6602 NP_705833 G1011E not found in SNVbox database
7001 NP_002531 E358K not found in SNVbox database
7807 NP_109597 R429T not found in SNVbox database
7958 NP_002531 D193V not found in SNVbox database
291 NP_705833 Q1015H not found in SNVbox database
1278 NP_705833 E62G not found in SNVbox database
1829 NP_705833 D911N not found in SNVbox database
1947 NP_705833 S279C not found in SNVbox database
2260 NP_705833 E404Q not found in SNVbox database
2870 NP_705833 L746V not found in SNVbox database
2999 NP_705833 Q322E not found in SNVbox database
3802 NP_705833 F104Y not found in SNVbox database
4578 NP_705833 K34N not found in SNVbox database
Sequencing variant TCGA-JX-A5QV-01A-22D-A28B-09 chr12:9265030 G>A maps to NM_000014.4 N124N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr12:8982338 C>T maps to NM_144670.3 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr12:9013792 C>T maps to NM_144670.3 L1134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr12:8997931 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr22:43089411 G>A maps to NM_017436.4 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr12:53703051 G>C maps to NM_015665.5 S275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr12:53702788 C>T maps to NM_015665.5 Q317Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr12:125591714 G>A maps to NM_023928.3 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:125587611 C>G maps to NM_023928.3 S251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr3:151532063 A>G maps to NM_001086.2 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr1:12726088 C>T maps to NM_001013630.1 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:170991779 G>A maps to ENST00000509167 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr4:170990360 A>C maps to ENST00000509167 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr15:67524188 C>T maps to NM_024666.3 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr2:69754431 G>A maps to NM_014911.3 D297D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr2:69709944 C>G did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr2:69757801 G>A maps to NM_014911.3 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:35346677 C>T maps to NM_012138.3 Q428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr17:79093811 C>T maps to NM_001080395.2 G1269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PI-01A-11D-A18J-09 chr17:79094810 G>A maps to NM_001080395.2 P975P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:79094732 G>A maps to NM_001080395.2 L1001L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr9:107593362 G>A maps to NM_005502.3 R579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr9:107578432 G>T maps to NM_005502.3 T1243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:67171597 G>A maps to NM_080282.3 I942I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:67186574 C>T maps to NM_080282.3 R685R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr2:215855599 A>C maps to NM_173076.2 Y1150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr2:215884457 C>T maps to NM_173076.2 E450E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr2:215875192 T>C maps to NM_173076.2 T778T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr2:215865462 G>A maps to NM_173076.2 Q1049*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A3L1-01A-11D-A21Q-09 chr2:215835045 G>A maps to NM_173076.2 R1881*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr2:215823080 G>A maps to NM_173076.2 Q2013*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:215876784 G>A maps to NM_173076.2 L677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr2:215802305 C>T maps to NM_173076.2 L2490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr2:215818591 C>G maps to NM_173076.2 L2211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr7:48315168 C>A maps to NM_152701.3 S1969*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr7:48273628 C>T maps to NM_152701.3 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr7:48349705 C>T maps to NM_152701.3 R3162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr7:48285127 G>A maps to NM_152701.3 E470E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr7:48318504 G>T maps to NM_152701.3 E2572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr7:48412031 C>T maps to NM_152701.3 L3691L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr7:48312256 C>T maps to NM_152701.3 I998I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LT-01A-11D-A18J-09 chr9:139915378 G>T maps to ENST00000355090 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M2-01A-21D-A18J-09 chr9:139912771 C>T maps to ENST00000355090 S647S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr9:139912144 C>T did not map to a codon.
Alternatively spliced codon TCGA-LP-A4AW-01A-11D-A243-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr9:139903453 C>A maps to ENST00000355090 V2323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R3-01A-11D-A28B-09 chr16:2339536 G>A maps to NM_001089.2 S866S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr16:2376197 C>T maps to NM_001089.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr16:2333225 G>A maps to NM_001089.2 L1332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr1:94487407 C>G maps to NM_000350.2 V1589V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:94508318 G>C maps to NM_000350.2 S1109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:94568587 G>A maps to NM_000350.2 Q185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:94461720 C>A maps to NM_000350.2 E2254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:94463473 G>A maps to NM_000350.2 S2224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:94467068 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr17:67246762 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr19:1049292 G>A maps to NM_019112.3 L803L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr19:1053487 G>A maps to NM_019112.3 L1127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:66871432 C>T maps to NM_007168.2 L1493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:66914282 G>C maps to NM_007168.2 S611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr17:67039791 A>T maps to NM_080283.3 L213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:67014660 G>C maps to NM_080283.3 S887*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr7:87133509 A>T did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr7:87179870 C>T maps to NM_000927.3 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr1:229667458 C>T maps to NM_012089.2 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:229653814 T>C did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr2:169847358 G>C maps to NM_003742.2 S287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr2:169801174 G>A maps to NM_003742.2 L850L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M1-01A-11D-A18J-09 chr7:87083891 C>T maps to NM_018849.2 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr7:87041263 G>A maps to NM_018849.2 R957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr7:20762742 G>C maps to NM_001163941.1 L842L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr23:74282250 C>T did not map to a codon.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr23:74295233 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:74295394 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr7:150739172 C>A maps to ENST00000297504 P598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZF-01A-11D-A28B-09 chr7:150730739 C>T maps to ENST00000297504 H65H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr7:150730661 C>T did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr7:150739121 G>A maps to ENST00000297504 V581V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A69L-01A-11D-A32I-09 chr6:43406529 C>G maps to NM_033450.2 L680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr6:43395874 G>C maps to ENST00000372530 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr6:43410727 C>T maps to NM_033450.2 L721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr16:48244924 G>A maps to NM_032583.3 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr16:48209284 G>A maps to NM_032583.3 P1194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr16:48125045 G>C maps to NM_033226.2 L1090L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr16:48130713 C>T maps to NM_033226.2 L1046L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr16:48172184 C>T maps to NM_033226.2 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73Q-01A-21D-A32I-09 chr16:48139109 G>A maps to NM_033226.2 F871F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A449-01A-11D-A243-09 chr10:101577117 G>A maps to NM_000392.3 K716K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr17:48761447 C>T maps to NM_003786.3 Q1365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr17:48742569 C>G maps to NM_003786.3 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr17:48738472 C>G maps to NM_003786.3 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr17:48745144 C>T maps to NM_001144070.1 P554P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr17:48746593 G>A maps to NM_003786.3 E677E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LC-01A-11D-A20U-09 chr13:95735502 G>A maps to NM_005845.3 A859A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr13:95695856 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr13:95696670 C>A maps to NM_005845.3 E1160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:183669664 G>A maps to NM_005688.2 R932*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:183685503 G>C maps to NM_005688.2 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:16255324 G>C maps to NM_001171.5 L1201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:16282744 G>C maps to NM_001171.5 L574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr16:16315643 C>G maps to NM_001171.5 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr16:16291889 G>C maps to NM_001171.5 V442V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr16:16248552 G>C maps to NM_001171.5 L1380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M2-01A-21D-A18J-09 chr12:22063159 G>A maps to NM_005691.2 V417V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr12:22061142 G>A maps to NM_005691.2 I441I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr12:21997452 G>A maps to NM_005691.2 L1093L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr23:152991451 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr23:153008475 T>C did not map to a codon.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr23:153008475 T>C did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:152994962 G>A did not map to a codon.
Sequencing variant TCGA-EA-A411-01A-11D-A243-09 chr23:152990940 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr23:152995017 G>A did not map to a codon.
Sequencing variant TCGA-HM-A3JK-01A-11D-A21Q-09 chr23:152990783 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:152991175 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr1:94972173 C>A maps to ENST00000454898 G631G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M1-01A-11D-A18J-09 chr1:94983782 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:94980662 C>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr4:146044713 T>G maps to NM_002940.2 V534V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A78R-01A-11D-A32I-09 chr7:150918699 G>A maps to NM_005692.3 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr21:43704741 C>T maps to NM_004915.3 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr11:119025601 C>T maps to NM_001142505.1 V221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr2:44053553 G>C maps to NM_022436.2 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr2:44051359 C>A maps to NM_022436.2 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr2:44051058 C>T maps to NM_022436.2 V439V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr2:44079963 C>T maps to NM_022437.2 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LS-01A-22D-A22X-09 chr2:44101012 C>T maps to NM_022437.2 F433F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr2:44104793 C>T maps to NM_022437.2 L617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr2:44104967 C>T maps to NM_022437.2 I646I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr3:111700727 C>T maps to NM_018394.2 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr14:51371086 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr3:52003447 G>A maps to NM_032750.2 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr3:52003870 G>A maps to ENST00000461108 Q181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr17:27889579 C>G maps to NM_198147.2 *469S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HQ-01A-11D-A20U-09 chr15:89731450 G>A maps to NM_152924.4 K281K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr15:89694979 G>A maps to NM_152924.4 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr18:19283675 G>A maps to NM_138340.4 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr19:17405542 G>A maps to NM_024527.4 F291F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr19:17405644 G>A maps to NM_024527.4 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:17405098 C>A maps to NM_024527.4 E383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HM-A3JK-01A-11D-A21Q-09 chr10:27112159 T>C maps to NM_005470.3 Q64Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr9:133730461 C>T maps to NM_007313.2 I195I. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-C5-A7CM-01A-11D-A33O-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EA-A3HR-01A-11D-A20U-09 chr9:133759591 C>T maps to NM_007313.2 R658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr9:133759497 G>A maps to NM_007313.2 K626K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr1:179077402 G>C maps to NM_007314.3 S1000*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3YQ-01A-11D-A22X-09 chr1:179095625 G>A maps to NM_007314.3 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U3-01A-11D-A28B-09 chr5:148622101 G>T did not map to a codon.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr3:38164398 G>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr18:47310230 G>A maps to NM_006111.2 Q394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr17:35562744 G>T maps to NM_198834.1 I1330I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr17:35766392 C>G did not map to a codon.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr17:35486320 G>T maps to NM_198834.1 R1972R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:109634907 C>T maps to NM_001093.3 L859L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr12:112130575 G>A maps to NM_001136538.1 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr12:112167694 G>C maps to NM_001136538.1 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr3:132294630 C>T maps to NM_032169.4 K662K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr3:128598505 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr3:128615307 G>A maps to NM_014049.4 Q161Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:211053738 A>G maps to NM_001608.3 G413G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:76226833 G>T maps to ENST00000370834 E358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:76226982 G>A maps to ENST00000370834 Q407Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr12:121176977 C>T maps to NM_000017.2 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr10:124800816 C>T maps to NM_001609.3 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:7125394 G>A maps to ENST00000356839 W295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:89391201 C>T maps to NM_013227.3 V555V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr15:89381936 G>A maps to NM_013227.3 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr3:195016552 G>T maps to NM_012287.5 S519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr6:160196399 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr17:43213570 G>A maps to NM_001135706.1 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr11:44069822 C>T maps to NM_001031854.2 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr11:44077811 T>C maps to NM_001031854.2 F421F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr11:44074224 C>T maps to NM_001031854.2 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr11:44079865 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr17:61559096 C>T maps to NM_000789.3 F372F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:61568381 G>C maps to NM_000789.3 S903S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr17:61557755 C>T maps to NM_000789.3 D238D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr14:23537772 G>T did not map to a codon.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr14:23532259 G>A maps to NM_014977.3 R979*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr14:23564375 C>G maps to NM_014977.3 R40R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr17:40061805 G>C maps to ENST00000401700 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr17:40025360 C>T maps to ENST00000401700 L1067L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr5:80626632 G>A maps to NM_130767.2 I506I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr6:24701841 G>A maps to NM_018473.3 *141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr1:6399595 G>A maps to NM_007274.3 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:23722843 C>G did not map to a codon.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr17:73975167 T>G did not map to a codon.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr3:58516239 G>A maps to NM_003500.3 I315I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr3:58508291 C>G maps to NM_003500.3 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr3:58490951 C>T maps to NM_003500.3 *682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr3:58490951 C>G maps to NM_003500.3 *682S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr19:11685967 G>A maps to NM_001111036.1 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZF-01A-11D-A28B-09 chr3:141011881 C>T maps to NM_001037172.1 V426V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr22:51183024 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr22:51183145 C>T maps to NM_001097.2 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr22:51183024 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr22:51182580 C>T maps to NM_001097.2 Q220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr12:6752713 G>A maps to NM_032489.2 F356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:70824091 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:70832406 G>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:70824304 C>G did not map to a codon.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr23:70824019 G>A did not map to a codon.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr23:70824020 C>G did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr23:70828884 C>G did not map to a codon.
Sequencing variant TCGA-MY-A5BE-01A-21D-A26G-09 chr15:78466843 C>T maps to NM_015162.4 G575G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr19:6183145 C>T maps to NM_030924.3 I395I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr17:48538694 C>G maps to ENST00000427954 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr4:185683649 G>A maps to NM_001995.2 Q517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr2:223789233 C>T maps to NM_203372.1 Q405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:223789178 C>T maps to NM_203372.1 I386I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:108911443 C>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:108904800 C>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:108906586 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:108887379 G>C did not map to a codon.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr23:108924277 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr16:20682920 C>G maps to NM_052956.2 G228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr16:20682932 G>A maps to NM_052956.2 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr16:20548638 G>A maps to NM_182617.3 Q559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A57G-01A-11D-A26G-09 chr16:20559409 G>A maps to NM_182617.3 R358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr16:20808369 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr20:25038480 G>A maps to NM_032501.2 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AX-01A-12D-A243-09 chr20:33513534 C>T maps to NM_001076552.2 I577I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr12:81568568 G>A maps to NM_024560.2 G367G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr1:229568793 G>A maps to NM_001100.3 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr1:229568026 G>A maps to NM_001100.3 F202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A4BA-01A-21D-A26G-09 chr7:5567196 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr7:5566883 C>T did not map to a codon.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr5:56778416 G>A maps to NM_001017992.2 R40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr15:35085532 G>A maps to NM_005159.4 Q123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr17:79478442 C>T maps to NM_001614.2 K191K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr17:79479368 C>T maps to NM_001614.2 E4E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr17:79479014 C>A maps to NM_001614.2 E93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr3:179294462 C>T maps to NM_004301.3 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr3:179305796 G>C maps to NM_004301.3 *430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr9:111625117 G>A maps to NM_006687.2 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr9:111625726 G>A maps to NM_006687.2 Q375Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:18153013 A>G maps to NM_030812.2 *367W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr19:8808988 G>C maps to NM_178525.3 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr14:69349242 C>A maps to NM_001130004.1 E629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr14:69349982 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr14:69350052 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr1:236883472 C>T maps to NM_001103.2 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:236925801 G>A maps to NM_001103.2 P856P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr19:39219658 C>T maps to NM_004924.3 I814I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr19:39219712 C>T maps to NM_004924.3 I832I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr19:39219928 G>T maps to NM_004924.3 E865*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr19:39219694 G>A maps to NM_004924.3 V826V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A6QX-01A-12D-A33O-09 chr19:39219709 C>T maps to NM_004924.3 F831F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:98275837 G>A maps to NM_005735.3 Q98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr2:65473824 C>T maps to NM_001005386.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VI-01A-11D-A28B-09 chr2:65473735 C>T maps to NM_001005386.2 R85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr7:152520587 C>T maps to NM_020445.4 F282F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr12:100603860 C>G maps to NM_022496.3 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr12:52387887 G>A maps to NM_020328.3 K545K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr2:158412761 C>G maps to NM_145259.2 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr2:158406725 C>T maps to NM_145259.2 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr2:148674877 C>G maps to NM_001616.3 Y233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr2:148654035 G>A maps to NM_001616.3 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr3:38519414 C>T maps to NM_001106.3 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr3:52021612 C>T maps to ENST00000463937 G399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2GZ-01A-11D-A17W-09 chr20:43249624 C>T did not map to a codon.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr20:43248485 G>A maps to NM_000022.2 Q361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr16:84229447 C>T maps to NM_139174.3 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr17:42851876 G>A maps to NM_002390.4 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr17:42850446 C>T maps to NM_002390.4 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr10:127724831 C>T maps to NM_003474.4 L807L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7X3-01A-11D-A351-09 chr1:155034079 C>A did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:155023352 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:155030784 C>T maps to NM_207197.1 I595I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr1:155028478 G>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:9645419 G>A maps to NM_003183.4 R473R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr2:9637282 G>A maps to NM_003183.4 F581F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr2:9667998 G>A maps to NM_003183.4 Q179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr8:39496007 G>T maps to NM_014237.2 V284V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr14:70926377 C>G maps to NM_003813.2 S721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PI-01A-11D-A18J-09 chr7:87762259 G>C maps to NM_021723.3 V357V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr2:207424740 G>A maps to NM_003812.2 K356K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr8:24181360 C>T maps to NM_014265.4 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr4:175896931 C>T maps to NM_014269.4 Q86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CJ-01A-11D-A32I-09 chr8:39142356 C>T did not map to a codon.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr8:38965216 C>G maps to ENST00000437682 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr20:3649568 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr8:24299984 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr8:24321393 G>A did not map to a codon.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr8:24342817 G>T maps to ENST00000380789 G302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr10:135084280 G>A maps to NM_001109.4 F531F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr8:38883374 C>G maps to NM_003816.2 S323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr19:8657676 C>T maps to NM_030957.2 T519T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr19:8670175 T>C maps to NM_030957.2 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr5:33881289 G>A maps to NM_030955.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr5:33616031 C>T maps to NM_030955.2 G763G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr10:72434399 G>A maps to NM_139155.2 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr10:72517979 G>A maps to NM_139155.2 T1042T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr5:5239839 C>T maps to NM_139056.2 R775R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R3-01A-11D-A28B-09 chr5:5235147 C>T maps to NM_139056.2 F624F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr15:100695465 G>C maps to NM_139057.2 S414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr16:77325240 C>T maps to NM_199355.2 E1108E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr5:129037111 C>T maps to NM_133638.3 R990*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr5:128983516 G>A maps to NM_133638.3 E638E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A69B-01A-11D-A32I-09 chr5:178559249 G>A maps to NM_014244.4 D757D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr12:43944891 C>T maps to ENST00000389420 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WH-01A-22D-A351-09 chr12:43822199 G>T maps to ENST00000389420 C1263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr12:43771256 C>A maps to ENST00000389420 E1636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr1:161165345 G>A maps to NM_005099.4 V390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:161166036 G>C maps to NM_005099.4 V338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr15:79058073 C>T maps to ENST00000258883 P1393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr15:79068582 T>A maps to ENST00000258883 S551S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr9:18639369 G>T maps to NM_001040272.4 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr9:18639369 G>T maps to NM_001040272.4 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr9:18639297 C>G maps to NM_001040272.4 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr9:18622251 C>T maps to NM_001040272.4 C162C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr9:18777069 C>G maps to NM_001040272.4 S948*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr9:18776962 G>A maps to NM_001040272.4 E912E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr9:136406067 C>T maps to ENST00000393061 D318D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZF-01A-11D-A28B-09 chr15:84657472 G>A maps to NM_207517.2 Q1249Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr1:150524267 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr1:150522693 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:150529704 G>C maps to ENST00000369039 R670R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr1:154561846 G>A maps to ENST00000292205 I963I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:154562687 G>C maps to ENST00000292205 S866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr10:1246191 A>G maps to ENST00000381310 D35D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr10:1262868 G>A did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr10:1779302 C>T maps to NM_018702.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A4BA-01A-21D-A26G-09 chr1:33567486 C>T maps to ENST00000341637 A373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr1:33546850 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:33549551 C>T did not map to a codon.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr1:33547747 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr14:78366916 G>T maps to ENST00000393639 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr7:45717776 C>T maps to NM_021116.2 Q605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr7:45726196 C>G maps to NM_021116.2 L793L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr1:167779062 G>C maps to NM_018417.4 S1562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr1:167852752 G>A maps to NM_018417.4 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr1:167825572 G>A maps to NM_018417.4 F667F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:167823648 G>C maps to NM_018417.4 L750L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr5:7692128 C>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:7802389 C>T maps to NM_020546.2 F896F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A411-01A-11D-A243-09 chr5:7396480 C>T maps to NM_020546.2 D24D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr2:25065202 C>A maps to NM_004036.3 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr2:25095468 C>T maps to NM_004036.3 K265K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr14:24787689 G>A maps to NM_139247.3 Q1056*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr14:24792558 G>A maps to NM_139247.3 I716I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr3:123044255 G>A maps to NM_183357.2 I667I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr3:123010070 G>C maps to NM_183357.2 V1072V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr3:123010070 G>A maps to NM_183357.2 V1072V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr12:49162767 C>T maps to NM_015270.3 V1111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr16:50344638 G>A maps to NM_001114.3 S734S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr8:131964193 G>A maps to NM_001115.2 I387I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr8:132002734 G>T maps to NM_001115.2 I338I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr8:132002737 G>A maps to NM_001115.2 F337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr8:131826398 C>G maps to NM_001115.2 L943L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VH-01A-11D-A28B-09 chr8:132052021 G>A maps to NM_001115.2 N186N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr8:131848626 C>T maps to NM_001115.2 L857L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr8:132051625 G>A maps to NM_001115.2 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr16:4163952 G>A maps to NM_001116.3 C497C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr4:2910283 C>T maps to NM_014189.2 Q551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr4:2877716 C>T maps to NM_014189.2 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr4:2906519 C>A maps to NM_014189.2 Y397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr4:2886369 C>T maps to NM_014189.2 Q163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr2:70890610 G>A maps to NM_001185054.1 F709F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr10:111881893 A>G maps to NM_016824.3 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:111892228 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr10:111884031 G>A maps to NM_016824.3 T467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr4:100237127 G>T maps to NM_000668.4 S165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr4:100239093 C>T did not map to a codon.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr4:100048483 C>T maps to ENST00000505590 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr4:100047842 G>A maps to ENST00000505590 D359D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr4:99993740 C>T maps to NM_000671.3 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr4:100137073 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr4:100129808 C>G did not map to a codon.
Sequencing variant TCGA-JW-A5VI-01A-11D-A28B-09 chr4:100129850 C>A maps to NM_001102470.1 E268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr3:186570918 G>A maps to NM_004797.3 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr12:1882006 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr10:76429980 G>A maps to NM_006721.2 Q306Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr20:49508891 C>A maps to NM_181442.1 E787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr20:49509638 C>A maps to NM_181442.1 E538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr20:49510334 G>A maps to NM_181442.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr18:77895866 G>A maps to NM_014913.3 V857V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr18:77896352 A>G maps to NM_014913.3 R1019R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr1:203134454 C>T maps to NM_001048230.1 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CH-01A-11D-A33O-09 chr1:112029267 G>C maps to NM_020683.6 S271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LB-01A-11D-A243-09 chr15:73044860 C>A maps to NM_031284.4 E438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A78R-01A-11D-A32I-09 chr3:119301228 G>T maps to NM_001125.2 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr13:114083291 G>T maps to NM_138430.3 C207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr8:26722240 G>A maps to ENST00000356368 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:112838143 C>G maps to NM_000681.3 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:112839031 C>T maps to NM_000681.3 F426F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr10:112839007 G>A maps to NM_000681.3 V418V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr10:112839109 C>T maps to NM_000681.3 F452F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr2:96781783 C>T maps to NM_000682.5 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr10:115804370 C>T maps to NM_000684.2 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr5:148207389 C>T maps to NM_000024.5 F332F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr11:67053973 G>C did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:67044811 G>A maps to NM_001619.3 Q61Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:67050285 G>A maps to NM_001619.3 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr22:40759014 C>T maps to NM_000026.2 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr22:40745945 G>A maps to ENST00000428371 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr7:44151817 C>G maps to NM_001129.3 L705L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr4:7873715 C>T maps to NM_001134647.1 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr4:7787926 G>A maps to NM_001134647.1 N508N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr5:148682037 G>T maps to NM_152406.2 E129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr5:148697430 C>A maps to NM_152406.2 A469A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr10:116064525 G>A maps to NM_001001936.1 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5O9-01A-11D-A28B-09 chr23:148055116 T>A did not map to a codon.
Sequencing variant TCGA-EA-A6QX-01A-12D-A33O-09 chr23:147733595 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr23:148037543 G>C did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:148037883 C>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:147743666 C>A did not map to a codon.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr2:100728974 G>A did not map to a codon.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr5:132272779 G>C maps to NM_014423.3 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr4:74321432 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr2:64800108 G>A maps to ENST00000422803 L767L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr10:88760445 A>C did not map to a codon.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr10:88760502 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr15:86697673 A>G maps to NM_152336.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr2:27276035 G>A maps to NM_021831.5 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr2:27276871 G>T maps to NM_021831.5 E166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr2:27278088 G>A maps to NM_021831.5 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr2:27278588 G>A maps to NM_021831.5 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr2:27278877 G>T maps to NM_021831.5 E413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr2:27276284 C>T maps to NM_021831.5 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr2:27281370 G>A maps to NM_021831.5 W592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr1:100340196 C>G did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:100347191 C>T maps to ENST00000311030 F752F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3TQ-01A-11D-A22X-09 chr1:15904320 C>T maps to NM_024758.3 K253K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr6:32137053 C>T maps to NM_032741.4 *284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr9:139571110 C>A maps to NM_006412.3 E172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr9:139568326 C>T maps to NM_006412.3 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr21:45374796 C>G did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr21:45374857 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr4:84525960 G>C did not map to a codon.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr1:984693 G>T maps to NM_198576.2 L1459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:979320 C>T maps to NM_198576.2 Y639Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr9:88307682 C>T maps to ENST00000395847 E26E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:88203304 G>C maps to ENST00000395847 L937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr1:247028618 G>T did not map to a codon.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr1:247061638 C>T did not map to a codon.
Sequencing variant TCGA-EA-A5ZE-01A-11D-A28B-09 chr1:247003180 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr1:247016503 C>T maps to ENST00000428671 L1522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr1:247024351 C>T maps to ENST00000428671 P1365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr1:247002959 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A5R3-01A-11D-A28B-09 chr20:32880200 G>A maps to NM_000687.2 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr1:27860954 C>T did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr1:27861164 C>G did not map to a codon.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr1:27875173 C>T maps to NM_001029882.2 Q1151Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:27861136 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr6:135769613 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr11:62284968 C>T maps to NM_001620.1 L5640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr11:62288061 G>A maps to NM_001620.1 G4609G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr11:62300589 C>T maps to NM_001620.1 K433K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:62286536 G>A maps to NM_001620.1 Q5118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KH-01A-21D-A22X-09 chr14:105417626 G>A maps to NM_138420.2 L1387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr14:105417014 G>A maps to NM_138420.2 L1591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr14:105411032 C>T maps to NM_138420.2 L3585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr14:105418844 C>T maps to NM_138420.2 E981E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr14:105412934 C>T maps to NM_138420.2 P2951P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr14:105409511 C>T maps to NM_138420.2 V4092V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr7:17379821 A>G maps to NM_001621.4 V791V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr5:428076 G>C maps to NM_020731.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:61413944 A>G did not map to a codon.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr1:222867560 T>A maps to NM_022831.2 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZF-01A-11D-A28B-09 chr1:222885351 G>C did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr9:133981649 C>T maps to NM_001185095.1 Q57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr23:129299533 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:129281545 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr22:21329098 C>T maps to NM_144704.2 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr22:21327624 G>T maps to NM_144704.2 E21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:106960254 G>T maps to NM_001624.2 R13R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:26663709 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr7:6057524 G>T maps to NM_006303.3 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr21:45711045 G>T maps to NM_000383.2 R316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr1:4834485 G>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:33490111 C>G maps to NM_001625.3 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:78024353 G>A maps to NM_174858.1 *563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q8-01A-11D-A21Q-09 chr1:77763548 T>C maps to NM_174858.1 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr14:96944800 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr14:96944934 C>T maps to NM_152327.2 I563I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr13:42891749 C>T maps to NM_016248.2 Q1831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr13:42877014 C>A maps to NM_016248.2 S1378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr15:86189139 C>G maps to NM_006738.4 L1443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr15:86228061 C>T maps to NM_006738.4 F1753F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr15:86123893 C>T maps to NM_006738.4 L865L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WI-01A-12D-A351-09 chr15:86123231 C>T maps to NM_006738.4 Q645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr15:86064768 G>T maps to NM_006738.4 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr15:86201774 C>T maps to NM_007200.3 R1585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr23:119037198 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2H1-01A-11D-A17W-09 chr9:112930800 C>T did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr12:4735735 G>A maps to NM_006422.2 Q778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A69L-01A-11D-A32I-09 chr12:4737914 C>T maps to NM_006422.2 K51K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr23:49955454 G>A did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr23:49958364 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr23:49958882 C>A did not map to a codon.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr23:49957834 T>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:49957941 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:49958259 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:49957242 G>C did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr14:33291445 C>G maps to NM_004274.4 S1476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr14:33292214 C>G maps to NM_004274.4 V1732V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A411-01A-11D-A243-09 chr19:15512269 G>T maps to NM_014371.2 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr9:117139084 C>T maps to NM_030767.4 Q334Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R9-01A-11D-A18J-09 chr9:117107282 C>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr9:117120223 G>A maps to NM_030767.4 R906*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr9:117108027 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr9:117119144 G>A maps to NM_030767.4 I948I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr9:117103901 C>T maps to NM_030767.4 W1326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr1:109394360 G>C maps to NM_152763.3 S309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:109391559 C>A maps to NM_152763.3 E386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr7:134254235 G>A maps to ENST00000418096 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr7:134261722 C>T maps to ENST00000418096 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OA-01A-11D-A16Y-08 chr10:5032036 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3L7-01A-21D-A20U-09 chr10:5041579 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr10:5238642 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr7:137790150 C>G maps to NM_005989.3 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr7:137801415 G>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:19633835 C>T maps to NM_003689.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:40771138 G>A maps to NM_001626.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr1:243952038 T>C did not map to a codon.
Sequencing variant TCGA-C5-A7CH-01A-11D-A33O-09 chr23:55047615 G>T did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:55043939 C>G did not map to a codon.
Sequencing variant TCGA-FU-A5XV-01A-11D-A28B-09 chr23:55041278 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr19:49965834 C>G maps to NM_153329.3 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr10:97396861 G>A maps to NM_002860.3 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr9:75524534 C>A maps to NM_000689.3 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr15:58287281 G>T maps to NM_003888.2 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr15:101440801 C>T maps to NM_000693.2 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr12:105456722 C>T maps to NM_001034173.3 K288K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr11:67795655 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr11:67438576 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr11:67434462 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr1:19216522 G>A maps to NM_003748.3 R47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr1:19204080 G>A maps to NM_003748.3 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr14:74534263 C>T maps to NM_005589.2 K287K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CJ-01A-11D-A32I-09 chr6:135254072 G>A maps to NM_022568.3 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr16:30077130 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr16:30077130 C>G did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr16:30077130 C>G did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr16:30081398 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr9:104184111 G>A maps to NM_000035.3 F358F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LT-01A-11D-A18J-09 chr23:110988035 G>T did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:110961479 T>C did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:110964868 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr23:111003066 G>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:110970136 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:110988026 C>T did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:110928225 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr3:125649456 C>T maps to NM_001195223.1 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:63894748 G>A maps to ENST00000263440 R428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr11:77812241 C>G did not map to a codon.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr11:77838403 C>T maps to NM_024079.4 E58E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr11:77850610 C>T maps to NM_024079.4 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr14:78140374 G>T maps to NM_006020.2 S317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr11:43911304 G>A maps to NM_139178.3 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr17:18098343 C>T maps to ENST00000261650 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr17:18087691 C>T maps to ENST00000261650 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr11:107431559 C>T maps to ENST00000417449 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr2:73613100 G>A maps to NM_015120.4 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr2:73716936 G>A maps to NM_015120.4 Q2616Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr17:4541559 G>A maps to NM_001140.3 F253F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr17:7942714 C>T maps to NM_001141.2 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:45924145 C>T maps to NM_000698.2 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr10:45878010 G>A maps to NM_000698.2 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr10:45938982 C>G maps to NM_000698.2 S524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RA-A741-01A-11D-A33O-09 chr10:45939494 G>A did not map to a codon.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr4:113352412 C>T maps to NM_025144.3 F570F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr18:56203890 G>T maps to NM_052947.3 P1176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr15:85400593 G>C maps to NM_020778.4 L1077L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr15:85370780 C>T maps to NM_020778.4 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr15:85383340 C>T maps to NM_020778.4 N479N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr15:85411340 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr2:202619286 C>A maps to NM_020919.3 E527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr2:202630301 C>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr2:202622380 C>T maps to NM_020919.3 V405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr3:46713022 G>A maps to NM_147129.3 P912P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr3:46716159 G>A maps to NM_147129.3 L775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr3:46713022 G>A maps to NM_147129.3 P912P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:46722598 G>C maps to ENST00000431015 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M1-01A-11D-A18J-09 chr2:202352335 C>T maps to NM_001168221.1 *1821*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr9:116823270 G>A maps to NM_001633.3 Q321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LS-01A-22D-A22X-09 chr11:46430213 C>T maps to ENST00000458649 L1084L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr11:46529872 G>C maps to ENST00000458649 S736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr6:111211455 G>C did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr16:2578498 C>T maps to NM_001145815.1 N303N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr16:2581196 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:11316903 C>G did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr12:53823279 G>A maps to NM_020547.2 Q337Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr12:53823406 G>T maps to NM_020547.2 E380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr11:118081244 G>A maps to NM_001098526.1 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:109561024 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr2:128628867 G>C maps to NM_031445.2 S158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr12:31882027 G>A did not map to a codon.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr12:31882027 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:31842022 C>G maps to NM_001113402.1 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr23:112066005 G>A did not map to a codon.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr23:112058972 T>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:112024237 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:112058693 A>G did not map to a codon.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr23:112058754 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:112054492 G>C did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr23:112058935 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr3:134080425 C>T maps to ENST00000514516 E559E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr3:134085179 C>T maps to ENST00000514516 R435R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr11:10483212 C>T maps to NM_000480.2 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr7:38432236 G>A did not map to a codon.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr7:38468040 A>G maps to ENST00000421537 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr7:38431443 G>A maps to NM_001635.3 Q595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:49454674 G>C did not map to a codon.
Sequencing variant TCGA-JW-A852-01A-11D-A351-09 chr1:104115770 C>T maps to ENST00000305865 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr2:112638297 C>T maps to NM_022662.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr10:73989993 C>T did not map to a codon.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr9:140082273 C>T maps to NM_013366.3 E133E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr9:140080857 C>G did not map to a codon.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr1:213173780 G>A did not map to a codon.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr8:6360663 C>T maps to NM_001147.2 S483S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr20:855044 G>T maps to NM_015985.2 V411V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VH-01A-11D-A28B-09 chr1:178822863 A>G maps to NM_004673.3 Y294Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr11:101771163 G>A maps to NM_178127.4 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr8:41563759 C>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr4:114117522 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr10:61835653 G>C maps to NM_020987.2 S1662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr10:61846552 C>T maps to NM_020987.2 R1210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr15:65212090 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr15:65204163 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr17:54535255 G>C maps to NM_153228.2 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:54543852 C>G maps to NM_153228.2 S568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DV-01A-11D-A32I-09 chr17:54526548 T>C did not map to a codon.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr17:4098306 G>A maps to NM_016376.3 R446R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr17:4120285 G>A maps to NM_016376.3 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr17:4088125 G>T maps to NM_016376.3 I562I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr5:14741992 T>G maps to NM_054027.4 T318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr5:139838436 C>T maps to ENST00000253810 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A69M-01A-11D-A32I-09 chr5:139838930 C>T maps to ENST00000253810 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr5:139884446 C>T maps to ENST00000253810 Q1016*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RL-01A-11D-A18J-09 chr11:113270973 C>T maps to NM_178510.1 A761A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr19:17397496 G>T maps to ENST00000438921 V589V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr13:111552899 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3QD-01A-32D-A22X-09 chr16:89352025 G>A maps to NM_013275.4 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr16:89367173 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr16:89350570 C>T maps to NM_013275.4 K793K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr16:89351173 C>T maps to NM_013275.4 V592V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr18:9255251 G>T maps to NM_015208.3 E663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr18:9258685 G>A maps to NM_015208.3 E1807E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr18:9255251 G>T maps to NM_015208.3 E663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WH-01A-22D-A351-09 chr18:9255689 G>T maps to NM_015208.3 E809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr18:9255241 G>A maps to NM_015208.3 E659E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr18:9257209 C>T maps to NM_015208.3 V1315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:27939912 C>T maps to NM_152345.4 I528I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr1:70819989 G>A maps to NM_030816.4 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr4:73956515 G>A maps to NM_032217.3 Q2277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr9:69420381 G>A maps to NM_001098805.1 T424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr19:4222692 C>T maps to ENST00000262970 F1156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr19:4217320 C>T maps to ENST00000262970 Q812*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HM-A4S6-01A-11D-A26G-09 chr19:4222783 C>T maps to ENST00000262970 Q1187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr10:27335120 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr10:27335391 C>T maps to NM_014915.2 S625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr10:27322177 C>T maps to NM_014915.2 K1261K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr19:33096836 C>T maps to NM_032139.2 S799S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BE-01A-21D-A26G-09 chr19:33135368 G>A maps to NM_032139.2 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr19:33149897 G>A maps to NM_032139.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr3:15717535 G>A did not map to a codon.
Sequencing variant TCGA-EA-A5ZE-01A-11D-A28B-09 chr10:37438769 G>A maps to ENST00000374660 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A770-01A-11D-A33O-09 chr5:94027875 C>T maps to NM_032290.3 L870L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr1:145474434 G>A maps to NM_001039888.2 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr1:145473675 C>A maps to NM_001039888.2 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr2:98206252 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr17:48784889 G>C maps to NM_052855.3 V42V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr2:197870439 C>T maps to NM_001195144.1 P775P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr11:94230224 G>A did not map to a codon.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr4:125591338 C>G maps to NM_020337.2 L1031L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr12:56641846 G>A maps to NM_173595.3 I646I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr2:71209787 G>A maps to NM_001115116.1 Q288Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HR-01A-11D-A20U-09 chr22:38229153 G>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr22:38227783 G>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr22:38227804 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr6:90312809 C>T maps to ENST00000339746 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr6:90276739 C>G maps to ENST00000339746 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr6:35021878 G>T maps to NM_015245.2 E672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr12:99128515 A>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr16:4750747 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr9:101546365 C>T maps to ENST00000375018 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr11:70028708 C>G maps to NM_018043.5 L835L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3L7-01A-21D-A20U-09 chr12:5685040 C>T maps to ENST00000356134 Q861Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr12:5672734 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr12:5908677 G>A maps to ENST00000356134 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr12:101437343 C>T maps to ENST00000392977 I394I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr12:101491723 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr11:22294415 C>T maps to NM_213599.2 R706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:22296233 G>A maps to NM_213599.2 L785L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr19:17444511 C>T maps to NM_020959.2 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr11:430148 G>A maps to NM_001012302.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr12:48866841 G>A maps to NM_012404.2 *132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:90349433 G>A maps to NM_001150.2 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr4:80828577 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr9:75783757 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr10:81926597 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr8:124696864 G>A maps to NM_001003954.1 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr8:124707746 G>A maps to NM_001003954.1 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A78R-01A-11D-A32I-09 chr4:122605887 G>A maps to NM_001154.3 R45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr5:150497333 G>A maps to NM_001155.4 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr1:150958851 C>A maps to NM_003568.2 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr17:41001223 G>C maps to NM_009590.2 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr2:201507421 A>C maps to NM_001159.3 P915P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3TQ-01A-11D-A22X-09 chr22:29727817 C>T maps to NM_001127.3 T799T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr22:29724827 C>T maps to NM_001127.3 E944E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr16:71798268 G>C maps to ENST00000423132 S324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr16:71841729 C>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr19:16337341 C>A maps to NM_001130524.1 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr23:15870499 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr23:15849591 C>G did not map to a codon.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr19:50295237 C>T maps to NM_014203.2 R174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr17:33984675 C>T maps to NM_001030006.1 Q619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr3:183899780 C>G maps to ENST00000411763 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr3:183898924 G>C maps to ENST00000411763 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A6QX-01A-12D-A33O-09 chr5:77338707 G>C did not map to a codon.
Sequencing variant TCGA-C5-A2M1-01A-11D-A18J-09 chr15:83349468 G>A maps to NM_004644.3 Y270Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr19:2102252 G>C maps to ENST00000355272 V1189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr19:2121283 G>A maps to ENST00000355272 I376I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RA-A741-01A-11D-A33O-09 chr19:2130440 G>T maps to ENST00000355272 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:114438787 C>G did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr1:114442772 G>A maps to NM_006594.2 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr1:114447339 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr1:114443927 G>A maps to NM_006594.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr15:51293236 C>G maps to NM_007347.3 S1037*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr12:99042619 C>T did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr12:99106098 C>T maps to NM_181861.1 L948L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr12:99120963 C>G maps to NM_181861.1 S1157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr12:99042546 C>T maps to NM_181861.1 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr19:3760025 G>T maps to NM_004886.3 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr11:6417048 G>A maps to ENST00000389906 A644A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr10:26856370 C>G maps to NM_019043.3 S652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:26851193 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr10:26802468 G>A maps to NM_019043.3 E231E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr5:139943249 C>T maps to ENST00000354402 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZE-01A-11D-A28B-09 chr5:112178154 G>A maps to NM_001127510.2 Q2288Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr5:112136974 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr19:1456385 C>T maps to NM_005883.2 Q267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr19:1465201 G>C maps to NM_005883.2 L634L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr18:10468598 G>A maps to ENST00000423585 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr14:20923755 G>A did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr14:20925477 C>G maps to NM_080649.1 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr23:55026965 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LC-01A-11D-A20U-09 chr23:55033704 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73Q-01A-21D-A32I-09 chr23:55028831 G>T did not map to a codon.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr1:150241156 G>A maps to NM_001077628.1 F18F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr1:150239366 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr1:150238975 G>A maps to NM_001077628.1 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr11:34877322 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr11:34912206 C>T did not map to a codon.
Sequencing variant TCGA-FU-A770-01A-11D-A33O-09 chr23:128782614 G>T did not map to a codon.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr11:57003623 G>A maps to NM_005161.4 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr11:129980539 A>C maps to NM_001642.2 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:156563344 C>G maps to ENST00000446584 S239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:116692247 G>A maps to NM_000482.3 Q176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr2:21256184 C>T maps to NM_000384.2 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr2:21252877 C>T maps to NM_000384.2 K454K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr2:21247861 C>T maps to NM_000384.2 Q793Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:21225909 C>T maps to NM_000384.2 V4128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr2:21260895 C>T maps to NM_000384.2 K157K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr12:7802148 C>T maps to NM_001644.3 W235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr22:39385581 G>C maps to ENST00000402182 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr22:39417538 C>A maps to NM_152426.3 I5I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr22:39421628 C>T maps to NM_152426.3 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr22:39427901 C>T maps to NM_152426.3 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr22:39477101 G>A maps to NM_021822.3 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr19:45419567 T>C maps to NM_001645.3 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr11:116701770 G>T did not map to a codon.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr12:56755761 G>A maps to NM_001638.2 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr22:36657727 G>T maps to NM_145343.2 E108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr22:36661427 C>T maps to NM_145343.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr22:36055123 C>T maps to NM_030641.3 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr23:84329356 A>G did not map to a codon.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr21:27543062 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr17:58539129 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr17:58603318 C>T did not map to a codon.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr12:105591667 G>A maps to NM_018171.3 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr12:105589109 C>T maps to NM_018171.3 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr1:154296279 C>T maps to NM_080429.2 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2GZ-01A-11D-A17W-09 chr1:154296881 C>T maps to NM_080429.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr1:154296431 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr11:77301504 G>A maps to NM_173039.2 K156K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr2:241622113 G>A maps to NM_001102467.1 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr12:50344909 C>T maps to NM_000486.5 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr12:50357351 C>T maps to NM_001651.2 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr9:33385028 C>A maps to NM_001170.1 E335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr5:115351378 A>C maps to NM_173800.4 I891I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr5:115298712 C>T maps to NM_173800.4 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr5:115351426 C>T maps to NM_173800.4 D907D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr5:115327935 C>T maps to NM_173800.4 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr5:115350167 C>T maps to NM_173800.4 D798D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:35166069 G>A maps to NM_014691.2 Q1186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr15:35176740 G>T maps to NM_014691.2 I1004I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr15:35159782 G>A maps to NM_014691.2 Q1266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr23:66765954 G>A did not map to a codon.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr23:66765449 C>T did not map to a codon.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr23:66766449 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr23:66943613 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:66863101 G>C did not map to a codon.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr23:66931423 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:66765337 C>T did not map to a codon.
Sequencing variant TCGA-JX-A3PZ-01A-11D-A21Q-09 chr23:66937347 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:66905905 G>A did not map to a codon.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr23:66766390 G>A did not map to a codon.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr23:47426650 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:47428868 G>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:72408142 G>C maps to NM_001040118.2 L1017L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr11:72404262 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr11:72408649 G>A maps to NM_001040118.2 R928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr11:72422480 A>G maps to NM_001040118.2 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr4:36230328 T>C maps to NM_015230.2 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr5:141033461 G>C did not map to a codon.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr5:141035267 G>A maps to NM_022481.5 Q1344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr5:141033522 G>C maps to NM_022481.5 L1543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr5:141052871 C>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr11:118473591 T>G did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:118472584 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr1:228285142 G>A maps to NM_001024228.1 Q83Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H6-01B-11D-A22X-09 chr12:49332474 G>T did not map to a codon.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr3:57582434 G>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:57582965 G>C did not map to a codon.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr7:127228575 C>G maps to NM_001662.3 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr14:50360594 C>T maps to NM_001663.3 F47F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr20:61915225 G>A maps to NM_175609.1 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr11:47187023 G>T did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr8:68165806 G>A maps to NM_006421.3 I859I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WH-01A-22D-A351-09 chr8:68150646 G>T maps to NM_006421.3 R1074R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr20:47592586 T>C maps to NM_006420.2 D603D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr20:47569352 C>T maps to NM_006420.2 Q179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HG-A2PA-01A-11D-A20U-09 chr20:47591379 G>T maps to NM_006420.2 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr20:47591313 G>A maps to NM_006420.2 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7X3-01A-11D-A351-09 chr4:153831233 C>T maps to NM_001025595.1 Q329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr4:153832972 G>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr11:6498962 G>A maps to NM_012402.2 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr11:46703638 G>T maps to NM_004308.2 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr15:30936860 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr10:32096153 C>G did not map to a codon.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr6:129950524 C>T maps to NM_033515.2 K253K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr10:24909043 G>A maps to NM_020824.3 Q594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr10:24874804 G>T maps to NM_020824.3 I1471I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A556-01A-11D-A26G-09 chr10:49791042 C>G maps to ENST00000417912 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:86916228 G>A maps to NM_001025616.2 T474T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr17:43483116 G>A maps to ENST00000428638 D330D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr17:43474288 C>T maps to ENST00000428638 P648P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VK-01A-11D-A28B-09 chr17:43482440 G>T maps to ENST00000428638 S366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr1:161021239 G>A maps to NM_001025598.1 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr3:119133737 C>T maps to NM_020754.2 Q988*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr11:128841050 G>A maps to NM_001142685.1 Q1339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr11:128858005 G>A maps to NM_001142685.1 Q390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr19:36271141 C>T maps to ENST00000007510 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr23:130218321 C>T did not map to a codon.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr23:130215716 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3QE-01A-21D-A21Q-09 chr23:130217838 C>T did not map to a codon.
Sequencing variant TCGA-EA-A5FO-01A-21D-A28B-09 chr23:130222711 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:130219940 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:130220319 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr23:130222681 C>T did not map to a codon.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr23:153176374 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr23:153176610 C>G did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:153186186 C>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:153186237 G>C did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:153187187 C>G did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr23:153178165 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr14:32619106 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr14:32560283 C>T maps to NM_001030055.1 Q137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr23:11157629 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr23:11207063 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr23:11207090 C>A did not map to a codon.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr23:11682475 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr23:11206922 G>C did not map to a codon.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr23:11308547 G>A did not map to a codon.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr23:11187766 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr23:11204448 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr23:11157356 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:11156997 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:11204523 C>T did not map to a codon.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr23:11162182 C>G did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr22:45210623 G>A maps to ENST00000352766 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZF-01A-11D-A28B-09 chr12:57867942 C>T maps to ENST00000393797 L690L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr12:57882490 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr17:79827244 C>A maps to NM_004309.4 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr17:79827731 G>C maps to NM_004309.4 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr19:42396557 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr8:1876768 G>A maps to ENST00000398564 V983V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr8:1774296 C>T maps to ENST00000398564 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr1:18023598 C>T maps to NM_018125.3 L1188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr1:156907207 G>A maps to NM_198236.1 Q1425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:156916477 C>T maps to NM_198236.1 E890E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr11:120312839 A>T maps to NM_015313.2 K411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A411-01A-11D-A243-09 chr11:120295077 T>G maps to NM_015313.2 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr11:120291540 C>T maps to NM_015313.2 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr11:120350708 G>A maps to NM_015313.2 L1269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr11:120318966 C>G maps to NM_015313.2 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr11:120348211 C>A maps to NM_015313.2 S1170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr17:8216306 C>G maps to NM_173728.3 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr17:8222399 A>G maps to NM_173728.3 G703G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr1:16535285 C>T maps to NM_153213.3 E88E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:16535522 G>C maps to NM_153213.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:16528972 G>A maps to NM_153213.3 F668F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:155934785 G>A maps to NM_001162383.1 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr1:155931935 C>T maps to NM_001162383.1 K393K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr1:155917025 G>C did not map to a codon.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr1:155932918 G>A maps to NM_001162383.1 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr1:155932756 G>A maps to NM_001162383.1 V314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr3:56766437 G>A maps to NM_001128615.1 F384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:56763298 C>G maps to NM_001128615.1 *559S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr5:148977373 G>A maps to NM_001001669.2 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr4:106580236 G>A maps to ENST00000420470 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R1-01A-11D-A28B-09 chr4:106566401 G>A maps to ENST00000420470 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr2:131798816 G>A maps to NM_015320.2 Q373Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr2:131797982 G>T maps to NM_015320.2 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CG-01A-11D-A32I-09 chr23:135763033 A>G did not map to a codon.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr23:135762922 G>T did not map to a codon.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr23:135763010 A>G did not map to a codon.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr13:111870158 G>A maps to NM_001113511.1 W222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr13:111927124 C>T maps to NM_001113511.1 F441F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr13:111918014 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr23:62863881 C>T did not map to a codon.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr23:62898256 A>T did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:62917101 A>C did not map to a codon.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr23:62974365 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr23:63005019 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:62885881 C>G did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr23:62944443 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr1:27100374 C>T maps to NM_006015.4 Q1363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:27059193 C>T maps to NM_006015.4 Q611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:27100987 C>T maps to NM_006015.4 Q1424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WH-01A-22D-A351-09 chr1:27088755 C>T maps to NM_006015.4 Q789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A4BA-01A-21D-A26G-09 chr1:27057819 C>T maps to NM_006015.4 Q510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:27106353 C>T maps to NM_006015.4 R1989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:27106363 C>A maps to NM_006015.4 S1992*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A57G-01A-11D-A26G-09 chr1:27057660 C>T maps to NM_006015.4 Q457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VH-01A-11D-A28B-09 chr1:27057987 C>T maps to NM_006015.4 Q566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr1:27092777 G>A maps to NM_006015.4 G933G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr6:157519968 T>G maps to ENST00000367148 Y1386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr6:157502140 G>A maps to ENST00000367148 T1098T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr12:46300165 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr12:46301282 G>C did not map to a codon.
Sequencing variant TCGA-JW-A5VI-01A-11D-A28B-09 chr12:46245831 C>G maps to NM_152641.2 S1309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr19:929433 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr19:964967 G>A maps to NM_005224.2 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr15:74890149 G>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:58832748 C>T maps to NM_002892.3 S1108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr14:58771669 G>C maps to NM_002892.3 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr14:58768398 G>A maps to NM_002892.3 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:235345847 C>A maps to NM_016374.5 E796*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr10:63845626 G>T maps to NM_032199.2 E456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr3:49002354 C>G maps to NM_006321.2 Y109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr3:49006069 C>T maps to NM_006321.2 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr3:49017053 C>T maps to NM_006321.2 F367F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr12:101801472 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr13:50204666 C>T maps to NM_138450.5 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr23:100245554 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr3:93768271 G>A maps to NM_182896.2 K349K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr5:53182186 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr17:41477528 G>A maps to NM_001661.3 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr2:152684678 G>C maps to NM_012097.3 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr10:18961607 G>T maps to NM_178815.3 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr16:18804600 G>C maps to NM_015161.1 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A6QX-01A-12D-A33O-09 chr3:5220572 C>G did not map to a codon.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr8:66539549 C>T maps to NM_018120.4 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr7:102716268 C>A maps to NM_031905.3 S62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr6:109274450 C>A maps to NM_032131.4 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:28283894 C>T maps to NM_018076.2 W59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr10:28283974 C>A maps to NM_018076.2 E33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr10:28250634 A>C maps to NM_018076.2 A416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr10:28273114 G>C maps to NM_018076.2 S227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr10:28273993 G>A maps to NM_018076.2 Q177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A44S-01A-12D-A26G-09 chr17:73125202 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr3:137960642 C>T maps to ENST00000469044 R286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr2:232079545 G>A maps to ENST00000359743 K60K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr2:232100030 C>T maps to ENST00000359743 H239H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:100808135 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr23:100911644 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr23:100910678 G>C did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:100910948 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:100911002 G>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:100912262 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:100911347 G>C did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:100878841 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:100880766 C>G did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:100880828 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3WB-01A-11D-A22X-09 chr23:101858742 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:101857526 G>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:150789273 C>A maps to NM_001668.3 E598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr15:80762741 C>A maps to NM_014862.3 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AX-01A-12D-A243-09 chr15:80762741 C>T maps to NM_014862.3 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr11:13399977 C>T maps to ENST00000403290 I503I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr7:98992155 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr7:98984027 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:183595670 G>A did not map to a codon.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr3:35835543 C>T did not map to a codon.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr3:35778725 C>T maps to ENST00000458225 Q472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr11:74994372 G>C maps to NM_004041.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:4622634 C>G maps to ENST00000412477 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr9:140508298 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr9:140508899 C>T maps to NM_152285.2 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr5:90669611 C>G maps to NM_020801.2 R359R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr5:90670951 G>T maps to NM_020801.2 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr19:4891273 G>A maps to NM_001080523.1 F271F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr23:2878446 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:3030565 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr23:2951221 G>A did not map to a codon.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr11:3681283 C>T maps to NM_004314.2 R179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R3-01A-11D-A28B-09 chr4:77020135 C>T maps to NM_001130016.1 N281N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr12:14993508 G>C maps to NM_021071.2 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr12:14993781 A>T maps to NM_021071.2 Y150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr11:3663062 G>A maps to NM_001079536.1 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr22:19967386 G>A maps to NM_001670.2 R425R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:25031390 C>G did not map to a codon.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr8:131200417 C>T maps to NM_018482.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr8:131249236 G>A maps to NM_018482.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr1:23760771 C>T maps to NM_017707.3 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:23765252 G>A maps to NM_017707.3 F363F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr7:150878058 G>A maps to ENST00000422024 G402G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr10:5683874 C>T maps to NM_024701.3 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr7:123276929 C>G maps to NM_080928.3 L554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr7:123264785 G>A maps to NM_080928.3 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr7:123256535 G>A maps to NM_080928.3 E93E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr7:123254658 G>T maps to NM_080928.3 E35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:76397628 C>T maps to NM_080868.2 K116K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr1:76384651 C>T maps to NM_080868.2 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr14:94405903 C>T maps to ENST00000434324 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3WB-01A-11D-A22X-09 chr2:53831949 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr7:95157137 C>T maps to NM_016116.2 N167N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:15266971 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr6:101312039 C>T maps to NM_006828.2 W47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr6:101095187 G>C maps to NM_006828.2 S1131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RE-01A-11D-A18J-09 chr12:108169228 C>T maps to NM_203436.2 N79N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr17:7017495 G>A maps to NM_080912.2 Q22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:155319337 C>T maps to ENST00000368346 K2477K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:155327444 G>A maps to ENST00000368346 P2302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BE-01A-21D-A26G-09 chr1:155327405 C>T maps to ENST00000368346 K2315K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R3-01A-11D-A28B-09 chr8:37978653 C>G maps to NM_004674.3 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A411-01A-11D-A243-09 chr7:65546866 C>T maps to NM_000048.3 Y30Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr7:65547434 G>A maps to NM_000048.3 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:1734096 G>A did not map to a codon.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr23:1551172 G>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:1561058 G>A did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr23:1531690 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr23:1540564 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr23:1531691 G>T did not map to a codon.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr19:12858249 G>A maps to NM_004317.2 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr2:190531166 G>A maps to NM_019048.2 K103K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr17:3397701 C>T maps to NM_000049.2 Y231Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A69M-01A-11D-A32I-09 chr14:104559920 C>A maps to NM_001080464.1 C95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr8:62416043 G>C maps to NM_004318.3 L717L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr16:29913116 G>T maps to NM_181718.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr22:26830048 C>G maps to NM_020437.4 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr22:26829793 C>T maps to NM_020437.4 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr1:197069808 G>A maps to NM_018136.4 Q2858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HF-01A-11D-A20U-09 chr1:197072215 T>C maps to NM_018136.4 R2055R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr1:197112772 G>A maps to NM_018136.4 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZE-01A-11D-A28B-09 chr1:197091366 C>T maps to NM_018136.4 R1221R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:197098340 G>A maps to NM_018136.4 L912L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:197094290 C>T maps to NM_018136.4 W989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr9:133352340 C>T maps to NM_000050.4 F227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr2:96803368 G>C maps to NM_001002036.3 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr1:176918331 G>A maps to ENST00000281881 L689L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr9:119249768 C>G maps to ENST00000313400 L1122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M2-01A-21D-A18J-09 chr20:31020681 G>T did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr20:31023126 C>G maps to ENST00000375687 S871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr2:26022383 C>T maps to NM_018263.4 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr2:25966687 G>A maps to NM_018263.4 L840L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr18:31319866 G>A maps to NM_030632.1 L833L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr18:31322917 C>T maps to NM_030632.1 R1036*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr7:117067508 C>T maps to NM_130768.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr8:124359380 C>T maps to NM_014109.3 Q721Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr8:124408480 G>C maps to NM_014109.3 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:1421178 C>T maps to NM_031921.4 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:1398012 G>A maps to NM_001039211.2 R338R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr17:29161431 G>A maps to NM_024857.3 K111K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M2-01A-21D-A18J-09 chr19:3907822 C>T maps to NM_033064.4 N150N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr19:3909585 G>A maps to NM_033064.4 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr10:123549561 C>G did not map to a codon.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr2:175957796 G>A maps to NM_001880.2 Q393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr1:212793750 T>G did not map to a codon.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr22:39917808 G>A maps to NM_182810.1 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr22:39917548 C>G maps to NM_182810.1 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr22:39917548 C>G maps to NM_182810.1 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr22:39917509 C>T maps to NM_182810.1 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr6:32083735 G>C maps to NM_004381.4 S631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VI-01A-11D-A28B-09 chr12:14613979 C>T maps to NM_018179.3 R904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr16:10575838 G>A maps to NM_024997.2 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr16:10551363 C>T maps to NM_024997.2 Q444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr16:10565997 G>T maps to NM_024997.2 E462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr5:81549225 T>C maps to NM_031482.4 D215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr5:115167551 G>A maps to ENST00000274459 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:72533172 G>A maps to NM_033388.1 Q159Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr11:64679411 G>T maps to ENST00000421419 S377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M2-01A-21D-A18J-09 chr14:96813613 G>T maps to NM_018036.5 S76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr23:107397093 C>G did not map to a codon.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr6:106650033 C>A did not map to a codon.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr3:11372812 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr3:11596301 T>C maps to NM_006395.2 D699D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr3:11596301 T>C maps to NM_006395.2 D699D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr7:150717311 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr7:150710471 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr7:150709587 G>C did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr14:51026869 G>C did not map to a codon.
Sequencing variant TCGA-JW-A5VG-01A-11D-A28B-09 chr11:108178703 C>T maps to NM_000051.3 Q1919*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A770-01A-11D-A33O-09 chr16:81077771 C>T maps to NM_015251.2 Q557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr16:81078777 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr12:7047951 C>A maps to NM_001940.3 L942L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr4:94750667 A>G maps to NM_005172.1 K197K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr2:86014108 C>T did not map to a codon.
Sequencing variant TCGA-EA-A44S-01A-12D-A26G-09 chr15:25966966 G>A maps to NM_024490.3 D400D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R3-01A-11D-A28B-09 chr15:25953177 G>A maps to NM_024490.3 S840S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr5:160114973 C>G maps to NM_025153.2 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R9-01A-11D-A18J-09 chr4:47584002 C>T maps to NM_020453.3 I1225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr13:113510281 G>A maps to NM_032189.3 L767L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr3:182575667 C>A maps to NM_014616.1 S285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LB-01A-11D-A243-09 chr3:182566280 G>T maps to NM_014616.1 G263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr23:139014190 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr23:138813882 G>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr13:25266733 C>A maps to NM_001185085.1 I418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr13:25262602 C>G maps to NM_001185085.1 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:17312721 C>G maps to NM_022089.2 L1179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:17322356 G>C maps to ENST00000375508 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:17313384 G>C maps to NM_022089.2 V1050V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr3:193210716 T>C maps to NM_032279.2 E174E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A3LQ-01A-21D-A21Q-09 chr3:193096462 C>A maps to NM_198505.2 E18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr3:193081924 C>A maps to NM_198505.2 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:160095079 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr19:42489497 C>T maps to ENST00000441343 E228E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr1:160156476 G>A maps to NM_144699.3 E1026E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr3:141644559 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A5R1-01A-11D-A28B-09 chr3:141644552 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr23:119509334 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:119513441 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr16:28893803 G>A maps to NM_173201.3 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr17:3839723 C>T maps to NM_174953.1 L787L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr3:10387121 G>A maps to NM_001001331.2 L883L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:10370483 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr3:10377944 G>A maps to ENST00000342354 Q1154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr3:10370259 C>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr3:10443973 G>A maps to NM_001001331.2 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr23:152807876 C>G did not map to a codon.
Sequencing variant TCGA-DS-A7WF-01A-11D-A351-09 chr23:152801867 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr23:152825249 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2R9-01A-11D-A18J-09 chr23:152815582 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:152806979 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr23:152808573 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:152807331 C>G did not map to a codon.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr1:203672792 C>T maps to NM_001001396.1 D317D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:203696816 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr1:203668789 C>T maps to NM_001001396.1 L198L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EA-A3HT-01A-61D-A21Q-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-C5-A7CG-01A-11D-A32I-09 chr16:84456297 G>T maps to ENST00000416219 E280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr19:36045925 C>T maps to NM_000704.2 K793K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr19:36054414 G>C maps to NM_000704.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr12:57033095 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr10:7842007 G>A maps to NM_001001973.1 K197K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr19:1242459 C>T maps to NM_001687.4 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:111992025 C>A did not map to a codon.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr4:668036 C>G did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr21:27102095 G>A maps to NM_001003701.1 Q12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:41944234 G>A maps to ENST00000417807 Q110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:153662560 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3QD-01A-32D-A22X-09 chr23:153657144 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3HQ-01A-11D-A20U-09 chr5:81613842 A>C maps to NM_001017971.1 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr5:81614026 C>T maps to NM_001017971.1 R195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:40464970 T>G did not map to a codon.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr17:40652733 G>A maps to NM_001130020.1 K570K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr17:40672679 G>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr17:40673240 C>T did not map to a codon.
Sequencing variant TCGA-JX-A3Q8-01A-11D-A21Q-09 chr17:40618525 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr12:124228763 C>T maps to NM_012463.3 I402I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr7:138455976 G>A maps to NM_130840.2 R6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr7:138482972 G>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:44441390 C>G did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr1:44441361 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:44442473 C>T maps to NM_004047.3 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr7:149571219 C>T maps to NM_001100592.1 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr7:149571036 C>T maps to NM_001100592.1 I10I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr7:149571219 C>T maps to NM_001100592.1 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:113507616 G>A maps to NM_001690.3 V258V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:71187138 C>T maps to NM_001692.3 D172D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr8:20070410 C>T maps to NM_001693.3 R308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:10914998 G>T maps to NM_001039362.1 E242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr2:46739841 C>G maps to NM_080653.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr9:117350072 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr6:31513119 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr23:77264737 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr23:77289249 G>T did not map to a codon.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr23:77254034 C>T did not map to a codon.
Sequencing variant TCGA-EA-A6QX-01A-12D-A33O-09 chr13:52511637 C>A maps to NM_000053.2 E1293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr13:52548825 G>C maps to NM_000053.2 S177*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-C5-A1BQ-01C-11D-A20U-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr13:26343297 C>T maps to NM_016529.4 H833H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr13:26501334 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr13:26501420 G>C did not map to a codon.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr13:26145784 C>T maps to NM_016529.4 G539G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr18:55362543 C>A maps to NM_005603.4 E267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3TX-01A-11D-A22X-09 chr18:55322502 G>A maps to NM_005603.4 R952*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr18:55319360 G>T maps to NM_005603.4 S1102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr1:154317601 C>T maps to NM_020452.3 D847D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr1:154306642 G>A maps to NM_020452.3 W250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr1:154304126 C>T maps to NM_020452.3 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:154306643 G>A maps to NM_020452.3 W250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr19:1785260 G>A maps to NM_138813.2 C1143C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr15:50271845 G>C maps to NM_024837.2 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr15:50294400 G>C maps to NM_024837.2 S152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AU-01A-32D-A243-09 chr20:50287702 C>T maps to NM_006045.1 T377T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr20:50225059 G>C maps to NM_006045.1 L914L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr17:17942393 C>T did not map to a codon.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr3:142272218 T>C maps to NM_001184.3 V885V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr3:48506951 G>A maps to NM_130384.1 *792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr20:3452161 C>T maps to NM_139321.2 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr20:3605169 C>T maps to NM_139321.2 Q1272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HR-01A-11D-A20U-09 chr10:117024751 C>T maps to NM_207303.2 N590N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr10:116919961 C>T maps to NM_207303.2 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A0TN-01A-21D-A14W-08 chr23:76814317 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr23:76938874 C>G did not map to a codon.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr23:76939254 C>G did not map to a codon.
Sequencing variant TCGA-DS-A7WH-01A-22D-A351-09 chr23:76763048 T>A did not map to a codon.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr23:76949325 G>A did not map to a codon.
Sequencing variant TCGA-EA-A50E-01A-21D-A26G-09 chr23:76776918 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr23:76874433 T>A did not map to a codon.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr23:76874308 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr23:76761673 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2RL-01A-11D-A18J-09 chr23:76778778 G>T did not map to a codon.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr23:76856126 C>A did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:76891544 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:76938672 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:76762743 C>T did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:76938515 C>T did not map to a codon.
Sequencing variant TCGA-EA-A6QX-01A-12D-A33O-09 chr12:111908475 C>T maps to NM_002973.3 A1023A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr12:111892861 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr16:28843579 C>A maps to NM_148414.1 S459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M2-01A-21D-A18J-09 chr23:13337276 G>A did not map to a codon.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr23:13337276 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr23:13337386 C>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:13337012 C>A did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:13337059 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr7:105254170 G>A maps to ENST00000388807 H756H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr7:105305652 C>T maps to NM_020725.1 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PI-01A-11D-A18J-09 chr1:110034535 C>T did not map to a codon.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr1:1309974 G>A did not map to a codon.
Sequencing variant TCGA-EA-A50E-01A-21D-A26G-09 chr1:1310001 C>T did not map to a codon.
Sequencing variant TCGA-UC-A7PD-01A-11D-A351-09 chr1:1310232 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr17:8109912 C>T maps to NM_004217.2 K194K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr19:57742676 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr7:70255357 C>T maps to NM_015570.2 I1052I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr7:70255459 G>A maps to NM_015570.2 R1086R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr7:70163661 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr7:70252203 C>G maps to NM_015570.2 S773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr12:63544013 G>A maps to NM_000706.3 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr23:153171490 C>G did not map to a codon.
Sequencing variant TCGA-HM-A3JK-01A-11D-A21Q-09 chr23:153172075 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr23:69460047 C>T did not map to a codon.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr23:69457006 C>T did not map to a codon.
Sequencing variant TCGA-DS-A7WF-01A-11D-A351-09 chr23:69455617 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:69456970 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr23:69458096 C>G did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr23:69269698 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:69264292 G>A did not map to a codon.
Sequencing variant TCGA-C5-A7CJ-01A-11D-A32I-09 chr16:348161 C>T maps to NM_003502.3 P448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr17:63533494 C>T maps to NM_004655.3 S553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr19:41759595 G>C maps to NM_021913.3 L673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr7:99564615 C>A did not map to a codon.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr3:28364160 T>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr3:28364320 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr8:103870314 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr19:829603 G>C maps to NM_001700.3 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr15:45007718 G>T maps to NM_004048.2 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr15:45007644 C>G maps to NM_004048.2 S31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A69M-01A-11D-A32I-09 chr6:33245261 C>T maps to NM_003782.3 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr13:31850909 T>C did not map to a codon.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr11:134253723 G>A maps to NM_054025.2 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr19:17919002 G>A maps to NM_014256.3 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr12:122692313 G>A did not map to a codon.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr3:182987730 A>T maps to NM_032047.4 R49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr19:41932014 G>C maps to NM_198540.2 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr16:67183554 G>A maps to NM_033309.2 Y278Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr17:80963068 C>T maps to NM_001009905.1 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr17:80972368 C>T maps to NM_001009905.1 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q8-01A-11D-A21Q-09 chr17:80972327 A>T did not map to a codon.
Sequencing variant TCGA-C5-A7UC-01A-11D-A351-09 chr12:58020691 G>A maps to NM_001478.3 V479V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr17:47236505 G>C maps to NM_153446.2 R262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U3-01A-11D-A28B-09 chr17:47218740 G>A maps to NM_153446.2 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr12:667744 G>C maps to NM_173593.3 R893R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr12:663002 C>T maps to NM_173593.3 F638F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr11:373248 C>T maps to NM_178537.4 D198D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr9:33135201 G>A maps to NM_001497.3 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:161141163 G>A did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr1:161141582 T>C did not map to a codon.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr3:118945760 G>A maps to NM_212543.1 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr20:48252849 C>G maps to NM_004776.3 *389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr20:48260131 G>C maps to NM_004776.3 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A69M-01A-11D-A32I-09 chr5:177031509 C>T maps to NM_007255.2 H127H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr21:42609508 C>T maps to NM_012105.3 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q8-01A-11D-A21Q-09 chr6:90647928 C>T maps to NM_001170794.1 A659A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73S-01A-11D-A33O-09 chr6:90718533 G>T maps to NM_001170794.1 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr11:64051745 G>C maps to NM_032989.2 S32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr10:121429617 C>T maps to NM_004281.3 Q146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr21:11060116 A>T did not map to a codon.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr21:11060167 G>A did not map to a codon.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr21:11038788 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr21:11038738 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr15:40750914 G>A maps to NM_014952.3 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QD-01A-32D-A22X-09 chr1:32221618 G>A maps to NM_001703.2 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr1:32202034 A>G did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:32201188 C>T maps to NM_001703.2 Q1115Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr6:69758161 G>A maps to NM_001704.2 W731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr6:69728347 G>T maps to NM_001704.2 G688G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr6:69703685 G>A maps to NM_001704.2 Q587Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr17:79073864 G>A maps to NM_017451.2 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr22:38504319 G>A maps to NM_025045.4 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr16:1392014 G>T maps to NM_003933.4 E304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr16:1392547 C>T maps to NM_003933.4 V361V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr16:1392625 C>T maps to NM_003933.4 I387I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr11:65771227 C>T maps to NM_003860.3 C85C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr4:102839163 G>T maps to NM_017935.4 E342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr16:88110230 G>A maps to NM_001173543.1 E508E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr16:88110454 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr16:88104767 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr3:52437781 G>C maps to NM_004656.2 S460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A44S-01A-12D-A26G-09 chr3:52439882 G>A maps to NM_004656.2 Q277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr3:52439882 G>A maps to NM_004656.2 Q277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr3:52437847 G>C maps to NM_004656.2 S438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:215646071 G>A maps to NM_000465.2 Q176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr1:91182629 C>T maps to NM_020063.1 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr1:91182266 G>A maps to NM_020063.1 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3EO-01A-11D-A20U-09 chr11:129312619 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RE-01A-11D-A18J-09 chr11:64756990 A>T maps to NM_138456.3 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr1:212870662 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr7:72922760 G>A maps to NM_032408.3 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr12:57000121 C>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:56994156 G>A maps to NM_013449.3 Q1576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:56995490 C>A maps to NM_013449.3 E1306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr2:160318978 G>C did not map to a codon.
Sequencing variant TCGA-EA-A556-01A-11D-A26G-09 chr2:160318093 G>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr2:160181436 C>A maps to NM_013450.2 E2080*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr2:160318946 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr19:47725143 G>A maps to NM_001127240.1 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr11:27136997 G>C did not map to a codon.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr16:56531747 G>T maps to NM_031885.3 I568I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr2:170349382 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr4:122749660 C>G did not map to a codon.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr4:122754425 G>A maps to NM_176824.1 Q546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr7:33545329 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr7:33312683 C>T maps to NM_198428.2 Q255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr3:107474451 C>G maps to NM_001142568.1 S278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr23:152981117 C>T did not map to a codon.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr16:75301815 G>A maps to NM_001170715.1 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2GZ-01A-11D-A17W-09 chr16:75263741 G>A maps to NM_001170714.1 N806N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr1:94047998 G>A maps to NM_003567.2 F515F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:94079452 G>C maps to ENST00000370247 S12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr17:59161922 C>G maps to ENST00000407086 S838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr12:24987041 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:24995102 G>A maps to NM_001178093.1 Q256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KH-01A-21D-A22X-09 chr12:50236729 G>A maps to NM_181708.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr3:165547699 A>C maps to NM_000055.2 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr3:165548613 G>A maps to NM_000055.2 R70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R9-01A-11D-A18J-09 chr6:80881079 G>T maps to NM_183050.2 E239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A770-01A-11D-A33O-09 chr16:31121605 C>G maps to NM_005881.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr1:85742017 C>A maps to NM_003921.4 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr2:60780444 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr2:60695968 C>G did not map to a codon.
Sequencing variant TCGA-RA-A741-01A-11D-A33O-09 chr2:60686966 T>C did not map to a codon.
Sequencing variant TCGA-DS-A1OA-01A-11D-A16Y-08 chr14:99640538 G>A maps to NM_138576.2 G878G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr20:30309775 G>C maps to NM_138578.1 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:114429233 C>T maps to NM_001010922.2 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OA-01A-11D-A16Y-08 chr19:45262838 G>A maps to NM_005178.4 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr3:187443391 G>T maps to NM_001706.4 I578I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:187447541 C>T maps to NM_001706.4 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A5XV-01A-11D-A28B-09 chr16:30846269 C>G maps to ENST00000380317 *243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A78R-01A-11D-A32I-09 chr1:147078584 C>T did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr1:147086291 C>G maps to NM_004326.2 S146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr11:118769062 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr6:136599910 A>G maps to NM_014739.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A410-01A-11D-A243-09 chr6:136599058 C>T maps to NM_014739.2 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr6:136582161 G>T did not map to a codon.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr16:81295870 C>T maps to NM_017429.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr11:112064656 C>T maps to NM_031938.4 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:39932326 G>T did not map to a codon.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr23:39932688 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:39922920 C>A did not map to a codon.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr23:39934232 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:39933797 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:39913548 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:39937174 G>C did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:39937174 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73R-01A-11D-A33O-09 chr23:39931727 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73R-01A-11D-A33O-09 chr23:39933164 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr23:129155080 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:129139209 G>A did not map to a codon.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr23:129148260 G>A did not map to a codon.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr23:129148723 C>A did not map to a codon.
Sequencing variant TCGA-FU-A57G-01A-11D-A26G-09 chr23:129148349 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:129173216 G>A did not map to a codon.
Sequencing variant TCGA-JX-A5QV-01A-22D-A28B-09 chr23:129171478 C>T did not map to a codon.
Sequencing variant TCGA-LP-A4AU-01A-32D-A243-09 chr23:129139194 G>A did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr23:129159283 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr22:23658360 T>C did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr22:23603577 C>T maps to NM_004327.3 Q535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr22:23523872 C>G maps to NM_004327.3 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A69B-01A-11D-A32I-09 chr22:23657999 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr22:23524280 C>T maps to NM_004327.3 F378F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr22:23637245 G>A maps to NM_004327.3 L972L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr2:219526521 G>A maps to NM_004328.4 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr3:197281578 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr14:96730150 C>T maps to NM_000710.2 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr14:96730333 C>T maps to NM_000710.2 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A5QV-01A-22D-A28B-09 chr14:96707123 C>T maps to NM_000623.3 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr11:27678711 C>G did not map to a codon.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr14:101005409 G>A maps to NM_020836.3 I226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr23:18189169 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr23:18183236 G>A did not map to a codon.
Sequencing variant TCGA-C5-A7CG-01A-11D-A32I-09 chr6:107391661 C>A maps to NM_001080450.2 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr6:107391785 C>T maps to NM_001080450.2 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr6:107392133 C>T maps to NM_001080450.2 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3PZ-01A-11D-A21Q-09 chr6:56846693 C>G maps to NM_152731.2 S29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr10:13489308 C>T maps to ENST00000396900 A397A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr10:13534812 G>C maps to ENST00000396900 S212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr11:61723283 C>T maps to NM_001139443.1 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr11:61730085 C>G maps to NM_001139443.1 S427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr19:12868587 G>T maps to NM_017682.2 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr12:70048687 C>T maps to NM_032735.2 *669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr12:70070806 C>G maps to NM_032735.2 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:45253356 G>A maps to NM_153274.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr7:93605248 C>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:101408942 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2PI-01A-11D-A18J-09 chr20:17475567 G>A maps to NM_001195.3 N383N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr23:152771462 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr23:152774522 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:152772339 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:102004335 A>G did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:5025280 C>T maps to NM_003670.2 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:95484982 C>T maps to NM_001003800.1 E187E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr9:95481750 C>T maps to NM_001003800.1 E392E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr2:127827587 G>A maps to NM_139343.1 Q132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr12:51686076 G>A maps to NM_016293.2 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr12:51686076 G>A maps to NM_016293.2 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr12:51686022 C>T maps to NM_016293.2 E289E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr8:22478973 G>A maps to NM_018688.4 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr8:22478788 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr8:22478838 C>G did not map to a codon.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr8:22494059 C>T maps to NM_018688.4 K46K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr11:102220626 G>A maps to NM_001166.3 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr2:32678918 C>T maps to NM_016252.3 F1554F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:32605300 C>G maps to NM_016252.3 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr2:32772924 G>T maps to NM_016252.3 V4273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr17:28614947 G>A maps to NM_000386.2 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr17:28601164 G>A maps to NM_000386.2 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr10:97959868 G>T maps to NM_013314.3 R353R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr19:45684651 C>T did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr10:22618359 C>T maps to NM_005180.6 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr8:22064466 C>A maps to NM_006129.4 S778S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:69093119 G>A maps to NM_014482.1 I306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr23:50659448 C>G did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:50653861 G>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr4:79772145 C>T maps to NM_198892.1 I273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr6:55625296 C>T maps to NM_021073.2 K354K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr6:7727733 C>G maps to NM_001718.4 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:33946487 C>T maps to NM_133468.3 D64D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr7:34125570 C>T maps to NM_133468.3 Q538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:96070068 C>G maps to ENST00000440890 S446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr2:203407067 G>A maps to NM_001204.6 Q437Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr23:15552382 G>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:15555354 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr15:59955923 C>G did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr5:173035295 C>T did not map to a codon.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr2:198621172 C>T maps to NM_197970.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr20:36948572 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr17:65888034 C>G maps to ENST00000321892 S773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr17:65907169 C>A maps to ENST00000321892 S1183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr7:140550006 C>T maps to NM_004333.4 W48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr7:140477861 C>T maps to NM_004333.4 V482V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:112119639 C>G did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr17:41223130 C>T maps to ENST00000471181 L1622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr13:32937314 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr13:32914966 C>T maps to NM_000059.3 Q2159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr13:32972341 C>A maps to NM_000059.3 S3231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:154305475 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3TX-01A-11D-A22X-09 chr23:154319065 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:154306950 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr9:136898585 C>T did not map to a codon.
Sequencing variant TCGA-DS-A3LQ-01A-21D-A21Q-09 chr9:136913300 G>A maps to NM_007371.3 Y330Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr9:136916714 A>G maps to NM_007371.3 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr9:136901376 G>T maps to NM_007371.3 P571P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr16:50353863 G>A maps to NM_001173984.2 R613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr14:105684014 G>A maps to NM_001519.2 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr14:105685527 C>T maps to NM_001519.2 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr7:97920827 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr17:59934416 A>C did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:36168469 C>G maps to NM_015695.2 S124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr6:36168128 G>A maps to NM_015695.2 Q10Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr23:135570305 G>C did not map to a codon.
Sequencing variant TCGA-C5-A7UC-01A-11D-A351-09 chr23:135574301 C>G did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:135574332 G>C did not map to a codon.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr23:135574217 C>G did not map to a codon.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr19:55815947 G>A maps to NM_032430.1 P459P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:1467068 C>A maps to NM_003957.2 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr23:79932386 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr23:79999552 G>A did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr23:79955473 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr23:80064056 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr23:79975054 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr23:79946589 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr23:79980504 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:79991581 A>G did not map to a codon.
Sequencing variant TCGA-IR-A3LC-01A-11D-A20U-09 chr23:79942411 G>T did not map to a codon.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr23:79999565 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:79999747 G>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:79965076 C>T did not map to a codon.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr23:79936928 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr1:32842232 C>T maps to NM_001143888.1 E279E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr19:581369 C>G maps to NM_001728.2 S283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr19:577915 C>G maps to NM_001728.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr19:579512 C>T maps to NM_001728.2 F143F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr19:577838 G>T maps to NM_001728.2 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr19:572633 C>A did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr3:49695362 C>T maps to NM_003458.3 Q2792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr3:49698952 G>A maps to NM_003458.3 Q3225Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HQ-01A-11D-A20U-09 chr3:49698697 C>T maps to NM_003458.3 A3140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr3:49695040 C>G maps to NM_003458.3 V2684V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:49700628 C>A maps to NM_003458.3 R3680R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr3:49688999 C>T maps to NM_003458.3 Q671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr1:55464879 C>T maps to NM_057176.2 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:55465029 C>A maps to NM_057176.2 Y57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr9:116116518 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr10:93757459 C>T maps to NM_003972.2 F1204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr10:93773677 G>T maps to NM_003972.2 L1492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr15:83735726 G>A maps to NM_025238.3 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr12:107914402 C>T maps to NM_001018072.1 I425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr12:107937844 C>T maps to NM_001018072.1 F473F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr12:108051307 C>G maps to NM_001018072.1 S1043*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A852-01A-11D-A351-09 chr12:108013934 G>A maps to NM_001018072.1 A875A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr10:124089057 C>T maps to ENST00000368994 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr6:38560592 T>C maps to NM_052893.1 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr5:72801061 G>A maps to NM_001037637.1 *207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr23:100604944 C>G did not map to a codon.
Sequencing variant TCGA-EA-A6QX-01A-12D-A33O-09 chr23:100613644 C>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:100613378 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr23:100608248 A>T did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr3:112198560 G>A maps to NM_181780.3 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr6:26465471 C>T maps to NM_007049.3 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr6:26468257 C>T maps to NM_007049.3 F355F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr6:26392862 C>T maps to NM_001197237.1 Q414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr6:26409929 G>A maps to NM_007048.5 W295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr6:26373522 C>T maps to NM_001197246.1 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:26444365 G>A maps to NM_006994.4 Q89Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr6:32364125 G>A maps to ENST00000468270 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr5:180431734 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr2:111419250 G>T maps to NM_004336.3 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A5XV-01A-11D-A28B-09 chr15:40498656 G>C maps to ENST00000412359 L683L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RA-A741-01A-11D-A33O-09 chr10:124914621 C>A maps to NM_004725.3 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RA-A741-01A-11D-A33O-09 chr11:116633812 G>T maps to NM_032725.3 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A6QX-01A-12D-A33O-09 chr6:105563702 C>A did not map to a codon.
Sequencing variant TCGA-JX-A3PZ-01A-11D-A21Q-09 chr6:105577277 C>T maps to NM_007073.4 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr17:56399683 G>A maps to NM_004758.2 V469V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr2:201686899 G>C maps to ENST00000452790 *452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr7:16736605 C>T maps to NM_014038.2 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr7:16737783 C>T maps to NM_014038.2 Q361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr10:77795879 C>T maps to NM_032024.3 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr10:98742022 G>C maps to NM_015652.2 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VK-01A-11D-A28B-09 chr10:98744689 G>A maps to NM_015652.2 L1181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr10:127414248 A>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr10:102748732 C>T maps to NM_021830.4 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr10:102753197 G>A maps to NM_021830.4 Q662Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr10:73520431 T>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr10:32872047 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2RL-01A-11D-A18J-09 chr10:118427792 G>A maps to ENST00000388884 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A4BA-01A-21D-A26G-09 chr10:128335206 C>G did not map to a codon.
Sequencing variant TCGA-DG-A2KH-01A-21D-A22X-09 chr11:2322039 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr11:68031152 C>T did not map to a codon.
Sequencing variant TCGA-EX-A69L-01A-11D-A32I-09 chr11:76253260 C>T maps to ENST00000393457 V854V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr11:76255553 C>G maps to ENST00000393457 L988L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr11:558612 C>T did not map to a codon.
Sequencing variant TCGA-JX-A3Q8-01A-11D-A21Q-09 chr11:62432617 G>A did not map to a codon.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr11:62430805 C>A did not map to a codon.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr11:111795060 C>G maps to NM_080659.2 S15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:111951135 G>A maps to NM_018195.3 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A0TN-01A-21D-A14W-08 chr11:122774914 G>T maps to NM_024806.2 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H1-01A-11D-A17W-09 chr11:122795697 C>T maps to NM_024806.2 Q320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HM-A4S6-01A-11D-A26G-09 chr11:82643345 G>C maps to NM_145018.3 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr11:82644095 A>C maps to NM_145018.3 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr11:63585349 G>A maps to NM_138471.1 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr11:111385665 C>T maps to NM_207430.2 Q53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr11:111179047 C>T maps to NM_001136105.1 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr11:111177314 C>T maps to NM_001136105.1 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:40040239 C>G maps to NM_001031748.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr12:103696205 G>A maps to NM_001099336.1 Q255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:117175741 G>C did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr12:4459045 C>G maps to NM_020375.2 S85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DV-01A-11D-A32I-09 chr12:48881834 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr12:64706453 C>T did not map to a codon.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr12:7052785 G>A did not map to a codon.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr12:48578441 C>T maps to NM_001013635.3 D179D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr12:48578078 G>C maps to NM_001013635.3 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:57938126 C>T maps to NM_018168.2 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr14:52466481 C>T maps to NM_016039.2 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr14:52458092 C>G maps to NM_016039.2 Y40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr14:77319572 G>A maps to NM_194287.2 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr14:73957910 G>C maps to NM_024644.2 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A69L-01A-11D-A32I-09 chr14:50470651 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr14:50472202 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr14:104380301 C>T maps to NM_001127393.1 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VH-01A-11D-A28B-09 chr14:105476632 G>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr14:105963728 G>A maps to ENST00000392523 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr14:23467812 G>A maps to NM_021944.2 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr15:83680350 C>T maps to NM_144597.2 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R1-01A-11D-A28B-09 chr15:83680347 G>A maps to NM_144597.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr15:40633047 A>G maps to NM_207380.2 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr15:40544783 C>A did not map to a codon.
Sequencing variant TCGA-EA-A50E-01A-21D-A26G-09 chr15:74032524 G>A maps to NM_001039614.1 D205D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VH-01A-11D-A28B-09 chr15:41062837 C>T maps to NM_001130448.2 R49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr16:684552 G>C maps to NM_001040160.1 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr16:29755963 C>G maps to NM_175900.3 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr16:2514076 G>A maps to NM_025108.2 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr16:19644445 C>T maps to NM_020314.5 V618V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr16:67179510 G>A maps to NM_025187.3 E363E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr16:9196860 C>T maps to NM_014117.2 R110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:49433131 C>G maps to NM_144602.2 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr16:49433074 C>A maps to NM_144602.2 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3PZ-01A-11D-A21Q-09 chr16:27079689 C>G did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr16:27079142 G>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr16:27079377 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A6DV-01A-11D-A32I-09 chr16:67700944 G>A maps to NM_001012984.2 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr16:5115921 C>T maps to ENST00000350219 E34E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr16:1470075 G>A maps to NM_001010878.1 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr16:1470399 G>C maps to NM_001010878.1 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr17:32904623 G>A maps to NM_207454.2 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A852-01A-11D-A351-09 chr17:32906119 G>A maps to NM_207454.2 C60C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A5QV-01A-22D-A28B-09 chr17:42232291 C>T maps to NM_024032.3 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LB-01A-11D-A243-09 chr17:65989226 G>A maps to NM_181655.2 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A5XV-01A-11D-A28B-09 chr17:80401642 C>T maps to ENST00000342572 W123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr17:62078826 G>A maps to NM_001164257.1 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr17:7329891 G>A maps to NM_175734.4 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr17:71243443 G>A maps to NM_017941.4 T598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:59489401 C>G maps to NM_203425.1 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr17:263128 G>A maps to NM_001013672.4 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr18:51892103 C>T maps to ENST00000382911 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr18:21109336 C>T did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr18:21111731 C>G did not map to a codon.
Sequencing variant TCGA-EA-A50E-01A-21D-A26G-09 chr19:30193593 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr19:58472917 G>A maps to NM_152474.4 R125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr19:2280830 C>T did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr19:7570448 G>A maps to NM_198534.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QE-01A-21D-A21Q-09 chr19:40827896 C>T maps to ENST00000357884 R387R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr19:36249076 G>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:36258751 G>A maps to NM_001039887.2 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr19:14003956 G>A maps to ENST00000454313 Q96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr19:49621984 G>A maps to NM_018111.2 Q99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr23:119760182 C>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:119760174 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:119760957 T>C did not map to a codon.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr23:119760655 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:22974164 G>A maps to NM_172369.3 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:22974170 G>A maps to NM_172369.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr17:43037647 C>A maps to NM_006688.3 E229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A6QX-01A-12D-A33O-09 chr11:119209985 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr11:119209809 G>T did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr22:37576361 G>A did not map to a codon.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr22:37578302 C>T maps to NM_182486.1 E254E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr12:7252369 G>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:244735746 C>T maps to NM_001130957.1 F541F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:244756712 C>T maps to NM_001130957.1 Q736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HQ-01A-11D-A20U-09 chr1:200860772 G>A maps to NM_018265.2 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QE-01A-21D-A21Q-09 chr1:200876962 G>A maps to NM_018265.2 E259E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr1:38148082 A>C did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:38156030 G>C did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:38148725 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr1:169798415 C>T maps to NM_018186.2 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr1:169806078 C>T maps to NM_018186.2 I517I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:207195734 C>A maps to NM_023938.5 P458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:207196771 C>A maps to NM_023938.5 E113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr1:38274836 C>T maps to ENST00000446260 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr1:53686186 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:53686128 C>T did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:53685870 G>A did not map to a codon.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr1:231374797 C>T maps to ENST00000421623 K85K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:231374578 T>C did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:1017587 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:1018004 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:1018228 C>T maps to ENST00000428805 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr1:112018184 C>G did not map to a codon.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr1:27278000 G>A maps to NM_152365.2 Q291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr1:27278442 G>C maps to NM_152365.2 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73R-01A-11D-A33O-09 chr1:27278789 C>A maps to NM_152365.2 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr1:75108727 G>A maps to NM_001002912.4 R100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr1:75038215 G>A maps to NM_001002912.4 R1060*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A69L-01A-11D-A32I-09 chr1:75038597 C>T maps to NM_001002912.4 E932E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr1:75078443 G>T maps to NM_001002912.4 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr1:55273257 G>A maps to NM_001110533.1 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:55277498 G>A maps to NM_001110533.1 E171E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr1:154178093 T>C maps to NM_001010979.1 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:159810560 G>A maps to NM_001134233.1 Q180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr1:43748629 G>C maps to NM_001164829.1 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:162353075 C>A maps to NM_001135240.1 S184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:162353430 C>G maps to NM_001135240.1 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr1:213009359 C>T maps to NM_001024601.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr1:228289822 G>T maps to NM_024319.2 S164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:228289721 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:228289606 G>C did not map to a codon.
Sequencing variant TCGA-EA-A3HQ-01A-11D-A20U-09 chr1:154186399 C>T maps to NM_001098616.1 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LC-01A-11D-A20U-09 chr1:154179793 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:154185137 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:154185144 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr1:43239084 G>C did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:150257221 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr1:151021204 C>T maps to NM_017860.3 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr1:156382264 C>T did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr1:156382477 C>T did not map to a codon.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr1:223567620 G>A maps to NM_152610.2 K268K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LS-01A-22D-A22X-09 chr1:156264185 C>T maps to NM_144580.1 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AX-01A-12D-A243-09 chr1:156263855 G>A maps to NM_144580.1 Q251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr1:2116534 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:2129632 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:60474326 C>T maps to ENST00000395552 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr1:34667793 C>G maps to NM_001134734.1 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:226784512 C>G maps to ENST00000366788 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr20:31108722 G>A maps to ENST00000375678 I25I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr20:31136381 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr20:35238036 C>G maps to NM_018840.4 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr21:45758159 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr21:45561287 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr21:47735420 C>T maps to NM_058180.3 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr21:33982259 C>T maps to NM_021254.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr22:29456576 C>T maps to NM_015370.1 K86K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr22:29456462 G>A maps to NM_015370.1 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr21:43334761 C>T maps to NM_015500.1 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PD-01A-11D-A351-09 chr21:43325860 G>A maps to NM_015500.1 V468V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PD-01A-11D-A351-09 chr21:43325881 G>A maps to NM_015500.1 I461I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr11:73825445 C>T maps to ENST00000334126 V571V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A5XV-01A-11D-A28B-09 chr11:73849867 C>G maps to ENST00000334126 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr11:73748733 C>T maps to ENST00000334126 L1890L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:73745581 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr2:27802540 C>G maps to NM_032266.3 L1034L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr2:106690477 C>T maps to NM_032411.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr2:70408571 C>T maps to NM_017880.1 Q182Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr2:105954073 C>T maps to NM_024093.1 C10C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:105954031 C>G maps to ENST00000437250 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr2:241830998 G>A maps to NM_001085437.1 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr2:85838417 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:85838863 C>G maps to NM_001013649.3 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr2:29294043 C>T maps to NM_001029883.1 T1028T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr2:54587430 C>G maps to NM_001100396.1 S199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr2:120069237 G>C maps to NM_001017927.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HQ-01A-11D-A20U-09 chr19:6707525 G>A maps to NM_000064.2 A666A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr19:6679457 C>T maps to NM_000064.2 L1502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:112724776 G>C maps to NM_015412.3 S437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr3:14770063 T>C maps to NM_032137.4 S603S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr3:14813663 C>T maps to NM_032137.4 A862A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:14731502 G>C did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr3:128292451 G>A maps to NM_007354.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr3:133647581 G>A maps to NM_025041.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr3:129007719 C>T maps to NM_001006109.1 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr3:111835487 G>C did not map to a codon.
Sequencing variant TCGA-C5-A7UC-01A-11D-A351-09 chr3:58898468 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr3:184800812 C>T maps to NM_001025266.1 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr3:184870594 G>T maps to NM_001025266.1 S6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr6:31963800 G>T maps to NM_007293.2 L1100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:207297627 C>A maps to NM_000715.3 S208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:113482021 C>T maps to NM_018392.4 L1609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr4:113460798 C>G maps to NM_018392.4 L2073L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr4:113510988 A>C maps to NM_018392.4 V1006V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr4:113474996 C>T maps to NM_018392.4 L1780L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U3-01A-11D-A28B-09 chr4:113541343 C>T maps to NM_018392.4 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr4:120219934 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr4:87809428 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr4:87809367 G>T maps to NM_144645.3 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr4:71008260 C>G did not map to a codon.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr9:123800209 C>T maps to NM_001735.2 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr19:47823990 C>T maps to ENST00000355085 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr5:43506469 C>T maps to NM_198566.2 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr5:37196094 G>A maps to NM_023073.3 R1226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr5:179280282 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr5:147281296 G>T maps to NM_206966.2 S37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr5:131811682 C>T did not map to a codon.
Sequencing variant TCGA-JW-A852-01A-11D-A351-09 chr5:131792779 G>A maps to ENST00000378947 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr5:41176762 T>A maps to NM_001115131.1 K328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr6:34214350 G>A maps to NM_178508.3 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr6:165695235 T>C did not map to a codon.
Sequencing variant TCGA-DS-A7WH-01A-22D-A351-09 chr6:88138519 G>A maps to NM_001031743.2 V379V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr6:2623873 G>C maps to NM_152554.2 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr6:4087922 G>A maps to NM_001085401.1 T16T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr6:43970469 G>A maps to NM_153246.4 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr6:71298316 G>T did not map to a codon.
Sequencing variant TCGA-HG-A2PA-01A-11D-A20U-09 chr6:170162584 T>C maps to NM_018341.1 F306F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr6:36853742 C>T did not map to a codon.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr6:36870109 C>T maps to NM_152734.3 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HM-A3JK-01A-11D-A21Q-09 chr5:40947852 C>T maps to NM_000587.2 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr5:40981527 G>A maps to NM_000587.2 S795S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr7:89936213 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr7:89909022 G>A maps to NM_001039706.2 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr7:89933281 G>T did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr7:89906409 G>A maps to NM_001039706.2 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr7:47698633 G>A maps to NM_001123065.1 Q88Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr9:139840396 C>T maps to NM_000606.2 Q98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr8:69243480 C>G maps to NM_052958.2 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr8:69537879 C>T maps to ENST00000325233 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr8:67592257 G>C did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr8:67591813 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr8:67428139 C>G maps to NM_152765.3 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr9:132084250 C>T maps to NM_001012715.3 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr9:131586154 G>A maps to NM_016390.2 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr9:131588513 C>G did not map to a codon.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr9:131591026 C>T maps to NM_016390.2 E65E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr9:130475770 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr9:130475901 C>T did not map to a codon.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr9:7799695 G>A maps to NM_033428.1 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A0TN-01A-21D-A14W-08 chr9:88836482 C>A did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr9:130925200 C>G did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr9:130922668 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr9:97686289 C>T maps to NM_001193329.1 Q463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr9:97694039 C>G did not map to a codon.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr9:91606128 G>A maps to NM_001001938.3 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr9:132375856 C>T maps to NM_199350.3 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:214586 C>G maps to NM_152569.2 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr9:214655 C>T maps to NM_152569.2 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr9:139008611 G>C maps to NM_152833.2 S70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr9:27548003 A>C did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr9:132590388 G>A did not map to a codon.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr9:114454374 G>C maps to NM_173521.3 V1230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr9:114490153 C>T maps to NM_173521.3 K467K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr9:114521009 G>A maps to NM_173521.3 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr9:95870052 G>C maps to NM_032310.3 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr9:117379409 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr9:117396097 G>C maps to ENST00000374049 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr9:136265574 G>A maps to NM_153710.3 V372V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr17:50235157 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr15:63619424 G>A maps to NM_001218.3 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr8:86158062 G>A maps to NM_198584.2 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr1:9034437 C>T maps to ENST00000377436 Q293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr1:9011497 C>A maps to ENST00000319474 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:9034806 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr8:61192271 G>A maps to NM_004056.4 Q90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HR-01A-11D-A20U-09 chr22:24562873 G>T maps to NM_012295.3 E1759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr22:24509659 C>T maps to NM_012295.3 L1415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr11:67287315 G>A maps to NM_016366.2 D195D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr11:67225897 G>A maps to NM_145200.3 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr18:21723169 C>G maps to NM_138644.1 S31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:65068491 C>T maps to ENST00000371073 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HM-A3JK-01A-11D-A21Q-09 chr1:65099845 C>T maps to ENST00000371073 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:65099936 C>T maps to ENST00000371073 Q334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:65157441 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:65157585 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr9:141010113 C>T maps to ENST00000277549 L1921L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr9:140807658 C>T maps to ENST00000277549 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QD-01A-32D-A22X-09 chr9:140878594 C>T maps to ENST00000277549 I555I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr9:140946582 G>C maps to ENST00000277549 L1251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:2719825 C>T maps to NM_199460.2 F1246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr12:2706418 T>G maps to NM_199460.2 V939V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A449-01A-11D-A243-09 chr12:2786272 C>T maps to NM_199460.2 T1662T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr12:2711063 G>C maps to NM_199460.2 R986R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr12:2690794 G>A maps to NM_199460.2 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr1:181453068 C>T maps to ENST00000357570 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr1:181706768 G>T maps to ENST00000357570 L1177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A556-01A-11D-A26G-09 chr1:181767480 C>A maps to ENST00000357570 T2151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73R-01A-11D-A33O-09 chr1:181680089 G>T maps to ENST00000357570 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HQ-01A-11D-A20U-09 chr23:49066139 T>A did not map to a codon.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr23:49087753 G>C did not map to a codon.
Sequencing variant TCGA-EA-A44S-01A-12D-A26G-09 chr23:49072950 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr23:49071931 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:49072854 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:49063284 G>A did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr23:49088167 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr17:48653073 C>G maps to NM_018896.3 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:48655897 C>A maps to NM_018896.3 L758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr16:1251943 G>A maps to NM_021098.2 Q498Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr16:1259399 C>T maps to NM_021098.2 D1244D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr16:1270950 C>G maps to NM_021098.2 S2340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr22:40061887 C>G maps to NM_021096.3 L1327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr22:40068992 C>G maps to NM_021096.3 V1563V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CJ-01A-11D-A32I-09 chr1:201031085 G>A maps to NM_000069.2 F1013F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A449-01A-11D-A243-09 chr1:201031121 G>A maps to NM_000069.2 L1001L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr1:201061235 G>A maps to NM_000069.2 F135F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr3:50402377 G>A maps to ENST00000435965 L1088L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:50412210 G>A maps to ENST00000435965 F647F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr3:55108241 G>A did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr3:55107696 G>A did not map to a codon.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr3:54604081 C>G maps to NM_018398.2 S280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr3:54798356 C>T maps to NM_018398.2 T453T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HM-A3JK-01A-11D-A21Q-09 chr3:54919572 G>A maps to NM_018398.2 A672A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr12:1910284 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr17:37331541 C>T maps to NM_000723.3 R567R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr17:37353712 G>T maps to NM_000723.3 Y12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A449-01A-11D-A243-09 chr17:37343053 G>A maps to NM_000723.3 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr17:37343682 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr2:152695760 G>A maps to NM_000726.3 Q479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr2:152698449 G>T maps to NM_000726.3 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr17:65050166 C>T maps to NM_000727.3 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr16:24358138 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr17:64876773 G>A maps to NM_014404.1 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr19:54515262 G>A maps to NM_145814.1 Q201Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr19:54445318 C>T maps to NM_031896.4 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr1:174973856 G>A maps to NM_014412.2 K41K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr2:27457540 C>T maps to NM_004341.3 V1258V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5FO-01A-21D-A28B-09 chr11:115375114 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr3:85008740 C>A did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr19:44129383 C>T maps to NM_145296.1 W258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr3:62556597 G>A maps to ENST00000383709 I531I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr3:62499349 G>A maps to NM_183394.2 V871V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HQ-01A-11D-A20U-09 chr6:7373451 G>A maps to NM_001170692.1 Q534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr12:54115829 C>T maps to NM_020898.2 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr17:46928957 G>T maps to ENST00000448105 E248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A50E-01A-21D-A26G-09 chr10:105215351 C>T maps to NM_001001412.3 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr10:105209515 G>A maps to NM_015916.4 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr2:47403564 C>G did not map to a codon.
Sequencing variant TCGA-DS-A3LQ-01A-21D-A21Q-09 chr19:47112430 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr19:13049555 C>G maps to NM_004343.3 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZE-01A-11D-A28B-09 chr7:128394424 C>T maps to ENST00000342367 R119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:44268526 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2PI-01A-11D-A18J-09 chr7:44268618 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr7:44259837 G>A maps to NM_001220.4 H608H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr7:44268518 G>A maps to NM_001220.4 P448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr4:114468802 C>T maps to ENST00000511664 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr10:75608804 G>A maps to ENST00000423381 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr10:75576467 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr3:183978916 G>A maps to NM_033259.2 R53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr3:183977944 C>T maps to NM_033259.2 *80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:134086561 C>T maps to NM_001745.2 F271F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr9:138758250 G>T did not map to a codon.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr1:7723698 C>T maps to NM_015215.2 S364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr1:7309667 C>G maps to NM_015215.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:7724547 G>A maps to NM_015215.2 V647V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr1:7723500 G>C maps to NM_015215.2 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:4883074 G>A maps to NM_015099.3 I514I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:12856709 C>T maps to NM_001162499.1 I359I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr5:179151710 G>A maps to ENST00000415618 V559V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr5:179134135 G>A maps to ENST00000415618 W118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr11:64950426 G>A maps to NM_005186.3 W85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr11:64956161 C>G maps to NM_005186.3 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr11:64950384 G>A maps to NM_005186.3 K71K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr2:241535884 C>T maps to NM_023083.3 D476D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R3-01A-11D-A28B-09 chr2:241535809 C>T maps to NM_023083.3 Y451Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr19:39224779 A>C did not map to a codon.
Sequencing variant TCGA-DG-A2KH-01A-21D-A22X-09 chr19:39230770 G>A maps to NM_144691.3 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr19:39234769 G>A maps to NM_144691.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr19:39230810 A>T maps to NM_144691.3 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A5XV-01A-11D-A28B-09 chr19:39232547 G>C maps to NM_144691.3 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LB-01A-11D-A243-09 chr19:39224991 G>A maps to NM_144691.3 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr2:30955385 C>T maps to ENST00000295055 V615V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:223947150 C>T maps to NM_001748.4 I499I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:223957628 C>T did not map to a codon.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr15:42676698 C>T maps to NM_000070.2 R110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr23:110491186 G>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:110497607 C>T did not map to a codon.
Sequencing variant TCGA-DS-A7WH-01A-22D-A351-09 chr23:110496435 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:110494901 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr23:110494280 C>T did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr11:34121473 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr11:34120901 G>A maps to NM_005898.4 Q706Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr11:34101276 C>G maps to NM_005898.4 S264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A3L1-01A-11D-A21Q-09 chr11:34074228 C>G did not map to a codon.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr11:34117895 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr12:30881671 C>T maps to NM_001002259.1 Q564Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr12:30881632 G>A maps to NM_001002259.1 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr12:30863276 T>A maps to NM_001002259.1 A981A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr12:30882049 G>A maps to NM_001002259.1 S438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr19:5914202 C>G maps to ENST00000394521 S87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr12:75765016 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr7:116544250 C>T maps to NM_006136.2 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr7:116528222 G>T maps to NM_006136.2 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr7:2952969 C>T maps to NM_032415.4 Q990Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr7:2972190 C>T maps to NM_032415.4 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr17:78176111 C>T maps to NM_024110.2 H704H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr17:78177624 C>T maps to NM_024110.2 Q742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr19:48689852 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3L7-01A-21D-A20U-09 chr11:3038338 C>T maps to NM_001014437.2 L638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr11:3050643 G>C maps to NM_001014437.2 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr17:38324109 C>T maps to NM_007359.4 F553F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr7:94166899 C>T maps to NM_022900.4 F320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:41390271 G>A did not map to a codon.
Sequencing variant TCGA-EA-A5FO-01A-21D-A28B-09 chr23:41419100 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr23:41416351 C>T did not map to a codon.
Sequencing variant TCGA-EX-A69M-01A-11D-A32I-09 chr23:41481886 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr23:41524687 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:41401970 C>G did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr16:2239140 G>A maps to NM_020764.3 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr17:73501031 G>A maps to NM_020753.3 I351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr17:73498413 G>C maps to NM_020753.3 S914*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr2:202074060 C>T maps to NM_032977.3 F397F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr10:115485289 C>T maps to NM_033338.4 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr2:202149750 C>T maps to NM_001080125.1 Q398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr2:202136247 C>T maps to NM_001080125.1 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr2:202136258 C>G maps to NM_001080125.1 S168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr2:202151269 C>T maps to NM_001080125.1 Q524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr2:202150038 C>T maps to NM_001080125.1 R494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr2:202149615 G>T maps to NM_001080125.1 E353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr6:90576284 G>A maps to NM_012115.3 V1092V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr6:90576584 G>A maps to NM_012115.3 L1192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr1:15833503 C>A maps to NM_001229.3 E174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr1:160171085 G>T maps to NM_001231.4 E371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr1:10720516 C>T maps to NM_001079843.1 Q194Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WH-01A-22D-A351-09 chr1:10699829 G>A maps to NM_001079843.1 R1483R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr1:10699535 C>T maps to NM_001079843.1 T1581T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3TQ-01A-11D-A22X-09 chr1:10720360 G>A maps to NM_001079843.1 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr1:10725311 G>T maps to NM_001079843.1 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr1:10713653 G>A maps to NM_001079843.1 L820L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr11:34492395 G>T did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:34472556 C>T maps to NM_001752.3 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr15:43928407 C>T maps to NM_172095.1 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr15:43931924 G>A maps to NM_172095.1 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr14:92102779 C>G maps to NM_024764.2 V577V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr19:38857866 G>A maps to NM_021185.4 T895T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr19:38860840 C>T maps to NM_021185.4 F1052F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr7:116140194 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr7:116139969 C>G maps to NM_001233.3 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr20:32224461 C>T maps to NM_005093.3 F424F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr16:88949137 G>T maps to NM_005187.5 I383I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr16:88968056 C>T maps to NM_005187.5 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr3:105377915 C>T maps to NM_170662.3 V949V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A69M-01A-11D-A32I-09 chr19:45295766 G>A maps to NM_012116.3 W378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr16:49313389 G>A maps to NM_004352.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZF-01A-11D-A28B-09 chr21:37443335 C>G maps to NM_001757.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr21:44488637 G>A maps to ENST00000398168 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr9:173312 C>A maps to NM_018491.3 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr9:161590 C>G did not map to a codon.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr9:70883976 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr17:46148889 C>T maps to ENST00000442683 K159K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:26242450 G>C did not map to a codon.
Sequencing variant TCGA-EA-A44S-01A-12D-A26G-09 chr7:26242432 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr22:39262279 G>A maps to NM_014292.3 F391F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr1:52822820 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr4:15482422 G>A maps to NM_001080522.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr4:15597792 C>G maps to NM_001080522.2 S1467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr10:97752361 C>T maps to ENST00000371198 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr10:70547682 G>A did not map to a codon.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr10:70507286 C>T maps to NM_018237.2 Q264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WH-01A-22D-A351-09 chr1:89430627 G>A maps to NM_001008661.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr2:55762943 C>T maps to ENST00000403007 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr2:219875664 G>A maps to NM_194302.2 T1337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HM-A3JK-01A-11D-A21Q-09 chr2:219897275 G>A maps to NM_194302.2 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr4:110585444 G>C did not map to a codon.
Sequencing variant TCGA-EA-A556-01A-11D-A26G-09 chr18:47792729 G>T maps to NM_145020.3 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr18:47753900 C>T maps to NM_145020.3 E465E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr18:47769345 C>T maps to NM_145020.3 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr19:48824025 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr3:46982548 C>A maps to NM_144716.3 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr23:48925126 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr23:48922113 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:48922602 C>G did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:48923077 G>A did not map to a codon.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr23:48924807 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr19:18047325 G>T maps to NM_001136203.1 E33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr5:68578571 G>C maps to NM_176816.3 S507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr7:23651036 C>T maps to NM_138771.3 Q35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr7:31683551 G>A maps to NM_194300.2 V856V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr7:31614226 G>T maps to NM_194300.2 E157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M1-01A-11D-A18J-09 chr3:42777312 C>G maps to NM_144719.3 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr3:42791399 G>C maps to ENST00000435327 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr3:42791311 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr19:13869864 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VH-01A-11D-A28B-09 chr22:42209804 A>T maps to NM_024821.2 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr22:42205901 G>A maps to NM_024821.2 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr16:57741509 G>T maps to NM_032269.5 E333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WH-01A-22D-A351-09 chr17:79634866 C>T maps to NM_199287.2 I81I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr2:179912013 G>C maps to NM_173648.3 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr17:20799132 G>A maps to NM_001004306.1 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr7:76908106 G>A maps to NM_020879.2 K493K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr7:76751980 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr10:106118344 C>T maps to NM_001008723.1 Q86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr2:159166126 G>A maps to NM_138803.3 Q310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr4:24810019 C>G maps to NM_001130726.2 V527V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:197504477 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2GZ-01A-11D-A17W-09 chr2:197565862 G>T maps to NM_001080539.1 E552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:197521509 C>G maps to NM_001080539.1 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr5:42769697 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr19:11464108 C>A did not map to a codon.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr23:133378998 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:133379428 A>G did not map to a codon.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr23:133379540 G>A did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr23:133379618 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:46086414 C>A maps to NM_001114938.2 E564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:93657577 C>T maps to NM_206886.2 Q280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr1:159842989 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:159857690 G>A maps to NM_012337.2 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:159846317 G>A did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr1:159869893 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3QD-01A-32D-A22X-09 chr23:49105662 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr23:49104952 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr1:44461378 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:3670735 C>T maps to NM_152492.2 R125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr1:32667665 C>T maps to ENST00000421922 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr10:13040404 G>C maps to NM_031455.3 S161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr15:74564042 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr3:126139025 C>T maps to ENST00000505024 Q347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr3:126151932 G>C maps to ENST00000505024 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:126137951 G>A maps to ENST00000505024 K229K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr3:126151923 C>T maps to ENST00000505024 V434V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr3:126133024 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:126142170 G>A maps to ENST00000505024 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr3:180381769 G>C maps to NM_181426.1 S32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr3:191047504 C>G maps to NM_178335.2 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr3:191075841 C>G maps to NM_178335.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R9-01A-11D-A18J-09 chr12:82750801 A>T maps to NM_014167.4 L134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr12:119954431 G>T maps to NM_178499.3 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H6-01B-11D-A22X-09 chr12:119772967 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr19:46520258 C>T maps to NM_001080402.1 F433F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr16:3080596 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr12:49312137 C>T maps to NM_033124.4 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A449-01A-11D-A243-09 chr11:93104220 C>T maps to NM_181645.3 Y188Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr10:32854532 G>A maps to NM_001026383.1 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr10:32807382 G>T maps to NM_001026383.1 E315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr3:49201116 G>A maps to NM_022903.3 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr2:132287645 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr12:539853 C>T maps to NM_032358.3 Q179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U3-01A-11D-A28B-09 chr12:521074 T>G maps to NM_032358.3 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr12:498526 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:498567 C>G did not map to a codon.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr16:773854 A>G did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr16:772970 C>T maps to NM_001031737.2 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73Q-01A-21D-A32I-09 chr3:112358467 C>A maps to ENST00000447230 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr11:96117182 G>C maps to NM_024725.3 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr2:56603036 C>T maps to NM_001080433.1 S513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr2:56603037 C>T maps to NM_001080433.1 Q514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr11:60610304 G>A maps to NM_024098.3 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr11:66358230 G>A maps to NM_018219.2 F752F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr11:66358233 G>A maps to NM_018219.2 F751F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr11:66358278 C>T maps to NM_018219.2 A736A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr2:55563906 C>T maps to ENST00000436346 Q522Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr11:64111689 G>A maps to NM_032251.5 E559E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr11:64112487 G>A maps to NM_032251.5 R825R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr11:64124659 A>G maps to ENST00000359902 G613G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr11:64119015 G>C maps to NM_032251.5 G1009G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A852-01A-11D-A351-09 chr11:64108933 C>T maps to NM_032251.5 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:91850870 C>G did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr14:91808752 G>A maps to NM_001080414.2 Q152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr11:82996674 G>T did not map to a codon.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr12:28605542 C>T maps to NM_018318.3 Q353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr12:28412326 G>T maps to NM_018318.3 E21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr12:28459677 C>T maps to NM_018318.3 Q91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr12:124428831 C>G maps to NM_025140.1 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R9-01A-11D-A18J-09 chr2:118709185 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr4:7043585 C>T maps to NM_153376.2 Q360Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr19:41825617 G>A maps to NM_052848.1 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr9:36170050 C>G maps to NM_005893.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:42305092 C>T maps to NM_000729.4 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr11:6291977 C>T maps to NM_176875.2 D252D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr16:57448994 C>T maps to NM_002987.2 R25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr17:32582376 C>A maps to NM_002982.3 V3V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr16:57397454 C>A maps to NM_002990.4 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr7:45104111 C>T maps to NM_001029835.2 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr7:45104162 C>T maps to NM_001029835.2 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr13:37014269 C>T maps to NM_003914.3 Q350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr13:37006086 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr14:20779660 C>G did not map to a codon.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr23:50052360 C>G did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:50028214 C>G did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:50052680 G>C did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:50028144 G>A did not map to a codon.
Sequencing variant TCGA-JW-A69B-01A-11D-A32I-09 chr23:50051744 G>A did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr23:50054312 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr19:30314668 G>T maps to NM_001238.1 G406G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HQ-01A-11D-A20U-09 chr16:2499398 C>T maps to NM_001761.2 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr16:2503297 C>T maps to NM_001761.2 I525I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr4:78082833 G>A maps to NM_004354.2 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr4:78082671 G>A maps to NM_004354.2 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr10:97820183 A>C did not map to a codon.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr10:97816695 G>A maps to NM_001134375.1 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr5:159680107 G>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:156870833 A>G maps to NM_020307.2 H200H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:156877262 C>G maps to NM_020307.2 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr1:1333623 C>G maps to NM_030937.4 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr1:1322817 G>A maps to NM_030937.4 C452C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr5:54527208 C>T maps to NM_021147.3 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:135710842 C>G maps to NM_058241.2 S273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr15:55669315 G>A maps to ENST00000442196 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr3:46398966 G>C did not map to a codon.
Sequencing variant TCGA-C5-A7CM-01A-11D-A33O-09 chr3:32994925 G>A maps to NM_005508.4 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr3:46415352 C>T maps to NM_001100168.1 F320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr17:38711119 G>C maps to NM_001838.3 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr17:38711533 G>C maps to NM_001838.3 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr3:39374121 G>A maps to NM_005201.3 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:45942948 C>T maps to NM_031200.2 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr4:139966096 G>A maps to NM_012118.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr11:66366698 C>G maps to NM_005125.1 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr1:156308087 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr1:156290800 G>T maps to NM_005998.4 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:156278945 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:156290679 C>A maps to NM_005998.4 E187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr7:56122147 C>G maps to NM_001762.3 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:73479987 G>A maps to NM_006429.3 *544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr1:117544452 C>G maps to NM_004258.3 S5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CM-01A-11D-A33O-09 chr5:140011842 G>A maps to NM_001174105.1 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr12:7637944 A>G maps to NM_004244.4 F842F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr6:109703434 G>A maps to NM_006016.4 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2GZ-01A-11D-A17W-09 chr1:27709083 G>T maps to NM_207397.2 C54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:27709026 G>A maps to NM_207397.2 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr19:43858503 C>T maps to NM_020406.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZF-01A-11D-A28B-09 chr16:28950042 C>G maps to NM_001178098.1 P512P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:158226846 C>T maps to NM_001763.2 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr1:158151384 C>T maps to NM_001766.3 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr1:158325177 G>C maps to NM_030893.3 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:158325753 C>T maps to NM_030893.3 Q255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr2:71058943 G>A maps to NM_015717.3 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73Q-01A-21D-A32I-09 chr19:35837089 G>A maps to NM_001771.3 P788P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QE-01A-21D-A21Q-09 chr18:67563261 C>A maps to NM_006566.2 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr1:167487675 C>T maps to NM_198053.2 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr17:72584926 T>G maps to NM_001115152.1 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr17:72691887 C>T maps to ENST00000412086 Q246Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr7:80292451 C>T maps to NM_001127444.1 Y192Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr19:49838724 C>G did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr12:6926359 G>A maps to NM_000616.4 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr20:44756861 C>T maps to NM_001250.4 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr23:135730505 C>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:135741262 A>G did not map to a codon.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr23:135732427 G>C did not map to a codon.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr11:35160832 C>G did not map to a codon.
Sequencing variant TCGA-C5-A7X3-01A-11D-A351-09 chr1:207967031 G>T did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr1:207940451 C>T maps to NM_172359.2 C256C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:207934771 T>C maps to NM_172359.2 R218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:207940685 C>A did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:207933080 C>G did not map to a codon.
Sequencing variant TCGA-EA-A3HR-01A-11D-A20U-09 chr3:107762964 C>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr3:107763024 T>G did not map to a codon.
Sequencing variant TCGA-IR-A3LB-01A-11D-A243-09 chr3:107764454 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:107762490 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:160651193 C>T maps to NM_001778.2 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr1:207527418 C>T maps to ENST00000391920 I383I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr1:117086980 C>A maps to NM_001779.2 E106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr19:6586410 G>A maps to NM_001252.3 Q68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr9:35612926 G>C maps to NM_001782.2 S251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr9:35610238 G>C did not map to a codon.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr9:35616189 C>T maps to NM_001782.2 K146K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr2:87016515 G>A maps to ENST00000456996 I226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr2:87085222 C>T maps to NM_172213.3 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:111264107 G>T maps to NM_198196.2 E93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr19:14516687 C>G maps to NM_078481.2 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr19:14513541 C>T maps to NM_078481.2 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr19:14517893 C>T maps to NM_078481.2 I743I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr19:14517902 C>T maps to NM_078481.2 L746L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr19:14518908 C>T maps to NM_078481.2 L828L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr19:14517944 C>T maps to NM_078481.2 F760F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr23:2609848 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr23:2638397 C>T did not map to a codon.
Sequencing variant TCGA-EX-A69M-01A-11D-A32I-09 chr23:2651448 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr23:2651453 G>A did not map to a codon.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr23:149999751 C>G did not map to a codon.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr23:149963741 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:149963686 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:149998023 G>T did not map to a codon.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr13:49822117 G>C did not map to a codon.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr15:43028185 G>A maps to NM_138477.2 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr10:12257791 C>T maps to NM_006023.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr9:99380951 G>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr9:99258568 C>G maps to ENST00000474602 *472Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr13:115011473 G>T did not map to a codon.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr1:43827909 A>C maps to NM_001255.2 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr5:54420850 G>C maps to NM_001170402.1 S332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr5:137534363 G>C maps to NM_004661.3 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:48228244 C>T maps to NM_001789.2 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr20:3783435 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr17:45219630 G>A maps to NM_001114091.1 Q454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr19:10514086 G>A maps to NM_007065.3 I23I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr1:227299833 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:227381438 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr14:103470288 G>A maps to NM_006035.3 Y141Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr14:103406261 G>A maps to NM_006035.3 D1538D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr14:103400154 G>C maps to NM_006035.3 S1677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M2-01A-21D-A18J-09 chr11:64608045 G>A maps to NM_017525.2 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:64609202 G>A maps to NM_017525.2 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr22:37964250 C>T maps to NM_152243.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr22:37964429 C>G maps to NM_152243.2 S260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr17:71282207 C>T maps to NM_012121.4 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr17:71302938 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr6:44387270 C>G maps to NM_001253.2 S393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZF-01A-11D-A28B-09 chr1:193220215 G>A did not map to a codon.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr8:25341480 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr8:25317768 C>G maps to ENST00000434814 S5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr12:6958093 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr12:6958993 C>G maps to NM_031299.4 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr7:21945149 G>A maps to NM_018719.4 R341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HG-A2PA-01A-11D-A20U-09 chr3:45132716 G>A maps to NM_022842.3 S647S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr1:54602316 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr16:68869293 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73Q-01A-21D-A32I-09 chr16:68868699 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr5:24535248 G>A maps to NM_006727.3 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr5:24511435 C>T maps to NM_006727.3 K334K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VH-01A-11D-A28B-09 chr5:24593377 G>A maps to NM_006727.3 Y74Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr5:24487403 C>A did not map to a codon.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr16:64984721 G>T maps to NM_001797.2 G614G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HR-01A-11D-A20U-09 chr16:65022215 G>A maps to NM_001797.2 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr16:64984691 G>C maps to NM_001797.2 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr16:64981643 C>T maps to NM_001797.2 V751V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PI-01A-11D-A18J-09 chr5:21752318 G>A maps to NM_004061.3 R638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr5:21975494 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr5:22078957 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr16:83817033 C>T maps to ENST00000268613 F697F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr16:83817048 C>T maps to ENST00000268613 V702V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr16:89245822 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr16:89251680 C>T maps to NM_004933.2 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7X3-01A-11D-A351-09 chr8:95164277 A>C maps to NM_001144663.1 P538P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CJ-01A-11D-A32I-09 chr5:19839102 T>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr18:64218333 C>A maps to NM_021153.2 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr18:25565687 G>A maps to NM_001792.3 I593I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr18:25583080 G>T maps to NM_001792.3 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr20:44869842 G>A maps to NM_021248.1 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M1-01A-11D-A18J-09 chr10:73472507 C>T maps to ENST00000398860 L1108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr10:73556743 C>G did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr14:23523478 G>A maps to NM_022478.3 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr16:68725653 C>T maps to NM_001793.4 F609F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr16:68732018 G>A maps to ENST00000429102 Q768Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr20:60511901 C>T maps to NM_001794.2 N884N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AX-01A-12D-A243-09 chr20:60498573 G>C maps to NM_001794.2 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr5:31267657 G>A maps to NM_004932.2 K26K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A69M-01A-11D-A32I-09 chr18:63511148 G>A maps to NM_004361.2 T361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr16:62055156 C>A maps to NM_001796.2 E51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr16:61952342 C>T did not map to a codon.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr16:61689422 G>A maps to NM_001796.2 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr16:61747889 T>G did not map to a codon.
Sequencing variant TCGA-FU-A5XV-01A-11D-A28B-09 chr5:26915831 C>T maps to NM_016279.3 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HQ-01A-11D-A20U-09 chr10:85974455 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr10:85968516 G>A maps to NM_033100.2 V400V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr10:85974064 C>G maps to NM_033100.2 L756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr10:85965625 C>T maps to NM_033100.2 I302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr7:105564465 A>G did not map to a codon.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr7:105669021 C>T maps to NM_152750.4 V766V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr3:49832786 C>T maps to NM_001007540.2 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr3:49831401 G>A maps to NM_001007540.2 N439N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr1:1636375 G>C maps to NM_024011.2 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr7:40132637 C>T maps to NM_003718.4 Q1164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:90419920 C>T maps to NM_012395.2 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr7:90338817 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr7:90338783 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr12:96676322 G>A maps to NM_002595.4 R474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr1:205501635 G>A did not map to a codon.
Sequencing variant TCGA-EA-A78R-01A-11D-A32I-09 chr1:205499705 G>C did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:205495891 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr1:205501486 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr1:205499655 G>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:205501517 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3HR-01A-11D-A20U-09 chr12:56365573 G>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr9:90589418 C>G did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr11:67275413 C>G did not map to a codon.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr11:67274908 G>A maps to NM_005851.3 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr12:58145320 C>T maps to NM_000075.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr2:219825345 C>T maps to NM_003936.3 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr2:219825153 G>C maps to NM_003936.3 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A410-01A-11D-A243-09 chr20:31984664 A>T maps to ENST00000357886 L69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr9:123202152 C>T maps to NM_018249.4 L1082L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr9:123165170 C>T maps to NM_018249.4 Q1740Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:46052531 C>G maps to NM_176096.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr17:46048632 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr17:46054076 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RL-01A-11D-A18J-09 chr7:92300822 G>A maps to NM_001145306.1 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr7:92462442 C>T maps to NM_001145306.1 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr5:68530840 G>A maps to NM_001799.3 E13E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr13:26959423 C>T maps to NM_001260.1 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr14:50844421 G>A maps to ENST00000356146 F460F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr14:50845054 G>A maps to ENST00000356146 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr4:76529027 G>C maps to ENST00000307465 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr23:18622090 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr23:18671621 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr23:18622354 C>T did not map to a codon.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr23:18593568 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:18622090 G>A did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr23:18668689 C>T did not map to a codon.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr23:18627005 T>A did not map to a codon.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr23:18627006 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr4:184367412 G>C maps to NM_017632.2 R192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr4:184368432 G>A maps to NM_017632.2 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr10:14879933 C>T maps to NM_001029954.2 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr11:125853857 G>A maps to ENST00000392693 I968I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:125880589 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr23:139866365 C>A did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr16:22361023 C>T maps to NM_001802.1 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr20:5171874 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr20:5169735 C>T maps to NM_003818.2 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr16:88871168 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2H1-01A-11D-A17W-09 chr23:72667525 C>G did not map to a codon.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr23:72674415 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73Q-01A-21D-A32I-09 chr6:4773343 G>C did not map to a codon.
Sequencing variant TCGA-EA-A6QX-01A-12D-A33O-09 chr19:43023355 G>A maps to NM_001712.4 I330I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr19:43016550 G>A maps to NM_001712.4 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr19:43031406 C>G maps to NM_001712.4 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr19:45213774 G>T maps to ENST00000396750 G490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr19:51981895 C>G maps to NM_001080405.1 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr19:45015097 G>C maps to NM_001102597.1 S576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr19:42092924 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr2:37444135 G>T maps to NM_005760.2 T733T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr2:37458671 C>T maps to NM_005760.2 K13K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr22:17688134 C>T maps to NM_017424.2 W123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr22:17670773 A>T did not map to a codon.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr22:17976527 C>T maps to ENST00000400579 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R9-01A-11D-A18J-09 chr22:17907427 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr22:18022112 C>T maps to ENST00000400579 R740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A852-01A-11D-A351-09 chr22:18020197 G>A maps to ENST00000400579 W510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr9:135946535 G>A maps to NM_001807.3 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr1:15783231 A>G did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr1:15789916 C>T maps to ENST00000375924 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr1:22329578 C>T maps to NM_005747.4 Q43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:22333385 C>T maps to NM_005747.4 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WF-01A-11D-A351-09 chr11:47510458 G>A maps to NM_001172639.1 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr10:11299827 G>C maps to NM_006561.3 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr10:11308600 G>A maps to NM_006561.3 Q193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr18:34855192 G>A maps to NM_020180.3 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr18:34839127 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LC-01A-11D-A20U-09 chr19:3290269 G>T maps to NM_021938.3 E410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr22:46787539 G>A maps to NM_014246.1 L2046L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr1:109816585 C>T did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr1:109794626 C>T maps to NM_001408.2 V642V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr1:109815024 G>A maps to NM_001408.2 L2684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:109803757 C>T maps to NM_001408.2 F1351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr1:109795250 C>G maps to NM_001408.2 V850V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr3:48679398 C>T maps to NM_001407.2 E2903E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:48699500 C>T maps to NM_001407.2 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr3:48681728 C>G did not map to a codon.
Sequencing variant TCGA-JW-A69B-01A-11D-A32I-09 chr3:48697841 G>A maps to NM_001407.2 V742V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr11:788162 C>T maps to NM_016564.3 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr20:3766323 G>A maps to NM_001810.5 V269V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr16:90038051 C>T maps to NM_145039.3 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr4:104084650 A>T maps to NM_001813.2 Y569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr4:104067179 C>A maps to NM_001813.2 E1407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73S-01A-11D-A33O-09 chr4:104027423 C>T maps to NM_001813.2 W2687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:214816096 C>T maps to NM_016343.3 L1472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:214792494 G>T maps to NM_016343.3 E169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:214830322 G>T maps to NM_016343.3 E2845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:214788401 G>A did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr1:214818771 C>G maps to NM_016343.3 L1953L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr23:100382212 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3QE-01A-21D-A21Q-09 chr23:100402753 A>G did not map to a codon.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr23:100356280 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3HQ-01A-11D-A20U-09 chr17:16246151 G>A maps to NM_181716.2 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr5:122754059 G>A maps to NM_153223.3 Q67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr4:56847536 A>T maps to NM_025009.3 K591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr4:56820460 C>G maps to NM_025009.3 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:49048134 G>A maps to NM_001194998.1 L1104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PI-01A-11D-A18J-09 chr15:49031342 C>T maps to NM_001194998.1 K1412K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr15:49085631 G>A maps to NM_001194998.1 Q240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr11:117266343 G>T maps to NM_014956.4 E999*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73R-01A-11D-A33O-09 chr11:117242154 G>T maps to NM_014956.4 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:243289743 G>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:243303300 G>A maps to NM_014812.2 Q1390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3YQ-01A-11D-A22X-09 chr20:34079139 C>T maps to NM_007186.3 Q953*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr20:34090756 G>A maps to NM_007186.3 Q1520Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr1:179989082 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr3:134256085 G>T maps to NM_025180.3 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:134278114 G>A maps to NM_025180.3 L599L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr2:65298778 C>G maps to NM_015147.2 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr3:138256056 G>A maps to NM_024491.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:138248111 G>C maps to NM_024491.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr5:635547 G>A maps to NM_018140.3 Q251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr5:633994 C>T maps to NM_018140.3 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr9:80855102 C>T maps to NM_001098802.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:101447777 G>A maps to ENST00000327230 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr1:111724618 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2R9-01A-11D-A18J-09 chr1:111721816 G>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:111725405 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:111727357 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr9:131193545 G>A maps to NM_016174.4 V389V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2GZ-01A-11D-A17W-09 chr22:47103758 C>G maps to NM_022766.5 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr16:66997225 C>G maps to NM_024922.5 S76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr16:66995224 G>A maps to NM_024922.5 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr18:580566 G>A maps to NM_004066.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr16:57017520 G>A maps to NM_000078.2 Q475Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr16:75445850 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr1:196884083 A>C did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:196876117 T>G did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr23:47489266 C>G did not map to a codon.
Sequencing variant TCGA-FU-A3TQ-01A-11D-A22X-09 chr23:47486558 G>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:47486688 G>A did not map to a codon.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr23:47486552 C>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:47487587 C>G did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:117232504 C>T maps to NM_000492.3 Q762*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr7:117251804 G>T maps to NM_000492.3 E1104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A5XV-01A-11D-A28B-09 chr19:49539052 C>A maps to ENST00000391869 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr19:49561976 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr1:151491198 C>G maps to NM_020770.2 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr1:151491313 C>T maps to NM_020770.2 Q107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:151508254 G>A did not map to a codon.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr15:57730625 G>T maps to NM_032866.3 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr2:27322669 C>T maps to NM_001166240.1 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr14:54996926 C>G maps to NM_006568.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr10:90967016 G>A maps to NM_003956.3 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr10:50821493 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr7:132481276 C>A maps to ENST00000448878 E201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr3:14154461 C>T maps to NM_144636.2 K131K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M2-01A-21D-A18J-09 chr3:126679199 G>A did not map to a codon.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr5:98212253 G>A maps to NM_001270.2 F1082F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr5:98236755 A>C maps to NM_001270.2 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A69B-01A-11D-A32I-09 chr1:146767151 C>T maps to NM_004284.3 Q886*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr15:93528870 C>T maps to NM_001271.3 L1127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr15:93515517 G>A maps to NM_001271.3 K792K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr15:93485093 C>T maps to NM_001271.3 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr15:93558025 C>G maps to NM_001271.3 S1598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr17:7804194 C>T maps to NM_001005271.2 R1061*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr12:6710827 G>A maps to ENST00000309577 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A4BA-01A-21D-A26G-09 chr12:6709698 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr12:6687668 C>T maps to ENST00000309577 Q1703Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr12:6687677 C>T maps to ENST00000309577 V1700V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:6687052 C>T maps to ENST00000309577 Q1781Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:6214951 G>C maps to NM_015557.2 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WH-01A-22D-A351-09 chr1:6170486 C>T maps to NM_015557.2 E1783E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:6169957 G>C maps to NM_015557.2 L1825L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr20:40084592 C>T maps to NM_032221.3 V952V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr20:40111953 C>T maps to NM_032221.3 Q821Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr20:40040786 C>T maps to NM_032221.3 L2416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AX-01A-12D-A243-09 chr8:61778086 T>C maps to NM_017780.2 A2863A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr16:53341656 C>G maps to ENST00000219084 S2282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr19:16643446 C>A maps to NM_006387.5 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr19:16631641 C>T maps to NM_006387.5 R732R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr19:16630140 G>A maps to NM_006387.5 L860L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr12:133485605 C>G did not map to a codon.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr12:133454167 G>C maps to NM_001161344.1 S69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:93396081 C>T maps to NM_001275.3 Q93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr14:93397860 C>T maps to NM_001275.3 Q208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:72901072 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr23:72901146 G>C did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:203186867 C>G maps to NM_003465.2 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr3:369909 G>A maps to NM_006614.2 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr3:384666 T>G maps to NM_006614.2 L227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2GZ-01A-11D-A17W-09 chr23:85218960 G>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:85218694 C>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:85117272 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A73S-01A-11D-A33O-09 chr23:85128099 G>C did not map to a codon.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr23:85211313 A>G did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr1:241798624 A>G maps to NM_001821.3 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr3:87302860 G>C did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr11:89944495 T>G did not map to a codon.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr12:102120185 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2PI-01A-11D-A18J-09 chr3:184104670 G>A maps to NM_003741.2 P745P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr3:184100680 C>T maps to NM_003741.2 H340H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:109924797 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:110002982 C>T did not map to a codon.
Sequencing variant TCGA-EA-A411-01A-11D-A243-09 chr15:30654960 G>A maps to NM_139320.1 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr15:30665322 G>A maps to NM_139320.1 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr7:136700394 G>A maps to NM_001006628.1 Q261Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr7:136556184 C>T did not map to a codon.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr7:136700955 G>A maps to NM_001006628.1 K448K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr1:240071326 T>A maps to NM_000740.2 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr15:34356037 C>T maps to NM_012125.3 Q374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr15:34356123 C>T maps to NM_012125.3 I402I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:175624353 G>A maps to NM_001039523.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr15:78894296 G>A maps to NM_000743.4 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr15:32460418 C>T maps to NM_001190455.1 G452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr15:32460292 C>T maps to NM_001190455.1 N410N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A50E-01A-21D-A26G-09 chr4:40351153 C>T maps to NM_017581.2 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A50E-01A-21D-A26G-09 chr4:40351426 G>A maps to NM_017581.2 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr17:7357836 C>T maps to NM_000747.2 Q348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:154543730 C>T maps to NM_000748.2 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr1:154548323 C>T maps to NM_000748.2 I475I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5FO-01A-21D-A28B-09 chr2:233394710 C>T maps to NM_000751.1 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr2:233407754 C>T maps to NM_005199.4 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr11:45671567 G>A maps to NM_003654.4 Y302Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr11:45671729 G>A maps to NM_003654.4 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr2:101010045 G>A maps to NM_004854.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:40764158 G>A maps to NM_130468.3 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr10:125804144 G>A maps to NM_015892.3 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr10:73767070 C>G maps to NM_004273.4 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OA-01A-11D-A16Y-08 chr16:71571632 C>T maps to NM_001166395.1 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:46433632 C>T did not map to a codon.
Sequencing variant TCGA-EA-A1QS-01A-61D-A22X-09 chr19:34263496 C>T maps to NM_022467.3 F268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A69L-01A-11D-A32I-09 chr19:34263475 C>T maps to NM_022467.3 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr5:129241193 C>T maps to NM_175856.4 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr16:69154217 C>T maps to ENST00000306585 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr10:101953848 G>A maps to NM_001278.3 L622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr15:78398015 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr2:26804231 C>T maps to NM_001029881.1 *186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr2:26863417 G>A maps to NM_001029881.1 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr19:42791513 G>A maps to NM_015125.3 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QD-01A-32D-A22X-09 chr14:24775180 G>A maps to NM_014430.2 Q167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr16:11001769 G>T maps to NM_000246.3 L807L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr16:11002910 C>T maps to NM_000246.3 L895L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr16:11010238 T>C maps to NM_000246.3 S995S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr16:11002972 C>T maps to NM_000246.3 F915F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A3LQ-01A-21D-A21Q-09 chr19:19654946 C>T maps to NM_153221.2 F531F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr16:69199374 G>A maps to NM_032830.2 P593P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr17:36890987 G>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:36890306 C>G did not map to a codon.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr17:36886893 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr23:71521705 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr9:130950163 G>C maps to NM_012127.2 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr9:130928434 G>C did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr9:130929265 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr9:130931158 C>T did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr9:130928413 G>T did not map to a codon.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr2:113522196 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr2:113498522 C>T maps to NM_152515.3 K628K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr12:106633119 G>T maps to NM_006825.3 P497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr12:106633845 G>A maps to NM_006825.3 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:46806153 G>A maps to ENST00000415402 Q680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr14:103988710 C>T maps to NM_001823.3 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr14:103986312 G>C maps to NM_001823.3 S345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr5:80554978 G>A maps to NM_001825.2 W307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:154951277 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:154951642 C>T did not map to a codon.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr2:122139866 C>T maps to NM_015282.2 A1136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr2:122139866 C>T maps to NM_015282.2 A1136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr19:40224975 G>A maps to NM_001828.4 Q84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr1:86904662 G>A maps to NM_006536.5 E359E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr1:87038328 C>T maps to ENST00000263723 Q465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QE-01A-21D-A21Q-09 chr1:109472736 G>A did not map to a codon.
Sequencing variant TCGA-EA-A410-01A-11D-A243-09 chr1:109479989 G>A maps to NM_001048210.1 G364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr1:109482748 G>T maps to NM_001048210.1 S271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr1:109472615 A>G did not map to a codon.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr7:143039070 G>T maps to NM_000083.2 V544V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr7:143017824 C>T maps to NM_000083.2 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:184071525 G>C maps to NM_004366.4 L593L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr23:10181773 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr23:10174518 C>A did not map to a codon.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr23:10174519 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr23:49855455 T>C did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:49855077 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr1:11897156 C>T maps to ENST00000376496 I694I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr1:11900255 G>A maps to NM_001286.2 L862L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:11894622 G>A maps to ENST00000376496 W590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:16350316 G>A maps to NM_004070.3 Q41Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr1:16358719 C>T maps to NM_004070.3 I593I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr3:170425950 G>T did not map to a codon.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr3:170425956 G>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr7:90099217 C>G did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:190120148 C>G maps to NM_006580.3 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr3:137729132 C>T maps to NM_016369.3 I22I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr3:137729204 C>T maps to NM_016369.3 Y46Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr23:106171763 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:106171610 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr6:155596972 C>T maps to NM_001001346.3 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr4:184240978 G>A maps to NM_001111319.1 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr11:113651086 A>G maps to NM_001101389.1 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OA-01A-11D-A16Y-08 chr7:73183782 G>A maps to NM_001306.3 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr16:3065629 C>G maps to NM_021195.4 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr17:6980274 C>T maps to NM_182906.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr19:51228561 C>T maps to NM_002975.2 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr14:38723949 G>A maps to NM_175060.1 H426H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:38724387 C>T maps to NM_175060.1 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr14:38724059 G>A maps to NM_175060.1 Q390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr19:14710942 C>T maps to ENST00000417570 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:14703134 C>G maps to ENST00000417570 S81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr16:74444525 G>T maps to NM_001011880.2 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr12:10007088 G>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr12:8289435 C>G maps to NM_016184.3 S168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr12:7882229 G>A maps to NM_130441.2 Q202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr2:71043159 G>A maps to NM_173535.2 V451V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr2:71043159 G>A maps to NM_173535.2 V451V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr2:71046973 G>A maps to NM_173535.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:7795303 G>A maps to NM_198492.3 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr19:7794813 G>A maps to NM_198492.3 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr7:141635691 T>C maps to NM_013252.2 E89E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr12:10279188 G>T maps to NM_197947.2 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr12:10194128 C>A did not map to a codon.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr9:139890113 C>T maps to NM_004669.2 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr6:45909282 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr6:45882183 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr6:46047622 G>A maps to NM_001114086.1 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr6:46047900 C>A maps to NM_001114086.1 E27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WH-01A-22D-A351-09 chr12:122794403 G>A maps to ENST00000302528 Q1167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A770-01A-11D-A33O-09 chr12:122835662 C>A maps to ENST00000302528 E466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:122763442 G>C maps to ENST00000302528 S1271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr7:73753045 C>T maps to NM_003388.4 F130F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr19:36508768 C>T maps to NM_015526.2 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr2:201722519 G>A maps to NM_001162407.1 F293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr1:155238499 T>A maps to ENST00000368361 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr1:155239278 C>T maps to ENST00000368361 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr5:178043941 G>A maps to NM_020666.2 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr14:95669684 A>G maps to NM_024734.3 R667R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr16:28502379 G>C did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr11:57427145 C>T maps to NM_006831.2 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr6:35762943 G>A maps to NM_001832.2 D106D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr19:45493812 C>G maps to NM_001294.2 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A69L-01A-11D-A32I-09 chr5:1341803 G>A maps to NM_030782.3 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr10:129682071 C>G maps to NM_152311.3 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr1:36230311 G>C maps to NM_022111.3 S46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:9791275 G>A maps to NM_001009566.1 V912V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr22:19213065 G>A maps to NM_007098.3 Q680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr22:19230406 G>C maps to NM_007098.3 S191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr16:3569994 G>A maps to NM_015041.1 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr8:62377356 G>A did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr6:123377006 C>T maps to NM_001010852.2 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3L7-01A-21D-A20U-09 chr5:10286562 G>A maps to NM_138809.3 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr16:81703845 C>T maps to NM_198390.2 Q309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr16:81703835 G>A maps to NM_198390.2 K305K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr12:108686037 G>A maps to NM_001142344.1 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr2:6988804 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr16:66612744 C>T maps to NM_052999.3 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr16:66670349 G>A maps to NM_178818.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr14:23847619 G>A maps to ENST00000339180 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:79027908 C>G maps to NM_153610.3 L1107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr5:79025922 A>G maps to NM_153610.3 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr5:79032669 G>A maps to NM_153610.3 V2694V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr5:79030218 C>T maps to NM_153610.3 V1877V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr5:79054712 C>T maps to NM_153610.3 Q3750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3PZ-01A-11D-A21Q-09 chr8:88249228 A>G maps to NM_173538.2 G220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr18:72223679 C>T maps to NM_032649.5 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr18:72250866 C>A maps to NM_032649.5 I460I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr4:47938938 G>A maps to NM_001142564.1 L593L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:150912868 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:150912702 G>T did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr11:6261554 T>C maps to NM_001037329.2 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr11:6265350 G>C maps to NM_001037329.2 V480V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr16:57949227 G>C maps to NM_001297.4 L743L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr16:57951354 G>A maps to NM_001297.4 F661F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr8:87590943 G>A maps to NM_019098.4 L692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr1:224918243 G>T maps to NM_152495.1 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UC-01A-11D-A351-09 chr1:224563705 G>A did not map to a codon.
Sequencing variant TCGA-C5-A2M1-01A-11D-A18J-09 chr23:21444769 T>C did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:21613111 C>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:21627322 G>C did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:21670429 G>C did not map to a codon.
Sequencing variant TCGA-LP-A4AU-01A-32D-A243-09 chr23:21581384 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr6:154727586 C>T maps to NM_173515.2 G523G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr19:1037781 C>G maps to NM_004368.2 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr1:95367348 G>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:95363402 G>A maps to NM_001839.3 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr10:101090616 C>T maps to NM_020348.2 D491D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UC-01A-11D-A351-09 chr10:101090571 G>A maps to NM_020348.2 V476V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr10:101090205 C>T maps to NM_020348.2 I354I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr10:104679238 C>G maps to NM_017649.3 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr2:97475252 G>A maps to NM_020184.3 *776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr2:97427597 C>T maps to NM_020184.3 Q288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PD-01A-11D-A351-09 chr16:58622717 G>C maps to NM_016284.3 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2GZ-01A-11D-A17W-09 chr5:154252150 G>A maps to NM_004779.4 R223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R9-01A-11D-A18J-09 chr5:154238368 G>A did not map to a codon.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr17:40120645 C>T maps to NM_033133.4 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr7:99722591 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr7:99722650 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr17:40961914 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr17:40962556 G>C did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr17:40956315 C>T maps to NM_173478.2 Q107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:40951156 G>A maps to NM_173478.2 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr19:40732341 C>G maps to NM_024877.3 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A5XV-01A-11D-A28B-09 chr9:17309220 C>T maps to NM_017738.2 Q438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr12:41337929 C>T maps to NM_001843.2 I547I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3L7-01A-21D-A20U-09 chr1:205033552 C>G maps to NM_005076.3 A448A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3PZ-01A-11D-A21Q-09 chr1:205039052 C>A maps to NM_005076.3 G765G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr11:99715930 C>T maps to NM_014361.2 Q172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr3:1444153 G>A maps to NM_014461.2 R990R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr3:1424825 G>C maps to NM_014461.2 L789L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr17:40844535 C>T maps to NM_003632.2 F850F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:40847809 C>T maps to NM_003632.2 F1088F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:147869394 G>C maps to NM_014141.5 V945V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R9-01A-11D-A18J-09 chr7:146818155 C>A maps to NM_014141.5 V280V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr7:147844581 G>A did not map to a codon.
Sequencing variant TCGA-EA-A5FO-01A-21D-A28B-09 chr16:76482703 C>T maps to NM_033401.3 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr2:125281943 G>A maps to NM_130773.2 T463T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:124999879 C>T maps to NM_130773.2 Y97Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:125671804 C>T maps to NM_130773.2 F1287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr17:40716555 C>T maps to NM_001042532.2 F365F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr17:40714663 C>T maps to NM_001042532.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr17:40715125 C>A maps to NM_001042532.2 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:165578670 G>A maps to ENST00000392717 Q342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr2:165586568 G>C maps to ENST00000392717 S134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr14:31358934 G>T maps to NM_004086.2 E531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr17:71192822 C>T maps to NM_018714.2 R165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:230823904 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr16:70542704 C>T maps to ENST00000393612 *338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr16:70530309 C>T maps to NM_015386.2 R502R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr16:70516652 G>A maps to NM_015386.2 S633S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr16:70515273 G>A maps to NM_015386.2 L741L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr16:69354270 G>C did not map to a codon.
Sequencing variant TCGA-EA-A3HQ-01A-11D-A20U-09 chr1:103474020 G>A maps to NM_080629.2 Q573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr1:103364275 C>T maps to NM_080629.2 Q1410Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:103474020 G>A maps to NM_080629.2 Q573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr6:33148096 G>A maps to NM_080680.2 R433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr6:75813484 G>A maps to ENST00000322507 I2769I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr6:75898135 G>A maps to ENST00000322507 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CJ-01A-11D-A32I-09 chr9:101748163 G>T maps to NM_001855.3 E140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr9:101832134 C>T maps to NM_001855.3 I1378I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr9:101748153 C>T maps to NM_001855.3 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr9:101747952 C>T maps to NM_001855.3 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr9:101751494 C>T maps to NM_001855.3 D253D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr10:105815741 C>T maps to NM_000494.3 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr10:105817940 C>G maps to NM_000494.3 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr21:46897680 G>A maps to ENST00000359759 Q756Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A69B-01A-11D-A32I-09 chr21:46888225 G>A maps to ENST00000359759 T474T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr21:46875881 G>A maps to ENST00000359759 E146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr21:46925095 C>T maps to ENST00000359759 Q1388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A6QX-01A-12D-A33O-09 chr6:70916909 G>T maps to NM_001858.4 G1121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr6:70875852 G>A maps to NM_001858.4 G807G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr17:48264088 G>A maps to NM_000088.3 I1242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr7:94039760 T>A maps to NM_000089.3 G373G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr20:61939374 C>G maps to ENST00000326996 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A50E-01A-21D-A26G-09 chr20:61947914 G>C maps to ENST00000326996 L852L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr6:55922388 C>G did not map to a codon.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr8:139606404 C>T maps to NM_152888.1 A1490A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U3-01A-11D-A28B-09 chr8:139734393 A>C maps to ENST00000341807 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr1:86590533 T>C maps to NM_152890.5 G495G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:86487946 C>T maps to NM_152890.5 G744G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:86361539 C>A did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr1:86591520 A>G maps to NM_152890.5 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr4:109767294 C>T maps to ENST00000333642 P505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr9:117052562 C>T maps to NM_032888.2 I1440I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr9:116930428 C>G maps to NM_032888.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr7:7472139 C>T maps to NM_001037763.2 P654P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr12:48393726 G>T maps to NM_001844.4 C89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr12:48369199 G>C maps to NM_001844.4 L1262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:48369280 G>A maps to NM_001844.4 P1235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr2:189862094 C>T maps to NM_000090.3 Q617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr13:110839652 C>T maps to NM_001845.4 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr13:110850841 A>G maps to NM_001845.4 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr13:110831666 A>G maps to NM_001845.4 V765V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr13:110819507 G>A maps to NM_001845.4 Q1316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr13:110859213 G>A maps to NM_001845.4 Q269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr13:110960451 C>T maps to NM_001846.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M1-01A-11D-A18J-09 chr13:111155757 G>T maps to NM_001846.2 G1356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr13:110960451 C>T maps to NM_001846.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr13:111160571 T>G did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr13:111088662 C>T maps to NM_001846.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:228121063 C>G maps to NM_000091.4 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr5:74677812 C>T maps to NM_001130105.1 W654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr5:74696107 C>T maps to NM_001130105.1 K472K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr2:227919322 C>A maps to ENST00000396625 L949L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr23:107834846 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr23:107683384 C>T did not map to a codon.
Sequencing variant TCGA-DS-A1OA-01A-11D-A16Y-08 chr23:107814649 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3QD-01A-32D-A22X-09 chr23:107920733 A>T did not map to a codon.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr23:107909763 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr23:107936119 C>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:107911726 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr23:107408145 G>A did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr23:107412839 G>A did not map to a codon.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr23:107414134 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:107431199 G>T did not map to a codon.
Sequencing variant TCGA-HG-A2PA-01A-11D-A20U-09 chr23:107418433 T>C did not map to a codon.
Sequencing variant TCGA-EA-A78R-01A-11D-A32I-09 chr9:137701007 G>C did not map to a codon.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr2:189904001 C>T maps to NM_000393.3 Q1307Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr2:189929374 G>A maps to NM_000393.3 Q542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr21:47406451 G>A maps to NM_001848.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr21:47423449 C>T maps to NM_001848.2 D870D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr21:47532337 C>G maps to NM_001849.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr21:47545433 G>A maps to NM_001849.3 E624E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:238261166 G>T maps to NM_004369.3 R2251R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr2:238296429 C>T maps to NM_004369.3 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A69B-01A-11D-A32I-09 chr3:130095512 G>T maps to ENST00000312481 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr3:130284199 C>T maps to NM_001102608.1 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WH-01A-22D-A351-09 chr3:130279231 C>T maps to NM_001102608.1 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr3:48601911 C>G did not map to a codon.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr3:99514613 C>T maps to ENST00000429802 T624T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr1:36563679 C>A maps to NM_005202.2 G534G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr6:70991092 G>A maps to NM_001851.4 D292D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5FO-01A-21D-A28B-09 chr1:40773117 C>T maps to NM_001852.3 A336A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr20:61453149 C>T maps to NM_001853.3 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr20:61467601 C>T maps to NM_001853.3 Q489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr20:61468388 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr20:61457203 G>A maps to NM_001853.3 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr20:61467601 C>T maps to NM_001853.3 Q489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr20:61460829 C>T maps to NM_001853.3 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr8:120118094 A>T maps to NM_006438.3 K167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr2:3691112 C>T maps to ENST00000418971 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3TQ-01A-11D-A22X-09 chr2:3691437 C>T maps to ENST00000418971 D196D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A852-01A-11D-A351-09 chr2:3691677 C>T maps to ENST00000418971 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr18:346406 C>T maps to NM_130386.2 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:15516910 C>G did not map to a codon.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr3:15531136 G>A maps to NM_005677.3 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr10:22606983 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr10:22607674 T>G did not map to a codon.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr15:75632154 A>C maps to NM_017828.3 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr13:76100689 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr13:76111744 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr13:76104528 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr20:31291245 G>A maps to NM_053041.2 Q181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr10:76994714 C>T maps to NM_144589.2 K161K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr19:19010502 G>A maps to NM_007263.3 Y304Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr19:19021650 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr19:19030097 G>A maps to NM_007263.3 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr7:99689396 C>T maps to NM_006833.4 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A770-01A-11D-A33O-09 chr6:99831698 A>G maps to NM_017421.3 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A770-01A-11D-A33O-09 chr6:99831700 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr9:131085385 C>T maps to NM_016035.3 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZF-01A-11D-A28B-09 chr16:19083256 A>G maps to NM_016138.4 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr16:57486730 C>T maps to NM_020312.3 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HQ-01A-11D-A20U-09 chr4:47644043 G>A maps to NM_006587.2 N697N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr16:30198162 G>C maps to NM_007074.3 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr9:100889064 C>T maps to NM_052820.3 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr9:100892172 C>G did not map to a codon.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr17:27943317 G>A maps to ENST00000345068 I418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr16:84600378 G>A did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr17:14063215 C>G maps to NM_001303.3 S216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr10:101476232 G>C did not map to a codon.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr16:85839283 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr20:30226890 C>G maps to NM_032609.2 S24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr15:75212767 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr2:98262629 G>C maps to NM_001862.2 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr2:98262629 G>C maps to NM_001862.2 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A4BA-01A-21D-A26G-09 chr2:42578284 A>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr2:42580341 C>G did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:77158373 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2GZ-01A-11D-A17W-09 chr7:130023299 C>T maps to NM_001868.2 V184V. Only missense variants will be evaluated by CHASM.
Reference base specified for sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr7:129962359 G>T does not match reference base at that coordinate in hg19.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr19:17108022 G>A maps to ENST00000443236 V388V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RL-01A-11D-A18J-09 chr19:17132954 C>G maps to ENST00000443236 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr19:17088209 G>A maps to ENST00000443236 Q633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr19:17039020 G>C maps to ENST00000443236 S1113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R3-01A-11D-A28B-09 chr19:17013536 C>T maps to ENST00000443236 W1593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7X3-01A-11D-A351-09 chr3:148577822 C>G did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr15:83226521 G>C maps to ENST00000261723 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr4:15004564 C>T maps to NM_001177382.1 Q90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr4:15004503 C>T maps to NM_001177382.1 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr10:93999171 G>C maps to NM_014912.4 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr5:173317424 C>G maps to NM_030627.2 S230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:173383210 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr20:34213973 C>T did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr8:87559983 C>T maps to NM_003909.3 Q289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QD-01A-32D-A22X-09 chr3:131404726 G>A maps to ENST00000502818 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr3:131756536 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr14:24545479 G>A maps to NM_006032.2 Q349Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr16:89645290 C>T maps to NM_014427.4 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr2:207804332 C>T maps to NM_173077.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr16:12758793 C>G maps to NM_018340.2 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:211447405 G>A maps to NM_001122633.1 Q204Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr2:211467044 C>T maps to NM_001122633.1 L615L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2GZ-01A-11D-A17W-09 chr8:145619867 G>A maps to NM_013291.2 I1186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr8:145625596 G>C maps to NM_013291.2 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr8:145624234 C>G maps to NM_013291.2 V524V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr8:145624240 C>T maps to NM_013291.2 Q522Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr14:92625342 C>G maps to NM_017437.1 S613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr1:1252785 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:1256018 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr7:99051699 C>T maps to NM_006693.2 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr7:99042427 C>T maps to NM_006693.2 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr12:69650494 T>C maps to ENST00000266679 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr11:68522293 G>C maps to NM_001031847.2 S754*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr22:51014665 C>T maps to NM_152245.2 Q220Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr19:50204794 C>T maps to NM_152359.2 F199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A50E-01A-21D-A26G-09 chr7:29105686 G>A maps to NM_031311.3 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr7:29111988 G>C maps to NM_031311.3 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr23:88008860 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:88009170 T>G did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr20:2777943 G>T maps to NM_019609.4 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr20:2777277 C>A maps to NM_019609.4 E314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr10:125506280 C>T maps to NM_198148.2 *757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:207780599 C>T maps to NM_000651.4 R1939*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr1:207871116 G>A maps to NM_175710.1 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr1:207881608 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:207884021 T>A did not map to a codon.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr1:207644372 C>A maps to NM_001006658.2 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr16:1720686 G>A maps to NM_020825.3 K1174K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RL-01A-11D-A18J-09 chr16:1664951 C>T maps to NM_020825.3 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr16:1676139 G>A maps to NM_020825.3 K171K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:197396582 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr1:197297587 C>G maps to NM_201253.2 S36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr9:126132811 C>T maps to NM_173689.5 Q494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HR-01A-11D-A20U-09 chr2:208461840 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr2:208462087 G>A did not map to a codon.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr7:137567264 G>A maps to NM_194071.2 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:153946136 C>T maps to NM_130898.2 F313F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr7:28844034 C>T maps to NM_182898.2 Q308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr16:3778627 C>T maps to NM_004380.2 Q2140Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QD-01A-32D-A22X-09 chr16:3779770 T>A maps to NM_004380.2 P1759P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr16:3794921 G>A maps to NM_004380.2 R1319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr16:3817783 C>A maps to NM_004380.2 E1063*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr16:3817798 C>A maps to NM_004380.2 E1058*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3TX-01A-11D-A22X-09 chr16:3801725 C>T did not map to a codon.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr16:3900709 G>T maps to NM_004380.2 S129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr16:3781797 G>T maps to NM_004380.2 A1623A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R9-01A-11D-A18J-09 chr11:85371270 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr11:85371509 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr2:102000164 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr10:35460215 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr10:35456682 C>T maps to ENST00000395887 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr10:35500775 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr8:67089289 G>C maps to NM_000756.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr5:76251688 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr7:30704802 C>T maps to ENST00000348438 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr2:36775708 G>A maps to NM_016441.2 K992K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr8:75925232 C>T maps to NM_031461.5 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr19:18704913 C>A maps to NM_004750.4 E406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr23:1331583 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr23:1315002 C>G did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr17:29111326 G>A maps to NM_015986.3 R403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr4:5830335 G>A maps to NM_001014809.1 I561I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:5862759 C>G maps to NM_001014809.1 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:152382128 C>A maps to NM_016190.2 E477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr1:17282521 G>A maps to NM_014675.3 Q1245Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr1:17285208 G>A maps to NM_014675.3 L1332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3WB-01A-11D-A22X-09 chr1:17280577 T>C did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:17273257 G>T maps to NM_014675.3 L762L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LB-01A-11D-A243-09 chr1:17277293 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:17275494 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr11:122722542 G>C maps to NM_019604.2 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr1:153920585 C>T maps to NM_181715.2 *694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr15:91083311 C>T maps to NM_022769.3 Y58Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr15:91141767 G>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr15:91141792 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73S-01A-11D-A33O-09 chr19:48337768 G>T maps to NM_000554.4 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:107391156 C>G maps to NM_004075.3 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr21:44590667 G>A maps to NM_000394.2 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr2:219855000 C>A maps to NM_057094.1 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr3:97655688 G>A maps to ENST00000182096 E866E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr3:97652614 G>C maps to ENST00000182096 V825V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr2:209010506 G>A maps to NM_005210.3 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:209007481 C>T maps to NM_005210.3 E136E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr2:208986567 G>A maps to NM_006891.3 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr2:208988952 G>C maps to NM_006891.3 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr1:75175916 T>A maps to NM_001889.3 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr12:56693955 G>C maps to NM_004077.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr12:53553492 C>A maps to NM_015989.4 E435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:151908882 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:115292555 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr1:115277085 G>A maps to NM_001130523.1 Q202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr20:47707557 G>A maps to NM_001316.2 K788K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr20:47689160 G>A maps to NM_001316.2 K331K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr20:47712751 G>A did not map to a codon.
Sequencing variant TCGA-LP-A4AX-01A-12D-A243-09 chr20:47691933 C>A maps to NM_001316.2 I404I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr1:110466721 C>T maps to NM_000757.4 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3TX-01A-11D-A22X-09 chr5:131409527 G>A maps to NM_000758.2 Q4Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5FO-01A-21D-A28B-09 chr22:37330013 G>A maps to ENST00000262825 A437A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr22:37333841 G>A maps to ENST00000262825 G670G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr10:43654205 C>G maps to NM_018590.3 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr8:3611472 C>A maps to NM_033225.5 G304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr8:4277553 C>T maps to NM_033225.5 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr8:3889496 G>A maps to NM_033225.5 H180H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr8:3351248 C>T did not map to a codon.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr8:3063031 C>A maps to NM_033225.5 E1660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr8:3351194 C>T maps to NM_033225.5 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr1:34076830 C>T maps to ENST00000373381 L2011L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CJ-01A-11D-A32I-09 chr1:34099118 G>A maps to ENST00000373381 F1661F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr1:34192167 G>T maps to ENST00000373381 P789P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:34049380 C>G maps to ENST00000373381 L2327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr8:113332154 C>T maps to NM_198123.1 L2407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr8:113317095 C>T maps to NM_198123.1 W2707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr8:114031407 C>T maps to NM_198123.1 W306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr8:113349921 G>T maps to NM_198123.1 R2231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr8:113649100 G>A maps to NM_198123.1 I1220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr8:113812430 G>A maps to NM_198123.1 D644D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr5:148899918 C>T maps to NM_001025105.1 K130K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr15:64496788 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr19:1979935 G>A maps to NM_001319.6 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr15:75975191 G>T maps to NM_001897.4 S1547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:75980336 G>T maps to NM_001897.4 I1023I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr15:75983123 C>T maps to NM_001897.4 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr15:75982482 G>T maps to NM_001897.4 S308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr15:75982031 C>T maps to NM_001897.4 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr3:47618348 C>T maps to ENST00000383738 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr8:68062106 C>T maps to ENST00000389042 L719L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr8:68026057 C>T maps to ENST00000389042 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr12:51470430 C>T did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr12:77259932 G>A maps to NM_001321.1 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr20:18143135 C>G maps to NM_020536.4 G406G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr20:18123369 G>A maps to NM_020536.4 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr20:23729715 T>A maps to NM_001898.2 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PI-01A-11D-A18J-09 chr20:23860154 G>A maps to NM_001900.4 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr11:65780822 C>T maps to NM_001323.2 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr20:54974254 C>G maps to NM_001033522.1 S293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr23:100088221 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr23:100087787 G>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:100077238 G>C did not map to a codon.
Sequencing variant TCGA-EX-A1H6-01B-11D-A22X-09 chr23:100081732 C>A did not map to a codon.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr10:53458330 G>A maps to NM_015235.2 R327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr11:33163445 G>C maps to NM_001326.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:33113886 C>T did not map to a codon.
Sequencing variant TCGA-DS-A7WF-01A-11D-A351-09 chr20:23420795 G>T did not map to a codon.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr23:134847422 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:134856889 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr23:134948145 G>T did not map to a codon.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr23:153880857 C>T did not map to a codon.
Sequencing variant TCGA-DS-A1OA-01A-11D-A16Y-08 chr18:19997690 G>A maps to NM_172241.2 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr18:19996017 G>C maps to NM_172241.2 S586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr7:143882863 T>C maps to NM_198495.2 Y756Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr14:39771448 C>G maps to ENST00000396158 Y309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr14:39815195 C>G maps to ENST00000396158 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr14:39736707 C>T maps to ENST00000396158 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr4:1219223 C>T maps to NM_001328.2 Q157Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A0TN-01A-21D-A14W-08 chr1:85040023 C>T maps to NM_004388.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr16:67670645 G>T maps to NM_006565.3 E631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr20:56082639 C>G maps to ENST00000432255 *484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr20:56098961 C>T maps to ENST00000423479 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:58240197 G>A maps to NM_005730.3 I7I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q8-01A-11D-A21Q-09 chr15:44783039 A>G maps to NM_016396.2 Q178Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr15:44719942 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr5:138268316 C>T maps to ENST00000355078 I783I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RL-01A-11D-A18J-09 chr2:80540712 G>A maps to ENST00000343114 Q9Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A69B-01A-11D-A32I-09 chr2:80816448 G>A maps to ENST00000402739 P676P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr10:68280426 G>A maps to NM_013266.2 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr1:9932073 G>A maps to ENST00000361853 Q91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5FO-01A-21D-A28B-09 chr1:9932073 G>A maps to ENST00000361853 Q91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr20:36470725 A>G did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr20:36500430 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr11:57569477 C>T maps to NM_001085458.1 I410I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A852-01A-11D-A351-09 chr11:57576857 T>C maps to NM_001085458.1 V785V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr5:11082930 G>A maps to NM_001332.2 R889*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr5:11364722 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr5:10972956 A>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr5:10972667 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr5:10972954 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr17:3552206 C>T maps to NM_001031681.2 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:3559813 G>C maps to NM_001031681.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr23:16701274 G>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:16720990 G>T did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr8:11704594 G>A maps to NM_147783.2 F253F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr11:1774825 G>C maps to NM_001909.3 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr15:79237101 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr15:79237224 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr1:150772082 G>A maps to NM_000396.3 R241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LS-01A-22D-A22X-09 chr11:65650280 C>T maps to NM_001335.3 F217F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr20:57570796 C>T maps to NM_001336.3 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr10:17146595 G>T maps to NM_001081.3 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr10:16981091 C>T maps to NM_001081.3 W1868*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr10:16975227 C>T maps to NM_001081.3 P1994P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HR-01A-11D-A20U-09 chr10:104183033 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr7:148454088 G>A maps to NM_003592.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A69L-01A-11D-A32I-09 chr7:148495069 G>A maps to NM_003592.2 L663L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr7:148484148 G>A maps to NM_003592.2 K472K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr10:35328006 G>A maps to NM_001198778.1 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr10:35349896 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr2:225365090 C>T maps to NM_003590.3 E533E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VK-01A-11D-A28B-09 chr2:225339094 T>A did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr13:113893807 C>T maps to NM_001008895.1 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr13:113899365 C>T maps to NM_001008895.1 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr23:119694467 G>T did not map to a codon.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr23:119678051 G>C did not map to a codon.
Sequencing variant TCGA-EA-A5ZF-01A-11D-A28B-09 chr23:119674273 T>G did not map to a codon.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr23:119678347 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr11:107943061 T>G maps to NM_003478.3 L293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr6:43006109 G>A maps to NM_001168370.1 D1640D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr6:43017775 G>C maps to NM_001168370.1 L582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr6:43018877 G>T maps to NM_001168370.1 S438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr6:43005528 G>C maps to NM_001168370.1 S1749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr6:43182815 G>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr6:43153910 C>T maps to ENST00000354495 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr7:101844946 C>T maps to ENST00000360264 D801D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr7:101844748 C>T maps to ENST00000360264 L735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr7:101882708 G>A maps to ENST00000360264 L1255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr7:101813742 G>A maps to ENST00000360264 Q258Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr7:101754976 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr12:111758155 C>T maps to NM_015267.3 D781D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr10:124593208 G>A maps to NM_022034.4 R544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr17:36962571 G>A maps to NM_017748.3 R327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr4:48988464 G>T maps to NM_025087.2 E7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr16:57416205 G>A maps to NM_002996.3 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr4:74964650 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr4:74903835 C>T maps to NM_002090.2 Q94Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr23:70837347 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr2:136872497 G>A maps to NM_001008540.1 R338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr2:136872365 C>A did not map to a codon.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr18:47810932 C>A did not map to a codon.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr18:47810185 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr23:30577855 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr23:30577709 G>A did not map to a codon.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr23:35993316 C>G did not map to a codon.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr23:35974250 A>G did not map to a codon.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr23:35937974 G>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:35966467 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr23:19947986 C>G did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:19973589 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr23:19973607 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:19935398 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2R9-01A-11D-A18J-09 chr23:37850382 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr23:37850283 C>T did not map to a codon.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr23:45051183 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:148627245 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr23:149100844 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:149102008 A>G did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:134292168 G>C did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:118676554 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:118699295 G>C did not map to a codon.
Sequencing variant TCGA-C5-A2LS-01A-22D-A22X-09 chr23:105905423 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:105876457 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:105881223 T>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:105855821 G>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:115593001 T>G did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr23:70326095 G>A did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr23:70326270 G>A did not map to a codon.
Sequencing variant TCGA-EA-A5ZF-01A-11D-A28B-09 chr23:139038830 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:139038519 G>C did not map to a codon.
Sequencing variant TCGA-MY-A5BE-01A-21D-A26G-09 chr3:50390808 C>T maps to NM_007022.3 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr16:69458596 C>G maps to NM_030579.2 S4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr16:69458699 G>A maps to NM_030579.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr1:202936327 C>T maps to NM_016243.2 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:202933825 G>C did not map to a codon.
Sequencing variant TCGA-FU-A5XV-01A-11D-A28B-09 chr1:202931827 C>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr11:7686581 A>C did not map to a codon.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr23:37663317 A>T did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr23:37663270 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:37642817 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr23:37668872 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr2:172378865 G>C did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr8:145151376 C>G maps to NM_001916.3 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr15:22990122 C>T maps to NM_014608.2 Q915*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr15:22990061 G>A maps to NM_014608.2 L894L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr15:22990103 C>T maps to NM_014608.2 F908F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr23:83127935 C>A did not map to a codon.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr23:83129329 C>G did not map to a codon.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr23:83128501 T>C did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr15:74630958 G>A maps to NM_000781.2 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr8:143961220 G>T maps to ENST00000377675 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr8:143995804 C>A maps to NM_000498.3 E277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OA-01A-11D-A16Y-08 chr15:75043621 C>T maps to NM_000761.3 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr2:204161617 C>G maps to ENST00000429815 S467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr6:32007218 C>T maps to NM_000500.5 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr6:32008516 G>A maps to NM_000500.5 T397T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AU-01A-32D-A243-09 chr6:32006937 C>T maps to NM_000500.5 H120H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A6QX-01A-12D-A33O-09 chr10:94834931 C>T maps to NM_000783.3 H244H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr10:94836398 G>T maps to NM_000783.3 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr19:41351906 G>C maps to NM_000762.5 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr19:41386522 G>A maps to NM_000764.2 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr19:41522626 C>T maps to NM_000767.4 F457F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A5XV-01A-11D-A28B-09 chr10:96580374 G>A maps to NM_000769.1 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr22:42525884 G>A maps to NM_000106.4 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr10:135345140 G>C maps to NM_000773.3 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr19:41627917 C>T maps to NM_000774.3 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr19:41627929 C>T maps to NM_000774.3 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:60377993 G>C did not map to a codon.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr19:41704765 C>T maps to ENST00000301173 V269V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr4:108871577 G>T maps to NM_183075.2 *545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr7:99436307 G>A maps to ENST00000417625 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr7:99311101 C>T maps to ENST00000292414 E285E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr7:99305593 G>A maps to ENST00000292414 F419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr1:47395690 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:47610226 G>A maps to NM_001010969.2 E301E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:47606477 G>C maps to NM_001010969.2 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:47278270 C>T maps to NM_001099772.1 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr19:16045203 G>A maps to NM_021187.3 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr19:16000292 G>A maps to NM_001082.3 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr19:15648398 C>T maps to NM_173483.3 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:15769097 C>T maps to NM_000896.2 F380F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PI-01A-11D-A18J-09 chr4:187115762 G>T maps to NM_207352.3 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:47571829 G>A maps to NM_178134.2 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr8:59405043 G>A maps to NM_000780.3 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr8:65509245 G>A maps to NM_004820.3 Q492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr23:77529173 G>C did not map to a codon.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr23:77528892 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr23:77528274 C>T did not map to a codon.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr17:76672040 G>A maps to ENST00000392457 F58F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr7:6204917 C>T maps to ENST00000396741 W372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr7:6209730 G>T did not map to a codon.
Sequencing variant TCGA-EA-A3QD-01A-32D-A22X-09 chr2:158300366 G>A maps to NM_004288.4 R56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr21:27852627 G>C maps to ENST00000435845 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr14:59789711 C>G maps to NM_014992.1 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:59782053 C>G maps to NM_014992.1 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr14:59806895 G>C maps to NM_014992.1 S701S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A410-01A-11D-A243-09 chr6:39846354 T>C maps to ENST00000398904 S512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr6:39843172 C>T maps to ENST00000398904 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:57480997 C>T maps to ENST00000371231 P367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr1:57481087 G>A maps to ENST00000371231 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr5:39394477 G>A did not map to a codon.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr9:124522648 C>T maps to ENST00000408936 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr9:124522190 C>T maps to ENST00000408936 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr9:124534963 C>T maps to ENST00000408936 V719V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QS-01A-61D-A22X-09 chr23:85769283 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:86067872 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:85404061 C>G did not map to a codon.
Sequencing variant TCGA-JW-A69B-01A-11D-A32I-09 chr23:85997719 G>T did not map to a codon.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr14:59112963 G>A maps to NM_016651.5 K541K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr14:59113005 C>T maps to NM_016651.5 V555V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr14:59113113 C>G maps to NM_016651.5 L591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:23043980 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr11:61504724 C>G maps to NM_006133.2 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr11:61491026 G>A maps to NM_006133.2 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr7:6487441 C>T maps to NM_139179.3 W11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H6-01B-11D-A22X-09 chr7:6474473 G>T maps to NM_139179.3 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr3:49053402 C>A maps to ENST00000440857 V315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr3:49053408 C>T maps to NM_001009996.1 E480E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3YQ-01A-11D-A22X-09 chr3:49054256 C>T maps to NM_001009996.1 V317V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HR-01A-11D-A20U-09 chr12:109277521 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr12:109270565 G>C did not map to a codon.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr13:106142424 G>T maps to NM_172370.3 E153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:155695198 G>C maps to NM_004632.3 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:155658956 C>A did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:155701229 C>T did not map to a codon.
Sequencing variant TCGA-LP-A4AU-01A-32D-A243-09 chr1:155658794 G>T did not map to a codon.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr1:155701848 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A73Q-01A-21D-A32I-09 chr1:155697371 G>A did not map to a codon.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr1:155701223 C>G did not map to a codon.
Sequencing variant TCGA-C5-A2M1-01A-11D-A18J-09 chr9:90296362 G>A maps to NM_004938.2 Q682Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr9:90301514 G>A maps to NM_004938.2 V758V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr15:64204181 G>A maps to NM_014326.3 F319F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr15:64215049 C>G did not map to a codon.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr15:64215458 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2GZ-01A-11D-A17W-09 chr15:64204321 G>T maps to NM_014326.3 V311V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr15:64217032 G>C maps to NM_014326.3 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr19:3964691 G>C maps to NM_001348.1 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr19:3964676 G>A maps to NM_001348.1 D125D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:3964694 G>A maps to NM_001348.1 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:3964823 G>A maps to NM_001348.1 I76I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5FO-01A-21D-A28B-09 chr4:100774414 G>A maps to NM_014395.2 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:159175723 C>A maps to NM_001122951.2 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr6:33288312 C>G maps to NM_001350.4 R365R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr3:16635204 G>C maps to NM_001190811.1 S251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A3LQ-01A-21D-A21Q-09 chr9:122011391 G>A maps to NM_014618.2 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr9:121929685 G>A maps to NM_014618.2 D654D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr9:121929661 C>G maps to NM_014618.2 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VG-01A-11D-A28B-09 chr9:121976224 G>A maps to NM_014618.2 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr7:87537138 C>T maps to NM_006716.3 D562D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R3-01A-11D-A28B-09 chr7:87537186 G>C maps to NM_006716.3 V578V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:42786152 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr9:136523567 G>A maps to NM_000787.3 *618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr7:44100681 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2RL-01A-11D-A18J-09 chr9:37863320 T>A did not map to a codon.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr9:37860307 G>C did not map to a codon.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr23:125685754 C>A did not map to a codon.
Sequencing variant TCGA-EA-A5ZD-01A-11D-A28B-09 chr23:125686154 T>C did not map to a codon.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr23:125685979 A>T did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr23:125299851 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:125299272 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:125298618 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:125298774 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:125299004 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr23:125298662 G>A did not map to a codon.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr4:17805706 C>A maps to NM_017741.3 E20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr4:17805987 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr4:41983832 C>T maps to NM_001029955.3 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr8:88885074 G>A maps to NM_152418.3 F375F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr17:61666704 C>G did not map to a codon.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr17:61670998 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr17:61671186 T>G did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr17:61666383 C>T maps to NM_005828.3 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:160188830 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:160208573 G>C did not map to a codon.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr23:27998106 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:27997786 C>G did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr23:27998203 G>A did not map to a codon.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr18:50683790 C>T maps to NM_005215.3 R443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr18:50705388 G>A maps to NM_005215.3 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr18:50832090 T>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr18:51056748 C>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr18:50985766 C>G maps to NM_005215.3 L1186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:32678162 C>T maps to NM_001099434.1 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr11:6661920 G>A maps to NM_003737.2 D308D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr11:6651104 T>C maps to NM_003737.2 Q1611Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HM-A3JK-01A-11D-A21Q-09 chr11:6653795 G>A maps to NM_003737.2 R983*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr11:6644959 G>C maps to NM_003737.2 L2649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr11:6650966 G>C maps to NM_003737.2 L1657L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr11:6650692 G>A maps to NM_003737.2 I1717I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:6643100 G>C maps to NM_003737.2 S3269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr11:6662201 G>A maps to NM_003737.2 R215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M1-01A-11D-A18J-09 chr4:155161742 G>T maps to NM_017639.3 V1980V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr4:155287389 C>T maps to NM_017639.3 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QE-01A-21D-A21Q-09 chr4:155411340 G>A maps to NM_001142552.1 G389G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A50E-01A-21D-A26G-09 chr4:155254248 G>C maps to NM_017639.3 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr4:155252849 G>A maps to NM_017639.3 I750I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VI-01A-11D-A28B-09 chr4:155155735 G>A maps to NM_017639.3 I2901I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr4:71888098 C>T maps to ENST00000504952 Q75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr13:36396958 G>A maps to NM_004734.4 D487D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr13:36413286 C>T maps to NM_004734.4 T354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr4:151174641 G>C maps to ENST00000411937 *696S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr10:115602141 G>A maps to NM_014881.3 V875V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:114456242 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr10:14995990 G>A maps to NM_001033855.1 Q7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr10:14976734 G>A maps to NM_001033855.1 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr3:53321416 C>T did not map to a codon.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr3:53321593 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr5:112320220 C>T did not map to a codon.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr5:112327821 C>T maps to NM_152624.4 F70F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr1:155020576 G>A maps to NM_152494.3 K600K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:155005215 G>A maps to NM_144622.2 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R9-01A-11D-A18J-09 chr16:23678901 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr16:20873535 C>A maps to NM_173475.2 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CH-01A-11D-A33O-09 chr23:110574145 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr23:110653587 C>G did not map to a codon.
Sequencing variant TCGA-C5-A7X3-01A-11D-A351-09 chr11:61070627 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr11:61096836 G>A maps to NM_001923.3 Q183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:47256435 G>T maps to NM_000107.2 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr7:50605580 C>A maps to NM_000790.3 G138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H6-01B-11D-A22X-09 chr8:38099758 C>G did not map to a codon.
Sequencing variant TCGA-DS-A1OA-01A-11D-A16Y-08 chr1:15978346 C>T maps to NM_032341.4 D380D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr1:15959932 G>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr10:74034831 C>T maps to NM_019058.2 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr10:74033755 C>T did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr4:101108881 C>T maps to NM_145244.3 K178K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr6:110714273 G>A maps to NM_003649.2 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:20987828 G>A maps to NM_005216.4 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr1:162748501 C>T maps to NM_006182.2 R806*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:162749933 C>T maps to NM_006182.2 D822D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr20:3185216 G>C maps to NM_023935.1 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr20:3183979 C>G maps to NM_023935.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr2:15743959 C>T maps to NM_004939.1 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr11:108811172 C>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:31244670 C>T maps to NM_030653.3 Q370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr22:38895462 C>T maps to NM_001098504.1 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr1:112305495 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:112303676 C>T maps to NM_007204.4 Q298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A6QX-01A-12D-A33O-09 chr10:70719875 G>A maps to NM_004728.2 K134K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr12:49224419 G>A maps to NM_004818.2 I765I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr11:125788627 C>T maps to NM_013264.3 Q382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UC-01A-11D-A351-09 chr23:134711301 C>G did not map to a codon.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr23:134711237 A>T did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr23:134681105 T>C did not map to a codon.
Sequencing variant TCGA-FU-A770-01A-11D-A33O-09 chr23:134716149 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:134713951 G>C did not map to a codon.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr23:134706649 G>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr20:47860345 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr20:47841460 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr16:68057078 G>C maps to NM_018380.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr16:68057069 G>C maps to NM_018380.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr9:135505739 G>A maps to NM_022779.7 T619T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr23:41202540 G>T did not map to a codon.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr23:41205854 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:41204677 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr23:41205782 C>T did not map to a codon.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr5:176938928 C>A did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr5:176942306 C>G maps to ENST00000509576 *202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr17:61894304 G>A maps to NM_203499.1 T697T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr5:134143546 G>C maps to ENST00000452510 L688L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr5:134116908 G>A maps to ENST00000452510 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr19:19035768 C>T maps to NM_019070.4 V336V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr17:62501869 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr10:70706373 G>T maps to NM_024045.1 R734R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr23:23019521 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr23:23019161 T>C did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr12:113618743 G>A maps to NM_001111322.1 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr12:113602036 G>A maps to NM_001111322.1 R591R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr7:44605534 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:200635688 G>A maps to NM_001031725.4 C60C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr4:169158511 C>A maps to NM_017631.5 E1446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr4:169411575 T>A did not map to a codon.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr8:91013776 C>T maps to NM_001359.1 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr1:161091922 G>A did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr1:161092116 G>A maps to ENST00000368005 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr8:6735346 G>C maps to NM_005218.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A5XV-01A-11D-A28B-09 chr6:49936401 G>T maps to NM_001037729.1 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr6:49928005 C>G maps to NM_001037499.1 *70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr20:29896333 G>A maps to NM_001037731.1 Q19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr20:29965027 G>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr20:30028539 C>G maps to NM_153324.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr20:238469 G>A maps to NM_207469.2 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr14:100615442 G>A maps to NM_206918.2 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LS-01A-22D-A22X-09 chr14:100615442 G>A maps to NM_206918.2 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr7:140273622 C>T maps to NM_015689.3 K477K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr7:140302121 T>G maps to NM_015689.3 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr1:115142026 C>T maps to ENST00000393274 P717P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr1:115166238 G>A maps to ENST00000393274 Q278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr1:153905690 G>A maps to NM_014856.2 F1145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr9:19352600 C>T maps to NM_017925.4 F1288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr9:19336795 C>T maps to ENST00000380432 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73Q-01A-21D-A32I-09 chr11:9182286 G>T maps to NM_015213.2 I803I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr12:31566464 A>G maps to NM_144973.3 D862D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr12:31579358 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3YQ-01A-11D-A22X-09 chr22:32242913 C>A maps to NM_001136029.1 S1030*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr8:124042856 G>A maps to NM_024295.4 R85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZF-01A-11D-A28B-09 chr22:24176925 G>A did not map to a codon.
Sequencing variant TCGA-EA-A5ZF-01A-11D-A28B-09 chr22:24176932 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr22:24179858 G>A maps to NM_001135751.1 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr22:24180755 G>C maps to NM_001135751.1 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:3782245 C>G maps to ENST00000378212 S94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr9:117170229 G>A maps to NM_015404.3 S565S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr9:117165216 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr9:117165577 C>T maps to NM_015404.3 K820K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr8:145540569 C>A maps to NM_012079.4 V419V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr23:69424300 A>G did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:69420190 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr22:19122625 C>T maps to NM_022719.2 K366K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr22:18898504 G>A maps to NM_005675.4 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr22:18899214 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr22:18894273 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr22:20302221 C>T maps to NM_033257.3 Q213Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr22:20079117 C>G maps to NM_022720.6 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr7:14758206 C>T maps to NM_004080.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr7:14216523 C>T maps to NM_004080.2 R749R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr13:42830422 C>T did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr13:42830662 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr7:137294338 G>C maps to NM_004717.2 S337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:137082126 C>A maps to NM_004717.2 E993*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5FO-01A-21D-A28B-09 chr7:137294322 C>T maps to NM_004717.2 K342K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZF-01A-11D-A28B-09 chr7:137271862 G>A maps to NM_004717.2 R469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:50213604 C>G did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:50131535 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:50167246 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:50213451 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:50111811 G>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:50213187 C>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:50213445 A>G did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:50127784 C>G did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr23:50130628 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr2:74173877 G>A maps to NM_080916.1 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:55352681 G>C maps to NM_014762.3 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr3:93780202 C>T maps to NM_001195643.1 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr13:52346017 C>T maps to NM_001031719.1 W166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr13:52348139 G>A maps to NM_001031719.1 Q132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A411-01A-11D-A243-09 chr1:12632816 G>A maps to NM_004753.4 Q255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr23:2161133 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr23:2184870 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2GZ-01A-11D-A17W-09 chr23:2161182 C>T did not map to a codon.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr23:2184918 A>T did not map to a codon.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr10:12160858 C>T maps to NM_018706.5 L838L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr10:12159689 C>T maps to NM_018706.5 Q780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr4:24534693 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr4:24585974 G>C maps to NM_001358.2 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr6:30633381 G>A maps to NM_003587.4 H265H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:54570468 G>C maps to NM_019030.2 S888*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr5:54585103 C>A maps to NM_019030.2 E354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr3:47884654 C>G maps to NM_138615.2 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:127542655 G>C maps to NM_018180.2 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr20:37653955 G>A maps to NM_021931.3 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HR-01A-11D-A20U-09 chr3:154018863 G>A maps to NM_020865.2 Q424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:154024009 G>T maps to NM_020865.2 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr16:72138924 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr16:72137933 C>T maps to NM_014003.3 L638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr16:72132677 C>T maps to NM_014003.3 R251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UC-01A-11D-A351-09 chr17:41585299 G>T maps to NM_004941.1 E745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr17:41582012 G>A maps to NM_004941.1 A516A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:96200543 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr23:95990783 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr23:96197125 C>T did not map to a codon.
Sequencing variant TCGA-EX-A1H6-01B-11D-A22X-09 chr23:96171542 C>T did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr13:60453397 G>A maps to NM_001042517.1 Q858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr13:60686167 G>A maps to NM_001042517.1 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LS-01A-22D-A22X-09 chr14:95574780 C>T maps to NM_177438.2 V772V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr14:95556867 G>C maps to NM_177438.2 L1912L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr14:95570074 G>A maps to NM_177438.2 Q1220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr14:95590579 G>A maps to NM_177438.2 C443C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr20:61542822 G>A maps to NM_033081.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr20:61510620 C>T maps to NM_033081.2 S2229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr20:61525015 A>T did not map to a codon.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr21:47929215 G>C maps to ENST00000318711 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr21:47969759 G>T maps to ENST00000318711 E868*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZD-01A-11D-A28B-09 chr12:51138528 G>A maps to NM_173602.2 P1546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:51128867 G>A maps to NM_173602.2 V1352V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr10:402354 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LC-01A-11D-A20U-09 chr10:486840 G>A maps to NM_014974.2 Q122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr3:122514353 C>T maps to NM_032839.2 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr3:122591346 C>G maps to NM_032839.2 V408V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr13:73337592 G>C maps to NM_014953.3 S708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr13:73345041 C>T maps to NM_014953.3 K585K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr2:232952240 T>C maps to NM_152383.4 Y137Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr2:233201338 G>C maps to NM_152383.4 *886S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:231830493 C>T maps to NM_001164537.1 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr1:223176652 G>A maps to NM_032890.2 G638G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr1:223176988 C>T maps to NM_032890.2 S750S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr15:40659611 C>G maps to NM_033510.1 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr15:40660757 C>G maps to NM_033510.1 L815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr15:40659863 G>A maps to NM_033510.1 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr11:111889884 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:111890286 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr23:154004500 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr10:54076459 G>T maps to NM_012242.2 E232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr4:107956607 A>G maps to NM_014421.2 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr11:11989991 G>A maps to ENST00000450094 Q160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr11:11985983 C>A did not map to a codon.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr8:42231856 G>A maps to NM_014420.2 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr11:111916682 G>T maps to NM_001931.4 E463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr11:111915923 C>T maps to NM_001931.4 F420F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr8:12958087 G>A maps to NM_182643.2 S586S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr8:13356681 G>C maps to NM_182643.2 S300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr8:12957628 C>T maps to NM_182643.2 Q739Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A50E-01A-21D-A26G-09 chr8:12946081 G>A maps to NM_182643.2 I1402I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr8:12943361 G>A maps to NM_182643.2 F1515F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AU-01A-32D-A243-09 chr8:12943866 G>T maps to NM_182643.2 S1466S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DV-01A-11D-A32I-09 chr8:12948838 C>T maps to NM_182643.2 K1281K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr8:12990538 G>T did not map to a codon.
Sequencing variant TCGA-DG-A2KH-01A-21D-A22X-09 chr3:38080892 C>T maps to NM_007335.2 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr3:38159077 C>T maps to NM_007335.2 L1487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr3:38136537 C>T maps to NM_007335.2 F696F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:38101275 G>A maps to NM_007335.2 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A44S-01A-12D-A26G-09 chr13:51287266 C>A did not map to a codon.
Sequencing variant TCGA-DS-A3LQ-01A-21D-A21Q-09 chr3:196876612 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr3:196807887 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr11:83252885 G>T maps to NM_001142699.1 Y652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr11:83877981 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr11:83874520 C>A maps to NM_001142699.1 E203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr23:69699013 G>C did not map to a codon.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr23:69670154 G>A did not map to a codon.
Sequencing variant TCGA-DS-A7WI-01A-12D-A351-09 chr23:69670050 A>C did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr17:7099653 C>G did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr10:79572014 G>A maps to NM_004747.3 I1382I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr10:79601770 G>A maps to NM_004747.3 I435I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr10:79569394 C>G maps to NM_004747.3 G1519G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr10:79552245 G>A maps to NM_004747.3 V1904V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr18:3729210 G>A maps to NM_004746.2 D505D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr18:3508606 C>T maps to NM_004746.2 Q844Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr1:35372981 C>G did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr20:35128772 G>A maps to ENST00000339266 Q757Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr14:55650366 G>A maps to NM_014750.4 R115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr14:101200863 C>G maps to NM_003836.5 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr6:170593004 G>A maps to NM_005618.3 N454N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr15:41222244 C>T maps to NM_019074.3 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr14:75348640 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr17:48072206 C>A maps to NM_005220.2 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr17:48051275 C>G maps to NM_138281.2 S231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr17:48051295 C>T maps to NM_138281.2 Q238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr17:48050453 C>T maps to NM_138281.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr10:124377809 C>G maps to ENST00000368915 L1723L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr10:124348624 C>A maps to ENST00000368915 S650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:124348772 C>T maps to ENST00000368915 V699V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr10:124402736 C>T maps to ENST00000368915 S2484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr22:38966094 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr23:32380949 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr23:32509431 C>T did not map to a codon.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr23:32486616 G>A did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr23:32591731 G>A did not map to a codon.
Sequencing variant TCGA-EA-A5FO-01A-21D-A28B-09 chr23:32360320 C>T did not map to a codon.
Sequencing variant TCGA-EA-A5FO-01A-21D-A28B-09 chr23:32717260 G>A did not map to a codon.
Sequencing variant TCGA-EA-A5O9-01A-11D-A28B-09 chr23:32408239 T>G did not map to a codon.
Sequencing variant TCGA-EA-A5ZF-01A-11D-A28B-09 chr23:31525525 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr23:32563426 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr23:32459401 C>A did not map to a codon.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr23:31747810 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr23:32382742 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr23:31462736 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:31196836 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:31496410 T>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:31950328 C>A did not map to a codon.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr23:33357378 C>T did not map to a codon.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr23:32383309 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:33229515 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:32360326 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr23:31645827 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:31893426 G>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q8-01A-11D-A21Q-09 chr23:32398676 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73Q-01A-21D-A32I-09 chr23:32632544 G>T did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr23:31190489 C>G did not map to a codon.
Sequencing variant TCGA-EA-A3HQ-01A-11D-A20U-09 chr19:35991427 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr19:35990936 G>A did not map to a codon.
Sequencing variant TCGA-C5-A2LS-01A-22D-A22X-09 chr9:916848 C>T maps to NM_021951.2 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr9:1053807 C>G maps to NM_181872.4 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr9:990869 C>T maps to NM_021240.2 R428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr9:990437 C>T maps to NM_021240.2 V284V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VH-01A-11D-A28B-09 chr19:42351693 C>T maps to ENST00000427618 C66C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr19:46289820 G>A maps to NM_004943.1 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr5:118584138 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr15:51778393 G>A maps to NM_001174116.1 F1786F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr15:51790821 G>A maps to NM_001174116.1 F1533F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr10:70209936 C>A maps to NM_001080449.1 E349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:52417974 G>A maps to ENST00000273600 L2750L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:52432097 C>T maps to ENST00000273600 I4067I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr3:52412642 C>T maps to ENST00000273600 F2408F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr3:52397150 C>G maps to ENST00000273600 L1745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr3:52384528 G>T maps to ENST00000273600 R884R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:52398682 G>A maps to ENST00000273600 V1758V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A852-01A-11D-A351-09 chr3:52417482 C>T maps to ENST00000273600 Q2675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr12:124270379 C>T maps to NM_207437.3 R379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr12:124256188 C>T maps to NM_207437.3 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr12:124382350 A>G maps to NM_207437.3 E2987E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr12:124272479 C>T maps to NM_207437.3 D456D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr12:124363858 G>A maps to NM_207437.3 L2689L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr12:124416303 C>G maps to NM_207437.3 L4228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr12:124267766 C>T maps to NM_207437.3 Q258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:21826258 G>A maps to NM_003777.3 L3212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr7:21603846 G>A maps to NM_003777.3 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr7:21827104 G>A maps to NM_003777.3 L3283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr7:21639598 G>A maps to NM_003777.3 E954E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr7:21604002 C>G maps to NM_003777.3 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A78R-01A-11D-A32I-09 chr3:57493376 G>C maps to NM_178504.4 S297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr3:57443850 C>A maps to NM_178504.4 E987*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr3:57528441 T>C maps to NM_178504.4 K52K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr17:76497913 G>A maps to ENST00000389840 N1733N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr17:76454788 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr17:76501503 G>C maps to ENST00000389840 L1605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr17:76488832 G>A maps to ENST00000389840 L2127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr17:76490198 C>G maps to ENST00000389840 L2095L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:76570851 G>C maps to ENST00000389840 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr17:7695327 G>T maps to NM_020877.2 E2332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr17:7690335 C>T maps to NM_020877.2 I2196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr17:7701880 A>T maps to NM_020877.2 K2802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr17:7682664 C>T maps to NM_020877.2 G1882G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr17:7681471 G>T maps to NM_020877.2 R1775R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr17:7721143 G>C maps to NM_020877.2 L3402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr16:20996704 G>A maps to NM_017539.1 Y2453Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QD-01A-32D-A22X-09 chr16:20974836 C>A maps to NM_017539.1 E3457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr16:21071587 G>C maps to NM_017539.1 V1270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr16:20981114 G>A maps to NM_017539.1 S2819S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr16:21086766 C>T did not map to a codon.
Sequencing variant TCGA-FU-A5XV-01A-11D-A28B-09 chr16:20976328 G>A maps to NM_017539.1 I2959I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr16:21156658 G>A maps to NM_017539.1 F97F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr16:21063144 G>A maps to NM_017539.1 L1362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr16:21053504 G>A maps to NM_017539.1 V1494V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr16:21082113 G>A maps to NM_017539.1 Q1040*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr5:13829759 G>A maps to NM_001369.2 F2101F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr5:13868026 G>A maps to NM_001369.2 H1303H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr5:13717459 G>A maps to NM_001369.2 F4223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr5:13922307 G>A maps to NM_001369.2 Q190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr2:196834743 A>G maps to NM_018897.2 D711D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr2:196642522 C>G did not map to a codon.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr2:196765059 G>A maps to NM_018897.2 Y1498Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr6:38790762 C>T maps to ENST00000327475 Q1213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr6:38893971 G>T maps to ENST00000327475 E3690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VI-01A-11D-A28B-09 chr6:38840901 C>T maps to ENST00000327475 L2474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr6:38790647 G>A maps to ENST00000327475 L1174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr6:38709539 C>G maps to ENST00000327475 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr6:38850714 C>T maps to ENST00000327475 Q2618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr17:11511459 C>T maps to NM_001372.3 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr17:11535954 C>T maps to NM_001372.3 R524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr17:11666897 C>T maps to NM_001372.3 I2379I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3TX-01A-11D-A22X-09 chr17:11701023 C>A maps to NM_001372.3 T2778T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3TX-01A-11D-A22X-09 chr17:11786910 C>T maps to NM_001372.3 L3605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A69B-01A-11D-A32I-09 chr17:11835465 G>T maps to NM_001372.3 G4081*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr17:11778337 C>T maps to NM_001372.3 Q3439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr9:34500822 C>G maps to NM_012144.2 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr17:72278036 G>C maps to NM_023036.4 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr17:72278136 G>T maps to NM_023036.4 E61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LB-01A-11D-A243-09 chr17:72308203 G>A maps to NM_023036.4 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AX-01A-12D-A243-09 chr17:72285875 G>T did not map to a codon.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr16:4506662 C>T did not map to a codon.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr19:14627858 C>T did not map to a codon.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr10:74103157 C>T maps to NM_017626.4 K175K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr4:100826836 C>T maps to NM_001031723.2 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr2:220147866 C>A maps to NM_006736.5 S153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:78444879 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr2:183581192 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:6695695 G>T did not map to a codon.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr3:132184865 C>T maps to NM_015268.3 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr3:132172522 G>A maps to NM_015268.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr12:56215781 C>T maps to NM_032364.5 V696V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr12:56222283 G>A maps to NM_032364.5 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr1:15896203 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:15863293 G>T maps to NM_015291.2 E187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr5:138749835 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr7:102956535 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr5:34950382 C>T maps to NM_194283.3 Q477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr12:49743275 C>A maps to NM_024902.2 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr2:25181413 A>G did not map to a codon.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr13:96439259 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr7:73097087 G>A maps to NM_032317.2 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:65858182 C>G maps to ENST00000371069 S513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:38027425 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:38027338 G>C did not map to a codon.
Sequencing variant TCGA-EA-A5FO-01A-21D-A28B-09 chr23:153631923 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:153631422 C>T did not map to a codon.
Sequencing variant TCGA-EX-A1H6-01B-11D-A22X-09 chr23:153631422 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr11:6530457 C>T maps to NM_144666.2 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr9:139257547 G>C maps to NM_001080849.1 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr12:32866192 C>T maps to ENST00000381000 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr19:10886547 C>T maps to NM_001005361.2 D185D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr19:10886382 G>A maps to NM_001005361.2 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr19:10262175 G>A maps to NM_001130823.1 V721V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr2:25469056 G>A maps to NM_175629.1 V467V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr20:44424003 G>A maps to NM_052951.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr1:94344777 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr10:129055716 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr10:128795092 C>T maps to ENST00000398025 F185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr10:129216660 G>A maps to ENST00000398025 E1561E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr10:128908535 C>G maps to ENST00000398025 L826L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr23:117695417 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr23:117739290 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr23:117739291 A>T did not map to a codon.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr23:117676769 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:117809941 A>C did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:117718725 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:117783037 G>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:117731497 G>A did not map to a codon.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr23:117748712 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:117817117 G>C did not map to a codon.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr5:169410109 G>A maps to NM_004946.2 Q946Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr5:169496193 G>A maps to NM_004946.2 L1566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr5:169506071 G>C maps to NM_004946.2 R1696R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr3:51251580 T>C maps to NM_004947.4 R385R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr19:11361762 C>G did not map to a codon.
Sequencing variant TCGA-HM-A3JK-01A-11D-A21Q-09 chr1:63052285 G>C maps to ENST00000371140 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr9:418176 G>A maps to NM_203447.3 L1270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr9:405009 G>A maps to NM_203447.3 L1109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr9:465198 T>G did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr9:414808 C>T maps to NM_203447.3 V1186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A78R-01A-11D-A32I-09 chr13:99554034 A>G maps to ENST00000428223 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr13:99567631 G>A maps to ENST00000428223 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr13:99537986 C>T maps to ENST00000428223 K745K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr2:74783589 C>G maps to NM_001381.3 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr5:176936487 G>T maps to NM_024872.2 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr18:67344968 G>A did not map to a codon.
Sequencing variant TCGA-EA-A556-01A-11D-A26G-09 chr6:83877983 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr6:83846970 C>T maps to NM_015018.2 L1070L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr6:83846970 C>T maps to NM_015018.2 L1070L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:2226836 C>T maps to ENST00000221482 L1439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A69B-01A-11D-A32I-09 chr19:2217768 A>G did not map to a codon.
Sequencing variant TCGA-LP-A4AX-01A-12D-A243-09 chr19:2210817 C>T maps to ENST00000221482 Q439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr10:103368687 C>T maps to NM_015448.1 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr10:103368657 G>A maps to NM_015448.1 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr6:30917484 C>G maps to NM_080870.3 S415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr11:65112087 G>C did not map to a codon.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr14:73140899 A>G did not map to a codon.
Sequencing variant TCGA-EA-A3QD-01A-32D-A22X-09 chr14:73238500 G>A maps to NM_012074.3 Q45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:16306187 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr9:130698033 C>A maps to NM_003863.3 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:155112440 G>A maps to NM_018973.3 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A69B-01A-11D-A32I-09 chr2:116101412 G>T maps to NM_020868.3 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr11:66264945 C>T maps to NM_005700.3 Q626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr11:66276796 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr7:154429553 A>C maps to NM_130797.2 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr9:140006563 C>T maps to NM_013379.2 Q350Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr15:65759486 G>C maps to NM_197960.2 Y553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr15:65743242 C>G did not map to a codon.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr19:4702153 G>C maps to ENST00000357909 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr19:4719936 C>T maps to ENST00000357909 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr12:7868016 T>G maps to NM_199286.2 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr3:109049374 G>T maps to NM_018189.3 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZF-01A-11D-A28B-09 chr1:168683559 C>A maps to NM_001937.4 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr7:35009107 G>A maps to NM_015283.1 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3TQ-01A-11D-A22X-09 chr7:34979921 A>G maps to NM_015283.1 F496F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr19:32954773 G>C did not map to a codon.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr1:97658666 C>T maps to NM_000110.3 Q860Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:97544575 C>A maps to NM_000110.3 E1012*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr8:26477450 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr5:146792218 C>T maps to NM_001197294.1 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr2:74746332 C>A maps to NM_133637.2 G611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr5:174869676 G>A maps to NM_000794.3 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr5:174870003 G>C maps to NM_000794.3 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr11:113283563 G>C maps to ENST00000355319 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A852-01A-11D-A351-09 chr3:113866345 G>T maps to NM_000796.3 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr4:9784378 C>T maps to NM_000798.4 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OA-01A-11D-A16Y-08 chr4:9783769 A>G maps to NM_000798.4 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A4BA-01A-21D-A26G-09 chr23:100492678 T>A did not map to a codon.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr23:100503169 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:100510234 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr21:41561045 G>A maps to NM_001389.3 R826*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H6-01B-11D-A22X-09 chr21:41385098 G>A maps to NM_001389.3 A1967A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CJ-01A-11D-A32I-09 chr11:117395798 C>T did not map to a codon.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr11:117392106 C>T maps to NM_020693.2 V377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HQ-01A-11D-A20U-09 chr11:117329617 G>A maps to NM_020693.2 G1200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr6:116757049 C>T maps to NM_013352.2 Y473Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M2-01A-21D-A18J-09 chr6:116720652 C>G maps to NM_013352.2 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr6:116754693 C>T maps to NM_013352.2 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr6:116756827 C>T maps to NM_013352.2 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr18:65180657 G>A maps to NM_032160.2 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr18:28911706 G>A maps to NM_001942.2 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr18:29046628 G>A maps to NM_001944.2 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr18:29049277 C>A maps to NM_001944.2 I621I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr18:29045394 C>T maps to NM_001944.2 I462I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:7582904 C>T maps to NM_004415.2 Q1804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr6:7583773 C>T maps to NM_004415.2 I2093I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr6:7581462 G>A maps to NM_004415.2 L1680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr6:7578089 C>T maps to NM_004415.2 Q986*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-C5-A1BN-01B-11D-A14W-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-C5-A1M9-01A-11D-A13W-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-C5-A1M9-01A-11D-A13W-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-C5-A3HE-01A-21D-A22X-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-EK-A3GK-01A-11D-A20U-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-EK-A3GK-01A-11D-A20U-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-EK-A3GN-01A-11D-A20U-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr4:88534421 G>T maps to NM_014208.3 E362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr4:88534378 C>G maps to NM_014208.3 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr6:56443710 G>A maps to ENST00000361203 Q4099*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr6:56458792 G>A maps to ENST00000361203 L3921L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr6:56506863 C>T maps to ENST00000361203 Q425Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr6:56366457 C>A maps to ENST00000361203 E6323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr6:56483272 G>T maps to ENST00000281662 I2417I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr6:56473209 G>A maps to ENST00000361203 L1861L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LC-01A-11D-A20U-09 chr6:56484706 A>G maps to ENST00000281662 N1939N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr6:56417461 G>A maps to ENST00000361203 F5165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr6:56465019 C>G did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr6:56504496 G>C maps to ENST00000361203 L687L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr6:56417203 G>A maps to ENST00000361203 I5251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr6:56471440 G>C maps to ENST00000361203 S2451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr1:205128677 C>T maps to NM_015375.2 L745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr20:18576745 C>A maps to NM_080820.4 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr18:32418087 G>A maps to NM_001390.4 Q375Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr2:25705726 C>T maps to NM_021907.3 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr12:113534596 G>C maps to NM_004416.2 S572S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr12:113533236 A>G did not map to a codon.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr7:76112110 C>T maps to NM_020892.2 I185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr12:58002421 C>T maps to NM_178502.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A5XV-01A-11D-A28B-09 chr11:58956668 G>A maps to NM_015177.1 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7X3-01A-11D-A351-09 chr15:45398749 C>A maps to NM_014080.4 E641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr15:45404064 G>A maps to NM_014080.4 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr15:45393431 G>C maps to NM_014080.4 V964V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr15:45411370 G>C maps to NM_144565.2 S322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R1-01A-11D-A28B-09 chr19:5789394 G>A maps to NM_020175.2 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr19:5785240 C>T maps to NM_020175.2 P642P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QD-01A-32D-A22X-09 chr8:33449680 C>T maps to NM_024025.1 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr8:33454934 C>T maps to NM_024025.1 E33E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:167097843 G>C maps to NM_001080426.1 *1159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr8:29194614 G>A maps to NM_001394.5 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr11:1580136 C>T maps to NM_004420.2 Q173Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr23:152913686 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr15:48623777 G>C maps to NM_001025248.1 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr19:57669799 G>A maps to NM_001012729.1 Q112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:1273751 C>T maps to ENST00000378888 R468R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:1273929 G>C maps to ENST00000378888 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr17:7132957 G>A maps to NM_004422.2 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr17:7133188 G>T maps to NM_004422.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr14:102466694 C>T maps to NM_001376.4 Q1345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr14:102477144 C>T maps to NM_001376.4 F2158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr14:102496560 G>A maps to NM_001376.4 Q3275Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A78R-01A-11D-A32I-09 chr14:102452448 G>A maps to NM_001376.4 Q629Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr14:102474549 G>A maps to NM_001376.4 V1951V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A69M-01A-11D-A32I-09 chr14:102514295 C>T maps to NM_001376.4 T4383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr14:102467325 G>C maps to NM_001376.4 L1370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73Q-01A-21D-A32I-09 chr14:102476246 C>T maps to NM_001376.4 F2015F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr7:95442583 G>T maps to NM_004411.4 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr2:172569310 C>T maps to NM_001378.1 Q124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr16:66785176 G>A maps to NM_006141.2 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr11:103026187 C>G maps to NM_001080463.1 L1234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A6QX-01A-12D-A33O-09 chr11:103116083 A>G maps to NM_001080463.1 R3348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr20:33122636 T>G maps to ENST00000417166 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A69L-01A-11D-A32I-09 chr20:33128383 G>T did not map to a codon.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr21:38739646 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:40319104 C>G maps to NM_004714.1 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr1:206810290 C>T did not map to a codon.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr12:4682342 A>C did not map to a codon.
Sequencing variant TCGA-UC-A7PD-01A-11D-A351-09 chr12:4682314 G>C did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr2:71828535 G>C did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr13:96234548 G>C maps to NM_198968.2 S848*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BE-01A-21D-A26G-09 chr13:96240000 G>A did not map to a codon.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr3:137800603 G>A maps to NM_173543.2 I402I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AU-01A-32D-A243-09 chr3:137787114 G>A maps to NM_173543.2 P570P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr3:108407540 C>T maps to NM_014648.3 L1124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr3:108403095 G>T maps to NM_014648.3 E973*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr20:32264971 T>C maps to NM_005225.2 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:23847436 G>A maps to NM_004091.3 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr8:86127980 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr8:86127141 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr8:86127136 G>A did not map to a codon.
Sequencing variant TCGA-FU-A5XV-01A-11D-A28B-09 chr12:77436898 G>A maps to NM_203394.2 R357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73R-01A-11D-A33O-09 chr14:34998643 C>T maps to NM_018453.3 K130K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr5:158126043 C>G did not map to a codon.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr8:25897611 G>A maps to NM_022659.2 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr8:25718726 G>A maps to NM_022659.2 R394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr10:131761041 C>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr10:131646735 C>A maps to ENST00000355311 E350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr10:131760526 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr1:43637889 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr1:43636552 G>C did not map to a codon.
Sequencing variant TCGA-C5-A7CG-01A-11D-A32I-09 chr23:48382320 G>A did not map to a codon.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr3:184001607 G>C maps to NM_014693.3 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:39306253 C>T maps to NM_001398.2 *329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr6:127611067 C>T maps to NM_001139510.1 W290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr1:53377454 A>G maps to ENST00000371522 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr1:53387258 C>T maps to ENST00000371522 E29E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr10:11797399 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr1:150482444 C>T maps to ENST00000369049 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr1:150485844 C>T maps to ENST00000369049 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr19:11617187 C>T maps to NM_016581.3 T369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr3:172536476 C>G maps to ENST00000427830 S901*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr3:172501695 C>G maps to ENST00000392692 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr6:139206713 G>A maps to NM_001195037.2 L700L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr6:139165615 A>G maps to NM_001195037.2 R221R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr6:139203878 G>A maps to NM_001195037.2 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr23:69176993 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:69177046 G>A did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr16:67917563 C>T maps to NM_014329.3 Q1315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr14:21238474 G>T maps to NM_022360.4 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr20:33706306 G>C did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr20:33706315 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr1:184681602 G>C maps to NM_025191.3 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr6:12294299 G>A maps to NM_001955.4 W120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:41949752 G>A maps to NM_001956.3 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr4:148407186 G>A maps to NM_001957.3 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr4:148463810 C>T did not map to a codon.
Sequencing variant TCGA-DS-A1OA-01A-11D-A16Y-08 chr6:74228825 G>A maps to NM_001402.5 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2GZ-01A-11D-A17W-09 chr20:62121918 G>A maps to NM_001958.2 N314N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr20:62126343 C>T maps to NM_001958.2 V145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr8:144671933 G>T maps to NM_032378.4 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr11:62327818 C>T maps to ENST00000378019 W372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr19:3977936 G>A maps to NM_001961.3 I649I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr19:3979964 C>T maps to NM_001961.3 T482T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:3984339 G>A maps to NM_001961.3 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr16:22268578 C>T maps to NM_013302.3 F258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RA-A741-01A-11D-A33O-09 chr16:22268677 G>T maps to NM_013302.3 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A4BA-01A-21D-A26G-09 chr11:831573 C>T maps to ENST00000327417 C420C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr12:3763513 C>A maps to NM_001144958.1 E304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr17:28320318 G>T maps to NM_198529.3 G302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr22:44063042 G>A maps to NM_022785.3 R642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr22:44193199 T>C did not map to a codon.
Sequencing variant TCGA-FU-A3YQ-01A-11D-A22X-09 chr1:63998423 C>T maps to NM_032437.2 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr2:56149651 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr11:65634129 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr3:19988413 G>T did not map to a codon.
Sequencing variant TCGA-EA-A5FO-01A-21D-A28B-09 chr6:52344531 G>A maps to NM_018100.3 A529A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr23:44091895 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:44101442 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:44101484 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:155100406 C>G did not map to a codon.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr1:155100461 C>T maps to NM_004428.2 F3F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr5:106717039 G>A maps to NM_001962.2 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr5:106716964 C>T maps to NM_001962.2 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:68058516 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:68059872 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr13:107145420 C>T maps to NM_004093.2 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr15:82512458 C>T maps to NM_024580.5 G468G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:82533677 G>C maps to NM_024580.5 S104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr17:42928701 G>A maps to NM_004247.3 F953F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr4:110897269 C>T maps to NM_001963.4 P644P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KH-01A-21D-A22X-09 chr23:13636148 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3QE-01A-21D-A21Q-09 chr23:13645278 C>T did not map to a codon.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr6:32135383 C>T maps to NM_030652.2 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr6:32134313 C>G maps to NM_030652.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr5:38407216 C>A maps to ENST00000354891 T372T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr7:55214392 C>G maps to NM_005228.3 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A6QX-01A-12D-A33O-09 chr7:55242422 G>A maps to NM_005228.3 W731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr7:55224460 C>T maps to NM_005228.3 F381F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr7:55249086 C>T maps to NM_005228.3 F795F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr5:137801470 G>A maps to NM_001964.2 E7E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr2:73520478 C>T maps to NM_001965.3 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr11:64627614 C>G maps to NM_006795.2 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr11:64627689 C>T maps to NM_006795.2 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R9-01A-11D-A18J-09 chr11:64622128 G>A maps to NM_006795.2 G427G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LB-01A-11D-A243-09 chr11:64627701 C>G maps to NM_006795.2 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr19:48244574 C>T maps to NM_014601.3 F506F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr19:48229264 C>A maps to NM_014601.3 Y233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:34668237 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr3:184953230 G>A maps to NM_001966.3 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr3:184971747 G>A maps to NM_001966.3 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr3:184935935 G>A maps to NM_001966.3 Q186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr9:140729281 C>T maps to NM_024757.4 C1258C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A852-01A-11D-A351-09 chr9:140672486 C>T maps to NM_024757.4 L724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr9:140605429 G>A maps to NM_024757.4 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr9:140622860 G>T maps to NM_024757.4 E235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr6:31855590 G>A maps to ENST00000395728 A688A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr6:31864228 C>T maps to ENST00000395728 K188K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr6:31848580 G>A maps to ENST00000395728 I1164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr11:125453660 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr17:39845182 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr17:39845440 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr17:39847104 T>A did not map to a codon.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr17:39847105 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr17:39847265 G>T did not map to a codon.
Sequencing variant TCGA-JW-A5VI-01A-11D-A28B-09 chr23:20156733 C>T did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:150293453 C>T maps to NM_032025.3 Q468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7X3-01A-11D-A351-09 chr7:6084229 G>T maps to NM_014413.3 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr7:6094175 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr7:6066549 G>A maps to NM_014413.3 Q525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr2:37334415 C>G maps to NM_001135651.1 *552Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr12:124111691 A>T maps to NM_001414.3 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr1:45363061 C>T maps to NM_020365.3 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr1:45347293 C>T maps to NM_020365.3 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A69M-01A-11D-A32I-09 chr1:45424468 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr20:32686324 C>A maps to NM_003908.3 E138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr23:24094871 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr10:120796820 C>T maps to NM_003750.2 R1243R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:120819415 C>G did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr10:120818979 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr7:2412416 G>A maps to ENST00000314800 K599K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr7:2419072 G>T maps to ENST00000314800 E796*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr22:36912932 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr8:109226921 C>T maps to NM_001568.2 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr19:39114770 G>T maps to NM_013234.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr11:32610233 G>A maps to NM_006360.3 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr17:7479840 G>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr3:186504950 G>A maps to ENST00000440191 E270E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr3:186502833 G>T maps to ENST00000440191 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R3-01A-11D-A28B-09 chr3:186505010 G>C maps to ENST00000440191 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr12:53410309 G>T maps to ENST00000438209 E23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:71777665 G>C did not map to a codon.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr11:10830401 C>A did not map to a codon.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr1:21391063 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:21296059 A>G maps to NM_001198801.1 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LC-01A-11D-A20U-09 chr1:21139649 C>G did not map to a codon.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr7:73609170 C>T maps to NM_022170.1 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr2:99999377 C>T maps to NM_015904.3 L755L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:100013319 C>T maps to NM_015904.3 Q1118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A50E-01A-21D-A26G-09 chr20:33867867 T>A maps to NM_002212.2 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr20:33867891 G>C maps to NM_002212.2 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HM-A3JJ-01A-21D-A21Q-09 chr19:8056668 C>A maps to ENST00000351593 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr9:23762103 G>A maps to ENST00000359598 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R1-01A-11D-A28B-09 chr9:23762090 G>A maps to ENST00000359598 Q76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr19:11565682 C>T maps to NM_001420.3 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr4:139980711 G>A maps to ENST00000379550 Q403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr1:201984417 G>A maps to NM_004433.4 W361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr1:201981104 G>T maps to NM_004433.4 E62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:201981254 C>T maps to NM_004433.4 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:201982910 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr1:201981364 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:201983059 C>T maps to NM_004433.4 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:129200914 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr11:34533106 G>A maps to NM_198381.1 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr22:37769909 G>C maps to NM_052906.3 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr23:47496288 G>A did not map to a codon.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr23:47498359 G>T did not map to a codon.
Sequencing variant TCGA-LP-A5U3-01A-11D-A28B-09 chr23:47500684 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr1:205589547 G>C maps to NM_001973.2 S209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr19:18557289 C>T maps to NM_006532.3 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr19:18632760 C>G maps to NM_006532.3 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr19:18572603 C>T maps to NM_006532.3 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr7:37298895 C>T maps to NM_014800.9 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr7:37311453 G>A maps to NM_014800.9 R76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2GZ-01A-11D-A17W-09 chr20:45023164 C>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr16:67233123 C>T maps to NM_024712.3 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BE-01A-21D-A26G-09 chr11:107463875 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr2:85598617 G>A maps to NM_001135023.1 K180K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr7:73483017 G>A maps to ENST00000358929 R789R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr7:73452043 G>T maps to ENST00000358929 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:43829598 G>A maps to NM_022821.2 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr6:80631438 T>C maps to NM_022726.3 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr6:53156761 C>G did not map to a codon.
Sequencing variant TCGA-EX-A1H6-01B-11D-A22X-09 chr6:53213753 C>A did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr4:111119452 G>A maps to NM_024090.2 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3YQ-01A-11D-A22X-09 chr18:33750154 C>T maps to ENST00000442325 Q801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VH-01A-11D-A28B-09 chr18:33713235 C>A maps to ENST00000442325 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr11:31669287 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr1:79412052 G>A maps to NM_022159.3 N77N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr1:79403948 C>A maps to NM_022159.3 E138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr4:101344471 G>A maps to NM_016242.3 Q169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr23:153608139 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr23:153609277 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr16:1825360 G>A maps to NM_001010865.1 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr12:7079947 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr2:27306542 G>T maps to NM_007046.3 E702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr2:27306551 G>T maps to NM_007046.3 E705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr14:100402636 C>T maps to NM_001008707.1 L706L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr14:100402641 C>G maps to NM_001008707.1 S708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:46144972 G>C maps to NM_001193268.1 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr2:42490403 C>G maps to NM_019063.3 S200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DV-01A-11D-A32I-09 chr14:89130939 G>T maps to ENST00000380664 S1102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr12:13366731 C>G maps to NM_001423.2 S98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr19:6901985 C>T maps to ENST00000381407 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:6908764 G>C maps to ENST00000381407 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr19:6937310 G>A maps to ENST00000381407 L815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr19:14866480 G>A maps to NM_013447.2 F467F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:14779547 G>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:14779641 G>C maps to NM_032571.3 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M1-01A-11D-A18J-09 chr10:119302807 C>T maps to NM_004098.3 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr10:119308876 C>G did not map to a codon.
Sequencing variant TCGA-EX-A1H6-01B-11D-A22X-09 chr10:119308318 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr10:119308191 G>A did not map to a codon.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr10:119308121 C>G did not map to a codon.
Sequencing variant TCGA-EA-A410-01A-11D-A243-09 chr1:225702423 A>T maps to ENST00000284563 P611P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr1:225707233 C>T maps to ENST00000284563 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr12:48107059 G>C maps to NM_001172439.1 S288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:130605494 G>A maps to NM_001114753.1 Q33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr1:8922947 G>A maps to NM_001428.2 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr12:7031193 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr12:7027273 C>A maps to NM_001975.2 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A78R-01A-11D-A32I-09 chr17:4859381 C>T maps to NM_053013.3 C337C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:4859939 C>T maps to NM_053013.3 F380F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr18:674173 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr18:697269 C>T maps to ENST00000319815 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr18:677388 C>G maps to ENST00000319815 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr13:43934080 G>A maps to NM_001127615.1 C165C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr23:129769011 T>C did not map to a codon.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr23:129799720 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr4:111397772 C>G maps to NM_001977.3 S68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr6:132172327 G>A maps to NM_006208.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr6:132189246 C>A maps to NM_006208.2 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr8:120583067 G>C maps to NM_006209.3 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr8:120628551 G>A maps to NM_006209.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr6:131995357 C>G maps to NM_005021.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr6:132004302 G>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr6:132061483 C>T maps to NM_005021.3 I807I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr6:46107442 G>A maps to NM_014936.4 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr4:185138865 G>C maps to NM_153343.3 S36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr4:185074748 G>A maps to NM_153343.3 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr9:139942725 G>T did not map to a codon.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr9:139946065 C>T maps to NM_203468.1 Q94Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr8:23243542 C>T maps to ENST00000356206 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr9:140330467 G>A maps to NM_001033113.1 F349F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr9:140330987 G>A maps to NM_001033113.1 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr8:110346686 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr22:41525926 C>G maps to NM_001429.3 S401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HQ-01A-11D-A20U-09 chr22:41537114 C>T maps to NM_001429.3 R648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr22:41533714 C>T maps to NM_001429.3 Q561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr22:41545821 C>T maps to NM_001429.3 Q813*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr22:41574357 C>T maps to NM_001429.3 Q2215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr22:41527551 G>A maps to NM_001429.3 P481P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr22:41572869 C>T maps to NM_001429.3 Q1719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3TQ-01A-11D-A22X-09 chr22:41556726 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr22:41489063 C>G maps to NM_001429.3 S19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr22:41521979 C>G maps to NM_001429.3 S281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr22:41543929 C>T maps to NM_001429.3 Q741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr22:41574468 G>T maps to NM_001429.3 E2252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr22:41547873 C>G maps to NM_001429.3 S952*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr22:41562601 G>C did not map to a codon.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr12:132445332 C>T maps to ENST00000333577 Q57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:132448184 C>T maps to ENST00000333577 Q482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr12:132498440 C>T maps to ENST00000333577 D1338D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr12:132445646 C>T maps to ENST00000333577 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr12:132466941 G>A maps to ENST00000333577 S652S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:46525032 C>G did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr2:46583933 G>C maps to NM_001430.4 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr2:46524938 C>G did not map to a codon.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr1:29379716 A>T maps to NM_001166005.1 K580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr1:29314293 G>A maps to NM_001166005.1 E115E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr20:34778275 C>T maps to NM_012156.2 I368I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr20:34810274 G>T maps to NM_012156.2 E866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr20:34763471 G>C did not map to a codon.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr18:5630527 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr18:5630550 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr18:5416293 C>T maps to NM_012307.2 R530R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr5:111576450 G>A maps to NM_022140.3 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A69B-01A-11D-A32I-09 chr10:32667507 C>A did not map to a codon.
Sequencing variant TCGA-FU-A3TQ-01A-11D-A22X-09 chr2:47596297 C>G maps to ENST00000426238 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr7:37989928 G>A maps to NM_017549.3 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr7:37960780 C>T maps to NM_017549.3 D200D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RA-A741-01A-11D-A33O-09 chr7:143087513 G>T did not map to a codon.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr1:16460101 C>A did not map to a codon.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr3:89391037 G>A maps to NM_005233.5 W368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:222294715 G>A maps to NM_004438.3 N884N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr2:222283897 G>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:222283736 C>G did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:222307657 C>T maps to NM_004438.3 L655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr2:222284719 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr4:66231718 G>A maps to NM_004439.5 Q661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr4:66201812 G>A maps to NM_004439.5 L897L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr4:66467428 C>A maps to NM_004439.5 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr3:97202826 C>T maps to NM_001080448.2 D708D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:22920081 C>G maps to NM_020526.3 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr3:184294912 G>A maps to NM_004443.3 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr3:184295444 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr3:184298863 C>G maps to NM_004443.3 L881L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr7:100414847 G>A maps to NM_004444.4 F518F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A5XV-01A-11D-A28B-09 chr7:100401196 G>A maps to NM_004444.4 I950I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr7:100401184 C>T maps to NM_004444.4 L954L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr7:100414871 G>A maps to NM_004444.4 R510R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr7:142561387 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr7:142566337 C>T maps to NM_004445.3 A709A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr1:226019652 G>A maps to NM_001136018.2 K119K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr3:37034247 G>T maps to NM_014805.3 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr19:56196967 G>A maps to NM_001130071.1 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A410-01A-11D-A243-09 chr19:56206236 G>A maps to NM_001130071.1 T556T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr19:56203148 C>T maps to NM_001130071.1 F350F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:19186875 C>G maps to NM_014964.4 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RA-A741-01A-11D-A33O-09 chr17:19186470 C>T maps to NM_014964.4 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr19:11491609 G>T maps to NM_000121.3 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr8:144945859 G>C maps to NM_031308.1 S521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr8:144943470 G>A maps to NM_031308.1 L1317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr8:144941886 G>A maps to NM_031308.1 I1845I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr8:144942234 G>A maps to NM_031308.1 F1729F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr8:144942954 G>A maps to NM_031308.1 L1489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr8:144942648 C>G maps to NM_031308.1 L1591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:220219794 G>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:220184322 G>A maps to NM_004446.2 Q524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr1:51912771 A>T maps to NM_001981.2 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr19:55594889 G>A maps to ENST00000310075 V435V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr19:55593877 G>A maps to NM_133180.2 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73Q-01A-21D-A32I-09 chr11:726666 C>T maps to NM_022772.3 L661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr13:43462599 G>C maps to NM_001002264.1 S340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr17:56276425 C>A maps to NM_000502.4 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr12:91366697 C>A maps to NM_004950.4 E134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr5:96139367 G>A maps to NM_016442.3 Q88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QD-01A-32D-A22X-09 chr23:48688085 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3QE-01A-21D-A21Q-09 chr17:37884254 G>A maps to NM_004448.2 T1242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr12:56495502 C>T maps to NM_001982.2 L1231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr3:55544663 G>C did not map to a codon.
Sequencing variant TCGA-JW-A5VI-01A-11D-A28B-09 chr3:55543686 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:128030509 C>T maps to NM_000122.1 Q586Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr16:14029048 G>A maps to NM_005236.2 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr16:14041675 C>G maps to NM_005236.2 L741L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A556-01A-11D-A26G-09 chr10:50740701 G>A maps to ENST00000515869 D103D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr10:50678925 G>C maps to NM_000124.2 S1027*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr23:71427937 G>A did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr23:71425619 G>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:71426885 C>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:71426081 T>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:71427102 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr23:71427446 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr5:60188026 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr5:60186717 G>A maps to NM_000082.3 Q347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr5:60189041 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr5:60240760 C>T maps to NM_000082.3 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:42753674 C>A maps to NM_006494.2 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2GZ-01A-11D-A17W-09 chr19:42752617 C>T maps to NM_006494.2 *549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr5:172324902 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr5:172324909 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr5:172341858 C>T maps to ENST00000326654 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr8:8973881 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr1:44687111 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr1:44778897 G>A maps to NM_024066.1 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr2:54028724 G>A maps to NM_015701.3 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr10:101923793 C>A maps to NM_001100626.1 E208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr8:37597897 G>T maps to NM_007175.6 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr2:158178247 C>T maps to NM_001009959.1 Q143Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr17:62149425 C>T maps to NM_001433.3 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R3-01A-11D-A28B-09 chr14:53112957 C>T maps to NM_014584.1 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr12:15068651 C>G did not map to a codon.
Sequencing variant TCGA-EA-A3QD-01A-32D-A22X-09 chr1:8073497 C>T maps to NM_018948.3 K387K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr8:27633890 C>T maps to NM_001017420.2 F22F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr12:53673568 G>A maps to NM_012291.4 L806L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr12:53662643 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr12:53680113 C>T maps to NM_012291.4 L1198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr12:53680359 C>T maps to NM_012291.4 L1280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr1:6500364 C>T maps to NM_031475.2 C180C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr1:6520729 C>G did not map to a codon.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr1:6521026 C>G did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:6511967 C>T maps to NM_031475.2 Q713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr2:239040198 C>T maps to NM_194312.2 L948L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr16:68266311 G>A maps to NM_024939.2 Q306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr16:68266312 C>A maps to NM_024939.2 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr11:64082559 C>G maps to NM_004451.3 S277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr14:76928888 G>T maps to NM_004452.3 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr14:76957919 C>T maps to NM_004452.3 I306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:216880804 C>T did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr1:216850523 C>T maps to NM_001438.2 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:103499057 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr12:56524183 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr12:56527949 G>A maps to NM_001184796.1 V520V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr12:56528197 G>T maps to NM_001184796.1 E550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:56531320 G>A maps to NM_001184796.1 L669L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr7:158526570 C>T did not map to a codon.
Sequencing variant TCGA-C5-A7UC-01A-11D-A351-09 chr3:138195300 C>G maps to NM_031913.3 S864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr3:138191230 G>C maps to NM_031913.3 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr3:138178867 C>T maps to NM_031913.3 Q244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr3:138195121 G>A maps to NM_031913.3 V842V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr2:67631407 C>T maps to NM_019002.3 Q532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr19:51857781 A>G maps to NM_001014763.1 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr19:51857828 T>G maps to NM_001014763.1 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr19:44030499 C>A maps to NM_014297.3 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr19:44012174 C>T maps to NM_014297.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr19:44012025 C>G did not map to a codon.
Sequencing variant TCGA-RA-A741-01A-11D-A33O-09 chr19:44012070 G>C did not map to a codon.
Sequencing variant TCGA-C5-A7CH-01A-11D-A33O-09 chr11:128359202 G>A maps to NM_001143820.1 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr1:157062806 C>A maps to NM_001004341.2 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr17:41610667 A>G maps to NM_001079675.1 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr17:41606045 G>A maps to NM_001079675.1 F432F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr3:185766532 G>A maps to NM_004454.2 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr4:5620290 G>A maps to NM_147127.4 R874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr4:5633690 A>C maps to NM_147127.4 S513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr1:93159885 C>G maps to NM_005665.4 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:93091305 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr19:7911451 C>A maps to NM_001159944.1 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr17:74018064 C>T maps to NM_001988.2 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr2:176947125 G>C maps to NM_001080458.1 S160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A69M-01A-11D-A32I-09 chr2:176948342 C>T maps to NM_001080458.1 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr15:41476476 C>T maps to NM_152596.2 E399E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr14:69707599 G>C did not map to a codon.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr9:140260772 C>G did not map to a codon.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr9:140242525 G>A maps to NM_017820.3 A665A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:446436 G>A maps to ENST00000315013 K49K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M1-01A-11D-A18J-09 chr19:45728158 C>T maps to NM_138568.3 E139E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr7:132959805 G>A maps to NM_021807.3 E52E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr14:57699548 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr10:94675655 G>T maps to NM_019053.4 E269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr2:72719497 C>G maps to NM_015189.1 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr2:72945399 C>T maps to NM_015189.1 E167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr17:74087298 G>A maps to NM_001145297.2 Q276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr1:231472603 C>T maps to NM_175876.3 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:231472833 G>A maps to NM_175876.3 Q220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr3:38583287 C>T maps to ENST00000358249 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr3:38565707 C>G maps to NM_005107.3 S321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr1:11141201 G>A maps to NM_001001998.1 R458R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:11141159 C>G maps to NM_001001998.1 R472R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr11:108380359 G>A maps to NM_015065.2 I1958I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr8:118825164 G>A maps to NM_000127.2 I556I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr8:28574931 C>T maps to NM_001440.2 F452F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr8:72128978 G>A maps to NM_000503.4 F436F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AX-01A-12D-A243-09 chr8:72129213 G>A maps to NM_000503.4 N395N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr20:45618726 C>T maps to ENST00000360649 D31D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr20:45607193 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr1:28415060 G>C did not map to a codon.
Sequencing variant TCGA-EX-A69M-01A-11D-A32I-09 chr6:133777754 A>G maps to ENST00000452339 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr6:65301415 G>A maps to ENST00000370616 F1448F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr6:64498953 C>T maps to ENST00000370616 L2525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr17:40880970 C>G did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr17:40857135 C>T maps to ENST00000264646 K638K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr7:148513786 C>T maps to NM_004456.3 K498K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr5:176832360 G>A maps to NM_000505.3 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr5:176830338 G>A maps to NM_000505.3 Q483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr5:176830383 G>A maps to NM_000505.3 Q468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr6:6174945 G>T maps to NM_000129.3 I538I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:94996027 C>T maps to NM_001993.4 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr1:169509974 G>T maps to ENST00000367796 L1456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:169512259 C>A maps to ENST00000367796 E695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr23:154158427 T>A did not map to a codon.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr23:154158443 G>T did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:154066023 A>G did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr23:154066020 G>C did not map to a codon.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr23:154066004 G>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:154156996 C>A did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:154175985 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:154221308 G>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:154159333 C>G did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:154115558 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:154115606 C>G did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:138643723 C>T did not map to a codon.
Sequencing variant TCGA-EA-A556-01A-11D-A26G-09 chr23:138633354 C>A did not map to a codon.
Sequencing variant TCGA-LP-A5U3-01A-11D-A28B-09 chr23:138633229 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr23:57405213 C>G did not map to a codon.
Sequencing variant TCGA-MY-A5BE-01A-21D-A26G-09 chr23:57405195 C>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr8:82391025 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2R9-01A-11D-A18J-09 chr11:70049619 G>T maps to NM_003824.3 E19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr11:61574163 G>T maps to NM_013402.4 Y316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr17:72878726 G>A maps to ENST00000310226 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr17:72889642 C>T maps to ENST00000310226 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A5XV-01A-11D-A28B-09 chr1:51032843 G>T maps to NM_007051.2 C391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr2:96071356 G>A maps to NM_016044.2 Q17Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr2:97749842 C>G did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr2:97747858 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr1:207078187 A>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr5:14609092 G>A maps to NM_019018.2 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr5:14601466 C>T maps to NM_019018.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:58612840 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr10:14816479 G>A maps to NM_031453.2 G61G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-C5-A1ML-01A-11D-A14W-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr11:58919991 C>A maps to NM_198847.2 S284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr4:38916591 C>T maps to NM_138389.2 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr5:153372601 G>C maps to ENST00000442256 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr17:47795076 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr17:47797792 G>A maps to NM_030802.3 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr2:203622078 A>G maps to NM_173511.3 T416T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr9:96289483 C>G maps to ENST00000333936 S517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr6:170627029 C>T maps to NM_032448.1 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr6:170627052 C>A maps to NM_032448.1 S192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr23:54161358 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73Q-01A-21D-A32I-09 chr9:71395259 G>A maps to NM_138333.3 R60R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:133923620 G>C did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:133931209 C>T did not map to a codon.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr23:133922793 G>A did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr23:133941541 C>A did not map to a codon.
Sequencing variant TCGA-FU-A3TQ-01A-11D-A22X-09 chr23:133941587 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr7:22985679 G>C maps to NM_032581.3 S365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr2:201846252 G>A maps to NM_173822.3 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QE-01A-21D-A21Q-09 chr23:134166457 G>A did not map to a codon.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr1:184764869 G>C maps to NM_052966.2 L676L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr3:184055356 G>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:16384779 G>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q8-01A-11D-A21Q-09 chr1:1177984 C>T maps to NM_001014980.1 G284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr23:92964578 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:92964552 G>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:92965018 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr8:139163663 C>T maps to NM_015912.3 E1018E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr2:70528852 C>G maps to ENST00000430566 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:89941645 G>C maps to NM_014883.2 S131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr4:89702329 G>A maps to NM_014883.2 Q482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr5:137292183 G>A maps to NM_001101801.1 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M1-01A-11D-A18J-09 chr5:137323273 C>A maps to NM_016603.2 E308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr8:53447150 T>C did not map to a codon.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr1:55075435 G>C maps to NM_176782.2 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr5:175520228 G>A maps to NM_001079529.2 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RE-01A-11D-A18J-09 chr5:175558736 G>A did not map to a codon.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr5:177480915 T>G did not map to a codon.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr15:82564164 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr13:108518439 C>A maps to NM_001080396.2 E169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R1-01A-11D-A28B-09 chr23:68749615 C>A did not map to a codon.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr23:68749582 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr11:6232576 G>C did not map to a codon.
Sequencing variant TCGA-EA-A5ZE-01A-11D-A28B-09 chr11:6239971 G>A maps to NM_032127.3 H431H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr8:21958968 C>G maps to NM_022749.5 P545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:179782209 G>C did not map to a codon.
Sequencing variant TCGA-EA-A50E-01A-21D-A26G-09 chr10:15255633 C>T maps to NM_001010924.1 A651A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A78R-01A-11D-A32I-09 chr10:15290683 C>T maps to NM_001010924.1 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr10:15290719 G>T maps to NM_001010924.1 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr10:15255564 G>A maps to NM_001010924.1 N674N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R1-01A-11D-A28B-09 chr15:93162637 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A5R1-01A-11D-A28B-09 chr15:93277232 C>T did not map to a codon.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr14:35546372 T>C maps to NM_173607.3 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr10:102675790 C>G maps to NM_001136123.1 S59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr10:102685752 G>A maps to NM_001136123.1 V673V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A3LQ-01A-21D-A21Q-09 chr2:97637862 C>T maps to ENST00000417561 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr2:29225480 G>C maps to NM_199280.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr14:45432170 C>T maps to ENST00000361462 Q183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr11:47609700 C>T maps to ENST00000356737 H130H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr14:94391700 G>A maps to NM_138344.3 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr6:119327697 G>A maps to NM_024581.4 Q577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr6:119297140 G>A maps to NM_024581.4 Q842*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr12:49994423 C>T maps to NM_032130.2 E333E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr15:29861725 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr15:29443941 G>A maps to NM_015307.1 Q209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr15:29418551 G>A maps to NM_015307.1 G382G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:155220085 G>A maps to ENST00000368370 I498I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr5:176959529 G>A maps to ENST00000442143 R397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr3:150384693 T>C maps to NM_152394.3 K536K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr3:150396311 G>A maps to NM_152394.3 Q381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr4:159092076 G>A maps to NM_001128424.1 Q151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr4:159048576 T>C maps to NM_001128424.1 V514V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr23:103430824 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:103434444 G>C did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr22:49145892 C>T did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:66538871 C>T maps to NM_017565.3 K297K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:179033475 G>A maps to NM_014864.3 K261K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr10:51889697 G>T maps to NM_001005751.1 E1203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr6:116875493 C>T maps to ENST00000368596 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3WB-01A-11D-A22X-09 chr23:153741233 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr10:120893114 C>A did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr1:27332977 G>A maps to NM_052943.3 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A6QX-01A-12D-A33O-09 chr1:27332617 C>T maps to NM_052943.3 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:79698857 G>T did not map to a codon.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr23:34148720 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr23:34149540 C>T did not map to a codon.
Sequencing variant TCGA-C5-A2LS-01A-22D-A22X-09 chr23:34149764 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:34148612 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VK-01A-11D-A28B-09 chr23:34148843 G>C did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr23:34961356 C>A did not map to a codon.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr23:34962464 C>G did not map to a codon.
Sequencing variant TCGA-EX-A449-01A-11D-A243-09 chr23:34961910 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:34962238 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr23:37026575 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr23:37027104 T>A did not map to a codon.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr23:37027641 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:37027434 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:37028025 T>C did not map to a codon.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr23:37027058 G>A did not map to a codon.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr23:37028658 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr23:37027933 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr2:16742801 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr8:130864411 G>C maps to NM_016623.3 S210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr8:130883698 C>T maps to NM_016623.3 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WH-01A-22D-A351-09 chr23:153677567 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr23:153674232 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:153678637 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr5:137673982 C>T did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:643788 C>T maps to NM_024792.1 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr23:152858019 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr1:177226387 A>T maps to NM_021165.2 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A3LQ-01A-21D-A21Q-09 chr1:177250920 G>A did not map to a codon.
Sequencing variant TCGA-DS-A3LQ-01A-21D-A21Q-09 chr1:190233993 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr1:190066939 A>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:150974869 G>C maps to NM_001163258.1 S123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr15:59080148 G>A maps to NM_001040450.1 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr15:59064304 C>T maps to NM_001040450.1 F237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2GZ-01A-11D-A17W-09 chr6:25042095 C>T did not map to a codon.
Sequencing variant TCGA-EX-A69M-01A-11D-A32I-09 chr6:25042140 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr6:24873920 G>A maps to NM_014722.2 Q70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr20:49226184 G>A maps to NM_080829.2 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A5XV-01A-11D-A28B-09 chr1:93309451 G>A maps to NM_001006605.3 Q259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:93309605 C>T maps to NM_001006605.3 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr18:72114128 G>A maps to NM_001044369.2 Y196Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr18:72114011 G>A maps to NM_001044369.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:212799757 G>A maps to NM_153606.3 W513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:78245411 G>A maps to NM_198549.2 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A44S-01A-12D-A26G-09 chr9:131804534 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LC-01A-11D-A20U-09 chr9:134134558 C>T did not map to a codon.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr9:134134487 G>C did not map to a codon.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr9:134134542 G>C did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr5:94764305 G>C did not map to a codon.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr8:124219597 C>T maps to NM_032899.4 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr20:33875237 G>A maps to NM_178468.4 R448R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr20:33875248 G>A maps to NM_178468.4 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr19:49116503 G>A maps to NM_017708.3 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr17:18907092 G>A maps to NM_001039999.2 Q88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr17:18907092 G>A maps to NM_001039999.2 Q88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr8:127569295 G>C maps to NM_174911.4 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr8:12041094 T>G did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr8:12040404 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr8:124797867 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr15:64385877 G>A maps to NM_032231.4 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr2:33820589 G>A maps to ENST00000395190 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr23:8764328 C>G did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:8761787 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr23:8995966 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:13061279 C>T did not map to a codon.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr16:89865581 C>T maps to NM_000135.2 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr16:89849302 G>C maps to NM_000135.2 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R1-01A-11D-A28B-09 chr16:89849268 C>A maps to NM_000135.2 E542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr23:14862066 G>C did not map to a codon.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr23:14883160 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr23:14863269 T>C did not map to a codon.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr23:14863134 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VG-01A-11D-A28B-09 chr9:98009762 A>G maps to NM_000136.2 I67I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr3:10142945 G>C maps to NM_001018115.1 *1452Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr3:10074514 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr2:163031422 G>A maps to NM_004460.2 F641F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr2:163051247 G>A maps to NM_004460.2 I471I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:163070561 G>A maps to NM_004460.2 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr12:29449987 C>T maps to NM_018099.3 Q134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr13:99101830 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr2:242350462 G>A maps to NM_014808.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A44S-01A-12D-A26G-09 chr2:242430485 G>T maps to NM_014808.2 E839*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr2:242407697 G>A maps to NM_014808.2 L679L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73Q-01A-21D-A32I-09 chr6:5368820 C>G maps to NM_006567.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr19:13033633 C>T maps to NM_004461.2 Q485Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr17:80040793 C>T maps to NM_004104.4 R1921R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr17:80042557 C>G maps to NM_004104.4 V1533V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr17:80043492 G>C maps to NM_004104.4 L1329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr17:80040814 C>T maps to NM_004104.4 L1914L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RA-A741-01A-11D-A33O-09 chr20:3128326 C>A maps to NM_021826.4 E464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr4:187629359 G>C maps to ENST00000260147 S541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr4:187540002 G>A maps to ENST00000260147 F2582F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QS-01A-61D-A22X-09 chr4:187540390 G>C maps to ENST00000260147 S2453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A78R-01A-11D-A32I-09 chr4:187527310 G>A maps to ENST00000260147 V3424V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr4:187525000 G>C maps to ENST00000260147 S3563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr4:187527349 G>A maps to ENST00000260147 L3411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr4:187542655 G>C maps to ENST00000260147 S1698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr5:150914119 G>A maps to NM_001447.2 R3093*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:150932739 G>C maps to NM_001447.2 S1385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr5:150923211 C>T maps to NM_001447.2 E2492E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr5:150947185 G>C maps to NM_001447.2 S436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr5:150946709 G>A maps to NM_001447.2 Q595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr5:150928859 C>T maps to NM_001447.2 L1595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr5:150932739 G>C maps to NM_001447.2 S1385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr11:92088451 T>C maps to ENST00000298047 I1058I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr11:92087286 C>A maps to ENST00000298047 S670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M1-01A-11D-A18J-09 chr4:126372316 A>G maps to NM_024582.4 R3382R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr4:126238992 C>G maps to NM_024582.4 S476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A449-01A-11D-A243-09 chr4:126408723 A>G maps to NM_024582.4 G4347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr4:126373321 C>T maps to NM_024582.4 L3717L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HM-A4S6-01A-11D-A26G-09 chr4:126369916 C>T maps to NM_024582.4 V2582V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr4:126411500 C>T maps to NM_024582.4 I4508I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr4:126337604 G>A maps to NM_024582.4 V2282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr4:126241222 A>T maps to NM_024582.4 I1219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73Q-01A-21D-A32I-09 chr4:126411465 G>T maps to NM_024582.4 E4497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr23:150884627 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr23:150889971 C>T did not map to a codon.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr17:73919312 C>A maps to ENST00000389570 E446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:16111164 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr22:45996324 G>C maps to ENST00000348697 *704S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr3:13612025 G>A maps to NM_001165035.1 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:13669377 C>T maps to NM_001165035.1 F826F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M1-01A-11D-A18J-09 chr2:112933424 C>G did not map to a codon.
Sequencing variant TCGA-EA-A556-01A-11D-A26G-09 chr15:48760654 G>A maps to NM_000138.4 D1512D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr15:48779634 C>T did not map to a codon.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr5:127866339 G>A maps to NM_001999.3 N128N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr5:127613632 G>T maps to NM_001999.3 G2470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr5:127686698 T>C did not map to a codon.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr19:8182453 C>G maps to NM_032447.3 L1119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr19:8182453 C>T maps to NM_032447.3 L1119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr19:8188851 A>G maps to NM_032447.3 D924D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr9:97369153 G>A maps to NM_001127628.1 Y216Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HR-01A-11D-A20U-09 chr7:102604085 C>T maps to NM_145032.3 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr16:745767 G>A maps to NM_153350.3 I263I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr16:744328 G>A maps to NM_153350.3 P462P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HR-01A-11D-A20U-09 chr17:37557640 C>T maps to NM_032875.2 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr17:37499486 G>C maps to NM_032875.2 S17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr17:37421663 G>A maps to NM_032875.2 R326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr15:63893569 G>C maps to NM_203373.2 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr13:77581723 G>A maps to NM_012158.2 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr9:37537856 C>T maps to NM_012166.2 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:48050302 G>C maps to NM_001190274.1 S532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr18:71790642 G>A maps to NM_001142958.1 F366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr18:71793245 G>A maps to NM_001142958.1 F292F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr8:28218598 G>A maps to NM_018660.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73Q-01A-21D-A32I-09 chr8:28314369 G>T maps to NM_172366.2 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr10:5945068 C>T maps to NM_032807.3 Q81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr10:5963483 C>T maps to NM_032807.3 A809A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HG-A2PA-01A-11D-A20U-09 chr10:5957375 G>A maps to NM_032807.3 K520K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr15:76209602 C>T maps to NM_147188.2 Q166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:100189464 C>T maps to NM_012172.4 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr7:100193256 C>T maps to NM_012172.4 I416I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr11:33795772 C>T did not map to a codon.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr6:146125681 G>T maps to NM_032145.4 V620V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr16:87364920 G>A maps to NM_024735.3 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr14:55738157 T>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr14:55817885 G>T maps to NM_152231.1 E260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr17:6683543 G>C maps to NM_153230.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CH-01A-11D-A33O-09 chr2:73495990 C>A maps to ENST00000295133 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A78R-01A-11D-A32I-09 chr8:101146589 C>A maps to NM_001029860.3 G559G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr8:101154310 G>C maps to NM_001029860.3 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr3:196304664 C>T maps to NM_001105573.1 N220N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr3:196311047 T>A maps to NM_001105573.1 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:46215970 G>A maps to NM_001080469.1 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:37099096 G>A maps to NM_001008777.2 F339F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr5:171299925 G>A maps to NM_012300.2 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr3:48423301 C>T maps to NM_207102.2 F366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PI-01A-11D-A18J-09 chr9:123540629 C>T maps to NM_012164.3 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr9:123555326 C>T did not map to a codon.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr10:103427676 G>A maps to ENST00000331272 R246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr9:139838385 G>A maps to NM_018998.2 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr4:153244184 G>T maps to NM_033632.2 R658R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CG-01A-11D-A32I-09 chr4:153268137 G>A maps to NM_033632.2 R224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr4:153247244 A>T maps to NM_033632.2 Y519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A50E-01A-21D-A26G-09 chr4:153253769 C>T maps to NM_033632.2 W321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr4:153251906 G>A maps to NM_033632.2 R367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr4:153247279 G>A maps to NM_033632.2 Q508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr12:117402549 C>T maps to NM_153348.2 Y242Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr19:12800191 G>C maps to ENST00000380339 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:12800030 C>T maps to ENST00000380339 *489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr1:161189037 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr14:75182713 C>T maps to NM_015962.4 H68H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr19:40398399 G>A maps to NM_003890.2 F2189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr19:40380154 G>A maps to NM_003890.2 F3720F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LS-01A-22D-A22X-09 chr19:40382451 C>T maps to NM_003890.2 A3478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr19:40402409 G>A maps to NM_003890.2 G1663G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr19:40421394 C>T maps to NM_003890.2 P842P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr19:40362850 G>A maps to NM_003890.2 F5073F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr19:40366169 C>T maps to NM_003890.2 A4688A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr19:40368435 G>A maps to NM_003890.2 F4304F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr19:40421421 G>A maps to NM_003890.2 V833V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73Q-01A-21D-A32I-09 chr19:40357709 G>T maps to NM_003890.2 S5201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr1:149755774 C>G maps to NM_000566.3 S90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr1:120928570 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:161487971 G>T did not map to a codon.
Sequencing variant TCGA-DS-A7WH-01A-22D-A351-09 chr19:50028010 G>A maps to NM_004107.4 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr19:50027767 C>A maps to NM_004107.4 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr5:72332991 G>A maps to NM_138782.2 K288K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr5:141021032 A>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr5:141020661 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr11:72554397 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr9:137801745 G>A maps to NM_002003.3 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:27700641 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr1:157789794 A>G did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr1:157776817 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr1:157769849 G>T maps to NM_052938.4 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr1:157776888 C>A did not map to a codon.
Sequencing variant TCGA-HG-A2PA-01A-11D-A20U-09 chr1:157767999 G>T maps to NM_052938.4 T355T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:157773647 C>T maps to NM_052938.4 Q102Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr1:157737270 G>A maps to NM_030764.3 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:157490281 G>A maps to NM_031281.2 L857L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:157512837 C>A maps to NM_031281.2 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr1:161680546 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:161680321 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr1:155288072 C>G maps to NM_001135821.1 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:155288526 C>T maps to NM_001135821.1 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr11:111746779 C>T maps to NM_138378.1 E247E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr11:111749419 G>A maps to ENST00000428306 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr15:68582994 C>T maps to NM_015322.3 V433V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr15:68582019 C>A maps to NM_015322.3 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LS-01A-22D-A22X-09 chr11:61563300 C>G maps to NM_004111.4 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr11:61563333 G>A maps to NM_004111.4 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr5:108281857 G>T maps to NM_005246.2 E422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr8:125078703 G>A maps to NM_001039112.2 R1197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr8:124998375 G>A maps to NM_001039112.2 R493R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr8:125131949 C>G maps to NM_001039112.2 L1831L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr8:125131973 C>T maps to NM_001039112.2 V1839V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr8:125035754 C>T maps to NM_001039112.2 I735I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HG-A2PA-01A-11D-A20U-09 chr8:125025690 G>A maps to NM_001039112.2 V614V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr8:124968230 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr7:19184565 G>A maps to NM_152898.2 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3WB-01A-11D-A22X-09 chr7:19184751 C>T maps to NM_152898.2 E78E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AX-01A-12D-A243-09 chr7:19184751 C>T maps to NM_152898.2 E78E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr20:6088187 C>T maps to NM_017671.4 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RA-A741-01A-11D-A33O-09 chr20:6057199 C>T did not map to a codon.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr14:53324532 T>G did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr14:53324869 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr14:53327240 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr11:63990962 G>C maps to NM_178443.2 *668S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:63990555 C>T maps to NM_178443.2 I573I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr11:63986824 C>T maps to NM_178443.2 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr15:91428289 C>T maps to NM_002005.3 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr15:91428561 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr15:91437205 C>T maps to NM_002005.3 I748I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:186358434 G>C maps to NM_014375.2 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr11:125315968 G>A did not map to a codon.
Sequencing variant TCGA-JW-A69B-01A-11D-A32I-09 chr11:125351441 G>T maps to NM_005103.4 C133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr7:121943726 G>T maps to NM_001024613.2 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr7:121942386 C>T maps to NM_001024613.2 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LB-01A-11D-A243-09 chr3:62357288 G>T maps to NM_018008.3 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr19:35850070 C>T maps to NM_005304.3 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A44S-01A-12D-A26G-09 chr23:54472597 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:54497875 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr6:36979600 C>T maps to NM_173558.3 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr9:95776210 G>C maps to NM_033086.2 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr3:14862554 G>A maps to NM_152536.3 L659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RA-A741-01A-11D-A33O-09 chr3:14861276 G>T maps to NM_152536.3 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr12:95604510 G>C maps to NM_018351.3 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr3:191888292 C>T maps to NM_021032.4 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr13:102520946 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RE-01A-11D-A18J-09 chr5:170876247 C>T maps to NM_003862.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RL-01A-11D-A18J-09 chr8:16859520 G>A maps to NM_019851.2 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr19:49259544 C>T maps to NM_019113.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr19:49260186 C>G maps to NM_019113.2 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr11:69625366 C>T maps to NM_005247.2 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr4:81208211 G>C did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr4:81189521 A>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr12:4554442 G>C maps to NM_020996.1 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr10:103534605 G>A maps to NM_033163.3 Q74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RA-A741-01A-11D-A33O-09 chr10:103530217 G>T maps to NM_033163.3 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr13:22275847 A>G did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr13:22275733 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr4:1807848 C>T maps to NM_000142.4 F636F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr4:1803223 C>T maps to NM_000142.4 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr3:59737841 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr23:135291509 G>A did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr23:135289173 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2R9-01A-11D-A18J-09 chr1:38471150 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr16:67271210 C>T maps to NM_013241.2 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr16:67265246 G>A maps to NM_013241.2 S837S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr16:67264117 G>C maps to NM_013241.2 S1022*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr18:34339098 G>T did not map to a codon.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr6:110146302 G>A maps to NM_014845.5 S853S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:15376223 G>T did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr2:164467450 G>A maps to NM_018086.2 G297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr6:76023429 C>T maps to NM_015687.2 L706L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr6:76022901 G>A maps to NM_015687.2 I882I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr6:76124533 G>C maps to NM_015687.2 S52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr6:76072463 G>T maps to NM_015687.2 S149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr19:56104928 G>C maps to NM_032836.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr11:35642191 C>G did not map to a codon.
Sequencing variant TCGA-FU-A3WB-01A-11D-A22X-09 chr11:35641434 C>T maps to NM_014344.3 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr9:115950805 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr9:115947058 G>C maps to ENST00000446284 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr20:1350325 A>C did not map to a codon.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr11:64010729 C>A maps to NM_057092.2 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:2908401 C>G maps to NM_002014.3 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr7:33014870 C>T maps to NM_007270.3 Q149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr6:32096555 C>T maps to NM_022110.3 K334K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr6:32096938 C>A maps to NM_022110.3 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr6:32096939 C>T maps to NM_022110.3 K206K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr9:108358964 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr9:108337406 T>C maps to NM_006731.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:154961003 G>T maps to NM_025207.4 E266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr1:152286054 G>C maps to NM_002016.1 S436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr1:152277070 G>A maps to NM_002016.1 Q3431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LC-01A-11D-A20U-09 chr1:152282255 A>G maps to NM_002016.1 D1702D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:152281156 G>A maps to NM_002016.1 Q2069*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr1:152327737 G>A maps to NM_001014342.2 Q842*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr23:153580314 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr23:153582587 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3QE-01A-21D-A21Q-09 chr23:153585974 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr23:153594729 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr23:153599550 G>C did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:153590068 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:153580008 G>A did not map to a codon.
Sequencing variant TCGA-FU-A57G-01A-11D-A26G-09 chr23:153581708 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:153581030 G>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:153582056 C>G did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:153590889 C>T did not map to a codon.
Sequencing variant TCGA-JX-A3Q8-01A-11D-A21Q-09 chr23:153589833 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr23:153579989 G>T did not map to a codon.
Sequencing variant TCGA-EA-A556-01A-11D-A26G-09 chr3:58127611 G>T maps to NM_001164317.1 E1744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr3:58109340 C>T maps to NM_001164317.1 F1216F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr7:128498543 C>T maps to NM_001458.4 V2715V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr7:128489419 G>T maps to NM_001458.4 E1663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3EO-01A-11D-A20U-09 chr7:128494889 T>C maps to NM_001458.4 G2353G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HG-A2PA-01A-11D-A20U-09 chr7:128486418 C>T maps to NM_001458.4 G1343G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr7:128475569 C>T maps to NM_001458.4 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A69B-01A-11D-A32I-09 chr7:128480701 G>A maps to NM_001458.4 T550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A410-01A-11D-A243-09 chr11:63885112 G>A maps to NM_013280.4 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr14:86092300 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr14:86092304 G>T did not map to a codon.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr14:86089522 G>A maps to NM_013231.4 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr13:28901604 G>C maps to NM_002019.4 L930L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr13:28942800 C>G did not map to a codon.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr13:28608482 G>T maps to NM_004119.2 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr13:28631599 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr5:180056291 G>A maps to NM_182925.4 R318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A44S-01A-12D-A26G-09 chr5:180041164 C>T maps to NM_182925.4 L1078L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr5:180056319 A>C maps to NM_182925.4 Y308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr16:2986311 C>G did not map to a codon.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr16:2948898 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr17:43320549 C>T maps to NM_005892.3 L692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr12:50059692 T>G did not map to a codon.
Sequencing variant TCGA-EA-A5O9-01A-11D-A28B-09 chr1:171239750 T>G did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:171244492 C>G maps to NM_002021.1 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr1:171165849 C>T maps to NM_001460.2 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:171165873 G>A maps to NM_001460.2 Q136Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:146680529 A>G maps to NM_001461.2 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:146672799 G>A maps to NM_001461.2 Q373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:146672887 G>C maps to NM_001461.2 V343V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr1:203316849 G>A maps to NM_002023.3 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr23:147025128 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr23:147026441 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr23:147010262 A>G did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:147014006 C>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:147027158 C>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:147011665 C>G did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr23:147027064 C>T did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:147090177 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr2:216272871 G>C maps to NM_212482.1 S826*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr2:216226709 G>A maps to NM_212482.1 Y2448Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:216298068 C>G maps to NM_212482.1 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr17:80706804 G>A maps to NM_022158.3 E181E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr9:132665170 G>A maps to NM_015033.2 R469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr3:171969134 C>A maps to NM_022763.3 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr3:171969125 G>A maps to NM_022763.3 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr3:172058909 G>A maps to NM_022763.3 Q620Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:33330059 C>A did not map to a codon.
Sequencing variant TCGA-C5-A2LS-01A-22D-A22X-09 chr11:49204789 A>G maps to NM_004476.1 Y277Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WF-01A-11D-A351-09 chr11:49221890 C>T maps to NM_004476.1 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HR-01A-11D-A20U-09 chr11:49204789 A>G maps to NM_004476.1 Y277Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A3L1-01A-11D-A21Q-09 chr11:49204789 A>G maps to NM_004476.1 Y277Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr11:89395389 A>G did not map to a codon.
Sequencing variant TCGA-EA-A411-01A-11D-A243-09 chr11:89392795 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr11:89392701 C>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:71903283 C>T maps to NM_016729.2 Q23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:71903324 C>G maps to NM_016729.2 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr2:28635080 C>T maps to NM_005253.3 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr20:22563210 G>A maps to NM_021784.4 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr6:1611075 C>G maps to NM_001453.2 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr1:47904448 C>T maps to NM_004474.3 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr9:117888 G>A maps to NM_207305.3 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr2:114257594 C>G maps to NM_012184.4 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr2:114257609 C>T maps to NM_012184.4 Y259Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:114257651 G>A maps to NM_012184.4 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr14:29237006 G>A maps to NM_005249.3 K174K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr8:145700623 G>A maps to NM_003923.2 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr5:169533306 G>T maps to NM_012188.4 E116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr5:169533236 G>A maps to NM_012188.4 Q92Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr5:169533236 G>A maps to NM_012188.4 Q92Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr17:74133685 G>A maps to NM_001454.3 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr17:80559591 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr17:80559806 C>G did not map to a codon.
Sequencing variant TCGA-LP-A5U3-01A-11D-A28B-09 chr16:86612400 G>A maps to NM_005250.2 E24E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr12:2968331 G>C maps to NM_202002.1 L626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr12:2968011 G>C maps to NM_202002.1 S733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr23:70321380 T>C did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:70316570 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:70320630 G>A did not map to a codon.
Sequencing variant TCGA-C5-A7X3-01A-11D-A351-09 chr3:71090576 T>A maps to NM_032682.4 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr3:71355067 G>A did not map to a codon.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr7:114329978 T>A maps to NM_148898.3 *741R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZF-01A-11D-A28B-09 chr23:49113248 G>A did not map to a codon.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr6:41555241 G>C maps to NM_001012426.1 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr6:41562606 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:55650924 G>A did not map to a codon.
Sequencing variant TCGA-JX-A3PZ-01A-11D-A21Q-09 chr23:55650326 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:55650351 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr23:55651040 G>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr22:36889850 C>T did not map to a codon.
Sequencing variant TCGA-JW-A852-01A-11D-A351-09 chr22:36886249 C>G maps to NM_001102371.1 L620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr9:130575576 C>G maps to NM_004957.4 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr19:52272801 C>T maps to NM_001005738.1 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr10:95431875 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr4:79396682 G>T maps to NM_025074.6 E2592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr4:79420975 C>T maps to NM_025074.6 Q3073*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr4:79461937 C>G maps to NM_025074.6 S3900*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3YQ-01A-11D-A22X-09 chr9:14784444 G>A maps to ENST00000380880 F1458F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr4:190882045 C>T did not map to a codon.
Sequencing variant TCGA-C5-A2LS-01A-22D-A22X-09 chr10:135439802 C>T maps to ENST00000443774 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr6:116325054 C>A maps to NM_002031.2 E151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr9:85881960 C>T maps to ENST00000328788 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr10:13743411 C>T maps to NM_018027.3 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr10:13852887 C>T maps to NM_018027.3 E44E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73R-01A-11D-A33O-09 chr10:13687646 T>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:69230519 G>C maps to NM_015123.1 S794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr3:69277539 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr15:44202143 G>C maps to NM_032892.3 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr15:44202143 G>C maps to NM_032892.3 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr14:52194512 C>T maps to ENST00000344768 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr14:52194647 G>A maps to ENST00000344768 Q590Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr10:49459668 C>A maps to NM_001018071.3 E31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr23:12734604 A>T did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr23:12736236 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LC-01A-11D-A20U-09 chr23:12734822 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:100181192 G>A maps to NM_001013660.2 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr6:41738418 G>A maps to NM_006653.3 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr13:32776659 C>T maps to NM_023037.2 F1338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr13:32776587 C>G maps to NM_023037.2 L1314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr13:32785124 C>T maps to NM_023037.2 P1515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr2:183731214 G>C maps to NM_001463.3 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A44S-01A-12D-A26G-09 chr14:44975705 G>C maps to NM_032135.3 S162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr14:44974137 G>A maps to NM_032135.3 L685L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr7:5642987 G>A maps to ENST00000340250 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr7:5643566 C>T maps to ENST00000340250 I401I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr7:5632992 C>G maps to ENST00000340250 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr17:79495604 C>T maps to NM_001077182.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr17:79503717 C>T maps to NM_001077182.2 F416F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr7:127231782 G>A did not map to a codon.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr2:49190834 C>T maps to NM_000145.3 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr2:186657506 G>T maps to NM_173651.2 E1971*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CH-01A-11D-A33O-09 chr2:186665465 T>C maps to NM_173651.2 C3900C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A44S-01A-12D-A26G-09 chr2:186670382 T>C maps to NM_173651.2 S5539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:186669522 G>T maps to NM_173651.2 E5253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr2:186655009 C>T maps to NM_173651.2 I1138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr2:186670250 C>T maps to NM_173651.2 F5495F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:681412 C>T maps to NM_005860.2 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr4:162307435 G>A maps to NM_020116.3 S669S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A852-01A-11D-A351-09 chr4:162376268 C>T maps to NM_020116.3 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R9-01A-11D-A18J-09 chr21:47570312 G>A maps to ENST00000397748 R255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr21:47558550 C>T maps to ENST00000397748 A438A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5O9-01A-11D-A28B-09 chr23:31089600 C>T did not map to a codon.
Sequencing variant TCGA-LP-A5U3-01A-11D-A28B-09 chr23:31089909 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr5:121187813 C>T maps to NM_177478.1 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr17:61904803 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr6:143816981 C>T maps to NM_032020.4 V422V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr16:70513186 C>T maps to NM_145059.2 L1012L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr23:44383367 G>C did not map to a codon.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr23:154282926 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:154279970 A>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr15:91419568 C>T maps to NM_002569.2 Q88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr19:49207014 G>T maps to NM_001097638.2 E268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr19:5844262 C>T maps to NM_001097641.1 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr19:5844385 G>A maps to NM_001097641.1 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr19:5867439 G>A maps to NM_002034.2 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr19:5867193 G>T maps to NM_002034.2 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr14:66096236 C>G maps to NM_178155.1 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr14:66208816 C>T maps to NM_178155.1 R473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr19:50314709 G>A maps to NM_025129.4 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr3:180688093 G>A maps to NM_005087.3 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr17:7495873 G>A maps to NM_004860.3 R591R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr10:43870965 G>C maps to NM_173160.2 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A0TN-01A-21D-A14W-08 chr5:39269863 A>G did not map to a codon.
Sequencing variant TCGA-C5-A2M1-01A-11D-A18J-09 chr3:46009301 G>T maps to NM_024513.2 V508V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr3:46008584 G>C maps to NM_024513.2 L747L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CJ-01A-11D-A32I-09 chr6:112041197 G>A maps to NM_153047.1 D19D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr12:130648506 G>A maps to NM_007197.3 K340K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr12:130648278 C>T maps to NM_007197.3 I264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr8:28385333 G>T maps to NM_017412.3 E353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr11:86665890 C>G maps to NM_012193.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr2:208633031 C>T maps to NM_003468.3 E144E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr10:35928929 C>T maps to NM_031866.2 Q476Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:3532041 C>G maps to NM_001136198.1 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:209849100 G>A maps to NM_015714.3 V24V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr4:76598497 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr17:41062953 C>T maps to NM_000151.2 F195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr2:169764722 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr23:153763456 G>T did not map to a codon.
Sequencing variant TCGA-Q1-A73R-01A-11D-A33O-09 chr23:153763557 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr17:78078693 C>T maps to NM_001079804.1 C103C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr17:78086485 G>T maps to NM_001079804.1 E622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr4:144359595 G>A maps to NM_207123.2 P346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr23:153941666 G>A did not map to a codon.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr23:153940974 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LB-01A-11D-A243-09 chr23:153944424 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr22:17444719 C>T did not map to a codon.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr22:17444719 C>T did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:75611122 C>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr6:29589054 A>G maps to NM_001470.2 R382R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr9:101235586 G>A maps to NM_005458.7 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AU-01A-32D-A243-09 chr1:151076067 C>G maps to NM_144618.2 S218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr5:161277834 C>T maps to NM_001127648.1 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr4:46973126 C>A maps to NM_000809.2 E283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr15:27114344 G>T did not map to a codon.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr5:161128673 G>A maps to NM_000811.2 Q419Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr5:161128680 C>T maps to NM_000811.2 R422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr5:160973754 A>G did not map to a codon.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr15:27017879 C>T maps to NM_021912.4 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr15:26866675 A>G maps to NM_021912.4 Y82Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr15:27184441 C>A did not map to a codon.
Sequencing variant TCGA-EA-A556-01A-11D-A26G-09 chr1:1961651 C>T maps to NM_000815.4 Y430Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr1:1961471 C>T maps to NM_000815.4 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:1956824 C>A maps to NM_000815.4 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7X3-01A-11D-A351-09 chr23:151123326 T>A did not map to a codon.
Sequencing variant TCGA-EK-A2R9-01A-11D-A18J-09 chr23:151121843 C>A did not map to a codon.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr23:151123463 G>A did not map to a codon.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr23:151127556 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr15:27572006 C>T maps to NM_033223.4 R108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:151821377 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:151818972 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:151818218 G>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:89895169 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr6:89974133 C>T maps to NM_002043.2 E386E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr2:171710456 C>T maps to NM_000817.2 Y446Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr2:171702014 G>A did not map to a codon.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr19:2477086 C>T maps to NM_015675.3 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr23:49173690 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr4:870334 G>A maps to NM_005255.2 T679T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr2:242743052 G>T maps to NM_022134.2 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr7:99764664 C>G maps to NM_024637.4 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VI-01A-11D-A28B-09 chr14:88452830 A>G did not map to a codon.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr17:73754154 G>T maps to ENST00000437911 A417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:73759141 G>A maps to ENST00000437911 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr16:88891255 G>A maps to NM_000512.4 G387G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr18:33267009 G>A maps to NM_020474.3 V240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr5:153755918 G>A maps to NM_198321.3 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr1:230398691 G>A maps to NM_004481.3 R418R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr2:158167844 A>G maps to NM_014568.1 K936K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr4:174169342 C>T maps to NM_017423.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr4:174242729 G>A did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr12:4848367 C>T maps to NM_017417.1 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr12:4870146 C>T maps to NM_017417.1 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr12:132811486 C>A did not map to a codon.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr4:173942727 C>G maps to NM_001034845.2 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr4:172734708 T>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr4:173150835 A>G maps to NM_001034845.2 Q56Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:74072989 C>G maps to NM_003857.2 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr17:74073163 G>A maps to NM_003857.2 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr17:74073112 C>T maps to NM_003857.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr9:34649555 G>T maps to NM_000155.2 E352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr19:1399899 G>A maps to NM_138924.1 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr11:62397702 C>T maps to NM_198335.2 W542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr15:42632032 C>T maps to NM_198141.2 I670I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr9:128112572 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr21:34883748 C>T maps to NM_001136006.1 R708R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr21:34892737 G>A maps to NM_001136006.1 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr22:29704118 C>T maps to NM_152236.1 I8I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr17:34072550 G>A maps to NM_139285.2 I655I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr17:34072388 C>G maps to NM_139285.2 L709L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QE-01A-21D-A21Q-09 chr12:100994245 C>T maps to NM_174942.1 Y35Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr12:101017745 C>G maps to NM_174942.1 S388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr13:114550996 A>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr13:114549989 G>A maps to ENST00000355761 Q23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WI-01A-12D-A351-09 chr17:9939843 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr17:9850222 G>A maps to NM_201433.1 C201C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr17:39872093 C>T maps to NM_000805.3 F92F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:48650369 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2R9-01A-11D-A18J-09 chr23:48652557 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:48649665 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr3:128200906 G>T did not map to a codon.
Sequencing variant TCGA-C5-A7CJ-01A-11D-A32I-09 chr3:128199903 G>A maps to NM_032638.4 F467F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A6QX-01A-12D-A33O-09 chr3:128199828 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:128200128 C>T maps to NM_032638.4 G392G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr15:45656203 G>T maps to ENST00000432007 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr7:99821294 G>C maps to NM_178831.6 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr7:99799677 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr22:30683472 C>T maps to ENST00000434291 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr10:104139677 G>A maps to NM_004193.2 E1614E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HR-01A-11D-A20U-09 chr10:104123067 C>T maps to NM_004193.2 G643G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr1:89521613 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:89524906 G>T did not map to a codon.
Sequencing variant TCGA-EA-A50E-01A-21D-A26G-09 chr1:89582882 A>T maps to NM_004120.3 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr1:89730575 G>A maps to NM_052942.3 V314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A6QX-01A-12D-A33O-09 chr1:89735175 C>T maps to NM_052942.3 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr1:89618014 C>G maps to NM_207398.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr2:237076491 G>A maps to NM_001485.2 Y41Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr2:237074502 C>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr2:237074606 T>G maps to NM_001485.2 R333R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr2:237074512 G>T did not map to a codon.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr7:127222898 G>T maps to NM_024523.5 A499A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr7:127222265 G>A maps to NM_024523.5 I710I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr2:109109214 C>T maps to NM_181453.3 L1472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:109087432 C>T maps to NM_181453.3 Q550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr2:109067509 C>T maps to NM_181453.3 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr2:163002165 G>A maps to ENST00000233604 H95H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr14:55313835 G>T maps to NM_001024024.1 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr2:27746300 C>T maps to NM_001486.3 Q625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr6:10621626 C>T maps to NM_145649.4 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr15:59911591 C>T maps to NM_004751.2 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr15:59910895 G>C maps to NM_004751.2 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H1-01A-11D-A17W-09 chr5:74324663 C>T maps to NM_016591.2 W400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr15:57921907 C>T maps to NM_001018090.3 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr9:74834421 C>T maps to ENST00000238018 N202N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr20:42907816 C>A maps to NM_024034.3 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr20:42907861 C>T maps to NM_024034.3 F342F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr20:42907876 C>G maps to NM_024034.3 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:118463025 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:118461267 G>A maps to NM_017686.3 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr10:48414294 G>A maps to NM_016204.1 F191F. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DR-A0ZM-01A-12D-A10S-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-EK-A3GN-01A-11D-A20U-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr20:34021778 G>A maps to NM_000557.2 F478F. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-LP-A4AW-01A-11D-A243-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-LP-A4AW-01A-11D-A243-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr8:97157726 C>A maps to NM_001001557.2 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr2:20871109 C>G maps to NM_182828.2 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:132197394 C>T maps to NM_005260.3 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr23:153670073 C>G did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:153670148 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2R9-01A-11D-A18J-09 chr23:153670140 G>T did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:69652905 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:69649619 A>C did not map to a codon.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr11:76928351 C>T maps to ENST00000376217 Q511Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr11:75154076 G>C did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr17:648333 G>A maps to NM_015721.2 F983F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr5:154272067 C>T maps to NM_015465.3 L1213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr5:154272082 C>T maps to NM_015465.3 L1208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr5:154317603 G>A maps to NM_015465.3 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HG-A2PA-01A-11D-A20U-09 chr2:39008895 C>T maps to NM_024775.9 D122D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr19:45593641 C>T maps to NM_024707.2 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:14027160 C>T did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr2:17941368 C>T maps to NM_001130009.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr7:933394 C>T maps to NM_015949.2 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr9:135865271 G>A maps to NM_004188.4 K264K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr6:13365253 G>T maps to NM_018988.2 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr2:69554096 C>T maps to ENST00000357308 V668V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr2:69575309 G>A maps to ENST00000357308 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HQ-01A-11D-A20U-09 chr5:179751885 G>A maps to NM_005110.2 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr5:179745955 G>A maps to NM_005110.2 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PI-01A-11D-A18J-09 chr10:117823974 C>G maps to NM_005264.4 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr5:137589023 G>C maps to NM_001496.3 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr5:137600193 G>C maps to NM_001496.3 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr22:38019459 G>T maps to ENST00000381756 E263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr16:23478654 C>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr16:23478640 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr17:73236103 G>T maps to NM_138619.2 S450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:85777675 A>G did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr8:63927959 C>T maps to NM_003878.2 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr22:25007113 C>T maps to NM_005265.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr22:25023583 C>G maps to NM_005265.2 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr22:25024697 C>T maps to NM_005265.2 T534T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr22:24621549 G>A maps to NM_001099781.1 R434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3YQ-01A-11D-A22X-09 chr20:33437773 C>A maps to NM_178026.2 L605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr17:40342752 G>A maps to NM_032484.4 R393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr5:42718805 C>T maps to NM_000163.2 F399F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr5:42719028 C>T maps to NM_000163.2 Q474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr11:59611400 C>T maps to NM_005142.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr7:100285843 G>C maps to NM_022574.4 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A69B-01A-11D-A32I-09 chr7:150417616 C>T maps to NM_130759.3 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr5:102423567 C>T did not map to a codon.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr16:85722473 C>A maps to NM_016095.2 E11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr16:85711931 C>T maps to NM_016095.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A4BA-01A-21D-A26G-09 chr1:78601339 C>T maps to NM_017655.4 D287D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr1:78560748 G>A maps to NM_017655.4 K180K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr19:46174546 C>T maps to NM_000164.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:121768310 G>A maps to NM_000165.3 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZE-01A-11D-A28B-09 chr6:121768442 G>T maps to NM_000165.3 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A69L-01A-11D-A32I-09 chr1:35260437 C>T maps to NM_002060.2 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr1:39341323 G>A maps to NM_030772.4 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:39340414 G>C maps to NM_030772.4 V452V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:70443860 G>C did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr1:35250431 C>T maps to NM_001005752.1 I23I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr1:35250932 C>T maps to NM_001005752.1 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WH-01A-22D-A351-09 chr1:35222960 G>A maps to NM_005268.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr13:20797328 G>C maps to NM_001110221.2 Y97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr1:228345524 C>T maps to NM_020435.2 F22F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CG-01A-11D-A32I-09 chr10:35897247 C>T maps to NM_153368.2 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr23:30712557 G>C did not map to a codon.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr23:30686130 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr4:80328007 G>A maps to NM_033214.2 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr3:141917645 C>A maps to NM_001039547.2 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr3:141884577 C>G maps to NM_001039547.2 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr9:86363352 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr23:100658842 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:100652820 C>T did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:100662882 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr3:33055754 C>T maps to NM_000404.2 W509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr3:33059990 G>C maps to NM_000404.2 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr11:134151279 G>A maps to NM_001080407.2 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr9:6534788 C>G did not map to a codon.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr9:6535984 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr9:131271284 C>G maps to NM_001003722.1 S77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr16:74503972 T>A did not map to a codon.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr16:74528656 C>A did not map to a codon.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr7:42088255 C>T maps to NM_000168.5 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr8:144356974 G>A did not map to a codon.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr12:75874743 C>T maps to NM_006851.2 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr9:36162778 T>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:54059921 C>T maps to NM_147193.2 K218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr16:4385081 C>T maps to NM_032575.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr16:4383432 A>G maps to NM_032575.2 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr16:4386903 C>T maps to NM_032575.2 G318G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr16:4387479 C>T maps to NM_032575.2 V510V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr16:4384929 C>G maps to NM_032575.2 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr9:4299596 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr9:3829393 C>A maps to NM_001042413.1 E858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VI-01A-11D-A28B-09 chr9:3827919 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr9:4125835 G>T maps to NM_001042413.1 S165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr17:685468 G>A maps to ENST00000397393 F212F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:48629374 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr6:39034010 C>T maps to NM_002062.3 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr17:9783805 C>T maps to NM_004246.1 F419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr23:14748343 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr23:14550432 C>T did not map to a codon.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr23:14627258 G>A did not map to a codon.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr4:175577899 T>C maps to NM_006529.2 S370S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr4:175644036 C>T did not map to a codon.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr23:102979866 C>A did not map to a codon.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr23:102979468 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr23:102968491 T>C did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr4:158091756 G>A maps to NM_001166060.1 K457K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr5:95158312 G>A maps to NM_002064.2 F18F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr14:96010553 G>C did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:191769882 G>A maps to NM_014905.3 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr12:56872958 C>G maps to NM_013267.2 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:56868638 G>C maps to NM_013267.2 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr12:104397060 C>A maps to NM_031302.3 E46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr12:104393267 C>G maps to NM_031302.3 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr1:1263336 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr17:4693080 C>T maps to NM_001014985.2 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:120182170 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:120182120 G>A did not map to a codon.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr23:120182356 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr1:182359684 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:182359957 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:182355305 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr1:182355366 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr11:58477547 C>T maps to NM_201648.2 Q194Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:150632827 C>T maps to NM_000405.4 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WI-01A-12D-A351-09 chr6:2116040 T>A maps to NM_001500.2 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:29018109 A>C maps to NM_006582.2 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr19:19753384 G>A maps to NM_016573.2 I21I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr19:19745467 G>T maps to NM_016573.2 I644I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr6:24784709 C>G maps to NM_015895.3 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr6:16295254 T>G maps to NM_006877.3 T292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr17:63052600 G>T maps to NM_006572.4 C37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr3:50296395 G>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr20:57428721 C>T maps to NM_080425.2 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr3:50232330 C>T maps to NM_000172.3 F332F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:110148946 G>C maps to NM_005272.3 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr1:110148666 G>A maps to NM_005272.3 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr22:19776197 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr22:19776255 G>T maps to NM_053004.2 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr22:19799873 C>G maps to NM_053004.2 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr12:6950483 G>A maps to NM_002075.2 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CJ-01A-11D-A32I-09 chr15:52418210 C>A maps to NM_016194.3 E315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr15:52472035 G>T maps to NM_016194.3 S56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr15:52416672 G>T maps to NM_016194.3 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr14:52344354 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr6:30522369 G>A maps to NM_005275.3 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr1:38061360 T>A maps to NM_013285.2 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr23:54578805 G>C did not map to a codon.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr1:231396395 G>A maps to NM_014236.3 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RL-01A-11D-A18J-09 chr1:231402066 C>T maps to NM_014236.3 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:231410859 G>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:231408082 C>T maps to NM_014236.3 F516F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr12:102159989 T>A maps to NM_024312.4 G497G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr16:1412295 C>T maps to NM_032520.4 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr16:1412896 G>T maps to NM_032520.4 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr20:3025089 C>G maps to NM_001501.1 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr12:65146510 G>A maps to ENST00000418919 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr12:65141671 G>A maps to ENST00000418919 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr9:127640715 C>T did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr9:127642417 C>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr12:133372578 G>T maps to NM_005895.3 I776I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:133365774 C>T maps to NM_005895.3 L883L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr3:37343795 G>T maps to NM_001172713.1 E425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:37284994 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr14:93282694 G>T maps to NM_005113.2 E474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HM-A3JK-01A-11D-A21Q-09 chr15:74363797 G>A maps to NM_001038640.2 T570T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr15:72954663 C>T maps to NM_018652.4 L307L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-IR-A3LK-01A-12D-A20U-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr3:121433718 C>A maps to ENST00000393667 E465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr3:121413300 T>C maps to ENST00000393667 Q2023Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr3:121383431 G>C maps to ENST00000393667 V3235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr9:88692353 G>A maps to ENST00000376023 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZE-01A-11D-A28B-09 chr9:88692497 G>A maps to ENST00000376023 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr5:32136350 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr5:32126045 G>T did not map to a codon.
Sequencing variant TCGA-DS-A7WH-01A-22D-A351-09 chr12:21668830 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:21668696 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr1:155753849 C>A maps to ENST00000368331 E607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr1:155754391 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr1:155755145 C>T maps to ENST00000368331 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H6-01B-11D-A22X-09 chr1:155735536 G>A maps to ENST00000368331 Q1243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:155733121 C>T maps to ENST00000368331 E1569E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:155823270 G>A maps to ENST00000368331 Q101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:155735228 A>G maps to ENST00000368331 C1345C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr1:155785974 G>C did not map to a codon.
Sequencing variant TCGA-FU-A3EO-01A-11D-A20U-09 chr6:117888188 C>T maps to NM_020399.3 E362E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:171786163 C>G did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr17:45102044 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr3:194117595 G>A maps to NM_004488.2 C472C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QE-01A-21D-A21Q-09 chr19:55543645 C>T maps to NM_001083899.1 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr8:145139175 C>T maps to NM_003801.3 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr8:145139651 C>G maps to NM_003801.3 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr10:113928263 G>A maps to NM_020918.4 R305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:96698049 G>A maps to NM_207328.2 R20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr19:33587165 C>T maps to NM_018025.2 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr1:217688210 C>A maps to NM_018040.2 V373V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr17:42475271 G>A maps to NM_001002909.2 I1391I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr17:42477227 G>A maps to NM_001002909.2 G739G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr17:42477648 G>C maps to NM_001002909.2 S599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr17:42478740 G>C maps to NM_001002909.2 S235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:46124623 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr7:99774885 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr23:132833992 G>A did not map to a codon.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr23:132730621 C>T did not map to a codon.
Sequencing variant TCGA-DG-A2KH-01A-21D-A22X-09 chr23:132548980 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr13:93518568 G>A maps to NM_004466.4 K532K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr13:94958239 C>T maps to NM_005708.3 Q339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr3:32207341 C>T maps to NM_015141.3 Y332Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr14:66976011 C>G did not map to a codon.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr19:34857701 C>T maps to NM_000175.3 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZE-01A-11D-A28B-09 chr19:34859588 G>A maps to NM_000175.3 K128K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr23:48976098 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr23:48979985 C>T did not map to a codon.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr23:48972639 G>A did not map to a codon.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr23:48973410 C>A did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:48976167 C>A did not map to a codon.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr6:24447151 G>A maps to NM_001503.2 S578S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr23:13803801 C>T did not map to a codon.
Alternatively spliced codon TCGA-Q1-A73Q-01A-21D-A32I-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr23:136113038 C>T did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:136113006 C>G did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr23:136112350 C>T did not map to a codon.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr9:132862906 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr6:46967978 G>A maps to ENST00000283297 Q906*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LB-01A-11D-A243-09 chr6:46967926 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr6:47646845 T>C maps to NM_153839.6 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr6:47645598 G>A maps to NM_153839.6 E31E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr6:47649620 G>A maps to NM_153839.6 E374E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr6:47650136 C>T maps to NM_153839.6 I546I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr23:135429207 A>G did not map to a codon.
Sequencing variant TCGA-C5-A2M1-01A-11D-A18J-09 chr23:135431358 T>A did not map to a codon.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr23:135430287 A>C did not map to a codon.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr23:135428589 A>T did not map to a codon.
Sequencing variant TCGA-EA-A5ZE-01A-11D-A28B-09 chr23:135426994 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr23:135431677 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:135488007 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr23:135480159 C>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:135405382 A>C did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:135435502 C>A did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:135391003 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:135405121 G>C did not map to a codon.
Sequencing variant TCGA-EA-A6QX-01A-12D-A33O-09 chr2:26534372 G>T maps to NM_001145168.1 A741A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr2:26532886 G>A maps to NM_001145168.1 L1055L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:57601500 C>T maps to ENST00000349457 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HQ-01A-11D-A20U-09 chr6:47682097 G>T maps to NM_153838.3 E373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr10:134942342 G>A maps to ENST00000368577 A877A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr8:37697139 G>A maps to NM_032777.9 A837A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr8:37696478 G>C maps to NM_032777.9 L755L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QE-01A-21D-A21Q-09 chr4:22437052 G>A maps to NM_145290.2 R442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A69L-01A-11D-A32I-09 chr4:22415239 C>T maps to NM_145290.2 V669V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr4:22403110 G>A maps to NM_145290.2 T808T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr6:142691546 C>G maps to NM_198569.2 S229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr3:100413634 G>A maps to NM_032787.2 Q728Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R1-01A-11D-A28B-09 chr3:100364820 C>T maps to NM_032787.2 Q327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M1-01A-11D-A18J-09 chr14:105517705 G>C maps to NM_013345.2 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr12:131471835 C>T maps to NM_198827.3 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr12:131623877 C>A did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr11:64055562 G>A maps to NM_001170726.1 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr17:72368288 C>G maps to ENST00000440684 L1276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr17:72365730 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr23:9727433 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:9693817 C>G did not map to a codon.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr23:9727433 G>A did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr11:67219208 C>T maps to NM_206997.1 E329E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr11:67219820 G>C maps to NM_206997.1 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr1:6313807 G>T maps to NM_207370.2 I252I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr1:6311455 G>C maps to NM_207370.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr1:6314905 G>C maps to NM_207370.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr2:175311386 C>T maps to NM_152529.5 L655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr2:175338009 G>A maps to NM_152529.5 N181N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr3:119892197 C>T maps to NM_153002.2 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr3:119900016 G>T maps to NM_153002.2 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr3:119886580 G>A maps to NM_153002.2 F581F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr10:25464454 C>T maps to NM_020752.2 R36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr10:25887398 T>G maps to NM_020752.2 S948S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr12:6933900 C>G maps to NM_019858.1 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr2:128409566 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73S-01A-11D-A33O-09 chr2:128409330 C>T did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr23:53106337 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr23:53106075 C>G did not map to a codon.
Sequencing variant TCGA-LP-A5U3-01A-11D-A28B-09 chr23:53106805 G>A did not map to a codon.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr23:78426932 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:78426873 T>G did not map to a codon.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr23:78426970 G>C did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr15:40099334 G>A maps to NM_007223.1 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CJ-01A-11D-A32I-09 chr17:36482458 C>T maps to ENST00000398597 Q2332Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr17:36484588 C>T maps to ENST00000398597 E1622E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr17:36486799 C>G maps to ENST00000398597 R885R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr17:36482658 C>A maps to ENST00000398597 E2266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr17:36499399 G>C maps to ENST00000398597 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr17:36499123 C>T maps to ENST00000398597 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RA-A741-01A-11D-A33O-09 chr17:36484665 C>A maps to ENST00000398597 E1597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr12:12815010 G>C maps to NM_006143.2 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr8:142367297 G>A maps to NM_005293.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HG-A2PA-01A-11D-A20U-09 chr1:27720958 C>T maps to NM_005281.2 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr6:167570452 G>A maps to NM_005299.2 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr6:167570419 G>C maps to NM_005299.2 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:41555199 T>G did not map to a codon.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr2:241569401 C>T maps to NM_001195381.1 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr7:124404619 C>T maps to NM_005302.2 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr2:133174896 C>T maps to NM_001508.2 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr19:46094536 G>C maps to NM_005282.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A411-01A-11D-A243-09 chr2:105858467 C>A maps to NM_007227.3 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZF-01A-11D-A28B-09 chr2:105858749 G>A maps to NM_007227.3 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A770-01A-11D-A33O-09 chr23:150348925 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr23:150349572 C>T did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr23:150348748 G>A did not map to a codon.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr1:174417842 C>T maps to NM_005684.4 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:19049107 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr23:19032053 T>C did not map to a codon.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr23:19024192 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr23:19046341 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:19017236 C>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:19021126 C>G did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr14:88477989 C>T maps to NM_003608.3 R267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr14:88477739 C>G maps to NM_003608.3 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr14:91701265 G>C maps to ENST00000238699 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HM-A4S6-01A-11D-A26G-09 chr14:91701058 G>C maps to ENST00000238699 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr4:8583011 C>T maps to NM_080819.2 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr4:8584564 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr16:57712221 C>T maps to NM_170776.4 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr5:90449159 G>A maps to NM_032119.3 L6249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr5:90055299 G>A maps to NM_032119.3 L4005L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:101909940 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr23:101910558 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr23:101911352 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr23:101909233 A>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:101911363 C>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:101909940 C>T did not map to a codon.
Sequencing variant TCGA-LP-A5U3-01A-11D-A28B-09 chr23:101910192 C>T did not map to a codon.
Sequencing variant TCGA-MY-A5BE-01A-21D-A26G-09 chr23:101911752 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr23:101911586 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr23:101970440 G>C did not map to a codon.
Sequencing variant TCGA-EX-A1H6-01B-11D-A22X-09 chr23:101970962 C>T did not map to a codon.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr23:101971103 G>C did not map to a codon.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr12:13061821 C>T maps to NM_003979.3 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr16:19884104 G>A maps to NM_016235.1 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr4:90169398 C>T maps to NM_198281.2 K621K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr4:90169500 C>T maps to NM_198281.2 K587K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr17:80011072 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr17:80014955 G>T maps to NM_212492.1 E513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr8:145730015 C>T maps to NM_005309.2 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr16:46943726 C>T maps to NM_133443.2 D236D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr16:46918770 C>T maps to NM_133443.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:53072634 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:53072634 C>T did not map to a codon.
Sequencing variant TCGA-LP-A4AU-01A-32D-A243-09 chr1:53072513 G>A maps to NM_015696.4 E99E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr5:54456008 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2R9-01A-11D-A18J-09 chr5:54460614 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr15:72454717 C>T maps to NM_001012642.2 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A0TN-01A-21D-A14W-08 chr12:52408604 C>T maps to NM_181711.2 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr2:165349468 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr2:11718522 G>A maps to NM_014668.3 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr1:240656727 C>T maps to NM_022469.3 V16V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr1:24668627 G>C maps to NM_021180.3 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:24664501 C>T maps to NM_021180.3 F292F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr5:153144152 C>T maps to NM_001114183.1 Y661Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr4:158257848 C>T maps to NM_000826.3 L598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr23:122551677 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr23:122387319 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr23:122319786 G>A did not map to a codon.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr23:122532562 A>G did not map to a codon.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr23:122538636 C>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:122387268 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:122387376 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A6DV-01A-11D-A32I-09 chr23:122336539 T>C did not map to a codon.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr23:122336582 C>A did not map to a codon.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr23:122387168 C>T did not map to a codon.
Sequencing variant TCGA-C5-A7CG-01A-11D-A32I-09 chr10:87484145 G>A maps to NM_017551.2 S607S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr10:87898650 C>G maps to NM_017551.2 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr10:87898608 G>A maps to NM_017551.2 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr4:93225801 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr4:94006334 C>G maps to NM_001510.2 S145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr21:30961185 G>A maps to ENST00000327783 N514N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr1:37271867 C>A maps to NM_000831.3 A717A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:120776192 G>C maps to NM_014619.2 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr11:120776102 C>G maps to NM_014619.2 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr11:120769287 C>A maps to NM_014619.2 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr11:120702684 C>T maps to NM_014619.2 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2GZ-01A-11D-A17W-09 chr19:42507725 C>T maps to NM_002088.3 E791E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr19:42569372 A>G did not map to a codon.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr19:42558572 G>A maps to NM_002088.3 R319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr19:42526473 G>A maps to NM_002088.3 I502I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr9:140053107 C>T maps to ENST00000371546 G404G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr9:140051345 G>A maps to ENST00000371546 K296K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr9:140033985 C>T maps to ENST00000371546 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr16:9858382 C>T maps to NM_000833.3 A1006A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZE-01A-11D-A28B-09 chr16:9916230 A>G maps to NM_000833.3 P686P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PI-01A-11D-A18J-09 chr16:9862722 G>C maps to NM_000833.3 L860L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr16:9858727 C>T maps to NM_000833.3 Q891Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr16:9916128 C>T maps to NM_000833.3 L720L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr12:13717246 C>G maps to NM_000834.3 L975L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr17:72842271 G>A maps to NM_000835.3 I761I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr17:72843458 G>T maps to NM_000835.3 L663L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr9:104448996 C>T maps to NM_133445.2 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr19:1008187 C>T maps to NM_138690.1 S788S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr19:1008172 C>T maps to NM_138690.1 L783L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr3:14533757 G>T did not map to a codon.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr3:14530658 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr3:14530729 G>T did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr3:14548434 C>A maps to ENST00000507975 E856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CH-01A-11D-A33O-09 chr3:14548414 C>T maps to ENST00000507975 L862L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr3:14535165 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr23:48840189 C>T did not map to a codon.
Sequencing variant TCGA-C5-A2M1-01A-11D-A18J-09 chr23:48839722 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:48855594 G>C did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:48841725 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:48841799 T>G did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:48830615 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:48844595 C>T did not map to a codon.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr10:121093340 G>T maps to ENST00000369106 E71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr3:141497719 G>T maps to NM_139209.2 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr19:47422774 G>C maps to NM_004491.4 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3TX-01A-11D-A22X-09 chr19:47423966 G>T maps to NM_004491.4 E679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A6QX-01A-12D-A33O-09 chr6:146755619 C>T maps to NM_000838.3 S1091S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr6:34071422 G>T did not map to a codon.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr5:178418889 G>A maps to NM_000843.3 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr5:178413373 G>C maps to NM_000843.3 L627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr5:178418865 A>C maps to ENST00000319065 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr3:7678035 C>T did not map to a codon.
Sequencing variant TCGA-EA-A6QX-01A-12D-A33O-09 chr7:126249490 G>A maps to NM_001127323.1 I473I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr5:148732526 T>G did not map to a codon.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr23:16170720 A>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:16142144 T>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:16170616 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:16142201 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:16168520 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr13:113980314 C>T maps to NM_024719.2 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr13:114018387 G>C did not map to a codon.
Sequencing variant TCGA-C5-A7CH-01A-11D-A33O-09 chr4:42965045 C>T maps to NM_001080476.2 N174N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr4:42965085 C>T maps to NM_001080476.2 R188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A69B-01A-11D-A32I-09 chr4:42895396 G>A maps to NM_001080476.2 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr17:38121934 G>C did not map to a codon.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr8:130760788 G>C maps to NM_031415.2 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr19:42735002 C>T maps to NM_019884.2 P465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr19:42736278 G>C maps to NM_019884.2 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr19:42736795 G>A maps to NM_019884.2 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr9:124091305 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr9:124073023 C>G maps to NM_000177.4 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr9:124079434 G>C maps to NM_000177.4 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr9:124074511 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:51487544 T>C did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr23:51488447 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr23:51488202 G>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:51488153 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr8:30539545 G>A maps to NM_000637.3 R396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr20:33533874 G>A maps to NM_000178.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:52761708 G>A maps to NM_000847.4 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A449-01A-11D-A243-09 chr6:52852196 C>A maps to NM_001512.3 E33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr6:52696762 C>T maps to NM_153699.1 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr4:106630021 C>T did not map to a codon.
Sequencing variant TCGA-FU-A770-01A-11D-A33O-09 chr1:110279793 G>A did not map to a codon.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr1:110199373 C>G maps to NM_000850.4 S26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr1:110256231 C>G did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr11:67353728 C>T did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:67353984 C>G maps to NM_000852.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WF-01A-11D-A351-09 chr22:24323193 G>A maps to NM_000854.3 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WF-01A-11D-A351-09 chr22:24302512 C>T maps to NM_000854.3 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr14:81659057 G>A maps to NM_015859.2 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr14:81659135 G>A maps to NM_015859.2 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr14:81670288 G>A maps to NM_015859.2 Q98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr8:30437887 G>A maps to NM_002095.4 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VH-01A-11D-A28B-09 chr19:6380387 G>A maps to NM_002096.2 S486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr13:45841510 G>T maps to NM_004128.2 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr11:18359718 C>T maps to NM_005316.3 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr12:124132554 C>T maps to NM_001516.3 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr12:124144780 G>C maps to NM_001516.3 *309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr7:74113411 C>T maps to NM_032999.2 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr7:74169839 G>C did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:74016759 G>C maps to NM_016328.2 *960Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RA-A741-01A-11D-A33O-09 chr7:73927290 C>A maps to NM_016328.2 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr16:27480780 C>T maps to NM_001520.3 V1635V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr2:27565899 G>T maps to NM_001521.2 S121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:135546242 C>T maps to NM_012204.2 I86I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr9:135553956 T>C maps to NM_012204.2 F317F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr9:135931306 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr6:111279990 G>T maps to NM_138408.3 E7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr22:39112086 G>A maps to NM_004286.4 E160E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr22:39117745 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr6:43596853 C>A maps to NM_019096.3 G16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr6:43591720 G>A maps to NM_019096.3 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr6:43588570 G>C did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr10:1046732 G>A maps to NM_012341.2 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr10:1042197 C>T did not map to a codon.
Sequencing variant TCGA-EA-A6QX-01A-12D-A33O-09 chr22:46725457 G>T maps to NM_016426.6 V710V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr12:54858832 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr6:42146127 C>T maps to NM_000409.3 N104N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr6:42141389 G>A maps to NM_000409.3 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr11:106810317 G>A maps to ENST00000282249 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr4:156643279 C>T maps to NM_001130684.1 L603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr4:156632144 G>A maps to NM_001130684.1 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr4:156711017 C>T maps to ENST00000502959 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr4:156723667 C>G maps to ENST00000502959 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr4:156724849 C>T maps to ENST00000502959 I518I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr4:156723363 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr12:14840905 G>C maps to NM_004963.3 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr12:14794076 G>A maps to NM_004963.3 I669I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr23:108673541 G>A did not map to a codon.
Sequencing variant TCGA-EA-A78R-01A-11D-A32I-09 chr23:108696941 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr23:108696909 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr23:108718758 G>C did not map to a codon.
Sequencing variant TCGA-EX-A69L-01A-11D-A32I-09 chr23:108696805 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:108652352 G>T did not map to a codon.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr4:44691409 C>T maps to NM_021927.2 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CG-01A-11D-A32I-09 chr1:228335272 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr1:228334422 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:228333447 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:228336138 G>C maps to ENST00000366720 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:2748122 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:2773192 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2RE-01A-11D-A18J-09 chr11:45949829 C>T maps to NM_152312.3 Y619Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr4:144940463 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr23:103268224 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:103268213 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr23:103267769 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr17:73774738 C>T maps to NM_005324.3 K116K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr1:9324431 C>G maps to NM_004285.3 S627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr10:115343958 C>T maps to NM_004132.3 Y430Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr10:115341869 C>T maps to NM_004132.3 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr9:99227723 C>T maps to NM_014282.2 D206D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr6:105232899 G>A maps to NM_020771.3 Q457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr4:108953507 C>T maps to ENST00000351726 N304N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr4:108948796 T>C did not map to a codon.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr16:784555 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr5:153857328 C>T maps to NM_004821.2 Q80Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr5:153857265 C>T maps to NM_004821.2 K101K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr20:7915152 G>A maps to NM_017545.2 D89D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HQ-01A-11D-A20U-09 chr20:7886946 G>C maps to NM_017545.2 S192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:39888583 C>T maps to ENST00000310778 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PI-01A-11D-A18J-09 chr19:19369455 G>A maps to NM_023002.2 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr19:19369518 G>A maps to NM_023002.2 N210N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr5:140062702 T>G maps to NM_002109.3 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr19:52222788 C>T maps to NM_001523.2 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr2:172823388 C>T maps to NM_003642.3 Q248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr14:23421629 C>T maps to NM_017815.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:36104781 G>A maps to NM_015302.1 K58K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr19:36106005 C>T maps to NM_015302.1 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr9:19082872 G>A maps to NM_017645.3 Q290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr9:19086755 A>G maps to NM_017645.3 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr23:152719931 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr1:154245994 C>T maps to NM_006118.3 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr6:135286428 C>T did not map to a codon.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr23:153224133 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:153220406 C>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:153223486 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:153225701 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:153225739 G>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:153215956 G>A did not map to a codon.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr12:104458472 C>T maps to NM_013320.2 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr12:104476566 C>T maps to NM_013320.2 G317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr12:104474573 C>T maps to NM_013320.2 R245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr20:30659514 C>G maps to NM_002110.3 S38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr3:121350297 G>T did not map to a codon.
Alternatively spliced codon TCGA-EK-A2RN-01A-12D-A20U-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr5:45645499 C>A maps to NM_021072.2 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:613850 G>C did not map to a codon.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr19:615960 G>A maps to NM_001194.3 P719P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr1:155258444 A>G did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:155258281 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr15:73615838 G>A maps to NM_005477.2 F865F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr15:73616099 G>A maps to NM_005477.2 I778I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A69B-01A-11D-A32I-09 chr15:73659972 G>A maps to NM_005477.2 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr1:32084963 C>T maps to NM_001525.2 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr22:50686383 A>G maps to NM_032019.5 V424V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZE-01A-11D-A28B-09 chr6:114274455 G>A maps to ENST00000398283 G302G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr2:240002873 G>A maps to NM_006037.3 P884P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:240048390 C>T did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr23:48676648 C>T did not map to a codon.
Sequencing variant TCGA-C5-A2M2-01A-21D-A18J-09 chr23:48681792 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:48663866 C>A did not map to a codon.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr23:48661071 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:48674574 C>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:71788728 A>C did not map to a codon.
Sequencing variant TCGA-Q1-A5R3-01A-11D-A28B-09 chr23:71792630 C>T did not map to a codon.
Sequencing variant TCGA-C5-A2M2-01A-21D-A18J-09 chr7:18868818 C>T maps to NM_178425.2 H786H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr15:50550606 G>A maps to NM_002112.3 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:156721267 G>T did not map to a codon.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr1:156712759 G>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:156712541 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:242168949 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:242168951 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:242168992 G>C did not map to a codon.
Sequencing variant TCGA-HG-A2PA-01A-11D-A20U-09 chr23:83724331 T>C did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:83588782 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr1:236716982 C>G maps to NM_018072.5 L2045L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:236750790 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr14:73974858 C>T maps to ENST00000334988 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr14:73987661 C>T maps to ENST00000334988 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr14:31863313 G>T maps to ENST00000389961 S233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr14:31774365 C>A maps to ENST00000389961 E1656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr17:58156275 C>G did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr14:31598190 C>T maps to NM_015382.2 R1462R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr10:93249461 G>C did not map to a codon.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr1:45471528 C>T maps to NM_024602.5 W624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr1:45469789 G>A maps to NM_024602.5 F763F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:45469600 C>T maps to NM_024602.5 R785R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:45470391 C>T maps to NM_024602.5 L674L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:45468858 G>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:45474373 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3WB-01A-11D-A22X-09 chr7:43508527 C>T maps to NM_015052.3 R975*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr7:43484019 G>T maps to NM_015052.3 E417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr7:43484405 G>A maps to NM_015052.3 V545V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr2:197085611 C>T maps to NM_020760.1 K1400K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr3:124739957 C>T maps to NM_020733.1 E310E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr3:124732409 A>G maps to NM_020733.1 S671S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr3:124731881 C>T maps to NM_020733.1 L847L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:84368044 C>T maps to NM_133636.2 V445V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr4:84376881 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr4:84358066 G>A maps to NM_133636.2 L664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr11:124793850 G>A maps to NM_152722.4 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr7:92848494 C>A maps to ENST00000453812 E140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr23:65486375 T>C did not map to a codon.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr23:65486298 A>T did not map to a codon.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr23:65486315 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr15:63916526 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr15:64039149 C>A maps to ENST00000261887 L829L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr15:63932559 G>A maps to ENST00000261887 Q3898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr15:63946434 G>A maps to ENST00000261887 L3391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr15:28525272 C>T maps to NM_004667.4 E161E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A3LQ-01A-21D-A21Q-09 chr15:28443554 A>T maps to NM_004667.4 S2660S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A5XV-01A-11D-A28B-09 chr15:28422656 T>C did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr15:28387978 G>A maps to NM_004667.4 F3846F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr15:28510987 G>A maps to NM_004667.4 R577R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr4:89628056 G>T maps to NM_014606.1 L1033L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr10:69682815 C>A maps to NM_022079.2 E1016*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr10:69726538 C>T maps to NM_022079.2 Q609Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr10:69832929 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr4:89407318 C>G maps to NM_016323.2 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr4:89326035 T>C maps to NM_017912.3 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr4:89304371 G>T maps to ENST00000502870 E31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr4:89363428 G>A maps to NM_017912.3 Q962Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr16:56966191 C>G maps to NM_014685.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr16:56966266 C>G maps to NM_014685.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr3:193855739 C>T maps to NM_005524.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:934942 C>T maps to NM_001142467.1 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr15:72638961 G>A maps to ENST00000457859 F423F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr5:73981267 C>T maps to NM_000521.3 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr17:80400179 C>G maps to NM_173620.2 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:80399094 C>G maps to NM_173620.2 S402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr17:43226811 G>C maps to NM_006460.2 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr8:80679866 G>T maps to NM_001040708.1 S11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr6:126080947 A>C maps to NM_012259.2 *338Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LS-01A-22D-A22X-09 chr1:91859872 G>A maps to NM_001017975.3 Q91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr1:91851245 G>A maps to NM_001017975.3 Q214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr1:91844727 C>T maps to NM_001017975.3 W350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr4:3446051 G>T maps to ENST00000511533 E205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr17:79667753 C>T maps to NM_004712.4 L682L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr8:43025772 C>T maps to ENST00000458501 Q255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr3:42735140 G>A maps to NM_020707.3 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr1:222712017 G>A maps to NM_024746.3 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DV-01A-11D-A32I-09 chr1:222717480 C>T maps to NM_024746.3 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr9:97177516 G>A maps to NM_032558.2 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr22:21799585 C>A maps to NM_015094.2 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr14:62193409 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr14:62193396 T>C did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr14:62193398 A>C did not map to a codon.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr10:102295783 C>G maps to ENST00000442724 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr10:102296253 A>C maps to ENST00000442724 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr5:130495250 C>G maps to NM_005340.5 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr7:75192304 G>A maps to NM_005338.4 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr7:75171283 G>C maps to NM_005338.4 S969*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr12:123335841 C>G maps to NM_003959.1 S192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:114505024 C>T maps to ENST00000426820 Q761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr19:40890034 G>A maps to NM_144685.3 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr19:40895761 G>C maps to NM_144685.3 V16V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr19:40895398 G>C maps to NM_144685.3 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr19:40895683 G>C maps to NM_144685.3 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr16:30005772 G>T maps to NM_003609.3 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr16:30006989 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr6:27834713 C>T maps to NM_005322.2 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr6:27834863 C>T maps to NM_005322.2 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr6:27834887 C>T maps to NM_005322.2 K140K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr6:27834713 C>T maps to NM_005322.2 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr6:26156663 G>T maps to NM_005321.2 E16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr6:26156683 G>A maps to NM_005321.2 K22K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr6:26156770 C>T maps to NM_005321.2 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr6:26157091 G>A maps to NM_005321.2 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OA-01A-11D-A16Y-08 chr6:25726559 G>A maps to NM_170745.3 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OA-01A-11D-A16Y-08 chr6:25726563 A>C maps to NM_170745.3 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr6:26033404 C>T maps to NM_003513.2 *131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr6:26217567 G>A maps to NM_021052.2 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr6:27101230 G>T maps to NM_021064.4 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A50E-01A-21D-A26G-09 chr6:27114915 A>G maps to NM_080596.1 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr6:27782445 G>A maps to NM_021066.2 Q25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr6:27805843 C>A maps to NM_003510.2 E92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr6:27114562 C>A maps to NM_080593.2 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr6:27775462 G>T maps to NM_003519.3 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr6:26197325 C>T maps to NM_003530.3 E51E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr6:26271486 G>A maps to NM_003534.2 Y42Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr6:27858574 G>C did not map to a codon.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr6:26104485 G>A maps to NM_003542.3 *104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3TQ-01A-11D-A22X-09 chr6:26240697 C>T maps to NM_003540.3 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr6:26240850 G>C maps to NM_003540.3 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr6:26247064 G>A maps to NM_003547.2 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr6:27798994 C>G maps to NM_003541.2 *104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr6:27798994 C>A maps to NM_003541.2 *104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr6:27841105 C>T maps to NM_003546.2 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:149859406 G>A maps to NM_175065.2 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr1:149857968 G>A maps to NM_003528.2 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:149857833 G>A maps to NM_003528.2 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:14923745 C>T maps to NM_175054.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr6:12121869 C>T maps to NM_002114.2 S614S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZD-01A-11D-A28B-09 chr6:12164276 G>A maps to NM_002114.2 E2580E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A6QX-01A-12D-A33O-09 chr6:12122773 G>T maps to NM_002114.2 G916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr6:12123369 A>G maps to NM_002114.2 Q1114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr6:143093706 G>A maps to NM_006734.3 I723I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr6:143092437 C>A maps to NM_006734.3 L1146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr6:143091570 C>T maps to NM_006734.3 L1435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3WB-01A-11D-A22X-09 chr6:143074249 T>C maps to NM_006734.3 L2445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr6:143091089 C>A maps to NM_006734.3 E1596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr6:143074954 G>C maps to NM_006734.3 V2210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr1:42048468 G>C maps to NM_024503.3 S667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr1:42047015 G>A maps to NM_024503.3 L1151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr2:75116396 C>T maps to NM_000189.4 R801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr2:75107454 C>T maps to NM_000189.4 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr5:176314514 G>A maps to NM_002115.2 R513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr10:70992571 G>A maps to NM_025130.3 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr19:37853491 G>A maps to NM_181786.2 K265K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr6:29910796 G>T maps to ENST00000376806 E113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr6:29910796 G>T maps to ENST00000376806 E113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr6:29911301 G>T maps to ENST00000376806 E201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr6:29910397 G>A maps to ENST00000376806 W23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:29910586 G>T maps to ENST00000376806 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A69L-01A-11D-A32I-09 chr6:29911897 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr6:29911953 G>C maps to ENST00000376806 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr6:29912834 G>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr6:29910743 C>G maps to ENST00000376806 S95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr6:29912275 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr6:29911301 G>T maps to ENST00000376806 E201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3TQ-01A-11D-A22X-09 chr6:31323000 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr6:31323240 G>A maps to ENST00000428231 Q320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr6:31323000 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr6:31323000 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr6:31324476 G>A maps to NM_005514.6 Q111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr6:31324680 C>A maps to ENST00000428231 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr6:31323126 C>A maps to ENST00000428231 E358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr6:31323159 C>A maps to ENST00000428231 E347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr6:31239772 C>G did not map to a codon.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr6:31238206 C>T maps to ENST00000383329 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr6:31239014 C>A maps to ENST00000383329 E152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr6:32917052 G>C maps to NM_006120.3 S259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr6:32906569 G>C maps to NM_002118.4 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr6:32906677 G>A maps to NM_002118.4 F40F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A78R-01A-11D-A32I-09 chr6:33048259 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr6:32609785 G>A maps to NM_002122.3 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr6:32713836 C>T maps to NM_020056.4 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr6:32629154 C>A maps to ENST00000374943 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr6:32487255 G>A maps to NM_002125.3 D181D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr6:32487168 C>T maps to NM_002125.3 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr6:29694150 G>A did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr6:29691561 G>A maps to NM_001098479.1 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr17:53392588 T>G maps to NM_002126.4 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr3:148756953 G>C maps to NM_003071.3 S893*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:148778606 G>C maps to NM_003071.3 S400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:221055496 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr1:186141186 G>A maps to NM_031935.2 K5246K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr1:186141186 G>A maps to NM_031935.2 K5246K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:185939557 C>T maps to NM_031935.2 G768G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr1:186017886 C>T maps to NM_031935.2 Q2165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr1:186113712 C>A maps to NM_031935.2 S4715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:3576257 G>C did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr6:34208658 G>A maps to NM_145899.2 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr13:31037402 G>A maps to NM_002128.4 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr1:24137115 G>C did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr6:55443817 G>A maps to NM_019036.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr5:74655363 C>T maps to NM_000859.2 Q814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr21:40719457 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr21:40720241 C>A maps to NM_004965.6 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7X3-01A-11D-A351-09 chr1:26801751 T>A did not map to a codon.
Sequencing variant TCGA-EK-A2H1-01A-11D-A17W-09 chr1:26801497 T>C did not map to a codon.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr1:26801752 A>T did not map to a codon.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr23:80370359 C>T did not map to a codon.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr19:1080507 C>G maps to NM_012292.2 S625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:1081907 C>A maps to NM_012292.2 S822*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:162902672 G>A maps to NM_001142556.1 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr5:162910272 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr17:73150527 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr12:121438964 C>T maps to NM_000545.5 I622I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr17:36093701 G>A maps to NM_000458.2 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CG-01A-11D-A32I-09 chr7:26235494 G>T maps to NM_031243.2 G243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr7:26230677 C>T did not map to a codon.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr23:100667592 G>A did not map to a codon.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr9:86585657 G>A maps to NM_031262.2 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr19:8553924 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr1:23634677 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr1:23670748 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:23670748 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:23636895 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr11:62488793 C>T maps to NM_001079559.1 R528R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr11:62491177 G>A maps to NM_001079559.1 Q258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R1-01A-11D-A28B-09 chr11:62489767 G>A maps to NM_001079559.1 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr19:19040314 G>C maps to NM_004838.3 V341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WF-01A-11D-A351-09 chr1:60294515 A>C maps to NM_015888.4 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr19:12875630 G>A maps to NM_013312.2 R608R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr8:42821732 G>C maps to NM_032410.3 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr1:150671334 A>G did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:150671182 G>A maps to NM_032132.4 Q378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr1:150671101 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr22:30517977 C>T maps to NM_152510.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UC-01A-11D-A351-09 chr7:27135384 G>A maps to NM_005522.4 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr7:27141771 G>A maps to NM_006735.3 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr7:27150229 C>G maps to NM_153631.2 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr7:27170292 G>A maps to NM_002141.4 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr7:27169113 C>T maps to NM_002141.4 E231E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr7:27194713 G>A maps to NM_006896.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr17:46620386 C>A did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr17:46622257 C>A maps to NM_002145.3 E6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr17:46627736 G>A maps to NM_002146.4 Q419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:46628394 C>T maps to NM_002146.4 Q199Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr17:46655231 C>T maps to NM_024015.4 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr17:46670954 C>G maps to NM_002147.3 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr17:46687941 C>T maps to NM_004502.3 Q113Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr12:54383745 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:54369372 G>A did not map to a codon.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr12:54333241 G>A maps to NM_017410.2 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr12:54422600 C>G maps to NM_004503.3 S99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr12:54403490 G>A maps to NM_022658.3 W141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr12:54404915 G>A maps to NM_022658.3 Q160Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R1-01A-11D-A28B-09 chr12:54405014 G>A maps to NM_022658.3 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr12:54396298 G>A maps to NM_006897.1 E208E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr2:176965364 G>A maps to NM_021193.3 Q230Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr2:177033964 C>T maps to NM_006898.4 Y41Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr2:177017630 G>A maps to NM_014621.2 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr2:177016483 G>A maps to NM_014621.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr2:177017825 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr1:40149740 G>A maps to NM_016257.2 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr12:122294312 C>A did not map to a codon.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr4:175414435 C>T maps to NM_000860.4 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:95223383 G>A maps to NM_014485.2 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr23:133609304 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr10:100177235 G>C did not map to a codon.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr3:148863258 G>A maps to NM_032383.3 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr11:18327892 C>A maps to NM_181507.1 E205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr11:534329 C>T did not map to a codon.
Sequencing variant TCGA-MY-A5BE-01A-21D-A26G-09 chr3:192980925 G>T maps to NM_020386.3 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr20:60790435 C>T maps to ENST00000317393 *454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr20:60791268 C>G maps to ENST00000317393 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr18:22056883 C>T maps to NM_021624.3 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr1:152188860 C>T maps to NM_001009931.1 S1748S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5FO-01A-21D-A28B-09 chr1:152188860 C>T maps to NM_001009931.1 S1748S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2GZ-01A-11D-A17W-09 chr1:152189049 C>T maps to NM_001009931.1 S1685S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr1:152192728 G>C maps to NM_001009931.1 S459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AU-01A-32D-A243-09 chr1:152186613 C>G maps to NM_001009931.1 S2497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:20838178 A>G maps to ENST00000402541 *214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WH-01A-22D-A351-09 chr16:22926814 C>T maps to NM_006043.1 R346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr17:13503858 G>A maps to NM_006042.1 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:13503885 G>A maps to NM_006042.1 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H6-01B-11D-A22X-09 chr17:14205133 C>A maps to NM_006041.1 S100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:132092452 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:131762894 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr23:131762917 T>C did not map to a codon.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr23:132090973 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:131842588 A>C did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:132091224 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr17:40706694 C>T maps to NM_000413.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr23:53459254 C>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr4:88258405 C>T did not map to a codon.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr4:88258412 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr11:43694602 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:43702326 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr4:88231401 G>A maps to NM_178135.3 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr19:49339659 C>T maps to NM_016246.2 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr5:118866972 C>T maps to NM_000414.3 Q623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M2-01A-21D-A18J-09 chr12:57167789 C>T maps to NM_003725.2 R52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr6:33173927 G>A maps to NM_014234.3 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr1:120056572 G>T maps to ENST00000235547 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:119964792 C>G maps to NM_000198.3 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr16:30999440 G>A maps to NM_025193.3 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr8:145515502 C>T maps to NM_005526.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr6:122743931 G>A maps to NM_004506.3 Q300Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr21:45012109 C>T maps to NM_007031.1 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr16:67200498 G>T maps to NM_001040667.2 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr17:56540517 C>T maps to NM_001080439.1 E389E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr17:56565422 G>A maps to NM_001080439.1 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr14:102552356 G>A maps to NM_001017963.2 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr6:44218332 C>T maps to NM_007355.2 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr10:118434522 G>T maps to NM_025015.2 V599V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr10:14886053 G>T did not map to a codon.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr10:14885842 C>T maps to ENST00000309584 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr6:31783742 G>A maps to NM_005345.5 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr6:31778930 C>T maps to NM_005527.3 K273K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WI-01A-12D-A351-09 chr9:128001704 G>A maps to NM_005347.4 N200N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:161495956 C>T maps to NM_002155.3 I503I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr1:161495803 C>G maps to NM_002155.3 T452T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:122931492 C>T maps to NM_006597.3 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr5:137903343 C>T maps to NM_004134.6 Q201Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr7:75933360 G>A maps to NM_001540.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:16345658 G>A maps to ENST00000375718 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A852-01A-11D-A351-09 chr2:198365388 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:22168564 G>A maps to NM_005529.5 F3041F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr1:22177950 C>G did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:22159061 C>T maps to NM_005529.5 G3711G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:22201524 G>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:22181342 G>C maps to NM_005529.5 S2044*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3PZ-01A-11D-A21Q-09 chr1:22170682 G>A maps to NM_005529.5 V2858V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:22170718 C>G maps to NM_005529.5 L2846L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:22202740 G>C maps to NM_005529.5 S995*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr13:31725796 T>C maps to NM_006644.2 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr23:135582898 G>C did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr23:135593293 G>A did not map to a codon.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr23:135585076 G>C did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:63256874 G>A maps to NM_000524.2 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HR-01A-11D-A20U-09 chr5:63257120 G>A maps to NM_000524.2 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr5:63257162 G>A maps to NM_000524.2 C128C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HR-01A-11D-A20U-09 chr1:23520070 G>A maps to NM_000864.4 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HG-A2PA-01A-11D-A20U-09 chr1:23519578 C>A maps to NM_000864.4 *378Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:23519980 G>A maps to NM_000864.4 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr13:47466696 A>G maps to NM_000621.3 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5O9-01A-11D-A28B-09 chr23:114141189 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:114141785 C>G did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr23:113961365 G>A did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr23:114141908 G>A did not map to a codon.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr11:113848496 G>A maps to NM_213621.3 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:113852022 C>T maps to NM_213621.3 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr3:183754186 C>T maps to NM_001145143.1 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr3:183756392 C>T maps to NM_001145143.1 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:183756155 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr3:183756705 C>G maps to NM_001145143.1 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr3:183821989 C>T maps to NM_182589.2 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr3:183815374 C>T maps to ENST00000415389 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr5:147889569 G>A maps to NM_001040173.2 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr5:147929785 C>T maps to NM_001040173.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr5:147845451 G>A maps to NM_199453.3 F371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AX-01A-12D-A243-09 chr5:147889203 G>A maps to NM_001040173.2 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr7:154863128 C>T maps to NM_024012.2 L174L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-LP-A5U3-01A-11D-A28B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr10:92508658 G>C maps to NM_019859.3 S411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr10:92508963 G>A maps to NM_019859.3 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A852-01A-11D-A351-09 chr10:124266385 C>T maps to NM_002775.4 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZE-01A-11D-A28B-09 chr4:3190798 C>T maps to NM_002111.6 L1783L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr21:33346884 G>C maps to NM_014586.1 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr6:656449 C>T maps to NM_148959.3 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr23:53589842 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr23:53579330 C>T did not map to a codon.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr23:53643956 C>T did not map to a codon.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr23:53564519 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:53672358 A>C did not map to a codon.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr23:53589157 C>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:53644393 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:53675224 T>G did not map to a codon.
Sequencing variant TCGA-FU-A3TX-01A-11D-A22X-09 chr23:53564616 G>A did not map to a codon.
Sequencing variant TCGA-HM-A3JK-01A-11D-A21Q-09 chr23:53615415 T>C did not map to a codon.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr23:53579731 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:53560325 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:53588726 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:53589103 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:53655821 G>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:53579707 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:53591560 C>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr7:123508681 C>T maps to NM_012269.2 Q119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr7:123514825 C>T maps to NM_012269.2 V322V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:71015348 C>T maps to NM_032821.2 L1484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr16:70908780 C>T maps to NM_032821.2 L3532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A4BA-01A-21D-A26G-09 chr16:70894770 C>T maps to NM_032821.2 P3936P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr16:71004491 C>T maps to NM_032821.2 K1849K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr16:71163620 T>C maps to NM_032821.2 R383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr11:118924882 C>T maps to NM_001130991.1 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr9:95003119 C>G did not map to a codon.
Sequencing variant TCGA-UC-A7PD-01A-11D-A351-09 chr9:95002908 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr1:220320874 C>A maps to NM_018060.3 V979V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr1:220269458 C>A maps to NM_018060.3 S94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:220311327 C>T maps to NM_018060.3 F706F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr1:220311205 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2GZ-01A-11D-A17W-09 chr7:8272303 C>T maps to ENST00000422063 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr7:8268264 C>T maps to ENST00000422063 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr7:8153553 C>T maps to ENST00000422063 *513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr19:10394331 C>T maps to NM_000201.2 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr17:62081144 C>A maps to NM_001099789.1 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr19:10446429 G>C maps to NM_002162.3 S189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr19:10398020 G>A maps to NM_001544.3 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr19:10402777 G>A maps to NM_003259.3 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CJ-01A-11D-A32I-09 chr20:30193561 G>T maps to NM_002165.2 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:8822501 C>T maps to NM_002166.4 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:23885559 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3QD-01A-32D-A22X-09 chr15:78449272 G>C maps to ENST00000379576 *38Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr20:2644839 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr20:2639176 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:153051682 G>A did not map to a codon.
Sequencing variant TCGA-JX-A5QV-01A-22D-A28B-09 chr23:153055287 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr10:1070525 C>T maps to NM_033261.2 E46E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A0TN-01A-21D-A14W-08 chr8:39836099 T>C did not map to a codon.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr8:39847323 C>T maps to NM_194294.2 Q225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr8:39847292 C>G maps to NM_194294.2 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr8:39862882 G>A maps to NM_194294.2 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr23:148579753 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:148568845 T>G did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:148585783 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr23:148585790 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr23:148571886 G>C did not map to a codon.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr23:148584732 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:148577935 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:148564587 C>T did not map to a codon.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr4:997844 G>A maps to NM_000203.3 A591A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73R-01A-11D-A33O-09 chr19:13264404 G>T maps to NM_004907.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:181058847 C>T maps to NM_016545.4 I270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr9:131939149 G>A maps to NM_203434.2 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr12:6649648 C>T maps to NM_001193457.1 *572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr1:158990291 G>C maps to ENST00000295809 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr1:159021542 G>A maps to ENST00000295809 V580V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr1:159021551 G>A maps to ENST00000295809 L583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:159021792 G>T maps to ENST00000295809 G664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:159002439 C>T maps to ENST00000295809 Q430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr17:41165086 C>T maps to NM_005533.4 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:79115875 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:79106758 C>T maps to NM_006820.2 Q368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr10:91163266 C>G maps to NM_001548.3 S412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr10:91143777 A>G maps to NM_001010987.2 G236G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A69B-01A-11D-A32I-09 chr12:25679783 G>T maps to NM_001145728.1 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr9:21166470 G>A maps to NM_002175.2 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr9:21304813 G>A maps to NM_002169.2 Q148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr9:21350316 T>G maps to NM_021002.2 *190Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr9:21409238 C>T maps to NM_002170.3 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr6:137519720 G>C maps to NM_000416.2 S306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr6:137519720 G>T maps to NM_000416.2 S306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr6:137519178 C>A maps to NM_000416.2 E487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:50327470 G>A maps to ENST00000336089 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr3:129236333 C>T maps to NM_052985.2 F1147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr3:129234392 C>T maps to NM_052985.2 N1123N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr16:1614147 C>G maps to NM_014714.3 V639V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr16:1642481 G>C maps to NM_014714.3 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr2:27684267 G>A maps to NM_015662.1 I770I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr22:37171856 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr22:37172222 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr12:110565220 C>G maps to NM_014055.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr23:69353868 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:69368660 C>G did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr15:99500352 C>T maps to NM_000875.3 I1262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr15:99500355 C>A maps to NM_000875.3 I1263I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr15:99472811 G>A maps to NM_000875.3 L936L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HG-A2PA-01A-11D-A20U-09 chr15:99465400 C>T maps to NM_000875.3 V742V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr15:99442727 G>A maps to NM_000875.3 E375E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr15:99482578 C>G maps to NM_000875.3 V1149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr15:99467896 C>T maps to NM_000875.3 F922F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A78R-01A-11D-A32I-09 chr11:2154261 G>T maps to NM_001127598.1 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr17:47123298 T>G maps to NM_006546.3 G481G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr17:47074976 C>T did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr17:47075052 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr3:185407162 G>A maps to NM_006548.4 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr7:23387307 C>T maps to NM_006547.2 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr19:46733398 C>T maps to NM_198541.1 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr19:46627225 G>A maps to NM_207393.1 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LT-01A-11D-A18J-09 chr19:46543438 G>T maps to NM_001002923.1 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr1:201169418 G>A maps to NM_001164586.1 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr1:201176006 A>G maps to NM_001164586.1 G662G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr11:68703760 C>A maps to NM_002180.2 R605R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr11:68701259 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr11:68702825 C>T maps to NM_002180.2 V564V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VK-01A-11D-A28B-09 chr19:51831093 C>T maps to NM_001101372.1 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr23:130410032 C>G did not map to a codon.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr23:130411001 C>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:130409549 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr23:130412690 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr3:151158440 A>C did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr3:151165247 C>A maps to NM_178822.4 E841*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr3:151161082 C>T maps to NM_178822.4 V1884V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:151164885 C>G maps to NM_178822.4 V961V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:118647441 G>C maps to NM_152538.2 S112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:18703403 C>T maps to NM_032880.4 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr11:18727640 G>A maps to NM_173588.3 H1211H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr11:18733674 C>G maps to NM_173588.3 V784V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr1:159901342 G>C maps to NM_001135050.1 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:159899720 G>A maps to NM_001135050.1 F703F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr1:159901457 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr11:133807324 G>A maps to NM_014987.1 R209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr11:133816073 G>A maps to NM_014987.1 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr11:133801383 G>A maps to NM_014987.1 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr11:133801564 C>T maps to NM_014987.1 A412A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:140041771 G>A maps to NM_006083.3 E540E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr12:99019971 C>T maps to NM_153687.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:111668765 C>T did not map to a codon.
Sequencing variant TCGA-EX-A3L1-01A-11D-A21Q-09 chr8:42174277 G>T maps to NM_001556.2 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr7:50467664 G>A maps to NM_006060.3 E300E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr2:213872481 C>A maps to ENST00000342002 E401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr2:214012327 G>A maps to ENST00000442445 Y87Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr3:159707993 C>T maps to NM_000882.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr19:18179256 G>A maps to NM_005535.1 H423H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr19:18184371 C>T maps to NM_005535.1 E246E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PD-01A-11D-A351-09 chr1:67861459 G>A maps to NM_001559.2 E759E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A44S-01A-12D-A26G-09 chr23:117900859 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:117925732 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr23:114245322 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:114251853 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr6:52053994 G>T maps to NM_002190.2 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr13:21277401 G>T did not map to a codon.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr13:21277371 C>T did not map to a codon.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr3:9959777 G>T maps to ENST00000440502 *100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:9974952 C>G maps to NM_153461.2 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr3:57139965 C>T maps to NM_017563.3 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr3:57135378 G>T maps to NM_017563.3 S331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr2:103040353 C>T maps to NM_003853.2 Q52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr2:102793101 G>A maps to NM_000877.2 W531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr2:102626318 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr2:102632494 G>A maps to NM_004633.3 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr2:102644706 G>A maps to NM_004633.3 W350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr3:190374254 C>T maps to NM_001167931.1 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:190322169 C>G maps to NM_002182.3 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr23:29301124 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:29301119 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3QD-01A-32D-A22X-09 chr23:104961410 C>G did not map to a codon.
Sequencing variant TCGA-EA-A411-01A-11D-A243-09 chr23:104961395 G>T did not map to a codon.
Sequencing variant TCGA-EA-A5ZE-01A-11D-A28B-09 chr23:104999270 G>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:105011022 A>G did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:104512090 G>C did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr2:102851513 C>G maps to NM_003854.2 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr1:207039220 C>T maps to NM_018724.3 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr12:56733800 C>G maps to NM_016584.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:23844998 G>A maps to NM_022789.3 E148E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr14:23844857 C>T maps to NM_022789.3 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr12:68619009 A>G maps to NM_018402.1 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q8-01A-11D-A21Q-09 chr12:68619363 A>G did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr19:14157027 G>A maps to NM_004843.2 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr10:6060062 C>A maps to NM_000417.2 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr22:37531390 G>T maps to ENST00000406505 I270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr23:1464224 C>G did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:1497562 G>C did not map to a codon.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr23:1471017 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr19:50394271 G>A maps to NM_172374.1 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A78R-01A-11D-A32I-09 chr16:27353577 C>T maps to NM_000418.2 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BE-01A-21D-A26G-09 chr16:27373941 C>T maps to NM_000418.2 C423C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A3LQ-01A-21D-A21Q-09 chr5:55264183 G>A maps to NM_002184.3 N137N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A69B-01A-11D-A32I-09 chr8:79648738 G>A maps to NM_000880.3 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr23:155231084 G>A did not map to a codon.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr23:155239719 G>A did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr23:155234189 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr23:155231059 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:155232552 C>G did not map to a codon.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr23:155235747 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:121741027 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:153634541 T>C did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:6631823 G>A maps to NM_001014795.1 E447E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73R-01A-11D-A33O-09 chr11:6631718 C>T maps to NM_001014795.1 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr2:239103228 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr2:239103497 C>T maps to NM_030768.2 Q23Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr19:15226401 G>A maps to NM_006844.3 N565N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr11:31477933 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr7:110526717 G>A maps to NM_032549.2 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr2:131103842 G>A maps to NM_033416.1 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr8:57905781 G>C maps to NM_017813.3 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HM-A3JK-01A-11D-A21Q-09 chr6:76712653 T>C maps to NM_001563.2 G424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr6:76631853 C>G maps to NM_001563.2 L782L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr3:100962777 T>A maps to NM_016247.2 A799A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr11:61919294 C>G maps to NM_001040694.1 L868L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M1-01A-11D-A18J-09 chr11:61914293 G>C maps to NM_001040694.1 R708R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr11:61914359 G>T maps to NM_001040694.1 R730R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:61897556 C>G maps to NM_001040694.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr14:105178821 C>T maps to ENST00000252520 L848L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr14:105180714 G>A maps to ENST00000252520 L1072L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A57G-01A-11D-A26G-09 chr13:111371895 C>T maps to NM_005537.3 Q296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr2:242660351 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr2:220437116 C>T maps to NM_002191.3 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr7:41731655 C>G did not map to a codon.
Sequencing variant TCGA-EA-A3QD-01A-32D-A22X-09 chr7:41729910 G>C maps to NM_002192.2 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr7:41729811 G>A maps to NM_002192.2 D239D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr2:121107167 C>G maps to NM_002193.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr2:121106681 C>T maps to NM_002193.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr12:57850120 G>A maps to NM_031479.3 E181E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr7:30795310 C>T maps to NM_006774.4 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R3-01A-11D-A28B-09 chr7:30739484 C>T did not map to a codon.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr15:41347513 C>A maps to NM_017553.1 E707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:41275975 G>A maps to NM_017553.1 V1407V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73Q-01A-21D-A32I-09 chr2:191236082 G>A maps to NM_002194.3 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr2:99198161 G>T maps to NM_001566.2 L936L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr4:143129637 C>A maps to NM_003866.2 E338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr4:143003323 C>T maps to NM_003866.2 L834L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:38397236 C>A maps to ENST00000440912 E294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr2:233998698 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr2:233944075 C>T maps to ENST00000359570 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73S-01A-11D-A33O-09 chr2:234104108 C>T maps to ENST00000359570 H887H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr10:121586538 A>T maps to NM_014937.2 V882V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:121569691 C>G maps to NM_014937.2 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr22:31522640 C>T maps to ENST00000331075 D476D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr22:31521298 G>T maps to ENST00000331075 E192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr7:155090261 C>G maps to ENST00000344756 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr7:155095545 C>T maps to ENST00000344756 F272F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:118865889 C>T maps to NM_016133.2 Q224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr2:118864262 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr2:118867465 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr19:17927707 G>A maps to NM_005543.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr19:7128912 G>T maps to NM_000208.2 V965V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr1:156821164 G>C maps to NM_014215.2 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr1:156814525 G>A maps to NM_014215.2 Y849Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr7:1525078 G>T maps to ENST00000389470 G1168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr7:1519191 G>A maps to ENST00000389470 I1605I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HQ-01A-11D-A20U-09 chr7:1535822 G>A maps to ENST00000389470 A688A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr7:1542627 C>T maps to ENST00000389470 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr7:1511262 G>A maps to ENST00000389470 L2281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr7:1512807 G>A maps to ENST00000389470 F2204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr7:1523758 G>C maps to ENST00000389470 L1270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr4:106604361 G>C maps to NM_020395.3 S306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr1:153745110 C>T maps to ENST00000512605 L800L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:153742318 C>G maps to ENST00000428986 L797L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:153735820 C>G maps to ENST00000428986 L584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr11:77629949 G>A maps to NM_033547.3 F613F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr11:77590060 G>A maps to NM_033547.3 I942I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr11:62416083 G>A maps to NM_030628.1 R490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr11:62414998 G>A maps to NM_030628.1 F851F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr13:51997185 T>C did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:212190328 C>T maps to NM_015434.3 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr1:212118245 C>T maps to NM_015434.3 L827L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr1:212180085 C>T maps to NM_015434.3 Q258Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr3:48731582 C>G maps to ENST00000450045 *152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CH-01A-11D-A33O-09 chr6:33690844 C>T maps to NM_054111.4 R295R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-C5-A1MI-01A-11D-A14W-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr6:154567852 G>A maps to NM_001130700.1 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H6-01B-11D-A22X-09 chr6:154480964 A>G maps to NM_001130700.1 *439R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr5:61822024 G>A maps to NM_001134779.1 L691L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VI-01A-11D-A28B-09 chr5:61747702 T>C maps to NM_001134779.1 H193H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr1:44433063 C>T maps to NM_014652.3 F897F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr14:24653558 G>A maps to ENST00000458132 Q568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr13:98664576 G>A maps to NM_002271.4 L729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr11:9424907 G>C maps to NM_006391.2 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr11:9424777 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr11:9431473 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:201843429 C>T maps to NM_018085.4 I921I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:201835971 C>G maps to NM_018085.4 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr1:46165595 G>T did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr9:95378212 G>C maps to NM_022755.5 V459V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QD-01A-32D-A22X-09 chr9:95378116 G>C maps to NM_022755.5 V491V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QD-01A-32D-A22X-09 chr9:95378125 G>A maps to NM_022755.5 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr3:121547405 G>A maps to NM_001023570.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr12:113638561 G>C maps to ENST00000416617 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr7:2608598 G>A maps to NM_152558.3 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr7:2637912 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr3:51897274 C>T maps to NM_203424.1 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr3:197616499 G>C maps to NM_001134435.1 S428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr3:197639563 G>A maps to NM_001134435.1 F315F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr3:197618336 C>A maps to NM_001134435.1 E393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr3:197616440 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr3:197619501 C>T maps to NM_001134435.1 K364K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:67664959 C>G maps to NM_001031715.2 S422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UC-01A-11D-A351-09 chr15:90996473 G>A maps to NM_003870.3 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:75866442 C>G maps to NM_006633.2 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr5:75970512 C>G maps to NM_006633.2 S1169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr5:75967718 C>T maps to NM_006633.2 I993I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr5:76003273 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr1:156534462 C>T maps to NM_178229.4 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr1:156539198 G>A maps to NM_178229.4 Q32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:156533584 G>A maps to NM_178229.4 Q157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr23:53278056 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr23:53276286 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr23:53272578 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VK-01A-11D-A28B-09 chr23:53296140 T>A did not map to a codon.
Sequencing variant TCGA-FU-A3TX-01A-11D-A22X-09 chr12:176518 G>A maps to NM_001170738.1 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr23:153282518 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:153278868 C>G did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:153282448 G>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q8-01A-11D-A21Q-09 chr3:10219597 G>A maps to NM_001570.3 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr12:66638415 C>T maps to NM_007199.2 I346I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H6-01B-11D-A22X-09 chr5:131823639 G>A maps to NM_002198.2 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr19:46388495 C>G maps to NM_015649.1 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr19:50168984 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:209963023 G>C maps to NM_006147.2 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr11:613209 G>A maps to NM_004031.2 F424F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PI-01A-11D-A18J-09 chr11:613862 C>A maps to NM_004031.2 E270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5O9-01A-11D-A28B-09 chr16:85952377 C>A maps to NM_002163.2 V319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr14:24635116 C>T maps to NM_006084.4 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr19:44222853 C>T maps to NM_019612.3 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr19:44222730 C>T maps to NM_019612.3 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A69L-01A-11D-A32I-09 chr19:44096996 G>A maps to NM_001007561.2 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:44097209 G>C maps to NM_001007561.2 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr2:227662863 C>T maps to NM_005544.2 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr13:110434809 G>A maps to NM_003749.2 G1197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr23:107979293 C>T did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr23:107976264 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:107978806 C>G did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:107979073 G>A did not map to a codon.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr5:3599343 G>A maps to NM_024337.3 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr5:3599745 C>T maps to NM_024337.3 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr5:2749784 C>T maps to NM_033267.4 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr16:55362885 G>A maps to NM_024335.2 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZE-01A-11D-A28B-09 chr16:55363209 G>A maps to NM_024335.2 P440P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr1:949716 C>T maps to NM_005101.3 D119D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:156697517 C>G did not map to a codon.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr5:50683467 G>A maps to NM_002202.2 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr5:50683410 C>T maps to NM_002202.2 I102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr15:74425397 C>G maps to NM_001130137.1 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr15:74426564 G>A maps to NM_001130137.1 A490A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LC-01A-11D-A20U-09 chr14:77951064 C>T maps to NM_199296.2 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WH-01A-22D-A351-09 chr5:128440650 C>G maps to NM_016048.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CJ-01A-11D-A32I-09 chr7:16255785 G>A maps to NM_001101426.3 Q386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr20:33030036 C>T maps to ENST00000262650 H339H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr16:47487998 G>A maps to NM_030790.3 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr5:52206173 G>C maps to NM_181501.1 P594P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr1:145532811 C>T maps to NM_003637.3 F377F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:145538295 C>T maps to NM_003637.3 L941L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QD-01A-32D-A22X-09 chr15:68649535 C>T maps to ENST00000423218 Q234Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3PZ-01A-11D-A21Q-09 chr15:68624759 C>G maps to ENST00000423218 V494V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr5:52386427 G>A maps to NM_002203.3 *1182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr5:52351381 C>G maps to NM_002203.3 S265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr17:48156606 C>G maps to NM_002204.2 L856L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr2:182363437 G>A maps to NM_000885.4 V543V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VK-01A-11D-A28B-09 chr2:182347103 T>A maps to NM_000885.4 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr2:182346368 G>T maps to NM_000885.4 E267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:173352120 G>C maps to ENST00000264106 L739L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr12:56094854 G>A maps to ENST00000347027 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr12:56090709 G>A maps to ENST00000347027 V614V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr10:15649713 T>A maps to NM_003638.1 K576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr10:15590564 A>G maps to NM_003638.1 N923N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr10:15617593 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr10:15561411 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr3:37544679 G>A maps to NM_002207.2 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A69M-01A-11D-A32I-09 chr3:37792020 A>T maps to NM_002207.2 S834S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr3:37785522 C>T maps to NM_002207.2 Q811*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr16:31424552 C>G maps to ENST00000444228 S677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U3-01A-11D-A28B-09 chr16:31434713 C>T maps to ENST00000444228 N983N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A5QV-01A-22D-A28B-09 chr17:3655126 G>A maps to NM_002208.4 P570P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr17:3655000 G>A maps to NM_002208.4 F612F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DV-01A-11D-A32I-09 chr17:3656604 G>A maps to NM_002208.4 Y549Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr16:30485562 C>T maps to NM_002209.2 F36F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr16:31282367 C>G maps to NM_001145808.1 S174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:187455217 C>T maps to NM_002210.3 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:187531486 G>A maps to NM_002210.3 V741V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr2:187465066 C>T maps to NM_001144999.1 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr16:31382736 C>T maps to NM_000887.3 Q642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr16:31368668 C>T maps to NM_000887.3 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:70521660 C>G did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:70524983 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr23:70523592 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr21:46330646 G>A maps to NM_000211.3 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr21:46320234 G>A maps to NM_000211.3 F299F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr17:45405718 G>C did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:63906587 A>C did not map to a codon.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr17:73738774 C>T maps to NM_001005619.1 I965I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:73738842 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr17:73726983 C>G maps to NM_001005619.1 S344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr3:124567328 G>C maps to NM_002213.3 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr2:160980320 C>T maps to NM_000888.3 A654A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QE-01A-21D-A21Q-09 chr2:160998512 G>A maps to NM_000888.3 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr12:53591318 G>A maps to NM_000889.1 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr12:53589845 G>C maps to NM_000889.1 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr3:52825551 C>T maps to NM_002215.2 I838I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AX-01A-12D-A243-09 chr3:52816047 C>T maps to NM_002215.2 Y260Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr3:52825554 T>G maps to NM_002215.2 G839G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr3:52860027 A>C maps to ENST00000485816 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr10:7679251 G>A maps to ENST00000256861 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A50E-01A-21D-A26G-09 chr10:7679251 G>A maps to ENST00000256861 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr10:7621935 G>A maps to ENST00000256861 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr23:78616653 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A73R-01A-11D-A33O-09 chr23:78622731 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr20:3190193 C>A did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr15:41795047 G>A maps to NM_002220.1 R391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr1:226829633 G>A maps to NM_002221.3 I813I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr3:4836776 C>T maps to ENST00000356617 R2277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr3:4847938 C>T maps to ENST00000356617 F2418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr3:4821244 G>A maps to ENST00000356617 S2099S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr6:33632873 C>T maps to ENST00000374316 I431I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr6:33655085 C>T maps to ENST00000374316 I2053I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr6:33655091 C>T maps to ENST00000374316 I2055I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WF-01A-11D-A351-09 chr2:96992534 G>T maps to ENST00000420728 E87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr2:24439052 C>T maps to NM_006277.2 Q1285Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr2:24521653 A>G maps to NM_006277.2 R458R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr1:152883055 A>G maps to NM_005547.2 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr1:185266927 T>C did not map to a codon.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr6:150716576 G>T maps to NM_001164695.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr20:10639290 G>A maps to NM_000214.2 N173N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr20:10653408 G>C maps to NM_000214.2 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr20:10620520 C>T maps to NM_000214.2 R1094R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr14:105618302 G>A maps to NM_002226.3 D337D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr1:65305415 C>T maps to NM_002227.2 Q904Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:65332605 G>A maps to NM_002227.2 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:65312459 C>G did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr9:5123013 G>T maps to NM_004972.3 E1024*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr9:5055738 C>G maps to NM_004972.3 S336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr9:5050790 G>T maps to NM_004972.3 E192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr9:5090885 G>T maps to NM_004972.3 E1012*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr19:17951036 A>G did not map to a codon.
Sequencing variant TCGA-FU-A770-01A-11D-A33O-09 chr4:6086677 G>A maps to NM_001099433.1 D283D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr4:6087284 C>T maps to NM_001099433.1 Q232Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr4:6042434 G>A maps to NM_001099433.1 F702F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr5:147040795 G>A maps to NM_014790.3 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr10:133955449 G>C maps to NM_001105521.2 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr10:133946875 C>T maps to NM_001105521.2 Q232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr11:134014898 C>G did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr6:15497207 C>T maps to NM_004973.2 F584F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr6:15517423 T>C maps to NM_004973.2 C1161C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr7:139791673 G>A maps to NM_030647.1 F887F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr14:59951217 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VI-01A-11D-A28B-09 chr10:64953103 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr15:42127258 G>T maps to NM_005090.3 E104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A5XV-01A-11D-A28B-09 chr5:78610438 T>G maps to NM_152405.4 P808P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr5:78586978 C>T maps to NM_152405.4 Q462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr8:75227565 A>T maps to NM_020647.2 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr16:87678344 C>T maps to NM_020655.2 Y288Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr16:87724056 C>T maps to NM_020655.2 F697F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr8:143740179 G>A did not map to a codon.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr11:96125363 G>A maps to NM_003772.3 Q517Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr1:59247747 C>G maps to NM_002228.3 *332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:59248412 G>A maps to NM_002228.3 F110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr19:12903535 C>T maps to NM_002229.2 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr19:12903627 G>C maps to NM_002229.2 *348S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:12902989 C>T maps to NM_002229.2 F135F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr19:18391925 G>A maps to NM_005354.4 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr17:39919564 C>T maps to NM_021991.2 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr17:39925390 C>G maps to NM_021991.2 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5O9-01A-11D-A28B-09 chr6:24358085 C>T maps to NM_181337.3 N73N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:8507778 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr3:123881187 G>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:124369773 G>A maps to NM_001024660.3 L1927L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr3:124398420 C>T maps to ENST00000462213 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr9:710903 C>G maps to NM_015158.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr9:745828 T>G did not map to a codon.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr9:731243 C>T maps to NM_015158.2 Q995*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr9:711530 G>A maps to NM_015158.2 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr19:11303836 G>A maps to NM_015493.6 Q307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr19:11303837 A>G maps to NM_015493.6 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr19:8397919 G>A maps to NM_198471.2 I638I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr19:8399295 G>A maps to NM_198471.2 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:62739080 C>T maps to NM_181712.4 K565K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:62738963 C>T maps to NM_181712.4 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr17:40271594 G>A maps to NM_021078.2 Q281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr13:30805525 G>A maps to NM_032116.3 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr18:44572877 G>A maps to ENST00000356157 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr16:57787336 C>G maps to NM_005886.2 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr3:127642674 C>T maps to NM_207335.2 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr3:127703142 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr7:32909520 C>T maps to NM_015483.2 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr11:105923633 G>A maps to NM_198439.2 C594C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr13:41768291 G>A maps to NM_032138.4 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr13:41768354 G>A maps to NM_032138.4 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr3:67048773 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr12:5020789 C>T maps to NM_000217.2 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr12:5020633 C>T maps to NM_000217.2 H30H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr12:5027213 G>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:111147188 G>A maps to NM_004974.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr11:30034063 G>A maps to NM_002233.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr11:30034509 A>G did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr11:30034992 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr12:5155076 C>G maps to NM_002234.2 V588V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr12:4920130 C>T maps to NM_002235.3 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr3:156192550 G>A maps to NM_172159.3 Q182Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr3:156254593 G>A did not map to a codon.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr3:155755531 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr8:73849924 G>T maps to NM_004770.2 G779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr8:73480145 G>A maps to NM_004770.2 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr11:17793408 C>T maps to NM_001112741.1 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:17793717 C>T maps to NM_001112741.1 F359F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr11:17758016 G>A maps to NM_001112741.1 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:50827006 G>C maps to NM_004977.2 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr1:110765969 C>T maps to NM_004978.4 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:110774855 C>T maps to NM_004978.4 L611L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:48826641 G>A did not map to a codon.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr7:120373013 G>A maps to NM_012281.2 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr7:120373061 C>A maps to NM_012281.2 S407S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr1:112525176 G>A maps to ENST00000315987 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:112525015 G>A maps to ENST00000315987 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr23:108867843 C>T did not map to a codon.
Sequencing variant TCGA-EA-A410-01A-11D-A243-09 chr20:49621097 C>T maps to NM_002237.3 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R3-01A-11D-A28B-09 chr20:49626581 G>A maps to NM_002237.3 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr18:77659698 C>T maps to NM_012283.1 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr18:77659101 C>T maps to NM_012283.1 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:210856727 G>A maps to NM_172362.2 L955L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr7:150648869 C>G maps to NM_000238.2 R537R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr12:49948276 C>T maps to NM_012284.1 F692F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr12:49951640 T>C maps to NM_012284.1 L1053L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A44S-01A-12D-A26G-09 chr12:49934757 C>T maps to NM_012284.1 D51D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3TX-01A-11D-A22X-09 chr17:40316183 G>A maps to NM_012285.2 G696G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr14:63175098 G>T maps to NM_139318.3 L698L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr14:63246616 G>A maps to NM_139318.3 I616I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr17:61611638 C>T maps to NM_030779.2 F356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr2:163694970 G>T maps to NM_033272.2 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr3:19190253 C>T maps to NM_144633.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr10:103587398 C>G maps to NM_173197.2 *185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr10:103586854 C>G did not map to a codon.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr4:21731536 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr11:128709382 G>A maps to NM_000220.2 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5FO-01A-21D-A28B-09 chr11:17408654 C>T maps to NM_000525.3 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr17:21318908 C>G maps to NM_021012.4 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LT-01A-11D-A18J-09 chr2:233633434 G>T maps to NM_002242.4 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr19:48965010 C>T maps to NM_170720.1 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr19:48965271 C>T maps to NM_170720.1 F97F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr17:68128779 C>T maps to NM_018658.1 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr17:68172112 C>T maps to NM_000891.2 C311C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M1-01A-11D-A18J-09 chr22:38823294 C>T maps to NM_152868.1 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr21:39086856 C>T maps to NM_002240.2 E201E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr21:39087249 C>G maps to NM_002240.2 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr1:160053897 G>A maps to NM_004983.2 E26E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr14:88729707 G>T maps to NM_138318.2 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr20:43378815 C>T maps to ENST00000372861 C110C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr6:39282795 C>T maps to NM_032115.3 K304K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3L7-01A-21D-A20U-09 chr1:215259780 G>A maps to NM_001017425.2 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr6:39158926 G>A maps to NM_003740.3 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A411-01A-11D-A243-09 chr6:39158872 G>A maps to NM_003740.3 D431D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr6:39158728 G>T maps to NM_003740.3 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr8:140630752 C>T maps to NM_016601.2 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZE-01A-11D-A28B-09 chr8:140630965 G>A maps to NM_016601.2 Y220Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr10:79396113 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr10:79396285 G>A did not map to a codon.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr3:178957771 C>T did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:154744506 G>A maps to NM_002249.4 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:154744743 G>A maps to NM_002249.4 F385F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:154687434 G>A maps to NM_002249.4 I582I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr19:44278345 C>T maps to NM_002250.2 E227E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr11:2797248 C>T maps to NM_000218.2 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr20:62076669 G>A maps to NM_172107.2 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr8:133492620 G>A maps to NM_004519.2 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H6-01B-11D-A22X-09 chr8:133141781 G>A maps to NM_004519.2 I782I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr6:73787561 T>C maps to NM_001160133.1 D290D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr6:73751727 C>T maps to NM_001160133.1 R187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5FO-01A-21D-A28B-09 chr20:43726319 G>A maps to NM_002251.3 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr2:18113429 C>T maps to NM_002252.3 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr9:138660688 C>T maps to ENST00000298480 I472I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr1:196195006 G>T did not map to a codon.
Sequencing variant TCGA-C5-A2LS-01A-22D-A22X-09 chr1:196295845 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr1:196309499 A>C maps to NM_198503.2 L585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:196196858 C>T did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr8:36766905 G>C maps to NM_001031836.2 P728P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2GZ-01A-11D-A17W-09 chr8:36780036 C>T maps to NM_001031836.2 Q876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr8:110980665 C>T maps to NM_014379.2 W385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr8:110980753 C>A maps to NM_014379.2 G356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr9:2718191 C>T maps to NM_133497.2 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr12:109898563 G>A maps to NM_031954.3 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr13:77459647 G>A maps to NM_138444.3 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr13:77460013 G>A maps to NM_138444.3 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3TX-01A-11D-A22X-09 chr11:77728118 C>T maps to NM_023930.3 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr19:34302351 G>A maps to ENST00000422820 E199E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr6:36452531 G>T maps to NM_173562.3 E300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr1:215760000 C>T maps to NM_016121.3 Q264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr13:45768492 C>T maps to NM_198404.2 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr3:58484429 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:23399796 C>T maps to NM_001009999.2 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr11:66975045 C>T maps to NM_012308.2 Q125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr11:66975146 G>A maps to NM_012308.2 Q158Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr11:66985141 G>C did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr11:67022513 G>A maps to NM_012308.2 Q1159Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr11:67024770 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr11:67021878 C>A maps to NM_012308.2 L1099L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr12:121947489 G>C maps to ENST00000377071 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr12:121880219 C>T maps to ENST00000377071 L1008L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:137754896 C>T maps to NM_016604.3 Q1231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr5:137763728 G>A maps to NM_016604.3 V1569V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr5:137762662 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr5:137762889 G>C maps to NM_016604.3 L1505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R1-01A-11D-A28B-09 chr5:137727606 C>G maps to NM_016604.3 L762L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R1-01A-11D-A28B-09 chr5:137727776 C>G maps to NM_016604.3 S819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr1:44132111 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr19:5144885 C>T maps to NM_015015.2 I998I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr19:5144296 C>T maps to NM_015015.2 V925V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr9:7103734 C>T maps to NM_015061.3 I825I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LB-01A-11D-A243-09 chr9:6893236 G>T did not map to a codon.
Sequencing variant TCGA-MY-A5BE-01A-21D-A26G-09 chr9:7174650 G>A maps to NM_015061.3 K1031K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr9:6893198 C>G maps to NM_015061.3 V296V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr11:94731207 A>G maps to NM_018039.2 E224E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr12:431664 G>A maps to NM_001042603.1 R782*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr12:465701 G>C maps to NM_001042603.1 S225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr12:416237 G>A maps to NM_001042603.1 F1316F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:419124 C>T maps to NM_001042603.1 L1074L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:202698922 G>C maps to ENST00000367264 S1506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr1:202702960 G>C maps to ENST00000367264 L1195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr1:202709924 C>T maps to ENST00000367264 L1023L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr1:202710712 C>T maps to ENST00000367264 E945E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr1:202743751 G>A maps to ENST00000367264 Q132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr1:202702903 G>A maps to ENST00000367264 I1214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr23:53228334 G>A did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr23:53228251 G>C did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:53222363 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr23:53253975 C>G did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:53253978 G>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:53223511 C>T did not map to a codon.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr23:44942756 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:44922853 T>G did not map to a codon.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr23:44938389 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:44928920 C>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:44928928 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:44929241 C>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:44929321 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:44929340 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:44929352 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:44929361 C>G did not map to a codon.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr23:44911047 G>A did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr23:44949030 G>A did not map to a codon.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr17:7752017 C>G maps to NM_001080424.1 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr17:7748247 G>A did not map to a codon.
Sequencing variant TCGA-EA-A5ZD-01A-11D-A28B-09 chr4:55973989 C>T maps to NM_002253.2 T442T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr6:74019362 G>T maps to ENST00000370384 I25I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr8:136659336 C>T did not map to a codon.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr19:6416893 C>G did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:2837401 C>G did not map to a codon.
Sequencing variant TCGA-JW-A5VK-01A-11D-A28B-09 chr9:2804206 G>T did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr17:26959123 C>T maps to NM_014680.2 K1313K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr17:26970292 G>A maps to NM_014680.2 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr17:26955503 C>T maps to NM_014680.2 W1458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr17:26962165 C>T maps to NM_014680.2 R813R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q8-01A-11D-A21Q-09 chr15:64669054 G>T maps to NM_014736.4 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr17:73481597 C>T maps to ENST00000375248 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr17:73482022 C>T maps to ENST00000375248 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr8:126085487 C>A maps to ENST00000377985 E358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr4:6862711 T>C maps to NM_014743.2 C201C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr14:70171393 C>T maps to NM_014734.3 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr6:24569027 G>A maps to NM_014809.3 L707L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7X3-01A-11D-A351-09 chr1:35906653 G>A maps to NM_024874.4 R986*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:35906602 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr19:34791602 C>T maps to NM_014686.3 D75D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr9:114140943 G>C maps to NM_001080398.1 L1468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr16:15704956 G>C maps to NM_014647.3 S1209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HR-01A-11D-A20U-09 chr16:27643923 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr16:27781219 C>G maps to NM_015202.2 V1338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr16:27751795 C>T maps to NM_015202.2 V726V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr1:39877563 C>T maps to NM_015038.1 L543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QD-01A-32D-A22X-09 chr16:67214569 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr1:155886622 A>C did not map to a codon.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr1:155891711 G>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:155899504 C>A maps to NM_014949.2 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr4:154513679 C>G maps to NM_001131007.1 L622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr4:154523327 T>G maps to NM_001131007.1 L764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:5457443 G>C did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr5:5464405 G>A maps to NM_015325.1 L1653L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr5:5464744 C>T maps to NM_015325.1 L1766L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr6:84913751 C>A maps to NM_014895.2 E212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M2-01A-21D-A18J-09 chr15:79760659 G>C maps to NM_015206.2 L895L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr12:105558477 G>A maps to NM_015275.1 K1138K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr4:123168400 C>T maps to NM_015312.3 Q1801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr5:175774644 G>C maps to NM_020444.3 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr15:81234255 C>G maps to NM_018689.1 G1158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr23:118222150 C>G did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:118222062 T>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:118227697 G>T did not map to a codon.
Sequencing variant TCGA-FU-A3WB-01A-11D-A22X-09 chr23:118223457 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:118223211 C>G did not map to a codon.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr23:118242372 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr4:57182676 G>A maps to NM_020722.1 P1003P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr4:57193850 G>T maps to NM_020722.1 E1195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr10:24835134 C>G maps to NM_019590.3 S1905*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr10:24820870 G>A maps to NM_019590.3 T1065T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr6:138613166 C>T maps to NM_020340.4 L1115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KJ-01A-11D-A18J-09 chr6:138613151 G>A maps to NM_020340.4 A1110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr6:138612945 C>T maps to NM_020340.4 Q1042*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr6:138640858 T>C maps to NM_020340.4 Y1498Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr3:128697044 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr10:70775880 A>G maps to NM_015634.3 R525R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr11:101815076 G>A maps to NM_020802.2 K110K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr3:113729735 C>T maps to NM_020817.1 K432K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr8:95500997 G>T maps to NM_015496.3 S1792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr4:186111574 G>C maps to NM_020827.1 S259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr4:186085306 C>T maps to NM_020827.1 V449V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr10:30316394 C>G maps to NM_020848.2 P894P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr12:13233557 G>T did not map to a codon.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr12:13208764 C>G maps to NM_020853.1 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R9-01A-11D-A18J-09 chr1:33236207 C>T maps to NM_020888.2 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr1:33234341 G>T maps to NM_020888.2 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:33237622 C>G maps to NM_020888.2 S948*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr3:108279558 C>T maps to NM_020890.2 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HM-A4S6-01A-11D-A26G-09 chr6:56917954 C>T maps to NM_020931.2 Q220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QE-01A-21D-A21Q-09 chr1:180913547 G>A maps to NM_020950.1 R1061R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:180907774 C>G maps to NM_020950.1 S949*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr22:44692658 G>C maps to NM_001099294.1 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr19:18376081 G>A maps to NM_001145304.1 L756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr19:18380274 C>T did not map to a codon.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr13:45563759 C>T did not map to a codon.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr20:36850987 C>T maps to NM_001029864.1 R760R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr20:36869137 C>T maps to NM_001029864.1 E465E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr20:36856602 G>A maps to NM_001029864.1 D637D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr1:233518364 C>T maps to NM_032435.2 Q1007*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr1:233489615 C>T maps to NM_032435.2 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A69M-01A-11D-A32I-09 chr1:233482308 C>A maps to NM_032435.2 A309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A5XV-01A-11D-A28B-09 chr1:233518244 C>T maps to NM_032435.2 Q967*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr2:61385089 C>T maps to ENST00000398622 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr6:111588063 G>T maps to NM_153369.2 G433G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr6:111587258 C>G maps to NM_153369.2 S165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr9:115421910 G>A maps to NM_133465.2 T571T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr9:115380202 C>T maps to ENST00000374244 I408I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr9:139700618 G>A maps to NM_001039374.4 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr9:139700648 G>A maps to NM_001039374.4 E356E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr9:139700699 G>A maps to ENST00000432628 G332G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr9:139694866 C>T maps to NM_001039374.4 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:11983499 G>A maps to ENST00000376576 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A3LQ-01A-21D-A21Q-09 chr3:113376115 C>T maps to NM_001009899.2 Q1471Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr3:113377146 C>A maps to NM_001009899.2 E1128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr23:73962691 G>A did not map to a codon.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr23:73963959 C>G did not map to a codon.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr23:73960741 C>T did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:73959274 C>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:73962042 C>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:73965412 C>A did not map to a codon.
Sequencing variant TCGA-LP-A4AX-01A-12D-A243-09 chr23:73962041 T>G did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr23:73960814 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr9:6007360 C>A maps to NM_001017969.2 E143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr9:5923061 C>T maps to NM_001017969.2 K978K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr9:6007496 G>A maps to NM_001017969.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr2:8934072 C>A maps to NM_020738.2 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr2:8967124 C>T maps to NM_020738.2 E33E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr2:8936987 C>T maps to NM_020738.2 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr2:8926070 G>A maps to NM_020738.2 L677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr2:8930013 G>A maps to NM_020738.2 F539F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr2:8930034 G>A maps to NM_020738.2 F532F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr10:94410248 C>A maps to NM_004523.3 S1005*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr9:116854203 G>A maps to ENST00000259410 G626G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A44S-01A-12D-A26G-09 chr6:17826020 G>A maps to NM_022113.4 I588I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr6:17826008 C>T maps to NM_022113.4 L592L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr8:28988055 G>A maps to NM_015254.3 L1023L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr8:28988169 C>T maps to NM_015254.3 V985V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr8:28932812 C>T maps to NM_015254.3 V1502V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VG-01A-11D-A28B-09 chr1:200528487 A>G maps to NM_014875.2 H1441H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr20:16360066 G>A maps to NM_024704.4 I860I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr1:20998568 C>A maps to NM_020816.2 E862*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr11:28056944 C>T maps to NM_031217.3 R831R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr17:72350664 G>T maps to NM_153209.3 R891R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A3LQ-01A-21D-A21Q-09 chr2:241700167 C>T maps to ENST00000373308 T786T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr2:241689948 C>G maps to ENST00000373308 L958L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OA-01A-11D-A16Y-08 chr1:10363822 G>A maps to NM_183416.3 L860L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:10425555 C>T maps to ENST00000377086 L1534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr17:4925559 C>T maps to NM_006612.5 I728I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr5:137518569 G>A maps to NM_005733.2 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr10:91469149 C>T maps to ENST00000416354 Q95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr10:91479208 G>T maps to ENST00000416354 E490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr10:91503596 G>A maps to ENST00000416354 L1346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr1:200974480 G>A maps to NM_017596.2 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A5XV-01A-11D-A28B-09 chr1:200942676 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr1:200977901 G>A maps to NM_017596.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr15:69728996 G>A maps to NM_138555.1 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A6QX-01A-12D-A33O-09 chr15:69732247 G>A maps to NM_138555.1 E573E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr9:34257872 A>G maps to NM_194313.2 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr6:168443352 G>A maps to NM_030615.2 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr6:168418688 C>A did not map to a codon.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr14:104641548 C>T maps to NM_015656.1 N808N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr1:245772751 G>A maps to NM_018012.3 S612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr1:245766082 C>T maps to NM_018012.3 Q519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr1:245850610 G>A maps to NM_018012.3 L1442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr9:86530455 G>A maps to NM_017576.1 C17C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr9:86498736 C>G maps to NM_017576.1 L812L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:45223225 A>C did not map to a codon.
Sequencing variant TCGA-EX-A3L1-01A-11D-A21Q-09 chr1:45216174 G>A maps to NM_006845.3 E126E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr1:45232559 C>G maps to NM_006845.3 T678T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr5:132036231 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr20:30915356 A>G did not map to a codon.
Sequencing variant TCGA-FU-A770-01A-11D-A33O-09 chr20:30898822 C>A maps to NM_004798.3 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr2:26152235 G>A maps to NM_002254.6 L742L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr2:26178493 G>A maps to NM_002254.6 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LS-01A-22D-A22X-09 chr23:69615616 G>T did not map to a codon.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr23:69521873 C>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:69516912 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr23:69594045 G>C did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:69595078 C>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:69561766 G>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:69625689 G>C did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr5:154396406 C>T maps to NM_001099293.1 L996L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr5:154395761 C>T maps to NM_001099293.1 L781L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr5:154393824 C>T maps to NM_001099293.1 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr12:57944126 C>T maps to NM_004984.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LB-01A-11D-A243-09 chr10:32311952 T>A maps to NM_004521.2 G579G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A4BA-01A-21D-A26G-09 chr2:149866722 C>T maps to NM_004522.1 R875R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:149838050 G>A maps to NM_004522.1 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr15:90152030 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr15:90190195 C>T maps to NM_198525.2 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr15:90192360 G>C maps to NM_198525.2 S256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr3:47281405 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr3:47277038 G>A maps to NM_182902.3 I762I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr6:33371528 G>T maps to NM_002263.3 G127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr6:33368140 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr6:33368153 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr6:33366153 C>T maps to NM_002263.3 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LS-01A-22D-A22X-09 chr16:57795348 C>A maps to NM_005550.3 V616V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr16:57819412 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr16:57831719 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr16:57806155 C>G maps to NM_005550.3 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr10:7798010 G>T did not map to a codon.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr19:55294398 G>A maps to ENST00000291633 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A449-01A-11D-A243-09 chr19:55284905 G>C maps to ENST00000291633 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr19:55263155 C>T maps to NM_015868.2 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr19:55263146 C>T maps to NM_015868.2 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr19:55329004 G>A maps to ENST00000355608 Q17Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RE-01A-11D-A18J-09 chr19:55333102 C>A maps to ENST00000355608 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UC-01A-11D-A351-09 chr19:36357422 C>T maps to NM_032123.5 I629I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr19:36348062 C>T maps to NM_199180.2 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr13:33635285 G>A maps to NM_004795.3 P690P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr4:39448913 G>A maps to NM_175737.3 L856L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr4:39448763 C>T maps to NM_175737.3 L806L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr4:39435942 G>C maps to NM_175737.3 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr11:66026209 G>T maps to NM_022822.2 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr11:66030327 C>T maps to NM_022822.2 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr19:45851406 G>A maps to NM_177417.2 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr1:44596346 G>A maps to NM_173484.3 K363K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CJ-01A-11D-A32I-09 chr4:38690501 C>T maps to NM_016531.5 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr4:38698704 G>T maps to NM_016531.5 E287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr13:73636561 G>A maps to NM_001730.3 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr10:3821733 G>C maps to NM_001300.5 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:56292145 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr6:42986398 T>C maps to NM_057161.2 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr16:87764167 C>A maps to NM_017566.3 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KH-01A-21D-A22X-09 chr1:18807594 G>A maps to NM_152375.2 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr22:50986891 G>C maps to NM_138433.3 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr3:49212501 G>A maps to NM_173546.2 W258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr13:70681765 G>A maps to NM_020866.2 F22F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr13:70681804 G>A maps to NM_020866.2 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:117053560 G>C did not map to a codon.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr23:117162392 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:117054301 A>C did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:117043456 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr18:30350038 G>A maps to NM_020805.1 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr18:30350521 G>A maps to NM_020805.1 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr23:24024243 C>T did not map to a codon.
Sequencing variant TCGA-EA-A5FO-01A-21D-A28B-09 chr23:24006424 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:24006132 C>T did not map to a codon.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr23:24006340 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:897277 C>T maps to NM_198317.2 Q188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R9-01A-11D-A18J-09 chr3:47364190 C>T maps to NM_025010.4 R132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr2:170592187 C>T maps to NM_144711.5 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr14:45398272 G>T maps to ENST00000355081 G572G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr14:45403316 C>A did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr5:136997700 G>C maps to NM_017415.2 S219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr23:21675599 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr16:84695381 C>T maps to NM_024731.2 I498I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr8:124658170 C>T maps to NM_001081675.2 V518V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr23:86868949 G>A did not map to a codon.
Sequencing variant TCGA-EA-A5FO-01A-21D-A28B-09 chr23:86890561 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr23:86772952 G>C did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:86772993 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr23:86890702 T>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:86869043 A>G did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:86873002 C>G did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr23:86873029 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr3:183209822 C>T maps to NM_130446.2 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr19:51530212 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr19:51537306 G>A maps to NM_019598.2 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CJ-01A-11D-A32I-09 chr19:51563190 C>A maps to NM_015596.1 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3PZ-01A-11D-A21Q-09 chr19:51584835 G>A maps to NM_022046.4 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr19:51410258 G>A maps to NM_004917.3 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr19:51499380 A>T maps to NM_144505.1 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr12:10601864 G>A maps to NM_213658.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr12:10603152 G>T maps to NM_213658.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr12:10464229 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr12:10464196 C>T maps to ENST00000381908 Q100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KH-01A-21D-A22X-09 chr7:139164444 C>A maps to NM_198508.2 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:241714341 C>T maps to NM_003679.3 Q104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CH-01A-11D-A33O-09 chr10:135015329 C>T maps to ENST00000368572 A1107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr10:135020477 G>A maps to ENST00000368571 P1135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr10:135011221 C>G maps to ENST00000368572 S619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LC-01A-11D-A20U-09 chr10:135015314 C>T maps to ENST00000368572 A1102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr3:186456901 G>A maps to NM_001102416.2 K315K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr12:123078604 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr12:123078722 G>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:123058850 C>G maps to NM_014708.4 S769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr12:123087421 G>A maps to NM_014708.4 S1624S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr3:122144681 T>C did not map to a codon.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr3:122145812 G>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:66040015 G>A maps to NM_002266.2 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr1:152732420 C>T maps to NM_001025231.1 Y119Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr7:149430666 G>A maps to NM_032534.2 W874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr22:29536303 C>T maps to NM_032045.4 I403I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr12:53069234 G>A maps to NM_006121.3 Y559Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WI-01A-12D-A351-09 chr12:53069219 G>A maps to NM_006121.3 G564G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr12:53071165 G>T maps to NM_006121.3 V354V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr17:38976837 C>T maps to NM_000421.3 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:39659971 C>T maps to NM_153490.2 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:39659977 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr17:39742948 G>A maps to NM_000526.4 Y46Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr12:53344641 C>T maps to NM_000224.2 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr17:39684454 G>A maps to NM_002276.4 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr17:39079241 C>T maps to NM_015515.3 *423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:39087626 G>C maps to NM_015515.3 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr12:53185153 G>A maps to ENST00000309505 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr17:39553569 C>T maps to ENST00000393998 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr17:39537388 C>G maps to NM_021013.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr17:39538342 G>A maps to NM_021013.3 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr17:39535334 G>A maps to NM_021013.3 Q366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr17:39635694 C>T maps to NM_002280.4 R205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:39634663 C>G maps to NM_002280.4 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:39118418 G>A maps to NM_213656.3 R331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PI-01A-11D-A18J-09 chr12:53202173 T>C maps to NM_002272.2 Q417Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr12:52914023 G>A maps to NM_000424.3 T19T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr12:52844260 G>A maps to NM_005555.3 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr12:52841347 G>A maps to NM_005555.3 G478G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr12:52842664 G>A maps to NM_005555.3 I388I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr12:52863515 G>C maps to NM_173086.4 V454V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr12:52641572 C>A did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr12:52627213 C>G maps to NM_005556.3 S45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr12:52631388 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr12:52943901 C>T maps to NM_033448.2 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:52940164 C>T maps to NM_033448.2 R410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A556-01A-11D-A26G-09 chr12:52980754 G>A maps to NM_080747.2 G440G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZF-01A-11D-A28B-09 chr12:52984670 G>A maps to NM_080747.2 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr12:52980736 C>G maps to NM_080747.2 V446V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr12:52981578 C>T maps to NM_080747.2 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr12:52967183 G>A maps to NM_175053.3 N126N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr12:52825339 G>T maps to ENST00000252245 S340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:52827902 G>C maps to ENST00000252245 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr12:53170901 G>A maps to NM_015848.4 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr12:53162760 G>A maps to NM_015848.4 V551V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr12:53216100 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr12:52760949 G>A maps to NM_002283.3 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr12:52699841 A>G did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr12:52695762 G>C maps to NM_002284.3 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HR-01A-11D-A20U-09 chr17:39190874 C>A maps to NM_030966.1 E67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PI-01A-11D-A18J-09 chr21:45959904 C>G maps to NM_198691.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr21:45977947 C>T maps to NM_198696.2 Q217Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr21:45978469 C>T maps to NM_198696.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr21:45994647 C>G maps to NM_198687.1 S338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R9-01A-11D-A18J-09 chr21:46011963 T>C maps to NM_198688.2 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr21:46012206 C>G maps to NM_198688.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr21:46021246 C>T maps to ENST00000380102 V242V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-IR-A3LA-01A-11D-A22X-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr11:1629042 T>C maps to ENST00000359229 K241K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:155142355 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr17:25919585 C>T maps to ENST00000268763 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LS-01A-22D-A22X-09 chr12:118298122 G>A maps to ENST00000339824 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr12:117993044 G>A maps to ENST00000339824 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr12:117914375 C>T maps to ENST00000339824 Q825Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr12:118199000 G>A maps to ENST00000339824 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3PZ-01A-11D-A21Q-09 chr14:56103990 C>G maps to NM_001079521.1 S542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr14:56103922 G>A maps to NM_001079521.1 Q519Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr14:56083233 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr3:134369691 C>G maps to NM_178554.4 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr2:143799740 G>A maps to NM_003937.2 *466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr23:153128961 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:153138084 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr23:153136341 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:153137668 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:153133895 G>A did not map to a codon.
Sequencing variant TCGA-JW-A852-01A-11D-A351-09 chr23:153132161 G>T did not map to a codon.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr23:153133906 G>C did not map to a codon.
Sequencing variant TCGA-JW-A69B-01A-11D-A32I-09 chr22:41621883 C>T maps to NM_031488.4 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:130374064 C>A maps to NM_032438.2 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A411-01A-11D-A243-09 chr6:130392141 C>A maps to NM_032438.2 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr6:130399705 T>C maps to NM_032438.2 C416C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr12:55027017 C>A did not map to a codon.
Sequencing variant TCGA-FU-A3YQ-01A-11D-A22X-09 chr15:63433477 G>C did not map to a codon.
Sequencing variant TCGA-EA-A3QD-01A-32D-A22X-09 chr1:201354846 G>A maps to NM_005558.3 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr19:54868124 G>C maps to NM_002287.3 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr18:6980552 C>A maps to NM_005559.2 E1992*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr6:129636635 G>T maps to NM_000426.3 E1191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A770-01A-11D-A33O-09 chr6:129618861 C>T maps to NM_000426.3 G963G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr6:129777515 G>C maps to NM_000426.3 L2248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A852-01A-11D-A351-09 chr6:129762060 C>G maps to NM_000426.3 L2062L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr6:129786307 G>T maps to NM_000426.3 E2392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr18:21492845 G>A did not map to a codon.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr18:21364000 C>T maps to ENST00000416669 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:112439101 C>G did not map to a codon.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr20:60905568 G>A maps to NM_005560.3 L1318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr7:107577712 A>G maps to NM_002291.2 I1257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr7:107626527 C>T maps to NM_002291.2 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr7:107591607 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr3:49160389 G>C maps to NM_002292.3 L1440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr3:49162312 G>C maps to NM_002292.3 S977*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr3:49162771 G>A maps to NM_002292.3 V878V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr3:49163433 G>A maps to NM_002292.3 I770I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr3:49166204 G>A maps to NM_002292.3 S593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr1:209791341 C>T maps to NM_000228.2 L987L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:209799069 C>T maps to NM_000228.2 Q633Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr1:209788693 C>T maps to NM_000228.2 L1147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HM-A4S6-01A-11D-A26G-09 chr1:183104286 G>A maps to NM_002293.3 L1370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:183177097 C>G maps to NM_005562.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:183206489 G>T maps to NM_005562.2 E869*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:183206632 G>A maps to NM_005562.2 G916G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr9:133962879 G>A maps to ENST00000355048 L1428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr23:119581703 G>A did not map to a codon.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr3:182880494 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr7:55492960 G>A maps to NM_018697.3 E341E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr23:37431656 G>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:37431521 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr4:17585202 C>T maps to NM_015907.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr4:17608477 C>T maps to NM_015907.2 V429V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr22:33712206 C>A maps to NM_133642.3 E439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr5:154092619 G>A maps to NM_015315.3 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr5:154173552 C>T maps to ENST00000377643 G354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr5:154191163 C>T maps to ENST00000377643 L1015L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr4:129120695 G>A maps to NM_018078.2 L702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H6-01B-11D-A22X-09 chr4:129100540 C>G did not map to a codon.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr10:909787 C>A maps to NM_015155.1 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr10:890927 G>A maps to NM_015155.1 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2GZ-01A-11D-A17W-09 chr10:871710 G>A maps to NM_015155.1 R409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr10:875462 C>A maps to NM_015155.1 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr15:71128663 C>T maps to NM_018357.2 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr15:71128789 C>T maps to NM_018357.2 W85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr4:113578652 A>G did not map to a codon.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr3:45554647 G>T maps to NM_015340.3 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr23:64752490 C>T did not map to a codon.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr23:64741095 G>C did not map to a codon.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr23:64738310 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr23:64741775 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr23:64741095 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr23:64741914 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:64742158 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:64742691 G>T did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr23:64732512 C>T did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr23:64749559 G>A did not map to a codon.
Sequencing variant TCGA-EA-A6QX-01A-12D-A33O-09 chr6:150005407 G>A maps to NM_004690.2 Q273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr6:150005604 G>C maps to NM_004690.2 S207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A69M-01A-11D-A32I-09 chr6:149997696 G>A maps to NM_004690.2 R924*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr6:150016266 G>A maps to NM_004690.2 R147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr6:150001485 C>A maps to NM_004690.2 V706V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr6:149997434 A>C maps to NM_004690.2 P948P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr13:21549038 C>T maps to NM_014572.2 Q1079Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr2:30457342 C>T maps to NM_030915.3 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr1:225606998 G>A maps to NM_194442.1 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr2:74726616 G>A maps to ENST00000377566 I16I. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-IR-A3LL-01A-11D-A20U-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr21:40777908 G>A maps to NM_152505.3 Q638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr21:40777979 G>C maps to NM_152505.3 S614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr21:40778143 G>A maps to NM_152505.3 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr16:67974268 G>A maps to NM_000229.1 H287H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:67974262 G>A maps to NM_000229.1 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:67974358 G>A maps to NM_000229.1 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:152800279 G>T maps to NM_178348.2 *111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H6-01B-11D-A22X-09 chr1:152659558 C>T maps to NM_014357.4 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:30748455 C>T maps to NM_182551.3 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr16:25162905 G>T maps to ENST00000380963 E148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr16:25162855 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr15:43622162 C>T maps to NM_014793.4 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr9:139650307 G>A maps to ENST00000392896 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr10:98714982 C>T maps to NM_001170765.1 F202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q8-01A-11D-A21Q-09 chr4:17885633 T>A maps to NM_001166139.1 G506G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:169689717 G>A maps to NM_005565.3 Q283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr5:169724597 C>T maps to NM_005565.3 V6V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr5:169697723 G>A maps to NM_005565.3 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr2:136564853 G>A maps to NM_002299.2 F1339F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr2:136566628 G>A maps to NM_002299.2 A1096A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr2:136547285 C>T maps to NM_002299.2 E1806E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr10:103870839 G>A maps to NM_001113407.1 Q79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr10:88494844 C>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:21790115 G>A maps to NM_002300.6 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr16:75148488 G>C maps to NM_153486.3 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr16:75150534 C>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr16:75148452 C>T maps to NM_153486.3 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr1:25894701 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr1:25893755 C>A did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr1:25894728 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3TQ-01A-11D-A22X-09 chr23:140270993 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr13:53277900 G>A maps to NM_007015.2 H278H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BF-01A-11D-A26G-09 chr1:226127175 G>A maps to NM_003240.3 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr3:156570670 C>T maps to NM_001004316.2 Q55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr3:156544665 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:156642385 G>C did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr3:156697068 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:66088676 A>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:66036335 C>G maps to NM_002303.5 S74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:43212308 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2R9-01A-11D-A18J-09 chr3:189705336 C>T maps to NM_018192.3 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr12:6948233 G>A maps to NM_014262.3 W658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RL-01A-11D-A18J-09 chr12:6948852 G>A did not map to a codon.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr22:38071706 A>G did not map to a codon.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr17:76970877 C>A maps to NM_005567.3 E90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr17:25958284 C>T did not map to a codon.
Sequencing variant TCGA-FU-A5XV-01A-11D-A28B-09 chr10:95518032 C>T maps to NM_005097.2 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr4:25014038 G>A maps to NM_018176.3 I246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr4:25005855 G>A maps to NM_018176.3 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr8:22009022 G>A maps to NM_139278.2 R270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr19:35625542 C>T maps to NM_139284.2 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr11:27395586 C>T maps to NM_018490.2 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:202250136 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr1:202287767 C>A maps to NM_001017403.1 I779I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:202288143 C>T maps to NM_001017403.1 Q905*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:49519366 C>T maps to NM_000894.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr2:48935992 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr23:111914585 G>A did not map to a codon.
Sequencing variant TCGA-EA-A5FO-01A-21D-A28B-09 chr23:111914461 G>T did not map to a codon.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr5:77784659 G>C did not map to a codon.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr5:77784641 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr3:9594297 G>A maps to NM_198560.2 I22I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr3:9543895 C>T maps to NM_198560.2 *248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr6:35773527 G>C maps to NM_182548.3 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr17:35298150 G>A maps to NM_005568.3 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr9:139096822 C>T maps to NM_178138.4 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr9:139092468 G>A maps to NM_014564.3 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr9:124989702 G>A maps to NM_014368.3 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr9:124988716 C>T maps to NM_014368.3 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr9:124979433 C>A maps to NM_014368.3 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:75608862 G>C maps to NM_001001933.1 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr22:30639681 C>T maps to NM_002309.3 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr5:38506636 G>A maps to NM_002310.5 G363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr13:108861174 T>A maps to NM_001098268.1 R814R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr13:108861663 G>A maps to NM_001098268.1 N651N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr19:55107365 G>A maps to NM_006863.1 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73Q-01A-21D-A32I-09 chr19:55107747 G>A maps to NM_006863.1 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr19:55086221 C>G maps to NM_001130917.1 S126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr19:55086304 C>T maps to NM_001130917.1 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr19:54804217 G>A maps to ENST00000391745 R3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr19:54822828 C>T maps to NM_021250.2 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr19:54822934 G>T maps to NM_021250.2 S154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr19:54783859 G>C maps to ENST00000391747 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A0TN-01A-21D-A14W-08 chr19:54722724 G>C maps to ENST00000245620 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr19:54723751 G>C maps to ENST00000407860 S449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr19:55160121 T>C did not map to a codon.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr19:54754900 T>C maps to ENST00000450632 A578A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr4:41635753 C>T maps to ENST00000503057 F673F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:45714189 A>G maps to NM_014240.2 Q550Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr20:62370084 C>G maps to NM_017806.2 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr7:73500114 G>A maps to NM_002314.2 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr22:31668595 C>A maps to NM_001031801.1 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr22:31668685 G>A maps to NM_001031801.1 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:26752836 C>G maps to NM_024674.4 S173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:36239656 C>G maps to NM_019104.1 S11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A0TN-01A-21D-A14W-08 chr4:83905635 G>T maps to NM_194282.2 S121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr4:83905682 C>T maps to NM_194282.2 Q105Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr1:226426769 C>A maps to ENST00000366807 E533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr1:226438592 T>A maps to ENST00000366807 K506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr15:77906550 G>A maps to NM_032808.5 I566I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr9:28295238 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr10:90983551 A>G maps to NM_000235.2 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CJ-01A-11D-A32I-09 chr15:58838163 C>T maps to NM_000236.2 H266H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr15:58853061 G>C did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr19:42930554 C>T maps to NM_005357.2 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:90427328 C>T maps to NM_001198829.1 Q47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr3:185252684 C>T maps to NM_139248.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr3:185229346 G>C maps to NM_139248.2 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr10:90492211 G>A maps to NM_001080518.1 K191K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr5:96443084 C>T maps to NM_153234.4 Q122Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:73552125 G>A did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr17:73559177 C>T maps to NM_001031803.1 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr18:56998761 C>A maps to NM_005570.3 E462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73R-01A-11D-A33O-09 chr18:57020468 G>A maps to NM_005570.3 R202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr2:97405603 C>T maps to NM_001142292.1 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr12:49496667 A>G did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr12:49504304 G>A maps to NM_018113.2 R12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A852-01A-11D-A351-09 chr12:49504416 C>A did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr6:70411821 G>T maps to NM_018368.3 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr22:50943259 C>A maps to NM_033200.2 E470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr22:50942058 G>A maps to NM_033200.2 Q629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr3:197748330 C>T maps to NM_001136049.2 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr1:156105655 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr19:2434312 G>A maps to NM_032737.2 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr11:8251848 G>A maps to ENST00000428101 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr11:8246192 G>A maps to ENST00000428101 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:16753786 G>C maps to ENST00000441439 S21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr13:76395532 C>T maps to ENST00000357063 Q740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr13:76395626 C>G maps to ENST00000357063 S771*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr7:97833403 G>A maps to NM_014916.3 P1463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr7:97821549 G>A maps to NM_014916.3 A591A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr7:97820150 C>T maps to NM_014916.3 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr19:49013841 G>A maps to NM_001080434.1 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:165173198 G>C maps to NM_177398.3 S356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr5:96322253 C>T maps to NM_005575.2 V337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr5:96350788 C>G maps to NM_005575.2 S789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr4:54347997 G>A maps to NM_001126328.1 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr4:54439887 G>A maps to NM_001126328.1 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr13:28122531 C>T maps to NM_153371.3 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr13:28155747 C>T maps to NM_153371.3 W31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr16:20857631 C>G maps to NM_030941.2 L738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LS-01A-22D-A22X-09 chr16:48385538 G>A maps to NM_031490.2 L795L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr2:100915695 G>A maps to NM_198461.3 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr23:118124431 G>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:118143098 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr23:118123582 C>A did not map to a codon.
Sequencing variant TCGA-FU-A3EO-01A-11D-A20U-09 chr1:153233505 C>T maps to NM_000427.2 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr8:23159626 G>C maps to NM_002318.2 T682T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr10:100013464 G>A maps to NM_032211.6 H560H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LY-01A-31D-A18J-09 chr9:113704130 C>T maps to NM_057159.2 W121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr23:78010488 C>G did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr12:6730126 C>T maps to ENST00000435659 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr5:1483581 C>T maps to NM_024830.3 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr16:55543251 G>A maps to NM_017839.4 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr16:55563839 C>A maps to NM_017839.4 S208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R1-01A-11D-A28B-09 chr16:55562472 C>T maps to NM_017839.4 R166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr12:7086370 G>A maps to NM_005768.5 F467F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr15:34654790 A>C maps to NM_153613.2 V289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:211966658 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2RE-01A-11D-A18J-09 chr19:14261735 C>T maps to NM_001008701.2 E1458E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr19:14266173 C>T maps to NM_001008701.2 K1102K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:82302630 C>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:82416114 C>T maps to ENST00000370717 Q481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr4:62936591 C>G maps to ENST00000506720 S1570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr2:11881503 C>T did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:11964763 G>A maps to ENST00000396099 V882V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr2:11945247 C>T maps to ENST00000396099 Q745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr18:2937747 C>T maps to NM_014646.2 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr18:2928603 C>T maps to NM_014646.2 Q535Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr8:19818549 C>T maps to NM_000237.2 F426F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A50E-01A-21D-A26G-09 chr17:56344896 C>A maps to NM_006151.2 L627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr17:56329550 C>T maps to NM_006151.2 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr17:56327978 C>T maps to NM_006151.2 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr17:56332226 C>T maps to NM_006151.2 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A78R-01A-11D-A32I-09 chr3:188327574 G>A maps to NM_005578.3 K352K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr19:11470165 C>T did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr19:11472091 C>T maps to NM_001170635.1 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr1:99771314 G>A maps to NM_014839.4 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr11:58318618 C>A maps to NM_004811.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr11:58295016 G>A maps to NM_004811.2 F357F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr4:151829833 G>T maps to NM_006726.3 S446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7X3-01A-11D-A351-09 chr13:47315856 C>T maps to NM_001164211.1 L722L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr13:47243272 C>T maps to NM_001164211.1 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CM-01A-11D-A33O-09 chr23:114399997 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:114414314 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:114391209 G>T did not map to a codon.
Sequencing variant TCGA-HM-A3JK-01A-11D-A21Q-09 chr23:114384484 G>T did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr23:114347795 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:114357164 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr3:197547200 G>A maps to ENST00000425562 V180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr7:100172786 G>A maps to NM_002319.3 F665F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:39798860 G>C maps to NM_020862.1 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:40400384 G>C maps to NM_020737.1 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr14:42077622 G>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:42361084 C>G maps to NM_152447.3 S673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr14:42077498 C>G did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr19:4538641 C>G maps to NM_052972.2 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr7:133881814 C>T maps to NM_144648.1 I501I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr7:133943056 T>C maps to NM_144648.1 C749C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr1:113667274 C>G did not map to a codon.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr1:113657442 C>T maps to NM_014813.1 V825V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:113667098 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:113616102 C>T maps to NM_014813.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr12:59266439 G>A maps to NM_153377.3 Q1092*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr12:59284454 G>C maps to NM_153377.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr10:85984188 G>A maps to NM_001017924.2 I264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A69B-01A-11D-A32I-09 chr10:85985197 C>A maps to NM_001017924.2 G27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr10:85984449 G>T maps to NM_001017924.2 Y177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr12:25186726 C>G did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr12:25185114 G>A did not map to a codon.
Sequencing variant TCGA-DS-A7WH-01A-22D-A351-09 chr12:57543505 C>T maps to ENST00000338962 H295H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr12:57559990 A>G maps to NM_002332.2 S932S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr12:57598988 C>T maps to NM_002332.2 F3764F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr12:57604558 G>A maps to NM_002332.2 V4271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr12:57538818 C>T maps to NM_002332.2 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A78R-01A-11D-A32I-09 chr8:105502133 T>C did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr8:105502516 G>T did not map to a codon.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr8:105502653 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr2:141243033 G>C maps to NM_018557.2 L3101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CG-01A-11D-A32I-09 chr2:141625762 C>T maps to NM_018557.2 G1413G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:141625356 C>A maps to NM_018557.2 E1461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr2:170135982 G>A maps to NM_004525.2 V488V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:170063719 C>T maps to NM_004525.2 L2170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HM-A3JK-01A-11D-A21Q-09 chr2:170048421 C>T maps to NM_004525.2 E2984E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr2:170011055 G>C maps to NM_004525.2 S4070*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr2:170029696 G>A maps to NM_004525.2 F3684F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr2:170127600 G>A maps to NM_004525.2 L711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:68125244 G>T maps to NM_002335.2 E206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr11:68192731 G>C maps to NM_002335.2 L1133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VH-01A-11D-A28B-09 chr11:68207254 C>T maps to NM_002335.2 C1453C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr22:25750773 G>A maps to NM_001135772.1 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr22:25750767 G>A maps to NM_001135772.1 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr4:3516583 G>A maps to NM_002337.2 H302H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr2:44123817 C>T maps to NM_133259.3 P1285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr2:44190815 C>A maps to NM_133259.3 E467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr2:44175580 C>T maps to NM_133259.3 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LB-01A-11D-A243-09 chr2:44175556 C>T maps to NM_133259.3 E612E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A3LQ-01A-21D-A21Q-09 chr6:53784277 A>T did not map to a codon.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr6:53784276 A>T did not map to a codon.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr5:191751 C>G maps to NM_001080478.1 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr6:25452490 C>T did not map to a codon.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr6:25435766 C>T maps to NM_017640.5 D102D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr6:25620362 C>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr6:25551206 C>T maps to NM_017640.5 R800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr14:24526136 C>T maps to NM_138360.3 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr7:102553459 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr10:50121492 G>T maps to NM_001006939.3 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr12:7019142 G>C maps to NM_201650.2 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr12:7023335 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:7016620 G>A maps to ENST00000433346 W211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr8:145747963 G>C maps to NM_001024678.3 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr10:134189076 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr10:134188812 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr16:67260934 G>T did not map to a codon.
Sequencing variant TCGA-C5-A3HF-01A-11D-A20U-09 chr18:7231198 G>A maps to NM_001105581.1 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:169587428 G>C maps to NM_024727.2 S56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr3:169571430 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr11:76368682 C>G did not map to a codon.
Sequencing variant TCGA-EA-A78R-01A-11D-A32I-09 chr16:67405105 G>T maps to NM_018296.5 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr16:67410676 C>T maps to NM_018296.5 Q570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr17:44374709 A>G maps to NM_014834.4 P737P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr17:44380066 C>T maps to NM_014834.4 L915L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr17:44632679 C>G maps to NM_001006607.2 L1648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr17:44626599 G>A maps to NM_001006607.2 L1365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:100626099 T>C maps to NM_144620.2 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr7:127669931 G>A maps to NM_022143.4 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr1:46764080 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:46745945 C>G maps to ENST00000254454 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr1:46751847 G>A maps to ENST00000254454 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr1:46750806 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:54417788 G>A maps to NM_052940.3 Q39Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr17:17896143 G>A maps to NM_031294.3 E170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr19:51022612 C>T maps to NM_001080457.1 K119K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr19:51022618 C>T maps to NM_001080457.1 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr19:51022612 C>T maps to NM_001080457.1 K119K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr19:51022459 G>A maps to NM_001080457.1 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr19:51021571 G>A maps to NM_001080457.1 S466S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr11:40137254 C>A maps to NM_020929.1 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr11:40137707 C>T maps to NM_020929.1 Q45Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:165514073 C>T maps to NM_001005214.3 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr11:544753 G>A maps to NM_198075.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:48474546 G>A did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr4:52861187 G>C maps to NM_001024611.1 S667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr4:52861484 G>C maps to NM_001024611.1 S568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr9:131671152 G>A maps to NM_001127244.1 Q570Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr9:131671152 G>A maps to NM_001127244.1 Q570Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr9:131670870 C>G maps to NM_001127244.1 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:90152109 G>C maps to NM_032270.4 V26V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr2:238657915 C>T maps to NM_001137552.1 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BE-01A-21D-A26G-09 chr3:37095398 C>T maps to NM_006309.2 L703L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr12:85517846 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:85546832 C>G maps to NM_001079910.1 S1484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr3:169540455 C>T maps to NM_001080460.1 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr15:101598291 C>G maps to NM_024652.3 S1542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr15:101597255 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr15:101523743 G>A maps to NM_024652.3 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr15:101565147 C>G maps to NM_024652.3 L736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr15:101589931 C>G maps to NM_024652.3 S1128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr15:101569239 C>T maps to NM_024652.3 L922L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr12:40728938 C>G maps to NM_198578.3 L1976L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr12:40671954 G>A maps to NM_198578.3 V711V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr1:204587428 G>A maps to NM_201630.1 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr20:6031428 G>A maps to NM_152611.3 Q286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr20:6022387 C>T maps to NM_152611.3 Q501Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr11:62455620 G>A maps to NM_203422.2 D120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr5:138210088 G>C maps to NM_015564.2 S54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A411-01A-11D-A243-09 chr9:130257660 G>T maps to NM_001005374.2 R554R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr9:130257501 G>A did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr9:130251772 G>A maps to NM_001005374.2 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr12:1944743 A>G did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr11:71819760 G>A maps to NM_001145309.1 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr3:115560716 G>A maps to NM_002338.3 V298V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr20:60697841 C>T maps to NM_144703.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr20:60702803 G>C maps to ENST00000253001 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr19:18418060 C>A did not map to a codon.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr11:1908066 C>T maps to ENST00000381758 Q403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr11:1887969 C>G maps to ENST00000381758 S89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr21:47639400 G>A maps to NM_002340.5 F212F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr6:31540805 C>T maps to NM_000595.2 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr6:31541298 C>G maps to NM_000595.2 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3WB-01A-11D-A22X-09 chr19:41105463 T>C did not map to a codon.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr12:6494465 C>T maps to NM_002342.1 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr12:6497462 C>G did not map to a codon.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr3:46480800 A>G maps to NM_002343.3 L632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr15:41797682 G>A maps to NM_002344.5 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr6:144184639 G>A maps to NM_032860.3 K468K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr17:48828530 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:23418234 G>A maps to NM_001142546.1 S840S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr11:24759790 G>A maps to NM_001009909.2 E92E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr6:31675807 C>T maps to ENST00000375834 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr8:143783123 G>A maps to ENST00000292430 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr2:160755556 G>A maps to NM_001198759.1 F36F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:160755556 G>A maps to NM_001198759.1 F36F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr1:160769447 G>A did not map to a codon.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr4:4281443 G>A maps to NM_017816.2 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr8:56910990 C>G maps to NM_002350.2 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr19:43965503 C>T maps to NM_014400.2 *347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr19:43967922 T>C did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr19:44302733 G>A maps to NM_001031749.2 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr6:5144478 T>C maps to NM_001164841.1 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr15:100269462 C>T maps to NM_152449.2 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr15:100256543 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:235944339 G>C maps to NM_000081.2 S1680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr1:235824370 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:235964365 G>A maps to NM_000081.2 F1248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:235850284 G>A maps to NM_000081.2 V3588V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RA-A741-01A-11D-A33O-09 chr1:235952023 G>T maps to NM_000081.2 P1555P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr10:30900894 C>A maps to NM_183058.2 E192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr1:9992943 G>A maps to NM_032368.3 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr8:20107233 C>T maps to NM_021020.2 *597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr13:36050011 G>A maps to NM_005584.4 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr13:36050077 G>A maps to NM_005584.4 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73Q-01A-21D-A32I-09 chr4:151504435 C>T maps to NM_006439.4 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr7:20198623 C>A maps to NM_182762.3 E454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr1:39753017 G>A maps to ENST00000361689 R528R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr1:39950487 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr1:39802261 C>T maps to ENST00000289893 F1774F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:39735229 G>C maps to ENST00000372900 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:39853529 G>T maps to ENST00000361689 E2944*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:39751355 C>G maps to ENST00000361689 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:39952334 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr6:43608104 C>T maps to NM_001003690.1 N252N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr19:498692 G>T maps to NM_130760.2 E179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr11:47296119 G>A maps to NM_003682.3 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr11:47297738 C>T maps to NM_003682.3 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr11:47306883 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:47346267 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr4:1293466 C>A did not map to a codon.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr4:1293499 C>A did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr4:1322571 C>T did not map to a codon.
Sequencing variant TCGA-JW-A69B-01A-11D-A32I-09 chr1:166959174 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr8:145160642 G>A maps to NM_032272.4 E19E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr22:38610545 C>G maps to NM_012323.3 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr23:152482139 G>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:148798205 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr23:148794828 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr23:151900160 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr23:151935840 A>T did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr23:151935274 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr23:151093051 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr23:151869984 G>A did not map to a codon.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr23:151870003 G>C did not map to a codon.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr23:151869755 T>C did not map to a codon.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr23:149013298 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:149013327 G>T did not map to a codon.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr23:148664666 G>A did not map to a codon.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr23:30269125 C>T did not map to a codon.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr23:30269338 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2R9-01A-11D-A18J-09 chr23:30268662 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:30268672 G>T did not map to a codon.
Sequencing variant TCGA-HG-A2PA-01A-11D-A20U-09 chr23:30269212 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr23:27840297 T>G did not map to a codon.
Sequencing variant TCGA-DG-A2KH-01A-21D-A22X-09 chr23:27839693 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr23:27839435 C>T did not map to a codon.
Sequencing variant TCGA-EA-A5O9-01A-11D-A28B-09 chr23:35820969 T>C did not map to a codon.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr23:35820489 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:35821127 G>A did not map to a codon.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr23:35820352 C>T did not map to a codon.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr23:26157300 G>A did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr23:26157792 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A6DV-01A-11D-A32I-09 chr23:30236903 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr23:30254898 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:30254170 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr23:30254215 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:30260590 G>A did not map to a codon.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr23:26212613 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:26212648 A>G did not map to a codon.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr23:26212430 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr23:140994897 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:140995696 C>T did not map to a codon.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr23:140994452 G>C did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:140993494 C>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:140994166 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3TX-01A-11D-A22X-09 chr23:140996028 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:140994538 C>G did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:140994801 G>C did not map to a codon.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr23:141290712 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr23:141291725 G>C did not map to a codon.
Sequencing variant TCGA-RA-A741-01A-11D-A33O-09 chr23:141290913 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr23:140969326 C>A did not map to a codon.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr23:140984700 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:140969243 T>C did not map to a codon.
Sequencing variant TCGA-EA-A50E-01A-21D-A26G-09 chr23:140969263 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr23:140984601 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr23:140967210 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr23:140984783 A>T did not map to a codon.
Sequencing variant TCGA-FU-A3TQ-01A-11D-A22X-09 chr23:140967149 A>G did not map to a codon.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr23:140983109 A>T did not map to a codon.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr23:140984708 C>T did not map to a codon.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr23:140985329 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr23:51640554 G>A did not map to a codon.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr23:51642269 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:51639895 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:51644957 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:51640995 G>C did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr23:51641679 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr23:54841755 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr23:54839586 G>A did not map to a codon.
Sequencing variant TCGA-RA-A741-01A-11D-A33O-09 chr23:54835683 G>T did not map to a codon.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr23:75649150 C>A did not map to a codon.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr23:75649185 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:75649010 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:75648351 G>A did not map to a codon.
Sequencing variant TCGA-HG-A2PA-01A-11D-A20U-09 chr23:75649282 G>A did not map to a codon.
Sequencing variant TCGA-HG-A2PA-01A-11D-A20U-09 chr23:75649306 G>A did not map to a codon.
Sequencing variant TCGA-HM-A3JK-01A-11D-A21Q-09 chr23:75651039 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr23:75648954 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr23:75649206 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:75649465 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr23:75648436 T>C did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr23:75003458 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:75004133 G>T did not map to a codon.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr23:75003784 G>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:184429174 C>T maps to NM_022149.4 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr23:55479284 G>C did not map to a codon.
Sequencing variant TCGA-FU-A3EO-01A-11D-A20U-09 chr23:55479013 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr3:65415612 C>T maps to NM_001033057.1 V583V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr7:77789555 G>C maps to NM_012301.3 G877G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:49022574 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr12:10762485 C>A maps to NM_018048.3 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr23:77150815 C>A did not map to a codon.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr23:77150968 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr23:77131013 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:77150955 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr6:10796314 C>G maps to NM_005906.3 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr6:10763240 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr2:95713816 G>A maps to NM_002371.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr8:120252533 C>T maps to ENST00000276681 Q145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr9:72727909 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr9:72741173 C>G maps to NM_153267.4 S248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr9:72741132 C>G maps to NM_153267.4 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr5:179221047 C>T did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr5:179201030 C>G maps to NM_014757.4 S735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr5:179201367 C>T maps to NM_014757.4 L847L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LS-01A-22D-A22X-09 chr11:95826264 G>A maps to NM_032427.1 F310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:95825809 G>C maps to NM_032427.1 S462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr23:149638348 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:149680842 C>A did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:149680409 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:149638142 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A73R-01A-11D-A33O-09 chr1:117910705 G>A did not map to a codon.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr9:139998223 A>G did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr9:139998617 C>A did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr1:25944780 C>T maps to NM_020379.2 Q165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr1:25944780 C>T maps to NM_020379.2 Q165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr15:91448605 C>A maps to NM_006122.2 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr15:75648959 C>T maps to NM_006715.2 L908L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:103610744 C>A maps to NM_005908.3 E316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UC-01A-11D-A351-09 chr6:96034515 C>T maps to NM_024641.2 I67I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:43515647 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:43698185 C>G did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:43654996 C>G did not map to a codon.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr23:43698136 C>T did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:43814639 C>G maps to ENST00000382031 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WH-01A-22D-A351-09 chr15:43813194 C>G maps to ENST00000382031 S150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr15:43817873 G>A maps to ENST00000382031 V1639V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr15:43821014 C>T maps to ENST00000382031 L2686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr5:71411576 C>G maps to NM_005909.3 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:71494087 C>T maps to NM_005909.3 Q1636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WH-01A-22D-A351-09 chr5:71491137 G>A maps to NM_005909.3 E652E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr5:71493363 T>G maps to NM_005909.3 V1394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr5:71491641 C>T maps to NM_005909.3 A820A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr5:71411576 C>G maps to NM_005909.3 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr5:71496105 C>G maps to NM_005909.3 V2308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A50E-01A-21D-A26G-09 chr20:33147997 G>A did not map to a codon.
Sequencing variant TCGA-JX-A3PZ-01A-11D-A21Q-09 chr20:33147554 G>C maps to NM_181509.1 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr19:17838523 G>A maps to NM_018174.4 L777L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:210594967 G>A maps to NM_002374.3 E1777E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr2:210594965 G>T maps to NM_002374.3 E1777*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr2:210517947 G>A maps to NM_002374.3 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr2:210561650 G>A maps to NM_002374.3 K1466K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr2:210594922 G>A maps to NM_002374.3 L1762L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr19:4099775 C>T did not map to a codon.
Sequencing variant TCGA-C5-A7CH-01A-11D-A33O-09 chr17:21215500 G>A maps to NM_145109.2 P274P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-FU-A2QG-01A-11D-A18J-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr17:11984675 G>A maps to ENST00000415385 E85E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr15:67838611 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr19:7977051 G>A maps to ENST00000425613 R408R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr5:56177813 G>A maps to NM_005921.1 E929E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr19:40710430 C>T maps to NM_002446.3 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A50E-01A-21D-A26G-09 chr19:40711972 G>A maps to NM_002446.3 E448E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr19:40698213 G>A maps to NM_002446.3 E92E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VK-01A-11D-A28B-09 chr11:65375231 C>T maps to NM_002419.3 Q375Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CH-01A-11D-A33O-09 chr17:43340705 G>A did not map to a codon.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr17:43351846 G>A maps to ENST00000344686 F467F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr17:43341843 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr17:43340692 T>C did not map to a codon.
Sequencing variant TCGA-Q1-A73Q-01A-21D-A32I-09 chr17:43348486 G>A maps to ENST00000344686 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr23:19482435 G>T did not map to a codon.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr23:19391728 G>A did not map to a codon.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr23:19378901 C>T did not map to a codon.
Sequencing variant TCGA-EA-A5O9-01A-11D-A28B-09 chr23:19449565 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr23:19418716 C>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:19418733 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr23:19392604 G>A did not map to a codon.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr23:19392604 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr2:128088059 G>A maps to NM_006609.3 Q96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LC-01A-11D-A20U-09 chr6:161491788 C>T maps to NM_005922.2 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr6:91225675 C>T did not map to a codon.
Sequencing variant TCGA-EA-A5ZF-01A-11D-A28B-09 chr6:91254328 G>A maps to NM_145331.1 G411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr14:71267555 G>C maps to NM_033141.2 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:47950972 G>A maps to ENST00000426837 S1663S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr3:47953285 C>T maps to ENST00000426837 L892L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr3:47963324 G>T maps to ENST00000426837 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr19:39100262 G>A maps to NM_001042600.1 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr11:64567649 G>A maps to NM_004579.2 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:64557880 G>A maps to NM_004579.2 L716L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr14:50895432 G>C maps to NM_198794.1 S758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A4BA-01A-21D-A26G-09 chr6:136698938 C>T maps to NM_001198609.1 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr6:136683706 A>C maps to NM_001198609.1 T499T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr1:36643630 G>T maps to NM_018067.3 E513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr23:20033419 C>A did not map to a codon.
Sequencing variant TCGA-EK-A2RE-01A-11D-A18J-09 chr23:20030617 C>A did not map to a codon.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr23:20074857 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr23:20082888 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:20029052 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:20043926 C>T did not map to a codon.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr23:135326894 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr23:135310927 T>G did not map to a codon.
Sequencing variant TCGA-EA-A3QD-01A-32D-A22X-09 chr23:135313039 G>C did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:135323431 T>G did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:135323394 C>A did not map to a codon.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr23:135328485 C>G did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr23:135323399 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr22:50705349 C>A did not map to a codon.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr22:50694088 C>T maps to NM_002969.3 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr6:36041851 G>A maps to NM_139012.2 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr14:55518384 G>C did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr15:52338059 T>G did not map to a codon.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr15:52356855 C>T maps to NM_002748.3 Q609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr17:19284340 C>G maps to NM_139034.2 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A449-01A-11D-A243-09 chr10:49634659 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr10:49639239 G>A maps to NM_139049.1 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr11:45919683 G>A maps to NM_005456.2 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr16:1793356 G>A maps to NM_015133.3 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr16:1818598 C>T maps to NM_015133.3 G1287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr16:1810462 T>C maps to NM_015133.3 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr5:179676111 C>T maps to NM_002752.4 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr1:206905166 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr1:206902306 G>C did not map to a codon.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr1:206905166 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr15:42116051 G>T maps to NM_001128608.1 E1342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr17:44068842 G>A maps to NM_001123066.3 T466T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr17:60814460 G>C maps to NM_152598.2 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:60799926 C>T maps to NM_152598.2 E712E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr17:60813356 G>A maps to NM_152598.2 F624F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A44S-01A-12D-A26G-09 chr2:217142479 G>A maps to NM_020814.2 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr10:94070945 G>A maps to NM_017824.4 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr2:119749365 G>A maps to NM_006770.3 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:220804456 C>T maps to NM_018650.3 F330F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr11:63670178 C>T maps to NM_001039469.2 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr14:103852003 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr12:57906125 C>T maps to NM_004990.2 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr12:57906035 C>T maps to NM_004990.2 F551F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr12:57906741 C>T maps to NM_004990.2 I654I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr16:71674335 C>T maps to NM_001017967.2 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr16:71675963 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr6:29454692 G>C maps to NM_052967.1 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr3:186978565 G>A maps to NM_139125.3 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr3:186944294 G>A maps to NM_001879.5 I485I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr3:186947581 C>T maps to NM_001879.5 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr3:186954179 G>C maps to NM_139125.3 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q8-01A-11D-A21Q-09 chr1:11106634 G>A maps to NM_006610.2 F130F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HM-A3JK-01A-11D-A21Q-09 chr19:12978424 G>A maps to NM_014975.2 L759L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:46496303 C>G maps to NM_015112.2 S860*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:46496372 C>G maps to NM_015112.2 S883*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr19:18257689 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr19:18239689 C>T maps to NM_015016.1 V355V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr19:18254621 C>T maps to NM_015016.1 Q768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr5:66398417 C>G maps to NM_001164664.1 V375V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:27454083 C>T maps to NM_001172303.1 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr10:27448576 C>G maps to NM_001172303.1 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr2:85766424 C>T maps to NM_005911.4 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr19:3784449 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr1:31189125 G>A maps to NM_002379.3 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr1:31194482 C>T maps to NM_002379.3 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr2:20205883 G>C maps to NM_002381.4 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr20:43929599 C>G maps to ENST00000372754 V354V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr14:65544130 C>G maps to NM_145113.1 *104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr14:65543310 G>T maps to NM_002382.3 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr16:29819889 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr19:1578485 C>T maps to NM_003926.5 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3YQ-01A-11D-A22X-09 chr19:1581161 C>T maps to NM_003926.5 K202K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr19:1581161 C>T maps to NM_003926.5 K202K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr3:129151413 C>A maps to NM_003925.1 E533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr2:149247487 G>A maps to ENST00000404807 Q1429Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr12:57921756 C>G maps to NM_052897.3 S788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr12:57919662 G>C maps to NM_052897.3 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr12:57919449 C>G maps to NM_052897.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr12:57919805 C>G maps to NM_052897.3 S352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr3:152017351 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr3:152018042 G>T maps to NM_021038.3 E21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr19:54691187 C>T did not map to a codon.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr17:49302480 G>A maps to ENST00000389496 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr17:49279024 G>A maps to ENST00000389496 F387F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr16:84099343 C>T maps to NM_003791.2 A794A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OA-01A-11D-A16Y-08 chr16:84103571 C>T maps to NM_003791.2 P618P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R9-01A-11D-A18J-09 chr16:84101351 G>A maps to NM_003791.2 N716N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr16:89985854 C>T maps to ENST00000304984 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr16:89981101 T>C maps to ENST00000331346 C158C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr16:89987152 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr16:89981137 T>C maps to ENST00000331346 C170C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr18:13884965 C>T maps to NM_000529.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H6-01B-11D-A22X-09 chr18:13884992 C>A maps to NM_000529.2 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr20:54824519 C>T maps to ENST00000371389 Y244Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr11:119185549 G>A maps to NM_006500.2 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr5:112389568 C>T maps to NM_001085377.1 K767K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr5:112437441 C>A maps to NM_001085377.1 R464R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WH-01A-22D-A351-09 chr5:70930871 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr23:138728983 A>G did not map to a codon.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr23:138678827 G>C did not map to a codon.
Sequencing variant TCGA-EA-A5FO-01A-21D-A28B-09 chr23:138774281 C>A did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr23:138698553 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:138711976 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr13:113708710 G>A did not map to a codon.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr13:113700994 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr3:183014772 G>C maps to NM_015078.2 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr22:41077811 C>T maps to NM_005297.3 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr6:100368917 G>A maps to NM_032503.2 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr6:100403984 G>A maps to NM_032503.2 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QD-01A-32D-A22X-09 chr1:150550969 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73S-01A-11D-A33O-09 chr1:150551970 G>T maps to NM_021960.4 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:127327820 G>A maps to NM_004526.2 V461V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr21:47690436 C>A maps to NM_003906.3 E836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr8:48880004 C>G maps to NM_182746.1 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr22:35804445 C>T maps to NM_006739.3 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr7:99695254 G>A maps to NM_005916.3 R367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr7:99693762 G>C maps to NM_005916.3 S410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr7:99696992 C>A maps to NM_005916.3 E104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr20:5974259 C>T maps to NM_032485.4 L783L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr19:7593568 C>T maps to NM_020533.2 R322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A6QX-01A-12D-A33O-09 chr19:7595353 C>T maps to NM_020533.2 I514I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr19:7595299 C>T maps to NM_020533.2 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr19:7595359 C>G maps to NM_020533.2 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:85462585 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr1:85510917 G>C maps to NM_018298.9 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr1:85510983 G>A maps to NM_018298.9 C20C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr8:6266850 C>G maps to NM_024596.3 S25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RA-A741-01A-11D-A33O-09 chr12:49953005 G>T maps to NM_001012300.1 R402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr15:94945135 C>G maps to NM_018349.3 S658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr15:94899418 C>G maps to NM_018349.3 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr6:30680934 G>A maps to NM_014641.2 Q262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr6:30681691 G>C maps to NM_014641.2 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr6:30681014 G>C maps to NM_014641.2 S235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr6:30680438 C>T maps to NM_014641.2 W427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M2-01A-21D-A18J-09 chr6:37605155 C>T maps to ENST00000297153 A955A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr14:47504460 G>C maps to NM_001113498.2 T524T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr2:207619772 C>T maps to NM_001039845.1 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr7:75677413 C>T did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr12:68719810 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr6:90422941 C>T maps to NM_014611.1 L2381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr6:90382014 C>T maps to NM_014611.1 V4566V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr14:24684983 G>A maps to NM_138476.3 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:153296199 G>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:153296612 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr17:37566918 G>A maps to NM_004774.3 Q519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr17:37565277 G>A maps to NM_004774.3 Q1066*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R3-01A-11D-A28B-09 chr17:37588193 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr5:6374448 G>A maps to NM_032286.2 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr23:70342152 C>A did not map to a codon.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr23:70348263 T>C did not map to a codon.
Sequencing variant TCGA-DS-A7WF-01A-11D-A351-09 chr23:70338670 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr23:70342456 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr23:70341486 C>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:70357068 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3TQ-01A-11D-A22X-09 chr23:70344124 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:70341572 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr23:70341567 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:70346187 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr3:151131026 C>T maps to NM_053002.4 Q2046*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:151067971 G>A maps to NM_053002.4 K757K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr3:151130965 C>T maps to NM_053002.4 G2025G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr3:151105722 C>T maps to NM_053002.4 Y1703Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr17:60039008 C>T maps to NM_005121.2 V1732V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:60040169 G>A maps to NM_005121.2 C1669C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BE-01A-21D-A26G-09 chr17:60050198 G>A maps to NM_005121.2 Q1286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr17:60038435 G>A maps to NM_005121.2 R1758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5O9-01A-11D-A28B-09 chr23:40571457 T>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:40518557 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:40539378 A>G did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:40541887 C>G did not map to a codon.
Alternatively spliced codon TCGA-EK-A2R8-01A-21D-A18J-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr22:20940942 C>T maps to NM_001003891.1 L773L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr19:879962 G>A maps to NM_005481.2 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:881595 G>C maps to NM_005481.2 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr19:872087 G>A maps to NM_005481.2 L646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr11:93517705 C>T maps to NM_004268.4 I9I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr11:93529608 C>G maps to NM_004268.4 S349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:57472621 C>T maps to ENST00000431606 K99K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr6:131908763 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr6:131917762 G>C maps to ENST00000403834 L897L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr6:131923424 G>A maps to ENST00000403834 L682L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr6:131919781 G>A maps to ENST00000403834 F786F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr17:38183200 G>A maps to NM_014815.3 I539I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr17:38176819 C>T did not map to a codon.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr19:50338816 G>T maps to NM_030973.3 G567G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WH-01A-22D-A351-09 chr19:50338831 G>T maps to NM_030973.3 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr19:39884191 G>C did not map to a codon.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr17:6553726 G>A maps to NM_016060.2 Q19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:17380525 G>C maps to NM_018019.2 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A69M-01A-11D-A32I-09 chr15:100211753 C>T maps to ENST00000346108 C96C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr1:156437233 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RE-01A-11D-A18J-09 chr5:126705680 C>A maps to NM_032446.2 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr19:42873721 C>T maps to ENST00000251268 C2227C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr9:123370232 C>T maps to ENST00000426959 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr10:15028920 C>T did not map to a codon.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr2:66794707 G>T did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr2:66664988 C>T maps to ENST00000407092 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R9-01A-11D-A18J-09 chr15:37183274 T>C did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr19:47910190 G>T maps to NM_020160.1 I390I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr9:36583687 C>T maps to NM_014791.2 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr11:64577149 G>A maps to NM_130804.2 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr17:41720863 C>A maps to NM_004527.3 E212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr18:29784240 C>G maps to NM_005925.2 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr7:100028534 C>A maps to NM_019606.5 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr4:88767935 C>G did not map to a codon.
Sequencing variant TCGA-FU-A770-01A-11D-A33O-09 chr15:90320499 C>T maps to NM_001039958.1 A304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RA-A741-01A-11D-A33O-09 chr12:58163157 C>A maps to ENST00000408972 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr10:126463296 G>A maps to NM_212554.2 Q116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr11:62432881 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VK-01A-11D-A28B-09 chr11:62432844 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr11:62434344 C>G maps to NM_001043229.1 S182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr7:128138113 G>A maps to NM_018396.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr2:172182596 G>A maps to NM_024770.3 R308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr16:21629231 C>T maps to NM_016025.3 Q135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:156047249 G>A maps to NM_001093725.1 I226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr18:48723051 C>T maps to NM_016626.4 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr19:1556817 C>A maps to NM_001174118.1 E234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr19:1556728 G>A maps to NM_001174118.1 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr15:44109623 C>T maps to NM_005926.2 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HQ-01A-11D-A20U-09 chr4:170912846 G>A maps to NM_021647.6 D304D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr4:170913056 G>A maps to NM_021647.6 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr15:89450572 G>A maps to NM_005928.2 N80N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr8:8750097 G>A maps to NM_004225.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr8:8643421 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr8:8643427 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr3:179082958 C>T maps to NM_033540.2 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73R-01A-11D-A33O-09 chr11:119212389 G>T maps to NM_031433.2 P536P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:2935542 G>C maps to NM_001146069.1 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr17:74735030 C>T maps to NM_024311.2 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:40433395 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:40431610 C>T maps to NM_001136493.1 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr2:24247078 C>A maps to ENST00000338315 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr2:24247120 C>T maps to ENST00000338315 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr2:191301099 C>T maps to NM_017694.3 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:128842678 C>T maps to NM_152778.2 Q450Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr4:128886249 G>C maps to NM_152778.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr15:41961628 C>G maps to ENST00000219905 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A69L-01A-11D-A32I-09 chr15:42058655 G>T maps to ENST00000219905 L2841L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U3-01A-11D-A28B-09 chr15:41961605 C>T maps to ENST00000219905 Q172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr7:141802439 G>C maps to ENST00000475668 G2659G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PI-01A-11D-A18J-09 chr7:141730554 G>T maps to ENST00000475668 E490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr7:141708378 C>A maps to ENST00000475668 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73S-01A-11D-A33O-09 chr14:50088483 G>T maps to NM_002408.3 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr22:39883519 C>T maps to NM_001098270.1 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr2:99260397 A>G maps to NM_012214.2 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr12:86373206 C>A maps to ENST00000393205 G462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr17:74865077 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2H1-01A-11D-A17W-09 chr17:74909777 G>A maps to ENST00000374998 E351E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr17:74902153 C>A maps to NM_198955.1 R315R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr10:103552509 G>A did not map to a codon.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr16:4730185 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr16:4731717 C>T maps to NM_015246.2 I433I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr16:4738830 C>T maps to NM_015246.2 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:222794558 G>A maps to NM_198551.2 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr22:18314622 C>A maps to NM_015241.2 E1018*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RL-01A-11D-A18J-09 chr22:18359610 T>G did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr22:18273682 C>G did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr22:18378150 G>A maps to NM_015241.2 Q450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr22:18387563 G>A maps to NM_015241.2 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr11:12316099 C>T maps to NM_032867.2 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RA-A741-01A-11D-A33O-09 chr22:38313729 C>A maps to NM_033386.2 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr7:1479624 G>A maps to NM_182924.3 I634I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr7:1474115 C>T did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr6:31474940 G>A maps to NM_005931.3 Q252Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:10535233 G>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:38664283 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr23:107084145 C>G did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr19:307173 G>A maps to NM_017550.1 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr5:56219368 C>T maps to ENST00000381226 V418V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:12089807 C>T did not map to a codon.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr3:97677936 G>A maps to NM_153182.2 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr17:4794896 G>A maps to NM_153827.4 T629T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr17:4795727 C>T maps to NM_153827.4 L707L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr17:4799782 G>A maps to NM_153827.4 E1225E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr17:4794979 G>A maps to NM_153827.4 W657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr14:37854915 C>A did not map to a codon.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr10:129917552 C>T maps to NM_002417.4 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr10:129906553 C>A maps to NM_002417.4 E1184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr10:129909844 A>C did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr10:129905147 G>C maps to NM_002417.4 L1652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:122493259 C>A maps to NM_032390.4 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A852-01A-11D-A351-09 chr22:40915230 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr7:131082108 C>T maps to NM_013255.4 Q162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr19:2041043 G>A maps to NM_199054.2 Q369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:2042431 G>C maps to NM_199054.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZE-01A-11D-A28B-09 chr15:23811384 G>A maps to NM_005664.3 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr17:56283701 C>G maps to NM_017777.3 R510R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr10:28023529 C>T maps to NM_173576.2 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr3:37055921 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr14:75515089 C>T maps to NM_001040108.1 Q423Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr14:75516265 G>A maps to NM_001040108.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr10:21962685 C>T maps to NM_004641.3 Q487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:20414064 G>C maps to NM_004529.2 S260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr9:20622290 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2GZ-01A-11D-A17W-09 chr6:168351978 G>A maps to ENST00000400822 Q1307Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr6:168273010 C>T maps to ENST00000400822 R177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr6:168272988 G>A maps to ENST00000400822 K169K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr13:49794658 G>T maps to NM_001507.1 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:238419643 C>T maps to NM_024101.5 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr2:238427251 C>A maps to NM_024101.5 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr12:122618097 C>T maps to NM_014938.3 F432F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr7:73008610 G>C maps to NM_032951.2 L811L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr4:146560410 T>C maps to NM_172250.2 C40C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr7:4959851 G>A maps to NM_001100600.1 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr7:4959869 G>T maps to NM_001100600.1 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr1:2542726 C>T maps to NM_033467.3 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:135047195 G>C did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:135056075 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr11:102649478 T>C maps to NM_002425.2 E166E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3YQ-01A-11D-A22X-09 chr22:24121513 C>T maps to NM_005940.3 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr11:102738637 C>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr11:102819835 C>T maps to NM_002427.3 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5FO-01A-21D-A28B-09 chr14:23312943 G>A maps to NM_004995.2 K292K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr8:89053781 G>A maps to NM_005941.4 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr8:89068394 C>T maps to NM_005941.4 W445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr8:89068414 A>C maps to NM_005941.4 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A852-01A-11D-A351-09 chr11:102447980 C>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:102477319 G>C maps to NM_004771.3 S300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A3L1-01A-11D-A21Q-09 chr20:33855065 G>A maps to NM_006690.3 R346R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A556-01A-11D-A26G-09 chr16:3105839 C>T maps to ENST00000325800 Q148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr11:5012685 C>G maps to NM_021801.3 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr11:102563729 C>T maps to NM_022122.2 Q412Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr20:44640372 C>T maps to NM_004994.2 F328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr4:90816727 C>T maps to NM_007351.2 F202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr4:90857905 G>C maps to NM_007351.2 L1025L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr10:99238090 G>A maps to ENST00000422291 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr22:28146819 G>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr22:28193384 C>T maps to NM_002430.2 V1049V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr15:56735843 G>A maps to NM_018365.2 Q299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr17:2290272 C>A maps to NM_020310.2 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr17:2291253 G>C maps to NM_020310.2 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr14:93649543 A>C maps to NM_022151.4 G348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr11:1492612 G>A maps to NM_001172223.1 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr18:33779771 G>C maps to NM_017947.2 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr6:39893500 G>A maps to ENST00000425303 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr2:74689730 G>A maps to NM_006302.2 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:49946584 C>T maps to NM_032355.3 V607V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr16:77228296 C>T maps to NM_014940.2 Q181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr12:62864488 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr12:62949937 C>A maps to ENST00000393630 I1126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr12:62860940 A>C did not map to a codon.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr3:108688568 G>A maps to NM_014429.3 L851L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr3:108813771 C>G maps to NM_014429.3 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr21:37741396 C>T maps to ENST00000290384 V578V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr21:37741837 C>T maps to ENST00000290384 I725I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr21:37741549 A>G maps to ENST00000290384 S629S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr21:37717217 A>C maps to ENST00000290384 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr21:37747581 C>T maps to ENST00000290384 I937I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:106186380 C>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:106199762 C>A did not map to a codon.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr15:79140358 G>A did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr15:79165367 G>A maps to NM_206839.1 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:102941729 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr12:122091037 C>T maps to NM_173855.4 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr23:134023169 G>A did not map to a codon.
Sequencing variant TCGA-EA-A6QX-01A-12D-A33O-09 chr23:14934347 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr1:113217533 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr22:50582542 G>A maps to NM_018995.2 P792P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr22:50599415 G>A maps to NM_018995.2 L1162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr22:50599220 G>A maps to NM_018995.2 L1143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr9:13126744 G>A maps to ENST00000319217 I1497I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr9:13223682 G>A maps to ENST00000319217 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A69B-01A-11D-A32I-09 chr9:13193261 C>A maps to ENST00000319217 L569L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr9:13224395 G>A maps to ENST00000319217 Q124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZE-01A-11D-A28B-09 chr2:71357944 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr12:123706422 T>A did not map to a codon.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr1:43812571 C>G maps to NM_005373.2 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr23:154033046 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr23:154020469 C>A did not map to a codon.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr17:41956723 G>A maps to NM_005374.3 F467F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5FO-01A-21D-A28B-09 chr17:41905134 G>A maps to ENST00000398393 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr17:41891625 G>A maps to ENST00000398393 Y396Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CJ-01A-11D-A32I-09 chr14:67786975 G>T maps to NM_022474.2 E467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:67799666 G>A maps to NM_022474.2 L674L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr14:67759226 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr14:67759339 G>A maps to NM_022474.2 Q160Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HM-A3JK-01A-11D-A21Q-09 chr14:67770294 G>A maps to NM_022474.2 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr10:28341767 C>T did not map to a codon.
Sequencing variant TCGA-C5-A7CJ-01A-11D-A32I-09 chr10:28420621 T>C did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr10:28358734 G>A maps to NM_173496.3 I390I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr18:11884234 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr18:11884270 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr22:43821021 C>T maps to NM_001044370.1 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr17:17000094 G>A maps to ENST00000395807 *94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A69L-01A-11D-A32I-09 chr22:37420681 C>T maps to NM_021126.4 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WF-01A-11D-A351-09 chr11:118130860 C>T maps to NM_144765.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr21:33684045 C>A maps to ENST00000445271 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr6:84772651 C>T maps to NM_138409.2 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr17:60749357 G>A did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr11:94192675 C>T maps to NM_005591.3 E466E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UC-01A-11D-A351-09 chr2:216809668 G>A maps to NM_018000.2 R188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:68773159 G>A maps to NM_145015.4 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr11:18956109 G>A maps to NM_147199.3 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr19:13875885 G>T maps to NM_001031727.2 E112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr4:78783988 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr6:43027091 G>A maps to NM_015950.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr1:1337573 G>A maps to NM_017971.3 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr11:68671239 C>A maps to NM_181514.1 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HM-A3JK-01A-11D-A21Q-09 chr5:154330429 C>T maps to NM_014180.3 R43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr17:48447380 G>A maps to ENST00000442592 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr16:420122 C>T maps to NM_006428.4 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr16:420170 C>T maps to NM_006428.4 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr16:419127 C>A maps to NM_006428.4 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr19:17417160 C>T maps to NM_023937.3 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr1:54649830 G>C did not map to a codon.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr19:10363048 C>G did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr19:10369969 G>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr19:10370057 G>C did not map to a codon.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr22:19423531 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr9:140446916 C>T maps to NM_032477.2 F128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr10:102746714 C>A maps to NM_176794.1 E86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U3-01A-11D-A28B-09 chr2:224824574 C>T maps to NM_022915.3 H168H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr15:89010587 C>T maps to NM_022163.3 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr11:64889735 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr9:104152782 G>A maps to NM_019051.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr2:74699581 C>A maps to NM_053050.3 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr1:151735517 C>A maps to NM_031420.2 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr1:151734850 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr1:151733962 C>T maps to NM_031420.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:36926862 A>C did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr6:30587277 C>G maps to NM_014046.3 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr5:44809105 G>A maps to NM_016640.3 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr2:105654621 C>T maps to NM_182640.2 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr1:19583620 C>T maps to NM_016183.3 Y85Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:19584269 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr11:60235877 G>A maps to NM_152866.2 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr11:60265179 C>T did not map to a codon.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr11:60183298 T>A maps to NM_032597.3 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr11:60541371 G>A maps to NM_001098835.1 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3EO-01A-11D-A20U-09 chr11:59828644 C>T maps to NM_006138.4 H4H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr11:59949161 C>T maps to NM_152852.1 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M1-01A-11D-A18J-09 chr8:72754892 G>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr8:72756050 G>A maps to NM_005098.3 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:47705645 C>T maps to NM_000251.1 Q816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QD-01A-32D-A22X-09 chr6:31729632 C>T maps to ENST00000375742 F757F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr6:31725964 G>C maps to ENST00000375742 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr2:48012057 G>C did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:48026984 G>C maps to NM_000179.2 L621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:48032839 G>T maps to NM_000179.2 E1214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr12:120789174 C>T maps to NM_002442.2 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:11790740 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr23:11776884 C>G did not map to a codon.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr16:816384 C>T maps to NM_013404.4 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr16:815695 C>T maps to NM_013404.4 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr16:828732 C>T maps to NM_001025190.1 W330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HQ-01A-11D-A20U-09 chr10:51556889 A>G did not map to a codon.
Sequencing variant TCGA-EA-A3QD-01A-32D-A22X-09 chr23:64953114 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:64958438 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:64949446 G>A did not map to a codon.
Sequencing variant TCGA-C5-A0TN-01A-21D-A14W-08 chr10:23384551 C>G maps to ENST00000277598 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr10:23384575 C>T maps to ENST00000277598 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr3:49723357 C>T maps to NM_020998.3 T395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr3:49723519 A>G maps to NM_020998.3 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr3:49924924 C>A maps to NM_002447.2 E1340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:131202296 T>G did not map to a codon.
Sequencing variant TCGA-HM-A3JK-01A-11D-A21Q-09 chr23:131208174 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:131207059 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LC-01A-11D-A20U-09 chr1:155716705 T>C did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:155580426 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr4:4864728 C>T maps to NM_002448.3 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73Q-01A-21D-A32I-09 chr4:4864434 G>A maps to NM_002448.3 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr16:56660657 C>T maps to ENST00000330439 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr16:56660708 G>A maps to ENST00000330439 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RL-01A-11D-A18J-09 chr16:56704433 C>T maps to NM_005951.2 C15C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr8:121553454 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr6:36949433 C>T maps to ENST00000373627 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr6:36949388 G>C maps to ENST00000373627 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr8:98718852 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr7:91502973 G>A maps to NM_006980.3 I378I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZE-01A-11D-A28B-09 chr2:242026908 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:38289466 G>C maps to NM_005955.2 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:93583964 A>G maps to NM_007358.3 Q232Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CJ-01A-11D-A32I-09 chr4:75147262 C>T maps to NM_001144978.1 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr4:75147262 C>T maps to NM_001144978.1 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:11855207 C>T maps to ENST00000376585 E367E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:68512460 G>C maps to NM_004923.3 S250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr11:68517981 G>A maps to NM_004923.3 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr11:68512504 G>C maps to NM_004923.3 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:149767132 T>G did not map to a codon.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr23:149931143 C>A did not map to a codon.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr23:149919522 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:149905768 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VH-01A-11D-A28B-09 chr15:31239428 G>T maps to NM_017762.2 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr1:149908228 G>C did not map to a codon.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr1:149900658 G>A did not map to a codon.
Sequencing variant TCGA-EX-A69M-01A-11D-A32I-09 chr22:30415897 G>A maps to NM_021090.3 L750L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr22:30394786 G>A maps to NM_021090.3 E166E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr17:56581220 G>A maps to NM_004687.4 L565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:56572508 C>G maps to NM_004687.4 L998L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr23:63564951 G>A did not map to a codon.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr8:11162519 G>A maps to NM_015458.3 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr6:74183256 G>A maps to NM_001123226.1 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr1:11182062 G>C maps to NM_004958.3 L2261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5O9-01A-11D-A28B-09 chr1:11181395 C>T maps to NM_004958.3 L2280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr1:11181395 C>T maps to NM_004958.3 L2280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:11174381 C>A maps to NM_004958.3 L2431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr1:11188177 G>A maps to NM_004958.3 L1972L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr10:30602410 G>C did not map to a codon.
Sequencing variant TCGA-DS-A1OA-01A-11D-A16Y-08 chr10:30654211 G>C maps to ENST00000358107 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr10:30654112 C>T maps to ENST00000358107 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr10:30657358 C>A did not map to a codon.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr10:30604918 G>A maps to ENST00000358107 F583F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr1:236973893 C>T maps to NM_000254.2 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr1:236958907 C>T maps to ENST00000418145 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr13:41834683 G>T maps to NM_004294.2 Y120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr6:153310987 G>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:100542385 C>T maps to ENST00000511045 F864F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr4:100534167 C>G maps to ENST00000511045 L723L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WF-01A-11D-A351-09 chr13:30077198 G>A maps to NM_001033602.2 L1332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr13:30071398 C>T maps to NM_001033602.2 Q1212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:155180434 G>C did not map to a codon.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr2:177188190 T>G maps to NM_006554.4 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr19:9059311 C>T maps to NM_024690.2 S9378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr19:9068287 G>C maps to NM_024690.2 V6386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr19:9084974 G>A maps to NM_024690.2 L2280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A50E-01A-21D-A26G-09 chr19:9083357 C>T maps to NM_024690.2 L2819L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr19:9082959 G>C maps to NM_024690.2 S2952*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr19:8976329 C>T maps to NM_024690.2 L14166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:9011001 G>A maps to NM_024690.2 F12972F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr19:9071028 G>A maps to NM_024690.2 Q5473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr19:9072599 G>T maps to NM_024690.2 S4949*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr19:9071032 G>A maps to NM_024690.2 I5471I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr19:9091664 C>T maps to NM_024690.2 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr19:9091808 C>A maps to NM_024690.2 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr19:9090941 G>A maps to NM_024690.2 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr7:100675896 C>T maps to NM_001040105.1 V400V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr7:100675494 A>G maps to NM_001040105.1 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr7:100676738 C>G maps to NM_001040105.1 S681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr7:100686384 G>C maps to NM_001040105.1 S3896S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr7:100676822 C>G maps to NM_001040105.1 S709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr7:100675172 C>G maps to NM_001040105.1 S159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr7:100679610 C>G maps to NM_001040105.1 V1638V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr11:1078303 G>A maps to ENST00000441003 Q197Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A4BA-01A-21D-A26G-09 chr11:1099466 T>C maps to ENST00000441003 P2436P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr11:1093676 C>T maps to ENST00000441003 S1832S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr11:1104214 C>T maps to ENST00000441003 G2802G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A852-01A-11D-A351-09 chr11:1092218 C>G maps to ENST00000441003 L1346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AU-01A-32D-A243-09 chr11:1079661 G>A maps to ENST00000441003 K293K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr11:1086012 G>A maps to ENST00000441003 T951T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:1082320 G>A maps to ENST00000441003 K592K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3TX-01A-11D-A22X-09 chr3:195346455 C>T did not map to a codon.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr3:195345577 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr3:195512102 G>A maps to NM_018406.5 T2116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr3:195515363 G>A maps to NM_018406.5 D1029D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr3:195475852 G>A maps to NM_018406.5 F5318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr3:195508148 G>A maps to NM_018406.5 S3434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M2-01A-21D-A18J-09 chr3:195488430 G>A maps to NM_018406.5 D4846D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr3:195490964 C>T maps to NM_018406.5 Q4665Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr3:195507161 G>C maps to NM_018406.5 V3763V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr3:195512139 G>C maps to NM_018406.5 S2104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr3:195512283 G>C maps to NM_018406.5 S2056*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr3:195512317 G>A maps to NM_018406.5 Q2045*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr3:195474047 C>G maps to NM_018406.5 *5413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr3:195474199 C>A maps to NM_018406.5 L5362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr3:195513627 G>T maps to NM_018406.5 S1608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr3:195517018 C>A maps to NM_018406.5 E478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr3:195513257 G>T maps to NM_018406.5 V1731V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr3:195513269 C>T maps to NM_018406.5 T1727T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr3:195510795 G>T maps to NM_018406.5 S2552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr3:195511419 G>C maps to NM_018406.5 S2344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr3:195509739 G>T maps to NM_018406.5 S2904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:195509547 G>C maps to NM_018406.5 S2968*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr3:195513668 G>C maps to NM_018406.5 S1594S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr3:195511899 G>C maps to NM_018406.5 S2184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R1-01A-11D-A28B-09 chr3:195492147 G>A maps to NM_018406.5 V4597V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr3:195508584 G>C maps to NM_018406.5 S3289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RA-A741-01A-11D-A33O-09 chr3:195512955 G>T maps to NM_018406.5 S1832*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr11:1267601 C>G maps to ENST00000447027 L3167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr11:1271507 G>A maps to ENST00000447027 T4469T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr11:1248314 C>A maps to ENST00000447027 Y172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CG-01A-11D-A32I-09 chr11:1269974 G>A maps to ENST00000447027 T3958T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7X3-01A-11D-A351-09 chr11:1255049 C>T maps to ENST00000447027 C786C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr11:1281215 C>T maps to ENST00000447027 S5611S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HR-01A-11D-A20U-09 chr11:1272202 C>G maps to ENST00000447027 S4701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr11:1263797 G>A maps to ENST00000447027 T1899T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr11:1271111 C>T maps to ENST00000447027 T4337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr11:1268332 C>G maps to ENST00000447027 S3411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr11:1276304 C>G maps to ENST00000447027 L5236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3PZ-01A-11D-A21Q-09 chr11:1265855 C>T maps to ENST00000447027 T2585T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr11:1269197 G>C maps to ENST00000447027 L3699L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr11:1267514 C>G maps to ENST00000447027 L3138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:1263911 C>T maps to ENST00000447027 P1937P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:1028328 G>A maps to NM_005961.2 I550I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:1028942 G>A maps to NM_005961.2 Q467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr11:1031827 G>C maps to NM_005961.2 S114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr4:71347021 G>A maps to NM_152291.2 E187E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr19:1371276 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr23:105451165 A>C did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr23:105451482 G>C did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:105449950 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:105451315 G>T did not map to a codon.
Sequencing variant TCGA-JW-A69B-01A-11D-A32I-09 chr23:105450198 C>T did not map to a codon.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr9:113550062 G>A maps to ENST00000189978 Q630Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A69L-01A-11D-A32I-09 chr6:49403180 C>T maps to NM_000255.3 V704V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr1:45805914 G>A maps to NM_001128425.1 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr16:88725117 G>A maps to NM_002461.1 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr16:88723973 C>T maps to NM_002461.1 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr12:110032987 T>C did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:110013876 C>G maps to NM_001114185.1 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr21:42774011 G>A maps to NM_002463.1 Q510Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr21:42771121 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr21:42762502 C>T maps to NM_002463.1 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73R-01A-11D-A33O-09 chr10:112039839 C>T maps to NM_130439.3 R241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr23:3238286 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr23:3228967 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr23:3241075 G>C did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr23:3229098 G>A did not map to a codon.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr23:3238157 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr23:3240794 G>C did not map to a codon.
Sequencing variant TCGA-EX-A69L-01A-11D-A32I-09 chr23:3242248 C>T did not map to a codon.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr23:3229027 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:3239577 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr23:3229383 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:3239348 G>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:3241580 C>T did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:3228084 G>A did not map to a codon.
Sequencing variant TCGA-RA-A741-01A-11D-A33O-09 chr23:3242778 C>A did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr17:74673768 C>T maps to NM_001008528.1 Q172Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr6:135539486 A>G did not map to a codon.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr12:102079531 C>T did not map to a codon.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr12:102038470 C>T maps to NM_002465.2 Q288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:50962465 C>T maps to NM_004533.3 F898F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr19:50958851 C>T maps to NM_004533.3 I763I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr19:50958396 C>T maps to NM_004533.3 Q683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr19:50961964 C>T maps to NM_004533.3 S820S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr19:50965289 G>A maps to NM_004533.3 P1075P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr19:50939935 C>T maps to NM_004533.3 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KH-01A-21D-A22X-09 chr8:128750879 C>T maps to NM_002467.4 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr13:77695486 G>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr13:77754363 C>T maps to NM_015057.4 L1677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VH-01A-11D-A28B-09 chr13:77677373 C>A did not map to a codon.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr2:241066088 G>C maps to NM_138336.1 S217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr12:81112733 C>T maps to NM_005593.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:81111255 G>C maps to NM_005593.2 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr17:10398361 C>T maps to NM_005963.3 E1784E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr17:10406093 C>T maps to NM_005963.3 L1024L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PI-01A-11D-A18J-09 chr17:8449918 C>G maps to ENST00000360416 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr17:8397164 C>G maps to ENST00000360416 L1365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:8424544 G>A maps to ENST00000360416 S672S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AX-01A-12D-A243-09 chr17:8381715 C>T maps to ENST00000360416 L1882L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr16:15917214 G>A maps to NM_001040114.1 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr16:15835412 C>T maps to NM_001040114.1 E929E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr17:10219249 C>G maps to NM_003802.2 L1277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr17:10248900 G>A maps to NM_003802.2 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr17:10263345 G>A maps to NM_003802.2 V192V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr17:10263482 G>A maps to NM_003802.2 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr17:10210288 G>A maps to NM_003802.2 N1754N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr17:10215383 C>A maps to NM_003802.2 E1459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BE-01A-21D-A26G-09 chr17:10235466 G>A maps to NM_003802.2 L749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr19:50760688 C>G maps to NM_001145809.1 L726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr19:50792781 A>T maps to NM_001145809.1 T1614T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr19:50781446 G>A maps to NM_001145809.1 R1311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr3:108195276 G>A maps to NM_014981.1 N420N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr3:108149737 T>A maps to NM_014981.1 K1105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr17:10428322 G>A maps to NM_017534.5 V1574V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr17:10430337 G>A maps to NM_017534.5 L1303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr17:10428319 C>T maps to NM_017534.5 K1575K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr17:10435165 G>A maps to NM_017534.5 F827F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr17:10541419 G>A maps to NM_002470.2 S1223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr17:10558293 G>A maps to NM_002470.2 Q30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr17:10542716 G>C maps to NM_002470.2 L1000L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr17:10535837 C>T maps to NM_002470.2 A1637A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr17:10360824 G>C maps to NM_017533.2 P603P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr17:10356552 C>T maps to NM_017533.2 Q1009Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr14:23866750 C>A did not map to a codon.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr14:23869467 C>T maps to NM_002471.3 E526E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DV-01A-11D-A32I-09 chr14:23866004 C>T maps to NM_002471.3 V730V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3TQ-01A-11D-A22X-09 chr14:23884924 G>A maps to NM_000257.2 A1690A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr14:23884897 C>T maps to NM_000257.2 R1699R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr14:23893301 C>T maps to NM_000257.2 K912K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr14:23902430 C>G maps to NM_000257.2 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A4BA-01A-21D-A26G-09 chr20:33567552 C>T maps to NM_020884.3 N138N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr17:10317336 G>T maps to NM_002472.2 G343G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr17:10302916 G>A maps to NM_002472.2 Q1269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr17:10297721 G>A maps to NM_002472.2 L1670L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr17:10312481 C>G did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr17:10300224 C>T maps to NM_002472.2 K1419K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr22:36718515 G>A maps to NM_002473.4 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CH-01A-11D-A33O-09 chr22:36697587 G>A maps to NM_002473.4 Q875*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr22:36680287 C>T maps to NM_002473.4 L1872L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr22:36684428 C>A maps to NM_002473.4 E1601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr22:36697734 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3L7-01A-21D-A20U-09 chr22:36685205 C>T maps to NM_002473.4 E1494E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr22:36691763 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr22:36744961 G>C maps to NM_002473.4 S107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr22:36745183 C>T maps to NM_002473.4 W33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr22:36691726 G>C maps to NM_002473.4 L1103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr12:56553367 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr3:123385155 C>T maps to NM_053025.3 Q1247Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr3:123419272 C>T maps to NM_053025.3 L1014L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr16:30388989 G>A maps to NM_013292.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr3:169496993 C>A maps to NM_018657.4 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr3:169496594 C>G maps to NM_018657.4 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr3:169492151 C>G maps to NM_018657.4 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr5:16703224 C>T maps to NM_012334.2 Q773Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr5:16818159 G>A maps to NM_012334.2 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr17:18025404 A>C maps to ENST00000205890 P1097P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr17:18052197 C>T maps to ENST00000205890 F2296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr17:18060372 C>T maps to ENST00000205890 R2903*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr17:18025404 A>C maps to ENST00000205890 P1097P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr17:18061907 C>G maps to ENST00000205890 L3013L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LB-01A-11D-A243-09 chr17:18055213 G>T maps to ENST00000205890 L2614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VI-01A-11D-A28B-09 chr17:18023394 C>T maps to ENST00000205890 H427H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr13:109793203 C>G maps to NM_015011.1 L1526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr13:109772764 C>G maps to NM_015011.1 L1140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A69B-01A-11D-A32I-09 chr13:109831944 G>T maps to NM_015011.1 S1771S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr13:109365048 C>A maps to NM_015011.1 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr17:27425863 C>A maps to NM_078471.3 E1254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr17:27438755 C>T maps to NM_078471.3 Q908Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:57433068 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr2:192227048 G>A maps to NM_001130158.1 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr17:1381434 G>A maps to NM_001080779.1 F449F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr17:1371351 G>C maps to NM_001080779.1 L942L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr17:1377927 G>A maps to NM_001080779.1 L591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr17:1370784 G>A maps to NM_001080779.1 I1018I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr17:30980881 G>C maps to NM_015194.1 L858L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr17:31048063 C>T maps to NM_015194.1 Q630Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:30981584 G>C maps to NM_015194.1 V800V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr15:59553682 G>C maps to NM_004998.2 S58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr15:59430492 G>A maps to NM_004998.2 Q1052*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr19:8587696 C>A maps to NM_012335.3 G957G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr19:8616751 C>A maps to NM_012335.3 E215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr12:109872884 G>T maps to NM_001101421.3 E687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr12:109878604 C>T maps to NM_001101421.3 R821R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr10:26500867 C>A maps to NM_017433.4 R1609R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr10:26417424 A>G maps to NM_017433.4 Q740Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UC-01A-11D-A351-09 chr2:171264295 G>A maps to NM_138995.3 L864L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr2:171262053 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr2:171258177 C>T maps to NM_138995.3 L702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr15:52697557 G>A maps to ENST00000358212 R327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr18:47500757 G>C maps to NM_001080467.2 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr18:47463689 C>G maps to NM_001080467.2 S610S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr15:52553090 C>T maps to NM_018728.3 Q427Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr11:76892541 C>G maps to NM_000260.3 V937V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr2:128380922 C>T maps to ENST00000389524 F1238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr2:128324315 C>T maps to ENST00000389524 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr2:128394376 C>G maps to ENST00000389524 L2047L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr2:128340009 C>T maps to ENST00000389524 F444F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R9-01A-11D-A18J-09 chr2:128335751 C>T maps to ENST00000389524 Y298Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr2:128350377 C>A maps to ENST00000389524 R668R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr2:128379603 C>T maps to ENST00000389524 F1165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr2:128341726 C>T maps to ENST00000389524 N458N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr15:72120254 C>A maps to ENST00000424560 E2456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr15:72172109 C>T maps to ENST00000424560 L1968L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr15:72311418 G>C maps to ENST00000424560 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr1:171605175 C>T maps to NM_000261.1 K468K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:171605065 C>T maps to NM_000261.1 *505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr1:171621373 C>T maps to NM_000261.1 R126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr17:12656107 G>A maps to NM_001146312.1 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr11:17741622 C>T maps to NM_002478.4 C98C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr10:95088618 G>A maps to NM_013451.3 Q1678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LC-01A-11D-A20U-09 chr10:95237969 T>G did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:203054798 C>T maps to NM_002479.4 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QD-01A-32D-A22X-09 chr18:3151752 G>A maps to NM_003803.3 F594F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr1:24413278 C>T maps to ENST00000330966 S552S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr19:46404854 G>T maps to NM_001012643.2 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr3:40192619 G>A maps to NM_015460.2 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr3:40085723 C>T maps to NM_015460.2 H98H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr3:40299696 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr3:40286040 G>A maps to NM_015460.2 A735A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr3:40299718 C>A did not map to a codon.
Sequencing variant TCGA-JW-A69B-01A-11D-A32I-09 chr1:59158364 G>A did not map to a codon.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr20:62867943 G>A maps to NM_004535.2 K978K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr2:1805481 T>A maps to ENST00000399161 K1088*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M2-01A-21D-A18J-09 chr2:1820040 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr2:2057783 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr2:1820501 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr2:1820057 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr2:1820469 C>T did not map to a codon.
Sequencing variant TCGA-LP-A4AX-01A-12D-A243-09 chr2:1921046 G>A maps to ENST00000399161 H516H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr2:1844768 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr2:1820142 C>T did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr13:32981745 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr13:33054765 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr21:30255319 G>A maps to NM_013240.3 Q70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3TX-01A-11D-A22X-09 chr4:80247016 G>A maps to NM_032693.2 N5N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr4:140264025 C>A maps to NM_057175.3 S150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HQ-01A-11D-A20U-09 chr4:140270689 G>T maps to NM_057175.3 E256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr4:140270727 C>G maps to NM_057175.3 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr13:41936627 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr12:112492279 G>A maps to NM_024953.3 R514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr12:112499081 C>G maps to NM_024953.3 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr12:112530884 C>T maps to NM_024953.3 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr14:57876232 G>A maps to NM_001011713.2 *363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr11:63706540 G>A did not map to a codon.
Sequencing variant TCGA-C5-A7CG-01A-11D-A32I-09 chr11:89891407 T>C did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr11:89892436 G>A maps to NM_005467.3 K307K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr11:64812805 G>C maps to ENST00000340252 L771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr12:57483007 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:57485123 G>A maps to NM_005967.3 Q100Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:57107410 C>T maps to NM_001113203.1 R1960R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr17:59668211 G>A maps to NM_199290.3 D110D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr11:71185635 C>G did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr11:71212396 G>C maps to NM_018161.4 *707S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZF-01A-11D-A28B-09 chr17:42084058 G>T maps to NM_153006.2 E360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr9:130829079 C>A maps to NM_197956.3 E101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr9:130825811 G>A maps to NM_197956.3 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr9:130829406 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr5:70308576 G>A maps to NM_004536.2 Q56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr13:102029362 G>T maps to NM_052867.2 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr13:101728268 G>A maps to NM_052867.2 G1303G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr13:101777026 G>A maps to NM_052867.2 R708R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr12:7945645 C>T maps to NM_024865.2 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr20:25597139 G>C maps to NM_152667.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr23:72432945 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr23:92928397 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3HQ-01A-11D-A20U-09 chr23:92927306 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:92927909 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:92928473 G>A did not map to a codon.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr23:92926241 C>T did not map to a codon.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr16:780647 C>T maps to NM_022493.1 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr16:780301 C>G did not map to a codon.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr18:55273951 G>A maps to NM_004539.3 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr19:55997215 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr17:72767863 C>T maps to NM_015654.3 *208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:201779861 C>T maps to ENST00000367296 F1591F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr11:20070574 C>T maps to ENST00000396087 Q1425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr12:78444741 G>T maps to NM_014903.4 S777S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr12:78444741 G>T maps to NM_014903.4 S777S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr12:78334046 G>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr12:78444580 G>T maps to NM_014903.4 E724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr12:78401165 C>T maps to NM_014903.4 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr2:15372595 C>T maps to NM_015909.2 L2062L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr2:15555686 G>A maps to NM_015909.2 Q974*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr2:15307269 C>A maps to NM_015909.2 E2340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr13:36229091 T>C maps to ENST00000400445 Y2691Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PI-01A-11D-A18J-09 chr13:36026232 G>T maps to ENST00000400445 T2103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr13:35622735 C>T maps to ENST00000400445 Q254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A3L1-01A-11D-A21Q-09 chr13:36220011 G>T maps to ENST00000379922 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr13:35747727 G>A maps to ENST00000400445 S1517S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr13:36026252 C>G maps to ENST00000400445 S2110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr13:35926394 G>A maps to ENST00000400445 Q2038Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr2:203948190 C>T maps to NM_001114132.1 Q312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr2:204073910 C>T maps to NM_001114132.1 Q2522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr2:204000414 C>T maps to NM_001114132.1 Q1248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr3:47033348 G>T maps to NM_015175.1 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3TQ-01A-11D-A22X-09 chr1:19981846 C>T maps to NM_182744.2 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:19981642 C>T maps to NM_182744.2 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr1:16903864 T>C maps to NM_017940.3 R617R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CJ-01A-11D-A32I-09 chr1:16889865 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr1:16890341 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:16935095 G>T did not map to a codon.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr1:16921145 T>C did not map to a codon.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr1:148594446 C>G maps to NM_001170755.1 S607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr1:21807445 G>T maps to NM_032264.2 E469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr8:102731653 G>A maps to NM_032041.2 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr8:102731623 C>T maps to NM_032041.2 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CH-01A-11D-A33O-09 chr11:113146828 G>C did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr11:113147596 T>G did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr11:113143754 C>G did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr11:113144008 C>T did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr11:113148182 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr21:22710835 G>A maps to NM_004540.2 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr21:22746205 C>T maps to NM_004540.2 V356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:134027949 C>A maps to NM_015261.2 L1349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:134047137 G>A maps to NM_015261.2 L999L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr11:134063984 G>A maps to NM_015261.2 L584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr4:17839397 C>T maps to NM_022346.3 Q814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr7:158458072 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr22:50956612 C>T maps to NM_001185011.1 C184C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr22:50959392 G>C did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr9:100423312 G>A maps to NM_002486.4 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr1:36023764 C>G did not map to a codon.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr7:74203028 G>A maps to NM_000265.4 Q344Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr7:74191961 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr1:183536380 C>T maps to NM_001127651.2 K271K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr2:106471653 C>A maps to NM_001004720.2 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr2:183826936 G>A maps to NM_205842.1 R617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr2:133489418 G>A maps to NM_207363.2 D1778D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr2:133887671 C>T maps to NM_207363.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr12:50195663 C>T maps to NM_001037806.3 Q106Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr19:3193401 C>T maps to NM_020170.3 Q166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr8:71128947 G>A maps to NM_006540.2 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr8:71036974 G>A maps to NM_006540.2 Q1348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr20:33356296 C>A maps to NM_014071.2 E162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QD-01A-32D-A22X-09 chr20:33345194 C>T maps to NM_014071.2 Q452Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:16021222 G>A maps to ENST00000395857 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr17:15976883 C>T did not map to a codon.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr17:16001721 G>A maps to ENST00000395857 L943L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr12:124862909 C>T maps to NM_006312.4 R680R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr12:124886951 G>C maps to NM_006312.4 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr19:55417655 G>A did not map to a codon.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr6:41310654 G>T did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:160326679 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr1:160326699 G>T did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr17:8347561 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr15:23932064 C>T maps to NM_002487.2 Q100Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr23:43809084 C>A did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr20:35288784 G>A maps to ENST00000373803 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr10:75567714 G>C maps to NM_003635.3 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr10:75567902 G>A maps to NM_003635.3 R82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:119007293 C>A did not map to a codon.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr22:42483074 G>A maps to NM_002490.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr22:42483069 G>C maps to NM_002490.3 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KH-01A-21D-A22X-09 chr9:124906635 G>A maps to NM_014222.2 R135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M1-01A-11D-A18J-09 chr6:97345679 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr14:92587951 C>T did not map to a codon.
Sequencing variant TCGA-EX-A449-01A-11D-A243-09 chr16:2011217 G>T maps to NM_004548.2 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr23:47003938 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr23:47001821 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr23:47002087 C>G did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:140404745 C>G did not map to a codon.
Sequencing variant TCGA-EX-A1H6-01B-11D-A22X-09 chr1:161184090 A>G did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:161179398 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr5:1802489 T>C did not map to a codon.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr11:67378576 C>G maps to NM_007103.3 S271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr11:67374474 G>C did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr11:67376091 G>A maps to NM_007103.3 W75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr2:152476024 G>A maps to NM_001164507.1 I3604I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr2:152586146 G>A maps to NM_001164507.1 Y20Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr2:152476074 G>A maps to NM_001164507.1 Q3588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr2:152419319 C>T maps to NM_001164507.1 L6232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:152348656 C>A maps to NM_001164507.1 E8338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:152518711 A>C maps to NM_001164507.1 Y1969*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr2:152394430 A>G maps to NM_001164507.1 R7019R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr10:21115384 A>G maps to ENST00000430741 N620N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr10:21097532 G>A maps to ENST00000430741 F891F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr10:21098822 G>A maps to ENST00000430741 L843L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr1:16767244 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr12:97330436 C>T maps to NM_001135175.1 F263F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R9-01A-11D-A18J-09 chr18:55981814 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RE-01A-11D-A18J-09 chr18:56034975 A>C did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr18:56024424 G>A did not map to a codon.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr22:29879484 G>A maps to NM_021076.3 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr8:24809848 T>G did not map to a codon.
Sequencing variant TCGA-EA-A50E-01A-21D-A26G-09 chr8:24771767 C>A maps to NM_005382.2 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr1:72400956 G>A maps to NM_173808.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr15:75644550 G>A maps to NM_024608.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr15:75641329 G>A maps to NM_024608.2 E28E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QD-01A-32D-A22X-09 chr4:170428889 C>T maps to ENST00000507142 R629R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr3:27387638 A>G maps to ENST00000396636 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:27343239 G>C maps to ENST00000396636 S372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr13:52667253 G>A maps to NM_199289.1 Q382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:27064322 G>C did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr14:75573249 G>A maps to NM_033116.4 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr14:75567839 C>T maps to NM_033116.4 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr11:20968932 G>T maps to NM_006157.3 E375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr12:44913799 G>A maps to NM_001145107.1 L846L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr12:45209911 G>A maps to NM_001145107.1 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:44915917 C>T maps to NM_001145107.1 E730E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr1:212619332 C>T maps to NM_013349.4 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr18:70526219 G>A maps to NM_153181.2 R103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr2:233899463 C>T maps to NM_005383.2 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr10:105344980 C>T maps to NM_004210.4 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr10:105330767 C>T maps to NM_004210.4 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr20:44517471 C>T maps to NM_080749.2 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A5QV-01A-22D-A28B-09 chr2:182543230 C>T maps to NM_002500.2 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr4:113436005 G>T maps to NM_024019.2 S209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CJ-01A-11D-A32I-09 chr4:113436222 C>A maps to NM_024019.2 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr17:29553643 C>T maps to NM_001042492.2 L731L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr17:29528440 C>T maps to NM_001042492.2 Q400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr17:29556484 T>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr17:29677226 C>T maps to NM_001042492.2 R2450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr17:29509566 G>T maps to NM_001042492.2 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr17:29546121 C>T maps to NM_001042492.2 Q543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:29652870 G>T maps to NM_001042492.2 L1623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R3-01A-11D-A28B-09 chr17:29585382 C>T maps to NM_001042492.2 Q1399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H1-01A-11D-A17W-09 chr22:30070876 G>T maps to NM_181832.2 E465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr22:42807593 C>T maps to NM_145912.5 Q90Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr1:204985780 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:204987178 T>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:204991892 A>C did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:204985892 C>T did not map to a codon.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr16:69727753 C>G maps to NM_138713.2 P1342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr16:69727883 C>T maps to NM_138713.2 Q1386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr18:77208810 G>A maps to NM_172387.1 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R9-01A-11D-A18J-09 chr18:77253551 G>C did not map to a codon.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr20:50139762 G>A maps to NM_012340.3 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr20:50179162 C>T maps to NM_001136021.1 Q2Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr16:68224712 C>G maps to NM_173165.2 S714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr14:24838984 G>A maps to NM_001136022.1 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr12:54686941 G>C maps to NM_001136023.1 S113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:46135814 C>G maps to ENST00000362042 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HM-A4S6-01A-11D-A26G-09 chr17:46136123 C>T maps to ENST00000362042 S499S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr2:178097217 C>A maps to NM_006164.3 E166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr2:178095887 G>A maps to NM_006164.3 F481F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr7:26225030 G>C maps to NM_004289.6 L571L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:61554152 C>T maps to NM_001145512.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr9:14116246 C>T maps to ENST00000397581 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3YQ-01A-11D-A22X-09 chr19:3453780 C>G maps to ENST00000269778 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr19:3434305 C>T maps to ENST00000269778 F247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr4:103518704 G>A maps to NM_003998.3 Q508Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr10:104154242 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr14:35872940 C>T maps to NM_020529.2 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr19:36381328 G>A maps to ENST00000352614 Q376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr20:34263074 G>A maps to NM_021100.4 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr9:33366760 C>T maps to NM_002504.4 V1058V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr9:33351828 C>T did not map to a codon.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr4:47853887 C>T maps to NM_152995.4 K831K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr2:233748710 C>T maps to NM_019850.2 V527V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr1:115829245 C>T maps to NM_002506.2 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr17:47590068 G>T did not map to a codon.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr2:220025454 G>C did not map to a codon.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr13:39613750 C>T maps to NM_001012754.2 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr23:17744528 C>T did not map to a codon.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr23:17745122 C>G did not map to a codon.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr23:17744356 G>A did not map to a codon.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr23:17743567 G>C did not map to a codon.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr23:17744186 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr23:17746793 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr23:17746201 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:17710459 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:17744254 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:17744155 C>T did not map to a codon.
Sequencing variant TCGA-LP-A5U3-01A-11D-A28B-09 chr23:17744068 G>A did not map to a codon.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr23:17744046 C>G did not map to a codon.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr23:17744196 C>G did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:71360612 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr1:236208916 C>A maps to NM_002508.2 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr14:52520401 C>A maps to NM_007361.3 E442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr20:25460853 C>G maps to NM_025176.4 L620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr20:25459788 C>T maps to NM_025176.4 E657E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr4:48037978 G>T maps to NM_207330.1 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr4:48037978 G>C maps to NM_207330.1 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr4:48038113 T>G maps to NM_207330.1 V386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr8:99208192 G>A maps to NM_024759.1 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr8:99264811 G>A maps to NM_024759.1 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr1:24787008 C>T maps to NM_020448.4 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr1:24768627 G>A maps to NM_020448.4 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr1:24771730 C>T maps to NM_020448.4 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M1-01A-11D-A18J-09 chr5:37006622 T>A maps to NM_133433.3 T1340T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M1-01A-11D-A18J-09 chr5:37006623 A>T maps to NM_133433.3 K1341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr5:36985279 C>T maps to NM_133433.3 S666S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr5:37038788 C>G maps to NM_133433.3 L2019L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr22:29956726 G>C maps to NM_003634.2 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr22:29956744 G>C maps to NM_003634.2 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr9:107531249 G>A maps to NM_018376.2 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr3:52521595 G>A maps to NM_007184.3 A696A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr3:52514408 C>T maps to ENST00000488380 F542F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:52522531 G>A maps to NM_007184.3 L1008L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:52524733 G>A maps to NM_007184.3 Q1209Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr6:124979387 G>A maps to NM_001040214.1 E110E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73R-01A-11D-A33O-09 chr6:124979591 G>A maps to ENST00000368416 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr23:119064009 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr23:119059327 C>T did not map to a codon.
Sequencing variant TCGA-HM-A4S6-01A-11D-A26G-09 chr23:119068473 C>G did not map to a codon.
Sequencing variant TCGA-EA-A78R-01A-11D-A32I-09 chr6:28227226 C>T maps to NM_001007531.1 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr16:50667158 C>T maps to NM_033119.3 R294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr5:1037711 A>C maps to ENST00000274150 R289R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr19:51875735 G>A maps to NM_005601.3 F18F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr23:118723424 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73R-01A-11D-A33O-09 chr23:118724033 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr14:36988460 G>A maps to NM_001079668.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr20:21492755 G>C maps to NM_002509.2 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr8:23538901 A>G maps to NM_006167.3 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr3:173998300 G>A maps to NM_014932.2 T560T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr17:7318955 C>G maps to NM_020795.2 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr23:70387000 C>G did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr23:70387279 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:70387590 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:70390051 T>C did not map to a codon.
Sequencing variant TCGA-EK-A2GZ-01A-11D-A17W-09 chr23:70389650 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr23:70390334 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr23:5811014 C>T did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr23:5821222 A>G did not map to a codon.
Sequencing variant TCGA-C5-A2M1-01A-11D-A18J-09 chr23:5821212 G>T did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:5821161 G>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:6069405 G>C did not map to a codon.
Sequencing variant TCGA-DS-A7WI-01A-12D-A351-09 chr23:6069277 G>T did not map to a codon.
Sequencing variant TCGA-JW-A5VH-01A-11D-A28B-09 chr23:5821412 G>A did not map to a codon.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr23:5827179 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr23:5821629 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr5:65077184 G>A maps to NM_020726.4 K253K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr16:3613848 G>C maps to ENST00000448023 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr16:3613353 G>C maps to ENST00000448023 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr16:3602270 C>T maps to ENST00000448023 K806K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr2:32475117 A>G maps to NM_021209.4 C605C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr2:32463278 G>A maps to NM_021209.4 L815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:32463228 G>T maps to NM_021209.4 C831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr16:57063769 T>G did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr16:57070016 C>A maps to NM_032206.3 S878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr16:57104512 G>A maps to NM_032206.3 W1550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr17:5485359 G>A maps to NM_033004.3 Y157Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr17:5440178 G>A maps to NM_033004.3 F984F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr17:5403370 C>T did not map to a codon.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr19:56312939 C>T maps to NM_145007.3 L723L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr19:56297127 T>A maps to NM_145007.3 R989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr19:56321255 G>A maps to NM_145007.3 V240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr19:56321471 C>T maps to NM_145007.3 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr19:54327206 G>C maps to ENST00000391773 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr19:54313718 G>A maps to ENST00000391773 F398F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr19:54299114 G>C maps to ENST00000391773 L1033L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr19:56424378 G>A maps to NM_176810.2 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr11:7083723 C>T maps to NM_176822.3 Q989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr19:55494073 G>A maps to NM_017852.3 T336T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:55508775 C>T maps to NM_017852.3 Q991*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr1:247582048 G>T did not map to a codon.
Sequencing variant TCGA-EA-A411-01A-11D-A243-09 chr1:247587314 C>T maps to NM_004895.4 I190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr19:56369914 G>T maps to NM_134444.4 E386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr19:56538690 C>T maps to NM_153447.4 F364F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr19:56539276 G>T maps to NM_153447.4 E560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DV-01A-11D-A32I-09 chr19:56538759 G>A maps to NM_153447.4 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr11:280448 G>T maps to NM_138329.1 E239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HM-A3JK-01A-11D-A21Q-09 chr11:284301 G>A maps to NM_138329.1 L758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr19:55449509 G>A maps to ENST00000446217 L705L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr19:56459459 C>T maps to NM_176811.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr19:56487501 G>A maps to NM_176811.2 L903L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3PZ-01A-11D-A21Q-09 chr19:56463941 G>T maps to NM_176811.2 G136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr19:56220298 C>T maps to NM_176820.2 K985K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr19:56220384 C>A maps to NM_176820.2 E957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr19:56235488 T>C maps to NM_176820.2 G672G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:119053982 C>A maps to NM_024618.2 L921L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr11:119042083 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr11:119050952 G>C maps to NM_024618.2 G741G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr11:119045733 G>C maps to NM_024618.2 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr5:137464198 C>T maps to NM_003551.2 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr3:48335897 C>T did not map to a codon.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr1:169293720 G>A maps to NM_013330.3 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr16:4511897 G>A maps to NM_020677.3 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr2:101097608 C>T maps to NM_001011717.1 R132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr17:43171153 C>T maps to NM_021079.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr17:43180326 G>A maps to NM_021079.3 K334K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr11:114183192 C>A maps to NM_006169.2 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr5:43659316 C>T maps to NM_182977.2 V833V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr5:43644760 C>T maps to NM_182977.2 Q383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:69776285 C>G maps to NM_014062.1 R396R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73Q-01A-21D-A32I-09 chr16:69786242 G>A maps to NM_014062.1 Y76Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr1:891553 C>T maps to NM_015658.3 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr10:96117814 G>T did not map to a codon.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr12:132636944 G>A maps to NM_024078.1 *517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr2:10729802 C>T maps to NM_024894.2 E499E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:10829969 G>A maps to NM_024894.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr17:65717521 C>G maps to NM_015462.3 S114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr17:65714107 G>C maps to NM_015462.3 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr9:33466915 C>G maps to NM_022917.4 L648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr9:95082609 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr1:6614165 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr16:18542929 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:70517279 G>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:70521006 T>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:70520932 G>C did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr23:70516457 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr15:34634297 C>G maps to NM_018648.3 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr12:6669684 C>T maps to ENST00000382421 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr20:2634825 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3L7-01A-21D-A20U-09 chr20:2635848 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr20:2636923 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr2:203155172 G>A maps to NM_015934.3 Q209Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:203147125 G>A maps to NM_015934.3 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr2:203155897 G>T maps to NM_015934.3 E229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr2:203149075 G>A maps to NM_015934.3 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr12:117658013 C>A maps to ENST00000338101 E1380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr12:117710210 G>A maps to ENST00000338101 N606N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:162326790 G>A maps to NM_014697.2 R268R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr17:26087700 G>A maps to NM_000625.4 I986I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:26108114 G>A maps to NM_000625.4 Q271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:26108138 G>A maps to NM_000625.4 Q263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CJ-01A-11D-A32I-09 chr7:150707744 G>T maps to NM_000603.4 E916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr7:150706115 G>A maps to NM_000603.4 L737L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr7:150706128 G>T maps to NM_000603.4 E742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RA-A741-01A-11D-A33O-09 chr7:150699019 G>T maps to NM_000603.4 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:50059840 C>G maps to NM_015953.3 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr2:169699593 G>A maps to NM_001171631.1 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:139397772 G>A maps to NM_017617.3 V1676V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:139418379 G>A maps to NM_017617.3 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr1:120462867 C>G maps to NM_024408.2 V1821V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZD-01A-11D-A28B-09 chr19:15299078 G>A maps to NM_000435.2 R487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr19:15276804 G>A maps to NM_000435.2 I1820I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A3L1-01A-11D-A21Q-09 chr19:15280980 C>T maps to NM_000435.2 K1705K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A69L-01A-11D-A32I-09 chr19:15295255 G>A maps to NM_000435.2 R806*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr19:15271473 C>G maps to NM_000435.2 *2322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr19:15272414 C>T maps to NM_000435.2 P2008P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr19:15299117 G>A maps to NM_000435.2 Q474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr6:32169255 G>A maps to NM_004557.3 C1259C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr6:32170025 C>T maps to NM_004557.3 P1194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr6:32163525 G>C maps to NM_004557.3 L1900L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr14:27018904 G>C did not map to a codon.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr23:100118507 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:100105260 G>A did not map to a codon.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr6:155764526 G>A maps to NM_015718.2 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr11:89133528 C>A maps to NM_016931.3 G289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr11:89155128 G>A maps to NM_016931.3 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3YQ-01A-11D-A22X-09 chr19:47548506 G>A maps to NM_002517.2 Q457Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr19:47535575 C>G maps to NM_002517.2 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr14:34270071 C>T maps to NM_001164749.1 F853F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr14:34268967 G>A maps to NM_001164749.1 E485E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr11:66188673 C>T maps to NM_178864.3 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr11:66189938 G>A maps to NM_178864.3 Q115Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr8:53852811 C>T maps to NM_005285.3 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr20:62737875 C>T maps to NM_005286.2 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr18:21119726 G>A did not map to a codon.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr7:44575552 G>A maps to NM_013389.2 D623D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr7:44560679 C>T maps to NM_013389.2 T997T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr7:44578915 G>A maps to NM_013389.2 V360V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A770-01A-11D-A33O-09 chr9:139935436 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3HR-01A-11D-A20U-09 chr17:45608749 C>T maps to NM_006310.3 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr4:73013315 C>G maps to NM_004885.2 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr3:132401566 C>T maps to ENST00000393156 L1264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr19:36330417 C>A maps to NM_004646.3 L969L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr19:36339023 C>T maps to NM_004646.3 Q453Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:182798812 G>A maps to ENST00000443789 *285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QD-01A-32D-A22X-09 chr17:79564318 G>A maps to NM_017921.2 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr8:21882272 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr8:21882800 G>C maps to NM_182795.1 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr1:153660529 G>A maps to NM_000906.3 E750E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr1:153665868 G>A maps to NM_000906.3 R1055R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:153665888 G>A maps to NM_000906.3 *1062*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:153657529 G>A maps to NM_000906.3 R525R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr5:32710860 C>T maps to ENST00000434067 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr16:167374 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr15:73925520 G>C maps to NM_012428.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RE-01A-11D-A18J-09 chr17:78449463 G>A maps to NM_002522.3 Q167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr4:156135546 C>T maps to NM_000910.2 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3TQ-01A-11D-A22X-09 chr23:30326792 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:30326418 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr23:30327071 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr11:47283408 G>C did not map to a codon.
Sequencing variant TCGA-EA-A5FO-01A-21D-A28B-09 chr11:47283253 C>T maps to NM_005693.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr11:47283258 G>A maps to NM_005693.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr11:47283300 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr11:47270220 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr12:95422187 C>T maps to NM_003297.2 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:15062305 C>T maps to NM_003298.3 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:15079633 C>G maps to NM_003298.3 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73S-01A-11D-A33O-09 chr3:15064800 G>T maps to NM_003298.3 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr19:19313681 G>C maps to ENST00000420605 S16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr15:72106368 G>A maps to NM_014249.2 K337K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M2-01A-21D-A18J-09 chr5:92929674 G>A did not map to a codon.
Sequencing variant TCGA-EA-A50E-01A-21D-A26G-09 chr5:92929439 C>T maps to NM_005654.4 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr15:96880845 C>T maps to NM_021005.3 Q414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr19:17355840 C>G maps to NM_005234.3 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WH-01A-22D-A351-09 chr5:142658931 G>A maps to ENST00000416954 I743I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr4:149356644 C>T maps to ENST00000511528 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3TQ-01A-11D-A22X-09 chr4:149035253 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3TX-01A-11D-A22X-09 chr4:149035254 G>A maps to ENST00000511528 D937D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr12:52435660 G>A maps to ENST00000360284 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr12:52449046 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr9:127287011 G>A maps to NM_033334.2 R448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr10:115364417 C>A maps to ENST00000369358 E1401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr10:115411591 C>T maps to ENST00000369358 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CJ-01A-11D-A32I-09 chr10:115350426 C>G maps to ENST00000369358 V1630V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr10:115405664 G>A maps to ENST00000369358 G343G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr8:144922148 G>A maps to NM_178564.3 I102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr8:144919846 G>A maps to NM_178564.3 F307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr7:107807497 C>A maps to ENST00000379032 E1112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:52277770 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr8:32606548 C>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr21:16337834 G>T maps to NM_003489.3 S893S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr12:2937119 C>T maps to NM_031474.2 E224E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr23:105152803 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr23:105153048 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr23:105168738 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr23:105168892 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr23:105193671 G>A did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr23:105132303 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr6:30655896 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr10:33483585 C>G did not map to a codon.
Sequencing variant TCGA-JX-A5QV-01A-22D-A28B-09 chr10:33559708 G>A maps to NM_003873.5 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr2:206630244 C>A maps to NM_201266.1 A785A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr2:206659476 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr2:206565457 C>T maps to ENST00000340626 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr6:24145978 A>T maps to NM_080723.4 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr20:334277 G>A maps to NM_024958.2 *205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr2:50147525 C>T did not map to a codon.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr2:51255078 G>A maps to ENST00000404971 D111D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr2:50765724 C>T maps to ENST00000404971 E643E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HQ-01A-11D-A20U-09 chr2:51149817 C>T maps to ENST00000404971 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr2:50148601 A>C did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr2:51255237 G>C maps to ENST00000404971 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr2:50573973 C>T maps to NM_138735.2 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr2:50733677 C>A maps to ENST00000404971 G858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr11:64428456 C>G maps to NM_015080.3 R651R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AU-01A-32D-A243-09 chr11:64421183 G>A maps to NM_015080.3 R800R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr14:79432548 G>A maps to NM_004796.4 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr14:78709691 C>T did not map to a codon.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr14:79434540 C>A maps to NM_004796.4 A625A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr5:74069848 T>C maps to NM_014886.3 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr5:176662834 G>A maps to NM_022455.4 E1270E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr5:176638816 T>A maps to NM_022455.4 S1139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr5:176687058 C>G maps to NM_022455.4 S1679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr5:176639053 G>A maps to NM_022455.4 L1218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr5:176687058 C>A maps to NM_022455.4 S1679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr5:176637739 G>C maps to NM_022455.4 S780S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr5:176637931 G>A maps to NM_022455.4 E844E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr5:176637991 G>A maps to NM_022455.4 L864L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr5:176638297 G>A maps to NM_022455.4 E966E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr5:176721265 C>T maps to NM_022455.4 L2299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LS-01A-22D-A22X-09 chr23:152018901 G>C did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:152031144 C>G did not map to a codon.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr23:152034374 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr17:44770330 G>A maps to NM_006178.2 Q336Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:212955581 T>G did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr10:123719110 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr5:6632821 G>A maps to NM_017755.5 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr3:93813014 G>C maps to NM_022072.3 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7X3-01A-11D-A351-09 chr1:46808525 G>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:46809450 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr1:46806551 C>T maps to NM_199044.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr1:46808702 C>T did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr1:46808638 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr7:72721670 C>T maps to NM_148956.2 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OA-01A-11D-A16Y-08 chr10:18937523 C>T maps to NM_182543.2 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr10:18837048 G>A maps to NM_182543.2 Q397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr4:40752790 G>C maps to NM_024677.4 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr17:73126732 C>T maps to NM_014595.1 Q152Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr2:18765968 C>T maps to ENST00000455492 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5FO-01A-21D-A28B-09 chr10:104913047 C>A did not map to a codon.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr10:104860426 G>A maps to ENST00000423468 Q25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:52558596 G>A maps to NM_001134231.1 T521T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr6:86176857 G>A maps to NM_002526.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr12:5603481 C>T maps to NM_001102654.1 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr11:132081970 T>C maps to NM_001144058.1 N152N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q8-01A-11D-A21Q-09 chr11:132205129 A>T did not map to a codon.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr12:96063913 C>A maps to NM_021229.3 E507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr12:96131748 G>A maps to NM_021229.3 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr1:107937832 C>T maps to NM_001113226.1 C315C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:107867343 C>T maps to NM_001113226.1 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RA-A741-01A-11D-A33O-09 chr1:107866902 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr9:135073663 C>T maps to NM_032536.2 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PD-01A-11D-A351-09 chr9:135102403 C>T maps to NM_032536.2 N342N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HR-01A-11D-A20U-09 chr1:156849867 C>T maps to NM_002529.3 S708S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr9:87325596 G>A maps to NM_006180.3 W158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr9:87570323 C>T maps to NM_006180.3 F688F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CJ-01A-11D-A32I-09 chr15:88576178 G>T maps to NM_001012338.1 P498P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr15:88680692 G>A maps to NM_001012338.1 Y188Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr12:86276128 C>G maps to NM_006183.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr12:106460990 C>T maps to NM_014840.2 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr1:205280878 C>T maps to ENST00000441520 E146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:205275363 G>C maps to ENST00000441520 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr14:32328427 G>A did not map to a codon.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr1:27271861 C>G did not map to a codon.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr1:27271870 C>A did not map to a codon.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr1:27272630 C>T maps to NM_006600.2 Q319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:27267964 C>T maps to NM_006600.2 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:51075856 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:51076120 G>T did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:105643315 C>T maps to NM_177533.3 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr16:4744304 G>C maps to ENST00000405142 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr1:145588597 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr11:63995092 G>A maps to NM_032344.2 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A69L-01A-11D-A32I-09 chr6:34261288 C>T maps to NM_006703.2 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr4:123843698 C>T maps to NM_007083.3 W10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr16:77756502 G>A maps to NM_001105663.1 E8E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr16:77775504 G>T maps to NM_001105663.1 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr1:163317605 G>A maps to NM_145697.2 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:163318777 C>T maps to NM_145697.2 R390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr13:45563517 G>T maps to NM_012345.2 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr14:73759576 G>A maps to NM_001005743.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr19:41179321 C>T maps to NM_004756.3 R321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr12:69083384 C>G maps to NM_020401.2 S58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr5:37331855 C>A maps to NM_153485.1 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr5:37341220 G>C maps to NM_153485.1 S406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr9:131752435 A>G maps to NM_015354.1 K857K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A50E-01A-21D-A26G-09 chr9:131768559 C>G maps to NM_015354.1 L1662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A50E-01A-21D-A26G-09 chr9:131768566 C>T maps to NM_015354.1 Q1665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr9:131747280 C>T maps to NM_015354.1 T688T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr9:131764002 C>T maps to NM_015354.1 Q1347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr9:131747302 G>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr9:131747322 G>C did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr9:131747406 G>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr9:131747419 G>A did not map to a codon.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr9:131742974 C>T maps to NM_015354.1 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr7:135300799 G>A maps to NM_015135.2 V1149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr7:135330312 G>A maps to NM_015135.2 S1927S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr7:135327943 C>A maps to NM_015135.2 T1799T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr7:135282129 G>A maps to NM_015135.2 V676V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr7:135262641 C>T maps to NM_015135.2 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr3:13381482 G>A maps to NM_024923.2 I1114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:154031135 C>A maps to NM_207308.2 E962*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HM-A3JK-01A-11D-A21Q-09 chr1:153995689 C>T maps to NM_207308.2 L1402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:154098849 C>G maps to NM_207308.2 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr9:134050875 C>T maps to ENST00000451030 Q1064*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr12:102512329 T>G did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr6:150067799 G>A maps to ENST00000367402 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr4:77051822 G>A maps to ENST00000458189 Q349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R3-01A-11D-A28B-09 chr19:50411684 C>T maps to NM_012346.4 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr17:5322970 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr15:41625244 G>A maps to NM_016359.3 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr15:41625062 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr15:41643259 C>T maps to NM_016359.3 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr16:67902435 C>T maps to NM_005796.1 I68I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:16926105 C>G maps to ENST00000438489 S1554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr19:16861133 G>T maps to ENST00000438489 E561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr19:16890253 C>T maps to ENST00000438489 I903I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr19:16860665 C>T maps to ENST00000438489 Q405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QD-01A-32D-A22X-09 chr11:62567919 C>T maps to NM_006362.4 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr11:62572854 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VI-01A-11D-A28B-09 chr11:62572854 C>T did not map to a codon.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr11:62567870 G>T maps to NM_006362.4 R332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr23:101572375 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:101620150 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr23:102337128 G>T did not map to a codon.
Sequencing variant TCGA-FU-A770-01A-11D-A33O-09 chr23:102338371 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr23:101095804 T>C did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:101096476 C>T did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:101096286 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr23:101095504 A>G did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr2:139428860 G>A maps to NM_007226.2 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr17:47656340 C>T maps to ENST00000513748 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:108781312 G>C did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:108785780 G>T did not map to a codon.
Sequencing variant TCGA-EA-A556-01A-11D-A26G-09 chr14:24879174 C>T maps to NM_025081.2 P725P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PI-01A-11D-A18J-09 chr14:24886633 C>T maps to NM_025081.2 F1893F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr14:24886650 G>T maps to NM_025081.2 *1899L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr14:24884523 C>G maps to NM_025081.2 S1190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VK-01A-11D-A28B-09 chr23:41333922 C>T did not map to a codon.
Sequencing variant TCGA-MY-A5BF-01A-11D-A26G-09 chr23:41333610 C>T did not map to a codon.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr12:113401135 C>T maps to NM_006187.2 P701P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R3-01A-11D-A28B-09 chr12:113403613 C>T maps to NM_006187.2 L823L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:121471366 C>G maps to NM_003733.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr10:126097340 G>A maps to NM_000274.3 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr10:126092459 C>T maps to NM_000274.3 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr15:64981337 C>T maps to ENST00000403937 E126E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr15:64981355 C>T maps to ENST00000403937 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VK-01A-11D-A28B-09 chr15:64980914 G>A maps to ENST00000403937 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HR-01A-11D-A20U-09 chr9:136083255 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr9:136081735 G>C maps to NM_014581.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr9:136083255 C>T did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr1:228492947 C>T maps to ENST00000366707 L1474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr1:228496034 C>T maps to NM_001098623.1 V4230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr1:228486165 C>T maps to ENST00000366707 R1010*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WF-01A-11D-A351-09 chr1:228464415 C>T maps to NM_001098623.1 T2162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr1:228560175 C>T maps to NM_001098623.1 Q7233*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-FU-A40J-01A-11D-A243-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr1:228461606 G>A maps to NM_001098623.1 E1758E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr1:228559530 C>T maps to NM_001098623.1 Q7018*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr1:228456234 C>T maps to NM_001098623.1 P1622P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr2:220427346 G>T maps to NM_015311.2 A910A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:220432575 C>T maps to NM_015311.2 E466E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr2:220419451 C>T maps to NM_015311.2 L1540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr15:28116341 C>A maps to NM_000275.2 L734L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A449-01A-11D-A243-09 chr15:28263671 C>T maps to NM_000275.2 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr4:48854007 G>C maps to NM_001079841.2 *188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr7:97617813 G>C maps to NM_006188.3 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr23:128695162 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:128722896 C>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:128710356 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr23:128696372 C>T did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:131262371 G>T maps to NM_153435.1 L840L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr9:131255084 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr9:131223279 G>C maps to NM_153435.1 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr11:198240 C>G maps to NM_053280.3 S118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr23:13779244 G>C did not map to a codon.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr23:13753461 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:13779288 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VI-01A-11D-A28B-09 chr23:13778395 C>G did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:13770893 G>A did not map to a codon.
Sequencing variant TCGA-LP-A4AU-01A-32D-A243-09 chr23:13775834 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr7:44706245 G>T did not map to a codon.
Sequencing variant TCGA-JX-A5QV-01A-22D-A28B-09 chr10:50966440 G>T maps to NM_018245.2 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr16:56500112 C>T maps to NM_018233.3 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr12:123459827 C>T maps to ENST00000228922 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr20:61442884 G>A maps to NM_007346.2 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr20:61444514 G>A maps to NM_007346.2 G516G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr3:9791866 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr3:9791866 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr9:95152239 C>A maps to NM_033014.2 E176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr9:95148527 G>T maps to NM_033014.2 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CH-01A-11D-A33O-09 chr23:70777113 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr23:70787860 G>C did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:70784468 A>C did not map to a codon.
Sequencing variant TCGA-HG-A2PA-01A-11D-A20U-09 chr23:70779274 G>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:70787859 C>T did not map to a codon.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr15:41601952 C>T maps to NM_007280.1 *230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr10:15115212 G>A maps to NM_018324.2 S314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr9:127557322 C>T maps to NM_182487.2 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr1:114522251 G>A maps to NM_020190.2 E38E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:114523273 C>G did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr18:55103897 C>A maps to NM_004852.2 S317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr3:193380645 G>A maps to NM_130837.2 K852K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr3:193332656 C>T maps to NM_130837.2 Q60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:46032592 G>A maps to NM_001017989.2 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr11:132307161 G>A maps to NM_002545.3 N206N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr11:133402238 C>T did not map to a codon.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr23:67432047 C>T did not map to a codon.
Sequencing variant TCGA-C5-A7CG-01A-11D-A32I-09 chr23:67272419 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:67283721 G>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:67316726 G>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr8:145111903 C>T maps to ENST00000360660 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:153461459 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr23:153459059 G>C did not map to a codon.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr23:153492788 G>T did not map to a codon.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr7:128414647 G>A maps to NM_001708.2 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:128414593 G>A maps to NM_001708.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:241753448 G>A did not map to a codon.
Sequencing variant TCGA-EA-A5ZF-01A-11D-A28B-09 chr6:47749897 G>A maps to ENST00000489301 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HQ-01A-11D-A20U-09 chr1:29189590 G>A maps to NM_000911.3 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:29185699 C>G maps to NM_000911.3 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr6:154567918 G>C maps to NM_001008503.1 *419Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OA-01A-11D-A16Y-08 chr6:154360930 G>T maps to NM_001145279.1 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr6:154412696 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr11:7949990 G>A maps to NM_001004461.1 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CH-01A-11D-A33O-09 chr11:55735636 C>T maps to NM_001005491.1 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AU-01A-32D-A243-09 chr11:55735342 C>T maps to NM_001005491.1 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:22102066 C>T maps to NM_001005466.1 *311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr14:22037975 C>G maps to NM_001005465.1 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr11:123909483 C>T maps to NM_001004463.1 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VK-01A-11D-A28B-09 chr11:123901165 G>A maps to ENST00000375021 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:15918292 C>T maps to NM_013940.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr19:15917989 G>C maps to NM_013940.2 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr19:15839494 C>T maps to NM_013939.2 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:15852819 C>T maps to NM_013938.1 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:15853002 C>A maps to NM_013938.1 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr19:16060197 C>T maps to NM_001004465.1 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr19:15905235 C>T maps to NM_001004466.1 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr1:159410018 G>T maps to NM_012351.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr1:159283819 T>A maps to NM_001004467.1 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr1:159283924 G>A maps to NM_001004467.1 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:159505755 G>A maps to NM_001004469.1 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:159505065 G>A maps to NM_001004469.1 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:159505653 G>A maps to NM_001004469.1 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:158390316 G>A maps to NM_001004476.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr1:158389869 G>A maps to NM_001004476.1 Q263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr11:57995863 G>A maps to NM_001004471.2 Q162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:158449972 C>T maps to NM_001004472.1 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr1:158368641 G>T maps to NM_001004475.1 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A852-01A-11D-A351-09 chr11:58034736 A>G maps to NM_207374.3 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr1:158549458 G>C maps to NM_001004477.1 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr1:158549539 G>C maps to NM_001004477.1 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:158549182 G>A maps to NM_001004477.1 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr1:158549458 G>C maps to NM_001004477.1 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:158576329 G>A maps to NM_001004478.1 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr6:29395166 C>T maps to NM_013937.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr14:19377961 T>C maps to NM_001013354.1 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr14:19377727 C>T maps to NM_001013354.1 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VH-01A-11D-A28B-09 chr10:45799324 C>A maps to NM_001004297.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr9:107366963 G>A maps to NM_001004481.1 F315F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr9:107298422 G>C maps to NM_001001961.1 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr9:107298509 T>C maps to NM_001001961.1 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr9:107457366 C>G maps to NM_001004484.1 S222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr9:107267220 G>C maps to NM_001004485.1 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZF-01A-11D-A28B-09 chr23:130678496 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr17:3101384 C>T maps to NM_012352.1 D191D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3YQ-01A-11D-A22X-09 chr9:125391127 G>A maps to NM_001004450.1 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr17:3301185 C>G maps to NM_003553.2 V173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr17:3301251 C>T maps to NM_003553.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr16:3254272 C>G maps to NM_012360.1 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr16:3254341 C>G maps to NM_012360.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr9:125281686 C>T maps to ENST00000444856 Q256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr9:125487176 G>A maps to NM_001005235.1 K303K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr19:9204405 G>A maps to ENST00000305465 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H6-01B-11D-A22X-09 chr9:125377519 C>T maps to NM_012364.1 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr11:57983166 C>T maps to NM_001004458.1 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr11:57982596 C>G maps to NM_001004458.1 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr11:57971059 G>A maps to NM_001004459.1 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr7:143772058 C>T maps to NM_001004488.1 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr7:143748006 C>A maps to NM_012365.1 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr7:99474452 G>C maps to NM_001005276.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LS-01A-22D-A22X-09 chr1:247752482 C>A maps to NM_001001915.1 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr1:247752383 C>T maps to NM_001001915.1 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr6:29556210 C>T maps to NM_007160.3 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr9:114090764 G>A maps to ENST00000374428 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:248202315 C>T maps to NM_001004686.2 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr1:248224123 C>T maps to NM_001004687.1 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr1:248112344 G>C maps to NM_001001963.1 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr1:248343928 C>A maps to NM_001004688.1 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:248366704 C>A maps to NM_001004689.1 C112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:248366380 G>A maps to NM_001004689.1 E4E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:248402985 C>T maps to NM_017504.1 Y252Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr1:248569549 C>T maps to NM_030904.1 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:248756598 G>A maps to NM_001004693.1 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:248616298 C>G maps to NM_001004136.1 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:248813927 C>T maps to NM_001001824.1 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr1:248737383 G>A maps to NM_001001821.1 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr1:248737419 G>T maps to NM_001001821.1 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:248551418 C>G maps to NM_001005471.1 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr1:247654731 C>G maps to NM_001004698.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr17:3195219 G>A maps to ENST00000397187 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr11:55111509 C>T maps to NM_001005274.1 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5FO-01A-21D-A28B-09 chr11:51412302 G>C maps to NM_001005272.3 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr11:55322126 C>T maps to NM_001001920.1 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr11:55340451 G>A maps to NM_001004701.2 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr11:48346647 C>T maps to NM_001004702.1 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr11:55432917 C>T maps to NM_001004704.1 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr11:59245561 C>A maps to NM_001004705.1 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A6QX-01A-12D-A33O-09 chr11:59225107 G>A maps to NM_001004708.1 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OA-01A-11D-A16Y-08 chr14:22133796 T>C maps to NM_001001912.1 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr15:102462416 C>A maps to NM_001004195.2 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3EO-01A-11D-A20U-09 chr14:20404679 C>A maps to NM_001004063.2 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr14:20404689 C>T maps to NM_001004063.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr14:20482424 G>A maps to NM_001004712.1 Q310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr15:22368877 C>G maps to NM_001004719.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr15:22382810 A>G maps to NM_001005241.1 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AU-01A-32D-A243-09 chr11:48327878 C>G maps to NM_001004725.1 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr11:48327897 C>T maps to NM_001004725.1 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr11:48286032 C>T maps to NM_001004726.1 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr11:48285588 C>T maps to NM_001004726.1 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A69L-01A-11D-A32I-09 chr11:4929286 T>C maps to NM_001004749.1 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr11:4661049 C>T maps to NM_001004751.2 I10I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr11:5462186 G>A maps to NM_001005288.2 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr11:5221009 C>T maps to NM_001004760.2 Q307Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr11:5220978 G>A maps to NM_001004760.2 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr11:5080665 G>A maps to NM_001005164.2 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr11:5566285 G>A maps to NM_001005289.1 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr11:6007923 G>C maps to NM_001005173.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr11:5809373 G>A maps to NM_001001913.1 Q225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr11:5799591 G>A maps to NM_001001922.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr11:6048724 G>C maps to NM_001001917.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr11:6048811 G>A maps to NM_001001917.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr11:6024246 G>A maps to NM_001005179.2 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:6024171 G>A maps to NM_001005179.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:6129416 C>T maps to NM_001005181.1 Q137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr11:56409222 G>T maps to NM_001002925.1 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr11:58275514 G>A maps to NM_001005218.1 Q22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr11:58275440 G>A maps to NM_001005218.1 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr11:58170012 C>G maps to NM_001005469.1 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr11:55587476 C>T maps to ENST00000395203 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr3:97888150 C>G maps to NM_001005515.1 S203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr3:97888337 G>A maps to NM_001005515.1 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr3:98002359 C>G maps to NM_001005482.1 S210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr3:97983233 C>T maps to NM_001005479.1 Q36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A50E-01A-21D-A26G-09 chr3:97983728 T>C maps to NM_001005479.1 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr11:55703783 G>C maps to NM_006637.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr11:55579853 G>C maps to NM_001004738.1 V304V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr11:55594996 C>T maps to NM_001004739.1 F101F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr11:55595000 T>C maps to NM_001004739.1 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr11:56380696 G>A maps to NM_001004740.1 Y94Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr11:56344765 C>A maps to NM_001004741.1 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr11:56309908 G>T maps to NM_001005245.1 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr11:56258534 G>A maps to NM_001005282.1 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr11:56000559 G>A maps to NM_001004746.1 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr11:55681194 C>G maps to NM_001001960.1 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr7:143701853 C>T maps to NM_001005281.1 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr2:240969075 G>A maps to NM_001005853.1 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OA-01A-11D-A16Y-08 chr12:55688302 G>A maps to NM_001005493.1 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr12:55886452 C>T maps to NM_001005519.1 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr12:55863490 G>A maps to NM_001005499.1 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr12:55641610 T>C maps to NM_001005490.1 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr12:55759218 G>T maps to NM_001005497.1 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr12:55820807 G>A maps to NM_001005183.1 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:158724676 G>A maps to NM_001005184.1 Q24Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:158724727 C>G maps to NM_001005184.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr1:158725552 C>T maps to NM_001005184.1 I316I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:123676286 C>T maps to NM_001005325.1 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr1:158735559 G>A maps to NM_001005185.1 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr1:158735608 G>A maps to NM_001005185.1 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr1:158736385 G>A maps to NM_001005185.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr11:57799098 C>T maps to NM_001005186.2 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr14:21109727 C>G maps to NM_001001968.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:123813597 C>T maps to NM_001005187.1 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr19:14991726 T>A maps to NM_030901.1 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr19:14938894 G>A maps to NM_017506.1 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr19:9226127 G>C maps to ENST00000293614 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr19:9225956 C>G maps to ENST00000293614 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr11:124253146 A>G maps to NM_001005468.1 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr11:124267082 G>C maps to NM_001005467.1 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr11:124310459 G>A maps to NM_012378.1 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZF-01A-11D-A28B-09 chr11:123777848 G>A maps to NM_001005197.1 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr11:55872566 G>T maps to NM_001005200.1 G17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3YQ-01A-11D-A22X-09 chr11:55872652 G>A maps to NM_001005200.1 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr11:55861447 C>G maps to NM_001003750.1 S222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr11:55861421 C>T maps to NM_001003750.1 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr11:55904864 C>T maps to NM_001004064.1 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr11:56113637 C>T maps to NM_001002907.1 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr11:55926965 C>T maps to NM_001004058.2 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr12:48919716 C>T maps to NM_001005203.2 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr11:56468522 C>T maps to NM_001013358.1 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr11:57947065 C>T maps to NM_001005212.3 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr11:57947065 C>T maps to NM_001005212.3 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CM-01A-11D-A33O-09 chr16:30964696 C>T maps to NM_152288.2 H140H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr11:69482386 C>A did not map to a codon.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr9:117085983 C>T maps to NM_000607.2 N52N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr9:117092309 G>A maps to ENST00000412657 W42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr12:56214127 G>A maps to NM_014182.4 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr12:56213205 C>T maps to NM_014182.4 H85H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr22:31266551 C>G maps to NM_030758.3 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr3:125271448 G>A maps to NM_022776.4 D410D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr3:125257329 C>T maps to NM_022776.4 V663V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr20:60854320 C>T maps to NM_144498.1 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr7:24854689 C>A maps to NM_015550.2 V720V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HM-A3JK-01A-11D-A21Q-09 chr7:24874251 C>T maps to NM_015550.2 R533R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr11:3128498 C>G maps to NM_020896.3 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr11:3125478 C>T maps to NM_020896.3 P396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr17:45886520 G>A maps to NM_145798.2 V697V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HG-A2PA-01A-11D-A20U-09 chr1:52238275 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr1:36883705 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr16:83999201 C>T maps to NM_013370.3 Q425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr8:90937186 C>T maps to NM_001126111.1 D359D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A78R-01A-11D-A32I-09 chr5:38884118 G>T maps to NM_003999.2 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr5:38876430 C>T maps to NM_003999.2 Q68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr2:19553113 G>C maps to NM_145260.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr6:108365367 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr23:38271133 C>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:38211945 G>T did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:38211865 C>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr16:21716721 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr16:21721390 C>A maps to ENST00000286149 I443I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr16:21721246 G>A maps to ENST00000286149 Q395Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr2:26690259 C>T maps to NM_194248.2 K1400K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr2:26691335 G>A maps to NM_194248.2 R1344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr3:161214768 C>G maps to NM_001080440.1 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:72921681 C>T maps to NM_178160.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr17:72926923 G>A maps to NM_178160.2 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr17:72931870 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr20:16729604 C>G maps to NM_020157.2 S70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr11:63756107 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:20230836 G>A maps to NM_015207.1 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr4:146059409 C>T maps to ENST00000447906 Q839Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr4:146065558 G>A maps to ENST00000447906 Q484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M1-01A-11D-A18J-09 chr23:48781174 G>T did not map to a codon.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr23:48792258 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:48792054 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VH-01A-11D-A28B-09 chr23:48801542 T>C did not map to a codon.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr23:69282719 G>C did not map to a codon.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr15:31851253 C>T maps to ENST00000382902 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:149921606 G>A maps to NM_020205.2 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A770-01A-11D-A33O-09 chr12:29639270 C>T maps to NM_183378.2 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr11:7716912 T>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr20:18038266 G>T maps to NM_021220.2 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:40235400 G>C maps to NM_022120.1 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr8:107695461 G>A maps to NM_001198533.1 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:25833166 C>G maps to NM_017897.2 S219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr17:3806870 G>A maps to NM_002558.2 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr17:3806894 G>A maps to NM_002558.2 F185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr12:133196043 A>T maps to NM_170683.2 K65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr11:57108107 C>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr12:121647981 C>T maps to NM_002560.2 C5C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A5QV-01A-22D-A28B-09 chr12:121622292 G>A maps to NM_002562.5 R492R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr23:78216863 G>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:69479358 G>A did not map to a codon.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr23:69479286 C>T did not map to a codon.
Sequencing variant TCGA-JX-A5QV-01A-22D-A28B-09 chr23:69478491 G>A did not map to a codon.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr23:1585078 C>T did not map to a codon.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr23:1585318 G>C did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:1584686 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr12:56504247 C>G maps to NM_006191.2 S232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr11:73611422 G>T maps to NM_025155.1 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr20:43565405 G>C did not map to a codon.
Sequencing variant TCGA-EA-A44S-01A-12D-A26G-09 chr13:25670977 C>T maps to NM_030979.2 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr13:25670506 G>A maps to NM_030979.2 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:40036805 G>A did not map to a codon.
Sequencing variant TCGA-EA-A411-01A-11D-A243-09 chr23:90691627 T>C did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr23:90690905 C>G did not map to a codon.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr23:90691094 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:90690778 T>C did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:90690683 G>A did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr23:90690972 C>T did not map to a codon.
Sequencing variant TCGA-EA-A1QS-01A-61D-A22X-09 chr14:105848349 C>T maps to ENST00000458164 N456N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UC-01A-11D-A351-09 chr11:47204044 G>A maps to NM_016223.4 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr1:17559360 C>T maps to NM_013358.2 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:17567242 C>T maps to NM_013358.2 F582F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr1:17422423 C>A maps to NM_007365.2 E131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr1:17394880 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:17395383 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:17409143 C>A maps to NM_007365.2 E352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:17601260 C>T maps to NM_016233.2 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:17597378 C>T maps to NM_016233.2 F279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr1:17672564 G>C maps to NM_012387.2 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr19:39879478 C>T maps to NM_019088.2 V221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr17:2570452 C>T maps to NM_000430.3 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr17:2585019 C>T did not map to a codon.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr17:2568718 C>A maps to NM_000430.3 S29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr8:81883061 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr8:81903728 C>T maps to NM_018440.3 E54E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr23:49459349 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:55102508 C>T did not map to a codon.
Sequencing variant TCGA-C5-A7CM-01A-11D-A33O-09 chr23:49597148 G>T did not map to a codon.
Sequencing variant TCGA-LP-A5U3-01A-11D-A28B-09 chr11:77090968 G>A maps to NM_001128620.1 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr3:196532221 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:196528861 C>T maps to NM_002577.4 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr23:110406214 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr19:39666056 C>T maps to NM_005884.3 I446I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr19:39663790 C>T maps to NM_005884.3 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr20:9546626 G>A maps to NM_177990.2 I465I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr20:9561028 C>T maps to NM_177990.2 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3PZ-01A-11D-A21Q-09 chr20:9561268 G>A maps to NM_177990.2 H171H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr16:23647105 G>C maps to NM_024675.3 S254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr16:23619252 C>G maps to NM_024675.3 V1094V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr16:23634402 C>T maps to NM_024675.3 L961L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr4:169433386 G>A maps to NM_001166108.1 Q244Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A411-01A-11D-A243-09 chr19:736064 C>T maps to NM_002579.2 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:736028 C>G maps to NM_002579.2 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr9:112898780 C>T maps to NM_007203.4 G319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr5:102262313 G>A maps to NM_000919.3 E156E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr11:35454017 C>T maps to NM_015430.2 W700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr12:56726778 G>A maps to NM_001127460.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr13:28834688 G>T did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr13:28794440 C>G maps to NM_175854.7 S309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HR-01A-11D-A20U-09 chr20:3904041 A>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr20:3904079 C>T did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:2445806 C>T maps to ENST00000425477 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:2453348 G>A maps to ENST00000502770 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WH-01A-22D-A351-09 chr1:2446786 C>T maps to ENST00000468002 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr22:50615962 G>A maps to NM_052839.3 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R9-01A-11D-A18J-09 chr22:50615968 C>T maps to NM_052839.3 R276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr11:124481633 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr16:50265072 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr14:97009199 C>G maps to NM_032632.3 S420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr2:61018983 C>T maps to NM_022894.3 Y495Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr9:118997559 C>T maps to NM_002581.3 V792V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:176525550 G>A maps to NM_020318.2 K31K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr4:108641219 G>C did not map to a codon.
Sequencing variant TCGA-EA-A3QD-01A-32D-A22X-09 chr10:89503209 C>T maps to NM_001015880.1 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr15:69652358 G>C did not map to a codon.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr6:52268055 C>T maps to ENST00000361841 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:142681902 G>A maps to NM_198504.2 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:142681917 G>A maps to NM_198504.2 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr10:34739376 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr10:34805960 G>A maps to NM_019619.3 Q117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr2:206166583 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr2:205983656 C>G maps to ENST00000406610 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr2:206036979 G>T maps to ENST00000406610 E556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr18:77918346 G>A maps to NM_032510.3 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr18:77917737 G>A maps to NM_032510.3 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5O9-01A-11D-A28B-09 chr6:162683698 G>A maps to NM_004562.2 N90N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr1:8030976 G>A maps to NM_001123377.1 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr1:226551835 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:226589951 C>T maps to NM_001618.3 Q83Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr12:3939162 C>A maps to NM_020367.4 E14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DV-01A-11D-A32I-09 chr7:139734129 G>T maps to NM_022750.2 A442A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:122432390 C>G maps to NM_017554.2 S1247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr3:122418793 C>T maps to NM_017554.2 Q465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:122447316 C>G maps to NM_017554.2 S1760*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A57G-01A-11D-A26G-09 chr14:20815063 C>T maps to NM_005484.3 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr3:122259322 C>T maps to NM_031458.2 S622S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr3:122247474 G>A maps to NM_031458.2 L767L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr3:122274228 C>T maps to NM_031458.2 K298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr22:44514991 T>A maps to NM_001003828.1 Y149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr23:150793971 C>T did not map to a codon.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr23:150841058 G>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:150840128 G>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q8-01A-11D-A21Q-09 chr23:150840914 G>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q8-01A-11D-A21Q-09 chr23:150840923 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr2:242047683 G>A maps to ENST00000358649 L1196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr22:31741128 C>A maps to NM_014323.2 E154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr12:80014938 G>A maps to NM_002583.2 R189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CG-01A-11D-A32I-09 chr20:21686348 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr20:21686448 C>T maps to NM_006192.3 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr20:21695219 C>A maps to NM_006192.3 R462R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr2:223158985 G>A maps to NM_181459.3 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr7:127255467 G>C maps to NM_006193.2 S36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr1:19062469 G>T maps to NM_002584.2 G500G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr2:113992972 G>C maps to NM_003466.3 S362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr14:37131132 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VI-01A-11D-A28B-09 chr14:37135650 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr10:70043942 C>T maps to NM_022129.3 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr3:52668756 G>A maps to ENST00000296302 Q388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr1:164610543 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr6:32154455 G>A maps to NM_002586.4 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr9:128697784 G>T maps to ENST00000373487 E248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr9:128729185 G>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:154924205 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr11:66616180 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr2:70315273 G>A maps to NM_006196.3 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr21:47337527 C>A maps to NM_020528.2 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr21:47333872 G>A maps to NM_020528.2 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr13:100741454 G>A maps to NM_000282.3 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr3:135979187 G>A maps to ENST00000468777 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr3:135980904 C>T maps to NM_001178014.1 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VI-01A-11D-A28B-09 chr5:141236898 G>A maps to NM_032420.2 L1079L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr5:141243225 C>T maps to NM_032420.2 K890K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr4:134073538 C>T maps to NM_032961.1 I748I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr4:134071546 C>A maps to NM_032961.1 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr4:134072555 C>T maps to NM_032961.1 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr23:91132648 C>T did not map to a codon.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr23:91873844 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3HR-01A-11D-A20U-09 chr23:91873932 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:91133868 C>T did not map to a codon.
Sequencing variant TCGA-HM-A3JK-01A-11D-A21Q-09 chr23:91090516 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:91133193 C>T did not map to a codon.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr23:91642929 C>T did not map to a codon.
Sequencing variant TCGA-C5-A7CJ-01A-11D-A32I-09 chr5:141335085 G>A maps to NM_016580.2 L777L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr5:141336488 G>A maps to NM_016580.2 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr5:141336210 C>T maps to NM_016580.2 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KH-01A-21D-A22X-09 chr10:55581941 G>A maps to NM_001142763.1 C1855C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:55698579 G>C maps to NM_001142763.1 S1128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr10:55600126 T>C maps to NM_001142763.1 A1317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr10:56089394 A>G maps to NM_001142763.1 Y227Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr10:55892703 G>A maps to NM_001142763.1 F621F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr10:55582733 C>T maps to NM_001142763.1 L1591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VH-01A-11D-A28B-09 chr10:55568612 C>A maps to NM_001142769.1 E1738*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr10:55626457 G>A maps to NM_001142763.1 Q1226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr13:58207444 C>T maps to NM_001040429.2 N255N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr13:58208548 C>G maps to NM_001040429.2 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr13:58208836 C>T maps to NM_001040429.2 L719L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr4:138453179 G>A maps to NM_019035.3 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr4:138451742 C>G maps to NM_019035.3 V500V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr23:99551215 G>A did not map to a codon.
Sequencing variant TCGA-DS-A1OA-01A-11D-A16Y-08 chr23:99663129 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr23:99662117 A>G did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:99597020 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:99663150 G>T did not map to a codon.
Sequencing variant TCGA-LP-A4AU-01A-32D-A243-09 chr23:99661980 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr23:99597060 G>C did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr23:99662727 G>A did not map to a codon.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr13:61987727 G>A maps to NM_022843.3 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R3-01A-11D-A28B-09 chr13:61987573 C>A maps to NM_022843.3 E220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr13:67801612 T>C maps to NM_203487.2 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr13:67800079 G>A maps to NM_203487.2 F831F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr5:140167431 A>G maps to NM_018900.2 A519A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr5:140167440 C>G maps to NM_018900.2 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr5:140167458 G>A maps to NM_018900.2 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LS-01A-22D-A22X-09 chr5:140165937 C>T maps to NM_018900.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr5:140167071 C>T maps to NM_018900.2 S399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr5:140167974 G>C maps to NM_018900.2 L700L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr5:140236853 G>A maps to NM_018901.2 V407V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr5:140237262 C>T maps to NM_018901.2 L544L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A0TN-01A-21D-A14W-08 chr5:140249107 G>T maps to NM_018902.3 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2GZ-01A-11D-A17W-09 chr5:140250025 C>T maps to NM_018902.3 D446D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A57G-01A-11D-A26G-09 chr5:140250199 G>A maps to NM_018902.3 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr5:140249473 C>G maps to NM_018902.3 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr5:140249734 C>T maps to NM_018902.3 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr5:140256418 G>A maps to NM_018903.2 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr5:140263676 G>A maps to NM_018904.2 S608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PI-01A-11D-A18J-09 chr5:140263676 G>A maps to NM_018904.2 S608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr5:140262968 C>T maps to NM_018904.2 I372I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr5:140262468 C>T maps to NM_018904.2 Q206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr5:140176741 G>A maps to NM_018905.2 A731A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr5:140176966 T>C maps to NM_031495.1 S806S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr5:140176360 C>T maps to NM_018905.2 N604N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OA-01A-11D-A16Y-08 chr5:140183219 C>G maps to NM_031497.1 S813*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr5:140182479 G>A maps to NM_018906.2 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr5:140182149 G>A maps to NM_018906.2 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr5:140180797 C>T maps to NM_018906.2 R6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr5:140187458 C>T maps to NM_018907.2 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr5:140202752 G>T maps to NM_018908.2 E465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:140208779 C>T maps to NM_018909.2 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr5:140209118 C>T maps to NM_018909.2 D481D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr5:140215533 G>A maps to NM_018910.2 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr5:140214534 A>C maps to NM_018910.2 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr5:140221088 G>A maps to NM_018911.2 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KH-01A-21D-A22X-09 chr5:140220968 C>T maps to NM_018911.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr5:140222138 C>T maps to NM_018911.2 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr5:140228211 C>T maps to NM_031857.1 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr5:140230161 G>T maps to NM_031857.1 V694V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr5:140347079 C>T maps to NM_018899.5 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr5:140573945 C>G maps to NM_018930.3 L607L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr5:140581380 G>A maps to NM_018931.2 P678P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A0TN-01A-21D-A14W-08 chr5:140589681 C>A maps to NM_018932.3 Y401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr5:140589897 C>T maps to NM_018932.3 I473I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr5:140590707 G>A maps to NM_018932.3 G743G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WF-01A-11D-A351-09 chr5:140595284 C>T maps to NM_018933.2 R530R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HR-01A-11D-A20U-09 chr5:140594525 G>A maps to NM_018933.2 E277E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LC-01A-11D-A20U-09 chr5:140595329 G>A maps to NM_018933.2 A545A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr5:140604873 C>T maps to NM_018934.2 N599N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr5:140603504 C>G maps to NM_018934.2 S143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr5:140626528 C>T maps to NM_018935.2 R461R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr5:140626408 C>T maps to NM_018935.2 I421I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr5:140562421 C>T maps to NM_020957.1 C96C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr5:140481795 C>T maps to NM_018937.2 Y521Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr5:140501900 G>T maps to NM_018938.2 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr5:140516881 G>A maps to NM_015669.2 E622E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr5:140532129 C>T maps to NM_018939.2 F764F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr5:140531421 C>T maps to NM_018939.2 R528R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr5:140530896 C>T maps to NM_018939.2 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AX-01A-12D-A243-09 chr5:140531439 C>T maps to NM_018939.2 R534R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr5:140554023 C>T maps to NM_018940.2 R536R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr5:140553825 C>T maps to NM_018940.2 I470I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr5:140554794 C>T maps to NM_018940.2 F793F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr5:140559612 C>A maps to NM_019120.2 G666G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr5:140559549 C>G maps to NM_019120.2 V645V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VI-01A-11D-A28B-09 chr5:140558958 C>T maps to NM_019120.2 N448N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5FO-01A-21D-A28B-09 chr5:140711084 G>A maps to NM_018912.2 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr5:140711802 C>T maps to NM_018912.2 R518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr5:140792798 G>A maps to NM_018913.2 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr5:140810712 T>C maps to NM_003735.2 N129N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr5:140719440 G>C maps to NM_018915.2 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr5:140720205 C>T maps to NM_018915.2 N556N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QE-01A-21D-A21Q-09 chr5:140720211 C>T maps to NM_018915.2 N558N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VK-01A-11D-A28B-09 chr5:140720391 G>A maps to NM_018915.2 S618S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr5:140719440 G>A maps to NM_018915.2 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:140723924 C>T maps to NM_018916.3 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr5:140725510 G>A maps to NM_018916.3 A637A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr5:140725573 C>T maps to NM_018916.3 V658V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr5:140736302 G>A maps to NM_018917.2 G512G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H6-01B-11D-A22X-09 chr5:140737031 C>T maps to NM_018917.2 H755H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr5:140744562 C>G maps to NM_018918.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr5:140745348 C>T maps to NM_018918.2 N484N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A449-01A-11D-A243-09 chr5:140745606 C>T maps to NM_018918.2 D570D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr5:140755392 C>T maps to NM_018919.2 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr5:140756056 G>T maps to NM_018919.2 E803*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr5:140764535 G>A maps to NM_018920.2 T690T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr5:140774554 C>T maps to NM_032088.1 L725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr5:140784702 C>A maps to NM_018921.2 T728T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr5:140730997 G>T maps to NM_018922.2 E391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr5:140741883 C>T maps to NM_018923.2 Q728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr5:140739719 G>A maps to NM_018923.2 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A411-01A-11D-A243-09 chr5:140769352 C>T maps to NM_003736.2 D634D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr5:140797791 G>T maps to NM_018927.2 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A852-01A-11D-A351-09 chr5:140797446 G>A maps to NM_018927.2 Q7Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr2:120362839 G>T maps to NM_001029996.3 E84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr11:82876721 T>A maps to NM_015885.3 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr11:82880509 C>T maps to NM_015885.3 Q1045*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr11:82879938 G>C maps to NM_015885.3 L854L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr11:82879497 C>T maps to NM_015885.3 F707F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr4:728783 G>A maps to NM_006315.4 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U3-01A-11D-A28B-09 chr4:727715 G>A maps to ENST00000430644 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:82545960 G>A maps to NM_033026.5 R3781*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr7:82595783 A>C maps to NM_033026.5 L1107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QD-01A-32D-A22X-09 chr7:82764744 C>T maps to NM_033026.5 V707V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr7:82764338 G>A maps to NM_033026.5 Q843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr8:17817610 C>G maps to NM_006197.3 S710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr20:62891508 C>G maps to NM_018257.2 S64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr20:5098123 C>A maps to NM_002592.2 E192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr3:101311686 G>A did not map to a codon.
Sequencing variant TCGA-C5-A7CH-01A-11D-A33O-09 chr21:47851508 G>T maps to NM_006031.5 E2711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr21:47831563 C>T maps to NM_006031.5 F1859F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A6QX-01A-12D-A33O-09 chr21:47845793 C>G maps to NM_006031.5 S2410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr21:47783728 C>A maps to NM_006031.5 S830*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr21:47851643 G>T maps to NM_006031.5 E2756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr21:47831137 G>A maps to NM_006031.5 L1717L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr21:47865278 G>A did not map to a codon.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr21:47786939 G>A maps to NM_006031.5 E1017E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr1:233431149 C>T maps to NM_014801.3 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr1:233431149 C>T maps to NM_014801.3 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:233394694 G>A maps to NM_014801.3 Q305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr11:65403089 C>T maps to NM_032223.2 Q1759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr11:65395031 C>T maps to NM_032223.2 L1227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr11:65394438 C>T maps to NM_032223.2 L1148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr7:100204156 C>T maps to NM_002593.3 Q282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr3:142542410 C>T maps to NM_013363.3 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr19:7696664 G>C maps to NM_174895.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R9-01A-11D-A18J-09 chr21:41255440 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr9:78973573 A>T maps to NM_001190482.1 P1773P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr9:78936490 G>A maps to NM_001190482.1 V1319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr15:101865103 C>T maps to NM_002570.3 E775E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr2:70504017 C>T maps to NM_016297.3 Q338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr3:195968875 C>T maps to NM_005017.2 A217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr23:24593429 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr23:24580053 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr17:79868880 C>T did not map to a codon.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr10:105201704 G>A maps to NM_014976.1 E1560E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr6:170892754 C>A maps to NM_002598.3 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr3:33906838 G>A maps to NM_001162429.1 A788A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr3:33896793 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr3:33896805 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr15:65412230 T>C maps to NM_005707.1 K357K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr6:165801876 G>A maps to NM_001130690.1 Y574Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr6:165746606 G>A maps to NM_001130690.1 L759L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr3:57542129 C>A maps to NM_177966.5 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr2:183099170 G>A maps to NM_005019.3 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:183387103 G>T did not map to a codon.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr12:54960779 T>C maps to NM_000924.3 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr7:31890314 G>C maps to NM_001191057.1 S264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr7:31917615 C>T maps to NM_001191057.1 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WI-01A-12D-A351-09 chr11:72308581 C>A maps to NM_002599.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr11:72301025 C>A did not map to a codon.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr12:20782868 C>G maps to NM_000921.3 S523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R9-01A-11D-A18J-09 chr12:20522787 C>T maps to NM_000921.3 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:20523042 G>A maps to NM_000921.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr19:18322661 G>A maps to NM_000923.3 A566A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr19:18331346 G>T did not map to a codon.
Sequencing variant TCGA-Q1-A5R1-01A-11D-A28B-09 chr19:18331126 G>A maps to NM_000923.3 F237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr1:144879255 C>A maps to NM_014644.4 L1398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr1:144915468 C>T maps to NM_014644.4 V652V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr1:144911894 G>C maps to NM_014644.4 P738P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:144911925 G>T maps to NM_014644.4 S728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr1:144891397 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3TX-01A-11D-A22X-09 chr1:144879120 C>T maps to NM_014644.4 Q1443Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:144859828 G>A maps to NM_014644.4 L2085L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:144931627 G>C maps to NM_001002811.1 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr1:145074996 G>A maps to ENST00000369345 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr5:149324191 C>T maps to NM_000440.2 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:647894 G>C maps to NM_000283.3 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr4:654371 C>T maps to NM_000283.3 G528G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr4:657638 G>A maps to NM_000283.3 T667T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr4:657656 C>T maps to NM_000283.3 F673F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr4:661665 G>T maps to NM_000283.3 E792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr4:657608 C>A maps to NM_000283.3 I657I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A4BA-01A-21D-A26G-09 chr2:232597736 G>A maps to NM_002601.2 N126N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr6:136512914 G>A maps to NM_018945.3 G430G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr15:85669514 G>A maps to NM_002605.2 L721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr4:157688962 G>A maps to NM_016205.2 Q295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr4:157684184 A>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr5:149501548 G>A maps to NM_002609.3 D746D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr5:149504302 G>C maps to NM_002609.3 V633V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr8:17447121 C>T maps to NM_006207.2 I67I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr23:19371081 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:19372690 C>A did not map to a codon.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr4:96761856 G>T maps to NM_005390.4 E186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:122821308 G>A maps to NM_006810.3 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:122865097 G>A maps to NM_006810.3 W378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr3:122865004 C>T maps to NM_006810.3 F347F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr16:20380945 G>T maps to NM_174924.1 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr16:20396078 G>T maps to NM_174924.1 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr23:24552120 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr23:24523380 C>A did not map to a codon.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr7:95218999 G>A maps to NM_002612.3 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr10:97050721 G>C did not map to a codon.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr10:97050681 G>A did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr4:186425696 C>T maps to NM_014476.4 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr4:186423480 G>A maps to NM_014476.4 G354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr5:176917896 C>T maps to NM_005451.3 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr8:94934992 C>T maps to NM_001161778.1 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr16:2651469 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr4:39924313 G>A maps to NM_001100399.1 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr6:107780476 G>A maps to NM_020381.3 Q5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr21:45165933 G>A did not map to a codon.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr21:45176058 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3EO-01A-11D-A20U-09 chr21:45176054 C>G did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:32091058 C>G maps to NM_178140.2 S2502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr5:32110195 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr5:32091008 G>C maps to NM_178140.2 L2485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RE-01A-11D-A18J-09 chr5:32089652 C>T maps to NM_178140.2 S2033S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr5:32053918 A>G maps to NM_178140.2 G610G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr5:32074401 G>T maps to NM_178140.2 E1064*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:153072747 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:153069803 C>G did not map to a codon.
Sequencing variant TCGA-JX-A5QV-01A-22D-A28B-09 chr23:153069982 G>T did not map to a codon.
Sequencing variant TCGA-Q1-A5R3-01A-11D-A28B-09 chr23:153070077 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr10:102770464 G>T maps to NM_001195263.1 P727P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr10:102771480 C>G maps to NM_001195263.1 T657T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73S-01A-11D-A33O-09 chr10:102770314 A>G maps to NM_001195263.1 R777R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr10:102780423 C>A maps to NM_001195263.1 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A5XV-01A-11D-A28B-09 chr1:145747057 C>T maps to NM_002614.3 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:47650857 G>A did not map to a codon.
Sequencing variant TCGA-C5-A0TN-01A-21D-A14W-08 chr12:41582514 C>T maps to NM_001164595.1 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr12:41871722 G>C did not map to a codon.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr12:41967169 C>T maps to NM_001164595.1 V863V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:156884501 C>G maps to NM_001080471.1 S1009*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr2:216930050 G>A maps to NM_018441.5 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr7:94298360 G>A did not map to a codon.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr19:57326752 G>A maps to NM_006210.2 Y1019Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U3-01A-11D-A28B-09 chr19:57328825 C>T maps to NM_006210.2 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HQ-01A-11D-A20U-09 chr5:52096722 G>A maps to NM_015946.4 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr17:4576053 C>T maps to ENST00000301396 G888G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr19:33904545 G>A maps to NM_000285.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr17:8046089 G>A maps to NM_002616.2 L1046L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr17:8050871 G>A maps to NM_002616.2 F471F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr17:8051104 G>A maps to NM_002616.2 I425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr2:239161690 G>A maps to NM_022817.2 L991L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A3L1-01A-11D-A21Q-09 chr1:7895970 G>T maps to ENST00000377532 E1122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:7863190 G>C maps to ENST00000377532 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr20:18122907 C>T maps to NM_001164811.1 N51N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr15:90233899 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr15:90233992 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr1:10678416 C>T maps to NM_004565.2 Y109Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:160249104 G>C did not map to a codon.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr8:77912229 G>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr8:77895826 G>C maps to NM_001172087.1 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr12:7361103 G>C maps to NM_001131023.1 V426V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr3:179526206 C>T maps to NM_016559.1 V457V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr3:179754388 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr3:179533759 C>T maps to NM_016559.1 K324K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A852-01A-11D-A351-09 chr20:52835608 C>T maps to NM_002623.3 Q109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr12:53691641 C>T maps to NM_002624.3 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr23:54982617 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:54984741 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VH-01A-11D-A28B-09 chr23:54985324 G>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr21:45736149 G>A maps to NM_002626.4 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr21:45733843 C>T maps to NM_002626.4 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr12:48528575 C>T maps to NM_001166686.1 D308D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr10:3147454 C>A did not map to a codon.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr2:24338427 T>G did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr2:24345291 G>A maps to NM_199346.1 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr7:44104590 C>T maps to NM_000290.3 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr7:44104527 G>A maps to NM_000290.3 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:133297419 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr2:197791250 G>A maps to NM_024989.3 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr2:197744873 G>A maps to NM_024989.3 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr1:249212357 G>A maps to NM_170725.2 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr1:230486820 C>T maps to ENST00000321327 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr1:230486790 C>T maps to ENST00000321327 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr5:114598461 G>A maps to NM_005023.3 F29F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr23:77378712 G>T did not map to a codon.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr23:77378487 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:77380790 C>T did not map to a codon.
Sequencing variant TCGA-JW-A852-01A-11D-A351-09 chr23:77381487 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr6:49754285 C>T maps to NM_138733.4 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HG-A2PA-01A-11D-A20U-09 chr19:15580364 G>A maps to ENST00000292609 A573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr19:15587258 C>T maps to NM_052890.3 W74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:64117279 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:74053661 G>A maps to NM_173582.3 F492F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr9:71098930 G>T maps to NM_021965.3 V482V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr9:70999423 G>T maps to NM_021965.3 E179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr23:118370403 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr23:118370415 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr1:28823240 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3QE-01A-21D-A21Q-09 chr1:28696258 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:28793214 C>T maps to NM_023923.3 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:28816355 G>A maps to ENST00000373838 V628V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr5:125939336 C>T maps to NM_032177.3 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr12:7077020 C>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr12:9089551 C>T maps to ENST00000433083 C918C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr1:33833010 G>A maps to ENST00000419414 R228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:33789882 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:33789940 C>G did not map to a codon.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr1:33832939 G>A maps to ENST00000419414 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr23:22239803 A>G did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:22051180 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:22115102 G>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:22112214 G>A did not map to a codon.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr23:22095638 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr6:33383742 G>T maps to NM_024165.2 G524G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr13:50097351 G>A maps to NM_001040443.1 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr17:27239782 C>T maps to NM_001033561.1 V602V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr17:27244305 C>T maps to NM_001033561.1 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:27240256 C>T maps to NM_001033561.1 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr7:11053395 G>A maps to ENST00000303905 E356E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr7:11101422 C>T maps to ENST00000303905 T829T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr5:133873702 C>G maps to ENST00000448712 S44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:46898450 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:46918323 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr23:46918302 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr4:129776798 C>T maps to NM_199320.2 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr4:129782959 C>T maps to NM_199320.2 F361F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr9:96398777 C>T maps to NM_005392.3 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr20:34526642 G>A maps to NM_016436.4 P775P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr8:133837519 G>T maps to ENST00000395386 E551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr8:133848894 G>T maps to ENST00000395386 E675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr8:133858143 G>A maps to ENST00000395386 Q1011Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CH-01A-11D-A33O-09 chr11:45992777 A>G maps to ENST00000257821 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr11:45992864 C>T maps to ENST00000257821 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr22:45309893 G>C maps to NM_138415.3 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr6:64422275 C>T maps to NM_015153.2 Q1598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:64395257 C>G maps to NM_015153.2 V545V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr23:133549135 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr23:54022199 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr23:54022193 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:54011585 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:53966696 G>A did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr23:54048781 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr23:54040925 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr1:120286678 G>T did not map to a codon.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr23:71825422 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr23:71932673 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3HR-01A-11D-A20U-09 chr23:71825219 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:71887264 G>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:71800866 G>T did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr23:18969234 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr23:18924857 G>A did not map to a codon.
Sequencing variant TCGA-C5-A7CM-01A-11D-A33O-09 chr23:18959774 G>T did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:18942508 G>A did not map to a codon.
Sequencing variant TCGA-EA-A5ZF-01A-11D-A28B-09 chr23:19002028 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2PI-01A-11D-A18J-09 chr23:18961873 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:18949832 C>A did not map to a codon.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr23:18919624 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A5R1-01A-11D-A28B-09 chr23:18944618 T>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr16:47621659 G>T maps to NM_000293.2 E286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr16:30768369 A>C maps to NM_000294.2 G391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr12:76424549 C>T maps to NM_007350.3 Q324Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:76424316 C>T maps to NM_007350.3 *402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr1:201437539 G>C maps to NM_012396.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr1:201435539 C>G did not map to a codon.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr1:201437539 G>C maps to NM_012396.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H6-01B-11D-A22X-09 chr1:201437554 G>A maps to NM_012396.3 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H6-01B-11D-A22X-09 chr1:201437740 G>A maps to NM_012396.3 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr1:201437749 G>A maps to NM_012396.3 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr3:111681102 T>C maps to NM_001134438.1 D1007D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr19:43999434 G>A maps to NM_198850.3 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LB-01A-11D-A243-09 chr18:60645814 C>T maps to NM_194449.2 S1435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr17:47302014 G>A maps to NM_001143804.1 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:139743862 G>C did not map to a codon.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr9:139743789 G>A did not map to a codon.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr9:139743845 G>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:606579 C>G maps to ENST00000264555 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:607351 C>T maps to ENST00000264555 F632F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr1:114254387 C>A maps to NM_006608.2 E343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr1:114256081 G>C did not map to a codon.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr7:77567157 G>T maps to ENST00000454592 V315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr7:77580941 C>G maps to ENST00000427986 L708L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr7:77538188 G>A maps to ENST00000427986 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr7:77484120 C>G maps to ENST00000427986 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr8:22081785 G>A maps to NM_014759.3 F137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr22:21188889 T>C maps to NM_058004.2 K51K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr22:21119957 G>A maps to NM_058004.2 I726I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr22:21174093 G>C maps to NM_058004.2 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr22:21075634 C>T maps to NM_058004.2 W1631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr1:151288810 C>T maps to NM_002651.2 Q61Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QD-01A-32D-A22X-09 chr1:151278697 G>A maps to NM_002651.2 R454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:145579295 C>G maps to NM_006099.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr13:73539530 G>A maps to NM_006346.2 E651E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr22:38469790 G>C maps to NM_012407.3 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr23:15349597 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:15349649 C>T did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr1:172412935 G>A did not map to a codon.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr1:172413190 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:172366305 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr4:493077 G>T did not map to a codon.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr1:77685078 G>A maps to NM_005482.2 V3V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:77557972 G>C did not map to a codon.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr9:35093125 G>A maps to NM_032634.2 I340I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RE-01A-11D-A18J-09 chr9:35095706 T>C did not map to a codon.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr9:35094191 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr9:35091214 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr16:624415 G>A maps to NM_148920.1 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr16:624233 C>T maps to NM_148920.1 Q54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A5QV-01A-22D-A28B-09 chr1:207112632 G>A maps to NM_002644.3 Y73Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr1:27117353 C>T maps to NM_017837.2 V16V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:196674918 G>T maps to NM_025163.2 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr11:111942360 G>C maps to NM_138789.3 S100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:98405364 C>A maps to NM_152309.2 E414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZF-01A-11D-A28B-09 chr10:98355334 C>G maps to NM_152309.2 *806S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr11:17191264 G>A maps to NM_002645.2 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr1:204408074 G>A maps to NM_002646.3 D1168D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:204400759 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr12:18435081 G>T maps to NM_004570.4 E23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr12:18715807 C>T maps to NM_004570.4 F1213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr12:18435272 G>A maps to NM_004570.4 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:18515720 G>C did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr3:138383903 C>T maps to NM_006219.1 L882L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:9784410 C>T maps to ENST00000361110 F956F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:9784990 C>T maps to ENST00000361110 L1022L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr7:106508779 G>C maps to NM_002649.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr5:67589547 C>G maps to ENST00000396611 V437V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr5:67589254 C>T maps to ENST00000396611 Q415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr19:18271290 C>G maps to NM_005027.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr19:18273797 G>C maps to NM_005027.2 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr1:46509192 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr1:46509303 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr3:130463840 C>G maps to NM_014602.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr2:209192950 C>T maps to NM_015040.3 F1222F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:209138438 C>A maps to NM_015040.3 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr7:99997547 C>T maps to ENST00000453419 Q225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr7:99997554 G>C maps to ENST00000453419 *227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr7:99949969 G>A did not map to a codon.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr7:99956688 C>G maps to ENST00000413850 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CG-01A-11D-A32I-09 chr6:37138992 G>A maps to ENST00000373507 E202E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr6:37141959 C>T did not map to a codon.
Sequencing variant TCGA-UC-A7PD-01A-11D-A351-09 chr23:48772317 C>G did not map to a codon.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr22:50355295 C>T maps to NM_001001852.3 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr23:71406220 G>A did not map to a codon.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr1:20977196 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr1:20977204 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr10:22825872 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr17:36935683 C>T maps to NM_003559.4 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R9-01A-11D-A18J-09 chr12:57985143 C>T maps to NM_024779.4 F24F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:151206944 C>T maps to NM_001135638.1 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr1:151220421 G>C maps to ENST00000414290 *199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr23:15408178 C>T did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:15509412 G>A did not map to a codon.
Sequencing variant TCGA-EX-A69M-01A-11D-A32I-09 chr23:15444054 G>A did not map to a codon.
Sequencing variant TCGA-EA-A50E-01A-21D-A26G-09 chr11:67260518 G>A maps to NM_004910.2 I1119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr12:123494553 G>A maps to NM_020845.2 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr17:6360958 G>A maps to NM_031220.3 I858I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr17:6381312 C>A maps to NM_031220.3 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr10:3185848 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr10:3180156 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr10:3180551 G>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:134364557 G>T maps to NM_002653.4 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:134364762 G>C maps to NM_002653.4 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr4:111542525 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr10:103990663 G>A maps to NM_005029.3 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr10:103990724 G>T maps to NM_005029.3 S152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr12:130842071 C>T maps to NM_004764.4 Q547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr12:130827567 C>T maps to NM_004764.4 Q38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr8:22141711 C>T maps to NM_001135721.1 Q224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr22:25115783 C>T maps to NM_001008496.2 T821T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr11:94337147 A>G did not map to a codon.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr11:94341822 C>T maps to NM_152431.2 C638C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr23:68383009 C>T did not map to a codon.
Sequencing variant TCGA-EA-A4BA-01A-21D-A26G-09 chr23:68382227 T>C did not map to a codon.
Sequencing variant TCGA-EX-A1H6-01B-11D-A22X-09 chr23:68381221 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr5:108704311 A>G maps to NM_014819.4 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr16:2157690 G>C did not map to a codon.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr16:2159881 G>T maps to NM_001009944.2 T1762T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr16:2169357 G>C maps to NM_001009944.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M2-01A-21D-A18J-09 chr16:2158330 G>A maps to NM_001009944.2 S2279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr16:2168329 G>C maps to NM_001009944.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr16:2159611 G>A maps to NM_001009944.2 V1852V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr16:2142995 G>A maps to NM_001009944.2 I3705I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr16:2158444 C>G maps to NM_001009944.2 L2241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr16:2161288 G>T maps to NM_001009944.2 V1293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr16:2158720 C>T maps to NM_001009944.2 P2149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr16:2161291 G>A maps to NM_001009944.2 F1292F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:47880141 G>A maps to NM_138295.3 D1823D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr7:47869021 C>A did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr16:81208267 G>A maps to ENST00000378597 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr4:88986630 C>T maps to NM_000297.2 R742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LS-01A-22D-A22X-09 chr10:102051080 G>A maps to NM_016112.2 R662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr10:102057140 C>G maps to NM_016112.2 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr5:137275820 G>C maps to NM_014386.2 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr2:42275815 C>T maps to NM_138370.2 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr22:46654349 G>A maps to NM_006071.1 L1624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr22:46654365 G>A maps to NM_006071.1 F1618F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr22:46655436 G>A maps to NM_006071.1 S1261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr22:46656321 G>C maps to NM_006071.1 L966L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr6:51735350 G>A maps to NM_138694.3 L2479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr6:51751998 G>C maps to NM_138694.3 L2347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr6:51907735 G>T maps to NM_138694.3 I1006I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M1-01A-11D-A18J-09 chr6:51503659 G>A maps to NM_138694.3 V3831V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr6:51907735 G>A maps to NM_138694.3 I1006I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr6:51921586 C>G did not map to a codon.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr6:51613065 C>A maps to NM_138694.3 L3116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr8:110478939 C>T maps to ENST00000426474 F2849F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr8:110498979 T>C maps to ENST00000426474 G3270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr8:110463246 G>A maps to ENST00000426474 G2073G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr8:110456021 C>G maps to ENST00000426474 S1561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr16:3025763 G>T maps to NM_004203.4 S143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr16:3026897 G>T maps to NM_004203.4 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr16:3022751 G>C maps to ENST00000431515 V464V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr19:14554354 G>A maps to NM_213560.1 E138E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr21:44448896 C>T maps to NM_004571.3 Q338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr1:201286770 C>T maps to NM_000299.3 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr1:201282403 C>T maps to NM_000299.3 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr12:32996149 C>A maps to NM_004572.3 T492T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr2:159314797 C>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr10:74714348 G>C maps to NM_032562.2 S32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr11:63342416 T>G maps to NM_001128203.1 *163Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:20305076 C>G did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:186901987 C>T maps to NM_024420.2 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:42446304 G>A maps to ENST00000397272 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr15:42442919 C>T maps to ENST00000397272 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr22:38559435 G>C maps to ENST00000445591 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr22:38559593 G>A maps to ENST00000445591 Q29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr22:38512121 G>A maps to NM_003560.2 F613F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HM-A3JK-01A-11D-A21Q-09 chr2:160901447 G>A maps to NM_007366.4 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:133700282 C>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr8:57079818 C>T maps to NM_002655.2 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr10:75673833 C>T maps to NM_002658.3 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr20:8769322 G>T maps to NM_015192.2 E1078*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr20:8632316 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr20:8745834 G>A maps to NM_015192.2 V920V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr15:40591116 G>A maps to NM_004573.2 F244F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr15:40591366 G>C maps to NM_004573.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr11:64026023 C>T maps to NM_000932.2 D364D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr11:64027603 G>C maps to NM_000932.2 L543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr11:64026146 C>G maps to NM_000932.2 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr20:9389807 C>A maps to NM_001172646.1 S660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr20:9438099 C>A maps to NM_001172646.1 I1012I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3L7-01A-21D-A20U-09 chr20:9460164 C>T did not map to a codon.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr3:38049576 C>A maps to NM_001130964.1 E726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr3:38065672 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr3:38049822 C>T maps to NM_001130964.1 K667K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr17:43198399 G>A maps to NM_133373.3 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr17:43197700 G>T maps to NM_133373.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr17:43196205 G>A maps to NM_133373.3 Q297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A69M-01A-11D-A32I-09 chr2:219499241 G>A maps to ENST00000432688 Q627Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr10:95848925 C>T maps to NM_001165979.1 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr10:96058364 G>A maps to ENST00000371380 P1799P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr20:39794457 C>G maps to NM_002660.2 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr3:155203487 G>A maps to ENST00000340059 L885L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr3:155271938 A>T maps to ENST00000340059 G360G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr3:155314019 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2PI-01A-11D-A18J-09 chr3:155206496 G>A maps to ENST00000340059 R819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr3:155200811 C>T maps to ENST00000340059 G1009G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr2:198949615 C>T maps to NM_006226.3 R459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr3:17052520 G>A maps to NM_001144382.1 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr23:207450 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr3:111439760 T>G did not map to a codon.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr5:41382226 G>A maps to NM_001005473.2 C171C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr5:41510615 G>A maps to NM_001005473.2 Q5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr3:171394594 C>G maps to NM_002662.3 R675R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5O9-01A-11D-A28B-09 chr3:171406540 G>A maps to NM_002662.3 D488D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VK-01A-11D-A28B-09 chr3:171406585 C>T maps to NM_002662.3 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:171453322 G>C maps to NM_002662.3 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:4711669 C>T maps to NM_002663.3 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr8:144998411 C>G maps to NM_201380.2 L2032L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr8:144993179 C>T maps to NM_201380.2 Q3740Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr8:144996563 C>G did not map to a codon.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr8:144994595 C>T maps to NM_201380.2 L3268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr8:144997376 C>T maps to NM_201380.2 L2377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr8:144997454 C>T maps to NM_201380.2 A2351A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A44S-01A-12D-A26G-09 chr8:145004626 C>T maps to NM_201380.2 L931L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr8:144995000 G>C maps to NM_201380.2 L3133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr8:144996800 C>T maps to NM_201380.2 Q2569Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr8:145004319 G>C maps to NM_201380.2 A1005A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr8:145024565 G>A maps to NM_201380.2 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr8:145024637 G>A maps to NM_201380.2 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr8:144996496 C>A maps to NM_201380.2 E2635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr8:145006128 C>T maps to NM_201380.2 L855L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr8:145009250 G>A maps to NM_201380.2 I388I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr14:67854155 G>A maps to NM_016445.1 Q318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr10:124184410 G>A did not map to a codon.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr10:124189978 A>G did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr10:124177429 G>A maps to NM_021622.4 K209K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr10:124172454 C>G maps to NM_021622.4 S121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr10:124191266 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr8:38830301 A>T did not map to a codon.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr2:179346648 C>T did not map to a codon.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr12:19282987 G>A maps to ENST00000429027 E31E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:204214040 G>T maps to ENST00000367191 S728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr11:16877406 G>A maps to ENST00000448080 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:16807924 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr7:30092482 G>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr7:30118401 G>C maps to ENST00000440706 *546S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr2:131890506 G>A maps to ENST00000409158 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr6:151089859 C>T maps to NM_001029884.1 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr14:65194405 G>C maps to ENST00000394691 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr14:65210857 G>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr14:65210908 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr14:65208124 G>A maps to ENST00000394691 G630G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr16:67315955 G>A maps to NM_001129729.1 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VI-01A-11D-A28B-09 chr16:67322303 G>T did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:143603 C>T maps to NM_052909.3 F243F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr12:93162805 C>T maps to NM_001004330.2 R328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr14:68029085 T>G maps to NM_020715.2 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BE-01A-21D-A26G-09 chr2:43965568 G>C maps to NM_172069.3 L1011L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr2:43924495 G>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr17:40820117 G>C did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr17:40828530 G>A maps to NM_024927.4 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr17:43513297 C>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr17:43516961 C>G maps to NM_014798.2 L980L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:16060402 C>T maps to ENST00000420314 R1115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5O9-01A-11D-A28B-09 chr1:150129151 G>A maps to ENST00000443480 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr6:161174002 T>C maps to NM_000301.3 G781G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M1-01A-11D-A18J-09 chr2:87240095 G>C did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr2:88047696 C>T maps to NM_001032392.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr9:19126394 C>T maps to NM_001122.2 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr9:19108574 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr9:19126025 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr19:4511412 C>T maps to NM_001080400.1 T839T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:4511859 G>C maps to NM_001080400.1 L690L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OA-01A-11D-A16Y-08 chr19:4510707 C>T maps to NM_001080400.1 P1074P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr19:4508869 C>T maps to NM_001080400.1 Q1190Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr19:4525652 G>A maps to NM_001013706.2 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr19:4525776 G>A maps to NM_001013706.2 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:4529813 G>A maps to NM_001013706.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr1:45270293 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:45270289 G>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:128811390 G>C maps to NM_014264.4 V610V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr4:128814467 C>T maps to NM_014264.4 F739F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr4:128814471 C>T maps to NM_014264.4 Q741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:12009903 G>A maps to ENST00000376369 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:12032749 G>A did not map to a codon.
Sequencing variant TCGA-MY-A5BE-01A-21D-A26G-09 chr1:12032699 C>T did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr23:103041592 C>G did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr23:103042604 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr23:103031868 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr23:103041100 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr23:103041063 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:49030741 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2PI-01A-11D-A18J-09 chr3:142430846 T>G maps to NM_001172312.1 *630E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr23:114880846 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:114868345 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr3:145913066 G>C maps to NM_020353.2 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr20:44536509 G>A maps to NM_006227.2 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R1-01A-11D-A28B-09 chr20:44540070 G>A maps to NM_006227.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr10:20466003 G>T maps to NM_032812.7 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr3:126737154 G>T maps to NM_032242.3 E1227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr3:126736416 C>T maps to NM_032242.3 T1142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr3:126723997 C>T maps to NM_032242.3 F603F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:208383783 G>A maps to NM_025179.3 F404F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HQ-01A-11D-A20U-09 chr1:208201415 C>A maps to NM_025179.3 E1843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:208383572 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:208218009 G>A maps to NM_025179.3 I1239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr23:153695475 G>A did not map to a codon.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr23:153694020 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:153694576 C>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:153697027 A>G did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:153696204 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr23:153698912 G>T did not map to a codon.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr23:153693146 G>A did not map to a codon.
Sequencing variant TCGA-EX-A69L-01A-11D-A32I-09 chr23:153698894 G>T did not map to a codon.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr23:153694353 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:153697542 G>A did not map to a codon.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr23:153692560 C>T did not map to a codon.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr23:153694816 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr7:131848963 G>A maps to NM_020911.1 G1479G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr7:132192822 C>T maps to NM_020911.1 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr7:131853271 G>A maps to NM_020911.1 I1359I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr3:48465444 G>A maps to NM_001130082.1 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr22:50719805 C>A maps to NM_012401.2 V1215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr22:50726394 G>C maps to NM_012401.2 P484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr22:50719907 C>T maps to NM_012401.2 E1181E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3TX-01A-11D-A22X-09 chr22:50724314 G>A maps to NM_012401.2 Q668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr23:153038719 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:153040414 G>A did not map to a codon.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr23:153039424 G>T did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr23:153032606 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr12:94676113 C>T maps to NM_005761.1 I1272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr12:94691183 G>A maps to NM_005761.1 K1353K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr12:94543448 C>T maps to NM_005761.1 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:94691156 C>T maps to NM_005761.1 F1344F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:205799286 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr1:156209490 G>A did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr16:72198701 G>A maps to NM_031293.2 D42D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr15:74315240 C>G maps to NM_033238.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:139313652 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr9:139311358 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:190738301 G>T maps to NM_000534.4 E852*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr7:6018284 C>T maps to NM_000535.5 L739L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr23:152935958 G>T did not map to a codon.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr23:152938099 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LB-01A-11D-A243-09 chr19:50364612 G>A maps to NM_007254.3 F486F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr19:50368511 G>A maps to NM_007254.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:50365330 G>A maps to NM_007254.3 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:50365342 G>T maps to NM_007254.3 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr19:50365824 C>T maps to NM_007254.3 K302K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HQ-01A-11D-A20U-09 chr6:160229829 G>A maps to NM_173516.1 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr10:118354276 C>T maps to NM_006229.2 C122C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CJ-01A-11D-A32I-09 chr10:118380912 G>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr10:118394402 C>G maps to NM_005396.4 S290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PD-01A-11D-A351-09 chr10:118404587 C>T maps to NM_005396.4 Q464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr10:118225614 G>T maps to NM_001011709.2 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr14:74180159 C>T maps to NM_006029.4 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr14:74179652 C>T maps to NM_006029.4 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr8:26366150 C>A maps to NM_007257.5 E41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A69B-01A-11D-A32I-09 chr23:152226469 C>T did not map to a codon.
Sequencing variant TCGA-EA-A5ZF-01A-11D-A28B-09 chr23:152159504 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr23:152158872 G>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr14:39651656 C>T did not map to a codon.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr2:68388846 G>C maps to NM_020143.2 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr8:28186790 C>T maps to NM_006228.3 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:20944589 C>T maps to NM_000270.3 R234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HQ-01A-11D-A20U-09 chr6:36269959 A>T maps to ENST00000457797 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr22:44319877 G>A maps to NM_025225.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WH-01A-22D-A351-09 chr22:44287688 G>A maps to ENST00000216177 H24H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr19:7619549 C>T maps to NM_001166111.1 R869*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr19:7606554 C>T maps to NM_001166111.1 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr19:7614938 C>T maps to NM_001166111.1 F594F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr9:140400155 C>T maps to NM_001098537.1 E461E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr9:140356867 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr9:140355118 G>A maps to NM_001098537.1 F1304F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr7:108154977 G>A maps to NM_015723.2 Q320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr7:108154977 G>A maps to NM_015723.2 Q320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3YQ-01A-11D-A22X-09 chr7:108142957 G>T maps to NM_015723.2 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr7:108136891 C>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr17:46020748 T>A maps to NM_018129.3 C72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr2:55883470 G>A maps to NM_033109.3 V440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:55906873 C>A maps to NM_033109.3 E208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr12:89890967 C>T maps to NM_172240.2 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr12:89860564 T>C maps to NM_172240.2 E338E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr12:89815012 G>T maps to NM_172240.2 R452R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:14042665 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr7:131195680 C>T maps to NM_001018111.2 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OA-01A-11D-A16Y-08 chr3:127358322 G>A maps to NM_015720.2 E102E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr21:46705579 C>G did not map to a codon.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr1:166810228 G>A maps to NM_017542.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr1:151379712 C>G maps to NM_015100.3 V810V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr1:151403233 G>A maps to NM_015100.3 Q123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:24859947 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr23:24759592 A>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:25013931 G>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:24717568 C>G did not map to a codon.
Sequencing variant TCGA-JW-A5VH-01A-11D-A28B-09 chr23:24745187 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr11:65064733 G>A maps to NM_002689.2 R597R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr11:65064745 C>G did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:50906814 C>T maps to ENST00000391817 F401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr19:50912853 G>C maps to ENST00000391817 V721V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr7:44155464 C>G maps to NM_006230.2 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:74323926 G>A maps to NM_006591.1 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr12:133256809 T>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr14:50154888 G>A maps to NM_002692.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr2:75196615 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr15:89864063 G>T maps to NM_002693.2 R972R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr17:62488864 C>T maps to NM_007215.3 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr18:51809298 G>T maps to NM_007195.2 E297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr5:74848347 C>T maps to NM_016218.2 R63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr5:74877065 G>T maps to NM_016218.2 E243*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-IR-A3LA-01A-11D-A22X-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr3:121208085 G>C maps to ENST00000393672 S1367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr3:121206961 G>A maps to ENST00000393672 Q1742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr3:121190911 G>A maps to ENST00000393672 Q2351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CH-01A-11D-A33O-09 chr2:86266015 C>A did not map to a codon.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr2:86258467 C>T maps to NM_015425.3 E1521E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr2:86265929 C>T maps to NM_015425.3 Q1309Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr2:86266479 C>T maps to NM_015425.3 K1282K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr2:86267660 C>T maps to NM_015425.3 L1198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr13:28196020 C>G did not map to a codon.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr13:28196056 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr13:28196056 C>T did not map to a codon.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr13:28240166 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr17:7406711 C>G maps to NM_000937.4 L979L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr17:7401105 C>G maps to NM_000937.4 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr17:7403989 G>A maps to NM_000937.4 S568S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:7416922 C>T maps to NM_000937.4 S1780S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr4:57891673 C>T maps to NM_000938.1 L1070L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr4:57876624 G>A maps to NM_000938.1 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:57503909 G>C maps to NM_032940.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr16:57496671 G>A maps to NM_032940.2 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr16:57496587 C>A did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr19:1090927 G>A maps to NM_002695.3 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr19:1093794 G>A did not map to a codon.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr19:1093960 G>T maps to NM_002695.3 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr22:38349777 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr7:102212862 G>A did not map to a codon.
Sequencing variant TCGA-C5-A7CH-01A-11D-A33O-09 chr1:145592731 G>A maps to NM_006468.6 F521F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr16:22343427 C>G maps to NM_018119.2 R664R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr16:22337137 C>T maps to NM_018119.2 Q469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr16:22337178 G>A maps to NM_018119.2 R482R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr16:22337466 G>A maps to NM_018119.2 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr16:22339865 G>A maps to NM_018119.2 Q634Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A0TN-01A-21D-A14W-08 chr20:18464303 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3HQ-01A-11D-A20U-09 chr20:18448222 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr7:72413867 G>A maps to ENST00000434423 G1112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr7:75050939 G>A maps to ENST00000257665 F1107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr7:53103780 C>T maps to NM_182595.3 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A69B-01A-11D-A32I-09 chr2:25384144 G>A maps to NM_001035256.1 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr2:25387629 C>T maps to NM_001035256.1 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr1:46657735 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr9:134386532 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr9:134397655 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr7:76239523 C>A did not map to a codon.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr7:76239479 C>A did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr7:95001494 G>A maps to NM_000940.2 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr19:30104847 C>T maps to NM_006627.2 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr23:48374528 C>T did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:48371090 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr23:48374453 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:48369722 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:48371044 T>G did not map to a codon.
Sequencing variant TCGA-EA-A3HQ-01A-11D-A20U-09 chr13:38145527 T>C maps to NM_006475.2 T719T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr13:38171337 G>T maps to NM_006475.2 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A0TN-01A-21D-A14W-08 chr2:132022030 C>T maps to NM_001083538.1 G1001G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr2:131984448 G>A maps to NM_001083538.1 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr2:131976376 C>T maps to NM_001083538.1 H134H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr22:16287381 C>T maps to NM_001136213.1 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr22:16287816 C>T maps to NM_001136213.1 K23K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr11:111249961 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr1:167190158 C>T maps to NM_002697.3 Q9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:167301705 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr19:42600012 G>A maps to ENST00000342301 F239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr19:42595859 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr11:120186098 C>G maps to NM_014352.2 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr11:120176481 C>T maps to NM_014352.2 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr6:99283887 C>A maps to NM_005604.2 S380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:82763443 C>A did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr5:93076345 G>C maps to NM_153216.1 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr5:93077197 C>T maps to NM_153216.1 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LS-01A-22D-A22X-09 chr7:39472872 C>T maps to NM_007252.3 P408P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A5XV-01A-11D-A28B-09 chr7:39446222 C>T maps to NM_007252.3 Q304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr1:57044972 G>C did not map to a codon.
Sequencing variant TCGA-FU-A5XV-01A-11D-A28B-09 chr1:57002686 A>G maps to NM_003713.4 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:56977717 G>C maps to NM_003713.4 S247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr8:38126362 C>T did not map to a codon.
Sequencing variant TCGA-FU-A5XV-01A-11D-A28B-09 chr9:4663040 G>C maps to NM_203453.2 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CG-01A-11D-A32I-09 chr6:35393786 G>T maps to NM_006238.4 R419R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr3:12458465 G>A maps to NM_015869.4 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr5:149215908 G>T maps to NM_133263.3 E631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:42922778 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr23:18748334 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr23:18845464 G>C did not map to a codon.
Sequencing variant TCGA-EX-A449-01A-11D-A243-09 chr23:18800494 C>T did not map to a codon.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr4:76794423 G>A maps to NM_006239.2 G454G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr4:76797519 C>A maps to NM_006239.2 E414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr4:76793175 G>A did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr11:70222678 C>T maps to NM_003626.2 V1119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr11:70221171 G>T maps to NM_003626.2 L1096L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:70171017 G>A maps to NM_003626.2 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr19:49652820 C>T maps to NM_003660.2 F1124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr19:49632668 C>T maps to NM_003660.2 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr1:203008213 C>T maps to ENST00000367238 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr15:64454325 C>A maps to NM_000942.4 E55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A69L-01A-11D-A32I-09 chr4:159634412 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:201750450 G>T maps to ENST00000422134 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr2:201736078 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr5:102491615 T>C maps to ENST00000451606 Y469Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr16:4960928 C>T maps to NM_002705.4 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr2:44459671 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr2:44396074 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr2:44396047 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr17:58740431 C>G maps to NM_003620.3 S446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr22:22287816 G>C maps to NM_014634.3 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr19:46003773 C>G maps to NM_001080401.1 S373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr1:161140466 C>T maps to NM_001122764.1 Q386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr1:161139703 G>T maps to NM_001122764.1 E293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr1:161139316 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr11:67168187 G>T maps to NM_001008709.1 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:67168223 G>A maps to NM_001008709.1 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr12:111160270 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr6:30573985 C>T maps to NM_002714.2 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr1:202550186 G>C did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:202471086 G>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:202471376 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr14:104224056 G>C maps to NM_015316.2 S129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr14:104219455 G>A maps to NM_015316.2 Q237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A69M-01A-11D-A32I-09 chr19:45895173 C>T maps to NM_001142502.1 P593P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:45895302 G>A maps to NM_001142502.1 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr19:49377386 C>G maps to NM_014330.3 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr8:145724336 C>T maps to NM_032902.5 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr12:54969541 A>G did not map to a codon.
Sequencing variant TCGA-IR-A3L7-01A-21D-A20U-09 chr2:182928495 G>C maps to ENST00000280295 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr7:113558803 C>T maps to NM_002711.3 W83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr7:113518223 C>A maps to NM_002711.3 E975*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr7:113518692 C>T maps to NM_002711.3 E818E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr23:49143336 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr23:49143299 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:49142902 C>G did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:28178051 C>T maps to ENST00000399118 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr7:94540009 T>C maps to NM_001166160.1 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr7:94540328 G>T maps to NM_001166160.1 E302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr17:48211891 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr17:48211940 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr8:30657145 C>T maps to NM_001009552.1 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A50E-01A-21D-A26G-09 chr19:52723026 G>C maps to NM_014225.5 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr11:111635534 A>G maps to NM_181699.2 C100C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr5:146070741 C>T maps to ENST00000394414 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr5:145969474 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr5:145969746 G>A maps to ENST00000394414 F431F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr4:6331053 G>C maps to NM_181876.2 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZF-01A-11D-A28B-09 chr23:301536 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr9:131882886 C>T maps to NM_178001.2 Q43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:212502485 C>A maps to NM_006243.3 S64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr11:64695768 C>A maps to NM_006244.3 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr11:64698936 G>A maps to NM_006244.3 E307E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr14:102368165 G>A maps to NM_002719.3 V321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr14:63888773 G>A maps to ENST00000422769 D197D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr4:102014970 G>A maps to NM_000944.4 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr10:75198055 G>A maps to NM_001142353.1 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr10:75204552 G>C maps to NM_001142353.1 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A449-01A-11D-A243-09 chr9:104356771 G>A maps to NM_147180.2 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr18:9570272 T>C maps to NM_001042388.1 P485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr18:9557314 C>T maps to NM_001042388.1 L698L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr19:46891688 C>G maps to NM_006247.2 S387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr10:103908291 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr1:40539718 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:48755724 G>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:48758477 G>C did not map to a codon.
Sequencing variant TCGA-HM-A3JJ-01A-21D-A21Q-09 chr23:48931628 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr1:12855772 C>G maps to NM_023013.2 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr1:12854276 C>G maps to NM_023013.2 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr1:12835063 G>A maps to NM_001080830.1 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:13448421 G>C maps to NM_001024661.1 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr1:13475009 C>T maps to NM_001099850.1 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr1:12921151 C>T maps to NM_023014.1 Q315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CM-01A-11D-A33O-09 chr1:13038326 G>T maps to NM_001100631.1 T464T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr1:12979857 G>A maps to NM_001012277.1 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr12:11545879 G>A maps to NM_006248.3 Q378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr17:74542942 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr11:82564296 C>T maps to NM_199418.2 E132E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr6:106555000 G>A maps to NM_001198.3 L706L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DV-01A-11D-A32I-09 chr11:129788547 G>A maps to NM_020228.2 A704A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr11:45245933 G>A maps to NM_020229.2 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr11:45241294 C>T maps to NM_020229.2 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr9:133556791 C>T maps to NM_021619.2 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr1:3319364 G>A maps to NM_022114.3 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:3313155 C>T maps to NM_022114.3 D225D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr1:3334453 G>A maps to NM_022114.3 S918S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr1:14108333 G>A maps to NM_012231.4 L1348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr1:14106830 C>G maps to NM_012231.4 V847V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:14105432 C>T maps to NM_012231.4 I381I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr12:108128299 C>G did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr4:121742342 G>C maps to NM_018699.2 S153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RA-A741-01A-11D-A33O-09 chr4:121702438 G>A maps to NM_018699.2 C434C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr16:90124846 G>C maps to NM_001098173.1 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr5:23524508 C>T maps to NM_020227.2 I339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr5:23526495 G>T maps to NM_020227.2 G433G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr5:23509645 G>A maps to NM_020227.2 W46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PD-01A-11D-A351-09 chr5:23526849 C>G maps to NM_020227.2 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:45980296 G>A maps to NM_181697.1 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr10:120928884 C>G did not map to a codon.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr11:64089123 C>T maps to NM_012094.3 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr1:173455458 G>A maps to NM_004905.2 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A0TN-01A-21D-A14W-08 chr5:145133733 C>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr20:47444177 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr1:186276584 A>C maps to NM_005807.3 P578P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A78R-01A-11D-A32I-09 chr12:42858227 C>T maps to NM_153026.2 S536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr23:49032206 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:49034709 C>G did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr6:41752605 C>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr12:57127957 G>A maps to NM_000946.2 R406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OA-01A-11D-A16Y-08 chr6:57512840 A>G did not map to a codon.
Sequencing variant TCGA-DS-A1OA-01A-11D-A16Y-08 chr6:57512873 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr6:57393102 T>G did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr6:57512725 C>G did not map to a codon.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr14:94245520 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:120118156 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr1:146631136 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:84644605 A>C did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr9:71628378 G>T maps to NM_002732.3 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:49399150 G>C did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr7:590219 C>T maps to NM_002735.2 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr17:64299115 C>T maps to NM_002737.2 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr16:24166138 G>A maps to NM_002738.6 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr16:24231364 C>T maps to NM_212535.2 I649I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr14:62017243 C>A did not map to a codon.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr19:11557089 C>A maps to ENST00000436195 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr1:1986918 C>T maps to NM_002744.4 F37F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr1:2087450 G>A maps to NM_002744.4 Q298Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2GZ-01A-11D-A17W-09 chr14:30100143 G>A maps to NM_002742.2 F492F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RL-01A-11D-A18J-09 chr14:30066910 C>A maps to NM_002742.2 R740R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr19:47197276 G>A maps to ENST00000449438 F477F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr8:48776015 T>C maps to NM_006904.6 Q1897Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr8:48777245 G>A maps to NM_006904.6 F1813F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr8:48740908 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr8:48794619 G>A maps to NM_006904.6 F1604F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr8:48839862 C>T maps to NM_006904.6 L770L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr8:48694967 C>T maps to NM_006904.6 R3788R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr8:48686799 C>G maps to NM_006904.6 L4106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr10:53667320 C>T maps to NM_001098512.1 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr4:82088332 G>A maps to NM_006259.1 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr4:82056353 C>T maps to NM_006259.1 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr4:82125985 G>C maps to NM_006259.1 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A5XV-01A-11D-A28B-09 chr7:102004774 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr7:102066992 G>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr7:102006470 C>G did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr7:102065729 G>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr7:102065803 G>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr7:102066383 G>T did not map to a codon.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr6:22294637 G>A maps to ENST00000397199 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr10:120353958 G>A maps to NM_004248.2 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr4:148605132 C>T maps to NM_138364.2 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr14:23394234 G>A maps to NM_006109.3 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HG-A2PA-01A-11D-A20U-09 chr14:23398531 G>A maps to NM_006109.3 R13R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr16:68371360 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr12:3703116 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A73Q-01A-21D-A32I-09 chr12:3677980 C>G maps to NM_019854.3 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr20:4705250 C>T maps to NM_012409.2 F18F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr20:4705592 C>G maps to NM_012409.2 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr20:4680615 G>C maps to NM_001080123.1 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:27037974 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:27037982 G>A did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr20:33764058 G>C maps to NM_006404.3 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr20:33764082 G>A maps to NM_006404.3 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr22:18910642 C>T maps to NM_016335.4 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr2:68882656 G>A maps to NM_138964.2 K377K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr20:5294781 G>A maps to NM_144773.2 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr20:5294985 G>A maps to NM_144773.2 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr20:5294943 G>C maps to NM_144773.2 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr4:15995621 G>C maps to NM_006017.2 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr2:95943220 C>T maps to NM_144707.2 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr2:95947743 C>T maps to NM_144707.2 I541I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr3:93646132 T>C maps to NM_000313.3 K65K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr3:93624963 G>A maps to NM_000313.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr8:37620215 C>T maps to NM_007198.3 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:214170275 C>G maps to NM_002763.3 S133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr14:75329295 C>T maps to ENST00000445876 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr10:13629113 C>A maps to NM_003675.3 R10R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr1:52882346 G>C maps to NM_032864.3 R308R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:52870414 T>G did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:52882337 G>A maps to NM_032864.3 K305K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:52882503 G>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:45564748 C>T maps to NM_017922.3 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr9:116045408 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr9:116045016 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr2:153533989 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr12:50028989 G>A maps to NM_001031698.1 Q348Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr6:4058960 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr20:62654201 C>T maps to NM_012469.3 A580A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr17:1556889 G>A maps to NM_006445.3 I2105I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr17:1557267 G>A maps to NM_006445.3 I2010I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr17:1554944 G>C maps to NM_006445.3 L2169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr12:49689216 C>G maps to ENST00000451891 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr23:12828218 T>A did not map to a codon.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr23:12838850 G>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr17:57270857 C>T maps to NM_018304.3 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr19:50100876 C>A maps to NM_020719.1 Y1095*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A78R-01A-11D-A32I-09 chr19:50102571 C>G maps to NM_020719.1 S1241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr19:50105123 C>T maps to NM_020719.1 F1574F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr16:30666706 C>G maps to NM_024031.2 S427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr5:119800237 G>T maps to ENST00000407149 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr2:240982051 C>G maps to NM_001080835.1 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr19:5783183 G>A maps to NM_001134316.1 F358F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr19:5783498 G>C maps to NM_001134316.1 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr3:138738972 C>T maps to NM_001013650.2 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr6:30525126 G>A maps to NM_025263.3 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr6:30525184 G>T maps to NM_025263.3 E22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HF-01A-11D-A20U-09 chr12:11001054 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr11:36484189 C>T maps to NM_001160167.1 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VH-01A-11D-A28B-09 chr11:36476881 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr23:37312799 G>A did not map to a codon.
Sequencing variant TCGA-C5-A2M1-01A-11D-A18J-09 chr23:37208596 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:37312501 C>G did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:150869354 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr16:29824353 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr1:170705269 G>C maps to NM_022716.2 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:170695369 C>T maps to NM_022716.2 Q143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr7:142459658 G>T maps to ENST00000486171 E93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr4:119204247 C>T maps to NM_003619.3 R686R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr11:86519255 C>T maps to NM_007173.4 R191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr16:31150459 C>T maps to NM_173502.3 *856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr1:228003830 C>T maps to NM_183062.2 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr4:152198350 G>A maps to NM_183375.2 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr3:46759248 G>A maps to NM_013270.4 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr15:55912410 T>G maps to NM_173814.4 V1084V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:151001296 C>G maps to NM_021222.1 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr9:79328480 G>A maps to NM_015225.2 Q305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr9:79259657 C>A maps to NM_015225.2 G2909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr9:79229481 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr9:79319880 G>A maps to NM_015225.2 R2437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr19:40904464 C>T maps to NM_020956.2 *148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr19:40901210 G>A maps to NM_181882.2 F1016F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:40901378 G>A maps to NM_181882.2 S960S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr8:143763115 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr10:104170844 G>A maps to NM_002779.3 L657L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr10:104180692 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr5:139201534 C>T maps to NM_032289.2 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr5:139201534 C>T maps to NM_032289.2 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr2:113915039 C>T did not map to a codon.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr2:113955394 C>T maps to NM_012455.2 H843H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr1:227079025 C>T maps to ENST00000391872 Q345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr19:43373184 C>T maps to NM_006905.2 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr19:43529134 G>T maps to ENST00000306308 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr19:43586752 G>T did not map to a codon.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr19:43579626 G>A maps to NM_031246.3 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr19:43586775 C>T did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr19:43411199 G>A maps to NM_002782.3 Q372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr19:43440461 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr19:43257301 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr19:43268272 G>A maps to NM_182707.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr19:43762459 G>C maps to NM_002784.3 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr9:15510233 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr8:87076346 A>C maps to ENST00000276616 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr11:14535159 G>C maps to NM_148976.2 S173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr14:58711622 C>G did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr14:58737186 C>T maps to NM_002788.2 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr17:4701365 G>C maps to NM_002798.1 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr17:4700800 C>G maps to NM_002798.1 S80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr17:61905259 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:107330967 G>T did not map to a codon.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr17:30771576 C>T maps to NM_002815.2 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AX-01A-12D-A243-09 chr17:65337162 G>A maps to NM_002816.3 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:151236292 G>C did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:122337766 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr17:40985911 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr20:1146840 G>C did not map to a codon.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr21:40550496 G>C maps to NM_003720.2 S178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr21:40551888 G>T maps to NM_003720.2 C139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr7:1607366 C>G maps to NM_001134340.1 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:109823693 C>T maps to ENST00000409138 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H6-01B-11D-A22X-09 chr15:77310553 G>A maps to NM_003978.3 K34K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr1:28476821 G>A maps to NM_001164721.1 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VK-01A-11D-A28B-09 chr1:28476616 C>A maps to NM_001164721.1 E306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:804854 G>A maps to NM_002819.4 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr19:807867 G>C did not map to a codon.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr1:97236445 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:97279083 T>G did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:97187331 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:97278930 G>C maps to ENST00000370197 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A852-01A-11D-A351-09 chr7:99032526 C>T maps to NM_001198879.1 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr9:98211362 G>A maps to NM_000264.3 F1264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr1:45293814 G>A maps to NM_003738.4 D586D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:45293981 G>C maps to NM_003738.4 L565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr23:23411549 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:23398155 T>A did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:23411481 C>T did not map to a codon.
Sequencing variant TCGA-LP-A4AX-01A-12D-A243-09 chr23:23397864 A>G did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:11561450 G>A maps to NM_020780.1 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr1:11575525 G>C maps to NM_020780.1 L518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr1:11589699 C>T maps to NM_020780.1 P962P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr1:11579819 G>T maps to NM_020780.1 E695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr10:27702726 C>T maps to NM_001034842.3 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A6QX-01A-12D-A33O-09 chr10:27702729 G>T maps to NM_001034842.3 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3TQ-01A-11D-A22X-09 chr10:27702693 G>A maps to NM_001034842.3 D162D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr8:97295860 A>C did not map to a codon.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr10:89717614 C>T maps to NM_000314.4 Q214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr10:89685299 C>G maps to NM_000314.4 Y65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr10:89711892 C>T maps to NM_000314.4 Q171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr10:89717660 C>G maps to NM_000314.4 S229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr10:89653924 C>A did not map to a codon.
Sequencing variant TCGA-EA-A5FO-01A-21D-A28B-09 chr10:89717671 C>T maps to NM_000314.4 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr10:89725042 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr10:89693161 G>C did not map to a codon.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr10:89717608 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3TQ-01A-11D-A22X-09 chr10:89624268 A>T maps to NM_000314.4 R15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VH-01A-11D-A28B-09 chr10:89690846 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr10:16526442 G>A maps to NM_030664.3 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr10:16526605 C>T maps to NM_030664.3 Q75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr14:52735041 C>T maps to NM_000953.2 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CJ-01A-11D-A32I-09 chr14:52735239 G>A maps to NM_000953.2 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr14:52734612 C>T maps to NM_000953.2 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WI-01A-12D-A351-09 chr9:139874617 T>A did not map to a codon.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr9:139875330 C>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr14:52781854 C>T maps to NM_000956.3 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr14:52781934 C>T maps to NM_000956.3 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:71512885 C>T maps to ENST00000354608 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HM-A3JK-01A-11D-A21Q-09 chr5:40681121 C>T maps to NM_000958.2 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr5:40681883 C>T maps to NM_000958.2 I263I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr5:40681721 G>A maps to NM_000958.2 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr5:40681916 C>T maps to NM_000958.2 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr5:40681883 C>T maps to NM_000958.2 I263I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr9:132502012 T>C maps to NM_004878.4 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr9:132510989 C>G maps to NM_004878.4 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr12:57081747 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr12:57057907 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr12:57057306 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr1:117509917 C>T maps to NM_020440.2 L675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr1:117509917 C>T maps to NM_020440.2 L675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr1:117532751 G>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:117509650 C>T maps to NM_020440.2 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr1:117509949 C>G maps to NM_020440.2 S686*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr9:114325401 C>G maps to NM_001146108.1 *330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr1:186645142 G>A maps to NM_000963.2 Q382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr1:186646908 T>G maps to NM_000963.2 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr2:209224739 C>G did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr8:141685662 C>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr20:62160942 G>A maps to NM_005975.2 F434F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr20:62163882 G>A maps to NM_005975.2 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr6:43112168 C>T maps to ENST00000473339 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A770-01A-11D-A33O-09 chr2:232576647 G>T maps to ENST00000409321 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr19:50363361 C>T maps to NM_017432.3 V387V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr6:64282608 G>A did not map to a codon.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr9:96857671 G>A maps to ENST00000434261 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:17636382 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr15:65868826 C>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr20:49191164 C>T maps to NM_002827.2 R156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr7:77256662 C>G maps to NM_002835.3 S556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:87685873 C>T maps to NM_080685.2 V1382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr4:87731117 T>G maps to NM_080685.2 L2432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr4:87671989 G>A maps to NM_080685.2 Q1006Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr4:87638210 C>T maps to NM_080685.2 S442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr1:214549656 G>A maps to NM_005401.4 R938*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr1:214706659 C>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr1:214706671 G>T did not map to a codon.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr1:214706238 C>A did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr14:88945914 G>T maps to NM_007039.3 V620V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:88983587 G>A maps to NM_007039.3 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3WB-01A-11D-A22X-09 chr1:114401659 A>G maps to NM_015967.5 D79D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M1-01A-11D-A18J-09 chr3:47454053 C>T maps to NM_015466.2 V1456V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr3:47451198 G>A maps to NM_015466.2 L668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:47449933 C>T maps to NM_015466.2 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr2:120658343 G>A maps to NM_002830.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr11:18751070 G>T maps to NM_032781.3 I511I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr20:2945627 C>T maps to NM_002836.3 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr12:70954691 G>A maps to NM_001109754.1 L1397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr12:70989913 G>A maps to NM_001109754.1 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr12:71029766 C>T maps to NM_001109754.1 R45R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr1:198701656 C>G maps to ENST00000271610 S705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr1:198700744 G>C did not map to a codon.
Sequencing variant TCGA-LP-A4AX-01A-12D-A243-09 chr1:198721824 A>T maps to ENST00000271610 K1145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr9:8518127 C>T maps to NM_002839.3 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PD-01A-11D-A351-09 chr9:8486256 G>A maps to NM_002839.3 Q854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZD-01A-11D-A28B-09 chr10:129883835 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr1:44087717 G>A did not map to a codon.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr1:44088217 G>C did not map to a codon.
Sequencing variant TCGA-EA-A44S-01A-12D-A26G-09 chr1:44088788 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:44044574 G>A maps to NM_002840.3 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr1:44088824 C>G did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:44019600 C>G maps to NM_002840.3 S123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:44089322 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr3:62180800 G>A maps to NM_002841.3 R428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr3:62267353 C>T maps to NM_002841.3 I1294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HM-A3JK-01A-11D-A21Q-09 chr3:62253427 G>A maps to NM_002841.3 W936*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZE-01A-11D-A28B-09 chr19:55702909 C>T maps to NM_002842.3 K781K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr19:55705543 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr19:55713637 G>A maps to NM_002842.3 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr19:55708497 G>A maps to NM_002842.3 L659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr11:48149587 G>T maps to NM_002843.3 V450V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr11:48186060 G>A maps to NM_002843.3 Q1283Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr6:128403633 C>T maps to ENST00000368210 T575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr6:128643076 G>C did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr18:8394575 G>A maps to NM_001105244.1 L1437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5O9-01A-11D-A28B-09 chr18:8406234 G>A did not map to a codon.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr18:8252484 G>T did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr18:8387203 C>T maps to NM_001105244.1 G1393G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr18:8143730 C>T maps to NM_001105244.1 L752L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr18:8394575 G>A maps to NM_001105244.1 L1437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr2:220154977 C>T maps to NM_002846.3 V970V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr2:220164720 G>A maps to NM_002846.3 I474I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr2:220172264 G>A maps to NM_002846.3 Q61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr7:157926523 G>A maps to NM_002847.3 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr7:157361624 C>T maps to NM_002847.3 L957L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr12:71050539 C>T maps to NM_002849.2 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr12:71286715 G>A maps to NM_002849.2 Q34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr19:5273570 T>G maps to NM_002850.3 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A6QX-01A-12D-A33O-09 chr19:5265144 G>T maps to NM_002850.3 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr19:5274290 G>A maps to NM_002850.3 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr19:5219478 C>T did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr19:5243945 G>C maps to NM_002850.3 L512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr20:41400149 C>T maps to ENST00000373198 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr20:41408921 G>C maps to ENST00000373198 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr20:40727168 G>A maps to ENST00000373198 F1268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr20:40944407 C>T maps to ENST00000373198 L698L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr20:41400169 G>A maps to ENST00000373198 R197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr20:40713385 G>A maps to ENST00000373198 R1380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr20:40877391 G>A maps to ENST00000373198 G768G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr20:40733325 C>T maps to ENST00000373198 L1163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr1:29652238 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr1:29652206 C>G did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:29585840 C>T maps to NM_005704.4 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:121659176 G>C did not map to a codon.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr7:121513404 A>C did not map to a codon.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr7:121513475 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2GZ-01A-11D-A17W-09 chr16:1538814 C>A did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr16:1536173 G>A maps to NM_001013658.1 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr8:144904724 C>G did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:31478833 G>A maps to ENST00000373741 Q232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr1:31438979 G>A maps to ENST00000373741 F681F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr1:31439029 G>A maps to ENST00000373741 Q665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr5:139494071 C>T maps to NM_005859.4 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr8:30889905 C>G maps to NM_013357.2 L131L. Only missense variants will be evaluated by CHASM.
Reference base specified for sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr2:61175311 C>G does not match reference base at that coordinate in hg19.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:1246425 C>G maps to NM_153339.1 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr11:119494209 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr11:119548546 C>A maps to NM_002855.4 E151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A6QX-01A-12D-A33O-09 chr19:45381603 G>A maps to NM_002856.2 R389R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A6QX-01A-12D-A33O-09 chr19:45381609 G>A maps to NM_002856.2 R391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:45391611 C>A maps to NM_001042724.1 V531V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr1:161043068 C>G maps to NM_030916.2 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr12:108086769 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr21:45547963 C>G maps to NM_005049.2 L764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:1653334 C>T maps to NM_012293.1 Q739Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:1652917 G>A maps to NM_012293.1 F878F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3TX-01A-11D-A22X-09 chr2:1667375 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr8:52384808 G>A maps to NM_144651.4 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr12:120650347 G>A maps to NM_001080855.1 F515F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr12:120659470 G>T maps to NM_001080855.1 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:79892975 G>A maps to ENST00000432920 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr20:25258980 G>A maps to NM_002862.3 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:51404507 C>T maps to NM_002863.4 Q97Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr11:64519471 G>A maps to NM_005609.2 F564F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr11:64518733 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr12:9322059 G>C maps to NM_002864.2 S656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr3:49137040 G>A maps to NM_005051.1 V476V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr3:49138859 G>A maps to NM_005051.1 F268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr3:49137067 G>T maps to NM_005051.1 Y467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:133769048 C>A maps to NM_198180.1 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr3:49094618 G>A maps to NM_198880.1 N338N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr17:74287141 G>A maps to NM_032134.1 A1056A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr17:74276490 G>A maps to NM_032134.1 V1335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr6:107110890 G>A maps to NM_018292.4 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr11:32948715 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr19:10823474 G>A maps to NM_031209.2 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr12:57677634 G>A maps to ENST00000438036 G399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr2:26257497 C>T maps to NM_016131.4 D7D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:66180229 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2GZ-01A-11D-A17W-09 chr19:8464927 C>T maps to NM_004218.3 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr8:37729589 G>C maps to NM_001002814.2 L910L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr8:37729372 C>A maps to NM_001002814.2 E983*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:119805359 G>C maps to ENST00000369199 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr17:29857423 C>G maps to NM_032932.3 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:73315527 C>G maps to NM_015470.2 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr2:73302589 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VG-01A-11D-A28B-09 chr1:153954807 C>T did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr1:153955951 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr1:153954966 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr9:123943694 C>T maps to NM_016322.3 Q209Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr2:238494053 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr7:140125874 G>C maps to ENST00000275874 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr7:140111669 C>G maps to ENST00000275874 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr11:66039340 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr13:111176395 G>C maps to NM_017817.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr6:57054533 A>G did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr16:2201869 C>G maps to NM_014353.4 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr14:21929393 C>T maps to NM_032846.3 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:129306123 C>A did not map to a codon.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr23:129306116 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr23:129306266 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr12:120541721 G>A maps to NM_006861.6 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:154490246 C>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr5:57879049 G>A maps to NM_138453.2 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr1:220440279 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:220363454 G>A maps to ENST00000358951 H555H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:220340970 G>A maps to ENST00000358951 F951F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:220440681 A>G did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:220363788 G>A maps to ENST00000358951 Q521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HF-01A-11D-A20U-09 chr23:102755558 C>T did not map to a codon.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr23:102192461 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr23:102192890 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73R-01A-11D-A33O-09 chr3:20017661 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:130737912 C>G maps to NM_032144.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UC-01A-11D-A351-09 chr19:16238843 C>G maps to NM_005370.4 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr9:125777840 G>C maps to NM_012197.3 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RA-A741-01A-11D-A33O-09 chr9:125860124 G>T did not map to a codon.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr1:174945276 G>A maps to ENST00000347255 E196E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr7:66274796 G>C did not map to a codon.
Sequencing variant TCGA-C5-A2M1-01A-11D-A18J-09 chr1:76252882 C>T did not map to a codon.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr1:76255552 C>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:76255786 A>C did not map to a codon.
Sequencing variant TCGA-JW-A5VI-01A-11D-A28B-09 chr1:202858202 G>A maps to NM_002871.3 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M1-01A-11D-A18J-09 chr2:114386171 A>G did not map to a codon.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr22:51208151 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr22:51205965 A>C did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:6441587 C>T maps to NM_018890.3 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr12:50384051 C>T maps to NM_013277.3 *633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr12:50410480 C>T maps to NM_013277.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr5:68666943 T>C did not map to a codon.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr8:117875498 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr8:117878869 G>A maps to NM_006265.2 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr9:110068755 C>T maps to NM_002874.3 Q109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr5:131923746 C>G maps to NM_005732.3 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr5:131893138 A>G maps to NM_005732.3 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr17:56809918 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr12:1022547 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr8:95470637 G>A maps to NM_012415.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr8:95390834 G>A maps to NM_012415.2 Q759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr8:95479677 C>G maps to NM_012415.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr7:4917598 G>A maps to NM_018059.4 Q58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:150210679 G>C maps to NM_139165.1 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RA-A741-01A-11D-A33O-09 chr6:150205623 C>A did not map to a codon.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr3:12660148 G>C maps to ENST00000415519 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr17:17713346 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr23:17819932 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:17818544 C>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:17818978 A>C did not map to a codon.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr14:36157724 C>G did not map to a codon.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr20:37153552 C>A maps to NM_020336.2 Y584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr20:37154151 C>G maps to NM_020336.2 V631V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr9:135973838 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr9:135979178 G>A maps to NM_006266.2 L571L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr9:135973187 C>T did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr9:135985047 G>A maps to NM_006266.2 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr9:135975586 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr8:85717003 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr17:40914674 C>T maps to ENST00000456272 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr17:40914698 C>T maps to ENST00000456272 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr17:40914698 C>T maps to ENST00000456272 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HG-A2PA-01A-11D-A20U-09 chr5:170722905 A>C maps to NM_022897.3 R1020R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr2:109380098 C>G maps to NM_006267.4 S1035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7X3-01A-11D-A351-09 chr1:21991719 G>A did not map to a codon.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr17:2808622 G>A maps to NM_015085.4 R42R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr3:152880787 C>T maps to NM_002886.2 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:131351212 G>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:131351093 C>G did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:131351136 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:131351086 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr9:134459712 C>T maps to NM_198679.1 Q965Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr12:48131379 G>C maps to NM_001098531.2 L914L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr2:173679323 A>G did not map to a codon.
Sequencing variant TCGA-C5-A2M1-01A-11D-A18J-09 chr5:130883757 C>T maps to ENST00000514667 E209E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr12:53608312 G>A maps to NM_000966.4 Q185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr3:158428575 G>A maps to NM_206963.1 Y162Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr5:86672328 C>T maps to NM_002890.1 R711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr5:86564632 C>A maps to NM_002890.1 S122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr5:86682698 C>T maps to NM_002890.1 I968I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr3:141291534 G>A maps to ENST00000452898 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:141292834 C>G maps to ENST00000452898 S470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr13:114762092 G>C maps to ENST00000389544 V692V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr13:114780742 C>G maps to ENST00000389544 P456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr13:114773064 C>T maps to ENST00000389544 S569S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr12:113537722 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:113537811 G>A maps to NM_001193520.1 L781L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:113553052 G>A maps to NM_001193520.1 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr1:178408664 G>A maps to ENST00000263528 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr19:15568599 C>A maps to NM_022904.1 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr17:17399273 G>C maps to NM_016084.3 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R1-01A-11D-A28B-09 chr22:35947703 C>T maps to NM_014310.3 N142N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr10:43692547 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr4:82377720 G>A maps to ENST00000436139 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr5:179545795 G>A maps to NM_175062.3 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr15:79327551 G>A maps to NM_002891.4 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr5:80383973 G>C did not map to a codon.
Sequencing variant TCGA-FU-A3EO-01A-11D-A20U-09 chr5:80497153 C>T maps to NM_006909.1 F933F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr5:80256694 C>T maps to NM_006909.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QE-01A-21D-A21Q-09 chr2:33736798 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr2:33783805 C>T maps to NM_170672.2 I591I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr19:49225249 C>T maps to NM_017805.2 W851*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr15:65350925 C>T maps to NM_016563.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HM-A4S6-01A-11D-A26G-09 chr3:50369017 G>C maps to NM_170714.1 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr3:50368086 G>A maps to NM_170714.1 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr20:4764156 G>C did not map to a codon.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr10:45480396 C>T maps to NM_032023.3 N170N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr10:45477982 G>A maps to NM_032023.3 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:206758445 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:206762591 C>T did not map to a codon.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr11:561797 G>C maps to NM_003475.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr11:562205 G>A maps to NM_003475.3 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr19:10432288 G>A maps to NM_133452.2 P410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr13:49039157 G>T maps to NM_000321.2 E746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr13:49039373 C>T maps to NM_000321.2 R787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr13:49050677 G>A did not map to a codon.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr13:49050706 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3HQ-01A-11D-A20U-09 chr13:48955381 G>C did not map to a codon.
Sequencing variant TCGA-EA-A5ZE-01A-11D-A28B-09 chr13:48955491 C>T maps to NM_000321.2 I536I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A852-01A-11D-A351-09 chr13:48942684 C>T maps to NM_000321.2 R358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr13:49030425 C>A maps to NM_000321.2 S634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr8:53626646 C>T did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr8:53569887 G>C maps to NM_014781.4 S834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr8:53570459 C>G maps to NM_014781.4 V643V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr7:5104370 C>G maps to NM_021163.3 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr16:24578502 G>A maps to NM_006910.4 Q543Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:16870687 C>T did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr18:20573282 C>A maps to ENST00000360790 S498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr18:20573290 C>T maps to ENST00000360790 Q501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr20:389368 T>C did not map to a codon.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr16:53504395 C>T maps to NM_005611.3 Q783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr16:53524766 C>T did not map to a codon.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr23:47040961 C>T did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:47034433 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3HR-01A-11D-A20U-09 chr23:47040951 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:47041149 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:47038523 G>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:47041163 C>T did not map to a codon.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr23:47045754 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr21:15596831 C>T maps to NM_144770.3 Q136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3PZ-01A-11D-A21Q-09 chr20:34242509 C>T maps to NM_001198838.1 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr8:94746937 G>A maps to NM_203390.2 F567F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr11:66384307 C>T maps to NM_001198845.1 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr11:66384487 C>T maps to NM_001198845.1 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr11:66384307 C>T maps to NM_001198845.1 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr11:66393086 C>T maps to NM_006328.3 R580R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:110882686 G>A maps to NM_022768.4 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WH-01A-22D-A351-09 chr1:110888940 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr1:110882123 C>T maps to NM_022768.4 Q33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:110889276 T>C did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr10:6139112 C>T maps to NM_001145547.1 Q29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A4BA-01A-21D-A26G-09 chr14:23371497 G>A maps to NM_001077351.1 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr13:79927341 A>G maps to ENST00000438737 S669S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CJ-01A-11D-A32I-09 chr5:145651102 C>T maps to NM_018989.1 R952*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZD-01A-11D-A28B-09 chr5:145665547 C>T maps to NM_018989.1 D1046D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr5:145648832 G>T maps to NM_018989.1 E839*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A57G-01A-11D-A26G-09 chr5:145603091 T>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr5:145613044 C>T maps to NM_018989.1 Q295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H1-01A-11D-A17W-09 chr23:48434777 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr23:48433774 C>T did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr23:48434069 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr1:235294964 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:235299400 G>C did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr20:34327243 T>C did not map to a codon.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr20:34297228 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr20:34330027 G>C did not map to a codon.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr20:34326958 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr20:34324512 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr20:34329875 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:36125186 G>A maps to NM_024321.3 K349K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr4:155719378 G>T maps to NM_144979.3 E190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr4:155718041 C>T maps to NM_144979.3 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A770-01A-11D-A33O-09 chr11:66444538 C>G maps to NM_031492.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:50005787 G>A maps to NM_005777.2 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr2:161130831 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:161157213 A>G maps to NM_016836.3 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:135955583 G>A did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr23:135961559 C>G did not map to a codon.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr23:129546419 C>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:129535994 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:129536099 G>A did not map to a codon.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr23:129543341 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr1:89449630 G>A did not map to a codon.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr10:48388080 G>A maps to NM_002900.2 L933L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr10:48388540 C>T maps to NM_002900.2 V779V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr12:7277326 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr1:10075888 G>A maps to ENST00000377192 *182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:26364132 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr4:26417193 C>T maps to NM_005349.2 Q98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5FO-01A-21D-A28B-09 chr20:43944933 G>A maps to NM_014276.2 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr8:30416464 G>T maps to NM_006867.2 *197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr9:125621234 G>A maps to NM_001100588.1 R666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr9:125667491 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr6:46424539 C>T maps to ENST00000405162 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr13:49075966 C>T maps to NM_001268.2 K385K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr1:28861791 G>A maps to NM_001048194.2 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QD-01A-32D-A22X-09 chr1:28862518 C>T maps to NM_001048194.2 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A78R-01A-11D-A32I-09 chr1:17735519 G>A did not map to a codon.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr14:103173770 G>A maps to NM_015156.2 E191E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:167666418 T>C maps to NM_052862.3 D186D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:167673908 T>C maps to NM_052862.3 T409T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr19:55558770 G>A maps to NM_001145971.1 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr12:57351165 C>T maps to NM_003708.3 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr17:34252521 G>A maps to NM_145654.3 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr14:24649098 C>T maps to NM_005132.2 F514F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr12:21624447 C>T maps to NM_032941.2 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:21629872 G>C maps to NM_032941.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr17:73654525 C>T maps to NM_004259.5 W334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr8:21995919 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr8:21995953 G>C did not map to a codon.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr19:1496285 C>A maps to ENST00000395479 C117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr2:79348028 G>A maps to NM_002909.4 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A4BA-01A-21D-A26G-09 chr2:79313498 T>G maps to NM_006507.3 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr1:120342437 C>T maps to NM_032044.3 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:65423152 C>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:65429491 G>A maps to NM_021975.3 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7X3-01A-11D-A351-09 chr19:45537559 G>C maps to ENST00000221452 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr19:45506231 G>A maps to ENST00000221452 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:45532203 C>T maps to ENST00000221452 C315C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr5:141017495 G>C did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr5:141017339 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr5:141018419 G>A maps to NM_173828.4 Q81Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr7:103268372 C>T did not map to a codon.
Sequencing variant TCGA-EA-A5ZF-01A-11D-A28B-09 chr7:103243749 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr7:103191722 A>T maps to ENST00000428762 T2031T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr7:103138564 C>G maps to ENST00000428762 V2934V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A5XV-01A-11D-A28B-09 chr7:103270623 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr7:103162495 C>T maps to ENST00000428762 A2547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr7:103183221 G>T maps to ENST00000428762 G2209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr1:204129705 G>A maps to NM_000537.3 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr1:204131239 A>G maps to NM_000537.3 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr6:139241453 C>G did not map to a codon.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr6:139229910 G>A maps to ENST00000367663 R704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:17095394 T>G did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:17092269 G>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:8426004 C>T maps to NM_012102.3 W438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:8716252 G>C maps to NM_012102.3 S35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:8415033 G>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:8568727 C>T maps to NM_012102.3 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3PZ-01A-11D-A21Q-09 chr12:18238555 G>A maps to NM_024730.2 Q62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr10:43608310 G>A maps to NM_020975.4 R553R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr10:43615039 G>A maps to NM_020975.4 E818E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr2:100040680 G>A maps to NM_016316.2 Q537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A770-01A-11D-A33O-09 chr6:111689104 A>G maps to NM_002912.3 N1962N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr19:1817260 G>C maps to NM_020695.3 S1053*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr19:1819020 C>T maps to NM_020695.3 L920L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr19:1816127 G>A maps to NM_020695.3 D1201D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:114320604 C>T maps to NM_015523.3 Q208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr11:114315253 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr9:136277935 G>A maps to NM_020385.2 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr9:136276149 C>T maps to NM_020385.2 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr7:73657530 G>A maps to NM_181471.1 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr12:118454685 G>A maps to NM_007370.4 R18R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr12:118469181 C>G did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr9:79002230 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr22:32586723 T>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:198480649 G>A maps to NM_144629.2 F368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:176133016 G>C maps to NM_022457.5 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A78R-01A-11D-A32I-09 chr19:14074707 G>A maps to NM_002918.4 L775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr19:6176277 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr19:6176352 C>A did not map to a codon.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr9:3275592 T>C maps to NM_134428.1 P331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr12:107126765 G>A maps to ENST00000357881 S521S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr12:107125950 C>T maps to ENST00000357881 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:151315474 G>T maps to NM_000449.3 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr1:151316235 G>A maps to NM_000449.3 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr6:117241489 C>T maps to NM_173560.3 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr15:56387633 G>T maps to NM_022841.5 V764V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr23:109696519 C>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr23:109696777 C>T did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:109695459 C>G did not map to a codon.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr23:109696639 C>A did not map to a codon.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr23:109697206 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:109696046 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:109696909 C>T did not map to a codon.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr23:71350358 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr23:71350408 G>A did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr23:71349693 C>T did not map to a codon.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr1:183874075 G>A maps to NM_015149.3 Q516Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HR-01A-11D-A20U-09 chr1:183891453 C>G maps to NM_015149.3 V736V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr19:11529982 C>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr9:35749826 C>T maps to ENST00000456972 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr9:35749381 G>A maps to ENST00000456972 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr9:35752744 G>A maps to ENST00000456972 W390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr10:86018408 G>C did not map to a codon.
Sequencing variant TCGA-EX-A69L-01A-11D-A32I-09 chr10:86008020 G>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr10:121295973 A>G did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr4:3344301 C>T maps to ENST00000306648 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr1:192614606 G>A did not map to a codon.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr1:192127614 G>A did not map to a codon.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr20:62708282 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr20:62705528 C>A maps to NM_005873.2 E144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr20:62705601 G>A maps to NM_005873.2 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr1:192779518 C>T maps to NM_002923.3 Q78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr8:101084452 G>C maps to NM_015668.3 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr8:100994307 G>A maps to NM_015668.3 Q1073*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr1:163042593 G>C did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:163044338 C>T maps to NM_001102445.2 Q300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:163045931 G>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:163045608 A>C did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:163046286 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:163187354 A>G maps to ENST00000367903 I10I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr14:72945010 T>C maps to NM_004296.4 C276C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr14:72818870 C>T maps to NM_004296.4 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr14:73006801 G>A maps to ENST00000404301 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr1:241099998 C>T maps to ENST00000407727 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr5:63802465 G>A maps to NM_001029875.1 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr1:182616019 C>T maps to NM_033345.2 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr17:63198171 C>G maps to NM_003835.3 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr7:75517727 G>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr7:75510756 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr16:109764 G>A maps to NM_022450.3 I594I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr17:74467960 G>A maps to NM_024599.5 F775F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr17:74475003 C>A maps to NM_024599.5 G215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr1:39361709 G>C maps to ENST00000372985 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:156354267 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:25715554 G>T maps to NM_020485.4 S284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr1:25633193 T>A maps to ENST00000357542 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr3:49405879 G>A maps to NM_001664.2 I86I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr3:49397642 C>T maps to NM_001664.2 *194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3EO-01A-11D-A20U-09 chr2:20647696 C>A maps to NM_004040.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr10:62632019 C>T maps to NM_014836.4 W615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr8:22862929 C>T maps to NM_001160036.1 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr8:22862929 C>T maps to NM_001160036.1 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr8:22865590 T>C maps to NM_001160036.1 F551F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr8:22852084 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr5:95067757 C>G maps to NM_014899.3 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr11:66838946 C>T maps to NM_014578.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr16:720882 C>T did not map to a codon.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr1:228871692 C>T maps to NM_021205.4 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:228879057 C>G maps to NM_021205.4 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr23:119249757 G>T did not map to a codon.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr23:119249758 A>G did not map to a codon.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr19:33502622 G>A maps to NM_033103.4 F185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KH-01A-21D-A22X-09 chr19:33493742 C>T maps to NM_033103.4 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr19:33490561 G>C maps to NM_033103.4 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr19:33470789 G>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr19:33493246 G>A maps to NM_033103.4 I337I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr23:53457906 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr11:213323 G>T maps to NM_021932.4 E467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr12:107208550 C>T maps to ENST00000392837 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr5:38957798 C>T maps to ENST00000296782 L818L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AU-01A-32D-A243-09 chr5:38954959 T>C maps to ENST00000296782 L871L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr5:38957825 G>A maps to ENST00000296782 L809L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr2:152266963 C>T maps to NM_018151.4 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr2:152285400 G>A maps to NM_018151.4 W297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr17:1551690 G>C maps to NM_031430.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr12:123920679 G>A maps to NM_145058.1 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A5XV-01A-11D-A28B-09 chr22:20457500 C>T maps to NM_015672.1 P1267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr22:20457821 C>T maps to NM_015672.1 Q1160Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr6:72975692 G>A maps to NM_014989.4 R1113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr6:72926937 C>G maps to NM_001168410.1 S16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr6:73110489 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr6:72984126 G>A maps to NM_014989.4 E1158E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr6:72678706 G>A maps to NM_014989.4 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr6:72678706 G>A maps to NM_014989.4 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr8:104973323 T>C maps to NM_001100117.2 S911S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr8:104933998 C>G maps to NM_001100117.2 S728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5FO-01A-21D-A28B-09 chr8:104513212 G>A maps to NM_001100117.2 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr8:104513287 C>A maps to NM_001100117.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr8:104780597 G>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr20:43438834 G>A maps to NM_182970.2 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr11:66102953 G>A maps to NM_004292.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr20:19916186 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr20:19982067 A>C did not map to a codon.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr20:19870109 G>C did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr14:93118692 C>T maps to NM_024832.3 G433G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr7:105177055 G>T maps to NM_021930.4 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr18:21061176 G>A maps to NM_003831.3 K498K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3L7-01A-21D-A20U-09 chr6:3078027 C>T maps to NM_003804.3 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr6:3077044 C>G did not map to a codon.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr8:90792330 G>A maps to NM_003821.5 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr14:24807136 C>T maps to NM_006871.3 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CG-01A-11D-A32I-09 chr1:155874116 G>T maps to ENST00000368322 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CJ-01A-11D-A32I-09 chr15:89760506 G>A maps to NM_000326.4 R64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr1:40705374 C>A maps to NM_012421.3 L1667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr23:73812277 G>T did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr23:73812296 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:73811718 A>C did not map to a codon.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr23:73812024 C>G did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr16:67688785 G>T maps to NM_001013838.1 E1230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr9:86617751 G>A maps to NM_024945.2 E617E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr14:21058828 C>T maps to NM_001024822.2 V18V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr14:21502045 G>C maps to NM_001012264.3 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr14:21502282 C>A maps to NM_001012264.3 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr14:21250154 C>A maps to NM_005615.4 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr14:21026809 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr2:3595525 G>A maps to NM_002936.3 Q257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr11:65487293 C>G did not map to a codon.
Sequencing variant TCGA-MY-A5BF-01A-11D-A26G-09 chr1:182555092 G>C maps to NM_021133.3 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr6:167347551 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr17:41178061 C>G maps to NM_005440.4 S63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr12:121014517 T>G did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr1:51737135 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr15:59387097 G>C maps to ENST00000434298 *1004S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr17:19318605 C>G maps to NM_007148.4 S435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:19318402 G>C maps to NM_007148.4 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr23:119005290 G>C did not map to a codon.
Sequencing variant TCGA-EX-A69L-01A-11D-A32I-09 chr23:119004828 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr3:49758727 C>A maps to NM_022064.2 S1312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CJ-01A-11D-A32I-09 chr18:29648334 G>A maps to NM_017831.3 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WF-01A-11D-A351-09 chr18:29598846 C>A maps to NM_017831.3 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr19:651747 A>C maps to ENST00000340092 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr23:105970451 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr23:105970627 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3EO-01A-11D-A20U-09 chr23:105937388 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr7:122338408 A>G maps to NM_139175.1 N188N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr11:10555623 G>A maps to NM_016422.3 R28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr5:158584522 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LC-01A-11D-A20U-09 chr5:158585860 G>A maps to NM_144726.2 V631V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr7:122342330 C>G maps to NM_198085.1 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr18:59560070 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr18:43914263 C>T maps to NM_152470.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr17:4844433 G>A maps to NM_015528.1 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr5:63621059 A>G maps to NM_001113561.1 E425E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr5:63496633 G>C did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr1:185069363 C>T maps to NM_007212.3 V314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr1:6270934 G>C maps to NM_207396.2 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr17:78318497 C>T maps to NM_020914.4 F2170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CH-01A-11D-A33O-09 chr17:78367414 G>A did not map to a codon.
Sequencing variant TCGA-C5-A7X3-01A-11D-A351-09 chr17:78317799 G>A maps to NM_020914.4 R2158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr17:78269549 C>G maps to NM_020914.4 S699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr17:78269595 C>T maps to NM_020914.4 I714I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:78328271 C>T maps to NM_020914.4 L3635L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr17:78332127 C>T maps to NM_020914.4 L3684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr17:78355465 C>T maps to NM_020914.4 I4688I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr17:78321461 C>T maps to NM_020914.4 Y3158Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr17:78337554 C>T maps to NM_020914.4 S3954S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr17:78261736 C>T maps to NM_020914.4 Q178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr17:78360056 C>A maps to NM_020914.4 I4898I. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-MY-A5BE-01A-21D-A26G-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-MY-A5BE-01A-21D-A26G-09 chr17:78326836 C>T maps to NM_020914.4 F3516F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr11:117109496 A>C maps to NM_207343.2 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr11:117150912 G>A maps to NM_207343.2 E361E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr7:5780711 A>G maps to NM_207111.2 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr7:5663693 C>T maps to NM_207111.2 K815K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr7:5800730 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr7:5779183 G>C maps to ENST00000389900 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr6:125284220 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr13:79190809 A>C maps to NM_024546.3 T362T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr1:45115221 G>C did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr1:45115371 G>C maps to ENST00000453887 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:119207070 C>T maps to NM_032015.3 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr16:30778081 G>A maps to NM_014771.2 Q438Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr16:30780683 G>T maps to NM_014771.2 E809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr17:56435411 G>A maps to NM_017763.4 V575V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5FO-01A-21D-A28B-09 chr17:56435252 G>A maps to NM_017763.4 D628D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr17:56434536 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr13:26788557 G>A maps to NM_005977.3 I487I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr6:37321863 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr6:89563356 G>A maps to NM_003800.3 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr11:494944 G>A maps to NM_203389.1 D412D. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-JW-A5VL-01A-11D-A28B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:685695 G>C maps to NM_018146.2 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr1:104068791 C>T maps to NM_017619.3 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:201970887 C>A maps to NM_020216.3 I473I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr2:241514235 G>A did not map to a codon.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr3:78734953 G>A maps to NM_002941.3 C428C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr3:78706262 G>A maps to NM_002941.3 Q867*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr3:77611800 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr18:18562726 G>A maps to NM_005406.2 F852F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr18:18586467 G>A maps to NM_005406.2 Q577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr18:18534771 C>T maps to NM_005406.2 K1275K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr20:34287610 C>T maps to NM_080748.2 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr9:94538028 G>A maps to NM_004560.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr9:94519830 C>G maps to NM_004560.2 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr15:61468388 A>G did not map to a codon.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr15:60803665 C>T maps to NM_134260.2 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr1:151785549 G>A did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr1:151785516 G>A maps to ENST00000392697 I451I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr1:151785498 G>A maps to ENST00000392697 F457F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr1:151785699 C>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:151783994 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:151780037 G>C maps to ENST00000392697 L543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QE-01A-21D-A21Q-09 chr6:117710545 G>A maps to NM_002944.2 Q576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr6:117622175 C>A maps to NM_002944.2 E2232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr6:117650502 G>A maps to NM_002944.2 I1785I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr8:55534095 C>T maps to NM_006269.1 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr8:55538850 T>A maps to NM_006269.1 P803P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr8:55542412 C>T maps to NM_006269.1 Q1991*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr8:10480213 C>T maps to NM_178857.5 Q166Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr8:10466720 G>C maps to NM_178857.5 L1629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr23:46719527 C>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr17:1798301 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr23:96139471 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr23:96139478 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr23:96139683 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr23:96139911 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr23:96139948 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr17:5324783 C>T maps to NM_001033002.3 Q84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr15:41812580 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr15:41812657 G>A maps to NM_015540.2 V1242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr15:41815044 G>C maps to NM_015540.2 S887*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:92789378 C>A maps to NM_024813.2 S301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr23:38156566 C>T did not map to a codon.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr23:38146174 C>G did not map to a codon.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr23:38146591 T>G did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:38135961 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:38156573 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:38146371 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:38132721 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:38146819 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:38158228 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr23:38180281 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:38146057 C>A did not map to a codon.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr23:38146663 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr14:21788327 C>T maps to NM_020366.3 Q487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr14:21780020 C>G maps to NM_020366.3 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WH-01A-22D-A351-09 chr14:21793409 C>T maps to NM_020366.3 F745F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H6-01B-11D-A22X-09 chr14:21769220 G>A maps to NM_020366.3 Q105Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr14:21756214 C>G maps to NM_020366.3 S27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr16:53729284 G>A did not map to a codon.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr12:113314456 G>C maps to NM_001143854.1 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr12:113285527 C>A maps to NM_001143854.1 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr2:88991296 C>T maps to NM_144563.2 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr23:153629108 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr6:35436226 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LC-01A-11D-A20U-09 chr6:35436195 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr6:35436279 C>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:24022862 A>C maps to NM_000975.3 *179Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:24022844 C>T maps to NM_000975.3 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr3:40503458 G>A maps to NM_001034996.1 K128K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr19:55899501 G>A maps to NM_001136134.1 W137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr19:55899663 G>A maps to NM_000991.4 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr3:52027808 G>A maps to NM_000992.2 Q146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr9:127623690 C>T did not map to a codon.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr19:5691503 G>T did not map to a codon.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr19:5691565 G>A maps to NM_015414.3 K84K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr23:118920603 C>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:118921284 C>T did not map to a codon.
Sequencing variant TCGA-EA-A50E-01A-21D-A26G-09 chr15:66793300 G>C maps to NM_000968.2 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr15:66797731 G>A did not map to a codon.
Sequencing variant TCGA-C5-A7CH-01A-11D-A33O-09 chr12:56510564 C>G did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr12:112843701 C>T maps to NM_001024662.1 R223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr8:74203305 G>A maps to ENST00000396470 I264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:136216354 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr9:136216848 G>A maps to NM_000972.2 E119E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr8:146015305 G>A maps to NM_000973.3 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5O9-01A-11D-A28B-09 chr12:120638790 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:120634584 G>C maps to NM_053275.3 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:128341189 G>C maps to NM_002950.3 V486V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:128345601 C>T maps to NM_002950.3 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr3:58303747 C>T did not map to a codon.
Sequencing variant TCGA-FU-A770-01A-11D-A33O-09 chr10:92631787 G>A maps to ENST00000458617 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr1:150443761 C>A maps to NM_015203.3 R780R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:150390096 C>G maps to NM_015203.3 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr19:39923927 C>T maps to NM_001020.4 Q142Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZE-01A-11D-A28B-09 chr6:33239879 C>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:42365219 C>A maps to NM_001022.3 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr19:42364870 G>C maps to NM_001022.3 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr16:2012213 C>T maps to NM_002952.3 W256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr20:60962390 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr5:81573525 G>A maps to NM_001025.4 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr2:55459971 C>T maps to NM_001177413.1 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QD-01A-32D-A22X-09 chr19:8386553 G>A maps to NM_001031.4 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A44S-01A-12D-A26G-09 chr19:8386419 C>T maps to NM_001031.4 D2D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr14:50050371 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr23:71495567 G>A did not map to a codon.
Sequencing variant TCGA-EA-A556-01A-11D-A26G-09 chr23:71493750 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr23:71495420 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:71494327 A>C did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:58906056 G>A maps to NM_001009.3 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R9-01A-11D-A18J-09 chr9:19376657 T>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr9:19378853 G>T maps to NM_001010.2 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:166918097 G>C maps to ENST00000510118 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5O9-01A-11D-A28B-09 chr6:166872943 C>T maps to ENST00000510118 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr6:166827356 G>A maps to ENST00000510118 L692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr23:20185771 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73R-01A-11D-A33O-09 chr23:20179861 T>A did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr23:83320048 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr23:83372121 C>T did not map to a codon.
Sequencing variant TCGA-LP-A4AU-01A-32D-A243-09 chr23:83351214 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:83351281 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A73Q-01A-21D-A32I-09 chr23:83357097 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73Q-01A-21D-A32I-09 chr23:83362645 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr11:67200647 G>A maps to NM_003952.2 W253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:67202363 C>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr11:67202295 C>T did not map to a codon.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr11:67200800 C>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr1:213414588 C>T maps to NM_012424.3 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr1:213446675 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr1:213446894 C>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr14:75377987 G>A maps to NM_031464.3 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr17:78939905 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr17:78518702 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr17:78796981 C>T maps to NM_020761.2 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr15:40865973 C>G maps to NM_152260.1 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PI-01A-11D-A18J-09 chr3:9885373 G>A did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr11:126081455 G>A maps to NM_032795.2 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr1:39318162 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr19:50139082 G>A maps to NM_006270.3 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr20:17596582 G>A maps to ENST00000377813 A1313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr20:17606198 G>T maps to ENST00000377813 I1004I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3TQ-01A-11D-A22X-09 chr20:17640440 G>A maps to ENST00000377813 Q238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr6:7229751 C>T maps to NM_001003699.3 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr11:4159524 C>G maps to NM_001033.3 S764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R3-01A-11D-A28B-09 chr11:4116009 C>A did not map to a codon.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr2:10262999 C>T maps to NM_001165931.1 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr2:10263581 C>T maps to NM_001165931.1 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr16:15155746 C>A maps to NM_018427.3 E604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PI-01A-11D-A18J-09 chr16:15188040 G>T maps to NM_018427.3 S17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PI-01A-11D-A18J-09 chr1:218475648 G>A maps to NM_016052.3 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr21:45104457 C>T maps to NM_015056.2 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr3:51970551 C>T maps to NM_004704.3 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr3:51967557 G>T maps to NM_004704.3 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr8:67342457 G>A maps to NM_015169.3 R364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr8:67342187 C>T maps to NM_015169.3 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr23:18662592 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr23:18662564 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:18660270 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr17:48559579 G>A maps to NM_018346.1 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr2:7033824 G>C maps to NM_080657.4 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2GZ-01A-11D-A17W-09 chr7:77326304 C>T maps to NM_198467.2 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A69L-01A-11D-A32I-09 chr11:77436744 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr11:77378487 G>C maps to NM_016578.3 S1267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr7:6825629 C>T maps to NM_173565.3 V603V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr7:6820457 C>T maps to NM_173565.3 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr8:108913362 C>T maps to NM_178565.4 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:12936534 G>A maps to NM_031429.1 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H1-01A-11D-A17W-09 chr22:23478485 C>T maps to ENST00000406876 *109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr20:62293290 C>G maps to ENST00000482936 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr20:62324336 G>A maps to ENST00000482936 K944K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr15:41768711 G>A maps to NM_015138.4 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr15:41772870 C>T maps to NM_015138.4 R707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr10:63957837 C>T maps to NM_145307.2 Q553Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr10:64028351 C>T maps to NM_145307.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr14:101348764 C>T maps to NM_001134888.2 V787V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5FO-01A-21D-A28B-09 chr19:45997640 C>T maps to NM_005619.3 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr19:45998372 G>C maps to NM_005619.3 S20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr2:55253893 G>A maps to NM_020532.4 F447F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr2:55201028 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr6:107076724 G>T maps to NM_032730.4 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr11:57235244 C>G maps to NM_178570.1 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr11:57244278 C>T maps to NM_178570.1 P386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr3:186917515 C>T maps to NM_153708.2 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr3:187416339 G>A maps to NM_001004312.2 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr18:67781754 G>A maps to NM_173630.3 V1203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr18:67718768 G>C maps to NM_173630.3 S1734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr18:67684777 G>A maps to NM_173630.3 L2096L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr18:67781754 G>A maps to NM_173630.3 V1203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr10:70139147 G>C did not map to a codon.
Sequencing variant TCGA-JW-A5VI-01A-11D-A28B-09 chr10:70103366 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr10:70105421 C>A did not map to a codon.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr4:71588331 C>T maps to NM_001037442.2 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:218938011 G>T maps to NM_198483.3 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr17:41143000 G>A maps to NM_173079.2 Q370Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr17:41143036 G>T maps to NM_173079.2 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr21:36228597 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr8:93004061 G>A maps to NM_175634.2 R266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr8:93027007 G>A maps to NM_175634.2 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr8:92988169 C>T maps to NM_175634.2 A437A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AX-01A-12D-A243-09 chr8:92982944 T>A maps to NM_175634.2 K494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr8:93026940 G>A maps to NM_175634.2 Q112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr8:93026983 G>A maps to NM_175634.2 F97F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr6:45390609 C>G maps to ENST00000359524 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr1:155294394 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr1:155295079 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:155300517 C>G did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:155296725 C>G maps to NM_001105203.1 V739V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr9:35560822 C>T maps to NM_001135999.1 Q1396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QD-01A-32D-A22X-09 chr19:49518397 G>C maps to NM_006666.1 R414R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr19:49510585 G>A maps to NM_006666.1 E141E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr21:30391661 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr1:95712056 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:95712056 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr13:32367058 C>T maps to NM_130806.3 V540V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr1:155912315 G>A maps to NM_181885.2 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr9:137330789 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr9:137330788 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr6:33162459 C>T maps to ENST00000374685 *538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr6:33168157 G>A maps to ENST00000374685 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr19:38976784 C>T maps to NM_000540.2 V1830V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr19:38991619 C>A maps to NM_000540.2 S2535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr19:39051943 C>T maps to NM_000540.2 R4158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CH-01A-11D-A33O-09 chr19:38948805 T>C maps to NM_000540.2 L681L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr19:38979845 G>A maps to NM_000540.2 V1859V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr19:38949864 C>T maps to NM_000540.2 L749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr19:38990367 C>G maps to NM_000540.2 S2374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:39055627 C>T maps to NM_000540.2 F4218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr19:38945894 G>C maps to NM_000540.2 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr19:39056335 C>T maps to NM_000540.2 L4454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr19:38973964 C>T maps to NM_000540.2 S1581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:237947566 G>A maps to NM_001035.2 K4185K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:237872192 C>T maps to NM_001035.2 Q3313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr1:237947389 G>A maps to NM_001035.2 L4126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr1:237936945 C>T maps to NM_001035.2 Q3925*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:237780710 C>T maps to NM_001035.2 V1947V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:237870321 C>T maps to NM_001035.2 I3218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr1:237919655 G>A maps to NM_001035.2 E3738E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:237617846 G>A maps to NM_001035.2 K483K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:237947563 G>A maps to NM_001035.2 E4184E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:33988602 C>T maps to NM_001036.3 I2015I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr15:34021063 C>A maps to NM_001036.3 S2347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr15:34113778 C>T maps to NM_001036.3 N3657N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A5QV-01A-22D-A28B-09 chr15:34112004 C>T maps to NM_001036.3 A3585A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr15:33927941 C>T maps to NM_001036.3 V1101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr1:153588399 G>C did not map to a codon.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr1:153520279 G>A maps to NM_002960.1 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr1:101704599 C>T maps to NM_001400.4 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr1:101705514 C>T maps to NM_001400.4 I325I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr19:10333440 G>T did not map to a codon.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr19:10625528 C>T maps to NM_001166215.1 E53E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr11:18105252 G>T maps to NM_138421.2 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr3:45751042 T>C maps to NM_014016.3 D129D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr13:23908102 G>C maps to NM_014363.4 L3304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr13:23914000 C>T maps to NM_014363.4 K1338K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr19:47658463 C>G maps to NM_005500.2 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr2:234229393 C>T maps to NM_000541.4 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:134991911 T>C did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:134994536 G>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:134989559 G>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q8-01A-11D-A21Q-09 chr23:134994495 C>G did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr23:134989156 C>T did not map to a codon.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr18:76754228 G>A maps to NM_171999.2 K746K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr20:50407562 G>A maps to NM_020436.3 Q487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr20:50408526 G>T maps to NM_020436.3 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr19:14200003 C>T maps to ENST00000269724 E272E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr6:130505719 C>T maps to ENST00000457563 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr19:39850654 C>G did not map to a codon.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr19:39868420 C>T maps to NM_018028.2 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr6:147830477 C>A maps to NM_001030060.2 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AU-01A-32D-A243-09 chr10:76910348 G>A maps to ENST00000372690 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr22:44368761 C>T maps to NM_015380.4 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr21:15858250 G>A maps to ENST00000285670 I436I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr2:128783856 G>A maps to NM_001145928.1 Q30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr2:128767908 G>C maps to NM_001145928.1 S294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CH-01A-11D-A33O-09 chr13:21720740 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr7:100170080 C>G maps to NM_001168682.1 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr4:174292223 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr9:136577742 G>A maps to NM_007101.3 I442I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr9:136583880 T>C did not map to a codon.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr1:109780428 T>C maps to ENST00000369923 H510H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H1-01A-11D-A17W-09 chr1:109779285 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr12:108942981 G>A maps to NM_014706.3 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:108919339 G>C maps to NM_014706.3 S806*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr6:148846468 C>T maps to NM_015278.3 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr23:128922005 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:128914079 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr23:128913962 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A6DV-01A-11D-A32I-09 chr23:128926433 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr1:100598422 C>T did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr1:100571328 C>G maps to NM_194292.1 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr2:200173587 C>A maps to NM_001172509.1 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr2:200213500 G>A maps to NM_001172509.1 Q366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A69M-01A-11D-A32I-09 chr23:84362390 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr7:66460332 C>T maps to NM_016038.2 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr11:9867226 G>A maps to NM_030962.3 Q999*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr11:10024134 G>A maps to NM_030962.3 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3EO-01A-11D-A20U-09 chr19:56042596 G>A maps to NM_001101401.2 Y123Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr12:123805112 G>A maps to NM_001167856.1 Q845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr19:1119066 G>A maps to NM_014963.2 I490I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr19:36017548 C>T maps to NM_001166034.1 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:50154542 G>A maps to NM_021228.2 E299E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr9:127828299 G>A maps to NM_173690.4 Q46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr1:155226554 C>T maps to NM_005698.2 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr6:28540338 G>A maps to NM_052923.1 F1109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr3:47465421 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A73Q-01A-21D-A32I-09 chr15:76998297 G>T maps to ENST00000324767 L731L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VH-01A-11D-A28B-09 chr8:27737164 C>T maps to NM_173833.5 K424K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr12:125298945 C>A maps to NM_005505.4 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr12:125296451 C>T maps to NM_005505.4 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr22:20786086 C>G maps to NM_153334.4 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr22:20784795 G>A maps to NM_153334.4 F374F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr1:246927546 G>A did not map to a codon.
Sequencing variant TCGA-EX-A449-01A-11D-A243-09 chr4:83601867 G>A maps to NM_001037582.2 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr4:83719651 G>A maps to NM_001037582.2 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr13:78176202 C>T maps to NM_144777.2 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr4:53752027 G>A maps to NM_152540.3 S616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr2:224462893 G>C maps to NM_003469.4 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr2:224462209 G>A maps to NM_003469.4 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3YQ-01A-11D-A22X-09 chr15:32972021 C>T maps to NM_001144757.1 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr6:25689738 A>G maps to NM_006998.3 K204K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr1:41651895 A>C did not map to a codon.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr23:17768234 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr23:18283731 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr3:38739814 C>T maps to NM_006514.2 V1632V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:38926867 G>C maps to ENST00000302328 S992*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr2:166848732 G>A maps to NM_001165963.1 Y1684Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr2:166211084 C>T maps to NM_001040142.1 L1101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZE-01A-11D-A28B-09 chr2:166167040 G>A maps to NM_001040142.1 G302G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:166246237 G>T maps to NM_001040142.1 S1974S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr2:166226733 G>A maps to NM_001040142.1 L1258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr2:166188011 C>G maps to NM_001040142.1 L774L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr17:62020420 C>T maps to NM_000334.4 T1351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr17:62020420 C>T maps to NM_000334.4 T1351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr17:62022989 C>T maps to NM_000334.4 V1150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr17:62022074 G>A maps to NM_000334.4 F1290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr17:62022107 G>A maps to NM_000334.4 I1279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr17:62019318 G>A maps to NM_000334.4 F1441F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr11:118006541 C>G did not map to a codon.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr3:38627472 G>A maps to NM_001099404.1 I832I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr3:38645226 C>T maps to NM_001099404.1 V622V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr3:38595845 C>A maps to NM_001099404.1 L1579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr2:167289235 C>T maps to NM_002976.2 V728V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr2:167319024 T>A maps to NM_002976.2 G319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VI-01A-11D-A28B-09 chr2:167328849 G>A maps to NM_002976.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr12:52180552 G>A maps to NM_014191.2 K1390K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr12:52168058 C>A maps to NM_014191.2 I1244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr2:167056374 C>A did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr2:167055592 C>T maps to ENST00000303354 E1853E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:167142953 C>T maps to ENST00000303354 E499E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr2:167138231 C>T maps to ENST00000303354 Q688Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr2:167108372 G>C maps to ENST00000303354 S1126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr1:151139287 G>A did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr12:6457039 C>T maps to NM_001159576.1 *729*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr16:23366648 C>T maps to ENST00000307331 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:1217633 C>G did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr16:23197693 C>G maps to NM_001039.3 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr16:23226540 G>A maps to NM_001039.3 Q567Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr22:50962088 G>T maps to NM_001169111.1 S251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:55065598 C>G maps to NM_021626.2 S165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr8:144891726 G>A maps to NM_182706.3 Y564Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr8:144896061 G>A maps to NM_182706.3 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:45918125 G>A maps to NM_138355.3 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:175260628 G>C did not map to a codon.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr22:43606202 G>T maps to NM_173050.2 I809I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr22:43608439 C>A maps to NM_173050.2 E738*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr22:43604186 G>A maps to NM_173050.2 Y875Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr11:9074757 C>T maps to ENST00000457346 V445V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:100704856 G>A maps to NM_017988.4 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr2:20402527 C>T maps to NM_001006946.1 *311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr8:97614701 A>G maps to NM_002998.3 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr20:43955981 C>T maps to NM_002999.2 K173K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr20:43959177 C>T maps to NM_002999.2 E91E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr9:139302310 C>T maps to NM_001039707.1 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr9:139298549 G>A maps to NM_001039707.1 Q389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr9:139299683 T>G did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:243579061 C>T maps to NM_006642.3 Q559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HR-01A-11D-A20U-09 chr17:26989105 C>A did not map to a codon.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr5:236601 G>A maps to NM_004168.2 E440E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr5:228352 G>C maps to NM_004168.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr1:17349635 T>A did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr1:17350560 G>C maps to NM_003000.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr1:161284264 G>C did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:161326587 C>T maps to NM_003001.3 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3EO-01A-11D-A20U-09 chr1:161326590 C>T maps to NM_003001.3 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3TX-01A-11D-A22X-09 chr11:111965692 G>C maps to NM_003002.2 *160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr17:71354290 G>A maps to NM_001144952.1 I1840I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr17:71429874 C>T maps to NM_001144952.1 Q436Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr12:57324158 C>G maps to NM_148897.2 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr17:26692211 G>A maps to NM_001080837.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr17:75186916 G>A maps to NM_001039573.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr22:30805240 C>G maps to NM_012429.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr22:30793104 G>T did not map to a codon.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr22:30867220 G>C maps to ENST00000434642 S33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr22:30866216 C>T maps to NM_174975.4 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr22:30890921 C>G maps to NM_174977.3 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H1-01A-11D-A17W-09 chr22:30887560 G>C maps to NM_174977.3 V360V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr22:30885863 C>G maps to NM_001161368.1 *361Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr9:139371509 C>T maps to NM_014866.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr9:139342932 G>A maps to ENST00000313084 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr9:139368803 G>A maps to NM_014866.1 P1088P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr9:139357482 C>A maps to NM_014866.1 T1583T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr9:139371805 G>A maps to NM_014866.1 Q88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7X3-01A-11D-A351-09 chr3:122920796 G>T did not map to a codon.
Sequencing variant TCGA-EA-A5FO-01A-21D-A28B-09 chr1:145116678 T>C did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:145116214 G>C did not map to a codon.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr5:134010892 C>G maps to NM_021982.1 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr5:134002534 G>A maps to NM_021982.1 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr10:75511671 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr10:75523301 G>T maps to NM_198597.1 G348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr10:75529388 G>T maps to NM_198597.1 L860L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr4:119653978 G>C maps to ENST00000379735 S863*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr4:83787986 G>A maps to ENST00000505472 R391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr4:83774806 G>A maps to ENST00000505472 L690L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A69B-01A-11D-A32I-09 chr10:102247513 G>T maps to NM_015490.3 A1133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr9:101984963 G>C did not map to a codon.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr9:91939383 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr20:13899728 G>A maps to NM_025229.1 D108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5FO-01A-21D-A28B-09 chr20:13894426 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr4:25848924 G>A maps to NM_015187.3 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr3:53925850 C>A did not map to a codon.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr1:169677747 T>G maps to NM_000655.4 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr1:169677816 C>T maps to NM_000655.4 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr1:169676571 G>C maps to NM_000655.4 S177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:169560701 C>T did not map to a codon.
Sequencing variant TCGA-EA-A5O9-01A-11D-A28B-09 chr7:83640559 T>C maps to NM_006080.2 K288K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr7:84751141 C>T maps to NM_152754.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7X3-01A-11D-A351-09 chr3:52476765 C>T maps to NM_020163.1 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:156126184 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr15:90768585 C>G maps to NM_198925.2 S493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr2:74902125 C>T maps to NM_004263.3 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr2:74902682 C>T maps to NM_004263.3 I468I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:74902650 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr10:102738362 G>A maps to NM_017893.2 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr5:9122802 G>A maps to NM_003966.2 C582C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr5:9197372 G>A maps to NM_003966.2 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr3:122634438 G>A maps to NM_001031702.2 F612F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr5:115822518 G>T maps to ENST00000257414 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr19:4550842 C>T maps to NM_032108.3 T363T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr1:151104756 C>T maps to ENST00000392792 E510E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr15:48056111 G>A maps to NM_153618.1 E271E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr15:48052057 C>T maps to NM_153618.1 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr15:74704300 G>A maps to NM_003612.3 F449F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr20:43836629 C>G maps to NM_003007.3 S231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr12:48482957 G>A maps to ENST00000339976 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:185344102 G>C maps to ENST00000427465 L618L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr6:76425308 G>A maps to NM_015571.2 *1113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr15:72432488 T>C maps to NM_145204.3 C175C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr16:30456154 G>C maps to ENST00000478753 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr16:30394216 G>T did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr16:30390801 C>T maps to NM_052838.3 G238G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr16:30392727 C>G maps to NM_052838.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr4:77917576 G>C did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr16:4833396 C>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr16:4833500 C>A maps to NM_144605.3 E230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr16:4835863 C>A maps to NM_144605.3 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr7:55902132 C>T maps to NM_207366.2 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr23:118763246 A>T did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:118763423 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr17:75370192 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr17:75478550 G>T did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr17:75398438 C>T maps to NM_001113491.1 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr1:67890584 G>C maps to NM_001018067.1 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr15:44092973 C>T maps to NM_016400.3 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr15:44092742 C>T did not map to a codon.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr11:17899777 G>C maps to NM_012139.2 S342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr1:31896550 C>T maps to NM_178865.4 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr1:31907412 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr5:79465308 G>A maps to NM_001174072.1 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr5:79465311 G>A maps to NM_001174072.1 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr3:150264651 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr3:150263565 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr13:44948220 G>A maps to NM_001010897.1 Q20Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr14:94849130 C>T maps to NM_001127707.1 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr14:95081042 C>T maps to ENST00000393080 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr14:95053974 G>A maps to NM_000624.4 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr14:94780391 G>C maps to NM_001756.3 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr23:105277519 C>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:105280683 T>C did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:105280794 G>A did not map to a codon.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr23:105279117 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr23:105279278 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr23:105281066 C>G did not map to a codon.
Sequencing variant TCGA-HG-A2PA-01A-11D-A20U-09 chr14:94945594 C>T did not map to a codon.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr6:2836095 C>T maps to NM_030666.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3PZ-01A-11D-A21Q-09 chr18:61322840 G>T did not map to a codon.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr18:61324220 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr18:61468246 G>T did not map to a codon.
Sequencing variant TCGA-C5-A7CJ-01A-11D-A32I-09 chr6:2890800 C>A maps to NM_004155.4 E243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:173878879 C>T maps to NM_000488.3 E321E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr11:75277831 C>T maps to NM_001235.2 F146F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3WB-01A-11D-A22X-09 chr11:75278008 C>T maps to NM_001235.2 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr3:167508189 C>G maps to NM_005025.4 S94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr19:40946981 C>G did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:28600016 C>G maps to NM_031459.3 S300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:28598237 G>A maps to NM_031459.3 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr1:28601430 C>T maps to NM_031459.3 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr11:94908717 T>A maps to NM_144665.2 R446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr9:131457726 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr9:131457172 T>G did not map to a codon.
Sequencing variant TCGA-FU-A3TQ-01A-11D-A22X-09 chr9:131454135 G>C did not map to a codon.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr9:131457119 G>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr18:42532103 C>G maps to NM_015559.2 L933L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WH-01A-22D-A351-09 chr16:30982736 C>T maps to NM_014712.1 L1019L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr16:30991902 C>T maps to NM_014712.1 I1502I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr14:99865318 C>T maps to NM_032233.2 E494E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr3:9476151 C>T maps to ENST00000407969 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr16:58550510 C>G maps to NM_001160305.1 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2GZ-01A-11D-A17W-09 chr12:123879786 C>A maps to NM_020382.3 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:123875254 C>T maps to NM_020382.3 Q71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:150917568 C>T maps to NM_001145415.1 V375V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:150923105 C>A maps to NM_001145415.1 R585R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZE-01A-11D-A28B-09 chr9:135150444 C>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr9:135205298 G>C maps to ENST00000372169 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A69L-01A-11D-A32I-09 chr9:135205160 C>G maps to ENST00000372169 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr9:135204701 C>T maps to ENST00000372169 S761S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr9:135205464 G>C maps to ENST00000372169 S507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr22:26565670 C>T maps to NM_021115.4 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A5XV-01A-11D-A28B-09 chr22:26707734 G>A maps to NM_021115.4 A561A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr22:26688507 G>A maps to NM_021115.4 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr16:29910334 C>T maps to NM_201575.2 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr16:29883599 G>A maps to NM_201575.2 Q871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr11:64536693 C>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr22:30736705 G>C maps to NM_005877.4 V389V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:38444714 G>A maps to NM_006802.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A50E-01A-21D-A26G-09 chr2:198260895 C>T maps to NM_012433.2 L1141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr11:65827431 C>T maps to NM_006842.2 F527F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr16:70590889 G>A maps to NM_012426.4 E656E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr22:32009452 C>T maps to NM_001007467.1 L893L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LS-01A-22D-A22X-09 chr3:53003240 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3TX-01A-11D-A22X-09 chr3:52962219 G>A maps to NM_016329.3 I345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr3:52939265 G>A maps to NM_016329.3 L829L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr10:7423843 G>C maps to NM_001018039.1 S6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZF-01A-11D-A28B-09 chr10:7318928 G>A maps to NM_001018039.1 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr10:7218003 C>T maps to NM_001018039.1 L644L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr1:27189708 G>A maps to NM_006142.3 E2E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RE-01A-11D-A18J-09 chr1:35645340 G>T did not map to a codon.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr8:41122838 G>C maps to NM_003012.4 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr10:99527271 C>T maps to NM_003015.3 *318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LS-01A-22D-A22X-09 chr8:22021505 C>T maps to NM_003018.3 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr8:22017203 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr10:104492658 C>T maps to NM_178858.4 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr10:120917550 C>T maps to NM_213649.1 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr2:73171778 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr13:23777967 C>T maps to NM_000231.2 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73R-01A-11D-A33O-09 chr1:66999881 C>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr8:8176254 G>A maps to NM_001080826.1 I1210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3PZ-01A-11D-A21Q-09 chr8:8185834 C>T maps to NM_001080826.1 V819V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr3:20202664 G>A maps to NM_001012410.3 R540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr10:72631649 C>G maps to NM_003901.3 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr10:72633154 G>A maps to NM_003901.3 K369K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr2:223423364 C>G maps to NM_152386.2 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr22:25289570 C>T maps to NM_001039948.2 I703I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr22:25297861 C>T maps to NM_001039948.2 C946C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PD-01A-11D-A351-09 chr22:25282578 C>T maps to NM_001039948.2 Q607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr19:2767200 C>T maps to NM_003021.3 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr5:64966099 G>A maps to NM_019072.2 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr8:19250841 C>G maps to NM_022071.3 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WH-01A-22D-A351-09 chr2:85660239 G>C did not map to a codon.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr2:85657722 C>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr15:78386531 C>T maps to NM_001101404.1 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3PZ-01A-11D-A21Q-09 chr22:38041471 C>T maps to NM_018957.3 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VI-01A-11D-A28B-09 chr4:2831493 C>T maps to NM_001145856.1 T344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:249105131 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr19:4361722 G>A maps to NM_003025.2 F327F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr19:4364096 C>T maps to NM_003025.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr23:19713766 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3HQ-01A-11D-A20U-09 chr23:19568180 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:19764467 G>C did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:19626094 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr5:171766799 G>A maps to NM_001017995.2 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HR-01A-11D-A20U-09 chr5:145317769 G>T maps to NM_152550.3 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr5:145379826 C>G maps to NM_152550.3 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr4:8229938 C>T maps to NM_018986.3 Q840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr5:148386524 T>G maps to NM_024577.3 P1198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr5:148406350 G>A maps to ENST00000394358 Q529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:70333106 C>T maps to ENST00000338508 R1091R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr11:70672690 C>T did not map to a codon.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr22:51113564 C>T maps to NM_001080420.1 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HG-A2PA-01A-11D-A20U-09 chr22:51117840 T>C maps to NM_001080420.1 C290C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr19:422298 G>A maps to NM_012435.2 H489H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A69B-01A-11D-A32I-09 chr19:434714 G>T maps to NM_012435.2 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr16:46655177 G>A maps to NM_024745.4 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr19:4284537 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr19:4283075 C>G maps to NM_020209.3 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr7:155604777 G>C maps to NM_000193.2 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:201860928 T>C maps to NM_198149.2 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr3:48509960 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr3:48538598 G>A maps to NM_016479.3 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr19:41083467 C>T maps to NM_138392.3 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr19:41083464 C>T maps to NM_138392.3 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A5XV-01A-11D-A28B-09 chr19:41083467 C>T maps to NM_138392.3 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr12:57628083 C>G maps to NM_005412.5 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr10:112771398 G>A maps to NM_007373.3 L524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RE-01A-11D-A18J-09 chr10:112679830 G>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr10:112724697 C>T maps to NM_007373.3 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr23:595404 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr3:157815851 C>G maps to NM_003030.4 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BE-01A-21D-A26G-09 chr17:3539498 C>T maps to NM_013276.2 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr3:72890221 G>A maps to NM_018130.2 R154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr5:132159473 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr5:132161161 G>C maps to NM_001172700.1 S224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr23:9864179 C>T did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr23:9864426 G>A did not map to a codon.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr23:9900722 C>A did not map to a codon.
Sequencing variant TCGA-DS-A7WI-01A-12D-A351-09 chr23:9864524 G>T did not map to a codon.
Sequencing variant TCGA-DS-A7WI-01A-12D-A351-09 chr23:9864525 A>G did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:9914962 G>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:77677799 G>A maps to NM_020859.3 Q1636Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr23:50341493 C>T did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr23:50350548 G>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr23:50378575 C>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:50345649 C>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:50350418 A>C did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:50377021 C>T did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:50351125 C>T did not map to a codon.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr3:164741480 G>A maps to NM_001041.3 S992S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr3:164714321 C>A did not map to a codon.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr3:113345004 C>T maps to ENST00000393830 F793F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr3:113345004 C>T maps to ENST00000393830 F793F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr11:117063943 C>T maps to NM_001040455.1 L727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:405937 G>A maps to NM_021805.2 A397A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr20:3677875 G>A maps to NM_023068.3 R746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr20:3684081 C>T maps to NM_023068.3 V330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HG-A2PA-01A-11D-A20U-09 chr20:3677953 G>A maps to NM_023068.3 Q720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr19:51917046 C>T maps to NM_033130.4 Q580Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr19:50453274 G>A maps to NM_052884.2 G683G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr19:52001467 G>A maps to NM_053003.2 V403V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr19:52002701 G>A maps to NM_053003.2 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr19:52002797 G>C maps to NM_053003.2 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr19:52001270 C>A did not map to a codon.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr19:52149137 G>T maps to NM_001098612.1 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr19:52115603 C>T maps to ENST00000222107 L512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr19:52033110 C>G maps to NM_001245.5 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr19:51958773 G>A maps to NM_014442.2 R317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A852-01A-11D-A351-09 chr19:51961225 A>T maps to NM_014442.2 L139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr19:51957936 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr19:51631764 C>T maps to NM_014441.2 Q401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr9:34636874 G>T did not map to a codon.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr21:44839822 G>C maps to NM_173354.3 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr11:111572231 G>A maps to NM_015191.1 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:111573943 C>T maps to NM_015191.1 R249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr11:116728695 G>C maps to ENST00000445177 S1155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr5:138282844 C>G maps to ENST00000509534 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr21:38081691 C>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr15:75682010 G>A maps to NM_001145357.1 I1001I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr19:16977348 C>T maps to NM_015260.1 I628I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:16986960 C>T maps to NM_015260.1 S928S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr11:65409787 G>A maps to NM_153253.29 E249E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr14:72196848 G>A maps to NM_015556.1 S1585S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr14:72054862 G>T maps to NM_015556.1 E92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr14:72090904 C>T maps to NM_015556.1 F590F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr14:72176351 C>T maps to NM_015556.1 F1414F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr1:232626796 C>T maps to NM_020808.3 L543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BE-01A-21D-A26G-09 chr1:232581532 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A73Q-01A-21D-A32I-09 chr1:232650404 A>G maps to NM_020808.3 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr19:38572046 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr19:38610311 C>T maps to NM_015073.1 I886I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73Q-01A-21D-A32I-09 chr19:38572483 G>A maps to NM_015073.1 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr19:38610011 C>T maps to NM_015073.1 F786F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr20:1902276 C>T maps to ENST00000400068 Q225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A50E-01A-21D-A26G-09 chr20:1918150 G>A maps to ENST00000400068 Q488Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3WB-01A-11D-A22X-09 chr20:1896051 C>T maps to ENST00000400068 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VG-01A-11D-A28B-09 chr20:1915397 C>T maps to ENST00000400068 Q422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr20:1532403 C>T maps to ENST00000381621 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr20:1615976 G>A maps to NM_018556.3 V339V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr10:69648777 C>G maps to NM_012238.4 S229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr12:120750453 C>G maps to NM_012240.2 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr12:120751012 C>G did not map to a codon.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr9:35649943 G>C maps to NM_014450.2 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr2:45169641 C>A maps to NM_005413.3 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr2:45169635 C>T maps to NM_005413.3 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr19:46268874 C>A maps to NM_175875.4 E702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr19:46271585 C>A maps to NM_175875.4 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr19:46268896 C>T maps to NM_175875.4 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A44S-01A-12D-A26G-09 chr14:60976682 G>A maps to ENST00000381716 K248K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr17:57189556 C>G did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr17:46214609 C>T maps to NM_003726.3 V356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:170079083 C>G maps to NM_005414.3 S322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr5:54696066 C>T maps to NM_015360.4 Q767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr5:54618186 C>G maps to NM_015360.4 S56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr5:36183986 C>T maps to ENST00000308927 I402I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr13:78320652 C>T maps to ENST00000389459 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:160604404 G>C maps to NM_003037.2 S233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:160616717 G>A maps to NM_003037.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:160721403 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr23:153717090 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr23:153716083 A>G did not map to a codon.
Sequencing variant TCGA-Q1-A5R1-01A-11D-A28B-09 chr23:153716977 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:51382140 C>T maps to NM_001174125.1 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr15:48539622 C>T maps to NM_000338.2 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr5:127449945 A>T maps to NM_001046.2 R307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:56918015 C>T maps to NM_000339.2 I575I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr16:56920998 C>T maps to NM_000339.2 L724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr20:44665957 C>T maps to NM_001134771.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr20:44681731 C>G maps to NM_001134771.1 L861L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73S-01A-11D-A33O-09 chr20:44669970 C>A maps to NM_001134771.1 I309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr5:1081830 C>T maps to NM_006598.2 A386A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VG-01A-11D-A28B-09 chr5:1078022 G>A maps to NM_006598.2 A518A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr3:124837624 C>G maps to NM_001195483.1 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr3:124802868 G>A maps to NM_001195483.1 I670I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr7:122755585 C>A maps to NM_022444.3 E592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr7:122774465 G>A maps to NM_022444.3 F310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr7:122787346 G>T maps to NM_022444.3 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr17:26820597 G>A maps to NM_001145975.1 K345K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr17:6604420 G>A maps to NM_177550.3 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr18:43224033 C>T maps to NM_007163.3 F420F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr18:43224123 C>T maps to NM_007163.3 S450S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr13:99361908 C>G maps to NM_005073.3 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr13:99356571 G>A maps to NM_005073.3 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr3:121647917 T>C maps to NM_021082.3 T477T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A5XV-01A-11D-A28B-09 chr3:121646561 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:121648192 G>C maps to NM_021082.3 V517V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr3:121647221 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr11:60714116 G>C maps to NM_016582.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr12:129299438 G>A maps to ENST00000376744 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr17:6945798 G>T maps to NM_153357.1 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr10:91195878 G>C maps to NM_213606.3 S409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr17:6940070 G>A maps to NM_201566.2 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr17:6940133 C>G maps to NM_201566.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:230910659 G>T maps to NM_152527.4 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr23:73740861 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr17:80195167 C>T maps to NM_001042423.1 Y174Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr17:80195569 G>A maps to NM_001042423.1 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LC-01A-11D-A20U-09 chr1:110919772 C>T maps to NM_004696.1 E347E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3TQ-01A-11D-A22X-09 chr17:73100197 C>T maps to ENST00000450736 V469V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr17:73096054 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr17:73094241 C>T maps to ENST00000450736 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:73101989 C>T maps to ENST00000450736 R500R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr6:25826751 C>T maps to NM_005074.3 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:25826703 G>A maps to NM_005074.3 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr6:25770362 C>T maps to NM_005495.2 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A5XV-01A-11D-A28B-09 chr11:22363304 C>T maps to NM_020346.2 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr11:22363241 C>T maps to NM_020346.2 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr19:49934388 C>A maps to NM_020309.3 V424V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr12:100787218 C>T maps to NM_139319.2 Y182Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A6QX-01A-12D-A33O-09 chr12:100787236 C>T maps to NM_139319.2 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr12:100784870 C>T maps to NM_139319.2 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr12:100813786 G>T maps to NM_139319.2 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr20:61598099 C>G did not map to a codon.
Sequencing variant TCGA-EX-A1H6-01B-11D-A22X-09 chr8:20036735 G>A maps to NM_001135691.2 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr8:20004822 G>A maps to NM_001135691.2 V470V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr10:50819082 G>A maps to NM_003055.2 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr10:50819880 T>G maps to NM_003055.2 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr21:46935895 C>T maps to NM_194255.1 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr21:46951726 G>A maps to NM_194255.1 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BE-01A-21D-A26G-09 chr1:169437991 G>A maps to NM_006996.2 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M1-01A-11D-A18J-09 chr2:228563509 C>T maps to NM_025243.3 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr2:228552883 G>A maps to NM_025243.3 Q438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr2:228552883 G>A maps to NM_025243.3 Q438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr9:4576645 T>G maps to NM_004170.5 L359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr5:36677064 G>C maps to NM_004172.4 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr19:47278772 G>C maps to NM_005628.2 V540V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr19:15067376 G>T maps to NM_005071.1 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr1:53580587 G>A maps to NM_006671.4 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:53600053 C>T maps to NM_006671.4 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr8:42286293 G>T maps to NM_006749.3 V592V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr8:42294922 C>T maps to NM_006749.3 E369E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LS-01A-22D-A22X-09 chr11:63072232 G>T maps to NM_001039752.3 T490T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr11:64366017 C>T maps to NM_144585.2 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr11:64366281 C>G maps to NM_144585.2 V319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr3:38316944 C>G maps to NM_004256.3 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr3:38354943 C>G maps to NM_004803.3 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr1:116534854 C>T maps to NM_018420.2 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr6:110759973 G>A maps to NM_033125.2 Y420Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr6:160638426 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr11:64993026 G>T maps to NM_001004326.4 E304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr11:64993247 C>T did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr6:3323945 C>G did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr6:3287168 G>A maps to ENST00000436008 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr5:131676381 G>A maps to NM_003059.2 Q523Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr11:62752072 C>T maps to NM_004790.3 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr11:62752042 G>A maps to NM_004790.3 F40F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr6:43267780 T>C maps to ENST00000372585 C268C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr11:63176207 C>G maps to NM_080866.2 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr20:4864394 C>T maps to NM_203327.1 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr2:220029971 G>C maps to NM_001144890.1 G370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr9:19786762 C>T maps to NM_020344.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr20:19701771 C>T maps to NM_020689.3 C641C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HG-A2PA-01A-11D-A20U-09 chr20:19666000 C>T maps to NM_020689.3 T440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr14:92923625 A>G did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr17:79674000 G>A maps to NM_002949.3 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr2:172648020 G>A maps to NM_003705.3 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A770-01A-11D-A33O-09 chr2:172691339 G>A maps to NM_003705.3 F216F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:129499592 G>C did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:129506940 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr10:70243194 G>C maps to NM_152707.2 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr22:41166797 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr5:140683186 G>A maps to NM_031947.2 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:794834 G>A maps to NM_001191061.1 I29I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr10:101370573 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr10:101371143 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr13:45971464 C>T maps to NM_001010875.2 K254K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr13:45975285 G>C maps to NM_001010875.2 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr8:104427123 C>T maps to NM_030780.3 W14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr8:104413814 G>A maps to NM_030780.3 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr1:9630369 C>T maps to NM_032315.2 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr17:8197762 G>A maps to NM_201520.1 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr17:8194263 G>A maps to NM_201520.1 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr8:23429091 C>T maps to NM_016612.2 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr8:23429134 C>T maps to NM_016612.2 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr4:186064506 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr7:87487977 G>C maps to NM_018843.3 S22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr19:6433694 G>A maps to NM_173637.3 Q4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr19:19221579 C>G maps to NM_178526.3 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr19:19221579 C>T maps to NM_178526.3 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr19:19216386 C>G maps to NM_178526.3 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr23:118588169 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr1:156177683 C>T maps to NM_014655.2 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr1:156163945 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:156169883 C>T maps to NM_014655.2 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr5:110089019 A>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr5:110091079 G>C did not map to a codon.
Sequencing variant TCGA-C5-A2M2-01A-21D-A18J-09 chr23:118604981 T>G did not map to a codon.
Sequencing variant TCGA-EA-A556-01A-11D-A26G-09 chr23:118603741 A>C did not map to a codon.
Sequencing variant TCGA-EA-A556-01A-11D-A26G-09 chr23:118603746 A>T did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:118604461 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A5R3-01A-11D-A28B-09 chr23:118603746 A>T did not map to a codon.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr23:1508323 G>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:1508374 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr4:983040 C>A maps to NM_213613.2 T562T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr12:58019064 C>T maps to NM_133489.2 T475T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A6QX-01A-12D-A33O-09 chr17:78196494 C>T maps to NM_173626.3 F92F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A6QX-01A-12D-A33O-09 chr17:78196635 C>G maps to NM_173626.3 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr17:78196985 C>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr5:149360292 T>C maps to NM_000112.3 I379I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:107434304 C>T maps to NM_000111.2 K51K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A50E-01A-21D-A26G-09 chr7:107431573 C>T maps to NM_000111.2 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr7:107303836 C>T maps to NM_000441.1 D87D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr7:107314772 C>T maps to NM_000441.1 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:48667572 G>A maps to NM_022911.2 I448I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr8:92374633 A>G maps to NM_134266.1 G456G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr8:92375747 G>A maps to NM_134266.1 V490V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:205892287 C>T maps to NM_134325.2 K565K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr19:17598091 G>A maps to NM_198580.1 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73Q-01A-21D-A32I-09 chr19:17611438 C>G maps to NM_198580.1 S490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr19:59010587 C>T did not map to a codon.
Sequencing variant TCGA-JX-A5QV-01A-22D-A28B-09 chr15:45559934 G>A maps to NM_004212.3 A380A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr9:86900260 G>T maps to NM_022127.2 S549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr6:44201201 C>T maps to ENST00000313248 F515F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U3-01A-11D-A28B-09 chr6:44197646 C>T maps to ENST00000313248 I185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr6:44197919 G>A did not map to a codon.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr6:44199823 C>T maps to ENST00000313248 I397I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr10:73115967 C>G maps to NM_018344.5 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:5331357 C>A maps to NM_153247.2 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr7:5342454 C>G maps to NM_153247.2 S493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr1:43392499 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr1:43392509 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:43395577 G>C maps to NM_006516.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr1:43395646 G>A maps to NM_006516.2 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DV-01A-11D-A32I-09 chr22:24227027 G>T maps to NM_030807.3 E502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr6:134349709 G>C maps to NM_145176.2 S418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr12:40422237 G>A maps to NM_052885.3 R264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr20:62374736 T>G did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:136340662 G>C maps to NM_017585.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr9:136338666 G>A maps to NM_017585.3 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr9:136343501 G>A maps to NM_017585.3 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr9:130166348 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr9:130167087 C>T did not map to a codon.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr4:9836555 G>A maps to NM_020041.2 T456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr4:9982226 G>A maps to NM_020041.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr1:220100373 G>A maps to NM_018713.2 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:220091630 C>T maps to NM_018713.2 Q308Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr1:26368272 G>A maps to NM_001004434.1 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:27480102 G>A maps to NM_003459.4 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr15:45814222 C>T maps to NM_013309.4 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr20:37356216 C>T maps to NM_080552.2 Y171Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr5:176824800 C>T maps to NM_003052.4 F478F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr5:176824812 C>A maps to NM_003052.4 I482I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr5:176824929 C>T maps to NM_003052.4 V521V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr4:25677794 C>T maps to NM_006424.2 I499I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr4:25677983 C>T maps to NM_006424.2 V562V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr9:140128913 C>T maps to NM_080877.2 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr9:140128657 C>T maps to NM_080877.2 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr23:48762064 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:48760735 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr1:100488413 C>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:100483335 C>T maps to ENST00000370153 I326I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr5:139946202 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr3:112299500 A>G maps to NM_017945.2 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr3:112301775 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr17:47781576 C>T maps to ENST00000415270 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr19:16664606 G>C maps to NM_024881.4 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr19:16664392 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VI-01A-11D-A28B-09 chr1:234444856 C>T maps to NM_173508.2 R207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr5:150714910 G>A maps to NM_181776.2 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr21:43955657 C>T maps to NM_018964.3 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr12:46591765 G>C maps to NM_030674.3 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr12:46599881 C>G maps to NM_030674.3 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DV-01A-11D-A32I-09 chr12:46589959 C>A did not map to a codon.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr17:79234146 G>A maps to NM_001037984.1 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr17:79226315 G>A maps to NM_001037984.1 L542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr17:79219517 C>T maps to NM_001037984.1 P1066P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr2:165755096 G>A maps to ENST00000409662 F357F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr12:46759015 C>G did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:50252125 C>T maps to NM_006841.4 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr23:48324405 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:48325233 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:48318138 G>A did not map to a codon.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr23:48317942 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr16:58712777 G>A maps to NM_018231.1 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A410-01A-11D-A243-09 chr5:55008362 G>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr5:55008343 G>T did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr10:18331701 G>A maps to NM_001145195.1 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr8:22262420 C>G maps to NM_001135153.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr19:2733270 C>T maps to NM_144564.4 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr19:2732802 G>C maps to NM_144564.4 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr12:56625234 G>A maps to NM_001135195.1 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr6:33169069 G>A maps to NM_006979.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr6:33171908 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr14:69864950 C>G did not map to a codon.
Sequencing variant TCGA-EX-A1H6-01B-11D-A22X-09 chr14:69864944 C>T did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr11:62648618 C>T maps to NM_001012661.1 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr11:62649361 C>T did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:190445310 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr2:190430188 G>A maps to NM_014585.5 C217C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WF-01A-11D-A351-09 chr1:205768157 G>A maps to NM_173854.4 H208H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3PZ-01A-11D-A21Q-09 chr1:205779627 C>G did not map to a codon.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr1:205764635 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr3:125727580 C>T maps to NM_001008485.1 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:108061568 C>T maps to NM_080546.3 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr19:10741982 C>T maps to NM_020428.3 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr19:10742317 C>T maps to NM_020428.3 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr19:10754059 G>A maps to NM_020428.3 *707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr19:10754000 C>T maps to NM_020428.3 F687F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr1:75683549 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr1:75702682 A>T maps to NM_152697.4 Y243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:75699773 C>G maps to NM_152697.4 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr1:8399733 C>A maps to ENST00000377479 L686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr1:8390365 C>T maps to ENST00000377479 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A770-01A-11D-A33O-09 chr1:8399604 C>T maps to ENST00000377479 I643I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr5:33963885 G>T maps to NM_016180.3 Y266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr9:115652151 A>G maps to NM_033051.3 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr13:29286974 G>C maps to NM_001135919.1 S301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr13:29275324 C>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr13:29287141 A>C maps to NM_001135919.1 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr13:29284945 G>A maps to NM_001135919.1 F365F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr17:19611825 G>C did not map to a codon.
Sequencing variant TCGA-DS-A1OA-01A-11D-A16Y-08 chr17:42335065 G>A maps to NM_000342.3 F464F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OA-01A-11D-A16Y-08 chr17:42335068 G>A maps to NM_000342.3 G463G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr17:42337836 G>A maps to NM_000342.3 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr2:162281185 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:162696378 G>T maps to NM_001178015.1 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr20:3210346 G>C maps to NM_001174090.1 S565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr20:3211113 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr2:27892131 C>G maps to NM_018158.2 S408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr2:27898426 G>A maps to NM_018158.2 W458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr7:150768845 C>T maps to NM_003040.3 F754F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr2:220502341 G>T maps to NM_201574.2 E886*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr2:220502407 G>T maps to NM_201574.2 E908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr4:72102353 G>T maps to NM_001098484.2 E21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr4:72412242 G>A maps to NM_001098484.2 V873V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr2:74486732 G>A maps to NM_021196.3 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr3:27427469 G>A maps to ENST00000454389 F1135F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr3:27427484 G>T maps to ENST00000454389 L1130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr12:51863469 C>G maps to NM_001039960.1 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr12:51888823 C>T maps to NM_001039960.1 F955F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr16:24902256 G>C maps to NM_052944.2 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A3L1-01A-11D-A21Q-09 chr16:24922823 C>T maps to NM_052944.2 C666C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:26732860 G>A maps to NM_178498.3 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr16:31496156 C>T maps to ENST00000431354 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr16:31500332 C>T maps to ENST00000431354 F471F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr16:31501801 C>G maps to ENST00000431354 L681L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3TX-01A-11D-A22X-09 chr22:32633297 C>T maps to NM_014227.2 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr2:27424682 G>C maps to NM_021095.2 V465V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr2:27429779 G>A maps to NM_021095.2 R142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HM-A3JK-01A-11D-A21Q-09 chr2:27426070 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr2:27430366 C>T maps to NM_021095.2 W51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr1:48713405 C>G did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr1:48703374 C>T maps to NM_001135181.1 V464V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr3:10960012 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73S-01A-11D-A33O-09 chr3:10976836 G>A maps to NM_014229.1 P566P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr12:369035 G>C maps to NM_016615.3 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr23:115574017 T>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:115582692 C>G did not map to a codon.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr1:110734775 C>T maps to NM_001010898.2 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr1:110734757 G>A maps to NM_001010898.2 T343T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R3-01A-11D-A28B-09 chr5:1219644 C>T maps to NM_001003841.2 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr16:55725924 C>G maps to NM_001043.3 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr16:55734064 C>G maps to NM_001043.3 V535V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr5:1409222 G>A maps to NM_001044.4 F472F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:20676573 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr11:20676506 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr11:20657922 C>T maps to NM_004211.3 I565I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr11:20623183 G>A maps to NM_004211.3 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr3:14486249 C>T maps to ENST00000435095 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr3:14499523 C>G maps to NM_001134367.1 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr5:149583534 G>A maps to NM_014228.3 K422K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr5:149576288 C>A maps to NM_014228.3 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr5:149581971 C>G maps to NM_014228.3 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr5:149576736 G>A maps to NM_014228.3 W161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M1-01A-11D-A18J-09 chr23:152957006 G>T did not map to a codon.
Sequencing variant TCGA-EA-A5ZF-01A-11D-A28B-09 chr23:152954232 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr23:152955983 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:152954236 G>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:152959914 G>C did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:152959017 A>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:152958161 C>G did not map to a codon.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr1:44490014 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr1:44466889 C>G maps to NM_201649.2 V500V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr13:30090362 G>T maps to NM_003045.4 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:33703232 G>A maps to NM_019849.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr3:170204043 G>A maps to NM_020949.2 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr3:170184914 C>T maps to NM_020949.2 K748K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr23:70148313 G>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:70145746 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr22:21385936 G>C maps to NM_004173.2 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr16:87872348 G>A maps to NM_003486.5 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr16:87902737 G>A maps to NM_003486.5 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr16:68328700 C>T maps to NM_003983.4 F372F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr19:33355544 G>C maps to NM_014270.4 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M2-01A-21D-A18J-09 chr19:33355559 C>T maps to NM_014270.4 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr19:33359428 A>G maps to NM_014270.4 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R9-01A-11D-A18J-09 chr2:40405621 G>T maps to NM_021097.2 S607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr19:47960515 G>A maps to NM_015063.2 I337I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr14:70512939 G>A maps to NM_183002.1 I836I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:27440752 G>C maps to NM_003047.3 S126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr1:27425850 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr2:103274407 C>T maps to NM_003048.3 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr2:103318927 C>G maps to NM_003048.3 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr16:2087933 C>T maps to ENST00000191922 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr2:103095451 C>A maps to NM_001011552.3 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr16:67283102 C>T maps to NM_004594.2 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr16:67290581 C>T maps to NM_004594.2 F374F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:135095118 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr23:135106632 T>C did not map to a codon.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr23:135080292 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:135067840 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr23:46541919 G>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:46522065 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:46513049 A>C did not map to a codon.
Sequencing variant TCGA-EA-A5O9-01A-11D-A28B-09 chr23:46618352 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:46466592 C>T did not map to a codon.
Sequencing variant TCGA-EA-A5O9-01A-11D-A28B-09 chr12:21355440 T>G maps to NM_006446.4 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr12:21028280 G>A maps to NM_019844.2 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr12:21242986 T>C maps to ENST00000381541 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr3:133661571 G>T maps to NM_005630.2 S501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr3:133664098 G>C maps to NM_005630.2 S434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:92459365 G>C maps to NM_013272.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr15:92706004 C>T maps to NM_013272.3 L591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr20:61290074 G>C maps to NM_016354.3 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr8:70744928 G>C did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr5:101813539 G>A maps to NM_173488.3 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr17:33690271 T>C maps to NM_152270.3 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A5QV-01A-22D-A28B-09 chr17:33592729 G>A maps to NM_144975.3 S833S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr1:41486317 C>T maps to NM_144990.3 K5K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr10:98794253 G>A maps to NM_003061.2 F804F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr4:20255563 C>T maps to ENST00000273739 H42H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr4:20597355 C>T maps to ENST00000273739 C1086C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr4:20597409 C>T maps to ENST00000273739 C1104C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QD-01A-32D-A22X-09 chr4:20569139 G>A did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr5:168199787 G>C maps to NM_003062.2 S486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr5:168176633 G>C maps to NM_003062.2 L660L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr5:168180966 G>A maps to NM_003062.2 F577F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr5:168620514 C>T maps to NM_003062.2 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr5:168151428 C>T maps to NM_003062.2 L777L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LS-01A-22D-A22X-09 chr13:84454532 C>T maps to NM_052910.1 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr13:84454214 G>T maps to NM_052910.1 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr13:84454367 G>T maps to NM_052910.1 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr13:84454439 G>A maps to NM_052910.1 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr13:84454448 G>A maps to NM_052910.1 Y398Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr13:84454520 G>C maps to NM_052910.1 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr13:84454934 G>A maps to NM_052910.1 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr13:84455051 G>A maps to NM_052910.1 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr13:84455408 G>A maps to NM_052910.1 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr13:84455447 C>A maps to NM_052910.1 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZF-01A-11D-A28B-09 chr23:144905445 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr23:144905848 G>A did not map to a codon.
Sequencing variant TCGA-C5-A2LS-01A-22D-A22X-09 chr3:164906467 G>A maps to NM_014926.2 G717G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr3:164906554 G>A maps to NM_014926.2 F688F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:142718309 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:142718887 T>C did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:142717612 C>G did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:142718329 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73S-01A-11D-A33O-09 chr23:142718807 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr13:88329805 C>T maps to NM_015567.1 G721G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3YQ-01A-11D-A22X-09 chr13:88329622 G>A maps to NM_015567.1 S660S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr13:88330294 C>T maps to NM_015567.1 P884P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr15:59186368 T>C maps to NM_024755.2 K467K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr8:143823320 G>A maps to NM_020427.2 Y26Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr4:146435947 G>A maps to NM_001003688.1 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr18:45374925 G>C maps to NM_001003652.2 S306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr15:67457306 G>A maps to NM_005902.3 W94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr18:48593410 C>T maps to NM_005359.5 Q388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A3L1-01A-11D-A21Q-09 chr18:48603031 C>T maps to NM_005359.5 R445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr5:135513102 C>T maps to NM_001001419.1 F444F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr5:135515181 G>T did not map to a codon.
Sequencing variant TCGA-EX-A1H6-01B-11D-A22X-09 chr15:67073398 C>T maps to NM_005585.4 H339H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr1:40879804 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:40887751 C>T maps to NM_022733.2 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:128615114 T>C did not map to a codon.
Sequencing variant TCGA-FU-A3WB-01A-11D-A22X-09 chr23:128582407 G>A did not map to a codon.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr9:2039778 G>A maps to NM_003070.3 Q223Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr9:2123738 G>C maps to NM_003070.3 R1261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr19:11172892 G>A did not map to a codon.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr19:11106995 G>T maps to NM_001128849.1 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr19:11105559 C>A maps to NM_001128849.1 S492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr19:11101917 C>T maps to NM_001128849.1 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73S-01A-11D-A33O-09 chr19:11129653 C>A maps to NM_001128849.1 Y820*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr19:11130307 G>A maps to NM_001128849.1 R849R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr4:144469251 C>T maps to NM_003601.2 Q982*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr4:144459761 C>T maps to NM_003601.2 F505F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr2:217347477 G>A maps to NM_014140.3 K881K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr22:24143247 G>A maps to NM_003073.3 K160K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr22:24129407 C>T maps to NM_003073.3 Q18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr22:24158953 C>T did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr22:24158945 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2GZ-01A-11D-A17W-09 chr3:47629583 G>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr3:47629596 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr12:56572821 G>C maps to NM_003075.3 S367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr12:56559332 G>A maps to NM_003075.3 Q970*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr12:50484355 C>T maps to NM_003076.4 I372I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr17:61910332 C>A maps to NM_001098426.1 E521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr7:150936712 G>C maps to NM_003078.3 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr17:38788619 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr23:53430513 C>T did not map to a codon.
Sequencing variant TCGA-C5-A7X3-01A-11D-A351-09 chr23:53438810 C>G did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:53407549 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:53439972 G>C did not map to a codon.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr23:53430535 T>G did not map to a codon.
Sequencing variant TCGA-C5-A3HF-01A-11D-A20U-09 chr9:106882374 G>A maps to NM_001042550.1 L688L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr9:106887245 G>T maps to NM_001042550.1 E771*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr3:160117443 G>C did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr3:160135674 C>G maps to NM_005496.3 L534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr2:17897484 G>A maps to ENST00000381272 Q491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr18:2697929 T>C maps to NM_015295.2 F411F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A411-01A-11D-A243-09 chr18:2728528 C>T maps to NM_015295.2 Q950*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3WB-01A-11D-A22X-09 chr18:2656257 C>T maps to NM_015295.2 Q62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr22:39910249 C>T maps to NM_019008.4 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr17:18219777 C>T maps to NM_144775.2 Y225Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5FO-01A-21D-A28B-09 chr17:18219720 G>A maps to NM_144775.2 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:91931635 C>T maps to ENST00000417249 L596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr2:55842569 G>C did not map to a codon.
Sequencing variant TCGA-EA-A5ZF-01A-11D-A28B-09 chr2:55804493 T>C did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr2:55842595 C>T maps to NM_001122964.1 Q63Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr2:55826042 C>A maps to NM_001122964.1 E144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr16:18937338 G>T maps to ENST00000389467 R9R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr16:18826563 G>A maps to ENST00000389467 V3519V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr16:18849987 G>C maps to ENST00000389467 V2323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr16:18849891 G>A maps to ENST00000389467 Y2355Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr16:18848734 G>A maps to ENST00000389467 L2482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr16:18860626 G>C maps to ENST00000389467 L1845L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr16:18881955 G>C maps to ENST00000389467 S823*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr16:18866112 C>A maps to ENST00000389467 E1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr16:18841281 G>A maps to ENST00000389467 F3033F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr1:156236368 G>A maps to NM_015327.2 G406G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr1:156228855 G>C maps to NM_015327.2 V794V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:156219816 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:156220032 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr17:2139834 C>G maps to NM_017575.4 L940L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:2195914 C>T maps to NM_017575.4 L756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr17:1990371 G>A maps to ENST00000354901 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3PZ-01A-11D-A21Q-09 chr17:1964522 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:183520228 G>A maps to ENST00000367537 E1115E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VI-01A-11D-A28B-09 chr7:128845479 G>A maps to NM_005631.4 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr20:4163253 C>T maps to ENST00000443211 F376F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr20:4168035 C>G maps to ENST00000443211 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr11:6412642 C>T maps to NM_000543.4 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:6412746 C>G maps to NM_000543.4 S151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr6:109763768 G>A maps to NM_003080.2 Q144Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr16:68398471 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr2:130910713 C>A maps to NM_017951.4 E725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr6:123130432 T>C maps to NM_006714.3 Y414Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7X3-01A-11D-A351-09 chr23:21990687 C>T did not map to a codon.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr23:21958933 C>T did not map to a codon.
Sequencing variant TCGA-EA-A6QX-01A-12D-A33O-09 chr22:31484485 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr22:31484502 C>T maps to ENST00000454496 Q123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr11:57310723 G>A maps to ENST00000457912 Q221Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr9:33073632 C>T maps to NM_018225.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr7:98638143 G>A maps to NM_020429.2 I495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QE-01A-21D-A21Q-09 chr2:88367421 C>T maps to NM_198274.3 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr2:88409910 C>T maps to NM_198274.3 F451F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr1:246670378 G>A maps to NM_001167740.1 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr17:1703352 G>C maps to NM_052928.2 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr2:73447239 G>A maps to NM_006062.2 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr20:48604489 C>G maps to NM_005985.3 S231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr16:88744856 C>T maps to NM_178310.3 *293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QE-01A-21D-A21Q-09 chr15:42821972 G>T maps to NM_003825.2 E176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr20:10258388 T>C did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr20:10287970 G>A did not map to a codon.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr22:21237834 C>T maps to NM_004782.3 H199H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:227921485 C>G did not map to a codon.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr1:227920970 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr6:84269882 G>A maps to NM_014841.2 V857V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr14:62248993 C>G maps to NM_003082.3 V285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr9:139276737 G>C maps to NM_003086.2 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr9:139290189 G>A maps to NM_003086.2 D70D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr9:139287210 C>T maps to NM_003086.2 Q217Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr5:121786381 G>T maps to ENST00000379533 E661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr5:121776322 G>T did not map to a codon.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr10:88719857 C>T maps to NM_003087.2 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr10:88722611 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr10:88719791 G>A maps to NM_003087.2 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr7:127725780 G>A maps to NM_014390.2 E751E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr7:127732188 A>C did not map to a codon.
Sequencing variant TCGA-EA-A5O9-01A-11D-A28B-09 chr7:127725825 C>T maps to NM_014390.2 Y766Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr7:127637780 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr2:241991560 G>A maps to NM_001080437.1 R652R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr17:47007746 T>C did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr1:38019743 C>T maps to NM_024700.2 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:38019728 G>C maps to NM_024700.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr16:11770037 C>T maps to NM_003498.5 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr2:96970570 G>A maps to NM_014014.3 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr2:96957550 G>A maps to NM_014014.3 L750L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr2:96944426 C>T maps to NM_014014.3 S1782S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr12:123956914 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr12:123956416 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr12:123956990 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:123956983 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:31754369 C>T did not map to a codon.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr19:49610935 C>G maps to NM_003089.4 S211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr18:19192398 C>G maps to NM_006938.2 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M1-01A-11D-A18J-09 chr18:19203859 G>C maps to NM_006938.2 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr19:46191814 G>C maps to NM_004597.5 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr8:121583572 C>G did not map to a codon.
Sequencing variant TCGA-DS-A3LQ-01A-21D-A21Q-09 chr8:121583519 G>T did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr16:69318091 G>A maps to NM_006750.3 R430R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr16:69318078 C>A maps to NM_006750.3 S426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr2:1357625 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr15:75897568 C>G did not map to a codon.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr15:75897568 C>G did not map to a codon.
Sequencing variant TCGA-EA-A78R-01A-11D-A32I-09 chr14:78205173 G>T maps to NM_012245.2 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OA-01A-11D-A16Y-08 chr17:46190130 T>C did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:70280809 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr7:17979954 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr6:86270987 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr6:86267720 C>A maps to NM_153816.3 E203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DV-01A-11D-A32I-09 chr6:86235931 C>A maps to NM_153816.3 L673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RA-A741-01A-11D-A33O-09 chr5:53815270 G>T maps to NM_052870.2 G497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr11:130749565 C>T maps to NM_014758.2 L933L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr16:50707547 G>A maps to NM_182854.2 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr16:50707415 G>A maps to NM_182854.2 F284F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr20:44470019 G>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr20:44470615 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr20:44470404 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr4:186180182 C>T maps to NM_031953.2 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr4:186168498 A>C did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr4:186284651 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:151665922 C>T maps to ENST00000458013 F514F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A852-01A-11D-A351-09 chr1:151611372 G>C maps to ENST00000458013 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U3-01A-11D-A28B-09 chr16:12093182 C>T maps to NM_032167.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr6:108582038 G>A maps to NM_003795.4 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr20:17922930 T>C did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr14:35037128 G>A maps to NM_152233.2 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr12:53509912 G>A maps to NM_003578.3 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr6:107955148 G>A maps to NM_018013.3 Q367Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr17:76354825 G>A maps to NM_003955.3 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr17:76354969 C>T maps to NM_003955.3 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr14:55509863 G>A maps to NM_199421.1 K35K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr14:55509924 G>T maps to NM_199421.1 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr2:46985884 G>A maps to NM_144949.2 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr18:67993285 C>A maps to NM_004232.3 S461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr18:67992740 C>T maps to NM_004232.3 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:36521233 G>A maps to NM_014598.2 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr21:33032015 C>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr13:36776104 C>T maps to ENST00000511166 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr21:34948918 C>G did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr21:34942132 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr10:97158830 C>T maps to NM_001034954.1 V367V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr10:97096726 G>A maps to NM_001034954.1 L1064L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr10:97154430 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr8:22419005 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr10:108337107 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr10:108434814 G>T maps to NM_001013031.1 L644L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr4:7725533 C>T maps to NM_020777.2 P845P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr4:7705978 G>C maps to NM_020777.2 L612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr10:106974211 T>C maps to NM_014978.1 I796I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr11:121491798 C>G maps to NM_003105.5 L1972L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr11:121391422 C>G maps to NM_003105.5 V423V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr1:109883465 G>A maps to NM_002959.4 R382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:109869777 G>A maps to NM_002959.4 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr2:39224137 C>T maps to NM_005633.3 E1002E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr14:50612205 G>C maps to NM_006939.2 L831L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr14:50605347 C>G maps to NM_006939.2 R980R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr2:5833653 G>A maps to NM_003108.3 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr17:7491863 G>T maps to NM_006942.1 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr3:181430397 G>T maps to NM_003106.2 E84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr23:139586892 C>T did not map to a codon.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr23:139586613 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr23:139586772 G>A did not map to a codon.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr23:139587209 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr12:24102510 G>A maps to NM_006940.4 Q9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr11:16119217 T>C maps to NM_001145819.1 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3WB-01A-11D-A22X-09 chr11:16760009 G>A did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr8:10689234 G>A maps to ENST00000354846 Q81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:231326076 T>G maps to NM_001080391.1 V307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr2:231115694 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr17:45994156 G>T maps to NM_003110.5 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr12:53722968 G>C maps to NM_001173467.1 S86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr11:124551304 G>T maps to NM_017425.3 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WI-01A-12D-A351-09 chr6:88767423 T>C maps to NM_030960.2 D120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr8:101196924 C>G maps to NM_003114.3 S222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr8:101178125 G>A maps to NM_003114.3 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr8:7308357 A>G maps to NM_058201.2 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:118629687 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:118514411 G>A did not map to a codon.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr20:34205118 G>C maps to NM_003116.1 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr20:34205751 C>G maps to NM_003116.1 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr10:22634676 G>A maps to ENST00000376603 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3EO-01A-11D-A20U-09 chr10:22634733 G>A maps to ENST00000376603 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr10:22678156 G>C maps to ENST00000376603 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr9:35811265 C>T maps to NM_001039592.1 W259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr9:35812147 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr23:140335817 C>T did not map to a codon.
Sequencing variant TCGA-C5-A7X3-01A-11D-A351-09 chr23:144337279 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr23:142795165 T>G did not map to a codon.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr23:142795176 T>C did not map to a codon.
Sequencing variant TCGA-FU-A57G-01A-11D-A26G-09 chr23:142795144 C>A did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:142113841 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr23:52826381 T>A did not map to a codon.
Sequencing variant TCGA-Q1-A73Q-01A-21D-A32I-09 chr4:88414907 G>A maps to NM_004684.4 G348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A411-01A-11D-A243-09 chr2:32339749 T>C maps to NM_014946.3 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AU-01A-32D-A243-09 chr17:48625392 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr17:48625788 C>T maps to NM_022827.2 Q91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr4:177114224 G>A maps to NM_144644.2 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr4:123949531 G>A maps to NM_145207.2 L687L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WF-01A-11D-A351-09 chr8:145094843 C>T maps to NM_198572.2 N82N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr8:145095182 G>A maps to NM_198572.2 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr12:49919879 C>T maps to NM_023071.3 Q494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr6:34507168 C>G maps to NM_012391.1 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A852-01A-11D-A351-09 chr6:34512079 G>A maps to NM_012391.1 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:29063287 C>G maps to NM_182756.3 S268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr2:29052077 T>C maps to NM_182756.3 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr20:3759527 C>T maps to ENST00000312411 *163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr20:3759455 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr5:35792493 G>A maps to NM_024867.3 L1500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HF-01A-11D-A20U-09 chr2:220348577 C>T maps to NM_005876.4 F2131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:220307971 G>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr2:220329157 G>A maps to NM_005876.4 L903L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr2:220354196 C>G maps to NM_005876.4 V2819V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:220357647 C>G did not map to a codon.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr17:7324763 C>G maps to NM_199339.2 S257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr1:16258353 G>A maps to NM_015001.2 E1873E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr1:16258746 G>A maps to NM_015001.2 P2004P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:16257905 C>G maps to NM_015001.2 S1724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:16261838 C>G maps to NM_015001.2 S3035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R9-01A-11D-A18J-09 chr1:16255854 G>A maps to NM_015001.2 V1040V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:16254825 C>A maps to NM_015001.2 Y697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:16255241 C>G maps to NM_015001.2 S836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:16256545 G>T maps to NM_015001.2 E1271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PD-01A-11D-A351-09 chr1:16262319 G>C maps to NM_015001.2 V3195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr13:46288425 G>A maps to NM_152719.1 A422A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr13:46288083 C>T maps to NM_152719.1 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr15:44944411 G>A maps to NM_025137.3 Q308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr15:44907616 G>A maps to NM_025137.3 L994L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr15:44864781 G>C did not map to a codon.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr15:44864782 A>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr15:44941198 G>C maps to NM_025137.3 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr13:36878516 C>T maps to NM_001142294.1 K662K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr16:89623344 G>A maps to NM_003119.2 E744E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:74381245 G>A maps to NM_182965.2 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:49131292 C>T maps to NM_020126.3 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr19:49133017 G>A maps to NM_020126.3 G651G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr19:49132816 C>T maps to NM_020126.3 F584F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr19:49132888 C>T maps to NM_020126.3 F608F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr2:228882202 C>A maps to NM_001142644.1 E1123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr2:228882251 C>T maps to NM_001142644.1 L1106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr9:91090482 C>A did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:57162265 C>T did not map to a codon.
Sequencing variant TCGA-EA-A78R-01A-11D-A32I-09 chr23:57146634 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr23:57021343 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr23:57021368 C>T did not map to a codon.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr19:38780920 G>T did not map to a codon.
Sequencing variant TCGA-C5-A2M2-01A-21D-A18J-09 chr18:12463426 G>A maps to NM_001128626.1 R521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr16:89925646 C>G maps to NM_032451.1 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr17:4434018 C>T maps to NM_001124758.1 F222F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr17:4439673 C>T maps to NM_001124758.1 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr17:4388364 G>A did not map to a codon.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr17:4389825 G>A maps to NM_182538.4 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr20:55917853 G>C maps to ENST00000371258 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr1:32280448 G>C maps to NM_144569.4 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr5:136315126 G>A maps to NM_004598.3 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr10:73828010 G>A maps to NM_014767.2 R175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QE-01A-21D-A21Q-09 chr17:47755312 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr2:139326584 C>T maps to NM_001001664.2 R372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr2:139308478 G>A maps to NM_001001664.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr4:88904113 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr4:88902910 G>A maps to NM_001040058.1 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr4:88901543 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr2:234967523 C>T maps to NM_006944.2 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr12:121220470 C>T maps to NM_139015.3 W163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr2:73118554 G>A maps to NM_003124.4 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr19:38886142 C>T maps to NM_001042522.1 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:152957715 C>T maps to NM_005987.3 Q4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U3-01A-11D-A28B-09 chr1:153004863 C>T maps to NM_003125.2 Q15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M1-01A-11D-A18J-09 chr23:155003759 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr23:155003587 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr1:158639537 G>A maps to NM_003126.2 D546D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr1:158627367 G>A maps to NM_003126.2 Q902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:158581037 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:158622382 A>G maps to NM_003126.2 N1083N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3TX-01A-11D-A22X-09 chr1:158627400 G>A maps to NM_003126.2 R891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KH-01A-21D-A22X-09 chr9:131387372 G>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:131361300 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr9:131346187 C>G maps to NM_001130438.2 T711T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr9:131362258 G>A did not map to a codon.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr9:131351131 C>G maps to NM_001130438.2 V972V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A5XV-01A-11D-A28B-09 chr9:131386726 C>T maps to NM_001130438.2 Q1985*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr9:131362263 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr9:131395164 G>A maps to NM_001130438.2 E2413E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr9:131386726 C>T maps to NM_001130438.2 Q1985*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr9:131346736 C>T maps to NM_001130438.2 F790F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr9:131348187 G>T maps to NM_001130438.2 E908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr14:65216119 C>T maps to ENST00000389723 A2301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr14:65268948 C>T maps to ENST00000389723 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr14:65259916 G>T maps to ENST00000389723 R826R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr2:54894739 G>C did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:66467040 G>C maps to NM_006946.2 L1204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr11:66461713 C>A maps to NM_006946.2 E1467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr11:66461723 C>G maps to NM_006946.2 S1463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:66457556 G>A maps to NM_006946.2 L1921L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QD-01A-32D-A22X-09 chr19:40998872 C>T maps to NM_020971.2 Q167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr19:41071419 G>T maps to NM_020971.2 E2003*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr15:42147811 G>A maps to ENST00000320955 F3051F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr15:42171993 C>T maps to ENST00000320955 L960L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr15:42143327 G>T maps to ENST00000320955 L3588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr15:42149152 G>T maps to ENST00000320955 A2902A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73S-01A-11D-A33O-09 chr15:42147039 C>T maps to ENST00000320955 Q3186Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M1-01A-11D-A18J-09 chr9:94830363 C>T maps to NM_006415.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr9:94877646 C>A maps to NM_006415.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr20:13029846 G>A did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr2:45704133 G>A maps to NM_018079.4 Q683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr2:45800395 G>A maps to NM_018079.4 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr20:36032760 G>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr20:36033163 G>C did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr20:36033335 G>T did not map to a codon.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr20:36031919 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr16:30748766 C>A maps to NM_006662.2 S2469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VI-01A-11D-A28B-09 chr16:30736066 G>A maps to NM_006662.2 S1774S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr17:36719743 C>T maps to NM_025248.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr17:36699364 A>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr7:76019543 G>A maps to NM_080744.1 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr7:76021281 G>A maps to NM_080744.1 D470D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5FO-01A-21D-A28B-09 chr2:31805819 C>T maps to NM_000348.3 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:31751094 G>C did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:56230310 C>T maps to NM_024592.3 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr22:42267030 C>T maps to NM_004599.2 Q287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr6:43143631 G>A maps to NM_003131.2 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr12:64491141 G>A maps to NM_020762.2 L600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr12:64458902 C>T maps to NM_020762.2 C343C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A411-01A-11D-A243-09 chr12:64456755 G>A maps to NM_020762.2 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr12:64410756 G>T maps to NM_020762.2 E152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr12:64521826 G>A maps to NM_020762.2 R909R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A69L-01A-11D-A32I-09 chr20:62178639 G>C maps to NM_080823.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr15:40331050 C>T did not map to a codon.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr17:74041398 G>A maps to NM_014230.2 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr17:74066477 C>A maps to NM_014230.2 G78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WH-01A-22D-A351-09 chr4:57355615 C>T maps to NM_006947.3 F429F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr1:225977057 G>A maps to NM_003133.5 E86E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr6:35806519 G>A maps to ENST00000373822 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr7:104773329 C>A maps to ENST00000336613 E585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:104909302 C>T maps to ENST00000482862 K33K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr7:104783726 C>T maps to ENST00000336613 K319K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr23:153050592 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:153049642 G>C did not map to a codon.
Sequencing variant TCGA-C5-A2LS-01A-22D-A22X-09 chr23:38031227 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:38016208 G>A did not map to a codon.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr23:99901355 C>G did not map to a codon.
Sequencing variant TCGA-EA-A411-01A-11D-A243-09 chr23:99920649 A>G did not map to a codon.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr23:99920344 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:99905896 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr16:2820871 G>A did not map to a codon.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr16:2815030 C>G maps to NM_016333.3 S1501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr16:2812361 G>T maps to NM_016333.3 R611R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr16:2813285 G>A maps to NM_016333.3 V919V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WH-01A-22D-A351-09 chr12:119594443 G>A maps to NM_194286.2 R559R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr12:119594443 G>A maps to NM_194286.2 R559R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A0TN-01A-21D-A14W-08 chr7:100482419 G>A maps to NM_015908.5 K334K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr7:100485022 G>A maps to NM_015908.5 Q686Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:170666791 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2RE-01A-11D-A18J-09 chr1:54692355 A>T did not map to a codon.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr12:109185926 G>A maps to NM_001161330.1 L676L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr17:27977721 C>T maps to NM_033389.2 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr17:27958149 G>C maps to NM_033389.2 L1327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr17:28011594 G>A maps to NM_033389.2 F128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr17:28022509 G>A maps to NM_033389.2 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LB-01A-11D-A243-09 chr17:27977703 C>T maps to NM_033389.2 W371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr17:27959007 C>T maps to NM_033389.2 L1041L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr7:149485712 G>A maps to NM_198455.2 P1342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr7:149488507 C>T maps to ENST00000262089 G697G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr7:149519677 C>T maps to NM_198455.2 Q4394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr7:149516581 C>T maps to NM_198455.2 F3999F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr1:155979342 C>T maps to ENST00000368312 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:155988143 C>T maps to ENST00000368312 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:155988068 C>T maps to ENST00000368312 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr23:153061913 C>T did not map to a codon.
Sequencing variant TCGA-EA-A411-01A-11D-A243-09 chr23:153059923 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr23:153063930 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:48121240 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr23:48270278 G>C did not map to a codon.
Sequencing variant TCGA-FU-A3TQ-01A-11D-A22X-09 chr23:48269516 C>A did not map to a codon.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr23:48047121 C>A did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr23:48047167 C>A did not map to a codon.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr23:52681346 G>T did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:52681982 T>G did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:130078418 C>T maps to NM_021978.3 F703F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr8:53092775 G>C maps to NM_014682.2 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr8:134488144 C>T maps to NM_173344.2 Q41Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr16:70415654 G>A maps to NM_006927.3 F330F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr1:44386146 C>T maps to NM_174963.2 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr3:98475281 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr3:98501743 C>T did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr3:98512550 C>T maps to ENST00000493584 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr11:8725067 G>A did not map to a codon.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr11:8720515 C>G maps to NM_005418.3 L968L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:8718157 C>T maps to NM_005418.3 E1036E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:74625171 C>T maps to NM_018414.3 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr17:74621486 C>T maps to NM_018414.3 W576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:74570584 G>A maps to NM_006456.2 Q75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr1:76540565 G>A maps to NM_152996.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr9:130678615 G>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:77528828 C>T maps to NM_030965.1 Q317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr9:130649000 G>T maps to NM_013443.3 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr9:130653220 G>A maps to NM_013443.3 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr7:116861991 C>G maps to ENST00000323984 S505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr7:116862961 G>A maps to NM_021908.2 K562K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr7:116830920 G>A maps to ENST00000323984 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R1-01A-11D-A28B-09 chr1:113162415 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr12:22354820 G>A maps to NM_003034.3 Q246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr15:92988085 G>T maps to NM_006011.3 E257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr18:55024206 G>C maps to NM_015879.2 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr5:100231455 G>C maps to NM_005668.4 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr5:100191849 G>A maps to NM_005668.4 R252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr3:52553335 G>C maps to NM_015136.2 V1697V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr3:52553416 G>A maps to NM_015136.2 P1724P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr12:104140423 G>A maps to NM_017564.9 K2062K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:104131461 C>T maps to NM_017564.9 L1867L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr12:104151982 C>T maps to NM_017564.9 G2341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr17:37370526 G>C maps to NM_198993.3 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr23:123164962 G>C did not map to a codon.
Sequencing variant TCGA-DS-A7WI-01A-12D-A351-09 chr23:123195681 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:123229268 C>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:123095674 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr23:123184048 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr7:99786600 C>G maps to NM_012447.2 S226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr7:66785109 C>T did not map to a codon.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr2:153001275 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr2:74077618 C>T maps to NM_213622.1 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr10:90733068 G>C maps to ENST00000371927 *462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A69B-01A-11D-A32I-09 chr10:90673019 C>T maps to NM_020799.2 R195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr11:72492046 C>T maps to NM_006645.2 E60E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr13:33703334 G>C maps to NM_178007.2 V485V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QE-01A-21D-A21Q-09 chr17:37819217 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3L7-01A-21D-A20U-09 chr18:51851220 C>T maps to NM_139171.1 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:67941567 G>C did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:67943509 G>T did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:67943674 G>C did not map to a codon.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr23:67940223 C>T did not map to a codon.
Sequencing variant TCGA-JX-A3Q8-01A-11D-A21Q-09 chr2:191841665 G>A maps to NM_007315.3 V653V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr12:56744662 C>T maps to NM_005419.3 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr12:56745188 C>T maps to NM_005419.3 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr12:56748603 C>T maps to NM_005419.3 K197K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr12:56749108 C>T maps to NM_005419.3 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr12:56740732 G>A maps to NM_005419.3 I577I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:56737277 C>T maps to NM_005419.3 P817P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr17:40500480 G>C maps to NM_139276.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr17:40500480 G>C maps to NM_139276.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr17:40467763 C>G maps to NM_139276.2 *771S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr2:191931241 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr2:191922762 G>C maps to NM_003151.2 S396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr2:191929648 C>T maps to NM_003151.2 E222E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr17:40441934 C>G maps to NM_003152.3 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr17:40353803 G>A maps to NM_012448.3 L772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr12:57493154 G>A maps to NM_003153.4 R605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr8:74333612 G>C maps to NM_001164380.1 A569A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr8:23702480 C>T maps to NM_003155.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr5:172745252 C>A did not map to a codon.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr1:47726193 T>A maps to NM_001048166.1 L949L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:47753325 C>A maps to NM_001048166.1 E344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr4:27009184 G>T maps to ENST00000382009 E425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr5:171544617 G>A maps to NM_005990.3 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr5:171614914 G>A maps to NM_005990.3 D44D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr19:1207151 C>G maps to NM_000455.4 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr19:1218457 C>T maps to NM_000455.4 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr2:220110703 G>A did not map to a codon.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr2:197004444 G>A maps to NM_004226.3 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr5:146722797 T>A maps to ENST00000398521 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr5:146703592 C>A maps to NM_001112724.1 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:5458577 C>T maps to NM_018401.1 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr2:219553556 G>A maps to NM_015690.3 L506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr2:219563735 C>T maps to NM_015690.3 L1157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr6:36483159 G>A maps to NM_007271.2 F208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr2:168811666 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr2:168811453 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:36809770 G>A maps to ENST00000373130 I283I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:26227119 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:26229916 G>C did not map to a codon.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr13:39542566 C>T maps to NM_145286.2 E207E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr13:39544497 G>A maps to NM_145286.2 Q114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr2:48808939 C>T maps to NM_172311.2 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:48808732 G>T maps to NM_172311.2 E321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr14:81837383 G>A maps to NM_033104.2 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr4:184931019 G>A maps to NM_020225.1 Q343Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr4:184931889 G>A maps to NM_020225.1 V633V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr15:74486260 G>T maps to ENST00000449139 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr17:61800728 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:202344894 C>T maps to NM_018571.5 F418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3PZ-01A-11D-A21Q-09 chr2:202344885 C>T maps to NM_018571.5 Y415Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr15:43892272 G>C maps to NM_153700.2 L1708L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr15:43893149 G>A maps to NM_153700.2 F1588F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr2:37082430 G>A maps to NM_003162.2 F634F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr23:7177408 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr23:7252033 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr16:731465 G>A maps to NM_005861.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr19:13260416 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr6:144508375 C>T maps to NM_003764.3 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr6:144508279 C>T maps to NM_003764.3 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:28148833 G>A maps to ENST00000373939 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr11:59560599 G>T maps to NM_004177.4 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr1:180942780 C>T did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr17:9448565 G>C maps to NM_004853.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr17:9448546 G>A maps to NM_004853.2 R89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr9:130425707 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr9:130425708 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr9:130438192 C>T maps to NM_003165.3 I407I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr9:130438201 C>G maps to NM_003165.3 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:109350079 G>A maps to NM_007269.2 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr17:53077095 G>T maps to NM_178509.5 G131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CJ-01A-11D-A32I-09 chr17:53077106 C>G maps to NM_178509.5 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr17:53120632 G>T maps to NM_178509.5 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr17:53124508 G>A maps to NM_178509.5 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr6:147635410 C>T maps to NM_001127715.1 I435I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr12:10782273 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr13:48562677 G>A maps to NM_003850.2 Q178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr2:84668472 G>A maps to NM_003849.3 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A556-01A-11D-A26G-09 chr2:84668456 G>A maps to NM_003849.3 Q149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr3:67579601 C>A maps to NM_003848.3 E79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr12:118852227 C>G maps to NM_022491.2 S326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr10:104375150 C>G maps to NM_016169.3 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr8:70550803 G>A maps to NM_001128206.1 E784E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr20:46290230 G>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr16:28619668 C>T maps to NM_177529.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr16:28606916 G>A maps to NM_001054.3 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr16:28606787 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr2:108881767 G>A maps to NM_001008743.1 K292K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr22:44234842 G>A maps to NM_014351.3 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr2:37410612 G>A maps to NM_001032377.1 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr2:37398706 A>T maps to NM_001032377.1 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr7:56147256 C>T maps to ENST00000395437 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr2:203084815 G>C maps to ENST00000409368 S9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr21:46226928 G>A maps to ENST00000411651 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CH-01A-11D-A33O-09 chr21:46226692 G>C did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr21:46225783 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr21:46228469 G>C maps to ENST00000397893 S79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr7:892252 C>T maps to ENST00000456758 R476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr22:39135416 G>A maps to ENST00000405018 I552I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr20:31573639 G>A maps to NM_080675.3 Q267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr12:56398436 G>T maps to NM_001032387.1 E422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr14:21829299 G>A maps to NM_007192.3 F622F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr14:21821724 C>G did not map to a codon.
Sequencing variant TCGA-EA-A3HR-01A-11D-A20U-09 chr6:44988297 C>T maps to NM_181356.1 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr17:56429475 C>T maps to NM_003168.1 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr19:39965348 C>T maps to NM_003169.3 R1005R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr19:39962365 C>G maps to NM_003169.3 S649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr10:70945776 G>A maps to NM_003171.3 K102K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr9:136227993 C>T maps to NM_017503.3 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr9:136230620 G>A maps to NM_033161.2 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr22:24579157 A>C maps to NM_019601.3 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr22:24582378 G>C maps to NM_019601.3 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr9:95847263 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr1:223396681 C>T maps to NM_017982.3 E451E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr1:223536671 C>G maps to NM_017982.3 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr1:223395528 C>G did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:223408321 G>C maps to NM_001037175.2 S282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr23:48558712 C>A did not map to a codon.
Sequencing variant TCGA-C5-A7CJ-01A-11D-A32I-09 chr10:14938927 G>A maps to NM_001193424.1 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr19:55858726 C>T maps to NM_032701.3 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr17:30302565 C>G maps to NM_015355.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr1:149876727 C>T maps to NM_014849.3 L689L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A5XV-01A-11D-A28B-09 chr1:149877556 G>A maps to NM_014849.3 F640F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:75581691 C>T maps to NM_014979.1 F378F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HQ-01A-11D-A20U-09 chr5:75581008 G>A maps to NM_014979.1 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3L7-01A-21D-A20U-09 chr5:75580984 A>G did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:113261351 C>T maps to ENST00000374463 W550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LB-01A-11D-A243-09 chr9:113170064 G>A maps to ENST00000374463 I2608I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr9:113141678 C>G maps to ENST00000374463 L3455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr10:29762859 G>C maps to NM_021738.2 V1812V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr10:29821085 C>T maps to NM_021738.2 E618E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr10:29843712 G>A maps to NM_021738.2 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr10:29821681 C>G maps to NM_021738.2 S538S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr11:22849395 C>A maps to NM_148893.1 E27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:22844581 A>G did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr7:138341200 A>G maps to NM_001139456.1 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr8:110654958 G>C maps to NM_001099744.1 S76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr10:135367771 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2RL-01A-11D-A18J-09 chr20:58496530 A>G did not map to a codon.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr19:15222449 C>G maps to NM_033025.4 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr19:15224539 C>T maps to NM_033025.4 C658C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:15223194 C>T maps to NM_033025.4 V539V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr1:85630293 G>C maps to NM_032184.1 V1000V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr19:46332235 C>T maps to NM_004819.2 Q659Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:47435780 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr23:47435555 T>G did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:47432360 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr22:32924938 C>T maps to NM_003490.3 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr22:32914294 G>A maps to NM_003490.3 Q449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:33147406 G>A maps to NM_001161708.1 F471F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr6:152470758 C>T maps to NM_182961.2 Q8165Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr6:152806071 C>T maps to NM_182961.2 K361K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HR-01A-11D-A20U-09 chr6:152763320 C>T maps to NM_182961.2 A1299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr6:152614827 C>T maps to NM_182961.2 Q5969Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr6:152651254 C>T maps to NM_182961.2 R4855R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr6:152443191 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr6:152671383 C>T maps to NM_182961.2 Q3940Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr6:152565760 C>A maps to NM_182961.2 E6535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr6:152599268 C>T maps to NM_182961.2 L6176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr6:152570388 C>G maps to NM_182961.2 L6493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr6:152765604 C>A maps to NM_182961.2 E1260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VI-01A-11D-A28B-09 chr6:152470697 C>A maps to NM_182961.2 E8186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr6:152603025 G>T maps to NM_182961.2 L6099L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr6:152652985 C>T maps to NM_182961.2 L4278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr14:64491094 C>T maps to NM_182914.2 Q1920*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr14:64685171 G>T maps to NM_182914.2 L6533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr14:64494307 C>T maps to NM_182914.2 L2171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr14:64593335 G>A maps to NM_182914.2 K4576K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr14:64488654 C>G maps to NM_182914.2 L1811L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr14:64691727 G>T maps to NM_182914.2 V6827V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:33402937 G>A maps to NM_006772.2 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr6:33420136 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RL-01A-11D-A18J-09 chr17:76167899 G>A maps to NM_004710.3 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A410-01A-11D-A243-09 chr6:158492660 G>A maps to NM_003898.3 T656T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr6:158492750 G>C maps to NM_003898.3 L686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr14:70839333 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr15:99666965 C>T maps to ENST00000336292 I324I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr15:99673535 G>A did not map to a codon.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr4:119952441 C>T maps to NM_133477.2 Q838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr4:119958342 G>A maps to NM_001128934.1 *1110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr10:75407372 G>C maps to NM_001114133.1 L679L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr3:63601101 C>G maps to NM_001130003.1 S268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr17:35879069 A>G maps to NM_007247.4 P1306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr17:35879063 G>A maps to NM_007247.4 L1308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:49054175 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr20:43995844 G>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr20:43995670 C>T maps to NM_033542.3 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr20:43995844 G>C did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr20:43994169 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr12:33559987 C>T maps to NM_198992.3 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:155851211 C>G maps to NM_152280.4 V403V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:155851250 G>A maps to NM_152280.4 E416E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr14:62550972 G>A maps to NM_031914.2 T498T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr16:19236107 C>T maps to NM_016524.2 F392F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H6-01B-11D-A22X-09 chr19:51128795 G>A maps to NM_001160329.1 I476I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr19:51133403 G>A maps to NM_001160329.1 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr19:51132705 C>A maps to NM_001160329.1 E376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr19:51132565 G>A maps to NM_001160329.1 I422I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73R-01A-11D-A33O-09 chr19:51128816 G>T maps to NM_001160329.1 P469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr18:40851808 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr18:40849932 G>T did not map to a codon.
Sequencing variant TCGA-JW-A5VK-01A-11D-A28B-09 chr18:40853811 G>T maps to NM_020783.3 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr18:40854011 C>A maps to NM_020783.3 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr19:55689699 G>C maps to NM_003180.2 S39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr19:55690438 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr11:61300490 G>A maps to NM_004200.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr11:61291311 G>A maps to NM_004200.2 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr11:61323614 G>A maps to NM_004200.2 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:61300490 G>A maps to NM_004200.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr11:1853068 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr11:1852697 C>G did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr1:27678210 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr1:27677684 G>C did not map to a codon.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr1:27679597 C>T did not map to a codon.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr1:27676638 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr11:85438849 A>G maps to ENST00000359152 D74D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr11:85436848 G>A maps to ENST00000359152 V741V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:85435305 G>A maps to ENST00000359152 Q1256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A6QX-01A-12D-A33O-09 chr6:159183154 G>T maps to ENST00000297239 G488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr23:99931136 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:99930369 G>T did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:99955936 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr11:64896205 G>C did not map to a codon.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr6:166580884 G>C maps to NM_003181.2 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:132910459 G>A maps to NM_003967.2 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr6:132910642 G>T maps to NM_003967.2 Y61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr6:132874748 T>C maps to NM_053278.1 N306N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:30872355 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3QD-01A-32D-A22X-09 chr23:30864731 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr23:30877609 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:30872549 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VH-01A-11D-A28B-09 chr23:30870895 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr23:30872912 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr4:1730121 G>C maps to NM_006342.1 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr4:1742568 G>A maps to NM_006342.1 Q693Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr4:1746445 G>T maps to NM_006342.1 E780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr10:71168821 G>A maps to NM_001057.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr4:104640292 C>T maps to NM_001059.2 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr1:59042150 G>A maps to NM_002353.2 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A5XV-01A-11D-A28B-09 chr1:166833159 T>A did not map to a codon.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr17:35830525 C>G maps to NM_001166105.1 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr17:35822180 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr4:7056572 C>G maps to NM_152293.2 S352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr3:9825713 C>T maps to NM_006354.2 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:70601675 G>C did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:70601683 T>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:70621403 T>G did not map to a codon.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr23:70683737 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:70613180 G>A did not map to a codon.
Sequencing variant TCGA-EX-A1H6-01B-11D-A22X-09 chr23:70603812 T>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:70597013 A>C did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr23:70618465 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr6:34848130 C>A maps to NM_005643.2 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr1:222732049 C>T maps to NM_005681.2 R435R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr2:10051015 C>G maps to NM_005680.2 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr9:32633288 C>T maps to NM_153809.2 E763E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr10:8006429 G>A maps to NM_031923.2 K319K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr10:7860773 C>G maps to NM_031923.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr10:8006326 C>G maps to NM_031923.2 S285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KH-01A-21D-A22X-09 chr20:60574119 G>A maps to NM_003185.3 L944L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr20:60585160 G>A maps to NM_003185.3 Q568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr18:23901073 G>C maps to ENST00000418698 V686V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr18:23854694 G>C maps to ENST00000418698 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr10:105141482 C>T maps to NM_006951.3 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr11:62554155 C>T maps to NM_006473.2 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A0TN-01A-21D-A14W-08 chr23:100538562 G>A did not map to a codon.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr23:100531424 C>G did not map to a codon.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr23:100531435 C>G did not map to a codon.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr23:100541590 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr5:68660981 G>A maps to NM_001015892.1 Q195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr5:68647888 C>G maps to NM_016283.4 *173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A556-01A-11D-A26G-09 chr23:77393272 G>A did not map to a codon.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr23:77387267 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr6:159457434 C>T maps to NM_054114.3 P540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr6:159457434 C>T maps to NM_054114.3 P540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr1:159889068 G>A maps to ENST00000368096 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr3:111719695 T>G maps to NM_001008272.1 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr2:160074020 C>T maps to NM_033394.2 A1086A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr2:160027047 C>T maps to NM_033394.2 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:27778619 C>G maps to NM_020791.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:27837949 G>C maps to NM_020791.2 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr16:29996796 G>A maps to NM_016151.2 R562R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr16:29997590 G>A maps to NM_016151.2 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr12:118615107 C>T maps to NM_016281.3 K531K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr12:118590139 G>A maps to NM_016281.3 L809L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr6:32816890 G>C maps to NM_000593.5 S478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr6:32818867 C>T maps to NM_000593.5 E361E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr6:32805779 G>A maps to ENST00000452392 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr6:32805351 G>C maps to ENST00000452392 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HR-01A-11D-A20U-09 chr6:33272197 G>A maps to NM_172208.2 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HR-01A-11D-A20U-09 chr6:33273055 G>C maps to NM_172208.2 S193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr6:33281141 G>A maps to NM_172208.2 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr6:33272262 G>A maps to NM_172208.2 Q341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr12:6570295 C>G did not map to a codon.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr1:234536925 C>A did not map to a codon.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr1:234527331 G>C maps to NM_005646.3 T1619T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr1:234529149 C>T maps to NM_005646.3 Q1506Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr1:234528169 G>T maps to NM_005646.3 L1563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr5:33448721 C>T maps to ENST00000455217 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HQ-01A-11D-A20U-09 chr1:150477119 C>T maps to NM_025150.3 A577A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PI-01A-11D-A18J-09 chr1:150464808 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr15:102201988 C>T maps to NM_152334.2 V666V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr15:102197160 G>A maps to NM_152334.2 R742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr15:102215847 C>A maps to NM_152334.2 P581P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QE-01A-21D-A21Q-09 chr1:6638779 G>A maps to NM_138697.3 P554P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr1:19180913 G>A maps to NM_152232.2 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr1:19180913 G>A maps to NM_152232.2 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:1269216 C>G maps to NM_152228.1 L644L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr1:1267262 C>A maps to NM_152228.1 S146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr5:9629838 G>A maps to NM_019599.2 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr5:9629466 C>T maps to NM_019599.2 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr12:11286060 G>A maps to NM_001097643.1 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr12:11286275 G>A maps to NM_001097643.1 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr7:141672739 G>T maps to NM_176817.4 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr7:141478325 C>G maps to NM_016944.1 S13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr12:11338901 C>T maps to NM_181429.1 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr12:11244101 G>A maps to NM_176884.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr12:11214391 G>A maps to ENST00000422992 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H6-01B-11D-A22X-09 chr12:11139425 G>A maps to NM_176890.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr3:10311954 C>T maps to NM_014760.3 F363F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr3:10312128 C>T maps to NM_014760.3 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr3:10312368 C>T maps to NM_014760.3 H501H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr4:38051421 C>T maps to NM_015173.2 Q605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr22:30722720 G>A maps to ENST00000403477 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr22:30722747 G>A maps to ENST00000403477 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3YQ-01A-11D-A22X-09 chr22:30688729 C>T maps to ENST00000403477 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr22:30714649 C>T maps to ENST00000433426 E2E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr11:67173469 C>G maps to NM_198517.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr17:77984011 G>A maps to NM_019020.2 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr19:50381378 C>T did not map to a codon.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr20:418072 G>T did not map to a codon.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr20:419230 C>A maps to ENST00000246077 *429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr22:47287218 G>T maps to NM_014346.2 E256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr6:37284603 C>T maps to NM_017772.2 Q431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr16:2547036 C>A maps to ENST00000434757 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr23:48418772 C>T did not map to a codon.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr23:48403315 T>C did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:48417640 T>C did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:48399806 C>T did not map to a codon.
Sequencing variant TCGA-RA-A741-01A-11D-A33O-09 chr23:48419229 T>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr15:78346324 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr13:76055552 G>A maps to ENST00000431480 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H1-01A-11D-A17W-09 chr13:75923386 G>A maps to ENST00000431480 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr3:17617958 A>T did not map to a codon.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr23:106116847 G>C did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:106066570 T>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:106070568 T>G did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:106093418 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr4:141555330 G>C maps to NM_015130.2 L839L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A50E-01A-21D-A26G-09 chr4:141590859 G>A maps to NM_015130.2 S455S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr5:179303025 G>A maps to NM_198868.2 I598I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr5:179306762 C>T maps to NM_198868.2 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr3:186274420 G>A maps to NM_001134415.1 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2GZ-01A-11D-A17W-09 chr17:80724216 C>T maps to NM_005993.4 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr1:235530758 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr12:64858233 C>T maps to NM_013254.3 R117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr17:45773696 G>A maps to NM_014726.2 E73E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr23:9673057 G>C did not map to a codon.
Sequencing variant TCGA-FU-A3TQ-01A-11D-A22X-09 chr23:9660203 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr14:55903418 T>G maps to NM_199047.2 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr2:162275533 C>T maps to NM_006593.2 I367I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr11:124500737 C>T maps to NM_032811.2 R312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr6:85446792 G>A maps to NM_001080508.1 F478F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr6:85447110 G>A maps to NM_001080508.1 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr6:85457705 C>A maps to NM_001080508.1 E291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr6:85473689 G>A maps to NM_001080508.1 D70D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:35284623 G>C maps to NM_001077653.2 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3EO-01A-11D-A20U-09 chr7:35293126 C>T maps to NM_001077653.2 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LS-01A-22D-A22X-09 chr23:79279575 C>T did not map to a codon.
Sequencing variant TCGA-C5-A7CM-01A-11D-A33O-09 chr23:79277788 G>A did not map to a codon.
Sequencing variant TCGA-DS-A7WH-01A-22D-A351-09 chr23:79278733 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:79286501 G>C did not map to a codon.
Sequencing variant TCGA-C5-A7CJ-01A-11D-A32I-09 chr17:59533880 C>T maps to ENST00000393853 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr19:3595826 G>A maps to NM_201636.2 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr19:3600353 G>A maps to NM_201636.2 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr7:139489298 G>T did not map to a codon.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr7:139717536 G>A maps to NM_001166253.1 R524R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr14:92278670 G>A maps to NM_001128596.1 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr1:23744602 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr1:23735132 G>T did not map to a codon.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr1:23724051 G>C maps to NM_003196.1 S217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr23:102884878 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:102863559 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:102864442 G>T did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr23:13681558 A>G did not map to a codon.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr23:13682751 C>G did not map to a codon.
Sequencing variant TCGA-EX-A69L-01A-11D-A32I-09 chr23:13682530 C>G did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr8:74868230 C>T maps to NM_005648.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr1:24078345 G>A maps to NM_003198.2 R443R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr1:24082353 C>T maps to NM_003198.2 Q631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr18:44560324 C>T maps to NM_016427.2 Q437Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr18:44561019 G>A maps to NM_016427.2 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr18:44555664 G>A maps to NM_145653.3 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr15:57578976 C>A did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr6:31129530 C>T maps to NM_007109.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr6:134212873 G>T maps to NM_003206.3 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:134210780 C>T maps to NM_003206.3 N82N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr16:89961511 C>T maps to NM_014972.2 Q299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr16:89977540 G>C maps to NM_014972.2 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr16:89977644 G>C maps to NM_014972.2 *677S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr16:89940058 C>G did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr16:89940068 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr10:114910864 C>T maps to NM_030756.4 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QS-01A-61D-A22X-09 chr20:61473403 G>A maps to NM_006602.2 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr1:152085167 C>A maps to NM_007113.2 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:152084507 C>G maps to NM_007113.2 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:152082062 C>T maps to NM_007113.2 R1210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:152084525 C>G maps to NM_007113.2 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr12:110346482 C>T maps to NM_032300.4 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr22:31008987 C>G maps to NM_000355.3 S129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr5:149755766 G>A maps to ENST00000451292 A672A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr5:149754644 G>T maps to ENST00000451292 G469G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr6:160210612 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr6:167772838 G>C maps to ENST00000366827 S284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr21:33949029 T>G did not map to a codon.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr21:33954590 C>T maps to ENST00000431216 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr3:49452401 G>C did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr6:44255655 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr6:44255449 G>C maps to NM_182539.3 S38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr6:170143220 G>A maps to NM_174910.1 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr6:170143220 G>A maps to NM_174910.1 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr1:67241844 G>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:67243158 C>G did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:124158263 C>T maps to NM_024809.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr12:124171411 C>T maps to NM_024809.3 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr6:24658979 A>C did not map to a codon.
Sequencing variant TCGA-JW-A5VG-01A-11D-A28B-09 chr10:115973874 T>C did not map to a codon.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr1:154516981 C>T maps to NM_001098475.1 H262H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr1:154520220 G>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:154516546 C>T maps to NM_001098475.1 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr1:179561977 G>A maps to ENST00000444136 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr6:46660916 G>A maps to NM_001010870.2 L1684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A57G-01A-11D-A26G-09 chr6:46656383 G>T maps to NM_001010870.2 V173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R3-01A-11D-A28B-09 chr1:151752565 G>A maps to NM_001083965.1 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr11:12901303 C>G maps to NM_021961.5 S127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73Q-01A-21D-A32I-09 chr11:12923609 G>T maps to NM_021961.5 E275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr7:97857363 C>T maps to ENST00000379795 E826E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr14:102900645 C>T maps to NM_014844.3 Q498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr14:102873790 G>C maps to NM_014844.3 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr14:102829406 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr11:121031100 G>A maps to NM_005422.2 Q1649Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr11:121037447 C>T maps to NM_005422.2 Q1849*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:120998860 C>T maps to NM_005422.2 D725D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr1:36550611 G>A maps to NM_014466.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr2:95542303 G>A maps to NM_144705.2 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q8-01A-11D-A21Q-09 chr16:10721426 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr12:53451365 C>T maps to NM_170754.2 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr12:53451428 C>G maps to NM_170754.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr12:53454750 C>T maps to NM_170754.2 R1021*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr14:20845580 T>A maps to NM_007110.4 V1982V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr14:20852328 G>A maps to NM_007110.4 F1134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr14:20841446 G>A maps to NM_007110.4 Q2266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr14:20854745 G>A maps to NM_007110.4 F907F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PD-01A-11D-A351-09 chr5:1293767 C>T maps to NM_198253.2 T411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr9:35607007 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr1:45810272 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:45809795 G>T did not map to a codon.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr10:70426845 C>T maps to NM_030625.2 V1502V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UC-01A-11D-A351-09 chr4:106157305 C>G maps to ENST00000513237 S757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr4:106158242 C>G maps to ENST00000513237 L1069L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr4:106164849 C>T maps to ENST00000513237 L1261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr2:74275302 C>T maps to ENST00000409262 S660S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr9:103065970 G>A maps to NM_017746.3 L873L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr23:69772049 A>G did not map to a codon.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr23:69774554 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr23:70073169 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:69945179 G>T did not map to a codon.
Sequencing variant TCGA-EX-A1H6-01B-11D-A22X-09 chr23:104464158 C>T did not map to a codon.
Sequencing variant TCGA-EA-A50E-01A-21D-A26G-09 chr23:107224919 C>G did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:107225194 C>A did not map to a codon.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr17:56661913 C>A maps to ENST00000240361 E1046*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr17:56682357 G>A maps to ENST00000240361 I445I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr8:30717449 C>A did not map to a codon.
Sequencing variant TCGA-EA-A3HQ-01A-11D-A20U-09 chr8:30695414 C>T maps to NM_031271.3 S2412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr8:30705206 C>A maps to NM_031271.3 E443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr17:62290373 G>A maps to NM_018469.3 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr3:133478067 G>A maps to NM_001063.3 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr6:50803852 C>T maps to ENST00000263046 G236G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HM-A3JK-01A-11D-A21Q-09 chr6:50803939 G>T maps to ENST00000263046 R265R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73Q-01A-21D-A32I-09 chr20:55212975 G>A maps to NM_003222.3 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr6:50740507 G>A maps to NM_172238.3 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr2:122007205 G>A maps to NM_014553.2 R78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AX-01A-12D-A243-09 chr2:121989524 C>G maps to NM_014553.2 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A556-01A-11D-A26G-09 chr13:114286075 G>C did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr13:114292056 T>C did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr13:114294629 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr23:132351491 C>T did not map to a codon.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr23:48887122 C>G did not map to a codon.
Sequencing variant TCGA-EA-A1QS-01A-61D-A22X-09 chr23:48889097 A>T did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:48895554 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:48891274 C>G did not map to a codon.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr23:48886989 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr21:43786544 G>T maps to NM_003225.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr21:43766556 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr7:100218698 G>A maps to NM_003227.3 F729F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr3:195799010 T>C maps to NM_001128148.1 E149E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr8:133919126 C>T maps to NM_003235.4 Q1277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HQ-01A-11D-A20U-09 chr13:95248441 A>G did not map to a codon.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr16:31488297 C>T maps to NM_001042454.2 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr16:31487833 C>T maps to NM_001042454.2 H307H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr16:31488809 C>T maps to NM_001042454.2 F433F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A4BA-01A-21D-A26G-09 chr14:76437562 G>C maps to NM_003239.2 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr9:101900342 C>T maps to NM_004612.2 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr3:30691761 G>A maps to NM_001024847.2 W113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A6QX-01A-12D-A33O-09 chr3:30713253 G>A maps to NM_001024847.2 R218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr3:30729967 C>T maps to NM_001024847.2 R522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr1:92184976 G>A maps to NM_003243.4 T486T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:92195495 C>T maps to NM_003243.4 K201K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr20:35207245 G>A maps to NM_021809.6 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr20:35207332 G>A maps to NM_021809.6 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:89177088 A>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:89177608 G>A did not map to a codon.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr20:36789840 G>T maps to NM_004613.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr20:36766608 G>C maps to NM_004613.2 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr20:2315843 G>C maps to NM_003245.3 V575V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr20:2293593 G>A maps to NM_003245.3 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr20:2315840 G>A maps to NM_003245.3 A574A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr3:44935067 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr20:2411090 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr2:85554083 A>C maps to ENST00000409015 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr2:85555055 C>T maps to ENST00000409015 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr2:43458381 G>C maps to ENST00000330266 S1857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr2:43801658 C>T maps to ENST00000330266 E515E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr2:43711416 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr8:42693359 G>C maps to NM_018105.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr22:21354219 C>T maps to NM_030573.2 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr22:21354543 C>T maps to NM_030573.2 Q185Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr4:83827475 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr1:155166958 G>A maps to NM_007112.3 L849L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr5:79335942 C>T maps to NM_003248.4 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:151861893 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr23:122745308 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:122778430 G>C did not map to a codon.
Sequencing variant TCGA-FU-A3EO-01A-11D-A20U-09 chr23:122765672 A>C did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:122754209 G>T did not map to a codon.
Sequencing variant TCGA-Q1-A73Q-01A-21D-A32I-09 chr23:122761591 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr5:175392150 G>A maps to NM_032361.2 N144N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr22:29908039 C>T maps to NM_003678.4 E589E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr3:63819875 C>G did not map to a codon.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr19:2805035 G>C maps to NM_003249.3 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr3:184090792 G>A maps to NM_000460.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr3:184090786 C>G maps to NM_000460.2 L192L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EK-A2H0-01A-11D-A17W-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr1:36762218 C>T maps to NM_005119.3 L717L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr1:36757079 T>G maps to NM_005119.3 A617A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:36752156 C>G maps to NM_005119.3 S109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr13:52952232 C>T maps to NM_018676.3 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OA-01A-11D-A16Y-08 chr15:72040914 C>T maps to NM_024817.2 L799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RE-01A-11D-A18J-09 chr7:11446664 G>A maps to ENST00000423059 R1312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr7:11446026 G>A maps to ENST00000423059 F1379F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr7:11630258 C>T maps to ENST00000423059 W427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr2:138413201 G>A maps to ENST00000272643 L1362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr2:137814667 C>G maps to ENST00000272643 S273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr2:138375965 G>A maps to ENST00000272643 W1193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr11:134118817 G>A maps to NM_199298.1 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr2:70454925 G>T maps to NM_022173.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr10:121356084 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr21:32598164 G>C maps to NM_003253.2 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr21:32638892 G>A maps to NM_003253.2 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr21:32537276 A>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr21:32554750 G>C maps to NM_003253.2 L958L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr21:32598200 G>A maps to NM_003253.2 V550V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr19:4816832 G>A maps to NM_182919.2 I519I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr19:4817189 G>C maps to NM_182919.2 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr1:43783116 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr1:43783485 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr1:43780909 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:43785208 G>C did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:43782883 C>A maps to NM_005424.2 I808I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:43783066 C>T maps to NM_005424.2 I869I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:43783156 C>G did not map to a codon.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr11:65124399 C>A maps to NM_145719.2 S374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr8:144681230 C>T maps to NM_032862.4 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr3:114014650 C>T maps to ENST00000481065 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:56815234 G>C maps to NM_003920.3 S923*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr12:56815543 G>A maps to NM_003920.3 Q898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr12:56817141 G>C maps to NM_003920.3 L736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr23:48750898 G>C did not map to a codon.
Sequencing variant TCGA-C5-A7CJ-01A-11D-A32I-09 chr19:7992964 G>A maps to NM_006351.3 V375V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr23:100603703 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr14:58875634 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr23:47445205 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr3:12198410 G>C maps to NM_003256.2 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HM-A3JK-01A-11D-A21Q-09 chr6:54214627 T>A maps to NM_014464.3 C338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3TQ-01A-11D-A22X-09 chr1:32050316 C>T maps to NM_022164.2 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:156395965 G>A maps to NM_015508.4 Q160Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr15:66671708 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr15:66672273 A>T did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr9:71861670 C>T maps to NM_004817.3 Q878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr3:53262156 C>G maps to ENST00000423516 L504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:153524260 G>A did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr23:153524224 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr4:164394280 G>A maps to NM_032136.4 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr4:164393644 G>A maps to NM_032136.4 I414I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr17:27051701 G>A maps to NM_138463.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr19:3015660 G>C maps to NM_003260.4 S223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr9:82286176 C>T maps to ENST00000462803 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr19:2987352 G>A did not map to a codon.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr17:60683571 G>T maps to ENST00000326270 V669V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr4:166965572 C>T maps to ENST00000507499 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr4:166976379 C>T maps to ENST00000507499 D582D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr10:98129926 C>T maps to NM_012465.3 R936R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LS-01A-22D-A22X-09 chr9:35713250 C>T maps to NM_006289.3 V1098V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr9:35699323 A>C did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr9:35704812 C>G did not map to a codon.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr9:35707157 G>A maps to NM_006289.3 V1622V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr15:62942298 C>T maps to NM_015059.2 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr15:62966061 G>A maps to NM_015059.2 Q275Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr4:38777921 G>A did not map to a codon.
Sequencing variant TCGA-EX-A69M-01A-11D-A32I-09 chr4:154624094 G>A maps to NM_003264.3 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr4:187000001 C>T maps to NM_003265.2 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:120466741 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr9:120476130 T>C maps to NM_138554.3 N575N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr1:223286247 G>C maps to NM_003268.5 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr23:12903658 A>T did not map to a codon.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr23:12904953 G>T did not map to a codon.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr23:12903914 C>G did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:12905597 C>G did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:12905744 C>G did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr23:12939945 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:12937372 G>C did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:12937615 C>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:12939887 A>C did not map to a codon.
Sequencing variant TCGA-Q1-A73Q-01A-21D-A32I-09 chr23:12939923 G>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr10:102896477 G>A maps to NM_005521.3 E267E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3WB-01A-11D-A22X-09 chr5:170738601 G>C maps to NM_021025.2 *292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr5:170736770 C>T maps to NM_021025.2 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr15:102191955 G>A maps to NM_078474.2 Q38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr15:83776461 C>T maps to NM_023003.3 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr10:98303714 G>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:219142176 C>G did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr12:66539730 G>A maps to ENST00000286424 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr20:2597897 C>G maps to NM_080751.2 L707L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr20:2597837 A>G maps to NM_080751.2 K687K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr20:2560635 C>T maps to NM_080751.2 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr15:81625473 G>A maps to ENST00000454937 I866I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr15:81635668 G>A maps to ENST00000454937 F555F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr19:54666431 G>A maps to NM_001145303.1 V498V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr19:54664721 G>A maps to NM_001145303.1 I628I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr19:54664212 C>T maps to NM_001145303.1 Q687Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VI-01A-11D-A28B-09 chr16:19451963 C>T maps to NM_001105248.1 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr16:19468107 C>G maps to NM_024780.4 S27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr17:76120083 G>A maps to NM_007267.6 I356I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr17:76120119 G>C maps to NM_007267.6 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr17:76116777 G>A maps to NM_007267.6 F557F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr17:76113950 G>A maps to NM_007267.6 V651V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr16:19070740 C>T maps to NM_024847.3 L677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr3:129389252 C>T maps to NM_001017395.3 E477E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr12:94965288 G>A maps to NM_020698.2 A452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr1:165738103 C>G did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:165697358 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr13:114150192 C>T maps to NM_017905.4 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr1:20009172 C>T maps to ENST00000375127 E564E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A770-01A-11D-A33O-09 chr1:20073673 C>A maps to NM_181719.4 G199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr19:10945989 C>A maps to NM_006858.2 E75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr7:44621745 G>A maps to NM_182547.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr2:193059223 C>T maps to NM_016192.2 Q9Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr17:53798407 C>T maps to NM_001099640.1 E8E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr17:42090493 G>A maps to NM_032376.2 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr17:7340050 G>T maps to NM_178518.2 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr17:72832423 C>T maps to NM_017728.3 F363F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr17:72832675 G>A maps to NM_017728.3 R447R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A449-01A-11D-A243-09 chr7:12255284 C>T maps to ENST00000453686 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr11:60690640 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr11:60690679 G>A did not map to a codon.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr12:44782996 T>A did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr7:75616634 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr7:75616591 G>A maps to NM_031925.2 C310C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr7:75621562 G>C maps to NM_031925.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr11:102323291 C>T maps to NM_052932.2 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr7:98460787 G>A maps to NM_001134450.1 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr2:98449873 A>C maps to NM_015348.1 L343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr2:98426210 C>T maps to NM_015348.1 V665V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr12:125811143 C>T did not map to a codon.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr12:129563183 C>T maps to NM_133448.2 V670V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr12:130184362 G>A maps to NM_133448.2 F320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr12:129558617 G>A maps to NM_133448.2 P1034P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr17:32953294 C>T maps to NM_207313.1 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr11:67231842 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3YQ-01A-11D-A22X-09 chr11:67232006 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr9:139686127 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr9:139686776 G>T maps to NM_032928.3 E94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr4:159140496 C>G maps to NM_018342.4 S123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr19:42818969 C>T maps to ENST00000406159 Y129Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr19:42820826 C>T maps to ENST00000406159 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr19:42820702 G>A maps to ENST00000406159 V253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr19:42821048 G>A maps to ENST00000406159 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr19:42821969 C>G maps to ENST00000406159 S351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr6:52541932 C>T maps to NM_014051.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr6:10749468 G>C did not map to a codon.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr6:10749476 G>A did not map to a codon.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr19:55824297 G>A maps to NM_001085488.1 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr11:66062523 G>A maps to NM_153266.3 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3TQ-01A-11D-A22X-09 chr4:39000443 C>T maps to NM_024943.1 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr5:87564616 G>C did not map to a codon.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr5:87494810 C>T maps to NM_153354.3 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr5:87498892 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr2:135214287 C>T maps to NM_030923.4 *290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:109247277 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr1:109637428 C>A did not map to a codon.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr1:109635590 C>G maps to NM_020141.3 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr7:112424577 G>A maps to NM_022484.4 F101F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:216964766 G>A maps to NM_138390.3 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr5:72419679 C>T maps to NM_173490.6 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr7:150500754 C>T maps to NM_018487.2 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr7:150491132 C>G maps to NM_014020.3 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr7:1588236 G>A maps to NM_001097620.1 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr4:148554077 G>A maps to NM_018241.2 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:153248008 G>A did not map to a codon.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr23:153248289 G>A did not map to a codon.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr12:57464514 G>A maps to NM_001130963.1 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr7:19812187 G>A maps to NM_152774.3 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr9:74361179 C>A maps to NM_013390.2 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr18:5891519 G>A maps to NM_001080209.1 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr15:72698976 C>A maps to NM_001080462.1 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr15:72700112 C>G maps to NM_001080462.1 S234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr9:140099704 G>A maps to NM_053045.1 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:1591970 C>A maps to NM_024600.4 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr22:25331425 G>C maps to ENST00000423535 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr6:37180456 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr11:123755272 C>T maps to NM_001013743.1 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3EO-01A-11D-A20U-09 chr11:118406230 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr6:75975014 G>A maps to NM_018247.3 Q129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr14:61748260 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr23:100334061 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr9:108510421 C>G maps to NM_018112.1 S204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr9:108510421 C>G maps to NM_018112.1 S204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr3:119150995 G>A maps to NM_018266.1 F433F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:32568451 T>G did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr1:32540601 G>T maps to NM_018056.2 E19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr3:12776200 G>T did not map to a codon.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr3:44905834 G>A maps to NM_144638.1 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr3:14170985 G>A maps to NM_024334.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr3:14170991 G>A maps to NM_024334.2 E31E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H6-01B-11D-A22X-09 chr3:194331717 G>C maps to NM_001166305.1 S362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:194344314 C>T maps to NM_001166305.1 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:100295884 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr23:34657408 G>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr21:34841093 C>T maps to NM_006134.5 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr1:45120219 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr1:33360938 C>G maps to NM_033504.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr1:33360406 C>G maps to NM_033504.2 *223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr1:54509138 G>A maps to ENST00000371338 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr19:18724917 C>T maps to NM_012109.2 C107C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WH-01A-22D-A351-09 chr1:226047209 G>A did not map to a codon.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr1:226054372 G>A maps to NM_014698.2 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73S-01A-11D-A33O-09 chr1:226065244 G>T maps to NM_014698.2 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr14:77686351 G>C maps to NM_020431.2 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr14:77712333 C>T maps to NM_020431.2 F500F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr8:29924374 G>A maps to NM_016127.4 Q254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr8:109796643 C>T maps to NM_153015.1 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr11:703086 C>T maps to ENST00000449452 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr11:700745 G>C did not map to a codon.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr1:16074125 G>A maps to NM_001013641.1 *344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr15:42556299 G>C maps to ENST00000389834 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr15:42531873 C>T maps to ENST00000389834 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr15:42531887 C>A maps to ENST00000389834 E222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A78R-01A-11D-A32I-09 chr2:112843657 G>T maps to NM_032824.2 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr2:112873752 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr9:136385317 C>G maps to NM_001080483.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr9:136385317 C>G maps to NM_001080483.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr17:48355919 C>G maps to NM_153229.2 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr17:48356299 C>T maps to NM_153229.2 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr17:48356376 C>G did not map to a codon.
Sequencing variant TCGA-EA-A50E-01A-21D-A26G-09 chr17:31260323 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VK-01A-11D-A28B-09 chr17:31267986 C>T maps to NM_015544.2 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr23:154842493 G>A did not map to a codon.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr23:154754248 G>T did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr9:100315614 G>A maps to NM_003275.3 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr9:100326398 G>C maps to NM_003275.3 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr15:52239399 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr12:98938001 G>C did not map to a codon.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr12:98931268 C>G maps to NM_001032283.2 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr4:68777059 T>G maps to NM_182606.3 *422Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3WB-01A-11D-A22X-09 chr4:68692990 G>A maps to NM_004262.2 Q314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr11:117789271 G>A maps to ENST00000413475 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr21:43792006 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr21:43802066 C>G did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr21:43792021 G>C did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr22:37480240 G>C maps to ENST00000442782 V439V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr3:111766715 C>G maps to ENST00000443106 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr19:2421913 C>A maps to NM_182973.1 I705I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr23:12994419 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr12:29936471 C>T maps to NM_001193451.1 W71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr12:29908756 G>A maps to NM_001193451.1 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr12:29659558 C>G did not map to a codon.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr12:29936561 G>T maps to NM_001193451.1 Y41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr12:88560201 C>A maps to NM_181783.3 S298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr12:88547150 A>G maps to NM_181783.3 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr13:101257340 G>A maps to NM_032813.2 I730I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr18:66344337 G>A maps to NM_019022.3 A399A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr20:7963052 G>A maps to NM_021156.2 Q299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr9:117817773 C>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr9:117848145 C>A maps to NM_002160.2 E622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr9:117815267 T>G did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr6:31544968 G>A maps to NM_000594.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr14:103592959 C>T maps to NM_006291.2 Q56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr6:138196078 G>A maps to NM_006290.2 K131K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr2:152226591 C>T maps to NM_007115.3 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr19:4640536 C>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr8:23082496 C>T maps to NM_003844.3 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr8:23004582 G>A maps to NM_003840.3 Q125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr8:23021421 C>T maps to NM_003840.3 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr18:60017105 G>A maps to NM_003839.2 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr16:3071953 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr17:16843019 C>T maps to NM_012452.2 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr17:16852097 C>T maps to NM_012452.2 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr17:16843712 G>A maps to NM_012452.2 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:2493179 C>G maps to NM_003820.2 S207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:2493275 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:1139438 C>T maps to NM_004195.2 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr12:6442924 G>C maps to NM_001065.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr12:6440005 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr12:6440010 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:12254072 C>T maps to NM_001066.2 I283I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr6:47200713 C>A maps to NM_014452.3 V585V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr20:62328437 C>T maps to NM_003823.2 H106H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HR-01A-11D-A20U-09 chr1:12202461 G>A maps to NM_001243.3 A554A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr1:12202342 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:12169641 G>A maps to NM_001243.3 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr13:43181039 C>T maps to NM_003701.3 R314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr13:108955664 G>A maps to NM_006573.3 E182E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr13:108959349 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr13:108922314 G>A maps to NM_006573.3 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WH-01A-22D-A351-09 chr9:117553052 T>C maps to NM_005118.2 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A78R-01A-11D-A32I-09 chr3:170781815 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:170928991 C>T maps to NM_015028.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr3:170841400 G>A maps to NM_015028.2 Q702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr4:122137567 A>C did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr17:7287071 G>A maps to NM_003985.3 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr3:195595032 C>A maps to NM_001010938.1 P775P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7X3-01A-11D-A351-09 chr8:9538265 C>T maps to NM_003747.2 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr8:9634218 C>T maps to NM_003747.2 T1319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr11:57080262 G>A maps to NM_033396.2 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr11:57077100 G>A maps to NM_033396.2 F1028F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr23:99854612 G>A did not map to a codon.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr23:99849346 G>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:175046841 G>A maps to NM_022093.1 Q96Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:175063327 C>A maps to NM_022093.1 V509V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr1:175086231 G>A maps to NM_022093.1 Q759Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HM-A3JK-01A-11D-A21Q-09 chr20:44453152 G>A maps to NM_003279.2 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr19:55669029 G>A did not map to a codon.
Sequencing variant TCGA-C5-A3HF-01A-11D-A20U-09 chr19:55668951 C>T maps to ENST00000344887 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:201341204 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:1956266 G>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr16:11362925 G>C maps to NM_005425.4 S65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr5:72204696 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr19:12826311 G>C maps to NM_001136196.1 S158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr1:175360460 C>T maps to NM_003285.2 Q490Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr7:5430071 C>G maps to ENST00000430504 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr16:24800640 G>A maps to NM_014494.2 K226K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:218686476 G>A maps to NM_022648.4 I1082I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr2:218758227 G>A maps to NM_022648.4 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr7:47323458 G>A maps to NM_022748.11 C1311C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr7:47451363 G>A maps to NM_022748.11 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73S-01A-11D-A33O-09 chr7:47408810 G>A maps to NM_022748.11 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr17:38645132 G>A maps to NM_032865.5 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr17:38638450 G>C maps to NM_032865.5 L534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr17:38644990 G>A maps to NM_032865.5 R224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr6:32035600 C>T maps to ENST00000375244 V2127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr6:32012816 C>T maps to ENST00000375244 K3631K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr6:32065756 G>A maps to ENST00000375244 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr6:32023868 C>T maps to ENST00000375244 L2742L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr22:41832380 G>A maps to NM_016272.3 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:45805811 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr11:1298481 C>T maps to ENST00000382211 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr22:35719505 C>T maps to ENST00000451197 F137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr22:35719850 C>T maps to ENST00000451197 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr17:17772739 G>A maps to NM_001082968.1 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R3-01A-11D-A28B-09 chr17:17801971 G>A maps to NM_001082968.1 R52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr20:43572096 G>C maps to NM_006809.4 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr1:161197765 G>A maps to NM_032174.4 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:161198385 C>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:161199824 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:161198296 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr1:161198485 C>T did not map to a codon.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr17:38556816 A>G maps to ENST00000357601 I957I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr17:38562848 G>C maps to ENST00000357601 V646V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr17:18194242 G>A maps to NM_004618.3 I460I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr22:22314108 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr3:133347255 C>T maps to NM_007027.3 K918K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr9:32542046 G>A maps to NM_005802.4 Q826*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr9:32542822 G>C maps to NM_005802.4 S567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr9:132569558 C>T maps to NM_014506.1 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr9:132569633 C>T maps to NM_014506.1 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr9:132566621 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr9:130496649 G>C maps to NM_001085347.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr1:179054979 C>T maps to NM_022371.3 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr17:7578381 G>C maps to NM_001126112.1 S183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr17:7573976 G>C maps to NM_001126112.1 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr17:7577064 C>T maps to NM_001126112.1 K291K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr17:7577076 C>T maps to NM_001126112.1 E287E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HM-A4S6-01A-11D-A26G-09 chr15:43784622 G>A maps to NM_001141980.1 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr20:33297289 C>G maps to NM_021202.1 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr20:44002618 C>G maps to NM_014477.2 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr3:189608647 C>T maps to NM_003722.4 Q575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr3:189612141 G>T maps to NM_003722.4 E632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr3:189585725 C>A maps to NM_003722.4 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A410-01A-11D-A243-09 chr1:3649570 C>T maps to NM_005427.2 G613G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5FO-01A-21D-A28B-09 chr1:3624292 G>T maps to NM_005427.2 G123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:3598992 C>T maps to NM_005427.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr1:3638613 C>T maps to NM_005427.2 C153C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr1:3645928 G>T maps to NM_005427.2 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr11:68822654 C>T maps to NM_139075.3 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr6:125541296 C>G maps to NM_003287.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A78R-01A-11D-A32I-09 chr6:125573170 T>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr9:6328702 C>G maps to NM_033516.5 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr11:18050789 A>G maps to ENST00000341556 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr12:6976717 C>T maps to NM_001159287.1 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3YQ-01A-11D-A22X-09 chr1:154143795 G>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:154145293 G>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr1:154130021 C>T did not map to a codon.
Sequencing variant TCGA-DS-A3LQ-01A-21D-A21Q-09 chr2:1491725 C>T maps to NM_000547.5 S577S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H1-01A-11D-A17W-09 chr2:1457570 G>A maps to NM_000547.5 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr2:1544401 G>A maps to NM_000547.5 S885S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr1:186292909 G>A maps to NM_003292.2 R2069*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr3:127294478 C>T did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr3:189033327 G>A did not map to a codon.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr19:48305208 G>A maps to NM_198479.2 F353F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R9-01A-11D-A18J-09 chr16:1277335 G>A did not map to a codon.
Reference base specified for sequencing variant TCGA-JW-A5VI-01A-11D-A28B-09 chr16:1306680 A>C does not match reference base at that coordinate in hg19.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr16:1272917 C>A did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr22:26937095 G>T maps to NM_003595.3 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr21:10996071 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr21:10906874 C>A did not map to a codon.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr20:30371594 C>T maps to ENST00000340513 T464T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr20:30385275 C>T maps to ENST00000340513 Q671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr7:23545178 C>T maps to NM_013293.3 *283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr3:185655768 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr9:139796833 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr9:139804385 C>T maps to ENST00000359662 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr9:139804463 C>A did not map to a codon.
Sequencing variant TCGA-FU-A3WB-01A-11D-A22X-09 chr6:111913049 G>C maps to ENST00000340026 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr6:111912596 G>C maps to ENST00000340026 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:209949291 G>T did not map to a codon.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr1:209953917 G>A maps to NM_025228.2 K472K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr17:27075425 C>G maps to NM_004295.3 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:27075393 C>T maps to NM_004295.3 Q193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr17:27076944 G>A did not map to a codon.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr1:211532936 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr3:49867118 G>A maps to NM_005879.2 V389V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr3:42132993 C>T maps to NM_001042646.1 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:42128644 C>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:202284116 A>C did not map to a codon.
Sequencing variant TCGA-C5-A7CJ-01A-11D-A32I-09 chr3:36874140 G>T maps to NM_014831.2 I2267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr3:36905815 G>A maps to NM_014831.2 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr3:36893236 G>C maps to NM_014831.2 L1576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr16:3715982 G>A maps to NM_016292.2 Q458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr17:7835147 C>G did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:7833971 C>T maps to NM_001166621.1 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr21:45499970 G>A maps to NM_003274.4 E562E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr21:45483603 G>T maps to NM_003274.4 E326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:36605229 T>G did not map to a codon.
Sequencing variant TCGA-Q1-A6DV-01A-11D-A32I-09 chr19:7747432 C>T maps to NM_001042461.1 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A0TN-01A-21D-A14W-08 chr8:140893936 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr8:140743267 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr8:141321455 G>A maps to NM_031466.5 Q603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr8:141468468 G>A maps to NM_031466.5 C65C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr3:108566026 C>T did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr11:118531413 G>C maps to ENST00000264029 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr6:41162209 G>A maps to ENST00000373108 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr6:41165886 G>A maps to ENST00000373108 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr6:42232540 C>G maps to NM_033502.2 L512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr6:42231040 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr23:152710752 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A6DV-01A-11D-A32I-09 chr3:129694731 C>T maps to NM_007117.3 Q25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RL-01A-11D-A18J-09 chr12:73012758 C>T maps to NM_013381.2 R759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr12:73046212 G>A maps to NM_013381.2 E884E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr12:72667019 C>G maps to NM_013381.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CJ-01A-11D-A32I-09 chr8:110100473 C>T maps to NM_003301.4 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73R-01A-11D-A33O-09 chr12:120883973 G>T did not map to a codon.
Sequencing variant TCGA-Q1-A5R1-01A-11D-A28B-09 chr2:12880514 C>T maps to NM_021643.3 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr7:28997038 G>A maps to NM_014817.3 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr7:28993034 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr7:28993115 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr1:228588757 G>A maps to NM_145214.2 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr9:100849772 G>A maps to NM_033219.1 I436I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr17:15539373 G>A maps to ENST00000455584 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr17:15584409 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr17:18638430 G>A maps to NM_001037330.1 Q235Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr17:18625637 C>G did not map to a codon.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr4:154216601 G>A maps to NM_015271.3 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A4BA-01A-21D-A26G-09 chr4:154197119 C>T maps to NM_015271.3 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr4:154216994 C>T maps to NM_015271.3 I439I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr4:154191651 C>T maps to NM_015271.3 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr11:5730381 C>G maps to NM_006074.4 S334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr17:54969327 G>A maps to NM_005082.4 L542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr6:28875229 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr19:59061166 C>T maps to NM_005762.2 L682L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr6:30071894 G>A maps to NM_007028.3 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr1:114947872 T>G did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr8:27145234 C>T maps to NM_171982.3 E438E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr8:27151767 G>A maps to NM_171982.3 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr8:27145093 G>A maps to NM_171982.3 I485I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr5:114462252 G>A maps to NM_018700.3 Q712*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr5:114466484 G>A maps to NM_018700.3 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LS-01A-22D-A22X-09 chr17:57106025 G>T maps to NM_015294.3 P669P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr17:57134234 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr6:25972170 G>A maps to NM_006355.2 E194E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr6:30309561 C>T maps to NM_021253.3 F361F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:30114944 C>T maps to ENST00000376724 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr3:140401672 C>T maps to NM_152616.4 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WH-01A-22D-A351-09 chr3:140401594 C>T maps to NM_152616.4 H211H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr2:96265242 G>A maps to NM_138800.1 K421K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr1:117663433 G>A maps to NM_025188.3 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr1:117660796 G>A maps to NM_025188.3 Q361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr1:155148616 C>T maps to NM_025058.3 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:155156671 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:155147101 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr11:89532886 G>A maps to NM_020358.2 R286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RA-A741-01A-11D-A33O-09 chr11:5686912 C>G did not map to a codon.
Sequencing variant TCGA-FU-A5XV-01A-11D-A28B-09 chr7:72732855 G>A maps to NM_178125.2 Q231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr5:180687438 C>A maps to NM_032765.2 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr8:67064639 C>T maps to NM_184085.1 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr7:100733755 T>G did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr7:100730883 G>A maps to NM_030961.1 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr7:100732122 C>T maps to NM_030961.1 I510I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr7:100732200 C>G maps to NM_030961.1 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr7:100732910 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr7:100732941 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr11:5624475 G>A maps to NM_001003819.3 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr11:5655129 G>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:33613038 G>A maps to NM_018207.2 I389I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr1:26394021 C>G did not map to a codon.
Sequencing variant TCGA-C5-A7CG-01A-11D-A32I-09 chr1:26394008 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr1:231298819 G>A maps to NM_001004342.3 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr1:231333182 C>T maps to NM_001004342.3 Q371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3TX-01A-11D-A22X-09 chr3:32915395 C>T maps to NM_001039111.1 Y313Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr16:31230471 G>A maps to NM_001008274.3 K149K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr16:31235904 C>T maps to NM_001008274.3 D421D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr14:51467499 G>A maps to ENST00000338969 N451N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr14:51467439 G>T maps to ENST00000338969 Y471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr4:189068345 C>T maps to NM_178556.3 V409V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr4:189060881 G>A maps to NM_178556.3 W57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:189026425 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr4:189022245 G>A maps to ENST00000326754 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr5:14316833 C>T maps to NM_007118.2 F571F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr22:38167739 G>A maps to NM_001039141.2 Q2311Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A411-01A-11D-A243-09 chr22:38120146 A>C maps to NM_001039141.2 T528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr22:38130480 G>T maps to NM_001039141.2 E1380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr22:38119409 C>T maps to NM_001039141.2 R283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr22:38130626 G>A maps to NM_001039141.2 Q1428Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:6751283 C>T maps to ENST00000420690 Q577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr14:92505915 C>A maps to NM_004239.3 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73R-01A-11D-A33O-09 chr14:92488176 T>C did not map to a codon.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr14:92484031 G>T maps to NM_004239.3 I217I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr2:230678651 G>T maps to ENST00000389044 I640I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr2:230650474 C>A maps to ENST00000389044 E1671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr2:230670550 G>A maps to ENST00000389045 R504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr2:230723834 G>C maps to ENST00000389044 S227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr2:230667173 A>G maps to ENST00000389044 G973G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr15:64680165 G>C did not map to a codon.
Sequencing variant TCGA-DS-A7WH-01A-22D-A351-09 chr1:40307501 G>A maps to ENST00000316891 Q440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr1:40315815 G>A maps to ENST00000316891 I226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr19:13227105 C>T maps to NM_001136035.2 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr19:13227099 C>T maps to NM_001136035.2 E38E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:100276200 C>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:100297125 A>C did not map to a codon.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr23:100275543 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr14:61446333 G>A maps to NM_020810.2 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr20:5924564 T>C did not map to a codon.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr23:54955745 C>G did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr23:54950196 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:54950190 G>T did not map to a codon.
Sequencing variant TCGA-JW-A5VG-01A-11D-A28B-09 chr23:54951466 A>G did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:54950073 C>T did not map to a codon.
Sequencing variant TCGA-RA-A741-01A-11D-A33O-09 chr23:54949049 C>G did not map to a codon.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr12:49717829 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr12:49717668 C>T maps to NM_005480.3 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr12:49720470 C>G maps to NM_005480.3 S246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr12:49724817 C>G did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr1:193038216 G>A maps to NM_004600.5 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:193054184 T>C did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:193044962 G>C maps to NM_004600.5 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr3:142462352 C>T maps to ENST00000476941 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr4:122853995 G>A maps to NM_001130698.1 N139N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CG-01A-11D-A32I-09 chr4:122872778 C>T maps to NM_001130698.1 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr4:122835997 C>A maps to NM_001130698.1 V426V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr4:122853863 G>A maps to NM_001130698.1 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr13:38225482 G>C maps to NM_003306.1 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr13:38266216 G>A maps to NM_003306.1 Q385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr13:38266157 C>T maps to NM_003306.1 W404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr20:33591060 C>T maps to NM_015638.2 W761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr23:111090480 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:111155611 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:111195356 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr23:111078179 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr11:101323780 C>A maps to NM_004621.5 E901*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr11:101347229 G>A maps to NM_004621.5 Q516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr15:31362145 G>A did not map to a codon.
Sequencing variant TCGA-C5-A2LS-01A-22D-A22X-09 chr15:31295002 G>A maps to NM_002420.4 N1278N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr15:31332542 G>A maps to NM_002420.4 F676F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr15:31341612 G>A maps to NM_002420.4 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr15:31341661 G>A maps to NM_002420.4 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr21:45862909 C>T did not map to a codon.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr21:45811189 C>T maps to ENST00000397932 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr21:45789053 C>A did not map to a codon.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr21:45837899 C>T maps to ENST00000397932 A1079A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr21:45815322 C>T maps to ENST00000397932 L607L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr19:49713651 C>T maps to NM_017636.3 L1106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr19:49713600 C>G maps to NM_017636.3 L1089L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr11:2439792 G>A maps to ENST00000452833 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr9:77427292 A>G maps to NM_017662.4 F455F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr9:77376683 G>A maps to NM_017662.4 V1571V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr9:77435248 G>A maps to NM_017662.4 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73S-01A-11D-A33O-09 chr9:77377511 C>A maps to NM_017662.4 E1359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr15:50903386 G>C maps to NM_017672.4 S728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr15:50868016 T>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:234869595 G>A maps to NM_024080.4 K513K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr8:116616497 G>A maps to NM_014112.2 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr8:116616304 G>A maps to NM_014112.2 Q631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr8:116616497 G>A maps to NM_014112.2 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5FO-01A-21D-A28B-09 chr11:63992434 G>A maps to NM_001160393.1 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr11:63992159 C>T maps to NM_001160393.1 E119E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr17:3477079 G>A maps to ENST00000399756 F661F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5O9-01A-11D-A28B-09 chr17:16335394 C>A maps to NM_016113.4 Y590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr12:110226261 G>A maps to NM_021625.4 L717L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr12:110221469 G>A maps to NM_021625.4 Q858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:110236472 G>A maps to NM_021625.4 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr7:142606660 G>A maps to NM_019841.4 F630F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr7:142575712 G>C maps to NM_018646.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr7:142573657 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr7:142575434 G>C maps to NM_018646.2 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr7:142573424 C>T maps to NM_018646.2 Q306Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr7:98609720 C>A maps to ENST00000359863 R3775R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr7:98579412 G>T maps to ENST00000359863 E2879*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr9:131071959 G>A maps to NM_015679.1 Q289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr9:131072038 G>A maps to NM_015679.1 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr9:131073193 G>A maps to NM_015679.1 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr9:135797307 G>C maps to NM_000368.4 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R1-01A-11D-A28B-09 chr9:135801120 G>C maps to NM_000368.4 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr16:2106736 C>T maps to NM_000548.3 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr16:2098750 G>A maps to NM_000548.3 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr16:2115599 G>T maps to NM_000548.3 V560V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr16:2108834 C>T maps to NM_000548.3 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr16:2131602 C>T maps to NM_000548.3 T1206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr16:2129354 G>A maps to NM_000548.3 T1070T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr16:2129131 C>T maps to NM_000548.3 L1022L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr16:2129167 C>G maps to NM_000548.3 V1034V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr16:2103359 C>G maps to NM_000548.3 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr13:45148541 G>A maps to NM_183422.2 Q557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr3:150127937 G>A maps to NM_014779.2 Q267Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:106959163 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3L7-01A-21D-A20U-09 chr23:107018612 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr12:58190248 G>A maps to NM_001172696.1 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr2:99695289 C>G did not map to a codon.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr2:99757575 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr7:130357680 G>C maps to NM_052933.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr14:81534645 C>T maps to NM_000369.2 F97F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr14:81422241 C>G did not map to a codon.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr18:72998081 C>T maps to NM_005786.4 F195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr18:72999995 G>A maps to NM_005786.4 E833E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr19:31770290 G>A maps to NM_020856.2 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WI-01A-12D-A351-09 chr19:31770278 C>T maps to NM_020856.2 Q140Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WH-01A-22D-A351-09 chr19:50266486 C>T maps to NM_021733.1 V6V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr19:50265446 C>G maps to NM_021733.1 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr19:50249908 C>T maps to NM_021733.1 W270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R1-01A-11D-A28B-09 chr19:50243365 G>A maps to NM_021733.1 D524D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr8:143361247 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr1:231699371 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr16:67855079 C>G maps to ENST00000339830 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr16:67841096 G>C maps to ENST00000339830 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr1:46651334 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr17:79613520 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr10:82267045 C>T maps to NM_030927.2 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr10:82279343 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr10:82277894 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr10:71267212 C>G did not map to a codon.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr12:58140208 G>A did not map to a codon.
Sequencing variant TCGA-EA-A411-01A-11D-A243-09 chr23:38533570 G>A did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr23:38535081 C>G did not map to a codon.
Sequencing variant TCGA-FU-A770-01A-11D-A33O-09 chr23:53114243 C>G did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:53113755 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2PI-01A-11D-A18J-09 chr6:116574252 G>A maps to ENST00000368611 R357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr6:116575097 G>C maps to ENST00000368611 S75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:54470859 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr2:3323592 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr2:3323593 A>G did not map to a codon.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr2:3323585 G>A did not map to a codon.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr2:3323587 A>C did not map to a codon.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr11:2424849 C>G maps to NM_005706.2 V329V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-C5-A7CJ-01A-11D-A32I-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr8:144696864 G>A maps to NM_003313.3 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr6:43251426 C>T maps to NM_032538.1 L983L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr6:43230634 C>T maps to NM_032538.1 R511R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr6:43237551 G>A maps to ENST00000393984 *623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr6:43237399 C>T maps to ENST00000393984 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:113212395 C>T did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:113230726 G>A maps to NM_017868.3 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr9:130493589 C>G maps to NM_144965.1 S843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr9:130486697 C>G did not map to a codon.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr9:130486937 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr9:130479948 C>G maps to NM_144965.1 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr11:43400839 G>T maps to NM_018259.5 E73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr10:75051772 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr10:75095276 G>A maps to NM_145170.3 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr3:39170290 G>A maps to ENST00000301819 L596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M1-01A-11D-A18J-09 chr3:39178359 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr3:39159649 T>C maps to ENST00000301819 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr2:166799845 G>A maps to NM_024753.3 H145H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr17:40094954 G>A maps to ENST00000377543 E257E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr2:32889466 G>A maps to NM_017735.4 E246E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr2:32855588 G>A did not map to a codon.
Sequencing variant TCGA-EA-A6QX-01A-12D-A33O-09 chr21:38505017 G>A maps to NM_003316.3 K465K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr21:38467757 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr21:38525249 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr2:178482346 G>A maps to NM_152275.3 F361F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:178416150 G>A maps to NM_152517.2 F447F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A69M-01A-11D-A32I-09 chr5:40728488 C>T maps to NM_012382.2 Q131Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:55197169 C>T maps to NM_004623.4 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr14:89341384 C>T maps to NM_144596.2 Q455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr19:40723220 G>C maps to NM_152479.5 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr9:135278097 G>A maps to NM_007344.2 F37F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:117626691 G>A maps to NM_003594.3 L652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr1:117638783 C>T maps to NM_003594.3 Q1017*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:117634489 C>G maps to NM_003594.3 S908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:117620613 T>C maps to NM_003594.3 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:117624634 T>C did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr6:80749468 C>T maps to NM_003318.4 Y729Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:113286900 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:113288820 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:113288910 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr9:124632837 G>A maps to NM_001139442.1 I647I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr22:43567738 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr15:90802005 C>G maps to ENST00000438251 S400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr14:76420865 C>T did not map to a codon.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr14:76243151 G>T maps to NM_015072.4 G782G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr17:46863558 C>T maps to NM_001130918.1 Q576Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:46868949 G>A maps to NM_001130918.1 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A69B-01A-11D-A32I-09 chr20:30467696 G>A maps to ENST00000375932 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr2:179614187 C>T maps to ENST00000375038 E4315E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr2:179395363 C>G maps to NM_133378.4 L32758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr2:179476177 C>G maps to NM_133378.4 L14358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr2:179483069 A>T maps to NM_133378.4 V13137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr2:179458766 A>G maps to NM_133378.4 R16883R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr2:179425301 A>G maps to NM_133378.4 N25951N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr2:179605179 C>T maps to NM_133437.3 A4089A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr2:179393093 G>A maps to NM_133378.4 R33194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr2:179517982 C>G did not map to a codon.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr2:179484534 G>C maps to NM_133378.4 L12935L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CJ-01A-11D-A32I-09 chr2:179482767 C>T maps to NM_133378.4 V13202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UC-01A-11D-A351-09 chr2:179582502 C>T maps to NM_133378.4 L7122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr2:179408346 G>C maps to NM_133378.4 S29550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:179449408 C>T maps to NM_133378.4 A19085A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr2:179427449 G>A maps to NM_133378.4 V25235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr2:179579851 C>T maps to NM_133378.4 K7443K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WH-01A-22D-A351-09 chr2:179498553 C>T maps to NM_133378.4 L11656L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr2:179460336 G>A maps to NM_133378.4 L16680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr2:179399218 C>T maps to NM_133378.4 E31473E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr2:179479454 C>T maps to NM_133378.4 V13694V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr2:179462436 G>C maps to NM_133378.4 V16556V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr2:179481955 G>A maps to NM_133378.4 T13354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr2:179410172 T>C maps to NM_133378.4 A29320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr2:179395465 C>G maps to NM_133378.4 L32724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr2:179424572 C>T maps to NM_133378.4 K26194K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr2:179424575 C>T maps to NM_133378.4 R26193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr2:179581861 G>T maps to NM_133378.4 I7289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr2:179606108 G>A maps to NM_133437.3 Q3780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3EO-01A-11D-A20U-09 chr2:179637916 G>A maps to NM_133378.4 L2592L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:179391858 G>A maps to NM_133378.4 D33384D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:179396050 T>C maps to NM_133378.4 E32529E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:179411049 G>A maps to NM_133378.4 R29102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:179454956 G>A maps to NM_133378.4 R17931*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:179481336 C>A maps to NM_133378.4 E13493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:179560598 G>T maps to NM_133378.4 V9156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:179579121 G>T maps to NM_133378.4 T7549T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:179584977 G>A maps to NM_133378.4 F6553F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:179594405 C>A maps to NM_133378.4 E4948*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:179599565 G>A maps to NM_133378.4 R3785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3TQ-01A-11D-A22X-09 chr2:179590681 C>T maps to NM_133378.4 P5545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HG-A2PA-01A-11D-A20U-09 chr2:179584116 G>T maps to NM_133378.4 A6756A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr2:179467111 C>G maps to NM_133378.4 L15771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr2:179418667 C>A maps to NM_133378.4 E27156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr2:179486626 C>A maps to NM_133378.4 E12440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr2:179501395 C>T maps to NM_133378.4 V11118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr2:179429006 G>C maps to NM_133378.4 V24716V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr2:179589075 G>C maps to NM_133378.4 S5765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:179635313 G>A maps to NM_133378.4 V2735V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:179666892 C>T maps to NM_133378.4 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr2:179407638 C>T maps to NM_133378.4 K29746K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr2:179440106 G>A maps to NM_133378.4 T21016T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr2:179427878 T>C maps to NM_133378.4 L25092L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr2:179641472 C>T maps to NM_133378.4 K1706K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr2:179547592 G>T maps to NM_133378.4 T9731T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73R-01A-11D-A33O-09 chr2:179582535 C>T maps to NM_133378.4 A7111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr8:63976818 G>A maps to NM_000370.3 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr8:63973936 G>A maps to NM_000370.3 F237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3WB-01A-11D-A22X-09 chr18:29175193 C>T maps to ENST00000432547 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr19:54947897 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr19:54932528 C>T maps to ENST00000391739 H128H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr12:49522589 G>A maps to NM_006082.2 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr12:49582663 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:49666529 G>A maps to NM_032704.3 E290E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr2:130953800 G>A maps to NM_207312.2 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr2:130949474 G>A maps to NM_207312.2 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A3L1-01A-11D-A21Q-09 chr22:18609309 C>T maps to NM_018943.2 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr22:18609337 C>G maps to NM_018943.2 S198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr6:30691825 G>A maps to NM_178014.2 Q329Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr6:30691294 C>T maps to NM_178014.2 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr20:57598815 C>T maps to NM_030773.3 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr6:3154870 A>C maps to NM_001069.2 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr6:3154969 G>A maps to NM_001069.2 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr6:3154873 G>A maps to NM_001069.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr6:3224670 C>A did not map to a codon.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr6:3224825 A>G did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:90001668 C>T maps to ENST00000304984 F617F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr10:93875 G>A maps to NM_177987.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr17:57958297 G>C maps to NM_016261.3 S165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr17:57937751 G>T maps to NM_016261.3 I431I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr6:112397150 G>A maps to NM_016262.4 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr17:40818754 C>T maps to NM_016437.2 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr10:135094895 G>A maps to NM_006659.2 F818F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr10:135110840 G>A did not map to a codon.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr10:135096698 G>A maps to NM_006659.2 G724G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:135112975 C>T maps to NM_006659.2 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr13:113213683 G>A maps to NM_006322.4 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr15:43695903 C>A maps to ENST00000399460 I586I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr15:43687351 G>A maps to ENST00000399460 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr15:22849170 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr15:22848315 A>C maps to NM_052903.4 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A69B-01A-11D-A32I-09 chr15:22867456 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr22:50664586 G>C maps to NM_020461.3 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr6:35473851 C>T maps to NM_003322.3 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr19:49392833 G>T maps to NM_003323.2 S190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M1-01A-11D-A18J-09 chr6:158923337 C>T maps to NM_020245.3 T881T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr6:158870080 A>G maps to NM_020245.3 R199R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr6:158834174 C>T maps to NM_020245.3 Q111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr11:62342748 C>A maps to NM_022830.2 L852L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr11:62343111 A>C maps to NM_022830.2 V731V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HM-A4S6-01A-11D-A26G-09 chr11:62344738 G>A maps to NM_022830.2 F433F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr7:19739761 C>A maps to NM_001002926.1 E180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr6:139609793 G>T maps to ENST00000358430 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr23:16859625 C>A did not map to a codon.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr23:16804695 G>A did not map to a codon.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr23:16804696 C>A did not map to a codon.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr23:16836837 G>A did not map to a codon.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr22:36863838 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr17:6545057 C>G did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr18:9886886 C>T maps to NM_001098529.1 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr6:7886213 G>A maps to NM_030810.3 F342F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr1:145441216 G>A maps to NM_006472.3 *392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:145442121 T>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:145442567 A>G did not map to a codon.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr1:145439807 T>C maps to NM_006472.3 Y118Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RL-01A-11D-A18J-09 chr18:54266501 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr12:104719206 G>A maps to NM_001093771.1 T436T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr22:19903311 G>A maps to NM_006440.3 C168C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr22:19906447 C>T maps to NM_006440.3 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr19:10472205 G>A maps to NM_003331.4 V676V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr19:10468251 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:10461838 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:10463227 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr22:50966023 G>A maps to ENST00000395681 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr18:672891 C>G maps to NM_001071.2 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr18:670728 C>G maps to NM_001071.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr11:88911390 G>A maps to NM_000372.4 Q90Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3YQ-01A-11D-A22X-09 chr11:88911210 G>C maps to NM_000372.4 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr19:36395530 G>C maps to NM_003332.3 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr9:12694280 C>T maps to NM_000550.2 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HM-A3JK-01A-11D-A21Q-09 chr10:71899625 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr7:66460412 T>C did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:75202090 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2PI-01A-11D-A18J-09 chr21:44527583 G>A maps to NM_001025203.1 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr15:70959509 C>T maps to NM_018003.2 Q1171Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A556-01A-11D-A26G-09 chr15:70959463 A>G maps to NM_018003.2 L1187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr15:70961396 C>T maps to NM_018003.2 L542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr15:70960112 C>T maps to NM_018003.2 Q970Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:162546700 C>T maps to ENST00000367925 Q139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:162560262 C>T maps to ENST00000367925 F440F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:47071824 G>A did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr23:47062947 G>C did not map to a codon.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr23:47060912 C>T did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr3:132395369 G>C maps to NM_024818.3 *405Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr4:68511734 C>G did not map to a codon.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr3:49847049 C>T maps to NM_003335.2 A671A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr3:49848800 C>A maps to NM_003335.2 E343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr9:138847246 G>A maps to NM_016172.2 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr9:33953363 G>A maps to NM_018449.2 F325F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr1:154241745 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr1:154241822 C>A did not map to a codon.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr1:154241828 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:154241465 C>T did not map to a codon.
Sequencing variant TCGA-RA-A741-01A-11D-A33O-09 chr1:154223746 C>T maps to NM_014847.3 Q482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr12:125397060 G>A maps to NM_021009.5 D419D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr12:125396262 G>C maps to NM_021009.5 V685V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr12:125396451 G>T maps to NM_021009.5 T622T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr4:103747766 C>G did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr4:103747822 C>G did not map to a codon.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr7:129497386 G>A maps to NM_003344.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr16:1358668 G>T maps to ENST00000339021 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr16:1374763 A>G maps to NM_194259.1 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:1203342 C>T maps to NM_194315.1 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr11:57321967 C>T maps to NM_004223.3 Q84Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr23:142967283 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr1:154527963 G>A maps to NM_017582.6 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:154524249 T>C maps to NM_017582.6 K357K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A5XV-01A-11D-A28B-09 chr15:76136659 T>C did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:202302442 G>A maps to NM_014176.3 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr12:109947442 C>T maps to NM_183415.1 F555F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QE-01A-21D-A21Q-09 chr7:157046951 T>C maps to NM_014671.2 G966G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr7:157023912 C>T maps to NM_014671.2 F791F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr7:157046682 T>A maps to NM_014671.2 P910P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr11:118247313 C>T maps to NM_004788.2 I499I. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DG-A2KL-01A-11D-A17W-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr16:23570964 G>T maps to ENST00000219638 E402*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EK-A2RJ-01A-11D-A18J-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr16:23568822 C>G maps to ENST00000219638 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr23:153713870 G>A did not map to a codon.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr1:110655650 G>A maps to NM_203412.1 E165E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HF-01A-11D-A20U-09 chr16:4910676 C>G maps to NM_016936.3 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr16:4921179 G>A maps to NM_016936.3 K528K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr20:3102561 C>T maps to NM_014948.2 E241E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr9:86297961 G>A maps to NM_013438.4 Q118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A5QV-01A-22D-A28B-09 chr23:56590600 C>T did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr11:5529678 G>A maps to NM_017481.2 S370S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr11:5537434 G>C maps to NM_145053.4 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr15:43270091 G>A maps to NM_174916.2 L1402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr15:43335479 T>C maps to NM_174916.2 E594E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr6:42600336 G>A maps to NM_015255.2 K443K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr2:170728793 C>T maps to ENST00000442603 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr2:170917914 C>T maps to ENST00000442603 Q1690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr1:19524207 G>A maps to ENST00000375267 F283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr1:19504089 G>A maps to ENST00000375267 V834V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A3L1-01A-11D-A21Q-09 chr1:19439130 C>T maps to ENST00000375267 L3896L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VK-01A-11D-A28B-09 chr1:19480330 C>T maps to ENST00000375267 P2187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:19401253 G>A did not map to a codon.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr1:19401340 C>T maps to ENST00000375267 L5200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:19490754 C>T maps to ENST00000375267 L1564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr1:19437113 C>T did not map to a codon.
Sequencing variant TCGA-EA-A5ZF-01A-11D-A28B-09 chr17:42292916 C>A did not map to a codon.
Sequencing variant TCGA-EA-A6QX-01A-12D-A33O-09 chr17:42293272 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr17:42289776 G>A maps to NM_014233.2 Q236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr1:26620813 G>A maps to NM_183008.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr2:24194274 G>A maps to NM_181713.3 Q57Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr2:24205897 A>T maps to NM_181713.3 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr2:136528139 G>C did not map to a codon.
Sequencing variant TCGA-EA-A5ZF-01A-11D-A28B-09 chr2:136519419 C>T maps to NM_014607.3 Q181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:136528182 G>T maps to NM_014607.3 E234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr19:4457625 G>C maps to NM_025241.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7X3-01A-11D-A351-09 chr9:134404407 G>A maps to NM_031432.2 R176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr9:134400276 G>C did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr20:62577387 G>A did not map to a codon.
Sequencing variant TCGA-HM-A3JK-01A-11D-A21Q-09 chr20:62575994 G>A maps to NM_017859.3 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr10:13275613 G>A maps to NM_145314.1 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr10:13275541 G>C maps to NM_145314.1 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr4:141484348 C>G maps to NM_021833.4 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr11:18558011 G>C maps to NM_001040697.1 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr22:19442307 G>A maps to ENST00000399525 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr4:39507310 G>A maps to NM_003359.3 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr2:128903519 C>T maps to NM_020120.3 F665F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr13:96506723 C>T maps to NM_020121.3 V1338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A5XV-01A-11D-A28B-09 chr2:234545341 C>T maps to NM_019075.2 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr2:234601814 G>A maps to NM_001072.3 E55E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A6QX-01A-12D-A33O-09 chr2:234590904 C>T maps to NM_019077.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:234590792 G>A maps to NM_019077.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:234581227 A>G maps to NM_021027.2 E216E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr4:70079879 C>T maps to NM_001073.1 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr4:70160415 G>C maps to NM_053039.1 V493V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr4:70361485 C>A maps to NM_021139.2 E32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr4:115589439 G>T maps to NM_003360.3 V414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RA-A741-01A-11D-A33O-09 chr4:115544656 C>A maps to NM_003360.3 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr1:162469973 G>A maps to NM_175866.4 W166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr1:162493116 G>C did not map to a codon.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr1:162467846 C>T maps to NM_175866.4 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr1:162493065 G>C did not map to a codon.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr19:4945949 C>A maps to ENST00000398240 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr19:4929292 C>A maps to ENST00000398240 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZF-01A-11D-A28B-09 chr6:34835143 C>G maps to NM_017754.3 L1185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A6QX-01A-12D-A33O-09 chr6:34827264 G>T maps to NM_017754.3 V1044V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr6:34835376 G>A maps to NM_017754.3 L1234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr12:100482792 C>T maps to NM_015054.1 V307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UC-01A-11D-A351-09 chr6:150290299 C>T maps to NM_025218.2 F143F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr17:19746513 G>A maps to NM_014683.3 Q189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr17:19680993 C>T maps to NM_014683.3 Q984Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr16:20355365 G>A maps to ENST00000424589 T470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr16:20348019 C>T maps to ENST00000424589 G623G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr21:43531074 C>T maps to NM_173568.3 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QD-01A-32D-A22X-09 chr19:17759738 C>T maps to ENST00000428389 T614T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr19:17738364 C>T maps to ENST00000428389 V1379V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr19:17751454 G>A maps to ENST00000428389 L972L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr19:17756546 G>A maps to ENST00000428389 F852F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr15:54630686 G>A maps to ENST00000260323 P1571P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr17:73838974 C>T maps to ENST00000412096 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr17:73831077 G>A maps to ENST00000412096 Q639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr15:91496405 C>T maps to NM_018671.3 Q815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73S-01A-11D-A33O-09 chr15:91488275 T>C maps to NM_018671.3 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr15:91479681 C>T maps to NM_018671.3 Q140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr4:96104151 G>A maps to NM_003728.3 L783L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr6:41002619 G>C maps to NM_173561.2 S65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RL-01A-11D-A18J-09 chr8:35624427 G>A maps to ENST00000416672 P779P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr6:167719470 C>T maps to NM_018974.3 D303D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr6:167711436 C>A maps to NM_018974.3 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr7:1273249 G>A maps to NM_001080461.1 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A0TN-01A-21D-A14W-08 chr12:109537061 C>T maps to NM_080911.2 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr12:109541278 C>T maps to NM_080911.2 Q222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr16:1453236 C>T maps to ENST00000508903 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr16:1463962 G>A maps to ENST00000508903 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R9-01A-11D-A18J-09 chr22:24923768 T>A did not map to a codon.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr19:18967004 C>T maps to ENST00000418384 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr19:18974273 G>A maps to ENST00000418384 P887P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:18968251 C>T maps to ENST00000418384 L709L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr10:11997476 G>A maps to NM_015542.2 R868R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr10:11971865 C>T maps to NM_015542.2 G1269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr23:118971799 C>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:118975125 C>A did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr23:118985825 C>T did not map to a codon.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr23:118979189 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr19:36164144 C>T maps to NM_007000.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr19:36164425 C>G maps to NM_007000.2 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A4BA-01A-21D-A26G-09 chr11:118828882 C>T maps to NM_006760.3 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr7:76144471 C>T maps to NM_030570.2 A289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr7:48146626 C>T maps to NM_003364.2 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:74523423 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr19:1605402 C>T maps to NM_006830.3 V2V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr3:48643247 C>T maps to NM_003365.2 E84E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr16:21994416 G>A maps to NM_003366.2 K429K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr5:132203225 C>T maps to NM_014402.4 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr1:229773069 T>C maps to NM_014777.2 L904L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr1:229773086 C>G maps to NM_014777.2 L909L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr7:43916663 G>A maps to NM_001077663.1 L800L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr7:43918599 C>T maps to NM_001077663.1 E154E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr9:131151898 G>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr9:131151911 G>A did not map to a codon.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr3:126218959 C>A maps to NM_001165974.1 E455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr3:126201219 C>A maps to NM_001165974.1 E727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr19:35770408 C>G did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr17:72915594 G>T maps to NM_173477.2 R446R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr1:216465553 T>C maps to ENST00000366943 G601G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr1:215987234 G>A maps to ENST00000366943 N3194N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr1:215955460 C>A maps to ENST00000366943 E3555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:216166365 C>T maps to ENST00000366943 P2267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr1:216380626 G>A maps to ENST00000366943 Q1102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr1:215807848 C>T maps to ENST00000366943 Q5083Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr19:17374920 G>A maps to NM_031941.3 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr16:84808823 C>G maps to NM_005153.2 L734L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr16:84793793 C>T maps to NM_005153.2 I489I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr23:47101545 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr23:47106742 G>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:47106540 C>G did not map to a codon.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr23:47104245 G>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:47106534 G>A did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr23:47098790 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:47106747 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr12:62798350 T>G did not map to a codon.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr3:49154040 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr9:132641780 G>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr9:132637225 C>G maps to NM_001008563.3 L680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr1:161131809 T>G did not map to a codon.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr17:20919104 G>A maps to ENST00000455117 F334F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr17:20919143 C>T maps to ENST00000455117 R321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:55569601 C>A maps to NM_015306.2 E1658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr1:55539504 G>A maps to NM_015306.2 Q2508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:55586324 G>A maps to NM_015306.2 L1484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:55680733 G>C maps to NM_015306.2 S18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr21:17246833 G>T maps to ENST00000285681 E962*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr23:132161142 G>T did not map to a codon.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr23:132161542 C>A did not map to a codon.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr23:132161098 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:132161382 A>G did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:132159900 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr23:132159589 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr23:132159936 T>G did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr11:113711321 G>A maps to NM_020886.2 Q178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr11:113685931 G>A maps to NM_020886.2 Q546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr11:113674599 C>G did not map to a codon.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr19:57641165 G>T maps to NM_020903.2 E375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr19:57640513 G>C maps to NM_020903.2 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr15:63880980 G>A maps to NM_006537.2 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr12:109505431 G>A maps to NM_032663.3 Q160Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr16:23117741 C>A maps to NM_020718.3 E280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr11:77911808 C>T maps to NM_020798.2 F384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr11:77921399 C>A maps to NM_020798.2 L833L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr2:219321884 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr2:219330899 C>A did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr2:85876360 G>C did not map to a codon.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr3:49331004 G>A did not map to a codon.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr7:6189272 G>A maps to ENST00000404835 S482S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr17:9596526 C>A maps to NM_153210.3 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PD-01A-11D-A351-09 chr17:9549281 C>T maps to NM_153210.3 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:22056233 T>C maps to NM_032236.5 Q421Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr23:55515231 C>T did not map to a codon.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr23:55513290 G>C did not map to a codon.
Sequencing variant TCGA-EA-A411-01A-11D-A243-09 chr23:55514363 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr23:55514504 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr23:55515181 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:55514413 G>A did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr23:55514408 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr4:120188513 C>T maps to NM_019050.2 R338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr4:120192584 C>T maps to NM_019050.2 Q524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr10:75258748 G>A maps to NM_152586.3 Q1565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr10:75277078 G>A maps to NM_152586.3 P1035P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr17:5032142 C>T did not map to a codon.
Sequencing variant TCGA-JW-A852-01A-11D-A351-09 chr17:5037190 G>T maps to NM_004505.2 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KH-01A-21D-A22X-09 chr15:50785053 C>T maps to NM_005154.3 N797N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr15:50776512 G>A maps to NM_005154.3 R615R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr23:41077745 G>A did not map to a codon.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr23:41055964 G>A did not map to a codon.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr23:41029360 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:40999951 G>A did not map to a codon.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr23:41075523 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:41055533 C>A did not map to a codon.
Sequencing variant TCGA-JW-A852-01A-11D-A351-09 chr23:41043694 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr13:31232649 C>A maps to NM_005800.4 S812S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr13:31205522 G>A maps to NM_005800.4 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr13:31205522 G>A maps to NM_005800.4 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr13:31227299 C>T maps to NM_005800.4 F418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr13:31232304 G>A maps to NM_005800.4 E697E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr13:31205522 G>A maps to NM_005800.4 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr1:38484133 A>G did not map to a codon.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr23:129041399 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:129042054 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr23:129047354 G>C did not map to a codon.
Sequencing variant TCGA-HM-A3JK-01A-11D-A21Q-09 chr23:129059021 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:129055460 G>C did not map to a codon.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr23:129042082 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr12:101684593 C>G maps to NM_014503.2 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr8:117861160 C>A did not map to a codon.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr17:30228607 G>A maps to NM_018428.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr6:145093094 C>T maps to NM_007124.2 Q2850*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr6:145079122 C>T maps to NM_007124.2 I2831I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr6:145079200 C>A did not map to a codon.
Sequencing variant TCGA-Q1-A73S-01A-11D-A33O-09 chr1:7906776 G>T maps to ENST00000377516 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:75776811 C>T maps to NM_003369.3 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr23:47518368 C>T did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:47511527 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr23:47516582 C>A did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr23:47516606 C>G did not map to a codon.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr16:70834761 G>A maps to NM_018052.3 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr12:6579754 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr2:85820263 C>G maps to NM_006634.2 S112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr1:160395020 G>A maps to NM_020335.2 K473K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:160393994 C>T maps to NM_020335.2 T409T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr20:56965215 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr20:57019855 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr6:31749934 G>A maps to NM_006295.2 Q724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr6:30882089 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr14:77242381 G>C maps to NM_014909.4 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:213125051 C>T maps to NM_024749.3 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr16:4432188 G>A maps to NM_138440.2 T437T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr16:4431255 C>T maps to NM_138440.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr19:6828464 G>A maps to NM_005428.2 K353K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr19:6828095 C>T maps to NM_005428.2 Q313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M1-01A-11D-A18J-09 chr9:136649440 G>C maps to NM_001134398.1 L544L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr9:136857229 G>C maps to NM_001134398.1 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A411-01A-11D-A243-09 chr1:108115881 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr1:101194864 C>T maps to NM_001078.3 N377N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr5:82817175 T>G maps to NM_004385.4 S1017S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:82832805 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr5:82815883 G>T maps to NM_004385.4 E587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr5:82876340 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr10:75757940 G>A did not map to a codon.
Sequencing variant TCGA-EA-A50E-01A-21D-A26G-09 chr8:67547563 G>T maps to NM_025054.4 G947G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr8:67576720 C>A maps to NM_025054.4 E825*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:6451977 T>C did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr23:8434328 C>T did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr23:8434153 G>C did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr23:8434033 G>C did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:76979067 C>T maps to NM_001184783.1 Q119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr8:42256270 A>G maps to ENST00000417062 K54K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr11:64003439 C>T maps to NM_003377.3 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr4:177713351 G>A maps to NM_005429.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr3:157213147 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr3:157206874 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr12:95676222 G>A maps to NM_017599.3 V377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr7:100807817 G>A maps to NM_003378.3 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr23:135630902 T>A did not map to a codon.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr23:135631025 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr3:11600914 C>T maps to NM_014667.2 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:38043240 G>T maps to NM_015873.3 E457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr3:38047733 G>A maps to NM_015873.3 E732E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr10:17276862 C>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr10:17278315 C>T maps to NM_003380.3 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr6:153073373 C>G maps to NM_003381.2 S21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M1-01A-11D-A18J-09 chr3:42576526 C>T maps to NM_004624.3 F357F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:36982178 G>T maps to NM_053276.3 E131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr2:37035658 C>T maps to NM_053276.3 S478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VI-01A-11D-A28B-09 chr7:65419184 C>T maps to NM_173517.3 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr9:2643292 C>T maps to NM_003383.3 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr19:53761979 G>T maps to NM_173856.2 G118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr19:53761996 C>G maps to NM_173856.2 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr19:53770597 G>A maps to NM_173857.2 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr6:133035099 G>A maps to NM_004666.2 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr7:55540724 C>T maps to NM_030796.3 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr3:51458161 G>A maps to ENST00000273612 I754I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr11:118938587 G>T maps to NM_021729.4 V18V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:118940947 C>T maps to NM_021729.4 F158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr9:79840895 G>T maps to ENST00000376646 E406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr9:79932559 G>A maps to ENST00000376646 Q1634Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr8:100155379 C>T maps to NM_017890.3 S610S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr8:100133457 C>T maps to NM_017890.3 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr8:100796655 G>A maps to NM_017890.3 A2656A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A411-01A-11D-A243-09 chr8:100844676 T>G maps to NM_017890.3 P3162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr8:100108603 C>G maps to NM_017890.3 S119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr8:100844847 C>T maps to NM_017890.3 L3219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr8:100712048 C>T maps to NM_017890.3 Q2140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr15:62283885 G>T maps to NM_020821.2 S490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr15:62173100 G>A maps to NM_020821.2 L3277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr15:62146685 C>T maps to NM_020821.2 V3744V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr15:62207972 G>C maps to NM_020821.2 V2768V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr1:12309610 A>G did not map to a codon.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr1:12359380 G>A maps to NM_015378.2 L2052L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:12414077 C>A maps to NM_015378.2 S3160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr20:2843295 G>A maps to NM_022575.2 Q381Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A852-01A-11D-A351-09 chr20:2845014 C>T maps to NM_022575.2 F575F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3PZ-01A-11D-A21Q-09 chr20:2845874 C>T maps to NM_022575.2 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr10:70883964 G>C did not map to a codon.
Sequencing variant TCGA-EA-A3QE-01A-21D-A21Q-09 chr8:145650984 G>A did not map to a codon.
Sequencing variant TCGA-DS-A7WH-01A-22D-A351-09 chr12:122745915 C>T maps to NM_022916.4 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr15:91549238 C>T maps to NM_018668.3 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr16:46706272 G>A maps to NM_018206.4 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr8:17155655 G>A did not map to a codon.
Sequencing variant TCGA-DG-A2KH-01A-21D-A22X-09 chr8:17137455 A>C did not map to a codon.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr11:60901631 C>T maps to NM_017966.4 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr15:42455912 T>C maps to ENST00000348544 E691E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr15:42457227 A>G maps to ENST00000348544 G632G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:150040826 G>A did not map to a codon.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr18:61074677 C>T maps to NM_004869.3 Q117Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZD-01A-11D-A28B-09 chr6:33239434 G>A maps to NM_022553.4 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr6:33239390 G>C maps to NM_022553.4 S21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr6:33218545 G>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr6:33239312 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr6:33232074 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr17:465782 G>A maps to NM_001128159.2 R506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HR-01A-11D-A20U-09 chr2:64147683 G>A maps to NM_016516.2 T649T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr1:151149167 G>T maps to ENST00000354473 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr1:151150621 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr3:184573497 G>C did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr3:184642660 G>A maps to ENST00000437079 E822E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr19:50498169 C>T maps to NM_016440.3 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:50482461 G>A maps to NM_016440.3 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr19:50512550 G>A maps to NM_016440.3 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr23:107319385 C>T did not map to a codon.
Sequencing variant TCGA-C5-A2M2-01A-21D-A18J-09 chr23:107320503 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr23:107315937 A>C did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:107320496 G>T did not map to a codon.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr23:107320569 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:107304671 C>T did not map to a codon.
Sequencing variant TCGA-LP-A5U3-01A-11D-A28B-09 chr12:118520133 G>A maps to NM_019086.5 N154N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr11:124618302 A>G maps to NM_014312.3 Y278Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M2-01A-21D-A18J-09 chr23:65242303 A>C did not map to a codon.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr23:65242171 G>T did not map to a codon.
Sequencing variant TCGA-EA-A44S-01A-12D-A26G-09 chr23:65253526 G>T did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr1:159827564 G>A maps to NM_001013661.1 Q208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr19:54551653 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr6:142519610 C>T maps to NM_016485.3 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr10:114287025 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr17:26695896 G>A maps to NM_000638.3 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr17:26696312 G>A maps to NM_000638.3 F222F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:116048874 C>T maps to NM_198496.1 F583F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr10:116048802 C>T maps to NM_198496.1 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr16:22132908 C>T maps to NM_173615.3 Q443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr16:22122306 C>T maps to NM_173615.3 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:98861918 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr2:98928685 G>A maps to NM_144992.4 A1253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr11:123989238 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr7:49815706 C>T maps to NM_198570.3 Q226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr11:61034993 G>A maps to NM_152718.2 I635I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3EO-01A-11D-A20U-09 chr12:6120957 G>A maps to NM_000552.3 P1889P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr12:6128107 C>T maps to NM_000552.3 R1492R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr10:28827294 G>C maps to ENST00000424883 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HQ-01A-11D-A20U-09 chr10:28821810 G>A did not map to a codon.
Sequencing variant TCGA-EA-A6QX-01A-12D-A33O-09 chr10:28900808 C>T maps to NM_016628.3 I465I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr10:28821933 G>T did not map to a codon.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr10:88196712 G>T did not map to a codon.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr10:88196318 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr10:88196032 C>T did not map to a codon.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr23:48547407 C>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr6:110423186 G>A maps to NM_003931.2 Q376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr6:110423275 G>C maps to NM_003931.2 S346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr7:123332689 G>C maps to NM_003941.2 S353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr2:74685708 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr2:74685749 G>C maps to ENST00000393972 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr2:74686630 C>G did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr22:42394814 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr13:41639316 G>A maps to NM_007187.3 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZF-01A-11D-A28B-09 chr7:74466871 G>A maps to NM_030798.3 N421N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr7:74486520 C>T maps to NM_030798.3 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HR-01A-11D-A20U-09 chr7:70597808 C>G maps to NM_022479.1 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr7:71177115 G>A maps to NM_022479.1 K594K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr7:71178133 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr7:71134985 C>T maps to NM_022479.1 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr7:71177238 C>G did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr13:52158942 C>T maps to NM_052950.3 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr4:85731123 G>C maps to NM_014991.4 S754*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr4:85710968 C>T maps to NM_014991.4 W1193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr4:10083052 C>A maps to NM_017491.3 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr4:10117965 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr10:122668849 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LC-01A-11D-A20U-09 chr10:122668663 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr10:122633396 G>C maps to NM_018117.11 L506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LS-01A-22D-A22X-09 chr23:48462648 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr23:48460335 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:48458939 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:48462651 C>T did not map to a codon.
Sequencing variant TCGA-MY-A5BE-01A-21D-A26G-09 chr23:48458813 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:48456173 G>A did not map to a codon.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr4:39246133 C>T maps to NM_025132.3 Y869Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr4:39271644 G>C maps to NM_025132.3 L1136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:39217799 C>T maps to NM_025132.3 R407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr16:737620 C>T maps to ENST00000248142 E330E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:224621579 G>A maps to NM_025160.6 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A0TN-01A-21D-A14W-08 chr6:169959694 C>A did not map to a codon.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr1:118477107 C>T maps to NM_006784.2 Q62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:118482164 G>A maps to NM_006784.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:118491032 G>A maps to NM_006784.2 G476G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr9:116098696 C>G did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:128471325 G>A maps to NM_018383.4 R1047*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr2:20189767 G>A maps to NM_001006657.1 F3F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr2:20113419 C>A maps to NM_001006657.1 E1149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WH-01A-22D-A351-09 chr5:110428129 G>A maps to NM_139281.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr5:110428116 C>G maps to NM_139281.2 S44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr10:1142134 C>T maps to ENST00000416775 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A78R-01A-11D-A32I-09 chr9:127618158 G>A maps to NM_001045476.1 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr21:44273713 G>A maps to NM_018669.4 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr21:44274709 G>A maps to NM_018669.4 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr2:29165187 C>A maps to NM_015131.1 S582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:29147998 C>T maps to NM_015131.1 Q356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr23:117480347 C>G did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:117528058 A>G did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:117528025 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:117532407 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr23:48934501 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:48934312 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:48935735 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:48932478 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr23:48932840 G>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:48932469 C>T did not map to a codon.
Sequencing variant TCGA-JW-A852-01A-11D-A351-09 chr23:48935158 G>C did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr6:33246900 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3TX-01A-11D-A22X-09 chr1:109514102 G>A maps to NM_001142550.1 F911F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QE-01A-21D-A21Q-09 chr3:39133112 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr3:39136443 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2RL-01A-11D-A18J-09 chr3:113120478 G>A maps to NM_001164496.1 F426F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:74652558 G>T maps to NM_032118.2 E272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr3:122134138 G>C maps to NM_019069.3 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr3:49051890 C>G maps to NM_018031.3 L944L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CJ-01A-11D-A32I-09 chr3:49049890 G>A maps to NM_018031.3 E338E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CJ-01A-11D-A32I-09 chr3:49049971 G>A maps to NM_018031.3 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:49049137 G>A maps to NM_018031.3 Q87Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A50E-01A-21D-A26G-09 chr3:49049119 G>C maps to NM_018031.3 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr3:49051432 C>T maps to NM_018031.3 P852P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:158723167 C>G maps to NM_018051.4 V836V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr15:78577610 G>A maps to NM_025234.1 Q274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr1:241904938 C>T maps to NM_144625.4 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr1:241875109 C>G maps to NM_144625.4 V317V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:241920749 C>T maps to NM_144625.4 Q636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr1:43647298 C>T maps to NM_001195831.1 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A852-01A-11D-A351-09 chr18:54694410 C>T maps to NM_015285.2 D1482D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R3-01A-11D-A28B-09 chr18:54606543 T>A maps to NM_015285.2 V1328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A69B-01A-11D-A32I-09 chr5:37392222 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr15:54003549 G>A maps to NM_182758.2 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr11:62601345 G>C maps to NM_018093.2 S280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr2:190329968 G>A maps to NM_032168.1 K426K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr1:67340543 G>C maps to NM_024763.4 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr17:1639341 C>T maps to NM_001163809.1 R1779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2GZ-01A-11D-A17W-09 chr17:1637013 C>T maps to NM_001163809.1 S1561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr17:1634414 G>A maps to NM_001163809.1 A1340A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr17:1629279 G>T maps to NM_001163809.1 E343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr17:1629455 G>A maps to NM_001163809.1 K401K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RA-A741-01A-11D-A33O-09 chr17:1629269 C>A maps to NM_001163809.1 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr7:151074055 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr16:705683 G>A maps to NM_145294.4 Q610Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr16:712706 C>T maps to NM_145294.4 L1392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A410-01A-11D-A243-09 chr16:707789 G>A maps to NM_145294.4 A834A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr15:90276273 T>C maps to NM_020212.1 C456C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U3-01A-11D-A28B-09 chr1:27608761 G>A maps to ENST00000319394 W55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr20:44258463 G>A maps to NM_080753.2 Q4Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr16:683819 C>T maps to NM_053284.2 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr16:682596 G>T maps to NM_053284.2 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr17:48917536 G>A maps to NM_175575.5 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr15:83485559 G>T maps to NM_001080435.1 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr4:1919927 G>T maps to NM_133335.3 E330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr4:1961445 C>G maps to NM_133335.3 V1078V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RL-01A-11D-A18J-09 chr8:38174708 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr8:38172264 C>T maps to NM_023034.1 L714L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr12:56295839 G>C maps to NM_032345.2 S144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr2:175431873 G>A maps to NM_003387.4 S460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr2:175436509 G>C maps to NM_003387.4 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr17:38421117 C>G maps to NM_133264.4 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr7:5254157 G>C maps to ENST00000315176 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr7:5267827 G>A maps to NM_015610.3 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr7:5256387 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr6:112389477 C>A maps to NM_198239.1 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr19:15539199 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr19:15547671 G>C maps to ENST00000389282 L847L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr19:15547785 G>A maps to ENST00000389282 I809I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr19:15547791 G>A maps to ENST00000389282 I807I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr19:15538982 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr12:978056 A>G maps to NM_001184985.1 Q1055Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr12:993813 G>A did not map to a codon.
Sequencing variant TCGA-JW-A852-01A-11D-A351-09 chr12:970492 C>T maps to NM_001184985.1 P645P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CJ-01A-11D-A32I-09 chr23:54263680 C>T did not map to a codon.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr23:54324624 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:54324667 T>G did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:54264791 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:54228425 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:54337696 G>A did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr23:54278032 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr17:40939477 C>T maps to NM_032387.4 V553V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr7:116962986 G>A maps to NM_003391.2 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr1:228194834 C>T maps to ENST00000366753 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr1:22448031 C>T maps to NM_030761.4 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3YQ-01A-11D-A22X-09 chr3:55504017 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:55504100 G>C maps to ENST00000442038 S120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WI-01A-12D-A351-09 chr22:46319121 G>A maps to NM_058238.2 R222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr17:44950036 C>T maps to NM_003396.1 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A411-01A-11D-A243-09 chr17:7604111 T>A maps to NM_018081.2 Y232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr8:31012234 C>T maps to NM_000553.4 I1261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr6:2785497 C>T maps to NM_020135.2 F660F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr6:2770430 C>G maps to NM_020135.2 V364V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3PZ-01A-11D-A21Q-09 chr6:2779556 C>T maps to NM_020135.2 D439D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr6:2779571 G>A maps to NM_020135.2 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr12:108603969 G>C maps to ENST00000261400 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr6:160176555 G>C maps to NM_004906.3 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr19:34991086 G>A maps to ENST00000270288 A626A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RE-01A-11D-A18J-09 chr19:34973056 G>T maps to ENST00000270288 E284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr23:10106898 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:10035325 G>C did not map to a codon.
Sequencing variant TCGA-C5-A7CL-01A-11D-A32I-09 chr16:69971534 C>T maps to NM_007014.3 Q775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr16:69974026 G>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:7689277 G>A maps to NM_020196.2 F292F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr19:7685818 C>T maps to NM_020196.2 Q628Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HQ-01A-11D-A20U-09 chr17:6659438 T>G did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:52893803 C>A did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr3:46063161 C>T maps to NM_005283.2 W93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr2:31572577 C>T maps to NM_000379.3 R981R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:123025118 G>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr3:39229160 C>T maps to NM_194293.2 Q592Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr3:39228398 C>T maps to NM_194293.2 L846L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73S-01A-11D-A33O-09 chr3:39230621 G>T maps to NM_194293.2 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr2:168106691 G>A maps to NM_152381.5 V2930V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr2:168102428 C>T maps to NM_152381.5 I1509I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr2:168115686 A>T maps to ENST00000420519 G910G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr2:168067269 G>A maps to NM_152381.5 E196E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr23:37587666 T>A did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:37545230 C>T did not map to a codon.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr22:17265192 C>G maps to NM_175878.3 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr8:56436428 C>T maps to NM_052898.1 A532A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HR-01A-11D-A20U-09 chr8:56015800 C>T maps to NM_052898.1 C251C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q8-01A-11D-A21Q-09 chr8:56436065 C>A maps to NM_052898.1 I411I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr1:28293329 C>G maps to NM_018053.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr1:28293344 C>T maps to NM_018053.2 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr8:71646349 T>A maps to NM_001011720.1 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr23:100177949 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3EO-01A-11D-A20U-09 chr23:100169812 G>A did not map to a codon.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr23:100169462 A>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr9:100449428 C>T maps to NM_000380.3 K168K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr10:111624806 T>G did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr10:111624694 G>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr10:111637620 G>A maps to NM_020383.3 Q416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr10:111651573 G>A maps to NM_020383.3 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RO-01A-11D-A18J-09 chr23:128902409 G>C did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:128885727 C>G did not map to a codon.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr23:128876101 C>A did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr22:41318402 C>G maps to NM_022098.2 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:28192331 G>C maps to NM_015171.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr8:21845356 C>T maps to ENST00000434536 F601F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr12:64813962 G>A maps to NM_007235.3 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr1:180849253 G>C maps to NM_004736.3 L617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr14:104165739 C>G maps to NM_005432.3 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr14:104166941 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr5:82606691 A>G did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:217002873 G>A maps to NM_021141.3 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr22:42049548 C>T maps to NM_001469.3 F382F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr20:21309245 C>G maps to NM_012255.3 S122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr20:21284092 C>T maps to NM_012255.3 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr20:21335436 C>T maps to NM_012255.3 L649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr20:21314411 G>A maps to NM_012255.3 W335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr20:21328884 G>A maps to NM_012255.3 T589T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr11:74651898 G>A maps to NM_182969.1 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UC-01A-11D-A351-09 chr11:74656093 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr11:74651875 C>G maps to NM_182969.1 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr11:74656104 T>G did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr16:17202794 G>A maps to NM_022166.3 L879L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WI-01A-12D-A351-09 chr16:17353100 G>A maps to NM_022166.3 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr16:17292211 G>T maps to NM_022166.3 R382R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr12:42629418 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr1:33245678 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:33256706 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:32908136 G>C maps to NM_001040436.1 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:7196798 G>T maps to NM_015982.3 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:183476668 C>T maps to NM_018023.4 I524I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr18:724572 G>A maps to NM_005433.3 Q495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:54354630 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr6:43483439 C>T did not map to a codon.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr5:143541825 C>T maps to NM_030799.7 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:67751725 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73S-01A-11D-A33O-09 chr19:19638111 G>T maps to ENST00000436926 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr7:44246080 G>A maps to NM_006555.3 E95E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr14:75266401 T>C did not map to a codon.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr14:75266119 C>T maps to NM_019589.2 R1374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr1:207222841 T>A maps to NM_018566.3 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr5:112902972 C>G maps to NM_022828.3 L1009L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr5:112917197 C>T maps to NM_022828.3 Q1147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr8:64122914 C>T did not map to a codon.
Sequencing variant TCGA-DS-A7WF-01A-11D-A351-09 chr8:64122716 A>G did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr8:64122559 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr8:64125041 C>G did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr8:64123779 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr8:64124493 C>G did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr22:32352574 C>T maps to NM_003405.3 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr14:100705961 C>T maps to NM_003403.3 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:155644833 G>C maps to ENST00000368339 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr23:21875257 T>A did not map to a codon.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr17:74077999 C>T maps to NM_180990.3 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr17:74076557 G>A maps to ENST00000425015 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr2:174055645 T>C maps to NM_016653.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr2:174074484 C>G maps to NM_016653.2 S258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr7:100355922 C>T maps to ENST00000349350 T1136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr7:100349806 G>A maps to ENST00000349350 T693T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr7:100389621 G>T maps to ENST00000349350 R2521R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr7:100344302 C>T maps to ENST00000349350 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr7:100365527 C>T maps to ENST00000349350 L1645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr7:100391774 C>G maps to ENST00000349350 L2673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A852-01A-11D-A351-09 chr2:98351724 C>T maps to NM_001079.3 D365D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr4:48494962 C>T maps to NM_175619.1 F355F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A50E-01A-21D-A26G-09 chr3:167086283 G>A maps to ENST00000307529 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr3:167090680 T>C maps to ENST00000307529 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:2408335 G>A did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr20:56191471 C>T maps to NM_030776.2 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3YQ-01A-11D-A22X-09 chr3:101383875 G>A maps to NM_014415.3 R519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr6:31868749 C>T maps to NM_181842.2 Q111Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RA-01A-11D-A18J-09 chr1:16271697 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:16268387 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:16269298 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:16270202 C>T maps to ENST00000375733 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:16271563 C>T maps to ENST00000375733 E265E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:16271599 C>T maps to ENST00000375733 E253E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:16272373 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3WB-01A-11D-A22X-09 chr3:114069160 G>A maps to NM_001164342.1 T588T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:114057932 G>A maps to NM_001164342.1 Y715Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr6:33284081 G>A maps to NM_001145338.1 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3YQ-01A-11D-A22X-09 chr6:33283916 C>T maps to NM_001145338.1 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KJ-01A-11D-A18J-09 chr6:109787777 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2GZ-01A-11D-A17W-09 chr11:62519843 G>A maps to NM_024784.3 F481F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZF-01A-11D-A28B-09 chr23:119388667 G>T did not map to a codon.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr23:119388942 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr23:119388903 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr1:173840187 G>T maps to NM_001122770.1 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:173839611 C>G maps to NM_001122770.1 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr3:141161571 G>A maps to NM_001080412.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr3:141162300 C>G maps to NM_001080412.2 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr3:141164490 C>T maps to NM_001080412.2 I1087I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr17:7365528 G>A maps to NM_020899.3 L924L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr17:7366071 C>T maps to NM_020899.3 K743K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr17:7366074 C>A maps to NM_020899.3 R742R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:22817949 C>G maps to NM_014870.3 S252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:22835629 G>C maps to NM_014870.3 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A5XV-01A-11D-A28B-09 chr1:197169635 A>G did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr9:129595498 C>T maps to NM_014007.3 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr11:130103258 C>A maps to ENST00000397753 E569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr19:59025615 G>C maps to NM_032792.2 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr20:62421189 G>A maps to NM_025224.2 F307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr3:42700891 G>T maps to NM_145166.3 E349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr9:125673271 C>T maps to NM_006626.4 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr19:4054348 C>A maps to NM_015898.2 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr19:4054918 C>A maps to NM_015898.2 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr1:154975262 G>A did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr1:33058777 C>T maps to NM_001040441.1 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr12:56512079 A>G did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr1:203819565 G>C did not map to a codon.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr1:203771245 C>G did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:203770988 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr1:203770892 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr1:203765596 G>A did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr1:203771388 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:37941278 C>A maps to NM_025079.2 S61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr1:37945918 C>A maps to NM_025079.2 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr23:64722634 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr23:64717049 A>G did not map to a codon.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr23:64709106 G>T did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:64722152 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr11:110030026 C>T maps to NM_033390.1 F320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr11:110008100 G>C maps to NM_033390.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr2:187373328 G>T maps to NM_018471.2 E384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr16:88694027 A>T did not map to a codon.
Sequencing variant TCGA-DS-A7WF-01A-11D-A351-09 chr19:47597686 C>A maps to NM_015168.1 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr19:47568443 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:113057489 G>T maps to NM_198581.2 E33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CJ-01A-11D-A32I-09 chr22:41716681 G>A maps to ENST00000351589 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr2:112995976 T>C maps to NM_032494.2 Q95Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:64136734 A>C did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:64141714 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr23:64136881 G>A did not map to a codon.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr23:117959930 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr23:117959557 G>A did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr23:73524430 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr23:73524600 G>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:111698091 G>T did not map to a codon.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr1:31836881 A>T maps to NM_016505.2 K190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:77913089 C>T did not map to a codon.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr23:77912936 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr9:88960658 G>A maps to NM_024617.3 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr9:37120658 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr12:122958742 G>C maps to NM_017612.2 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CH-01A-11D-A33O-09 chr2:207169839 C>T maps to NM_020923.1 N196N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr2:207170955 C>T maps to NM_020923.1 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr16:67432777 G>C maps to NM_013304.2 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr5:848730 G>A maps to NM_024786.2 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A852-01A-11D-A351-09 chr5:825287 C>T maps to NM_024786.2 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CG-01A-11D-A32I-09 chr9:131483964 C>T maps to ENST00000372667 Q163Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HM-A3JK-01A-11D-A21Q-09 chr9:131486102 G>C did not map to a codon.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr11:19197383 G>A maps to NM_019028.2 Q582Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr11:19192108 C>G maps to NM_019028.2 L542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:74725671 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr13:21950738 G>A did not map to a codon.
Sequencing variant TCGA-C5-A0TN-01A-21D-A14W-08 chr3:113681777 T>C did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr3:113672892 C>T maps to NM_173570.3 Q170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr3:113678540 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr3:113672892 C>T maps to NM_173570.3 Q170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr11:66311237 G>A maps to NM_207340.1 R166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr3:44959379 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr10:114194091 C>T maps to NM_022494.1 W289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LB-01A-11D-A243-09 chr16:85011578 C>T maps to NM_001145548.1 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr22:20127391 G>T maps to NM_013373.3 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:128947659 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr10:31815697 C>T maps to NM_001174096.1 Q962*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr2:145157220 G>A maps to NM_014795.3 V511V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr2:145275289 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr2:145147235 C>A maps to NM_014795.3 E1143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr9:131497625 G>A maps to NM_006336.2 L709L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr9:131503816 C>T maps to NM_006336.2 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PI-01A-11D-A18J-09 chr6:38120553 G>A did not map to a codon.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr9:74969853 C>A did not map to a codon.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr9:74970852 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr9:74969815 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr12:72038797 G>A maps to NM_144982.4 Q380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr12:72021565 G>C maps to NM_144982.4 L1365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr16:72992895 G>A maps to NM_006885.3 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr16:72821170 G>A maps to NM_006885.3 L3668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr16:72821212 C>G maps to NM_006885.3 S3654S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr16:72828825 G>A maps to NM_006885.3 A2585A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr16:72993678 C>T maps to NM_006885.3 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr16:72828477 G>A maps to NM_006885.3 F2701F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr16:72828797 G>A maps to NM_006885.3 Q2595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr16:72845842 C>T maps to NM_006885.3 S1208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr16:72845490 C>T maps to NM_006885.3 E1283E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr16:72984826 G>A maps to NM_006885.3 G919G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr16:72827609 G>A maps to NM_006885.3 Q2991*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr16:72829028 G>A maps to NM_006885.3 Q2518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr8:77763458 C>T maps to NM_024721.4 F1434F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr8:77768237 C>T maps to NM_024721.4 F3027F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr8:77767016 C>G maps to NM_024721.4 L2620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PI-01A-11D-A18J-09 chr8:77763575 C>T maps to NM_024721.4 S1473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr8:77618005 C>T maps to NM_024721.4 D561D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr8:77776072 G>T maps to NM_024721.4 E3375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr8:77767197 C>T maps to NM_024721.4 R2681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr19:57066328 C>A maps to NM_020828.1 G725G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr19:57065695 C>T maps to NM_020828.1 F514F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr14:69256774 G>A maps to NM_004926.2 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:69262693 C>G maps to NM_207442.2 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr14:69259640 G>A maps to NM_004926.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr2:43452372 C>T maps to NM_006887.4 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr2:43452528 C>T maps to NM_006887.4 Q138Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr9:115806339 C>T maps to NM_003408.1 Q186Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr9:115805336 G>A maps to NM_003408.1 Q521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:188923975 G>A maps to NM_174900.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr6:29641065 G>A maps to NM_001109809.2 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr16:68592276 G>C did not map to a codon.
Sequencing variant TCGA-EA-A3QD-01A-32D-A22X-09 chr11:64853950 C>T maps to NM_006782.3 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr8:106646568 C>T maps to NM_012082.3 C172C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr8:106431432 C>A maps to NM_012082.3 I34I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr5:32355731 C>G did not map to a codon.
Sequencing variant TCGA-FU-A3WB-01A-11D-A22X-09 chr19:3827624 C>T maps to NM_015174.1 Q293Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr23:24225965 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr23:24229098 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr23:24225502 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr23:24197539 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:24197733 G>A did not map to a codon.
Sequencing variant TCGA-HM-A4S6-01A-11D-A26G-09 chr14:73444864 G>A maps to NM_021260.2 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr14:68265154 C>T maps to NM_015346.3 K608K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr14:68251079 G>A maps to NM_015346.3 L1199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:68257343 C>A maps to NM_015346.3 R900R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr14:68221928 G>A maps to NM_015346.3 F2275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr14:68229099 G>A maps to NM_015346.3 T2063T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RA-A741-01A-11D-A33O-09 chr10:99516959 G>T did not map to a codon.
Sequencing variant TCGA-FU-A3YQ-01A-11D-A22X-09 chr4:2307162 C>A maps to NM_020972.2 G302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr4:2343312 G>A maps to NM_020972.2 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr19:10416085 G>C maps to NM_001103167.1 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr8:124279615 T>C did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr8:124266325 T>A maps to NM_007222.3 K621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr8:124267820 C>G maps to NM_007222.3 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr8:124268337 C>A did not map to a codon.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr8:123966101 G>A maps to NM_014943.3 E784E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr3:147128258 C>G maps to NM_003412.3 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr3:147128759 C>T maps to NM_003412.3 Y287Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr23:136649871 G>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr23:136649492 C>T did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:136649737 C>T did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:136649776 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr23:136649776 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A6DV-01A-11D-A32I-09 chr23:136659319 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr3:147106137 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr3:147106078 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr3:147121822 C>T maps to NM_001168378.1 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr7:99627903 C>A maps to NM_003439.1 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H1-01A-11D-A17W-09 chr7:99621383 G>T maps to NM_003439.1 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr16:25251137 C>G maps to NM_001012981.4 *968S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr6:28327423 G>T maps to NM_024493.2 E21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr6:28213015 G>A maps to NM_019110.3 Q506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr7:99129641 C>T maps to NM_014569.3 Q764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WH-01A-22D-A351-09 chr23:101139636 T>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:101138740 T>C did not map to a codon.
Sequencing variant TCGA-EA-A411-01A-11D-A243-09 chr23:101141646 C>A did not map to a codon.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr23:101139181 C>G did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr23:101139057 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr8:40532226 C>T maps to NM_024645.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr10:81070928 G>A maps to NM_020338.3 E1028E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr7:44804561 C>T maps to NM_031449.3 L651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr1:40726593 C>G maps to NM_005857.3 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:40737687 G>A maps to NM_005857.3 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr1:40723959 C>A maps to NM_005857.3 S6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:35579237 C>T maps to NM_024772.3 R603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CH-01A-11D-A33O-09 chr23:70468077 G>A did not map to a codon.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr23:70470477 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr23:70472919 G>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:70473059 G>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:70469442 C>G did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr23:70461084 G>A did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr1:35853071 C>T maps to NM_005095.2 F710F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:35469540 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr3:50382635 C>T maps to NM_015896.2 E40E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr1:42898672 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr17:4649283 G>C maps to NM_001136046.1 *743S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr19:19790232 A>G maps to NM_033204.2 Q145Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr19:19788737 T>C maps to NM_033204.2 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OA-01A-11D-A16Y-08 chr7:64439462 T>C maps to NM_015852.3 E162E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr7:6731191 C>A maps to ENST00000330442 G518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr7:6731025 G>C maps to ENST00000330442 S573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr7:6731055 G>C maps to ENST00000330442 S563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr7:6732155 G>C maps to ENST00000330442 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr19:58945829 G>A maps to NM_003433.3 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr19:58948492 C>T maps to NM_003433.3 E51E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr20:18296265 C>T maps to ENST00000401790 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr20:18297584 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr20:18297520 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr19:19822545 G>C maps to NM_021030.2 S515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OA-01A-11D-A16Y-08 chr19:19823159 T>C maps to NM_021030.2 K310K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr19:36728008 C>T maps to NM_007145.2 Q223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr19:58214144 G>A maps to NM_001085384.1 Q58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr19:44500375 C>T maps to NM_003445.2 Q123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr23:47269680 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr23:47272357 C>G did not map to a codon.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr23:47270143 G>C did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr23:47272494 G>T did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:47272076 G>C did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr23:47272384 G>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:47272520 G>T did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr8:146157668 C>T maps to NM_006958.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RK-01A-11D-A18J-09 chr9:97055556 C>G did not map to a codon.
Sequencing variant TCGA-EK-A2H1-01A-11D-A17W-09 chr19:9491579 C>T maps to NM_001172651.1 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr17:11881614 G>A maps to NM_144680.2 Q437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr17:11895969 C>T maps to NM_144680.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr19:45001413 G>A maps to NM_013256.3 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr19:44982159 G>A maps to NM_013256.3 Q180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr23:47837063 C>G did not map to a codon.
Sequencing variant TCGA-EA-A3QD-01A-32D-A22X-09 chr23:47835796 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:47842378 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr23:47836510 T>A did not map to a codon.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr6:27419368 G>A maps to NM_007149.2 L657L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr6:27420476 G>A maps to NM_007149.2 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr6:27419273 A>G maps to NM_007149.2 H688H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr23:152089260 C>T did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr23:152106655 G>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr9:104171025 C>T maps to NM_003452.2 R326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr16:71512830 G>A maps to NM_006961.3 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A852-01A-11D-A351-09 chr16:71509102 G>T maps to NM_006961.3 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:3380801 G>C maps to NM_001130520.1 S479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr3:44685486 G>A maps to NM_006991.3 E955E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr16:3274469 G>A maps to NM_198088.2 R204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr11:123611149 A>G did not map to a codon.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr11:123601371 C>T maps to NM_003455.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RA-A741-01A-11D-A33O-09 chr11:123599866 T>C maps to NM_003455.2 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WH-01A-22D-A351-09 chr17:30700348 T>A did not map to a codon.
Sequencing variant TCGA-EK-A2IP-01A-11D-A17W-09 chr19:22115996 C>T did not map to a codon.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr16:3191191 G>A maps to NM_001134655.1 K408K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr10:45499193 C>A maps to NM_006963.4 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr19:44571243 C>G maps to NM_013361.4 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr19:44635873 G>A maps to NM_013362.2 E369E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr19:44740264 C>G maps to NM_182490.1 S561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr19:44740133 G>A maps to NM_182490.1 E517E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr19:44740721 G>A maps to NM_182490.1 E713E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr19:44732431 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr19:44934109 C>T maps to NM_014518.2 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr16:71481923 C>G did not map to a codon.
Sequencing variant TCGA-C5-A2M1-01A-11D-A18J-09 chr19:44514809 C>T maps to NM_006300.3 Q207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr19:44662098 C>T maps to NM_006630.2 R644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr18:74587575 C>T maps to NM_007345.3 Q264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr18:74649141 C>A maps to NM_007345.3 S1540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr18:74593359 G>T maps to NM_007345.3 E435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr18:74580681 G>A maps to NM_007345.3 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr10:38120187 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr10:38121766 C>T maps to NM_021045.1 E172E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr10:38265468 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr10:38242110 G>C maps to NM_145011.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr8:145948192 C>G maps to NM_138367.1 R284R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr19:24289359 C>T maps to NM_203282.2 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr19:22271010 C>G maps to NM_033468.2 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr19:37005777 T>A maps to NM_001166038.1 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr16:3335109 C>T maps to NM_005741.4 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr16:31926595 C>T maps to NM_003414.4 I342I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HL-01A-11D-A20U-09 chr12:133780221 G>T maps to NM_001165881.2 T650T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr7:64349230 C>G did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr19:58718432 G>A maps to NM_133502.1 W201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:152612884 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr23:152612966 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr19:53304955 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr19:53303789 C>T maps to NM_006969.3 E436E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr22:22868859 G>A maps to NM_080740.3 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr19:44590139 C>G maps to NM_001037813.2 S170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr5:150275564 G>A maps to NM_001172831.1 T428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr19:35175899 A>T maps to ENST00000221282 K399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UC-01A-11D-A351-09 chr6:43307343 C>T maps to NM_014345.2 P1464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PI-01A-11D-A18J-09 chr6:43307898 C>T maps to NM_014345.2 K1279K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr6:43305621 G>C maps to NM_014345.2 V2038V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr6:43325331 G>A maps to NM_014345.2 I240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr10:44139650 C>T maps to NM_006973.2 R223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:53382787 C>G did not map to a codon.
Sequencing variant TCGA-C5-A2LX-01A-11D-A18J-09 chr19:58967303 C>T maps to NM_207395.2 H331H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:90487840 C>G maps to NM_182976.2 V446V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr19:54040625 C>A did not map to a codon.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr20:44592363 C>G did not map to a codon.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr20:44580950 C>T maps to NM_022095.3 P1008P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr10:38343651 G>A maps to NM_006954.1 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr10:43078390 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr8:145999028 C>T maps to NM_030580.3 V435V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A43B-01A-81D-A243-09 chr8:145998847 G>A maps to NM_030580.3 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr20:32358056 C>T maps to ENST00000375200 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr20:2464232 C>T maps to NM_024325.4 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr20:2465218 G>A maps to NM_024325.4 Q130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CH-01A-11D-A33O-09 chr19:37383798 C>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr19:37368457 T>G maps to NM_003419.3 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr19:53652616 G>A maps to NM_001172674.1 Q7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr3:44700919 C>T maps to NM_003420.3 I355I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr19:52468864 G>A maps to NM_021632.3 Q281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr5:178506305 G>A maps to NM_014594.1 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr19:7585259 C>T maps to NM_018083.4 Q378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr19:7584277 C>G maps to NM_018083.4 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr19:7584331 G>A maps to NM_018083.4 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr10:64162064 C>G did not map to a codon.
Sequencing variant TCGA-FU-A3EO-01A-11D-A20U-09 chr10:64160272 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr10:64135972 G>A maps to NM_199451.2 E7E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr5:71756369 G>A maps to NM_152625.1 F318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr5:71740118 C>G did not map to a codon.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr10:38403717 C>T maps to NM_003421.2 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr10:38407181 C>A maps to NM_003421.2 S368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr19:37118329 C>T maps to NM_032825.3 Q511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:37733786 C>T maps to NM_152604.1 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:37734032 C>T maps to NM_152604.1 Q299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr19:37734224 G>T maps to NM_152604.1 E363*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-C5-A1M6-01A-11D-A13W-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr12:6776899 C>A maps to NM_001135734.1 E572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:6782422 C>T maps to NM_001135734.1 E290E. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-JW-A5VJ-01A-11D-A28B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr12:6787339 G>T maps to NM_001135734.1 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr2:180306847 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr3:22414019 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr3:21465553 G>A maps to NM_024697.2 H285H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr7:99097647 C>T maps to NM_032164.2 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr18:32954013 C>T maps to NM_145756.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr18:32825269 G>T maps to NM_001135178.2 E201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr18:32823309 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr18:32823309 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr11:46726059 G>A maps to NM_024741.2 Q270Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr23:47307880 G>C did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:47307792 C>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:47307960 T>A did not map to a codon.
Sequencing variant TCGA-FU-A770-01A-11D-A33O-09 chr23:47307756 T>C did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:47308715 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:47308801 G>C did not map to a codon.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr19:8578211 G>C maps to NM_001146175.1 S6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr19:53612191 G>C maps to NM_001164309.1 S369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:58438813 G>A maps to NM_133460.1 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr19:58004284 C>G maps to NM_001098491.1 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr19:58004449 C>T maps to NM_001098491.1 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr16:49671685 G>A maps to NM_015069.2 H459H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr7:148802631 C>A maps to NM_001001661.2 E111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OA-01A-11D-A16Y-08 chr19:21720462 T>C maps to NM_001001415.2 P536P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr19:21712560 G>A maps to NM_001001415.2 E35E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr19:52538019 G>C maps to NM_014650.2 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr19:52537253 G>A maps to NM_014650.2 Q560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr19:11978580 G>T maps to NM_152262.2 E233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZF-01A-11D-A28B-09 chr19:12359150 G>A maps to ENST00000426973 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MY-A5BD-01A-11D-A26G-09 chr19:12384319 C>T maps to NM_001164276.1 E298E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr19:11891820 T>C maps to NM_152355.2 C394C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr19:11891038 C>T maps to NM_152355.2 Q134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A7WI-01A-12D-A351-09 chr19:12461053 G>A maps to NM_030824.2 R449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr19:12542058 A>G maps to NM_005815.4 Y309Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr19:12542451 G>A maps to NM_005815.4 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A5XV-01A-11D-A28B-09 chr19:58989541 G>A maps to NM_017908.2 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:134493903 T>G did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr23:134483046 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:44418648 G>A maps to NM_003425.3 F313F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr19:44418461 G>A maps to NM_003425.3 Q376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr6:56993562 G>T maps to NM_001031623.2 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HT-01A-61D-A21Q-09 chr9:109691646 C>T maps to NM_021224.4 P1818P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr9:109691938 G>T maps to NM_021224.4 E1916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr9:109691271 G>A maps to NM_021224.4 K1693K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr19:53344688 G>C maps to NM_001008801.1 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr19:57088789 G>A maps to NM_001001668.3 Q331Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr19:57036218 C>G maps to NM_020813.2 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QS-01A-61D-A22X-09 chr19:50550226 C>T maps to NM_015428.1 Q843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr19:50549916 C>T maps to NM_015428.1 F739F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LB-01A-11D-A243-09 chr5:121488159 C>T maps to NM_207317.1 Q159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr7:57188192 G>C maps to NM_033273.1 S310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr16:30409038 C>T maps to ENST00000495929 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr16:30409680 C>G maps to ENST00000495929 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5O9-01A-11D-A28B-09 chr16:30409620 C>G maps to ENST00000495929 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr19:52803700 G>A maps to NM_144684.2 K12K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A7HU-01A-11D-A33O-09 chr19:52825334 C>T maps to NM_144684.2 Q278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr9:114304894 C>T maps to NM_133464.2 F560F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:95610230 C>A maps to NM_031486.1 E280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AW-01A-11D-A243-09 chr9:95609814 C>T maps to NM_031486.1 G418G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OA-01A-11D-A16Y-08 chr19:20308379 C>T maps to ENST00000428290 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr19:20308811 G>A maps to ENST00000428290 E425E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R1-01A-11D-A28B-09 chr19:12721467 G>A maps to NM_020714.2 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr19:22846668 G>A maps to NM_020855.2 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr19:21607217 C>G maps to NM_001076678.2 S586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr19:21606430 G>T maps to NM_001076678.2 E324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7X3-01A-11D-A351-09 chr1:247492544 C>T maps to NM_032752.1 Q112Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RL-01A-11D-A18J-09 chr1:247471183 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr16:4812280 G>A maps to NM_021646.1 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr3:44776203 G>C maps to NM_145044.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr3:44762969 C>T maps to NM_033210.4 R221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HY-01A-11D-A21Q-09 chr19:19905634 G>C maps to NM_001099269.2 S354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr19:32843798 G>A maps to NM_014910.4 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr19:32838120 G>C did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr9:99522048 G>A maps to NM_014930.1 Q355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr10:135125333 C>A maps to NM_145806.2 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr10:135125360 C>T maps to ENST00000359035 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GN-01A-11D-A20U-09 chr20:62595897 C>T maps to NM_020713.1 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr2:95815400 G>A maps to NM_032788.1 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr18:74092248 C>T maps to ENST00000443185 P607P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr18:74074244 T>C did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr8:146032958 C>T maps to NM_213605.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr10:97917656 T>C maps to NM_014803.3 S526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr10:97922158 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2PM-01A-11D-A18J-09 chr18:14105613 G>A maps to NM_145287.3 Q309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr18:14105019 G>A maps to NM_145287.3 Q507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr18:14105109 G>A maps to NM_145287.3 Q477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr18:22806009 T>A maps to NM_015461.2 G624G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VG-01A-11D-A28B-09 chr18:22805592 G>A maps to NM_015461.2 N763N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AU-01A-32D-A243-09 chr18:22805421 C>T maps to NM_015461.2 A820A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr19:37865088 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr19:37865091 G>A did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr19:37862021 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr19:52919121 T>G maps to NM_032423.2 Y339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr19:52909927 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr19:52905261 C>G did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr19:58117822 C>T maps to NM_020880.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr19:58117825 T>A maps to NM_020880.3 I311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:58117123 G>A maps to NM_020880.3 Q77Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr18:56615334 C>T maps to NM_018181.4 F914F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr18:56606736 T>C maps to NM_018181.4 G863G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr18:56606769 T>C maps to NM_018181.4 I874I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr19:52942557 C>T maps to NM_001143939.1 F628F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr19:52954653 C>T maps to ENST00000424032 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr19:30935509 C>T maps to NM_014717.1 C347C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZF-01A-11D-A28B-09 chr19:31039804 C>T maps to NM_014717.1 S1093S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2GZ-01A-11D-A17W-09 chr19:30934828 C>T maps to NM_014717.1 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QS-01A-61D-A22X-09 chr19:57839192 C>G maps to NM_213598.3 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr19:40513242 C>T maps to NM_178544.3 D78D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RB-01A-11D-A18J-09 chr19:57910878 C>T maps to NM_001172773.1 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr19:58063841 G>A did not map to a codon.
Sequencing variant TCGA-EA-A5O9-01A-11D-A28B-09 chr19:58071045 G>A did not map to a codon.
Sequencing variant TCGA-EA-A3HR-01A-11D-A20U-09 chr19:2852401 C>A maps to NM_152791.4 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr19:2877792 C>T maps to NM_024967.1 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr19:8932740 G>A maps to NM_144693.1 Q20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HE-01A-21D-A22X-09 chr19:9730239 T>C did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr19:12432089 G>A maps to NM_145276.2 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr19:12637493 G>C maps to NM_144976.3 P476P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr19:36964288 C>T maps to NM_001145343.1 Q27Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr19:37211353 C>T maps to ENST00000423498 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A770-01A-11D-A33O-09 chr19:37487753 G>A maps to ENST00000444991 R387R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr19:37904284 G>A maps to NM_152484.2 F425F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr19:37958830 G>C did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr19:37961247 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr19:37974925 T>G maps to NM_144694.1 Y134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr19:37961244 G>T did not map to a codon.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr19:37961254 G>T did not map to a codon.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr19:52391204 G>T did not map to a codon.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr19:52364163 G>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:52376892 G>C maps to NM_032679.2 S117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr19:53014381 C>T maps to NM_001099694.1 Q250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr19:56089505 G>A maps to NM_152600.2 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UC-01A-11D-A351-09 chr19:56901418 G>A maps to NM_144690.1 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr19:56935047 C>T maps to NM_001159861.1 Q341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr19:37643543 G>A maps to ENST00000356958 F419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr19:37676173 G>A maps to NM_152279.3 F755F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr19:58290284 C>T maps to NM_017652.2 H110H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr19:58325932 C>G did not map to a codon.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr17:5085837 G>A maps to NM_032530.1 Q572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr17:5085174 C>A maps to NM_032530.1 E793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr17:5086045 G>C maps to NM_032530.1 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OA-01A-11D-A16Y-08 chr4:86924 A>G maps to NM_182524.2 V510V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr4:85883 T>C maps to NM_182524.2 H163H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HG-A2PA-01A-11D-A20U-09 chr4:60293 T>C did not map to a codon.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr8:183046 G>C did not map to a codon.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr19:35250658 C>T maps to NM_001007248.2 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr19:53269067 G>A maps to NM_198457.2 F647F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr19:58491315 A>G maps to NM_025027.3 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr19:38200718 G>C maps to NM_032689.4 S5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A4AV-01A-11D-A243-09 chr5:123984459 C>T maps to NM_020747.2 E539E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr15:64791778 C>G maps to NM_015042.1 S54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr15:64973555 C>G maps to NM_015042.1 S1404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr15:64966713 C>G maps to NM_015042.1 S554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr19:53208776 T>A maps to NM_001161500.1 K511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr19:53217356 G>C maps to NM_001161500.1 S34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OA-01A-11D-A16Y-08 chr19:52443520 C>T maps to NM_001031721.3 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr19:52443954 C>T maps to NM_001031721.3 I76I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:52443469 G>A maps to NM_001031721.3 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr19:52496663 G>C maps to ENST00000354939 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr19:52618220 G>A maps to NM_178523.3 L732L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QE-01A-21D-A21Q-09 chr9:116790995 G>C did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr9:116812419 C>T maps to ENST00000374126 L946L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:40528734 C>G maps to NM_001145082.2 S285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr3:40523817 G>A maps to NM_001145082.2 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr3:40529413 C>T maps to NM_001145082.2 F511F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr3:40529423 C>T maps to NM_001145082.2 Q515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr3:40557889 C>T maps to NM_175888.2 Q269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr5:16465641 C>A maps to NM_033414.2 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HM-A4S6-01A-11D-A26G-09 chr5:16465735 G>A maps to NM_033414.2 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A3HD-01B-11D-A20U-09 chr8:144733544 C>T maps to NM_014789.3 N501N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr19:11727566 C>T maps to NM_145295.3 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A51Y-01A-11D-A26G-09 chr19:11725658 C>T maps to NM_145295.3 Q50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr19:55994437 C>A maps to NM_033113.2 I622I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr16:30793805 G>A maps to NM_001080417.1 R615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UE-01A-11D-A33O-09 chr23:47919005 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr23:47918788 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr23:47918821 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:47918394 C>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:47918814 C>A did not map to a codon.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr23:47919231 C>A did not map to a codon.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr23:47917922 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr2:71602546 C>T did not map to a codon.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr2:71635302 C>T maps to NM_014497.3 L1063L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr2:71620687 G>A maps to ENST00000411930 K948K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr2:71658312 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr1:91403561 A>G maps to NM_201269.1 H1056H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KM-01A-11D-A17W-09 chr23:22291648 C>G did not map to a codon.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr23:22291583 C>T did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr23:22291430 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr16:31091076 G>A maps to NM_014699.3 P1144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr16:31090080 C>T maps to NM_014699.3 V812V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr16:31090134 C>T maps to NM_014699.3 F830F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr16:31089784 G>T maps to NM_014699.3 E714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr7:99173861 G>C did not map to a codon.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr7:99169958 C>T maps to NM_001083956.1 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73R-01A-11D-A33O-09 chr7:99172796 G>T did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr9:40768502 C>T did not map to a codon.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr9:40774574 G>A maps to NM_033160.5 Q234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr9:40773897 C>G maps to NM_033160.5 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A6DT-01A-11D-A32I-09 chr19:53669310 G>A maps to NM_024733.3 S144S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-C5-A1BI-01B-11D-A13W-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr16:31075396 G>A maps to NM_001172669.1 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr19:58233777 G>A maps to ENST00000335820 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VI-01A-11D-A28B-09 chr1:249142780 C>T maps to NM_024836.1 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr23:46359522 C>T did not map to a codon.
Sequencing variant TCGA-C5-A7UC-01A-11D-A351-09 chr23:46382533 G>C did not map to a codon.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr19:53740237 G>C maps to NM_182609.2 S581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H6-01B-11D-A22X-09 chr7:63981580 G>A maps to NM_178558.4 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr7:64023444 G>C did not map to a codon.
Sequencing variant TCGA-DS-A1OA-01A-11D-A16Y-08 chr19:23926944 T>C maps to NM_138286.2 K469K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A57G-01A-11D-A26G-09 chr19:23926851 A>G maps to NM_138286.2 H500H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr19:20150173 C>A did not map to a codon.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr1:41012966 G>A maps to NM_152373.3 E324E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MU-A5YI-01A-11D-A32I-09 chr16:30581407 G>A maps to NM_145271.3 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr16:30615815 C>T maps to NM_138447.1 S424S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr19:12014479 G>C maps to ENST00000429654 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr1:247163259 C>T maps to NM_020394.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2LZ-01A-11D-A20U-09 chr8:144375237 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:120168532 G>C maps to NM_001080470.1 S64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73S-01A-11D-A33O-09 chr19:9407493 C>A maps to NM_198535.1 E196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr8:146068093 C>T maps to ENST00000446747 F544F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr8:146067953 C>T maps to ENST00000446747 Q498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CK-01A-11D-A32I-09 chr19:53059186 G>C did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr8:37556023 G>T maps to NM_025069.1 R535R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A57G-01A-11D-A26G-09 chr8:37556104 G>T maps to NM_025069.1 P562P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5ZE-01A-11D-A28B-09 chr8:144773222 G>A did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr8:144776765 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr19:12606283 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr19:57133524 C>T maps to NM_021216.4 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr19:57133911 C>T maps to NM_021216.4 F419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr23:84525753 G>A did not map to a codon.
Sequencing variant TCGA-DS-A5RQ-01A-11D-A28B-09 chr23:84502591 G>T did not map to a codon.
Sequencing variant TCGA-EA-A3HQ-01A-11D-A20U-09 chr23:84525769 C>T did not map to a codon.
Sequencing variant TCGA-EA-A439-01A-11D-A243-09 chr23:84526708 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr23:84526760 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73P-01A-11D-A32I-09 chr23:84520159 G>A did not map to a codon.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr22:20755624 G>A maps to NM_003426.2 W102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3QE-01A-21D-A21Q-09 chr7:149171620 G>A maps to NM_001163474.1 R598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3NI-01A-11D-A21Q-09 chr7:149171492 G>A maps to NM_001163474.1 T640T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr7:149172452 G>A maps to NM_001163474.1 F320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr19:57956144 C>G maps to NM_001023561.2 L543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr19:57946914 C>G did not map to a codon.
Sequencing variant TCGA-LP-A5U2-01A-11D-A28B-09 chr17:80789923 G>T maps to NM_024702.2 S136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U3-01A-11D-A28B-09 chr17:80789322 T>A maps to NM_024702.2 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LP-A5U3-01A-11D-A28B-09 chr17:80789325 G>A maps to NM_024702.2 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr17:80790160 G>C maps to NM_024702.2 S57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3EO-01A-11D-A20U-09 chr16:3361823 G>A did not map to a codon.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr16:3358638 G>T did not map to a codon.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr23:134421466 C>T did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr23:134427772 C>T did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:35260388 G>A maps to NM_003427.3 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3TQ-01A-11D-A22X-09 chr6:35260670 C>T maps to NM_003427.3 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr19:53958417 G>A maps to NM_001008401.3 E219E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr19:53960272 G>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr19:53960250 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr16:30567087 C>G maps to NM_033410.3 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5O9-01A-11D-A28B-09 chr19:53926629 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr19:53911452 C>T maps to NM_001040185.1 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr19:52794062 C>G maps to NM_001010851.2 S340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3Y4-01A-51D-A243-09 chr16:30536770 C>T maps to NM_024671.3 E230E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr19:2934413 C>T maps to NM_021217.2 Q237Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PL-01A-11D-A18J-09 chr19:2933927 C>T maps to NM_021217.2 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr19:2934813 C>T did not map to a codon.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr15:35274378 C>T maps to NM_014106.3 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A5FO-01A-21D-A28B-09 chr15:35275293 G>A maps to NM_014106.3 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr15:35274572 G>A maps to NM_014106.3 Q355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr19:58016763 G>T maps to NM_198542.1 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A50E-01A-21D-A26G-09 chr15:90903468 G>T maps to NM_001004309.2 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr7:149129367 C>T maps to ENST00000440594 T666T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A50E-01A-21D-A26G-09 chr7:149152525 C>T maps to ENST00000440594 E196E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr16:89294117 G>A maps to NM_182531.2 E446E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr19:56599961 G>A maps to NM_001002836.2 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LF-01A-21D-A22X-09 chr19:56614300 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr9:130207190 C>T maps to NM_007135.2 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr19:12739989 G>A maps to NM_153358.2 E549E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr19:12739204 C>T maps to NM_153358.2 R288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr19:38024379 C>G did not map to a codon.
Sequencing variant TCGA-DG-A2KL-01A-11D-A17W-09 chr19:12502747 G>C maps to NM_001080821.2 S155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr19:58806466 G>A maps to NM_021089.2 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr19:58797540 G>T maps to NM_021089.2 E87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr7:127014975 A>C maps to NM_176814.3 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A40J-01A-11D-A243-09 chr7:88966313 G>T maps to NM_181646.2 E1340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr7:88966145 C>T maps to NM_181646.2 Q1284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A5QV-01A-22D-A28B-09 chr7:88964909 C>T maps to NM_181646.2 Q872*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q1-A73O-01A-11D-A32I-09 chr23:47755274 C>G did not map to a codon.
Sequencing variant TCGA-R2-A69V-01A-11D-A32I-09 chr23:47755251 G>T did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr23:47774736 C>A did not map to a codon.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr23:47775373 C>T did not map to a codon.
Sequencing variant TCGA-EK-A2RN-01A-12D-A20U-09 chr19:53993927 C>T maps to NM_001004301.3 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr4:146791580 C>T maps to ENST00000508784 E599E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7X3-01A-11D-A351-09 chr19:37383007 G>A maps to NM_001171979.1 Q310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HR-01A-11D-A20U-09 chr19:37382766 G>C maps to NM_001171979.1 S390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr19:37399291 G>A maps to NM_001171979.1 Q137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KH-01A-21D-A22X-09 chr19:53117016 T>G maps to NM_018300.3 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GJ-01A-21D-A20U-09 chr19:53116854 C>T maps to NM_018300.3 E321E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2H0-01A-11D-A17W-09 chr17:33288932 G>A maps to NM_052857.3 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr20:57768902 C>T maps to NM_178457.1 L943L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DG-A2KK-01A-11D-A17W-09 chr20:57768912 C>T maps to NM_178457.1 Q947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr20:57768812 C>T maps to NM_178457.1 P913P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WL-A834-01A-11D-A351-09 chr20:57767393 C>T maps to NM_178457.1 I440I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr14:102793112 G>A maps to NM_018335.3 T360T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr7:149557787 G>A maps to NM_001099220.1 V513V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:12155222 C>T maps to NM_001080404.1 K378K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr19:23489881 C>T did not map to a codon.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr19:23542270 C>T maps to NM_003430.2 A1170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7CO-01A-11D-A351-09 chr19:20044222 C>G maps to NM_031218.3 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H6-01B-11D-A22X-09 chr19:20026189 G>A maps to NM_031218.3 E35E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr19:22585687 T>A did not map to a codon.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr19:22715224 C>T did not map to a codon.
Sequencing variant TCGA-DS-A1OA-01A-11D-A16Y-08 chr19:22939434 C>T maps to ENST00000397104 G912G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr20:47872367 G>A maps to NM_021035.2 L927L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr22:29446271 G>A maps to NM_032173.2 W601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr19:5456110 G>A maps to NM_181710.3 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2PG-01A-11D-A18J-09 chr19:5455847 C>T maps to NM_181710.3 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr19:5456143 G>T maps to NM_181710.3 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr16:21221008 G>A maps to NM_003460.1 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr16:21215707 G>A maps to NM_003460.1 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JX-A3Q0-01A-11D-A21Q-09 chr7:50097645 G>A maps to NM_007009.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr1:71530061 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr1:71544391 C>T did not map to a codon.
Sequencing variant TCGA-IR-A3LI-01A-11D-A20U-09 chr23:15818014 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr19:58564882 G>T maps to NM_182572.3 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:58565154 G>A maps to NM_182572.3 P321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr19:58565040 G>A maps to NM_182572.3 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr16:3140072 G>A maps to NM_032805.1 H399H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A2M2-01A-21D-A18J-09 chr19:58596126 C>T maps to NM_001145542.1 A542A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr19:58601750 G>A maps to NM_001145542.1 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GM-01A-11D-A20U-09 chr15:85165834 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A5R2-01A-11D-A28B-09 chr15:85164940 C>T maps to NM_181877.3 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr1:33960202 C>G maps to NM_145238.3 L753L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:33960286 C>G maps to NM_145238.3 L781L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A3GK-01A-11D-A20U-09 chr19:58850040 G>A maps to NM_181846.2 K275K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:43658611 C>T maps to NM_152455.3 Q306Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R7-01A-11D-A18J-09 chr19:58187557 G>A maps to NM_152677.2 E15E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr19:56778129 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BQ-01C-11D-A20U-09 chr19:56701339 G>A maps to NM_001080456.2 F448F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr19:56701804 C>G maps to NM_001080456.2 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H6-01B-11D-A22X-09 chr19:56702269 C>T maps to NM_001080456.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RJ-01A-11D-A18J-09 chr2:187693430 A>C maps to NM_182521.2 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr20:44506246 C>G maps to NM_080752.3 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr20:44507086 C>G maps to NM_080752.3 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UC-A7PF-01A-11D-A351-09 chr20:44506549 G>A maps to NM_080752.3 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RD-01A-12D-A20U-09 chr19:13930180 C>T maps to NM_023072.2 F528F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JW-A5VL-01A-11D-A28B-09 chr1:45671716 G>A maps to NM_020883.1 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr6:116988228 C>A maps to NM_145062.2 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr11:113631296 C>A maps to NM_004724.2 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2R8-01A-21D-A18J-09 chr11:113610022 G>A maps to NM_004724.2 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr10:58118055 C>G did not map to a codon.
Sequencing variant TCGA-IR-A3LL-01A-11D-A20U-09 chr10:58118683 C>A maps to NM_032997.2 E169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A2QG-01A-11D-A18J-09 chr23:57935543 C>T did not map to a codon.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr23:57936103 C>T did not map to a codon.
Sequencing variant TCGA-JW-A5VJ-01A-11D-A28B-09 chr23:57620101 G>A did not map to a codon.
Sequencing variant TCGA-JW-A852-01A-11D-A351-09 chr23:57619631 G>A did not map to a codon.
Sequencing variant TCGA-Q1-A6DW-01A-11D-A32I-09 chr23:57620521 T>C did not map to a codon.
Sequencing variant TCGA-C5-A7UH-01A-11D-A351-09 chr3:126193877 G>A maps to NM_025112.4 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr7:143079494 G>A maps to NM_001010972.1 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LA-01A-11D-A22X-09 chr7:143080070 C>T maps to NM_001010972.1 Q227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr17:3989911 G>A maps to NM_015113.3 L794L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A3HU-01A-11D-A20U-09 chr17:3919732 G>T maps to NM_015113.3 R2677R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A3HZ-01A-11D-A20U-09 chr17:3969794 C>A maps to NM_015113.3 E1399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IR-A3LH-01A-21D-A20U-09 chr17:3928304 G>A maps to NM_015113.3 L2334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EK-A2RC-01A-11D-A18J-09 chr1:78030555 G>C did not map to a codon.
Sequencing variant TCGA-IR-A3LK-01A-12D-A20U-09 chr1:78034070 C>T maps to NM_015534.4 Q804Q. Only missense variants will be evaluated by CHASM.
