4957 NP_001070868 N771T not found in SNVbox database
5611 NP_001070868 F303V not found in SNVbox database
5997 NP_001070868 M45I not found in SNVbox database
725 NP_001070868 R346W not found in SNVbox database
1004 NP_001070868 S642L not found in SNVbox database
1132 NP_001070868 V60L not found in SNVbox database
1220 NP_001070868 S352C not found in SNVbox database
1987 NP_001070868 P786S not found in SNVbox database
2478 NP_001070868 R268Q not found in SNVbox database
2872 NP_001070868 P371S not found in SNVbox database
3333 NP_001070868 T674I not found in SNVbox database
4103 NP_001070868 I312M not found in SNVbox database
4260 NP_001070868 K773N not found in SNVbox database
4337 NP_001070868 P206T not found in SNVbox database
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr12:9264988 G>T maps to NM_000014.4 Y138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr3:151545575 G>T maps to NM_001086.2 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr2:69741752 C>T maps to NM_014911.3 Q542Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2I-01A-32D-A417-09 chr7:121716629 G>T maps to NM_005763.3 P898P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr17:67212427 G>T maps to NM_080282.3 S201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr2:215851336 G>T maps to NM_173076.2 L1364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr2:215851336 G>T maps to NM_173076.2 L1364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr7:48318054 G>T maps to NM_152701.3 E2422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr7:48443438 G>A maps to NM_152701.3 R4011R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZD-A8I3-01A-11D-A417-09 chr7:48327659 G>A maps to NM_152701.3 A2980A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2H-01A-31D-A417-09 chr16:2347793 G>A maps to NM_001089.2 I675I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr1:94486812 C>T maps to NM_000350.2 Q1667Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y4-01A-11D-A417-09 chr19:1052001 G>A maps to NM_019112.3 V1008V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZU-A8S4-01A-11D-A417-09 chr19:1065136 G>A maps to NM_019112.3 E2084E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr17:66878814 T>G maps to NM_007168.2 P1211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr2:169820751 A>C maps to NM_003742.2 V714V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr2:169792944 T>C did not map to a codon.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr2:169792944 T>C did not map to a codon.
Sequencing variant TCGA-ZH-A8Y8-01A-51D-A417-09 chr7:87053266 C>T maps to NM_018849.2 G722G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2H-01A-31D-A417-09 chr23:74375942 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr16:48249189 G>T maps to NM_032583.3 I339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr17:48745810 G>C maps to NM_003786.3 R601R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr17:48753043 C>A maps to NM_003786.3 R923R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y4-01A-11D-A417-09 chr13:95816667 G>T maps to NM_005845.3 V713V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr16:16315465 G>T maps to NM_001079528.3 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr12:22089572 T>C maps to NM_005691.2 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr23:153006140 T>A did not map to a codon.
Sequencing variant TCGA-ZU-A8S4-01A-11D-A417-09 chr4:89060946 G>T maps to NM_004827.2 I67I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA33-01A-11D-A417-09 chr1:179077424 G>A maps to NM_007314.3 L993L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr11:34194736 C>T maps to NM_145804.2 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W6-AA0S-01A-11D-A417-09 chr1:1237393 C>T maps to NM_030649.2 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y8-01A-51D-A417-09 chr14:23549703 C>A maps to NM_014977.3 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr17:40049389 G>A maps to ENST00000401700 A543A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr16:20448430 C>A maps to NM_017888.2 R456R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr16:20451132 A>C maps to NM_017888.2 A516A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr12:81536973 C>A maps to NM_024560.2 S290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W6-AA0S-01A-11D-A417-09 chr9:111625684 C>T maps to NM_006687.2 C361C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr1:236912524 G>A maps to NM_001103.2 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr1:236912524 G>A maps to NM_001103.2 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr7:152497655 T>C maps to NM_020445.4 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr12:52377792 C>A maps to NM_020328.3 T315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr4:175898004 C>T maps to NM_014269.4 C443C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr4:175898004 C>T maps to NM_014269.4 C443C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr8:38854668 G>T maps to NM_003816.2 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr9:136305516 T>G maps to NM_139025.3 P613P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr5:5318294 C>T maps to NM_139056.2 L1154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2H-01A-31D-A417-09 chr9:136404933 C>T maps to ENST00000393061 C226C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr7:140373609 G>A maps to NM_052853.3 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr1:167873152 G>T maps to NM_018417.4 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr2:25043664 G>A maps to NM_004036.3 H1060H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W6-AA0S-01A-11D-A417-09 chr14:24787681 G>A maps to NM_139247.3 C1058C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y1-01A-11D-A417-09 chr4:100125184 C>T did not map to a codon.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr10:76285054 G>T maps to NM_006721.2 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y5-01A-11D-A417-09 chr10:112838329 C>T maps to NM_000681.3 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr11:67051371 C>T maps to NM_001619.3 D481D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Z-01A-11D-A417-09 chr5:132232700 C>A maps to NM_014423.3 E541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr5:132219203 G>A maps to NM_014423.3 G1064G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-YR-A95A-01A-12D-A417-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr1:100346960 C>T maps to ENST00000311030 I706I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2R-01A-11D-A417-09 chr23:115303766 T>C did not map to a codon.
Sequencing variant TCGA-WD-A7RX-01A-12D-A417-09 chr23:115304156 A>T did not map to a codon.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr6:135763820 G>T maps to NM_017651.4 S604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2T-01A-12D-A417-09 chr5:434621 C>T maps to NM_020731.3 H611H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr2:61413902 G>T maps to ENST00000389584 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr6:143382349 G>T did not map to a codon.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr6:143382349 G>T did not map to a codon.
Sequencing variant TCGA-ZH-A8Y2-01A-11D-A417-09 chr7:6062934 G>T maps to NM_006303.3 V192V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr1:33476434 C>A did not map to a codon.
Sequencing variant TCGA-W5-AA2T-01A-12D-A417-09 chr6:151674610 G>T maps to NM_005100.3 P1695P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr7:91729134 G>A maps to NM_005751.4 L3616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr9:117105994 C>T maps to NM_030767.4 Q1250Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr1:19632583 G>T maps to NM_003689.2 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr13:52598852 G>A maps to NM_001004127.2 K329K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr2:73676230 G>T maps to NM_015120.4 A858A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr17:7976094 A>G maps to NM_001139.2 S700S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVE-01A-11D-A417-09 chr15:85400848 G>A maps to NM_020778.4 L1162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr9:116840381 A>G maps to NM_001633.3 N36N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr11:46564498 C>T maps to ENST00000458649 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr2:128628429 G>T maps to NM_031445.2 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WD-A7RX-01A-12D-A417-09 chr1:104160124 A>T maps to NM_000699.2 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr8:41550702 G>T maps to ENST00000415018 A1183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W6-AA0S-01A-11D-A417-09 chr8:41571688 C>T maps to ENST00000415018 P595P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr10:61994460 G>T maps to NM_020987.2 I294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr10:61900192 A>C did not map to a codon.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr17:4113217 T>G maps to NM_016376.3 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2W-01A-11D-A417-09 chr5:139885403 C>T maps to ENST00000253810 R1120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2R-01A-11D-A417-09 chr11:113270028 G>T maps to NM_178510.1 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2R-01A-11D-A417-09 chr11:113270028 G>T maps to NM_178510.1 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr12:133331414 G>T maps to NM_015114.1 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr11:67068426 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr11:67068426 G>T did not map to a codon.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr19:17435832 A>G maps to NM_020959.2 P1008P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr19:17435832 A>G maps to NM_020959.2 P1008P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WD-A7RX-01A-12D-A417-09 chr15:90336303 G>T maps to NM_001150.2 T737T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZD-A8I3-01A-11D-A417-09 chr2:69420522 G>T maps to NM_032208.2 V470V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA34-01A-11D-A417-09 chr15:60644600 G>A maps to NM_001002858.2 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr5:150484838 G>C maps to NM_001155.4 L602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVB-01A-31D-A417-09 chr19:50303256 C>T maps to NM_014203.2 Y435Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVA-01A-11D-A417-09 chr8:42015515 G>T maps to NM_006803.3 E111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr12:99106134 T>C maps to NM_181861.1 T960T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr5:112155041 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA2R-01A-11D-A417-09 chr1:154296075 T>G maps to NM_080429.2 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W6-AA0S-01A-11D-A417-09 chr2:241621969 G>A maps to NM_001102467.1 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVA-01A-11D-A417-09 chr5:115351065 T>A maps to NM_173800.4 I856I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr15:35185920 G>T maps to NM_014691.2 S838S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr15:35185920 G>T maps to NM_014691.2 S838S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2T-01A-12D-A417-09 chr23:66765909 G>A did not map to a codon.
Sequencing variant TCGA-ZH-A8Y2-01A-11D-A417-09 chr23:47426126 C>T did not map to a codon.
Sequencing variant TCGA-ZH-A8Y4-01A-11D-A417-09 chr23:47426126 C>T did not map to a codon.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr4:36152625 C>T maps to NM_015230.2 L931L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVB-01A-31D-A417-09 chr14:68114847 G>T maps to NM_001172.3 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y5-01A-11D-A417-09 chr10:99024581 C>T did not map to a codon.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr1:94650574 G>A maps to NM_004815.3 V654V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Z-01A-11D-A417-09 chr23:130218320 C>G did not map to a codon.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr4:106552106 C>G maps to ENST00000420470 Y187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2T-01A-12D-A417-09 chr2:131797698 C>G maps to NM_015320.2 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr13:111953839 C>A maps to ENST00000218789 T652T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr1:27106010 C>T maps to NM_006015.4 C1874C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr19:19162648 T>C maps to ENST00000392336 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr12:27573422 G>T maps to NM_020183.3 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2R-01A-11D-A417-09 chr23:2825479 G>A did not map to a codon.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr23:2836253 C>T did not map to a codon.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr23:2876370 C>G did not map to a codon.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr23:2945414 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr23:2945414 G>T did not map to a codon.
Sequencing variant TCGA-ZH-A8Y5-01A-11D-A417-09 chr11:3661208 G>T maps to NM_001079536.1 C150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr17:42248324 C>T maps to NM_080863.4 C56C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr10:73956735 G>A maps to NM_001198800.1 Q108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr16:29912807 C>T maps to NM_181718.3 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2T-01A-12D-A417-09 chr1:197115507 C>G maps to NM_018136.4 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZU-A8S4-01A-11D-A417-09 chr8:124340547 A>G maps to NM_014109.3 N1250N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr2:24118773 G>A maps to NM_017552.1 Q95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr1:1431001 C>A maps to NM_031921.4 P584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr1:1398006 C>T maps to NM_001039211.2 Y336Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr17:29220579 T>A maps to NM_024857.3 L1570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr19:50436093 C>T maps to NM_001193646.1 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2R-01A-11D-A417-09 chr1:161816250 G>A maps to NM_007348.2 Q400Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr12:14576920 G>A maps to NM_018179.3 Q24Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2I-01A-32D-A417-09 chr11:108218090 A>G maps to NM_000051.3 L2890L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZU-A8S4-01A-11D-A417-09 chr11:108115751 A>G maps to NM_000051.3 K300K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr12:7043190 G>T maps to NM_001940.3 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr12:7045884 A>G maps to NM_001940.3 Q485Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W6-AA0S-01A-11D-A417-09 chr13:113530135 C>T maps to NM_032189.3 L1070L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr23:138899054 A>G did not map to a codon.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr13:25274913 G>T maps to NM_001185085.1 E585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr19:19765460 G>A maps to NM_020410.2 H568H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WD-A7RX-01A-12D-A417-09 chr1:17316708 G>A maps to NM_022089.2 I775I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr3:194167664 G>A maps to NM_024524.3 C496C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr3:194152558 T>A maps to NM_024524.3 K770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr18:55336581 T>A maps to NM_005603.4 K689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr19:1811726 A>T maps to NM_138813.2 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr20:50290699 G>A maps to NM_006045.1 I343I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr10:116853363 C>T did not map to a codon.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr10:116853363 C>T did not map to a codon.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr22:46125304 A>G maps to NM_013236.3 R243R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZU-A8S4-01A-11D-A417-09 chr20:54963210 C>G did not map to a codon.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr17:63526144 C>A maps to NM_004655.3 V827V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr11:66114614 C>A maps to NM_006876.2 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVA-01A-11D-A417-09 chr11:76751603 T>C maps to ENST00000354301 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2W-01A-11D-A417-09 chr20:48256336 C>T maps to NM_004776.3 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WD-A7RX-01A-12D-A417-09 chr5:177035586 C>T maps to NM_007255.2 D229D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WD-A7RX-01A-12D-A417-09 chr5:177035586 C>T maps to NM_007255.2 D229D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVB-01A-31D-A417-09 chr11:117186289 G>T maps to NM_012104.3 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W6-AA0S-01A-11D-A417-09 chr21:11021152 G>A did not map to a codon.
Sequencing variant TCGA-W6-AA0S-01A-11D-A417-09 chr21:11021152 G>A did not map to a codon.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr8:143599536 C>T maps to NM_001702.2 I952I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2H-01A-31D-A417-09 chr22:38504286 C>T maps to NM_025045.4 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr3:52437804 G>A maps to NM_004656.2 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr3:52439929 T>C did not map to a codon.
Sequencing variant TCGA-W5-AA2W-01A-11D-A417-09 chr3:52440306 T>A maps to NM_004656.2 K249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr3:52440915 C>T maps to NM_004656.2 W196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr19:45262070 G>T maps to NM_005178.4 E384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr3:187439687 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr1:147096003 C>T maps to NM_004326.2 G1175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA34-01A-11D-A417-09 chr1:147084714 T>C maps to NM_004326.2 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr11:112065434 G>T maps to NM_031938.4 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr23:39933622 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr23:39933622 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr23:39921600 A>G did not map to a codon.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr5:70754622 C>A maps to NM_018429.2 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y1-01A-11D-A417-09 chr19:12865558 G>C maps to NM_017682.2 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr23:152771326 G>T did not map to a codon.
Sequencing variant TCGA-ZH-A8Y1-01A-11D-A417-09 chr2:127821522 C>T maps to NM_139343.1 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr2:32667183 T>C maps to NM_016252.3 V1332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y8-01A-51D-A417-09 chr2:32774510 C>T maps to NM_016252.3 L4369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr20:61870740 G>T maps to NM_139317.1 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr8:11415528 G>T maps to ENST00000427279 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr19:45683096 C>A maps to NM_212550.3 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr23:50659358 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr20:6759624 C>T maps to NM_001200.2 C360C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr4:79832211 C>A maps to NM_198892.1 L837L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr4:79832211 C>A maps to NM_198892.1 L837L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVE-01A-11D-A417-09 chr20:55777537 C>T maps to NM_001719.2 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr2:203383552 C>T maps to NM_001204.6 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr8:26240231 A>C did not map to a codon.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr6:3127474 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr13:32971138 G>A maps to NM_000059.3 P3202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Z-01A-11D-A417-09 chr16:50368661 C>A maps to NM_001173984.2 E283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr5:864588 C>T maps to NM_001009877.2 K543K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2R-01A-11D-A417-09 chr21:40668257 G>T maps to NM_018963.3 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr23:79946605 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr23:79941033 C>G did not map to a codon.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr11:62460155 G>A maps to NM_001130702.1 Y248Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr10:124036304 G>A maps to ENST00000368994 Q7Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr1:92573558 G>T did not map to a codon.
Sequencing variant TCGA-3X-AAVE-01A-11D-A417-09 chr6:26393053 T>C maps to NM_001197237.1 T477T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr6:26411340 A>G maps to NM_007048.5 G323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr5:180477172 C>G maps to NM_152547.4 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr10:103294589 G>T maps to NM_033637.2 G424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y2-01A-11D-A417-09 chr10:50396359 G>A maps to ENST00000374148 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr10:127429149 C>A maps to ENST00000356792 S700S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr10:99350106 T>C maps to NM_001009997.2 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr10:50530859 G>T maps to NM_001135196.1 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA33-01A-11D-A417-09 chr11:111796802 C>A maps to NM_080659.2 C84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr11:111385535 T>A maps to NM_207430.2 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr12:53700881 C>T maps to NM_021640.3 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y4-01A-11D-A417-09 chr14:91666202 C>T maps to NM_001102368.1 D466D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WD-A7RX-01A-12D-A417-09 chr16:4796982 C>T maps to NM_139170.2 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA34-01A-11D-A417-09 chr16:49412406 C>T maps to NM_144602.2 D99D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr17:79514061 A>C maps to NM_025161.5 T682T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr17:35746209 C>T maps to NM_173625.3 C221C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr19:41248652 A>T maps to NM_198476.3 A247A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-ZD-A8I3-01A-11D-A417-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-ZD-A8I3-01A-11D-A417-09 chr13:24895264 C>T maps to NM_178540.3 Q121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr12:7261801 G>T did not map to a codon.
Sequencing variant TCGA-ZH-A8Y2-01A-11D-A417-09 chr1:169796305 G>A maps to NM_018186.2 Q321Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr1:27278442 G>T maps to NM_152365.2 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr1:3807597 T>G maps to NM_207356.2 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr2:70392714 C>T maps to NM_017880.1 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr3:111828388 G>A did not map to a codon.
Sequencing variant TCGA-W5-AA33-01A-11D-A417-09 chr6:170179307 G>C maps to NM_018341.1 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVB-01A-31D-A417-09 chr7:148288050 G>T maps to NM_145304.2 E12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVE-01A-11D-A417-09 chr1:57409393 G>A maps to NM_000066.2 C403C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr9:74526742 G>A maps to NM_182505.3 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr9:136270412 G>A maps to NM_153710.3 K637K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2R-01A-11D-A417-09 chr17:49825139 G>T maps to NM_001082534.1 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZU-A8S4-01A-11D-A417-09 chr17:49710966 G>T maps to NM_001082534.1 I278I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2W-01A-11D-A417-09 chr1:181765856 G>T maps to ENST00000357570 E2088*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Z-01A-11D-A417-09 chr1:181686265 G>A maps to ENST00000357570 K451K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr1:181767936 G>A maps to ENST00000357570 L2303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr23:49062180 G>A did not map to a codon.
Sequencing variant TCGA-W5-AA33-01A-11D-A417-09 chr23:49079210 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA2H-01A-31D-A417-09 chr10:18690926 C>T maps to NM_201596.2 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr22:37098603 T>G maps to NM_006078.3 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVB-01A-31D-A417-09 chr7:71868297 G>A maps to NM_031468.3 D19D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Z-01A-11D-A417-09 chr19:16593512 C>T maps to NM_145046.3 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVE-01A-11D-A417-09 chr9:138703284 G>T maps to ENST00000409386 S1571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZU-A8S4-01A-11D-A417-09 chr12:67700163 C>T maps to NM_018448.3 Q906*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr11:34074071 C>T maps to NM_005898.4 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2W-01A-11D-A417-09 chr23:41469245 C>T did not map to a codon.
Sequencing variant TCGA-3X-AAVB-01A-31D-A417-09 chr5:96073606 G>T maps to ENST00000508830 E252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2W-01A-11D-A417-09 chr14:92105594 C>T did not map to a codon.
Sequencing variant TCGA-ZH-A8Y2-01A-11D-A417-09 chr17:42979873 G>T maps to NM_213607.1 G140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr7:31617534 G>T maps to NM_194300.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVB-01A-31D-A417-09 chr7:128446398 C>A maps to NM_022742.3 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr2:109405306 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr12:113593195 C>T maps to NM_001144872.1 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr17:80151669 C>T maps to ENST00000445854 Q271Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2H-01A-31D-A417-09 chr19:46511418 C>T maps to NM_001080402.1 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr12:123262118 C>T maps to NM_201435.3 R40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y8-01A-51D-A417-09 chr3:56653887 C>T maps to NM_001141947.1 R907*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr3:112357185 C>A maps to ENST00000447230 E534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W6-AA0S-01A-11D-A417-09 chr23:50085218 C>T did not map to a codon.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr2:62100223 A>T maps to NM_006430.2 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr7:56119583 C>A maps to NM_001762.3 R15R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA33-01A-11D-A417-09 chr22:17072591 G>T maps to NM_014406.4 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y1-01A-11D-A417-09 chr1:158152689 C>T maps to NM_001766.3 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y8-01A-51D-A417-09 chr19:35832641 G>T maps to NM_001771.3 G603G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr11:60780932 C>A maps to NM_006725.3 R397R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2I-01A-32D-A417-09 chr11:2416707 C>T maps to NM_004356.3 D139D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr1:193094240 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA33-01A-11D-A417-09 chr16:83520259 G>A maps to ENST00000268613 E320E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr20:44879705 C>A maps to NM_021248.1 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr10:73569790 C>T maps to ENST00000398860 L2984L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr20:58564140 T>C maps to NM_177980.2 I402I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZD-A8I3-01A-11D-A417-09 chr18:63489458 C>T maps to NM_004361.2 N256N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr5:26885774 G>T maps to NM_016279.3 G610G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y2-01A-11D-A417-09 chr5:176002398 C>A maps to NM_001171976.1 S247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2T-01A-12D-A417-09 chr23:18622315 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA2T-01A-12D-A417-09 chr23:18622315 G>T did not map to a codon.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr23:18638034 G>T did not map to a codon.
Sequencing variant TCGA-ZD-A8I3-01A-11D-A417-09 chr23:72674414 C>T did not map to a codon.
Sequencing variant TCGA-WD-A7RX-01A-12D-A417-09 chr1:15802635 C>T maps to ENST00000442979 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr18:34853024 G>A maps to NM_020180.3 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y2-01A-11D-A417-09 chr20:3765894 C>T maps to NM_001810.5 E412E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y5-01A-11D-A417-09 chr1:214818018 C>A maps to NM_016343.3 L1702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr20:34091509 C>T maps to NM_007186.3 L1771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr12:88530506 G>T maps to NM_025114.3 C118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr2:65299501 G>A maps to NM_015147.2 R424R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr2:65299501 G>A maps to NM_015147.2 R424R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W6-AA0S-01A-11D-A417-09 chr2:65309724 C>T maps to NM_015147.2 H720H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2I-01A-32D-A417-09 chr3:101451411 C>A maps to ENST00000327230 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr16:75339061 G>T maps to NM_006324.2 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr1:196759346 A>T maps to NM_021023.5 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr4:110663683 G>A maps to ENST00000394635 Y507Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr23:47487613 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr7:117232261 G>T maps to NM_000492.3 E681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y4-01A-11D-A417-09 chr1:146724302 G>T maps to NM_004284.3 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr17:7798769 C>T maps to NM_001005271.2 P598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr20:40161870 C>T maps to NM_032221.3 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr8:61734398 C>T maps to NM_017780.2 S916S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr14:21896184 G>T maps to NM_001170629.1 R482R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZD-A8I3-01A-11D-A417-09 chr16:53191284 A>G maps to ENST00000219084 S428S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr20:5903816 G>T maps to NM_001819.2 E343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2I-01A-32D-A417-09 chr1:203148987 G>A maps to NM_001276.2 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr3:383703 T>G maps to NM_006614.2 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr7:136700367 C>T maps to NM_001006628.1 D252D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2T-01A-12D-A417-09 chr1:240072088 A>C maps to NM_000740.2 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr17:7357772 T>C maps to NM_000747.2 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Z-01A-11D-A417-09 chr3:142840191 G>A maps to NM_004267.3 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr16:71571734 C>A maps to NM_001166395.1 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y2-01A-11D-A417-09 chr16:845948 G>A maps to ENST00000317063 V985V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr15:65489605 C>A maps to NM_003613.3 L1006L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr12:120135558 G>T maps to ENST00000392521 S1929S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr12:120135558 G>T maps to ENST00000392521 S1929S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZD-A8I3-01A-11D-A417-09 chr12:120172045 G>A maps to ENST00000392521 V1091V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y2-01A-11D-A417-09 chr12:106633700 C>A maps to NM_006825.3 E304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr3:33592748 G>T maps to ENST00000359576 R1059R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr23:10176630 G>A did not map to a codon.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr23:49840559 G>T did not map to a codon.
Sequencing variant TCGA-W6-AA0S-01A-11D-A417-09 chr23:49851057 G>A did not map to a codon.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr1:16383401 C>T maps to NM_000085.3 A685A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y8-01A-51D-A417-09 chr17:7164179 G>A maps to NM_001185022.1 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr4:141321604 G>T maps to NM_004362.2 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y5-01A-11D-A417-09 chr2:29404627 G>T maps to ENST00000379543 G665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr2:201718690 G>T maps to NM_001162407.1 R458R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr15:74922182 G>T maps to NM_001130028.1 E626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2T-01A-12D-A417-09 chr11:77336766 G>T maps to NM_001293.2 S120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr10:129676684 C>T did not map to a codon.
Sequencing variant TCGA-W5-AA33-01A-11D-A417-09 chr18:72251795 T>A maps to NM_032649.5 *508K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr23:21534641 G>C did not map to a codon.
Sequencing variant TCGA-W5-AA2I-01A-32D-A417-09 chr1:95364929 G>A maps to NM_001839.3 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2I-01A-32D-A417-09 chr1:95364929 G>A maps to NM_001839.3 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr9:17273831 T>C maps to NM_017738.2 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr11:100095500 C>A maps to NM_014361.2 T654T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y1-01A-11D-A417-09 chr3:1427410 C>T maps to NM_014461.2 S878S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr7:147964168 C>T maps to NM_014141.5 S1142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr17:7840510 T>G maps to NM_001037144.4 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y1-01A-11D-A417-09 chr17:71192845 G>A maps to NM_018714.2 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y1-01A-11D-A417-09 chr17:71192845 G>A maps to NM_018714.2 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr16:23415149 T>C maps to NM_153603.3 K556K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2W-01A-11D-A417-09 chr1:103455076 G>A maps to NM_080629.2 D809D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr10:105819418 G>T maps to NM_000494.3 S400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVE-01A-11D-A417-09 chr20:61944198 C>A maps to ENST00000326996 V670V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr8:139815132 C>T maps to NM_152888.1 K513K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVE-01A-11D-A417-09 chr9:116931157 G>T maps to NM_032888.2 R441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr7:7476073 C>G maps to NM_001037763.2 G604G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y8-01A-51D-A417-09 chr2:228148933 T>C maps to NM_000091.4 P918P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Z-01A-11D-A417-09 chr23:107842053 A>G did not map to a codon.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr23:107909788 G>A did not map to a codon.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr23:107909788 G>A did not map to a codon.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr9:137582890 G>A maps to NM_000093.3 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2T-01A-12D-A417-09 chr9:137710725 G>A maps to NM_000093.3 P1457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr9:137650126 C>T maps to NM_000093.3 G640G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y8-01A-51D-A417-09 chr2:238268787 C>T maps to NM_004369.3 P2075P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y4-01A-11D-A417-09 chr19:18901407 C>T maps to NM_000095.2 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y4-01A-11D-A417-09 chr19:18901407 C>T maps to NM_000095.2 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr1:160269047 G>A maps to NM_001098398.1 H567H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr15:49420220 G>A maps to NM_001143887.1 R427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVB-01A-31D-A417-09 chr2:232653435 G>T maps to NM_022730.1 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVB-01A-31D-A417-09 chr2:232653435 G>T maps to NM_022730.1 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZU-A8S4-01A-11D-A417-09 chr4:47625640 G>T maps to NM_006587.2 G829G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr3:148899804 A>C maps to NM_000096.3 T847T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr8:68658283 C>A maps to NM_020361.4 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr17:28750569 G>T maps to NM_001304.4 V568V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr2:211460257 G>A maps to NM_001122633.1 Q443Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr8:145618577 G>A maps to NM_013291.2 I1429I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr8:145623959 G>A maps to NM_013291.2 G569G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr20:2776023 C>A maps to NM_019609.4 E587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y2-01A-11D-A417-09 chr20:2777839 G>T maps to NM_019609.4 S277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr1:207643299 C>A maps to NM_001006658.2 R360R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr16:1675955 C>T did not map to a codon.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr16:1675955 C>T did not map to a codon.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr1:197313408 A>G did not map to a codon.
Sequencing variant TCGA-ZU-A8S4-01A-11D-A417-09 chr11:122733140 G>T did not map to a codon.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr5:149450019 T>C maps to NM_005211.3 R399R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr10:43659314 G>T maps to NM_018590.3 E328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr8:2886949 A>C maps to NM_033225.5 A2582A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZD-A8I3-01A-11D-A417-09 chr8:2976041 G>C maps to NM_033225.5 Y2103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVA-01A-11D-A417-09 chr1:33985236 C>A maps to ENST00000373381 E3553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr8:113349921 G>T maps to NM_198123.1 R2231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr13:37679177 G>T maps to NM_145203.5 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr15:75968448 G>T maps to NM_001897.4 P2137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr15:75968448 G>T maps to NM_001897.4 P2137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr15:75968340 C>T maps to NM_001897.4 V2173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y4-01A-11D-A417-09 chr10:68381521 G>T maps to NM_013266.2 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr20:36396409 G>A maps to NM_030877.3 Q238Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y4-01A-11D-A417-09 chr5:11199611 C>T maps to NM_001332.2 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr11:10785961 T>G maps to NM_014633.3 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y8-01A-51D-A417-09 chr11:65647689 G>A maps to NM_001335.3 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr1:112999055 A>G maps to NM_018704.2 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr10:17164816 A>G maps to NM_001081.3 C190C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y5-01A-11D-A417-09 chr10:17026202 G>A maps to NM_001081.3 Q1476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y1-01A-11D-A417-09 chr7:101845270 C>T maps to ENST00000360264 T909T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr12:111747905 C>A maps to NM_015267.3 P440P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y1-01A-11D-A417-09 chr10:124594544 G>A maps to NM_022034.4 I353I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y8-01A-51D-A417-09 chr11:107325250 T>C maps to NM_152434.2 K88K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr4:48988657 T>G did not map to a codon.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr23:105876174 G>T did not map to a codon.
Sequencing variant TCGA-WD-A7RX-01A-12D-A417-09 chr11:7686606 A>T maps to NM_016229.3 *277K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr23:37653033 T>G did not map to a codon.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr8:145151138 G>T maps to NM_001916.3 E147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr6:31975462 T>C maps to NM_000500.5 *316Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr6:31975462 T>C maps to NM_000500.5 *316Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVB-01A-31D-A417-09 chr19:41355848 A>G maps to NM_000762.5 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2W-01A-11D-A417-09 chr19:41628797 C>T maps to NM_000774.3 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr19:41633959 T>A maps to NM_000774.3 P483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr7:99247743 T>C maps to NM_000777.3 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2T-01A-12D-A417-09 chr1:47395906 C>T maps to ENST00000371904 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA33-01A-11D-A417-09 chr1:47608984 C>A maps to NM_001010969.2 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr1:47264866 G>A maps to NM_001099772.1 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr19:15651395 C>T maps to NM_173483.3 D269D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr19:15760953 C>A maps to NM_000896.2 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr23:77529103 A>G did not map to a codon.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr13:106142520 G>C did not map to a codon.
Sequencing variant TCGA-W5-AA33-01A-11D-A417-09 chr2:136664944 A>G maps to NM_001349.2 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr12:2062322 T>C maps to NM_152640.3 Q261Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr12:2062322 T>C maps to NM_152640.3 Q261Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr12:2062322 T>C maps to NM_152640.3 Q261Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr8:30013851 C>G did not map to a codon.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr11:47256384 A>G maps to NM_000107.2 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr1:20979148 G>T maps to NM_005216.4 R396R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2H-01A-31D-A417-09 chr12:31242072 T>C maps to NM_030653.3 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr12:31256768 G>A maps to NM_030653.3 *907*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W6-AA0S-01A-11D-A417-09 chr17:62496865 G>T maps to NM_004396.3 I414I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr23:23018969 G>A did not map to a codon.
Sequencing variant TCGA-W5-AA2I-01A-32D-A417-09 chr11:674556 G>A maps to NM_021008.2 H494H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2I-01A-32D-A417-09 chr11:674556 G>A maps to NM_021008.2 H494H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y8-01A-51D-A417-09 chr8:6873577 G>A maps to NM_004084.3 C73C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA33-01A-11D-A417-09 chr7:140246697 G>T maps to NM_015689.3 A693A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr8:142160983 G>T maps to NM_014957.2 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA33-01A-11D-A417-09 chr1:153907308 C>T maps to NM_014856.2 Q900Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y4-01A-11D-A417-09 chr11:33054929 G>T maps to NM_001077242.1 E489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr2:179325878 G>T maps to NM_001042702.3 G313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr22:20073624 G>T maps to NM_022720.6 E47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr3:186038224 G>T maps to NM_001346.2 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr3:186038224 G>T maps to NM_001346.2 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WD-A7RX-01A-12D-A417-09 chr19:49447640 G>T maps to NM_014475.3 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr6:30638650 C>T maps to NM_003587.4 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr6:30638650 C>T maps to NM_003587.4 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr23:96048620 C>A did not map to a codon.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr23:96212894 G>A did not map to a codon.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr23:96212894 G>A did not map to a codon.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr10:387245 G>T maps to NM_014974.2 A1159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y5-01A-11D-A417-09 chr19:49878125 C>T maps to NM_014419.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr11:111933225 G>A maps to NM_001931.4 K637K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr11:84865695 C>A did not map to a codon.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr1:35370531 C>G maps to NM_001080418.1 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr6:170597855 C>A maps to NM_005618.3 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr6:170597585 T>G did not map to a codon.
Sequencing variant TCGA-W5-AA2Z-01A-11D-A417-09 chr1:44684373 G>T maps to NM_019100.4 E223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr22:38917698 C>A maps to NM_007068.2 G289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr23:32519900 G>T did not map to a codon.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr23:32519900 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA2I-01A-32D-A417-09 chr23:32361349 A>T did not map to a codon.
Sequencing variant TCGA-ZH-A8Y5-01A-11D-A417-09 chr9:22451583 G>T maps to NM_022160.2 G397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr15:51766721 C>T maps to NM_001174116.1 L2344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr10:70206163 G>A maps to NM_001080449.1 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr7:21630879 G>A maps to NM_003777.3 L784L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2R-01A-11D-A417-09 chr17:7661811 G>T did not map to a codon.
Sequencing variant TCGA-W6-AA0S-01A-11D-A417-09 chr17:7630468 G>T maps to NM_020877.2 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZD-A8I3-01A-11D-A417-09 chr17:7705317 C>A maps to NM_020877.2 L2985L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr5:13859643 C>A maps to NM_001369.2 E1623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA33-01A-11D-A417-09 chr5:13919409 G>A maps to NM_001369.2 R284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y1-01A-11D-A417-09 chr2:196759762 T>C maps to NM_018897.2 P1611P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVA-01A-11D-A417-09 chr16:4497002 G>T maps to NM_005147.4 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr16:4484494 G>T maps to NM_005147.4 E108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr11:73679406 A>G maps to NM_153614.2 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2W-01A-11D-A417-09 chr1:15886124 T>C maps to NM_015291.2 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2W-01A-11D-A417-09 chr1:15886124 T>C maps to NM_015291.2 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr1:15855657 C>T maps to NM_015291.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr21:34860753 A>C maps to NM_001040192.1 L316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr1:65855272 C>T maps to ENST00000371069 Y477Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr23:153631920 A>G did not map to a codon.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr16:2287817 G>C maps to NM_001374.2 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr10:101716492 G>T maps to ENST00000342239 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2T-01A-12D-A417-09 chr23:117777437 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr6:31938790 C>A maps to NM_005510.3 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr11:66258757 G>A maps to NM_005700.3 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2I-01A-32D-A417-09 chr2:162875263 C>A maps to NM_001935.3 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y4-01A-11D-A417-09 chr19:32968451 G>A maps to NM_001172774.1 V574V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2R-01A-11D-A417-09 chr1:111663215 G>A maps to NM_178454.4 Q147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr4:9783916 T>C maps to NM_000798.4 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr18:28710754 C>T did not map to a codon.
Sequencing variant TCGA-W5-AA2R-01A-11D-A417-09 chr21:41452121 T>C maps to NM_001389.3 P1459P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-W5-AA2O-01A-11D-A417-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-WD-A7RX-01A-12D-A417-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-WD-A7RX-01A-12D-A417-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-WD-A7RX-01A-12D-A417-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-WD-A7RX-01A-12D-A417-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-ZH-A8Y2-01A-11D-A417-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-3X-AAVA-01A-11D-A417-09 chr1:205132931 G>A maps to NM_015375.2 V492V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Z-01A-11D-A417-09 chr1:205132086 C>T maps to NM_015375.2 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr17:7129306 C>T maps to NM_004422.2 V696V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Z-01A-11D-A417-09 chr12:4700464 G>A did not map to a codon.
Sequencing variant TCGA-W5-AA2T-01A-12D-A417-09 chr3:121575995 C>A maps to NM_018456.4 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr8:25716015 G>T maps to NM_022659.2 Y449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr13:78492578 C>A maps to ENST00000377211 E134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr12:93226361 C>A maps to NM_003566.3 E394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y2-01A-11D-A417-09 chr6:8097529 G>T maps to NM_004280.4 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr3:128060584 G>A maps to NM_021937.3 R432R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA34-01A-11D-A417-09 chr17:42937900 C>A maps to NM_004247.3 E540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y2-01A-11D-A417-09 chr5:38407066 T>C maps to ENST00000354891 A322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZU-A8S4-01A-11D-A417-09 chr7:55249089 C>T maps to NM_005228.3 G796G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr2:31457586 C>T maps to NM_014600.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr11:65767102 C>T maps to NM_032325.2 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr7:2411438 C>A maps to ENST00000314800 R548R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr2:233422640 T>G maps to NM_004846.2 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr22:31854516 C>A maps to NM_019843.3 G303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr2:100007023 G>C maps to NM_015904.3 G868G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr19:8056615 A>T maps to ENST00000351593 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVB-01A-31D-A417-09 chr23:129205392 G>T did not map to a codon.
Sequencing variant TCGA-3X-AAVB-01A-31D-A417-09 chr23:129205392 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr23:129201165 C>A did not map to a codon.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr23:47496462 C>G did not map to a codon.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr5:95236432 A>G maps to NM_012081.5 P306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr7:73470730 C>A maps to ENST00000358929 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr7:73474784 T>C maps to ENST00000358929 G602G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr7:73474787 T>C maps to ENST00000358929 V603V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y5-01A-11D-A417-09 chr5:60060156 G>T maps to NM_024930.2 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y2-01A-11D-A417-09 chr2:42483695 T>C maps to NM_019063.3 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr4:71510218 G>T maps to NM_031889.2 E1026*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr13:43930058 C>T maps to NM_001127615.1 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2T-01A-12D-A417-09 chr8:120602790 A>G maps to NM_006209.3 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr10:97599459 C>T maps to NM_001098175.1 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr12:132547143 G>A maps to ENST00000333577 Q2780Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2T-01A-12D-A417-09 chr12:132514440 C>T maps to ENST00000333577 F1895F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y5-01A-11D-A417-09 chr12:132547143 G>A maps to ENST00000333577 Q2780Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr5:111594967 G>A maps to NM_022140.3 H251H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr2:120925068 C>A maps to NM_020909.3 R664R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZU-A8S4-01A-11D-A417-09 chr2:120861692 C>T maps to NM_001184938.1 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr1:16462175 T>A maps to NM_004431.3 K468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr12:91371910 G>T maps to NM_004950.4 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVB-01A-31D-A417-09 chr9:5825097 G>T maps to NM_024896.2 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr17:62142631 A>G maps to NM_001433.3 V286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr12:53677188 C>T maps to NM_012291.4 Q982*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr8:95655628 T>C maps to NM_017697.3 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr23:103495186 C>A did not map to a codon.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr12:56524867 A>G maps to NM_001184796.1 K204K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr1:157062557 G>T maps to NM_001004341.2 G323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr1:157062557 G>T maps to NM_001004341.2 G323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr17:74003246 C>T maps to NM_001988.2 A2013A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVE-01A-11D-A417-09 chr15:41483651 T>C maps to NM_152596.2 Q226Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr4:56759747 A>G maps to NM_018261.3 K585K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr8:28573667 G>A maps to NM_001440.2 W31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y8-01A-51D-A417-09 chr6:66005907 G>T maps to ENST00000370616 S624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr6:159197490 G>T maps to NM_001111077.1 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr4:187194272 G>T maps to NM_000128.3 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr4:187194272 G>T maps to NM_000128.3 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y2-01A-11D-A417-09 chr5:76128776 C>T maps to NM_005242.4 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVA-01A-11D-A417-09 chr23:154194708 G>A did not map to a codon.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr23:138642997 A>G did not map to a codon.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr12:50294990 C>A maps to NM_012306.2 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2H-01A-31D-A417-09 chr1:207087179 G>A maps to NM_005449.4 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr11:58893429 A>G maps to NM_198947.3 V620V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr23:133938243 G>T did not map to a codon.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr2:201846199 G>T maps to NM_173822.3 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr23:134166534 C>A did not map to a codon.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr1:16385006 C>T maps to NM_182623.2 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr6:71195945 A>G maps to NM_020819.4 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y1-01A-11D-A417-09 chr5:177434137 G>A did not map to a codon.
Sequencing variant TCGA-ZD-A8I3-01A-11D-A417-09 chr5:10227606 G>T maps to NM_199133.2 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZU-A8S4-01A-11D-A417-09 chr2:29274736 C>T maps to NM_199280.2 S946S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr4:2698242 C>T maps to ENST00000324666 Q853*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr23:37028704 A>T did not map to a codon.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr16:67572724 G>T maps to NM_001193523.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr6:24836026 G>A maps to NM_014722.2 T725T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr6:24836026 G>A maps to NM_014722.2 T725T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2I-01A-32D-A417-09 chr7:128315769 T>C maps to NM_001012454.3 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y8-01A-51D-A417-09 chr1:78272786 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr15:38776826 T>A maps to NM_173611.2 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZD-A8I3-01A-11D-A417-09 chr6:5545473 C>T maps to NM_006567.3 I322I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr11:92532859 T>C maps to ENST00000298047 P2227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Z-01A-11D-A417-09 chr11:92534617 C>A maps to ENST00000298047 V2813V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr19:40331278 G>A maps to NM_001436.3 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2I-01A-32D-A417-09 chr5:127624881 C>A maps to NM_001999.3 G2192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2W-01A-11D-A417-09 chr9:37537627 G>T maps to NM_012166.2 R300R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr1:224345384 A>G maps to NM_015176.2 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr6:153296424 A>G maps to NM_012177.3 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr5:72378650 A>T maps to NM_138782.2 G748G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr5:108382828 C>A maps to NM_005246.2 P618P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr2:97370410 T>C maps to NM_001113382.1 L2088L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2H-01A-31D-A417-09 chr8:125081640 G>T maps to NM_001039112.2 G1253G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr8:125110055 T>G maps to NM_001039112.2 T1605T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr8:124989719 G>T maps to NM_001039112.2 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVE-01A-11D-A417-09 chr7:19184751 C>T maps to NM_152898.2 E78E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr7:19184745 C>T maps to NM_152898.2 E80E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr7:19184745 C>T maps to NM_152898.2 E80E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr20:6093270 C>T did not map to a codon.
Sequencing variant TCGA-ZH-A8Y5-01A-11D-A417-09 chr19:35850646 C>T maps to NM_005304.3 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr23:76709750 G>A did not map to a codon.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr3:99568866 G>C maps to NM_001042459.1 T551T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr4:54257251 G>A maps to NM_030917.3 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y8-01A-51D-A417-09 chr14:24600886 G>T maps to NM_203402.2 G39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr19:18648518 C>T maps to NM_012181.3 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVE-01A-11D-A417-09 chr19:47258781 G>A maps to NM_024301.4 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr1:152283923 G>A maps to NM_002016.1 H1146H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVB-01A-31D-A417-09 chr23:153595858 C>A did not map to a codon.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr3:58095322 C>T maps to NM_001164317.1 S740S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVB-01A-31D-A417-09 chr3:58090843 C>T maps to NM_001164317.1 Q550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Z-01A-11D-A417-09 chr7:128496612 G>T maps to NM_001458.4 V2431V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA34-01A-11D-A417-09 chr13:28631552 C>A maps to NM_004119.2 G139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr13:28610127 C>A maps to NM_004119.2 S454S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr1:240371624 G>A maps to ENST00000406993 A1314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr1:240374461 T>A maps to ENST00000406993 L1474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr1:240371321 C>T maps to ENST00000406993 P1213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WD-A7RX-01A-12D-A417-09 chr1:240371687 A>T maps to ENST00000406993 G1335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WD-A7RX-01A-12D-A417-09 chr1:240371687 A>T maps to ENST00000406993 G1335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr2:216243984 G>A maps to NM_212482.1 S1830S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVE-01A-11D-A417-09 chr13:49719948 C>A maps to NM_001079673.1 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr11:71850155 C>A maps to ENST00000442948 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr3:71179759 G>T maps to ENST00000491238 Y25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y1-01A-11D-A417-09 chr11:126139307 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr4:79204118 C>A maps to NM_025074.6 S418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y5-01A-11D-A417-09 chr13:39454560 C>T maps to NM_207361.4 S3049S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr5:132561380 T>G maps to NM_015082.1 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr6:37441250 T>C maps to NM_015050.2 T565T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr15:91421360 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr7:90894458 A>G maps to NM_003505.1 Q88Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y1-01A-11D-A417-09 chr2:208632293 G>T maps to NM_003468.3 C390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y8-01A-51D-A417-09 chr4:46930464 G>T maps to NM_000809.2 S481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y1-01A-11D-A417-09 chr2:171702543 G>T maps to NM_000817.2 E325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVB-01A-31D-A417-09 chr23:49179681 C>T did not map to a codon.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr7:151802438 C>T maps to NM_022087.2 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr7:151818668 C>T maps to NM_022087.2 C578C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr2:31168694 G>A maps to NM_024572.2 N232N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2R-01A-11D-A417-09 chr2:31178585 A>T maps to NM_024572.2 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr12:89916733 C>T maps to NM_003774.4 W531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr7:151680103 G>A maps to NM_145292.3 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr4:173804048 C>T maps to NM_001034845.2 I344I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr9:128094334 G>T maps to NM_015635.2 V768V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr9:128094334 G>T maps to NM_015635.2 V768V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr9:130026086 G>A did not map to a codon.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr7:30662039 C>T maps to NM_002047.2 C525C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr7:30662039 C>T maps to NM_002047.2 C525C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W6-AA0S-01A-11D-A417-09 chr3:81539563 C>T maps to ENST00000264326 P701P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA34-01A-11D-A417-09 chr10:104123465 G>T did not map to a codon.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr1:89650996 A>T maps to NM_052941.4 T621T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2H-01A-31D-A417-09 chr1:89616211 G>T maps to NM_207398.2 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2W-01A-11D-A417-09 chr12:120622661 G>T maps to NM_006836.1 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr6:10621587 T>C maps to NM_145649.4 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZD-A8I3-01A-11D-A417-09 chr23:153667149 T>C did not map to a codon.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr11:76954812 G>A maps to ENST00000376217 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr17:40344492 C>A maps to NM_032484.4 E219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y5-01A-11D-A417-09 chr2:233708928 G>A maps to ENST00000373566 Q1043Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y4-01A-11D-A417-09 chr7:150389905 C>T maps to NM_015660.2 R178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVE-01A-11D-A417-09 chr1:39340248 G>T maps to NM_030772.4 R508R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr2:220102657 G>T maps to NM_024506.3 R455R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr2:220102657 G>T maps to NM_024506.3 R455R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr11:134188523 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr16:74526936 C>T maps to NM_012201.5 R384R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2H-01A-31D-A417-09 chr2:121732607 G>T maps to NM_005270.4 E431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WD-A7RX-01A-12D-A417-09 chr9:4286059 A>G maps to NM_001042413.1 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr23:14748366 C>T did not map to a codon.
Sequencing variant TCGA-WD-A7RX-01A-12D-A417-09 chr23:14708891 G>C did not map to a codon.
Sequencing variant TCGA-ZH-A8Y2-01A-11D-A417-09 chr12:110295407 G>T maps to NM_016433.3 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA33-01A-11D-A417-09 chr19:48198731 G>C did not map to a codon.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr22:19808753 G>T maps to NM_053004.2 S42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr1:150667290 G>T maps to ENST00000369003 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr1:204170900 C>A maps to NM_198447.1 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr1:155732106 C>A maps to ENST00000368331 R1595R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2H-01A-31D-A417-09 chr1:217604609 T>C maps to NM_018040.2 R488R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2H-01A-31D-A417-09 chr1:217604609 T>C maps to NM_018040.2 R488R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr23:133119349 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr23:133119349 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA2R-01A-11D-A417-09 chr6:24448364 G>A maps to NM_001503.2 C506C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr23:13801542 C>A did not map to a codon.
Sequencing variant TCGA-ZH-A8Y4-01A-11D-A417-09 chr6:46977649 G>T maps to ENST00000283297 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2H-01A-31D-A417-09 chr10:134916322 G>A maps to ENST00000368577 P667P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2H-01A-31D-A417-09 chr4:22390065 G>T maps to NM_145290.2 P1076P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr12:131476786 C>A maps to NM_198827.3 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr3:154055682 C>T maps to NM_001038705.1 G667G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVA-01A-11D-A417-09 chr3:169802125 G>T maps to NM_014373.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2T-01A-12D-A417-09 chr1:168073857 G>T maps to NM_153832.1 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVE-01A-11D-A417-09 chr2:128407627 A>G maps to NM_005291.2 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVA-01A-11D-A417-09 chr17:36483727 C>T maps to ENST00000398597 L1909L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr17:36489223 G>A maps to ENST00000398597 D650D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr17:36491144 C>T maps to ENST00000398597 Q473Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W6-AA0S-01A-11D-A417-09 chr17:36495365 G>T maps to ENST00000398597 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr7:124404433 C>T maps to NM_005302.2 K199K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA34-01A-11D-A417-09 chr23:19021008 T>C did not map to a codon.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr16:57719584 C>T maps to NM_170776.4 Y429Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr5:89948369 A>G maps to NM_032119.3 V1208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr5:89948369 A>G maps to NM_032119.3 V1208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr5:90079723 A>G maps to NM_032119.3 L4501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr23:101910212 A>G did not map to a codon.
Sequencing variant TCGA-ZH-A8Y4-01A-11D-A417-09 chr17:72436466 C>T maps to NM_022036.2 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr2:11735402 G>T maps to NM_014668.3 E575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr2:11720941 G>T maps to NM_014668.3 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr6:102124679 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr9:140053111 G>T maps to ENST00000371546 E406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr16:9857877 C>A maps to NM_000833.3 E1175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVA-01A-11D-A417-09 chr10:121184541 G>T maps to NM_005308.2 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr19:47423516 C>A maps to NM_004491.4 R529R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr7:86394779 G>T maps to NM_000840.2 E107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr11:88323784 G>T maps to NM_001143831.2 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA34-01A-11D-A417-09 chr7:126086279 C>A maps to NM_001127323.1 V859V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr8:130777903 C>T maps to NM_031415.2 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y2-01A-11D-A417-09 chr19:42737288 A>G maps to NM_019884.2 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr7:73927157 A>G did not map to a codon.
Sequencing variant TCGA-W6-AA0S-01A-11D-A417-09 chr9:135564266 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr4:156632289 G>T maps to NM_001130684.1 E325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr23:108641913 C>A did not map to a codon.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr7:65425889 A>G maps to NM_000181.3 F650F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr23:2799128 G>A did not map to a codon.
Sequencing variant TCGA-3X-AAVE-01A-11D-A417-09 chr20:23349408 T>C maps to NM_022482.3 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr1:9305082 G>T maps to NM_004285.3 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr1:9305082 G>T maps to NM_004285.3 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr16:777489 G>A did not map to a codon.
Sequencing variant TCGA-W5-AA2T-01A-12D-A417-09 chr15:89424837 C>T maps to NM_178232.2 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr16:69148715 G>T maps to NM_005329.2 R403R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr16:69148715 G>T maps to NM_005329.2 R403R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2T-01A-12D-A417-09 chr19:613927 C>T maps to NM_001194.3 S634S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr23:48661353 A>C did not map to a codon.
Sequencing variant TCGA-ZH-A8Y4-01A-11D-A417-09 chr1:156714047 G>A maps to NM_001126050.1 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr19:4493797 T>C maps to ENST00000301284 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2I-01A-32D-A417-09 chr23:83581278 C>A did not map to a codon.
Sequencing variant TCGA-W5-AA2I-01A-32D-A417-09 chr23:83581278 C>A did not map to a codon.
Sequencing variant TCGA-ZH-A8Y1-01A-11D-A417-09 chr23:83723900 A>C did not map to a codon.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr7:814754 C>A maps to NM_017802.3 S732*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr16:50118141 T>C maps to NM_182922.2 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y2-01A-11D-A417-09 chr23:65476100 C>T did not map to a codon.
Sequencing variant TCGA-ZH-A8Y1-01A-11D-A417-09 chr11:93834377 G>T maps to NM_001098672.1 E818*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Z-01A-11D-A417-09 chr15:63967057 G>T maps to ENST00000261887 G2443G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W6-AA0S-01A-11D-A417-09 chr10:69785434 T>A did not map to a codon.
Sequencing variant TCGA-ZH-A8Y4-01A-11D-A417-09 chr1:222715436 G>T maps to NM_024746.3 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr22:19344492 G>A maps to NM_003325.3 L772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr22:19373052 A>G maps to NM_003325.3 D440D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVA-01A-11D-A417-09 chr6:27776313 G>A maps to NM_003509.2 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr6:27107239 C>A maps to NM_003495.2 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr6:29693308 C>T maps to NM_001098479.1 V324V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr1:185902702 G>T maps to NM_031935.2 V525V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZD-A8I3-01A-11D-A417-09 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr1:120302535 T>A maps to NM_005518.3 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2W-01A-11D-A417-09 chr19:1068618 C>T maps to NM_012292.2 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr19:8528545 C>T maps to NM_005968.3 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr4:57547690 T>C did not map to a codon.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr7:27210429 T>G did not map to a codon.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr17:46622341 T>C did not map to a codon.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr17:46673136 G>A did not map to a codon.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr2:177016417 G>T maps to NM_014621.2 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr2:176993749 T>C maps to ENST00000313266 K52K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr11:18313247 G>A maps to NM_181507.1 C727C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr4:84222114 G>T maps to NM_006665.5 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA33-01A-11D-A417-09 chr10:100481427 G>A maps to NM_021828.4 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2T-01A-12D-A417-09 chr4:11401503 G>A maps to NM_005114.2 R42R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr6:114379056 G>T maps to NM_153612.3 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2W-01A-11D-A417-09 chr14:102548745 G>A maps to NM_001017963.2 C719C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2W-01A-11D-A417-09 chr14:102548745 G>A maps to NM_001017963.2 C719C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr6:44221322 A>G maps to NM_007355.2 E721E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y2-01A-11D-A417-09 chr4:128743938 C>T maps to ENST00000438626 Q640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr5:137894310 C>A maps to NM_004134.6 V482V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr3:122459461 G>A maps to NM_024610.4 S399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr1:22214553 G>A maps to NM_005529.5 Q194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr4:70918807 C>T maps to NM_002159.2 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2R-01A-11D-A417-09 chr2:231973539 G>T maps to NM_000867.4 V379V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr11:113813744 G>A maps to NM_006028.3 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr11:113813744 G>A maps to NM_006028.3 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y4-01A-11D-A417-09 chr4:3076695 T>G maps to NM_002111.6 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr23:53570920 C>A did not map to a codon.
Sequencing variant TCGA-W5-AA34-01A-11D-A417-09 chr3:50332982 C>T maps to NM_003549.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr16:71015306 G>A maps to NM_032821.2 P1498P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2R-01A-11D-A417-09 chr12:21526360 G>T maps to NM_000415.2 E26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA33-01A-11D-A417-09 chr1:23885890 G>T maps to NM_002167.3 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y8-01A-51D-A417-09 chr1:158985756 G>T maps to ENST00000295809 E121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Z-01A-11D-A417-09 chr2:27702378 G>A maps to NM_015662.1 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr20:42264631 G>A maps to NM_016004.2 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr15:99460003 C>T maps to NM_000875.3 C700C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr3:185542733 A>C maps to NM_006548.4 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr6:160511103 A>C maps to NM_000876.2 G2208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr11:133802004 G>A maps to NM_014987.1 V357V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y8-01A-51D-A417-09 chr23:155232672 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA34-01A-11D-A417-09 chr2:131103673 C>A maps to NM_033416.1 Y226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y8-01A-51D-A417-09 chr14:105180790 G>T maps to ENST00000252520 E1098*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WD-A7RX-01A-12D-A417-09 chr7:30793365 G>A maps to NM_006774.4 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W6-AA0S-01A-11D-A417-09 chr15:41297826 G>T maps to NM_017553.1 S1154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr16:30007576 G>A did not map to a codon.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr16:30007576 G>A did not map to a codon.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr10:121587135 T>A maps to NM_014937.2 V1081V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr4:106604262 G>T maps to NM_020395.3 S339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Z-01A-11D-A417-09 chr17:59981822 G>T maps to NM_020748.2 V443V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZD-A8I3-01A-11D-A417-09 chr8:95841227 G>T maps to NM_017864.2 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y1-01A-11D-A417-09 chr13:98671934 C>A maps to NM_002271.4 I997I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y2-01A-11D-A417-09 chr13:98652791 G>A did not map to a codon.
Sequencing variant TCGA-3X-AAVB-01A-31D-A417-09 chr16:19745075 G>T maps to NM_153208.1 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr15:90972898 G>T did not map to a codon.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr3:10268071 C>T maps to NM_001570.3 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr5:3599508 C>T maps to NM_024337.3 H149H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr15:76632809 C>A maps to NM_145805.1 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVB-01A-31D-A417-09 chr15:74427080 C>T maps to NM_001130137.1 G662G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr15:74425466 G>A maps to NM_001130137.1 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr22:35481518 C>T maps to NM_001008494.1 Q191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr19:18548726 G>A maps to NM_016368.4 I21I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr10:15649687 G>A maps to NM_003638.1 I584I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVA-01A-11D-A417-09 chr16:31372508 G>T maps to NM_000887.3 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr17:45368458 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr2:160964273 G>A maps to NM_000888.3 C728C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr12:53588034 C>A maps to NM_000889.1 E419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W6-AA0S-01A-11D-A417-09 chr12:26755322 G>A maps to NM_002223.2 L1220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W6-AA0S-01A-11D-A417-09 chr12:26755370 G>A maps to NM_002223.2 Q1204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W6-AA0S-01A-11D-A417-09 chr12:26755404 G>A maps to NM_002223.2 L1192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W6-AA0S-01A-11D-A417-09 chr12:26755634 G>C maps to NM_002223.2 S1156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2T-01A-12D-A417-09 chr10:106074384 G>A maps to NM_033397.2 H475H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr1:152883127 C>G maps to NM_005547.2 Y285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Z-01A-11D-A417-09 chr1:152883025 G>A maps to NM_005547.2 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA34-01A-11D-A417-09 chr2:128284020 G>A did not map to a codon.
Sequencing variant TCGA-W5-AA34-01A-11D-A417-09 chr2:128284020 G>A did not map to a codon.
Sequencing variant TCGA-W5-AA2W-01A-11D-A417-09 chr5:146970682 C>T did not map to a codon.
Sequencing variant TCGA-W6-AA0S-01A-11D-A417-09 chr5:147029993 G>C maps to NM_014790.3 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr10:64966862 T>A maps to NM_032776.1 V1522V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr10:64968448 T>G maps to NM_032776.1 R994R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr17:40266619 G>T maps to NM_021078.2 I674I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr2:85280313 G>T maps to NM_020122.4 E310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZD-A8I3-01A-11D-A417-09 chr3:156175300 C>A maps to NM_172159.3 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr12:75436134 G>A maps to NM_139136.2 V600V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr12:49935524 C>T maps to NM_012284.1 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y1-01A-11D-A417-09 chr12:49948259 G>T maps to NM_012284.1 E687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr19:48967865 C>T maps to NM_170720.1 F381F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr14:90650698 C>T maps to NM_022054.2 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y4-01A-11D-A417-09 chr6:39285609 G>T maps to NM_032115.3 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y2-01A-11D-A417-09 chr6:39278777 G>A maps to NM_031460.3 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVE-01A-11D-A417-09 chr11:64064726 C>T maps to ENST00000422670 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr11:64060510 G>A maps to ENST00000422670 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr10:78704652 G>T maps to NM_001161352.1 S927*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr3:178560604 G>A maps to NM_005832.3 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Z-01A-11D-A417-09 chr19:18092606 C>T maps to ENST00000222249 C213C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y5-01A-11D-A417-09 chr1:154842332 C>T maps to NM_002249.4 Q36Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr8:36793038 G>T maps to NM_001031836.2 V1017V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr8:36675276 G>T maps to NM_001031836.2 E369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr9:2718783 C>T maps to NM_133497.2 Q349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr2:27310210 G>A maps to NM_006488.2 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WD-A7RX-01A-12D-A417-09 chr4:6863222 G>T maps to NM_014743.2 E372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr14:75179686 G>T maps to ENST00000338772 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr14:75179686 G>T maps to ENST00000338772 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVB-01A-31D-A417-09 chr9:114133912 C>T maps to NM_001080398.1 T1753T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2T-01A-12D-A417-09 chr5:5463257 C>T maps to NM_015325.1 Q1271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr15:79750675 G>A maps to NM_015206.2 S729S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr4:123210345 T>C maps to NM_015312.3 S3129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y4-01A-11D-A417-09 chr4:123107279 G>T maps to NM_015312.3 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2I-01A-32D-A417-09 chr15:81212523 T>A maps to NM_018689.1 L629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WD-A7RX-01A-12D-A417-09 chr1:109714601 C>T maps to NM_020775.3 Y194Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y8-01A-51D-A417-09 chr2:61319610 G>A maps to NM_001129993.1 W367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr3:113376106 C>T maps to NM_001009899.2 Q1474Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZD-A8I3-01A-11D-A417-09 chr3:113376106 C>T maps to NM_001009899.2 Q1474Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZU-A8S4-01A-11D-A417-09 chr9:6007400 G>A maps to NM_001017969.2 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y4-01A-11D-A417-09 chr5:132070087 G>T maps to ENST00000403231 S30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr18:30260288 C>T maps to NM_020805.1 G477G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVE-01A-11D-A417-09 chr1:173743533 A>G maps to NM_014458.3 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2W-01A-11D-A417-09 chr19:51518100 G>T maps to NM_001077500.1 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr19:51585889 G>T maps to NM_022046.4 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y8-01A-51D-A417-09 chr19:51412608 C>T maps to NM_004917.3 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr1:47013132 C>T did not map to a codon.
Sequencing variant TCGA-ZH-A8Y8-01A-51D-A417-09 chr17:8274669 G>T maps to NM_213597.2 Y61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVA-01A-11D-A417-09 chr16:3016344 C>A maps to NM_172229.1 C127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr12:53070969 T>G did not map to a codon.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr12:53294403 C>A maps to NM_002273.3 E220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZD-A8I3-01A-11D-A417-09 chr21:46020607 C>T maps to ENST00000380102 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr21:31709644 C>T maps to NM_001077711.1 Q114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr17:39334272 C>G maps to ENST00000458321 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr17:39324094 G>A maps to NM_033187.1 C110C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr11:1651114 A>G maps to NM_001001480.2 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Z-01A-11D-A417-09 chr17:39389205 C>T maps to NM_031962.2 Y151Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr19:35978353 C>T maps to NM_207392.1 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y4-01A-11D-A417-09 chr1:62672855 G>T maps to NM_019079.4 G186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr6:129588264 G>A maps to NM_000426.3 R741R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr6:129588264 G>A maps to NM_000426.3 R741R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr18:21513817 C>T maps to ENST00000416669 C2929C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr6:112510360 G>T maps to NM_001105206.1 C255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Z-01A-11D-A417-09 chr1:183093838 C>T maps to NM_002293.3 C825C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Z-01A-11D-A417-09 chr1:183093838 C>T maps to NM_002293.3 C825C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr9:133942410 C>A maps to ENST00000355048 P804P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr3:45500305 A>T maps to NM_015340.3 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr1:152785257 G>A maps to NM_178349.1 Q112Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA34-01A-11D-A417-09 chr10:98708963 C>T maps to NM_001170765.1 N50N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr10:88477867 G>T maps to NM_001171610.1 P613P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr19:11230845 T>C maps to NM_000527.4 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVA-01A-11D-A417-09 chr4:109086280 G>A maps to NM_016269.4 H84H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2T-01A-12D-A417-09 chr10:95557553 C>T maps to NM_005097.2 S556S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W6-AA0S-01A-11D-A417-09 chr17:33310392 G>T maps to NM_013975.3 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr19:55106238 G>A maps to NM_006863.1 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVA-01A-11D-A417-09 chr19:55146733 G>A maps to ENST00000427581 Q578Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA34-01A-11D-A417-09 chr19:55179364 G>A maps to ENST00000391733 Q415Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr12:50625493 C>T did not map to a codon.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr2:109150328 A>G did not map to a codon.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr1:145498116 T>G maps to NM_153713.1 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2I-01A-32D-A417-09 chr5:126156634 G>T maps to NM_005573.3 V398V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZU-A8S4-01A-11D-A417-09 chr7:123303793 C>T maps to NM_207163.1 R547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr3:100170609 G>A maps to ENST00000489752 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr13:28122524 G>A maps to NM_153371.3 Q674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr9:91266947 C>T did not map to a codon.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr9:91266947 C>T did not map to a codon.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr8:23198668 T>G maps to NM_002318.2 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2I-01A-32D-A417-09 chr4:62845390 G>T maps to ENST00000506720 G972G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr2:11913796 C>T maps to ENST00000396099 N222N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr2:11913796 C>T maps to ENST00000396099 N222N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2H-01A-31D-A417-09 chr18:2923828 C>T maps to NM_014646.2 Q706Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y4-01A-11D-A417-09 chr23:114357149 T>C did not map to a codon.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr8:105510176 G>A maps to NM_013437.4 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr2:141128374 G>T maps to NM_018557.2 R3638R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2T-01A-12D-A417-09 chr2:141528561 G>A maps to NM_018557.2 C1838C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2T-01A-12D-A417-09 chr2:141528561 G>A maps to NM_018557.2 C1838C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WD-A7RX-01A-12D-A417-09 chr12:12300323 G>T maps to NM_002336.2 R1125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr6:53764613 G>T maps to NM_018214.4 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y5-01A-11D-A417-09 chr3:46563074 G>T maps to NM_024512.3 R335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr7:127669003 G>T maps to NM_022143.4 R564R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr12:122685441 G>T maps to NM_001098519.1 V590V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr12:122685441 G>T maps to NM_001098519.1 V590V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2I-01A-32D-A417-09 chr17:17907738 C>T maps to NM_031294.3 C354C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y1-01A-11D-A417-09 chr15:71341746 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr1:165513518 T>C did not map to a codon.
Sequencing variant TCGA-W6-AA0S-01A-11D-A417-09 chr11:56949738 G>A maps to NM_001005210.2 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2T-01A-12D-A417-09 chr1:70504281 T>C maps to NM_020794.2 P887P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr1:90049513 T>C maps to NM_015350.2 N435N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2T-01A-12D-A417-09 chr8:86022347 A>T did not map to a codon.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr8:86038932 G>T maps to NM_033402.4 E428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZD-A8I3-01A-11D-A417-09 chr2:238683053 A>G maps to ENST00000391999 A577A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA34-01A-11D-A417-09 chr12:40668731 G>T maps to NM_198578.3 L626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr10:68686685 T>C maps to NM_178011.3 N4N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr2:77745439 A>G maps to NM_024993.4 *519R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr2:33540336 G>T did not map to a codon.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr15:100272029 C>T maps to NM_152449.2 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y5-01A-11D-A417-09 chr13:36048561 T>G did not map to a codon.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr23:152482527 T>G did not map to a codon.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr23:152482527 T>G did not map to a codon.
Sequencing variant TCGA-3X-AAVA-01A-11D-A417-09 chr23:27840134 C>T did not map to a codon.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr23:140994601 A>T did not map to a codon.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr23:140995728 C>A did not map to a codon.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr23:140984708 C>A did not map to a codon.
Sequencing variant TCGA-W5-AA2I-01A-32D-A417-09 chr23:51640333 A>T did not map to a codon.
Sequencing variant TCGA-W5-AA33-01A-11D-A417-09 chr23:51640346 A>G did not map to a codon.
Sequencing variant TCGA-W5-AA33-01A-11D-A417-09 chr23:51640346 A>G did not map to a codon.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr23:51644871 C>A did not map to a codon.
Sequencing variant TCGA-ZH-A8Y1-01A-11D-A417-09 chr23:51639968 A>G did not map to a codon.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr23:75650879 A>T did not map to a codon.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr23:55479370 T>G did not map to a codon.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr9:139754377 C>A maps to ENST00000392881 G1161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2W-01A-11D-A417-09 chr11:95825220 C>T maps to NM_032427.1 Q658Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr11:95825220 C>T maps to NM_032427.1 Q658Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr11:95825406 C>T maps to NM_032427.1 Q596Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZD-A8I3-01A-11D-A417-09 chr11:95825253 C>T maps to NM_032427.1 Q647Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y2-01A-11D-A417-09 chr11:95825253 C>T maps to NM_032427.1 Q647Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y8-01A-51D-A417-09 chr11:95825253 C>T maps to NM_032427.1 Q647Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr4:140811119 C>T maps to ENST00000509479 Q490Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr1:26079973 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA2R-01A-11D-A417-09 chr23:43652719 C>T did not map to a codon.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr5:71491849 G>T maps to NM_005909.3 E890*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y4-01A-11D-A417-09 chr5:71491936 G>T maps to NM_005909.3 G919*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr5:56178365 C>T maps to NM_005921.1 F1113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W6-AA0S-01A-11D-A417-09 chr17:61767702 C>T maps to NM_203351.1 D412D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr2:102490596 C>A maps to NM_145686.2 R978R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2H-01A-31D-A417-09 chr22:50694523 G>T maps to NM_002969.3 Y203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y8-01A-51D-A417-09 chr15:52338591 G>T did not map to a codon.
Sequencing variant TCGA-ZH-A8Y8-01A-51D-A417-09 chr15:52338591 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA2T-01A-12D-A417-09 chr4:164466874 G>T maps to ENST00000514618 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr19:8486774 C>T maps to NM_016496.4 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr5:10402697 G>A maps to NM_005885.2 W392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr19:45790747 G>T maps to NM_031417.3 T440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr5:66427644 A>G maps to NM_001164664.1 G653G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y4-01A-11D-A417-09 chr19:3778216 G>A maps to NM_002378.3 A497A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2H-01A-31D-A417-09 chr20:43932931 G>T maps to ENST00000372754 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVA-01A-11D-A417-09 chr16:29821449 A>G maps to NM_002383.2 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y2-01A-11D-A417-09 chr23:131526198 G>T did not map to a codon.
Sequencing variant TCGA-3X-AAVB-01A-31D-A417-09 chr11:119181067 C>T maps to NM_006500.2 P634P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr3:182756843 T>A maps to NM_020166.3 T449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr20:5974194 G>T maps to NM_032485.4 E762*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr12:69229764 G>T did not map to a codon.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr6:84061832 G>T maps to NM_002395.4 R130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2H-01A-31D-A417-09 chr23:70349588 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA2T-01A-12D-A417-09 chr12:116399130 G>T maps to NM_015335.4 C2191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2T-01A-12D-A417-09 chr11:57472099 G>T maps to NM_153450.1 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr1:156450643 C>T maps to NM_005920.2 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVE-01A-11D-A417-09 chr22:42191437 T>C maps to NM_152513.3 S1186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr2:112656267 T>G did not map to a codon.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr4:99916972 C>A maps to NM_015143.2 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr15:42046765 G>A did not map to a codon.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr5:180219932 G>T maps to NM_001114617.1 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA34-01A-11D-A417-09 chr12:86373132 C>T maps to ENST00000393205 R486R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr16:4733263 C>T maps to NM_015246.2 Q508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr12:16516727 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr19:41281790 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr6:109769502 C>T maps to NM_022765.3 V586V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr22:18379579 A>C maps to NM_015241.2 T372T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr23:10422988 C>A did not map to a codon.
Sequencing variant TCGA-ZU-A8S4-01A-11D-A417-09 chr7:7625409 G>T maps to NM_019005.3 E598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr17:56293484 G>T maps to NM_017777.3 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr17:56293484 G>T maps to NM_017777.3 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr3:158315943 G>T maps to NM_001195432.1 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr4:185638301 A>T maps to NM_024629.3 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVB-01A-31D-A417-09 chr7:151891213 C>G did not map to a codon.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr7:151921113 A>T maps to ENST00000355193 C1103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2I-01A-32D-A417-09 chr7:151921113 A>T maps to ENST00000355193 C1103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr7:151921113 A>T maps to ENST00000355193 C1103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y2-01A-11D-A417-09 chr7:151921113 A>T maps to ENST00000355193 C1103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr7:104719313 C>T maps to NM_182931.2 F384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr9:20414312 G>A maps to NM_004529.2 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr6:168307885 T>C maps to ENST00000400822 S561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2R-01A-11D-A417-09 chr1:2540787 G>A maps to NM_033467.3 C175C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr11:102592252 G>A maps to NM_002424.2 H167H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y1-01A-11D-A417-09 chr18:33831178 C>T maps to NM_017947.2 G699G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZD-A8I3-01A-11D-A417-09 chr23:14936833 C>A did not map to a codon.
Sequencing variant TCGA-W5-AA2T-01A-12D-A417-09 chr6:132645228 T>A maps to NM_015529.2 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr9:13176149 G>T maps to ENST00000319217 P972P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr9:13176275 A>G maps to ENST00000319217 T930T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr10:28413007 G>A maps to NM_173496.3 N189N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr10:28413007 G>A maps to NM_173496.3 N189N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr6:84772625 G>T maps to NM_138409.2 G48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y4-01A-11D-A417-09 chr11:3249153 G>A maps to ENST00000328215 D292D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr11:18955599 C>T maps to NM_147199.3 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr2:86437739 C>T maps to NM_016622.3 Y172Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y4-01A-11D-A417-09 chr17:36453188 A>C maps to NM_032351.3 R14R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr12:27863844 C>T maps to NM_021821.3 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr1:19584344 A>G maps to NM_016183.3 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y1-01A-11D-A417-09 chr11:10597536 C>T did not map to a codon.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr11:60561563 C>T maps to NM_206893.3 Y160Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr11:60152622 C>A maps to NM_206939.1 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr23:64956742 A>G did not map to a codon.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr23:64958960 G>A did not map to a codon.
Sequencing variant TCGA-ZH-A8Y1-01A-11D-A417-09 chr23:64949501 C>A did not map to a codon.
Sequencing variant TCGA-W5-AA34-01A-11D-A417-09 chr23:149818339 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr23:149814335 G>A did not map to a codon.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr5:7885966 G>T maps to NM_024010.2 G380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WD-A7RX-01A-12D-A417-09 chr19:9090830 A>G maps to NM_024690.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y4-01A-11D-A417-09 chr19:9090830 A>G maps to NM_024690.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Z-01A-11D-A417-09 chr7:100681473 A>G maps to NM_001040105.1 S2259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Z-01A-11D-A417-09 chr7:100681509 T>C maps to NM_001040105.1 T2271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr11:1092842 C>G maps to ENST00000441003 G1554G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr11:1092842 C>G maps to ENST00000441003 G1554G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZD-A8I3-01A-11D-A417-09 chr11:1092614 C>T maps to ENST00000441003 S1478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZD-A8I3-01A-11D-A417-09 chr11:1092614 C>T maps to ENST00000441003 S1478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr3:195509558 G>A maps to NM_018406.5 T2964T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2I-01A-32D-A417-09 chr3:195508970 T>C maps to NM_018406.5 S3160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr3:195508901 C>G maps to NM_018406.5 T3183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr3:195512372 G>T maps to NM_018406.5 S2026S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZD-A8I3-01A-11D-A417-09 chr3:195512267 G>A maps to NM_018406.5 D2061D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y2-01A-11D-A417-09 chr3:195509126 A>G maps to NM_018406.5 T3108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y2-01A-11D-A417-09 chr3:195509126 A>G maps to NM_018406.5 T3108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y4-01A-11D-A417-09 chr3:195505862 G>A maps to NM_018406.5 T4196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y8-01A-51D-A417-09 chr3:195505862 G>A maps to NM_018406.5 T4196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr11:1255535 G>T did not map to a codon.
Sequencing variant TCGA-ZH-A8Y1-01A-11D-A417-09 chr11:1269860 A>G maps to ENST00000447027 T3920T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr9:113449409 C>A maps to ENST00000189978 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVB-01A-31D-A417-09 chr20:42315649 C>A maps to NM_002466.2 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr12:102061630 C>T maps to NM_002465.2 S826S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr13:77672822 A>C maps to NM_015057.4 P2822P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr22:36717866 C>A did not map to a codon.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr7:44179934 C>T maps to ENST00000457314 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2T-01A-12D-A417-09 chr3:123339081 C>T maps to NM_053025.3 P1780P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2T-01A-12D-A417-09 chr3:123339081 C>T maps to NM_053025.3 P1780P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr3:123332737 T>C did not map to a codon.
Sequencing variant TCGA-W6-AA0S-01A-11D-A417-09 chr2:171371509 C>T maps to NM_138995.3 C1150C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr18:3067472 T>A maps to NM_003803.3 S1615S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr12:57113582 G>T maps to NM_001113203.1 S577S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr4:164050117 A>G maps to NM_138386.2 P472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr4:164050117 A>G maps to NM_138386.2 P472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr4:164050123 T>G maps to NM_138386.2 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr4:164050123 T>G maps to NM_138386.2 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA34-01A-11D-A417-09 chr4:164050123 T>G maps to NM_138386.2 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA34-01A-11D-A417-09 chr4:164050123 T>G maps to NM_138386.2 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVB-01A-31D-A417-09 chr7:105894815 G>T maps to NM_005746.2 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZD-A8I3-01A-11D-A417-09 chr1:201749555 G>T maps to ENST00000367296 E412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr11:19890523 C>A maps to ENST00000396087 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W6-AA0S-01A-11D-A417-09 chr12:78520945 G>T did not map to a codon.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr2:204000455 G>T maps to NM_001114132.1 V1261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2R-01A-11D-A417-09 chr2:106471557 C>T maps to NM_001004720.2 Y13Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2T-01A-12D-A417-09 chr8:71068238 C>T maps to NM_006540.2 E787E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr20:46279832 G>A maps to NM_181659.2 Q1253Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2T-01A-12D-A417-09 chr20:46279832 G>A maps to NM_181659.2 Q1253Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr20:46279832 G>A maps to NM_181659.2 Q1253Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr12:124839410 C>T maps to NM_006312.4 L1159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr13:52684524 C>A maps to NM_199289.1 G140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVE-01A-11D-A417-09 chr10:5496409 A>G maps to NM_001047160.1 K317K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y2-01A-11D-A417-09 chr2:242757380 G>A maps to NM_001167599.1 W167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr20:44518855 A>C did not map to a codon.
Sequencing variant TCGA-3X-AAVB-01A-31D-A417-09 chr17:7232438 G>A maps to NM_032442.2 Q65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2I-01A-32D-A417-09 chr2:182542720 C>T maps to NM_002500.2 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr22:30054253 G>T did not map to a codon.
Sequencing variant TCGA-W6-AA0S-01A-11D-A417-09 chr22:30064436 T>G did not map to a codon.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr1:204956668 G>A did not map to a codon.
Sequencing variant TCGA-W5-AA2T-01A-12D-A417-09 chr7:26224871 G>T maps to NM_004289.6 G518G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr7:26224961 T>C maps to NM_004289.6 P548P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr10:104157318 G>T maps to NM_001077494.1 E180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y8-01A-51D-A417-09 chr2:233756100 G>A maps to NM_019850.2 F413F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr6:18122099 G>A maps to NM_198586.2 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr1:236205366 G>A maps to NM_002508.2 Y326Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr1:236175344 T>C did not map to a codon.
Sequencing variant TCGA-WD-A7RX-01A-12D-A417-09 chr14:52520800 A>G maps to NM_007361.3 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA34-01A-11D-A417-09 chr15:23049092 G>T maps to NM_144599.4 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WD-A7RX-01A-12D-A417-09 chr4:48037900 A>T maps to NM_207330.1 T315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W6-AA0S-01A-11D-A417-09 chr3:173322867 C>T maps to NM_014932.2 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W6-AA0S-01A-11D-A417-09 chr3:173999083 C>A maps to NM_014932.2 T821T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr1:247588562 G>T maps to NM_004895.4 L606L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr19:56515294 C>T maps to NM_153447.4 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr19:56477639 C>T maps to NM_176811.2 Q759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr11:119050622 C>G maps to NM_024618.2 L631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr5:43704460 A>G maps to NM_182977.2 T1072T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr1:6593397 C>T maps to NM_024654.4 V393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y1-01A-11D-A417-09 chr1:6610486 G>T maps to NM_024654.4 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA33-01A-11D-A417-09 chr23:70516448 C>T did not map to a codon.
Sequencing variant TCGA-W5-AA2R-01A-11D-A417-09 chr12:117660626 G>A maps to ENST00000338101 Q1324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr17:26101405 G>A maps to NM_000625.4 Y451Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr7:150698923 C>A maps to NM_000603.4 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr15:69325388 C>A maps to NM_024505.3 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr17:79526287 G>T maps to NM_017921.2 T608T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZU-A8S4-01A-11D-A417-09 chr15:73889441 G>A maps to NM_012428.3 N120N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr4:164246816 G>A maps to NM_000909.4 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr12:95416117 C>A maps to NM_003297.2 E567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr6:108501553 G>T maps to ENST00000368983 E261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr7:107824715 G>T maps to ENST00000379032 S758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr2:50699450 C>A maps to ENST00000404971 E1117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr2:50723151 C>T maps to ENST00000404971 Q1027Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr5:176721679 A>G maps to NM_022455.4 K2437K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WD-A7RX-01A-12D-A417-09 chr20:1445014 C>T maps to ENST00000476071 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WD-A7RX-01A-12D-A417-09 chr1:46810540 G>A maps to NM_199044.2 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr2:18766067 G>A maps to ENST00000455492 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZD-A8I3-01A-11D-A417-09 chr10:104866416 C>A maps to NM_001134373.1 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr12:104171792 G>T maps to NM_001031701.2 T487T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr15:88690582 C>A maps to NM_001012338.1 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr7:151072980 T>A maps to ENST00000355851 P481P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2H-01A-31D-A417-09 chr23:51076023 G>A did not map to a codon.
Sequencing variant TCGA-W5-AA2Z-01A-11D-A417-09 chr23:51076023 G>A did not map to a codon.
Sequencing variant TCGA-ZD-A8I3-01A-11D-A417-09 chr23:51076023 G>A did not map to a codon.
Sequencing variant TCGA-ZU-A8S4-01A-11D-A417-09 chr23:51076023 G>A did not map to a codon.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr11:63994324 C>G maps to NM_032344.2 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr19:41183173 C>T maps to NM_004756.3 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr7:135286255 G>T did not map to a codon.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr19:16855308 C>T maps to ENST00000438489 D92D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr23:101096286 G>A did not map to a codon.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr1:228480449 C>T maps to NM_001098623.1 C3610C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr8:133044206 G>T maps to ENST00000262283 R530R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr23:128724135 T>G did not map to a codon.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr8:103564206 A>G maps to NM_024410.3 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr9:131256877 A>G maps to NM_153435.1 Q678Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr7:44737335 G>A maps to ENST00000444676 R786R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr3:193372781 G>A maps to NM_130837.2 W715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr20:62724276 G>C maps to NM_000913.3 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA34-01A-11D-A417-09 chr14:22038257 C>A maps to NM_001005465.1 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr11:123893736 C>A maps to NM_001001953.1 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr19:15918727 C>A maps to NM_013940.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr19:16060515 C>T maps to NM_001004465.1 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr23:130678377 G>T did not map to a codon.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr7:143748126 C>A maps to NM_012365.1 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr1:247752207 G>T maps to NM_001001915.1 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZU-A8S4-01A-11D-A417-09 chr1:248202087 C>T maps to NM_001004686.2 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr1:248458418 G>C maps to NM_001004692.1 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZU-A8S4-01A-11D-A417-09 chr1:248436681 C>T maps to NM_001004695.1 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr17:56247069 G>A maps to NM_001004707.3 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVE-01A-11D-A417-09 chr11:4967988 G>T maps to NM_001005329.1 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y8-01A-51D-A417-09 chr11:4842746 T>C maps to NM_001004753.1 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr11:5878457 G>A maps to NM_001005168.1 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr11:5878457 G>A maps to NM_001005168.1 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr11:5878457 G>A maps to NM_001005168.1 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y1-01A-11D-A417-09 chr11:5878457 G>A maps to NM_001005168.1 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr11:59132146 C>G maps to NM_001004729.1 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr11:55703318 C>T maps to NM_006637.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA34-01A-11D-A417-09 chr2:240984496 G>T maps to NM_173351.1 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr12:55846881 G>T maps to NM_054105.1 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr7:142749877 G>A maps to NM_001001667.1 W147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr19:14938183 A>G maps to NM_017506.1 Y290Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W6-AA0S-01A-11D-A417-09 chr11:124266926 A>G maps to NM_001005467.1 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y4-01A-11D-A417-09 chr11:124266859 A>G maps to NM_001005467.1 L130L. Only missense variants will be evaluated by CHASM.
Reference base specified for sequencing variant TCGA-ZD-A8I3-01A-11D-A417-09 chr11:56086146 G>A does not match reference base at that coordinate in hg19.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr11:56086519 G>A maps to NM_001005202.1 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2W-01A-11D-A417-09 chr23:48801511 G>T did not map to a codon.
Sequencing variant TCGA-3X-AAVB-01A-31D-A417-09 chr8:92096313 G>T maps to NM_016023.3 E287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y4-01A-11D-A417-09 chr11:7716912 T>A did not map to a codon.
Alternatively spliced codon TCGA-W6-AA0S-01A-11D-A417-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr23:49458701 C>A did not map to a codon.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr23:49458701 C>A did not map to a codon.
Sequencing variant TCGA-ZH-A8Y2-01A-11D-A417-09 chr23:55102522 G>A did not map to a codon.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr8:145059958 A>C maps to NM_032789.3 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZD-A8I3-01A-11D-A417-09 chr14:20820418 G>T maps to NM_005484.3 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y5-01A-11D-A417-09 chr2:242051785 G>A maps to ENST00000358649 I1141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr11:59418264 G>T maps to NM_152716.2 R516R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr7:154785434 C>T did not map to a codon.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr7:154785434 C>T did not map to a codon.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr3:52668816 C>A maps to ENST00000296302 E368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr3:52651495 G>A maps to ENST00000296302 R534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr3:52651333 C>A maps to ENST00000296302 E588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr3:52661361 T>A maps to ENST00000296302 R490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y1-01A-11D-A417-09 chr3:52678789 T>A maps to ENST00000296302 K277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y4-01A-11D-A417-09 chr3:52662938 G>A maps to ENST00000296302 R472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr11:66639208 C>A maps to NM_022172.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2I-01A-32D-A417-09 chr23:91133147 G>A did not map to a codon.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr13:61985615 G>T maps to NM_022843.3 I872I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr5:140188640 C>T maps to NM_018907.2 R623R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2I-01A-32D-A417-09 chr5:140517099 C>A maps to NM_015669.2 S695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr5:140530548 C>T maps to NM_018939.2 N237N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr5:140725273 C>T maps to NM_018916.3 N558N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr5:140725546 C>T maps to NM_018916.3 H649H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y1-01A-11D-A417-09 chr7:82545127 T>G maps to NM_033026.5 G4058G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr1:233275578 G>A maps to NM_014801.3 F1180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr1:233270845 G>A maps to NM_014801.3 F1250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr20:17462333 G>T maps to NM_002594.2 T512T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr1:55505551 A>G maps to NM_174936.3 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr1:55529043 G>T maps to NM_174936.3 V622V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr17:53852192 G>T maps to NM_021213.3 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr9:125588972 G>A maps to NM_005388.4 R32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr11:775134 C>A maps to NM_182612.2 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVB-01A-31D-A417-09 chr6:136512842 C>A maps to NM_018945.3 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr5:32093090 C>A maps to NM_178140.2 T2602T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr5:32071523 G>A maps to NM_178140.2 K856K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr2:239166977 G>T maps to NM_022817.2 V613V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr11:45939027 C>T maps to NM_057174.2 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y5-01A-11D-A417-09 chr5:114566718 C>T did not map to a codon.
Sequencing variant TCGA-W5-AA2T-01A-12D-A417-09 chr6:13053669 C>T maps to NM_030948.1 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr5:133871603 C>T maps to ENST00000448712 D35D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr5:133887779 G>T maps to ENST00000448712 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr8:133816129 C>T maps to ENST00000395386 R192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr6:64416711 A>C maps to NM_015153.2 A1219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr23:71839077 G>A did not map to a codon.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr23:71932694 A>G did not map to a codon.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr23:71825198 C>A did not map to a codon.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr23:18924874 G>A did not map to a codon.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr11:118499245 G>T maps to NM_015157.2 V569V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr3:111604231 A>G maps to NM_001134438.1 R436R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr9:131704025 C>T maps to NM_174933.3 P296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr9:131704025 C>T maps to NM_174933.3 P296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZU-A8S4-01A-11D-A417-09 chr8:75737720 C>A maps to NM_015886.3 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr22:21153978 G>A maps to NM_058004.2 Y542Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZU-A8S4-01A-11D-A417-09 chr22:38463727 C>T maps to NM_012407.3 H100H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2I-01A-32D-A417-09 chr1:207107995 C>A maps to NM_002644.3 E492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr18:39629496 G>T maps to ENST00000398870 G732*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr3:130452665 A>G maps to NM_014602.2 C392C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y5-01A-11D-A417-09 chr8:10677705 G>A maps to NM_017884.4 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2W-01A-11D-A417-09 chr9:130688239 G>A maps to NM_001135219.1 C223C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr8:22145049 G>T maps to NM_001135721.1 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr23:68382846 A>G did not map to a codon.
Sequencing variant TCGA-ZH-A8Y5-01A-11D-A417-09 chr16:2160403 G>A maps to NM_001009944.2 C1588C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr16:81248668 A>T maps to NM_052892.3 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr6:51921498 G>A maps to NM_138694.3 R564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr1:155271108 G>T maps to ENST00000423816 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr1:155271108 G>T maps to ENST00000423816 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZU-A8S4-01A-11D-A417-09 chr1:155271159 G>T maps to ENST00000423816 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2I-01A-32D-A417-09 chr11:125280124 G>T maps to NM_022062.2 G208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr1:201286845 C>T maps to NM_000299.3 I331I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W6-AA0S-01A-11D-A417-09 chr15:42292454 G>A maps to NM_001080490.1 N204N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr12:14664305 C>A maps to NM_024829.5 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA33-01A-11D-A417-09 chr3:17084421 C>T maps to NM_001144382.1 I1021I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr3:171394503 C>T did not map to a codon.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr8:144991672 C>A maps to NM_201380.2 E4243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA34-01A-11D-A417-09 chr1:6529205 C>T maps to NM_198681.2 E792E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr19:4511679 A>G maps to NM_001080400.1 D750D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr3:145788921 G>T maps to NM_182943.2 Y676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr17:7297796 T>C did not map to a codon.
Sequencing variant TCGA-WD-A7RX-01A-12D-A417-09 chr23:153040490 G>A did not map to a codon.
Sequencing variant TCGA-ZH-A8Y4-01A-11D-A417-09 chr23:152936620 G>A did not map to a codon.
Sequencing variant TCGA-ZD-A8I3-01A-11D-A417-09 chr23:7868820 A>G did not map to a codon.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr2:55874588 C>A did not map to a codon.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr2:55874588 C>A did not map to a codon.
Sequencing variant TCGA-W5-AA2T-01A-12D-A417-09 chr1:53535703 C>T maps to NM_153703.4 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr23:24741358 C>T did not map to a codon.
Sequencing variant TCGA-ZH-A8Y8-01A-51D-A417-09 chr23:24712121 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr12:133244234 C>A did not map to a codon.
Sequencing variant TCGA-3X-AAVB-01A-31D-A417-09 chr7:44113247 G>A maps to NM_013284.2 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVB-01A-31D-A417-09 chr7:44113247 G>A maps to NM_013284.2 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y8-01A-51D-A417-09 chr22:38363153 G>T maps to ENST00000407936 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2W-01A-11D-A417-09 chr22:41928663 G>A maps to NM_138338.3 H98H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr7:72416718 C>T maps to ENST00000434423 T1232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W6-AA0S-01A-11D-A417-09 chr14:19553529 C>T maps to NM_001005356.2 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W6-AA0S-01A-11D-A417-09 chr14:19553529 C>T maps to NM_001005356.2 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr4:147560456 T>C maps to NM_004575.2 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y2-01A-11D-A417-09 chr10:71978549 T>C maps to NM_021129.3 E49E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W6-AA0S-01A-11D-A417-09 chr22:46594337 G>T maps to NM_001001928.2 E20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr12:27832994 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr16:4935048 G>T maps to NM_002705.4 R1203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr17:57046943 G>T maps to NM_014906.3 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y4-01A-11D-A417-09 chr12:63042369 G>A maps to NM_020700.1 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr12:54976555 C>T maps to NM_006741.3 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr10:75255629 C>A maps to NM_001142353.1 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr9:127915866 C>T maps to NM_001123355.1 W242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y2-01A-11D-A417-09 chr1:13669137 A>G maps to ENST00000334600 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y2-01A-11D-A417-09 chr1:13669137 A>G maps to ENST00000334600 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y5-01A-11D-A417-09 chr11:129784862 G>T maps to NM_020228.2 L863L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr6:100062583 A>G maps to ENST00000359773 T701T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZU-A8S4-01A-11D-A417-09 chr21:43279218 T>G maps to NM_022115.3 R384R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA34-01A-11D-A417-09 chr20:47258998 G>T maps to NM_020820.3 I1210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2I-01A-32D-A417-09 chr1:186276305 T>C maps to NM_005807.3 T485T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZD-A8I3-01A-11D-A417-09 chr23:49034448 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr1:146639503 C>G maps to NM_005399.3 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr17:64685165 G>A did not map to a codon.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr19:11560244 T>G did not map to a codon.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr19:11560244 T>G did not map to a codon.
Sequencing variant TCGA-W5-AA2Z-01A-11D-A417-09 chr8:48710795 A>G did not map to a codon.
Sequencing variant TCGA-ZH-A8Y8-01A-51D-A417-09 chr10:53893620 C>T maps to NM_001098512.1 N304N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVA-01A-11D-A417-09 chr2:179306335 C>T did not map to a codon.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr23:3573312 G>A did not map to a codon.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr16:11367211 G>T maps to NM_021247.1 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr16:68355327 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr16:68380155 T>C maps to NM_019023.2 T388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WD-A7RX-01A-12D-A417-09 chr3:93605208 G>T maps to NM_000313.3 R432R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y8-01A-51D-A417-09 chr3:93605179 C>T maps to NM_000313.3 P441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr10:13629125 C>T maps to NM_003675.3 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr1:109238705 T>C maps to NM_018061.2 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr14:45571896 G>A maps to NM_017922.3 Q245Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr23:106885651 G>T did not map to a codon.
Sequencing variant TCGA-ZH-A8Y2-01A-11D-A417-09 chr23:106888556 C>T did not map to a codon.
Sequencing variant TCGA-ZH-A8Y2-01A-11D-A417-09 chr23:106888556 C>T did not map to a codon.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr2:240981682 A>G maps to NM_001080835.1 H239H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr7:142459666 G>A maps to ENST00000486171 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr9:79270372 G>T maps to NM_015225.2 G2774G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr19:43674290 C>T did not map to a codon.
Sequencing variant TCGA-WD-A7RX-01A-12D-A417-09 chr9:15468837 G>T maps to NM_001128217.1 R404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVE-01A-11D-A417-09 chr1:109964510 G>A maps to NM_002790.3 Q23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr1:109944657 C>A maps to NM_002790.3 E235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr16:67968567 G>T maps to NM_002801.2 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y4-01A-11D-A417-09 chr3:64008457 C>T maps to ENST00000492933 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y4-01A-11D-A417-09 chr3:64008457 C>T maps to ENST00000492933 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr12:122326824 C>T maps to NM_002813.4 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr2:54101580 G>T maps to NM_014614.2 L1665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVB-01A-31D-A417-09 chr23:23411590 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr11:488602 G>A maps to NM_030783.1 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr1:71512789 C>G maps to ENST00000354608 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr11:47591272 G>T maps to NM_175732.2 E93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr1:214557313 G>A maps to NM_005401.4 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr1:198710996 G>T did not map to a codon.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr10:129861357 G>T maps to NM_006504.4 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr6:128304394 G>A maps to ENST00000368210 Q1145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr21:46271540 G>A maps to NM_004339.2 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA34-01A-11D-A417-09 chr21:46271540 G>T maps to NM_004339.2 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y4-01A-11D-A417-09 chr2:1668820 A>G maps to NM_012293.1 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr8:52321347 G>A maps to NM_144651.4 R946*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr12:120649931 G>C did not map to a codon.
Sequencing variant TCGA-ZH-A8Y1-01A-11D-A417-09 chr3:49137443 A>G maps to NM_005051.1 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y1-01A-11D-A417-09 chr3:49137443 A>G maps to NM_005051.1 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr19:8467131 T>C maps to NM_004218.3 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr18:52556640 C>A maps to NM_004163.3 C218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2W-01A-11D-A417-09 chr12:70178543 G>T maps to NM_175623.2 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr9:125760960 C>G maps to NM_012197.3 V430V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr5:131931433 G>A maps to NM_005732.3 K713K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2R-01A-11D-A417-09 chr2:17698680 G>T maps to NM_001099218.2 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA34-01A-11D-A417-09 chr8:95479632 C>T maps to NM_012415.2 E45E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA34-01A-11D-A417-09 chr3:51675864 C>T maps to NM_015106.2 R778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2R-01A-11D-A417-09 chr14:36094619 C>T maps to NM_194301.2 L1786L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WD-A7RX-01A-12D-A417-09 chr14:36192383 C>T maps to NM_194301.2 S651S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr20:37191222 G>T maps to NM_020336.2 E1194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr1:178745907 A>C maps to NM_152663.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVB-01A-31D-A417-09 chr12:131359124 G>A maps to ENST00000392369 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZU-A8S4-01A-11D-A417-09 chr2:109379748 G>A maps to NM_006267.4 P918P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr12:48131421 A>T maps to NM_001098531.2 A900A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr11:47464330 C>G maps to NM_005055.3 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr12:53607313 T>A maps to NM_000966.4 T328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr5:86672322 C>T maps to NM_002890.1 R709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr11:13031683 C>T maps to ENST00000340901 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr8:53568652 G>A maps to NM_014781.4 L1246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr23:47030428 T>C did not map to a codon.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr12:56982714 G>T did not map to a codon.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr12:56982714 G>T did not map to a codon.
Sequencing variant TCGA-3X-AAVE-01A-11D-A417-09 chr23:135958703 G>C did not map to a codon.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr23:135958730 C>A did not map to a codon.
Sequencing variant TCGA-ZH-A8Y1-01A-11D-A417-09 chr23:135956306 T>C did not map to a codon.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr15:91504866 C>T maps to NM_033544.2 G333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr9:36091178 T>G maps to NM_021111.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y2-01A-11D-A417-09 chr8:145739897 C>T maps to ENST00000428558 L544L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr2:61149150 G>C maps to NM_002908.2 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVA-01A-11D-A417-09 chr19:45532158 A>G maps to ENST00000221452 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr7:103124179 G>A maps to ENST00000428762 N3367N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr11:114310339 C>T maps to NM_015523.3 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2R-01A-11D-A417-09 chr12:107103189 C>T maps to ENST00000357881 R315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr16:320813 G>A maps to NM_183337.1 F332F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZD-A8I3-01A-11D-A417-09 chr8:54852269 T>A maps to NM_170587.2 C215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr1:240979679 G>A maps to ENST00000407727 H240H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2R-01A-11D-A417-09 chr5:63802564 C>T maps to NM_001029875.1 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr6:49574863 T>G maps to NM_000324.2 T379T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr8:144462003 A>G maps to ENST00000422773 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr8:104897648 T>G maps to NM_001100117.2 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr20:19956129 C>T maps to ENST00000255006 F536F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr5:96503499 C>A maps to NM_018343.2 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr16:67681420 C>T maps to NM_001013838.1 R263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr2:86831625 G>T maps to NM_005667.3 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr5:141353305 C>T maps to NM_183399.1 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr18:44015311 C>T maps to NM_152470.2 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVA-01A-11D-A417-09 chr1:201965298 C>T maps to NM_020216.3 C254C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVA-01A-11D-A417-09 chr1:201965298 C>T maps to NM_020216.3 C254C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr20:34287658 G>A maps to NM_080748.2 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr9:77300434 G>T maps to ENST00000396204 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr8:55537425 C>T maps to NM_006269.1 D328D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr8:55542174 T>C maps to NM_006269.1 Y1911Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y8-01A-51D-A417-09 chr1:84948632 C>T maps to NM_025065.6 N107N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr16:53726056 G>T maps to NM_015272.2 Y150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y1-01A-11D-A417-09 chr20:36687878 G>T maps to NM_021215.3 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr23:20179854 A>G did not map to a codon.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr23:20183168 T>C did not map to a codon.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr17:78727808 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr11:126079516 C>T maps to NM_032795.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y2-01A-11D-A417-09 chr7:6006555 A>G maps to NM_173565.3 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVE-01A-11D-A417-09 chr19:12939520 T>C maps to NM_031429.1 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr15:41749982 G>T maps to NM_015138.4 E191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZU-A8S4-01A-11D-A417-09 chr11:57243729 C>T maps to NM_178570.1 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr17:42392344 C>T maps to NM_001144825.1 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr6:45390462 G>A maps to ENST00000359524 Q132Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr6:45390462 G>A maps to ENST00000359524 Q132Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr1:25229098 C>T maps to NM_001031680.2 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVA-01A-11D-A417-09 chr9:35546733 T>A maps to NM_001135999.1 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr19:39062861 G>A maps to NM_000540.2 L4650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr1:237777617 G>A maps to NM_001035.2 T1730T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr1:237880646 G>T maps to NM_001035.2 L3491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZU-A8S4-01A-11D-A417-09 chr1:237732450 C>A maps to NM_001035.2 R1144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVA-01A-11D-A417-09 chr15:34018688 C>T maps to NM_001036.3 L2339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZD-A8I3-01A-11D-A417-09 chr23:134986715 C>T did not map to a codon.
Sequencing variant TCGA-ZH-A8Y5-01A-11D-A417-09 chr16:51173911 G>T maps to ENST00000251020 R741R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W6-AA0S-01A-11D-A417-09 chr7:92734777 G>T maps to NM_017654.3 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr13:21714708 C>T maps to NM_005870.4 V6V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr23:84358921 C>A did not map to a codon.
Sequencing variant TCGA-WD-A7RX-01A-12D-A417-09 chr23:84362914 G>A did not map to a codon.
Sequencing variant TCGA-ZU-A8S4-01A-11D-A417-09 chr14:51107520 A>C maps to NM_021818.2 Y299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr11:9801362 G>A did not map to a codon.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr1:246929441 G>A did not map to a codon.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr15:32988765 A>T maps to NM_001144757.1 K199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WD-A7RX-01A-12D-A417-09 chr2:166231392 G>T maps to NM_001040142.1 E1391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr17:62020344 G>A maps to NM_000334.4 Q1377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y1-01A-11D-A417-09 chr3:38592469 C>T maps to NM_001099404.1 W1798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2T-01A-12D-A417-09 chr11:9101051 G>A maps to ENST00000457346 I87I. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-W5-AA39-01A-11D-A417-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr1:243663077 T>A maps to NM_006642.3 S711S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVA-01A-11D-A417-09 chr17:75210104 G>A maps to NM_001143998.1 *716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr9:139341748 G>T maps to NM_014866.1 L2209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr1:145116151 C>T did not map to a codon.
Sequencing variant TCGA-ZU-A8S4-01A-11D-A417-09 chr6:108214764 A>T maps to NM_007214.4 L532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2H-01A-31D-A417-09 chr15:49304060 C>A did not map to a codon.
Sequencing variant TCGA-W5-AA2H-01A-31D-A417-09 chr15:49304060 C>A did not map to a codon.
Sequencing variant TCGA-3X-AAVB-01A-31D-A417-09 chr1:169564102 G>T maps to NM_003005.3 S705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr3:150340939 G>A maps to NM_016275.3 W120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA34-01A-11D-A417-09 chr5:9202071 G>T maps to NM_003966.2 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA33-01A-11D-A417-09 chr5:115782914 G>A maps to ENST00000257414 Y846Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVA-01A-11D-A417-09 chr15:48063948 A>G maps to NM_153618.1 P1063P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2H-01A-31D-A417-09 chr15:48052507 G>A maps to NM_153618.1 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr3:101049207 C>A maps to NM_020654.3 S907S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2R-01A-11D-A417-09 chr4:77949911 G>T maps to ENST00000510515 E372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr1:31905888 A>G maps to NM_178865.4 T363T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-W5-AA38-01A-11D-A417-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr19:40929000 G>A maps to NM_013376.3 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr9:135202916 G>T maps to ENST00000372169 P1356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr19:2248133 G>A maps to NM_007165.4 G328G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr19:2248142 C>T maps to NM_007165.4 P331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr19:2248148 T>C maps to NM_007165.4 A333A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr1:38444661 G>C maps to NM_006802.2 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr2:198269867 C>A maps to NM_012433.2 E491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr2:198288621 A>C maps to NM_012433.2 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA34-01A-11D-A417-09 chr5:155935642 A>G maps to NM_000337.5 K75K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr2:201407334 A>T maps to NM_152524.5 K141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr19:4362633 G>C maps to NM_003025.2 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr23:19725064 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr23:19725064 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA2Z-01A-11D-A417-09 chr19:51165464 C>T maps to ENST00000391814 L2089L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA34-01A-11D-A417-09 chr11:70332551 G>A maps to ENST00000338508 Y1276Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr11:70332548 C>T maps to ENST00000338508 E1277E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr19:41086735 G>T maps to NM_138392.3 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2R-01A-11D-A417-09 chr23:50350730 C>T did not map to a codon.
Sequencing variant TCGA-W5-AA2R-01A-11D-A417-09 chr23:50350733 C>T did not map to a codon.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr20:3687243 G>A maps to NM_023068.3 D53D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr20:3687243 G>A maps to NM_023068.3 D53D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr19:51628377 C>A maps to NM_014441.2 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVE-01A-11D-A417-09 chr11:111572282 G>A maps to NM_015191.1 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVA-01A-11D-A417-09 chr19:38579445 G>A maps to NM_015073.1 E540E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Z-01A-11D-A417-09 chr20:1532454 G>T maps to ENST00000381621 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr17:57232318 G>T maps to NM_001100595.1 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr6:31935498 C>A maps to NM_006929.4 S864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr5:36181925 T>G maps to NM_005983.2 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr8:134062163 C>T maps to NM_006748.3 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y8-01A-51D-A417-09 chr1:160458957 C>A maps to NM_001184714.1 E267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr15:48580289 A>T maps to NM_000338.2 K894*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZU-A8S4-01A-11D-A417-09 chr5:127522245 G>T maps to NM_001046.2 E1188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr6:111498822 A>C maps to NM_018593.4 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr6:25850685 C>T did not map to a codon.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr19:15063765 C>T maps to NM_005071.1 T491T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y1-01A-11D-A417-09 chr8:42287685 C>T maps to NM_006749.3 W535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr5:131630428 G>T maps to NM_003059.2 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr20:4839935 T>G maps to NM_203327.1 P573P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr2:220029917 G>T maps to NM_001144890.1 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr2:220029917 G>T maps to NM_001144890.1 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr15:65918175 C>T maps to NM_004727.2 S586S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr6:46630145 T>G maps to NM_004277.3 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WD-A7RX-01A-12D-A417-09 chr5:110096915 C>A maps to NM_138773.1 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WD-A7RX-01A-12D-A417-09 chr23:1506181 C>A did not map to a codon.
Sequencing variant TCGA-W5-AA2H-01A-31D-A417-09 chr6:134350692 G>T maps to NM_145176.2 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2H-01A-31D-A417-09 chr6:134350692 G>T maps to NM_145176.2 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr6:118598678 C>T maps to NM_001029858.3 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVE-01A-11D-A417-09 chr5:150853232 G>T did not map to a codon.
Sequencing variant TCGA-3X-AAVE-01A-11D-A417-09 chr5:150853232 G>T did not map to a codon.
Sequencing variant TCGA-ZU-A8S4-01A-11D-A417-09 chr11:57184112 T>C maps to ENST00000428603 E247E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr2:162807339 G>A maps to NM_001178015.1 R841R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA33-01A-11D-A417-09 chr22:32500774 C>G maps to NM_000343.3 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr17:18880178 C>A maps to NM_152351.3 R287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y5-01A-11D-A417-09 chr19:33701908 C>T maps to ENST00000424731 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr8:17415879 G>T maps to NM_001164771.1 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr23:70149682 G>T did not map to a codon.
Sequencing variant TCGA-ZH-A8Y2-01A-11D-A417-09 chr23:46541897 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA2Z-01A-11D-A417-09 chr5:101582975 A>G maps to NM_180991.4 P597P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2T-01A-12D-A417-09 chr17:33749504 G>A maps to NM_018042.3 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2R-01A-11D-A417-09 chr4:20530585 C>A maps to ENST00000273739 R497R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y2-01A-11D-A417-09 chr23:144904918 C>T did not map to a codon.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr20:57611615 T>C maps to NM_016045.2 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr8:143823220 C>A maps to NM_020427.2 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr4:144451679 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA34-01A-11D-A417-09 chr4:144474310 G>T maps to NM_003601.2 G1045*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA33-01A-11D-A417-09 chr3:47702802 G>T maps to NM_003074.3 P767P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr12:56578657 C>T maps to NM_003075.3 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr17:61914838 C>T maps to NM_001098426.1 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr10:112352926 G>T maps to NM_005445.3 E637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr3:160150975 C>A maps to NM_005496.3 S1231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr9:72967111 G>A maps to NM_015110.3 L1057L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y2-01A-11D-A417-09 chr2:17906562 C>T maps to ENST00000381272 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y4-01A-11D-A417-09 chr23:21996163 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr1:214503533 C>A maps to NM_020197.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr2:241979570 C>T maps to NM_001080437.1 C375C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2I-01A-32D-A417-09 chr2:241976735 C>T maps to NM_001080437.1 C337C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2I-01A-32D-A417-09 chr2:96961291 C>T maps to NM_014014.3 K592K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr2:1168796 C>T maps to NM_018968.3 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y4-01A-11D-A417-09 chr16:50707592 G>A maps to NM_182854.2 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr16:12093199 G>T maps to NM_032167.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVE-01A-11D-A417-09 chr16:12136878 G>T maps to NM_032167.2 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr16:12220545 G>T maps to NM_001080530.2 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr1:179312000 T>C maps to NM_003101.4 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr14:55510679 C>T maps to NM_199421.1 T307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2H-01A-31D-A417-09 chr21:34948696 A>G maps to NM_138927.1 R2416R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr10:97106173 A>C maps to NM_001034954.1 A806A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr3:181432146 G>T did not map to a codon.
Sequencing variant TCGA-WD-A7RX-01A-12D-A417-09 chr23:139586718 G>A did not map to a codon.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr17:3370840 C>T maps to NM_001170695.1 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr1:229440934 C>A maps to NM_006542.3 C18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr19:49132948 T>A maps to NM_020126.3 Y628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA33-01A-11D-A417-09 chr2:228996761 C>T maps to NM_001142644.1 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr16:89920722 G>T maps to NM_032451.1 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2W-01A-11D-A417-09 chr1:32280313 C>T maps to NM_144569.4 K207K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVA-01A-11D-A417-09 chr4:1161433 C>T maps to NM_012445.3 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVA-01A-11D-A417-09 chr4:1161433 C>T maps to NM_012445.3 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVE-01A-11D-A417-09 chr9:131348106 C>T maps to NM_001130438.2 Q881*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2R-01A-11D-A417-09 chr2:54858075 C>T maps to NM_003128.2 C964C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2R-01A-11D-A417-09 chr2:54858075 C>T maps to NM_003128.2 C964C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr2:54877116 G>T maps to NM_003128.2 L1856L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr11:66463944 G>A maps to NM_006946.2 L1361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr5:139931629 A>T maps to NM_001035235.2 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr2:45807032 G>A maps to NM_018079.4 Y351Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr16:30722103 G>A maps to NM_006662.2 Q388Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr16:30722103 G>A maps to NM_006662.2 Q388Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr2:31751120 A>G did not map to a codon.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr17:17722482 A>G maps to NM_001005291.2 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr5:121362643 A>T maps to NM_152546.2 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr12:64505697 T>C maps to NM_020762.2 T692T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr12:64505655 T>C maps to NM_020762.2 H678H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr23:99925823 G>T did not map to a codon.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr23:99925823 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr23:99921899 C>A did not map to a codon.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr7:149503931 C>T maps to NM_198455.2 Y2921Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZD-A8I3-01A-11D-A417-09 chr20:23016851 C>T maps to NM_001052.2 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y1-01A-11D-A417-09 chr1:44303968 G>T maps to NM_174963.2 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y2-01A-11D-A417-09 chr1:44290441 C>T maps to NM_174963.2 D98D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr1:77334297 G>A maps to NM_030965.1 Q44Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA33-01A-11D-A417-09 chr3:52536049 C>A maps to NM_015136.2 C120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr12:104100718 C>A maps to NM_017564.9 A1382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr3:136059371 A>G maps to NM_005862.2 D1211D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVB-01A-31D-A417-09 chr23:123220533 G>A did not map to a codon.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr23:123200252 A>C did not map to a codon.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr19:4327372 C>T maps to ENST00000314714 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr12:56743969 G>T maps to NM_005419.3 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr11:63965023 G>T maps to ENST00000358794 E334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y4-01A-11D-A417-09 chr2:220473348 G>T maps to NM_052902.2 E561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr4:184931277 G>T maps to NM_020225.1 V429V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr4:184931277 G>T maps to NM_020225.1 V429V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr4:184931985 C>T maps to NM_020225.1 P665P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr4:184931985 C>T maps to NM_020225.1 P665P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr2:202344885 C>T maps to NM_018571.5 Y415Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr2:202344885 C>T maps to NM_018571.5 Y415Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr15:43893653 G>T maps to NM_153700.2 I1547I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr11:59554566 A>T maps to NM_004177.4 K58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr17:27001322 C>T maps to NM_003170.3 N44N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y2-01A-11D-A417-09 chr2:27878430 G>T maps to NM_014860.1 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr1:149879664 G>T maps to NM_014849.3 R491R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVE-01A-11D-A417-09 chr5:75428096 C>T maps to NM_014979.1 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr9:113205825 A>T maps to ENST00000374463 P1546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y8-01A-51D-A417-09 chr9:113166720 C>T maps to ENST00000374463 P3187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2W-01A-11D-A417-09 chr12:109334558 C>T did not map to a codon.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr20:58470490 C>T did not map to a codon.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr22:33376641 G>T maps to NM_003490.3 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr6:86351133 T>C maps to NM_006372.4 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W6-AA0S-01A-11D-A417-09 chr21:34045775 G>T maps to NM_003895.3 R573R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr20:43996520 G>A did not map to a codon.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr12:33579332 G>A maps to NM_198992.3 C83C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVB-01A-31D-A417-09 chr11:7334707 G>T maps to NM_175733.3 G194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr6:159104021 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr4:1729638 T>C maps to NM_006342.1 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr17:35827571 C>A maps to NM_001166105.1 R280R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr8:120754807 G>C maps to NM_003184.3 P1101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr10:8019212 G>T maps to NM_031923.2 E748*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-W6-AA0S-01A-11D-A417-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-W6-AA0S-01A-11D-A417-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr2:160035179 G>A maps to NM_033394.2 Q672Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZD-A8I3-01A-11D-A417-09 chr2:162081139 A>T did not map to a codon.
Sequencing variant TCGA-ZD-A8I3-01A-11D-A417-09 chr2:162081139 A>T did not map to a codon.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr6:32815403 C>A maps to NM_000593.5 E657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr1:234569296 G>T maps to NM_005646.3 C751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr12:10962374 A>C maps to NM_023917.2 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr1:235602122 C>A maps to NM_003193.3 R386R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr11:120957510 T>C maps to NM_152715.3 Y327Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2H-01A-31D-A417-09 chr6:170871015 G>A maps to NM_003194.4 Q64Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WD-A7RX-01A-12D-A417-09 chr6:170871015 G>A maps to NM_003194.4 Q64Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr2:162273322 C>T maps to NM_006593.2 H134H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr23:101382095 A>G did not map to a codon.
Sequencing variant TCGA-WD-A7RX-01A-12D-A417-09 chr5:145859642 A>G maps to NM_006706.3 K624K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVA-01A-11D-A417-09 chr18:52895477 G>T maps to ENST00000398339 S767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr10:114901067 C>A maps to NM_030756.4 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr4:156831266 T>G maps to NM_005651.2 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr7:97852436 G>C maps to ENST00000379795 P933P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2I-01A-32D-A417-09 chr11:120979960 C>T maps to NM_005422.2 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr2:74274264 T>C maps to ENST00000409262 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Z-01A-11D-A417-09 chr17:62248511 G>T maps to NM_018469.3 G880G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y2-01A-11D-A417-09 chr17:62271114 C>T maps to NM_018469.3 P660P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr6:50696635 T>C maps to NM_172238.3 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr3:30686281 G>A maps to NM_001024847.2 K71K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2T-01A-12D-A417-09 chr2:105897080 G>A maps to NM_004257.4 Y407Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2R-01A-11D-A417-09 chr18:3447748 G>A maps to NM_173207.1 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr14:24729729 G>T maps to NM_000359.2 S228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WD-A7RX-01A-12D-A417-09 chr16:67876819 G>A maps to NM_020457.2 Q121Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr2:242572710 T>A maps to NM_015963.5 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr4:76452235 G>T maps to NM_144721.4 E161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr6:169632767 C>T maps to NM_003247.2 T641T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y4-01A-11D-A417-09 chr3:184091268 G>A maps to NM_000460.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZU-A8S4-01A-11D-A417-09 chr15:71952876 C>T maps to NM_024817.2 G387G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2T-01A-12D-A417-09 chr2:137814608 G>A maps to ENST00000272643 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr3:9406698 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr3:9406698 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr4:153691680 G>T maps to NM_145720.2 S159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y2-01A-11D-A417-09 chr14:24710310 C>T maps to NM_001099274.1 V173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr4:187004483 C>T maps to NM_003265.2 H548H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr23:12939079 C>A did not map to a codon.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr3:52255289 G>A maps to ENST00000494383 T1167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr3:149051001 T>C maps to NM_138786.3 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y2-01A-11D-A417-09 chr17:4675352 C>T maps to NM_003963.2 Q46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr1:165728807 C>T maps to NM_019026.3 K54K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr12:124069353 C>T maps to NM_006815.3 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr12:124069353 C>T maps to NM_006815.3 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr14:77810057 G>A maps to NM_213601.1 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr4:4242109 A>G maps to ENST00000382753 Y112Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr2:85826689 G>T maps to NM_001031738.2 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZD-A8I3-01A-11D-A417-09 chr2:120439253 C>T maps to NM_030577.2 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr7:1587390 C>T maps to NM_001097620.1 K333K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVE-01A-11D-A417-09 chr4:148539205 C>T maps to NM_018241.2 C33C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVE-01A-11D-A417-09 chr4:148539205 C>T maps to NM_018241.2 C33C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr9:74300265 T>C maps to NM_013390.2 S1333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr1:212538673 G>T maps to NM_001198862.1 G373G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr9:108456997 C>A maps to NM_018112.1 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr1:54512946 A>G maps to ENST00000371338 C107C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2R-01A-11D-A417-09 chr17:28643708 C>A did not map to a codon.
Sequencing variant TCGA-W5-AA2W-01A-11D-A417-09 chr12:98927570 G>A maps to NM_003276.2 Q512Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr7:5352832 G>A maps to NM_001080495.2 S2563S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr16:24826537 T>G maps to NM_014494.2 T1581T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr17:38560514 T>C maps to ENST00000357601 P760P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr3:25675376 T>C maps to ENST00000264331 K327K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr16:52473514 C>T maps to ENST00000407228 Q451Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr15:43708492 C>A maps to NM_001141980.1 L1601L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y8-01A-51D-A417-09 chr1:154144579 G>A maps to NM_153649.3 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA33-01A-11D-A417-09 chr11:6638858 G>T maps to ENST00000453338 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA33-01A-11D-A417-09 chr11:6638858 G>T maps to ENST00000453338 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr11:6637269 T>G maps to ENST00000453338 R380R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr1:186312594 G>A maps to NM_003292.2 R1205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W6-AA0S-01A-11D-A417-09 chr1:186281175 T>A did not map to a codon.
Sequencing variant TCGA-W5-AA2T-01A-12D-A417-09 chr21:10941921 T>A maps to NM_199261.2 R261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr2:239242654 C>T maps to NM_015650.3 R348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2H-01A-31D-A417-09 chr1:211533364 C>T maps to ENST00000427925 R175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVE-01A-11D-A417-09 chr3:42260986 G>A maps to NM_001042646.1 A655A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr8:141415701 T>A maps to NM_031466.5 K426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr8:110131446 C>A maps to NM_003301.4 Y320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2R-01A-11D-A417-09 chr8:126445608 G>T maps to NM_025195.2 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr13:50590788 G>T did not map to a codon.
Alternatively spliced codon TCGA-W5-AA2R-01A-11D-A417-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-W5-AA2R-01A-11D-A417-09 chr5:114483089 G>T maps to ENST00000508894 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y1-01A-11D-A417-09 chr3:140407353 C>T maps to NM_152616.4 Y610Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y1-01A-11D-A417-09 chr3:140407353 C>T maps to NM_152616.4 Y610Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZD-A8I3-01A-11D-A417-09 chr7:100732026 G>T maps to NM_030961.1 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y1-01A-11D-A417-09 chr11:4626748 C>T did not map to a codon.
Sequencing variant TCGA-W5-AA2R-01A-11D-A417-09 chr15:45059568 C>T maps to NM_182985.3 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr14:51492032 C>A maps to ENST00000338969 E290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr5:14399005 G>T maps to NM_007118.2 E1481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr22:38120875 C>A maps to NM_001039141.2 S771S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr14:92470475 T>A maps to NM_004239.3 K1282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr23:54950953 C>T did not map to a codon.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr23:111155895 G>T did not map to a codon.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr23:111155895 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA34-01A-11D-A417-09 chr23:111155790 C>A did not map to a codon.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr9:77470477 A>T maps to NM_017662.4 C39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2R-01A-11D-A417-09 chr8:116631412 C>T maps to NM_014112.2 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr10:116734972 G>A maps to NM_139169.4 W295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr11:18536389 T>A did not map to a codon.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr8:143425474 C>A maps to ENST00000445818 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr8:143436076 G>T maps to ENST00000445818 Y3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr11:44941489 C>T maps to ENST00000425677 D185D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr11:2424012 C>T maps to NM_005706.2 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr3:180320909 A>T did not map to a codon.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr3:39154058 G>T maps to ENST00000301819 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr2:32891801 T>C maps to NM_017735.4 T302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Z-01A-11D-A417-09 chr5:94852863 G>T maps to NM_014639.3 L759L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr1:51754560 A>G maps to ENST00000447632 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA34-01A-11D-A417-09 chr17:46868790 G>T maps to NM_001130918.1 I391I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVE-01A-11D-A417-09 chr2:179569096 C>T maps to NM_133378.4 L8756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr2:179447085 C>A maps to NM_133378.4 E19465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr2:179511838 C>A maps to ENST00000429997 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr2:179615543 C>T maps to ENST00000375038 K3863K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr2:179615543 C>T maps to ENST00000375038 K3863K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr2:179529379 C>T did not map to a codon.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr13:19751498 G>T maps to NM_006001.1 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZU-A8S4-01A-11D-A417-09 chr6:30691486 G>A maps to NM_178014.2 K216K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZD-A8I3-01A-11D-A417-09 chr10:135107109 C>T maps to NM_006659.2 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZD-A8I3-01A-11D-A417-09 chr6:35479509 G>A maps to NM_003322.3 Y88Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr16:11785749 C>T maps to ENST00000356957 W459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr14:52978008 C>T maps to NM_020784.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr22:19865951 G>A maps to NM_006440.3 H428H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr9:12708980 G>T maps to NM_000550.2 R471R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y5-01A-11D-A417-09 chr19:36233567 C>T maps to NM_144987.2 Q180Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZU-A8S4-01A-11D-A417-09 chr9:33989029 G>T maps to NM_018449.2 S128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr2:238934041 A>G maps to NM_080678.1 E114E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr11:57322033 C>T maps to NM_004223.3 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr12:109927742 G>T maps to NM_183415.1 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr1:10205033 G>A maps to NM_001105562.2 W800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2I-01A-32D-A417-09 chr7:138978117 C>G maps to NM_173569.3 P1270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr7:138968746 G>A maps to NM_173569.3 S1032S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr6:42644578 T>G maps to NM_015255.2 A1482A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVE-01A-11D-A417-09 chr2:170780437 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr17:42293339 T>G maps to NM_014233.2 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr1:161123895 C>T maps to NM_016406.3 Q37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr19:4954680 G>C maps to ENST00000398240 A672A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr5:176396233 G>A maps to ENST00000377219 N174N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA34-01A-11D-A417-09 chr19:17756909 G>T maps to ENST00000428389 A773A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr5:176304912 G>T maps to NM_133369.2 E552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr22:45681855 T>G maps to NM_006953.3 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y4-01A-11D-A417-09 chr23:74494296 G>A did not map to a codon.
Sequencing variant TCGA-W5-AA33-01A-11D-A417-09 chr1:229779332 T>C maps to NM_014777.2 L1230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr3:126208212 C>T maps to NM_001165974.1 P598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y5-01A-11D-A417-09 chr1:216591857 G>A maps to ENST00000366943 Q217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr13:27669905 T>G maps to NM_182488.3 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr11:119243851 G>A maps to NM_004205.4 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr1:22063113 C>T maps to NM_032236.5 G332G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr17:5040989 G>T maps to NM_004505.2 V290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr17:5040989 G>T maps to NM_004505.2 V290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2H-01A-31D-A417-09 chr15:50785053 C>T maps to NM_005154.3 N797N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2T-01A-12D-A417-09 chr15:50785053 C>T maps to NM_005154.3 N797N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr15:50785053 C>T maps to NM_005154.3 N797N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA33-01A-11D-A417-09 chr23:41043818 A>G did not map to a codon.
Sequencing variant TCGA-ZU-A8S4-01A-11D-A417-09 chr23:41088539 C>T did not map to a codon.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr1:116206775 C>A maps to NM_001172412.1 I233I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr1:108247683 C>A did not map to a codon.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr10:75860837 C>A maps to NM_014000.2 R669R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr9:35060887 C>T maps to NM_007126.3 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y5-01A-11D-A417-09 chr10:135053261 C>T maps to NM_014468.2 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr3:10191634 C>A maps to NM_000551.2 R210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr6:133034963 C>T did not map to a codon.
Sequencing variant TCGA-W5-AA2H-01A-31D-A417-09 chr6:133070862 C>A maps to NM_004665.2 E448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y5-01A-11D-A417-09 chr3:51449831 C>G did not map to a codon.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr10:70916898 C>A maps to NM_004896.3 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y5-01A-11D-A417-09 chr11:134113054 G>C maps to NM_052875.3 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2W-01A-11D-A417-09 chr15:91557063 G>A maps to NM_018668.3 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr15:42465948 G>T maps to ENST00000348544 S365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr1:150054916 G>T maps to NM_007259.3 E352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr6:33236869 G>A maps to NM_022553.4 R157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVA-01A-11D-A417-09 chr2:64189235 T>C maps to NM_016516.2 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVA-01A-11D-A417-09 chr23:107319374 G>T did not map to a codon.
Sequencing variant TCGA-3X-AAVB-01A-31D-A417-09 chr6:110423268 A>G maps to NM_003931.2 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr17:73847680 T>A maps to NM_012478.3 K46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WD-A7RX-01A-12D-A417-09 chr4:85678261 G>A maps to NM_014991.4 N1747N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr10:122661796 G>T maps to NM_018117.11 E906*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA34-01A-11D-A417-09 chr23:48457848 A>G did not map to a codon.
Sequencing variant TCGA-ZU-A8S4-01A-11D-A417-09 chr4:39226501 A>T did not map to a codon.
Sequencing variant TCGA-ZU-A8S4-01A-11D-A417-09 chr4:39226501 A>T did not map to a codon.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr1:224599140 C>T maps to NM_025160.6 W382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVA-01A-11D-A417-09 chr1:118495208 C>A maps to NM_006784.2 S692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr23:117480528 C>T did not map to a codon.
Sequencing variant TCGA-ZD-A8I3-01A-11D-A417-09 chr3:113063554 G>A maps to NM_001164496.1 R1024*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr7:158704267 C>T maps to NM_018051.4 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr15:78582400 A>G maps to NM_025234.1 Y120Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2I-01A-32D-A417-09 chr18:54424283 C>T maps to NM_015285.2 C820C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W6-AA0S-01A-11D-A417-09 chr11:62601269 C>T maps to NM_018093.2 E305E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr2:68371714 A>C did not map to a codon.
Sequencing variant TCGA-ZD-A8I3-01A-11D-A417-09 chr8:38157086 G>T maps to NM_023034.1 S878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr17:38421060 G>A maps to NM_133264.4 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y4-01A-11D-A417-09 chr17:66417949 G>A maps to NM_017983.5 C435C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr6:112389432 G>A maps to NM_198239.1 W223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr9:96070760 G>T maps to ENST00000297954 V2174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y8-01A-51D-A417-09 chr12:49360089 G>A maps to NM_003394.3 R320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr3:55504230 G>T maps to NM_003392.3 Y344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y5-01A-11D-A417-09 chr17:7606343 C>T maps to NM_018081.2 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr23:52893906 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr23:52893877 C>T did not map to a codon.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr22:29195029 C>T maps to ENST00000403532 K113K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr22:29195029 C>T maps to ENST00000403532 K113K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr2:168104886 C>T maps to NM_152381.5 L2329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr22:17288750 G>A maps to NM_175878.3 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y2-01A-11D-A417-09 chr23:128881716 G>T did not map to a codon.
Sequencing variant TCGA-W5-AA2R-01A-11D-A417-09 chr6:43519109 G>T maps to NM_020750.2 C551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr16:17228427 G>A maps to NM_022166.3 S643S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W6-AA0S-01A-11D-A417-09 chr11:102100577 G>T maps to NM_001130145.2 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr1:33246689 G>T maps to NM_003680.3 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr3:183528368 T>C maps to NM_018023.4 *1423R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr22:22064925 G>T maps to NM_013313.3 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr17:57474461 G>T maps to NM_001005404.3 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr17:74077645 G>A maps to NM_180990.3 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W6-AA0S-01A-11D-A417-09 chr3:167023496 G>T maps to ENST00000307529 S553S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-W5-AA39-01A-11D-A417-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr11:114121243 A>T maps to NM_001018011.1 I663I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WD-A7RX-01A-12D-A417-09 chr17:7369565 C>T maps to NM_020899.3 W185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr6:149772004 T>C maps to NM_207360.2 S466S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr2:187351162 A>G maps to NM_018471.2 K18K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WD-A7RX-01A-12D-A417-09 chr7:138768748 C>T maps to ENST00000464606 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W6-AA0S-01A-11D-A417-09 chr16:87443921 G>A maps to NM_015144.2 Y938Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr4:25363482 A>C maps to NM_024936.2 V338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA30-01A-31D-A417-09 chr23:77912768 A>G did not map to a codon.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr3:28562601 G>T maps to NM_001040432.1 E302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr5:825359 T>C maps to NM_024786.2 K314K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr10:114200369 A>G maps to NM_022494.1 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr10:114190584 C>A maps to NM_022494.1 E407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr2:220072730 T>C maps to NM_138802.1 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr12:72024646 G>A maps to NM_144982.4 C1186C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2R-01A-11D-A417-09 chr8:77775450 T>A maps to NM_024721.4 P3167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2O-01A-11D-A417-09 chr15:42740763 G>T maps to NM_022473.1 R858R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr6:29640987 G>T maps to NM_001109809.2 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y8-01A-51D-A417-09 chr5:32407028 A>T maps to NM_016107.3 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2I-01A-32D-A417-09 chr15:41099909 A>G maps to NM_001077268.1 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y4-01A-11D-A417-09 chr14:68275964 A>G maps to NM_015346.3 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y2-01A-11D-A417-09 chr23:136649398 G>A did not map to a codon.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr16:25258432 C>A maps to NM_001012981.4 E362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W6-AA0S-01A-11D-A417-09 chr6:28333605 G>A maps to NM_024493.2 K387K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA34-01A-11D-A417-09 chr7:99123688 C>T maps to NM_014569.3 G342G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr23:101153156 G>T did not map to a codon.
Sequencing variant TCGA-3X-AAVB-01A-31D-A417-09 chr1:40724002 C>T maps to NM_005857.3 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr19:58945595 G>A maps to NM_003433.3 C405C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr23:47272742 G>T did not map to a codon.
Sequencing variant TCGA-W6-AA0S-01A-11D-A417-09 chr23:47272698 A>G did not map to a codon.
Sequencing variant TCGA-W5-AA2W-01A-11D-A417-09 chr8:146156247 G>T maps to NM_006958.2 S642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr19:52090211 G>T maps to NM_007147.2 E210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr19:9491916 A>C maps to NM_001172651.1 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2G-01A-11D-A417-09 chr17:11896083 G>A maps to NM_144680.2 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAV9-01A-72D-A417-09 chr19:22157033 G>A maps to NM_007153.3 Q268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVE-01A-11D-A417-09 chr19:22154451 A>G maps to NM_007153.3 L1128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2T-01A-12D-A417-09 chr19:44564660 G>T maps to NM_013361.4 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y8-01A-51D-A417-09 chr19:24289440 C>A maps to NM_203282.2 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr19:57723024 C>A maps to NM_003417.4 S187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2W-01A-11D-A417-09 chr12:133764549 G>T maps to NM_001165881.2 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y2-01A-11D-A417-09 chr16:89805161 T>C did not map to a codon.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr17:16455208 C>T maps to NM_020653.2 Q749Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Q-01A-11D-A417-09 chr19:9271877 G>T maps to NM_020933.4 T519T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr19:37368143 A>C maps to NM_003419.3 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr5:178154000 C>G maps to NM_005649.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr1:33741757 C>A maps to NM_152493.2 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2X-01A-11D-A417-09 chr1:33741757 C>A maps to NM_152493.2 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr19:52538067 G>T maps to NM_014650.2 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2U-01A-11D-A417-09 chr23:134494602 C>T did not map to a codon.
Sequencing variant TCGA-W5-AA31-01A-11D-A417-09 chr19:44417592 A>G maps to NM_003425.3 D665D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2R-01A-11D-A417-09 chr19:53344780 G>A maps to NM_001008801.1 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr19:52825570 G>T maps to NM_144684.2 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y4-01A-11D-A417-09 chr10:44104180 G>T maps to NM_145312.3 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3X-AAVC-01A-21D-A417-09 chr20:62594089 C>T maps to NM_020713.1 P671P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr2:27601101 G>A maps to NM_144631.4 F312F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y6-01A-11D-A417-09 chr18:74090964 C>G maps to ENST00000443185 A1035A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y8-01A-51D-A417-09 chr18:22669522 A>T maps to NM_015461.2 L1271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr19:42729172 C>T maps to NM_133444.1 C206C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr19:31039276 C>A maps to NM_014717.1 S917S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA33-01A-11D-A417-09 chr19:57888622 C>T maps to NM_173631.2 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr19:37904938 A>G maps to NM_152484.2 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZU-A8S4-01A-11D-A417-09 chr19:37905041 G>T maps to NM_152484.2 S173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr19:56934338 G>T maps to NM_001159861.1 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA38-01A-11D-A417-09 chr15:64968456 T>G did not map to a codon.
Sequencing variant TCGA-ZD-A8I3-01A-11D-A417-09 chr19:52497155 C>T maps to ENST00000354939 Q402Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2H-01A-31D-A417-09 chr17:16527620 G>T maps to NM_020787.3 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr23:47918880 T>G did not map to a codon.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr19:12014750 T>C maps to ENST00000429654 Y74Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2Z-01A-11D-A417-09 chr8:146067376 G>A maps to ENST00000446747 Q305Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr15:35274077 T>G maps to NM_014106.3 R520R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y4-01A-11D-A417-09 chr19:40540575 G>A maps to NM_001005851.2 C730C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2H-01A-31D-A417-09 chr19:12739911 C>A maps to NM_153358.2 P523P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y8-01A-51D-A417-09 chr19:35450227 C>T maps to NM_175872.4 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZO-01A-12D-A417-09 chr2:185802285 T>A maps to NM_194250.1 T721T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr16:71901863 G>A maps to ENST00000425432 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y2-01A-11D-A417-09 chr19:37382534 C>A maps to NM_001171979.1 G467G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA2T-01A-12D-A417-09 chr20:57769547 G>A maps to NM_178457.1 T1158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZH-A8Y5-01A-11D-A417-09 chr19:21132555 C>A maps to NM_003429.4 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W5-AA39-01A-11D-A417-09 chr19:23544196 T>C maps to NM_003430.2 R528R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZD-A8I3-01A-11D-A417-09 chr19:22574572 C>T maps to NM_001098626.1 K488K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4G-AAZT-01A-11D-A417-09 chr19:22952119 A>G maps to ENST00000397104 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YR-A95A-01A-12D-A417-09 chr19:58596276 G>A maps to NM_001145542.1 G492G. Only missense variants will be evaluated by CHASM.
