T>C maps to NM_007009.2 Q338Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-5871-01A-12D-1705-08 chr23:15827370 A>G did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:58549308 A>G maps to NM_182572.3 E35E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TD-01A-12D-A34A-08 chr19:58549410 C>G maps to NM_182572.3 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr16:3139433 G>A maps to NM_032805.1 C612C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S9-A7IS-01A-11D-A34A-08 chr16:3140075 C>T maps to NM_032805.1 A398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:28358596 A>G maps to ENST00000396827 I490I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr6:28093346 A>G maps to NM_025231.1 Q42Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr19:58596147 C>T maps to NM_001145542.1 P535P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FG-A87Q-01A-11D-A36O-08 chr15:85164511 C>T maps to NM_181877.3 Y362Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:33960017 G>T maps to NM_145238.3 E692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:33960238 C>A maps to NM_145238.3 P765P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7606-01A-11D-2086-08 chr1:33960424 T>G maps to NM_145238.3 P827P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E1-A7YH-01A-11D-A34A-08 chr7:99661834 A>G maps to NM_145914.2 K339K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:56734041 C>T maps to NM_024303.1 Q219Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7620-01A-11D-2253-08 chr19:56704395 C>T maps to NM_001080456.2 W9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-A61A-01A-11D-A29Q-08 chr19:56704283 A>G maps to NM_001080456.2 N46N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:44511608 C>T maps to NM_080603.4 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-5275-01A-01D-1468-08 chr2:187702142 G>A maps to NM_182521.2 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DH-5144-01A-01D-1468-08 chr2:187712477 C>T maps to NM_182521.2 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7860-01A-11D-2395-08 chr2:187693518 T>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr20:44506741 G>A maps to NM_080752.3 E515E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr19:13941041 T>C maps to NM_023072.2 Y716Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VW-A7QS-01A-12D-A33T-08 chr19:13941470 G>A maps to NM_023072.2 R859R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DB-A64U-01A-11D-A29Q-08 chr11:113608371 C>A maps to NM_004724.2 V646V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-A7TI-01A-11D-A33T-08 chr15:66813413 T>C maps to NM_017975.3 Y206Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr10:58118441 G>A maps to NM_032997.2 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr23:57936082 G>A did not map to a codon.
Sequencing variant TCGA-FG-7643-01A-11D-2086-08 chr23:57934556 C>T did not map to a codon.
Sequencing variant TCGA-RY-A83Z-01A-11D-A36O-08 chr23:57936019 C>T did not map to a codon.
Sequencing variant TCGA-RY-A83Z-01A-11D-A36O-08 chr23:57935759 G>A did not map to a codon.
Sequencing variant TCGA-DU-8158-01A-11D-2253-08 chr23:57620230 G>A did not map to a codon.
Sequencing variant TCGA-E1-A7YN-01A-11D-A34A-08 chr23:57619830 C>T did not map to a codon.
Sequencing variant TCGA-QH-A65X-01A-11D-A32B-08 chr23:57618945 G>A did not map to a codon.
Sequencing variant TCGA-S9-A6U1-01A-21D-A33T-08 chr23:57619096 G>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:126178580 C>A did not map to a codon.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr3:126178502 G>A maps to NM_025112.4 S735S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-7882-01A-11D-2395-08 chr17:3937517 G>A maps to NM_015113.3 N2125N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HT-8564-01A-11D-2395-08 chr17:3999983 C>T maps to NM_015113.3 T561T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TQ-A7RH-01A-12D-A34A-08 chr17:3974137 C>A maps to NM_015113.3 G1305G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DU-6392-01A-11D-1705-08 chr1:78041866 A>G maps to NM_015534.4 H739H. Only missense variants will be evaluated by CHASM.
