Sequencing variant TCGA-SR-A6MU-01A-11D-A35I-08 chr17:66979977 G>A maps to NM_080283.3 S1504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70A-01A-11D-A35D-08 chr13:95818471 C>T maps to NM_005845.3 S658S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A7CZ-01A-11D-A35D-08 chr7:150913091 G>A maps to NM_005692.3 I454I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70A-01A-11D-A35D-08 chr19:17412053 C>T maps to NM_024527.4 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7WL-01A-11D-A35I-08 chr6:160184038 T>G maps to NM_005891.2 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MY-01A-11D-A35I-08 chr14:23531642 T>C maps to NM_014977.3 K1049K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P8-A5KD-01A-11D-A35D-08 chr5:80643654 G>A maps to NM_130767.2 H197H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7WO-01A-11D-A35I-08 chr23:70823568 G>C did not map to a codon.
Sequencing variant TCGA-PR-A5PH-01A-11D-A35D-08 chr2:98275012 G>A maps to NM_005735.3 H178H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70A-01A-11D-A35D-08 chr17:42854138 C>T maps to NM_002390.4 D531D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6H4-01A-11D-A35D-08 chr5:5239325 C>T maps to NM_139056.2 N739N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7WW-01A-11D-A35I-08 chr12:43886327 G>A maps to ENST00000389420 D352D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A67X-01A-11D-A35D-08 chr4:73280585 T>A maps to NM_014243.1 R203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7WN-01A-12D-A35I-08 chr15:79059039 A>G maps to ENST00000258883 N1071N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A7IN-01A-11D-A35D-08 chr5:7766828 C>A maps to NM_020546.2 I708I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SP-A6QG-01A-12D-A35I-08 chr16:4015940 C>T maps to NM_001116.3 T1299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7X1-01A-11D-A35I-08 chr4:100234995 G>A maps to NM_000668.4 I270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7WM-01A-12D-A35I-08 chr2:64800180 A>G maps to ENST00000422803 T791T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A703-01A-11D-A35D-08 chr11:47712200 C>T maps to ENST00000357610 W353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A7CZ-01A-11D-A35D-08 chr6:32150434 T>C maps to ENST00000375070 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A700-01A-11D-A35D-08 chr21:45401060 G>A maps to NM_001037553.1 V345V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70Q-01A-13D-A35D-08 chr20:32878370 G>A maps to NM_000687.2 D280D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A69Q-01A-11D-A35D-08 chr11:62287728 C>T maps to NM_001620.1 K4720K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6H3-01A-11D-A35D-08 chr14:105409426 G>A maps to NM_138420.2 L4121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XK-01A-11D-A35D-08 chr14:105413381 G>A maps to NM_138420.2 A2802A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XN-01A-11D-A35D-08 chr14:105409426 G>A maps to NM_138420.2 L4121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A817-01A-11D-A35I-08 chr14:105409976 G>A maps to NM_138420.2 D3937D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RT-A6YC-01A-12D-A35D-08 chr7:17382666 G>A maps to NM_001621.4 L842L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A67V-01A-11D-A35D-08 chr23:129265713 G>A did not map to a codon.
Sequencing variant TCGA-RW-A680-01A-11D-A35D-08 chr6:151672063 G>A maps to NM_005100.3 V846V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A700-01A-11D-A35D-08 chr23:49963359 C>T did not map to a codon.
Sequencing variant TCGA-WB-A81W-01A-11D-A35I-08 chr7:91711855 T>C maps to NM_005751.4 H2680H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6GY-01A-11D-A35D-08 chr6:109818699 A>G maps to NM_001145128.2 C1761C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7WQ-01A-12D-A35I-08 chr1:19615022 G>A maps to NM_012067.2 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7WT-01A-12D-A35I-08 chr12:112223105 C>A maps to NM_000690.2 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W2-A7H7-01A-11D-A35I-08 chr5:125903981 T>C maps to NM_001182.3 K280K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XO-01A-11D-A35D-08 chr14:78174290 C>T maps to NM_006020.2 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W2-A7H5-01B-11D-A35I-08 chr2:73675528 A>G maps to NM_015120.4 R624R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7X2-01A-12D-A35I-08 chr17:4535049 C>A maps to NM_001140.3 E612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RX-A8JQ-01A-11D-A35D-08 chr17:7948674 C>T maps to NM_001141.2 C323C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7WT-01A-12D-A35I-08 chr2:202606481 A>G maps to NM_020919.3 L756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A708-01A-11D-A35D-08 chr17:33520579 G>A maps to NM_152462.2 D249D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XL-01A-11D-A35D-08 chr17:33520468 T>C maps to NM_152462.2 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RM-A68W-01A-11D-A35D-08 chr23:112021834 C>A did not map to a codon.
Sequencing variant TCGA-XG-A823-01A-11D-A35I-08 chr17:54559862 C>T maps to NM_153228.2 L749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70A-01A-11D-A35D-08 chr5:139908665 T>G maps to ENST00000253810 S2045S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81Q-01A-11D-A35I-08 chr5:139889714 G>A maps to ENST00000253810 V1351V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70T-01A-11D-A35D-08 chr11:113266944 G>T did not map to a codon.
Sequencing variant TCGA-RM-A68T-01A-11D-A35D-08 chr5:55407047 C>A maps to NM_024669.2 V509V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81H-01A-11D-A35I-08 chr6:34935027 G>A maps to NM_015245.2 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TT-A6YP-01A-21D-A35I-08 chr12:5963271 G>A maps to ENST00000356134 H186H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A822-01A-11D-A35I-08 chr11:22296293 G>C did not map to a codon.
Sequencing variant TCGA-QR-A70X-01A-11D-A35D-08 chr19:17444304 G>A maps to NM_020959.2 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81S-01A-11D-A35I-08 chr15:90335437 C>T maps to NM_001150.2 K827K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A706-01A-11D-A35D-08 chr7:99701078 C>T maps to ENST00000429084 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MQ-01A-11D-A35I-08 chr12:99117514 A>G maps to NM_181861.1 S1101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SA-A6C2-01A-11D-A35I-08 chr2:21229683 G>T maps to NM_000384.2 T3352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81N-01A-11D-A35I-08 chr23:66765160 A>T did not map to a codon.
Sequencing variant TCGA-W2-A7UY-01A-11D-A35I-08 chr5:141053008 G>A maps to NM_022481.5 Q311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SP-A6QG-01A-12D-A35I-08 chr4:148653478 C>T maps to NM_024605.3 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A686-01A-11D-A35D-08 chr1:94639988 C>T maps to NM_004815.3 Q1074Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SQ-A6I4-01A-11D-A35I-08 chr11:73021125 C>T maps to NM_014786.3 D481D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81V-01A-11D-A35I-08 chr12:46245244 G>A maps to NM_152641.2 G1113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A817-01A-11D-A35I-08 chr19:971938 C>T maps to NM_005224.2 G552G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W2-A7HA-01B-11D-A35I-08 chr11:64781693 C>T maps to NM_001667.3 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A7CZ-01A-11D-A35D-08 chr23:100880327 C>G did not map to a codon.
Sequencing variant TCGA-SR-A6MV-01A-11D-A35I-08 chr11:13402801 G>A did not map to a codon.
Sequencing variant TCGA-RW-A67Y-01A-11D-A35D-08 chr2:9540190 G>T maps to NM_003887.2 P908P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6GR-01A-11D-A35D-08 chr23:63445428 C>T did not map to a codon.
Sequencing variant TCGA-S7-A7WT-01A-12D-A35I-08 chr23:15267053 G>A did not map to a codon.
Sequencing variant TCGA-QR-A7IN-01A-11D-A35D-08 chr8:124382193 A>G maps to NM_014109.3 D266D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W2-A7HC-01A-11D-A35I-08 chr14:96798921 C>T maps to NM_018036.5 G426G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7X2-01A-12D-A35I-08 chr7:150713793 C>A maps to NM_173681.5 E802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XP-01A-11D-A35D-08 chr11:108173734 A>G maps to NM_000051.3 Q1825Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81J-01A-11D-A35I-08 chr4:47570851 A>G did not map to a codon.
Sequencing variant TCGA-W2-A7HB-01A-11D-A35I-08 chr23:119505019 G>C did not map to a codon.
Sequencing variant TCGA-QR-A6GT-01A-11D-A35D-08 chr16:28909394 C>A maps to NM_173201.3 C498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A8AZ-01A-11D-A35D-08 chr16:28909759 C>T maps to NM_173201.3 F584F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MU-01A-11D-A35I-08 chr16:2569715 C>T maps to NM_001694.3 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A706-01A-11D-A35D-08 chr23:77258625 C>G did not map to a codon.
Sequencing variant TCGA-QR-A6GY-01A-11D-A35D-08 chr4:42629112 T>A maps to NM_006095.2 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70A-01A-11D-A35D-08 chr23:76931777 G>C did not map to a codon.
Sequencing variant TCGA-RW-A680-01A-11D-A35D-08 chr23:76855942 G>A did not map to a codon.
Sequencing variant TCGA-RT-A6YA-01A-12D-A35D-08 chr12:111894042 G>A maps to NM_002973.3 A1178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A680-01A-11D-A35D-08 chr19:57743155 G>T did not map to a codon.
Sequencing variant TCGA-RT-A6Y9-01A-12D-A35D-08 chr7:32582853 C>T maps to NM_015060.1 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70T-01A-11D-A35D-08 chr23:69457053 G>C did not map to a codon.
Sequencing variant TCGA-RW-A7CZ-01A-11D-A35D-08 chr23:69458181 C>A did not map to a codon.
Sequencing variant TCGA-PR-A5PF-01A-11D-A35D-08 chr11:375705 G>C maps to NM_178537.4 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A688-01A-11D-A35D-08 chr1:32204530 G>A maps to NM_001703.2 L835L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A688-01A-11D-A35D-08 chr1:32204531 C>T maps to NM_001703.2 P834P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W2-A7HB-01A-11D-A35I-08 chr9:135458231 C>T maps to NM_020064.3 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RT-A6Y9-01A-12D-A35D-08 chr9:134357837 G>A maps to NM_013318.3 Q1688Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SP-A6QK-01A-11D-A35I-08 chr4:122774227 A>G maps to NM_176824.1 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A700-01A-11D-A35D-08 chr16:75263908 C>A maps to NM_001170714.1 E751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MX-01A-11D-A35I-08 chr14:99737528 C>G maps to NM_138576.2 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A689-01A-11D-A35D-08 chr12:12240320 G>A did not map to a codon.
Sequencing variant TCGA-QR-A6GO-01A-11D-A35D-08 chr23:39937136 T>G did not map to a codon.
Sequencing variant TCGA-QR-A6GX-01A-11D-A35D-08 chr23:39911405 C>G did not map to a codon.
Sequencing variant TCGA-RW-A68F-01A-11D-A35D-08 chr5:70757729 T>C maps to NM_018429.2 Y192Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70C-01A-21D-A35D-08 chr12:70048983 G>A maps to NM_032735.2 S570S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A685-01A-11D-A35D-08 chr17:76212109 C>A maps to NM_001012271.1 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A8AZ-01A-11D-A35D-08 chr2:32693032 C>G maps to NM_016252.3 Y1878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70G-01B-11D-A35D-08 chr3:112987284 C>A maps to ENST00000273395 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7WM-01A-12D-A35I-08 chr4:13600881 C>A maps to NM_148894.2 E2548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A7CZ-01A-11D-A35D-08 chr1:92430245 T>C maps to ENST00000347608 N97N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W2-A7HA-01B-11D-A35I-08 chr23:79999586 T>C did not map to a codon.
Sequencing variant TCGA-W2-A7HC-01A-11D-A35I-08 chr2:201681959 A>G maps to ENST00000452790 K210K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6GT-01A-11D-A35D-08 chr7:16734586 G>A maps to NM_014038.2 K260K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A80L-01A-11D-A35I-08 chr12:27067049 T>C maps to NM_018164.2 L477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XL-01A-11D-A35D-08 chr13:37269241 A>T maps to NM_203451.2 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A7IP-01A-11D-A35D-08 chr14:50092334 A>G maps to NM_018139.2 S813S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81T-01A-11D-A35I-08 chr14:91639742 C>T maps to NM_001102368.1 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70I-01A-11D-A35D-08 chr16:67168284 C>T maps to NM_025187.3 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6H1-01A-11D-A35D-08 chr7:7283231 C>T maps to NM_020156.3 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A815-01A-11D-A35I-08 chr1:151020748 T>C maps to NM_017860.3 N142N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81G-01A-11D-A35I-08 chr1:2125337 G>A maps to ENST00000359030 C70C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7WV-01A-11D-A35I-08 chr20:257756 G>C maps to NM_153269.1 R251R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A700-01A-11D-A35D-08 chr11:73760381 C>A maps to ENST00000334126 L1787L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W2-A7H7-01A-11D-A35I-08 chr4:57832875 G>A maps to NM_032313.2 V558V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70K-01A-12D-A35D-08 chr5:175764120 G>C maps to ENST00000443967 L776L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W2-A7HC-01A-11D-A35I-08 chr5:43446326 G>C maps to NM_022483.4 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SP-A6QI-01A-12D-A35I-08 chr6:151790031 G>A maps to NM_024573.1 R371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MU-01A-11D-A35I-08 chr6:127911361 C>T maps to NM_001010905.1 R269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70O-01A-11D-A35D-08 chr7:31736576 A>T did not map to a codon.
Sequencing variant TCGA-SR-A6MQ-01A-11D-A35I-08 chr9:99417013 C>G maps to NM_153698.1 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PR-A5PG-01A-11D-A35D-08 chr3:53839012 A>G maps to NM_001128840.1 Q1863Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6GW-01A-11D-A35D-08 chr23:49071912 G>A did not map to a codon.
Sequencing variant TCGA-SP-A6QJ-01A-11D-A35I-08 chr23:49062199 G>A did not map to a codon.
Sequencing variant TCGA-WB-A81V-01A-11D-A35I-08 chr17:48650205 C>A maps to NM_018896.3 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A819-01A-11D-A35I-08 chr1:201029809 G>T maps to NM_000069.2 L1130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A706-01A-11D-A35D-08 chr12:2017137 G>A maps to NM_172364.4 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7WQ-01A-12D-A35I-08 chr6:7373787 C>A maps to NM_001170692.1 E422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70O-01A-11D-A35D-08 chr2:85628998 C>T maps to NM_001747.2 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A7CZ-01A-11D-A35D-08 chr1:230930957 G>A maps to NM_006615.2 A640A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SP-A6QF-01A-12D-A35I-08 chr1:230914847 C>G maps to NM_006615.2 G361G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7X0-01A-12D-A35I-08 chr7:2968245 G>A maps to NM_032415.4 D580D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A8AZ-01A-11D-A35D-08 chr4:186379808 A>G maps to NM_152775.3 L644L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70P-01A-11D-A35D-08 chr17:16665776 T>C maps to NM_014695.1 L1273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A80Y-01A-11D-A35I-08 chr3:180365981 A>G maps to NM_181426.1 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A681-01A-11D-A35D-08 chr12:120510312 A>G did not map to a codon.
Sequencing variant TCGA-WB-A80P-01A-11D-A35I-08 chr15:43483810 G>C maps to NM_012142.3 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A815-01A-11D-A35I-08 chr1:117564513 T>C maps to NM_004258.3 A779A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A7U0-01A-11D-A35D-08 chr3:112546337 A>G maps to NM_001008784.2 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81K-01A-11D-A35I-08 chr1:160801172 G>A maps to NM_001166663.1 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A68D-01A-11D-A35D-08 chr17:41926250 C>T maps to NM_145273.3 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A7CZ-01A-11D-A35D-08 chr11:118175675 G>A maps to NM_000733.3 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SQ-A6I4-01A-11D-A35I-08 chr11:44640633 G>A maps to NM_002231.3 R254R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XK-01A-11D-A35D-08 chr19:14507919 G>A maps to NM_078481.2 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PR-A5PG-01A-11D-A35D-08 chr17:45219307 A>G maps to NM_001114091.1 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SP-A6QG-01A-12D-A35I-08 chr17:45234322 T>C maps to NM_001114091.1 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A816-01A-11D-A35I-08 chr1:193219825 C>A maps to NM_024529.4 S527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SQ-A6I6-01A-11D-A35I-08 chr16:89261331 C>T maps to NM_004933.2 D738D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A80N-01A-11D-A35I-08 chr16:66942311 G>A maps to NM_004062.2 L825L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6GY-01A-11D-A35D-08 chr16:66437024 C>T maps to NM_001795.3 L770L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XK-01A-11D-A35D-08 chr5:31299602 C>T maps to NM_004932.2 R226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A69Q-01A-11D-A35D-08 chr11:618713 G>A maps to NM_021924.4 P615P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6GU-01A-11D-A35D-08 chr6:110942542 G>A maps to NM_015076.3 Q381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70C-01A-21D-A35D-08 chr17:46053345 C>T maps to NM_176096.1 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81E-01A-11D-A35I-08 chr23:18616727 T>C did not map to a codon.
Sequencing variant TCGA-W2-A7UY-01A-11D-A35I-08 chr16:80667071 C>T maps to NM_152342.2 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SP-A6QJ-01A-11D-A35I-08 chr19:42231223 T>G maps to NM_004363.2 V699V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81Q-01A-11D-A35I-08 chr19:42265394 G>A maps to NM_002483.4 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70T-01A-11D-A35D-08 chr2:37455267 A>G maps to NM_005760.2 D356D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A815-01A-11D-A35I-08 chr18:13049393 A>G maps to NM_032142.3 T868T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TT-A6YN-01A-12D-A35I-08 chr20:40076588 G>A maps to NM_032221.3 L1236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MX-01A-11D-A35I-08 chr19:16632348 G>A maps to NM_006387.5 H699H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81D-01A-11D-A35I-08 chr3:382546 A>G maps to NM_006614.2 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A689-01A-11D-A35D-08 chr1:154548320 C>A maps to NM_000748.2 T474T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MX-01A-11D-A35I-08 chr19:42791284 G>T maps to NM_015125.3 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70P-01A-11D-A35D-08 chr11:46791573 G>A maps to ENST00000415402 P1087P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MS-01A-11D-A35I-08 chr4:170618773 C>G maps to NM_173872.2 V484V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A681-01A-11D-A35D-08 chr19:7831055 A>G maps to NM_014257.4 Q249Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81R-01A-11D-A35I-08 chr5:1325910 T>C maps to NM_030782.3 A367A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A821-01A-11D-A35I-08 chr3:74383969 C>A maps to NM_020872.1 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A8AZ-01A-11D-A35D-08 chr9:39118251 T>C maps to NM_033655.3 G695G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A67X-01A-11D-A35D-08 chr16:76569592 C>T maps to NM_033401.3 C968C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A816-01A-11D-A35I-08 chr16:23456407 G>A maps to NM_153603.3 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70N-01A-12D-A35D-08 chr1:103400016 T>G maps to NM_080629.2 P1208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A681-01A-11D-A35D-08 chr6:75811732 T>C maps to ENST00000322507 P2817P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MQ-01A-11D-A35I-08 chr6:75841697 G>A maps to ENST00000322507 R1965R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MV-01A-11D-A35I-08 chr6:70854155 G>A did not map to a codon.
Sequencing variant TCGA-QR-A6H6-01A-11D-A35D-08 chr6:56044742 G>A maps to NM_030820.3 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SP-A6QF-01A-12D-A35I-08 chr12:48387609 C>T maps to NM_001844.4 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70D-01A-11D-A35D-08 chr23:107936077 C>T did not map to a codon.
Sequencing variant TCGA-RW-A68F-01A-11D-A35D-08 chr23:107930800 C>A did not map to a codon.
Sequencing variant TCGA-RW-A67V-01A-11D-A35D-08 chr23:107413897 G>A did not map to a codon.
Sequencing variant TCGA-W2-A7H7-01A-11D-A35I-08 chr3:130282278 G>A maps to NM_001102608.1 E144E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7WV-01A-11D-A35I-08 chr1:160261695 G>A maps to NM_001098398.1 C1066C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MX-01A-11D-A35I-08 chr16:4408409 C>T maps to NM_024535.3 Q805Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6GU-01A-11D-A35D-08 chr16:57155596 G>A maps to NM_152727.5 E264E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70K-01A-12D-A35D-08 chr7:99054071 C>T maps to NM_006693.2 H253H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SQ-A6I6-01A-11D-A35I-08 chr12:107391081 G>A maps to NM_004075.3 S525S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A67X-01A-11D-A35D-08 chr2:208993025 C>T maps to NM_020989.3 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7WT-01A-12D-A35I-08 chr1:115272877 C>T did not map to a codon.
Sequencing variant TCGA-WB-A80M-01A-11D-A35I-08 chr1:115267955 T>A did not map to a codon.
Sequencing variant TCGA-WB-A81N-01A-11D-A35I-08 chr23:1407668 G>T did not map to a codon.
Sequencing variant TCGA-W2-A7UY-01A-11D-A35I-08 chr17:61950685 G>A maps to NM_020991.3 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P8-A5KC-01A-11D-A35D-08 chr1:34090178 C>T maps to ENST00000373381 P1815P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A7CZ-01A-11D-A35D-08 chr8:113237068 G>A maps to NM_198123.1 N3685N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PR-A5PG-01A-11D-A35D-08 chr15:75982727 T>C maps to NM_001897.4 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6H2-01A-11D-A35D-08 chr13:113888240 T>C maps to NM_001008895.1 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XP-01A-11D-A35D-08 chr23:119672575 C>A did not map to a codon.
Sequencing variant TCGA-RW-A685-01A-11D-A35D-08 chr6:43167851 C>T maps to ENST00000354495 L1114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MV-01A-11D-A35I-08 chr7:101559399 A>G maps to ENST00000360264 E23E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6GW-01A-11D-A35D-08 chr12:111729282 T>C maps to NM_015267.3 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6ZZ-01A-11D-A35D-08 chr23:35989874 T>A did not map to a codon.
Sequencing variant TCGA-QR-A6GR-01A-11D-A35D-08 chr23:19983716 G>T did not map to a codon.
Sequencing variant TCGA-W2-A7HD-01A-11D-A35I-08 chr23:23956666 T>A did not map to a codon.
Sequencing variant TCGA-WB-A80K-01A-11D-A35I-08 chr5:156787348 C>T maps to ENST00000442283 C984C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TT-A6YK-01A-11D-A35I-08 chr6:31975462 T>C maps to NM_000500.5 *316Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XO-01A-11D-A35D-08 chr19:41387997 G>A maps to NM_000764.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6GY-01A-11D-A35D-08 chr19:41516035 T>C maps to NM_000767.4 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A80M-01A-11D-A35I-08 chr4:108866588 A>T maps to NM_183075.2 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A700-01A-11D-A35D-08 chr1:47407090 C>G maps to ENST00000371904 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A80V-01A-12D-A35I-08 chr1:47402418 G>A maps to ENST00000371904 R143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MT-01A-11D-A35I-08 chr11:61110892 C>A maps to NM_015533.3 T315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XL-01A-11D-A35D-08 chr23:125685937 C>T did not map to a codon.
Sequencing variant TCGA-QR-A700-01A-11D-A35D-08 chr8:88886082 G>A maps to NM_152418.3 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A67X-01A-11D-A35D-08 chr18:50734158 T>C maps to NM_005215.3 D611D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A68F-01A-11D-A35D-08 chr18:50734114 C>T maps to NM_005215.3 R597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A80N-01A-11D-A35I-08 chr13:36385000 G>A maps to NM_004734.4 Y553Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70M-01A-11D-A35D-08 chr7:50595870 C>T maps to NM_000790.3 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81A-01A-11D-A35I-08 chr2:118582523 T>C maps to NM_006773.3 V405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A67W-01A-11D-A35D-08 chr23:41205820 G>A did not map to a codon.
Sequencing variant TCGA-SQ-A6I6-01A-11D-A35I-08 chr11:9187391 G>A maps to NM_015213.2 C758C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A821-01A-11D-A35I-08 chr7:24784269 G>A maps to NM_001127453.1 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TT-A6YK-01A-11D-A35I-08 chr20:61542655 G>C maps to NM_033081.2 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81R-01A-11D-A35I-08 chr20:61511022 G>T maps to NM_033081.2 P2095P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81D-01A-11D-A35I-08 chr3:122545709 A>G maps to NM_032839.2 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81H-01A-11D-A35I-08 chr11:111853097 G>A maps to NM_001037954.2 R268R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A706-01A-11D-A35D-08 chr22:38916081 A>T maps to NM_007068.2 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P8-A5KD-01A-11D-A35D-08 chr17:76457711 G>A maps to ENST00000389840 Q3071*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81P-01A-11D-A35I-08 chr17:76510972 G>A maps to ENST00000389840 A1328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7X0-01A-12D-A35I-08 chr5:13793657 C>T maps to NM_001369.2 T2730T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6GR-01A-11D-A35D-08 chr6:38881623 G>A did not map to a codon.
Sequencing variant TCGA-S7-A7WR-01A-11D-A35I-08 chr6:38841073 C>T maps to ENST00000327475 V2502V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MX-01A-11D-A35I-08 chr17:11543596 G>A maps to NM_001372.3 P599P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70V-01A-11D-A35D-08 chr17:72285857 C>A maps to NM_023036.4 S198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6ZZ-01A-11D-A35D-08 chr1:84878059 C>T maps to NM_021233.2 N192N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A817-01A-11D-A35I-08 chr2:230272008 G>A maps to NM_139072.3 N554N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A684-01A-12D-A35D-08 chr5:169454923 G>T maps to NM_004946.2 E1147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P7-A5NX-01A-11D-A35D-08 chr3:51393610 C>T maps to NM_004947.4 R1447R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70U-01A-11D-A35D-08 chr7:111484934 C>A maps to ENST00000428084 E874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70K-01A-12D-A35D-08 chr9:441993 C>T maps to NM_203447.3 I1825I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PR-A5PH-01A-11D-A35D-08 chr13:99538836 G>A maps to ENST00000428223 S695S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A819-01A-11D-A35I-08 chr20:49551758 A>G maps to ENST00000449701 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70Q-01A-13D-A35D-08 chr3:109050578 A>G did not map to a codon.
Sequencing variant TCGA-S7-A7WT-01A-12D-A35I-08 chr6:56504747 G>A maps to ENST00000361203 L655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70A-01A-11D-A35D-08 chr11:58959665 A>G maps to NM_015177.1 R439R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XJ-01A-11D-A35D-08 chr15:45440568 A>G maps to NM_175940.1 E914E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A815-01A-11D-A35I-08 chr18:46858297 G>T maps to NM_017653.3 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81I-01A-11D-A35I-08 chr11:103027114 A>G did not map to a codon.
Sequencing variant TCGA-W2-A7H7-01A-11D-A35I-08 chr12:68051586 G>A maps to NM_006482.2 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81F-01A-11D-A35I-08 chr10:131639195 A>G maps to ENST00000355311 N491N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70M-01A-11D-A35D-08 chr1:21573844 G>A maps to NM_001397.2 P344P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W2-A7UY-01A-11D-A35I-08 chr6:12290894 G>T maps to NM_001955.4 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SP-A6QG-01A-12D-A35I-08 chr8:16962936 C>G maps to NM_181723.2 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MZ-01A-11D-A35I-08 chr4:110925778 G>C did not map to a codon.
Sequencing variant TCGA-WB-A81M-01A-11D-A35I-08 chr19:48239780 G>A maps to NM_014601.3 Q357Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6H3-01A-11D-A35D-08 chr7:6085710 A>C maps to NM_014413.3 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A80Q-01A-11D-A35I-08 chr19:10229615 G>A maps to NM_003755.3 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81E-01A-11D-A35I-08 chr19:39127526 A>C did not map to a codon.
Sequencing variant TCGA-P8-A6RY-01A-12D-A35D-08 chr19:853363 C>T maps to NM_001972.2 Y109Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A684-01A-12D-A35D-08 chr20:39990876 C>T maps to NM_052846.1 G444G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A689-01A-11D-A35D-08 chr19:14752290 C>T maps to NM_032571.3 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70C-01A-21D-A35D-08 chr4:71500136 C>G maps to NM_031889.2 S108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6GY-01A-11D-A35D-08 chr23:129803979 T>G did not map to a codon.
Sequencing variant TCGA-XG-A823-01A-11D-A35I-08 chr23:129759352 C>G did not map to a codon.
Sequencing variant TCGA-QR-A6GZ-01A-11D-A35D-08 chr1:23235624 C>T maps to ENST00000400191 S821S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MZ-01A-11D-A35I-08 chr1:23232561 T>C maps to ENST00000400191 I616I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7WL-01A-11D-A35I-08 chr7:100320668 C>T maps to NM_000799.2 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XJ-01A-11D-A35D-08 chr19:11492638 G>A maps to NM_000121.3 R132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A688-01A-11D-A35D-08 chr23:71425180 G>T did not map to a codon.
Sequencing variant TCGA-RW-A67W-01A-11D-A35D-08 chr21:39817409 G>A maps to NM_001136154.1 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PR-A5PG-01A-11D-A35D-08 chr6:11105080 G>A maps to NM_207582.2 Q155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XN-01A-11D-A35D-08 chr23:103495313 G>T did not map to a codon.
Sequencing variant TCGA-QR-A70H-01A-12D-A35D-08 chr6:36343732 G>A maps to NM_016135.2 C74C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6H1-01A-11D-A35D-08 chr4:5720979 C>T maps to NM_153717.2 D60D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PR-A5PG-01A-11D-A35D-08 chr23:154159642 C>T did not map to a codon.
Sequencing variant TCGA-QR-A7IP-01A-11D-A35D-08 chr23:55172536 G>A did not map to a codon.
Sequencing variant TCGA-WB-A81I-01A-11D-A35I-08 chr11:58877136 C>T maps to NM_198947.3 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6GT-01A-11D-A35D-08 chr23:133948878 G>A did not map to a codon.
Sequencing variant TCGA-QR-A702-01A-11D-A35D-08 chr23:63412959 C>A did not map to a codon.
Sequencing variant TCGA-RW-A681-01A-11D-A35D-08 chr23:63412783 G>A did not map to a codon.
Sequencing variant TCGA-RM-A68W-01A-11D-A35D-08 chr23:134156378 G>T did not map to a codon.
Sequencing variant TCGA-WB-A81W-01A-11D-A35I-08 chr10:61083854 A>G maps to ENST00000442566 H134H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A67Y-01A-11D-A35D-08 chr23:68749681 C>T did not map to a codon.
Sequencing variant TCGA-PR-A5PF-01A-11D-A35D-08 chr14:24610467 G>A maps to NM_016049.3 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RM-A68T-01A-11D-A35D-08 chr9:140139812 C>A maps to NM_001001710.1 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W2-A7HB-01A-11D-A35I-08 chr8:11282012 C>A maps to NM_053279.2 E172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A80N-01A-11D-A35I-08 chr10:126523308 T>C maps to NM_032182.3 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70P-01A-11D-A35D-08 chr2:29225513 C>T maps to NM_199280.2 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A708-01A-11D-A35D-08 chr14:45523650 A>G maps to ENST00000361462 P1486P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MU-01A-11D-A35I-08 chr19:35718938 G>A maps to NM_152481.1 Y215Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6GX-01A-11D-A35D-08 chr3:150377879 C>T maps to NM_152394.3 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XL-01A-11D-A35D-08 chr23:79698959 G>A did not map to a codon.
Sequencing variant TCGA-QR-A6GY-01A-11D-A35D-08 chr23:34149313 C>T did not map to a codon.
Sequencing variant TCGA-QR-A6GY-01A-11D-A35D-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-QR-A70O-01A-11D-A35D-08 chr23:37026996 A>C did not map to a codon.
Sequencing variant TCGA-SR-A6N0-01A-11D-A35I-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-RW-A68A-01A-11D-A35D-08 chr20:49247339 G>A maps to NM_080829.2 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70P-01A-11D-A35D-08 chr1:212798287 C>T maps to NM_153606.3 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A80V-01A-12D-A35I-08 chr1:120854563 C>A maps to NM_001100910.1 S143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A68D-01A-11D-A35D-08 chr9:97864023 G>A maps to NM_000136.2 R548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XG-A823-01A-11D-A35I-08 chr14:45650702 A>G maps to NM_020937.2 K1431K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81W-01A-11D-A35I-08 chr10:127693554 G>A maps to ENST00000368692 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6GY-01A-11D-A35D-08 chr4:187630129 A>G maps to ENST00000260147 G284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MS-01A-11D-A35I-08 chr17:73909900 C>T did not map to a codon.
Sequencing variant TCGA-TT-A6YP-01A-21D-A35I-08 chr19:8130916 G>C maps to NM_032447.3 T2772T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W2-A7HA-01B-11D-A35I-08 chr18:71740824 G>A maps to NM_001142958.1 Y468Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A68B-01A-11D-A35D-08 chr19:39522615 G>A maps to NM_178820.3 H84H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XG-A823-01A-11D-A35I-08 chr1:159778166 T>C maps to NM_001004310.2 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XJ-01A-11D-A35D-08 chr17:72868220 G>A maps to ENST00000442102 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6H5-01A-11D-A35D-08 chr15:68581942 A>G did not map to a codon.
Sequencing variant TCGA-S7-A7WR-01A-11D-A35I-08 chr19:35940789 G>C maps to NM_005306.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70K-01A-12D-A35D-08 chr23:76709701 A>G did not map to a codon.
Sequencing variant TCGA-RW-A68A-01A-11D-A35D-08 chr15:49776571 A>C maps to NM_002009.3 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81W-01A-11D-A35I-08 chr5:176523688 G>A maps to NM_213647.1 S700S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MX-01A-11D-A35I-08 chr23:135288721 G>A did not map to a codon.
Sequencing variant TCGA-SP-A6QD-01A-12D-A35I-08 chr6:110036318 A>G maps to NM_014845.5 K35K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6H6-01A-11D-A35D-08 chr19:18648509 C>T maps to NM_012181.3 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7WW-01A-11D-A35I-08 chr1:154961059 A>G maps to NM_025207.4 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TT-A6YK-01A-11D-A35I-08 chr1:152280503 G>A maps to NM_002016.1 H2286H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6GS-01A-11D-A35D-08 chr1:152327954 G>A maps to NM_001014342.2 S769S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XO-01A-11D-A35D-08 chr17:18150575 C>G maps to NM_002018.2 G861G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P8-A6RX-01A-11D-A35D-08 chr9:84608004 C>T maps to NM_001001670.2 R874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A7D0-01A-11D-A35D-08 chr13:28919664 C>A maps to NM_002019.4 E758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70T-01A-11D-A35D-08 chr15:33358927 T>C maps to NM_001103184.2 P386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P8-A5KC-01A-11D-A35D-08 chr2:216273108 C>T maps to NM_212482.1 L780L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A685-01A-11D-A35D-08 chr2:216264045 G>A maps to NM_212482.1 Y1094Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XK-01A-11D-A35D-08 chr14:75746641 G>A maps to NM_005252.3 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MT-01A-11D-A35I-08 chr7:114269972 A>G maps to NM_148898.3 Q195Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A80N-01A-11D-A35I-08 chr7:114269972 A>G maps to NM_148898.3 Q195Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A684-01A-12D-A35D-08 chr10:13712495 G>A maps to NM_018027.3 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6GW-01A-11D-A35D-08 chr23:12712507 G>A did not map to a codon.
Sequencing variant TCGA-QT-A5XO-01A-11D-A35D-08 chr23:12735859 C>G did not map to a codon.
Sequencing variant TCGA-SR-A6MZ-01A-11D-A35I-08 chr23:12735148 C>T did not map to a codon.
Sequencing variant TCGA-SP-A6QF-01A-12D-A35I-08 chr16:53859930 G>A maps to NM_001080432.2 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W2-A7HH-01A-11D-A35I-08 chr19:5867556 A>G maps to NM_002034.2 N60N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A680-01A-11D-A35D-08 chr17:42153350 C>T maps to NM_138387.3 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MX-01A-11D-A35I-08 chr17:78083826 C>T maps to NM_001079804.1 N470N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TT-A6YO-01A-11D-A35I-08 chr5:160763708 C>T maps to NM_021911.2 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SP-A6QK-01A-11D-A35I-08 chr23:49355892 C>G did not map to a codon.
Sequencing variant TCGA-QR-A6GU-01A-11D-A35D-08 chr4:843540 G>A maps to NM_005255.2 Q1286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A67X-01A-11D-A35D-08 chr2:155102327 A>G maps to NM_052917.2 K230K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XK-01A-11D-A35D-08 chr4:72629625 G>A maps to ENST00000504199 Y186Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W2-A7HH-01A-11D-A35I-08 chr19:19747567 G>A maps to NM_016573.2 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7WM-01A-12D-A35I-08 chr12:6954871 G>T maps to NM_002075.2 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W2-A7H7-01A-11D-A35I-08 chr1:155723051 C>A maps to ENST00000368331 E1929*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7WP-01A-11D-A35I-08 chr17:45016026 G>A maps to NM_054022.2 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MP-01A-11D-A35I-08 chr17:45012513 G>A maps to NM_054022.2 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W2-A7H7-01A-11D-A35I-08 chr13:92346009 T>C maps to NM_004466.4 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W2-A7UY-01A-11D-A35I-08 chr6:142764555 C>T maps to NM_198569.2 V1219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W2-A7HA-01B-11D-A35I-08 chr2:131486786 C>T maps to NM_207364.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A700-01A-11D-A35D-08 chr13:95278278 C>T maps to NM_180989.4 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PR-A5PG-01A-11D-A35D-08 chr23:150345210 G>A did not map to a codon.
Sequencing variant TCGA-WB-A80K-01A-11D-A35I-08 chr23:150349266 C>G did not map to a codon.
Sequencing variant TCGA-QR-A6GS-01A-11D-A35D-08 chr23:19027844 T>C did not map to a codon.
Sequencing variant TCGA-RW-A67Y-01A-11D-A35D-08 chr11:94113422 C>T maps to NM_016540.3 K388K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SP-A6QH-01A-21D-A35I-08 chr23:101911810 G>C did not map to a codon.
Sequencing variant TCGA-SR-A6MY-01A-11D-A35I-08 chr16:19873269 G>A maps to NM_016235.1 N352N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A80Q-01A-11D-A35I-08 chr4:90170127 G>C maps to NM_198281.2 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81R-01A-11D-A35I-08 chr3:14536428 T>C maps to ENST00000507975 K1062K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MV-01A-11D-A35I-08 chr6:52658985 T>C maps to NM_145740.3 K117K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SP-A6QG-01A-12D-A35I-08 chr6:43589787 G>A maps to NM_019096.3 H528H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XM-01A-11D-A35D-08 chr23:103267770 G>A did not map to a codon.
Sequencing variant TCGA-WB-A815-01A-11D-A35I-08 chr1:9322244 G>A maps to NM_004285.3 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MT-01A-11D-A35I-08 chr17:39884514 G>A maps to ENST00000310778 Q380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A68A-01A-11D-A35D-08 chr2:239988459 G>A maps to NM_006037.3 C982C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81Q-01A-11D-A35I-08 chr6:138726292 T>C maps to NM_014320.2 Y38Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W2-A7HA-01B-11D-A35I-08 chr17:65074568 C>T maps to NM_014877.3 A1876A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70R-01A-11D-A35D-08 chr11:124789687 C>T maps to NM_001037558.2 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A819-01A-11D-A35I-08 chr17:80400117 C>A maps to NM_173620.2 R470R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70T-01A-11D-A35D-08 chr1:114514512 C>T maps to ENST00000426820 T1098T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P8-A6RY-01A-12D-A35D-08 chr12:66221788 C>T maps to NM_003483.4 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P7-A5NY-01A-12D-A35D-08 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-P8-A5KD-01A-11D-A35D-08 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-SQ-A6I6-01A-11D-A35I-08 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-SR-A6MY-01A-11D-A35I-08 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-W2-A7HA-01B-11D-A35I-08 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-WB-A81F-01A-11D-A35I-08 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-SR-A6N0-01A-11D-A35I-08 chr17:36099430 G>A maps to NM_000458.2 Q182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70O-01A-11D-A35D-08 chr5:179044052 G>A maps to NM_005520.2 Y372Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SP-A6QG-01A-12D-A35I-08 chr17:46629485 G>A maps to NM_002146.4 C117C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W2-A7HE-01A-11D-A35I-08 chr3:148884978 G>A maps to NM_032383.3 P916P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XK-01A-11D-A35D-08 chr3:186395479 T>C maps to NM_000412.2 P462P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6H6-01A-11D-A35D-08 chr1:152192787 G>A maps to NM_001009931.1 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A7IP-01A-11D-A35D-08 chr2:20818911 C>T maps to NM_022460.3 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81H-01A-11D-A35I-08 chr17:14204903 G>A maps to NM_006041.1 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XO-01A-11D-A35D-08 chr14:102552236 A>T maps to NM_001017963.2 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A80O-01A-11D-A35I-08 chr6:44221298 C>T maps to NM_007355.2 G713G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A8AZ-01A-11D-A35D-08 chr6:31777994 G>A maps to NM_005527.3 V585V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7WN-01A-12D-A35I-08 chr14:65007788 G>A maps to NM_021979.3 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7X0-01A-12D-A35I-08 chr1:22157965 G>A maps to NM_005529.5 S3814S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70T-01A-11D-A35D-08 chr1:20005097 C>T maps to NM_000871.1 D251D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70A-01A-11D-A35D-08 chr23:53570842 G>A did not map to a codon.
Sequencing variant TCGA-QR-A70E-01A-11D-A35D-08 chr23:53588817 T>C did not map to a codon.
Sequencing variant TCGA-SP-A6QJ-01A-11D-A35I-08 chr23:53602645 C>A did not map to a codon.
Sequencing variant TCGA-SP-A6QH-01A-21D-A35I-08 chr2:8822537 G>A maps to NM_002166.4 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81P-01A-11D-A35I-08 chr22:23915575 G>A maps to NM_020070.2 Y173Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RM-A68W-01A-11D-A35D-08 chr23:130408638 G>A did not map to a codon.
Sequencing variant TCGA-QR-A7IP-01A-11D-A35D-08 chr11:18732255 G>A maps to NM_173588.3 R840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SP-A6QK-01A-11D-A35I-08 chr23:117892070 A>G did not map to a codon.
Sequencing variant TCGA-RW-A68D-01A-11D-A35D-08 chr15:81591745 C>T maps to NM_172217.3 H693H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A7IN-01A-11D-A35D-08 chr16:27357863 G>A maps to NM_000418.2 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XK-01A-11D-A35D-08 chr11:31477877 T>G maps to NM_144981.1 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70R-01A-11D-A35D-08 chr7:120607661 A>G maps to NM_019071.2 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A689-01A-11D-A35D-08 chr2:99170840 G>A maps to NM_001134224.1 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P8-A5KC-01A-11D-A35D-08 chr2:234102470 T>C maps to ENST00000359570 I820I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PR-A5PF-01A-11D-A35D-08 chr1:156816314 A>T maps to NM_014215.2 P602P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6GT-01A-11D-A35D-08 chr1:156815541 G>A maps to NM_014215.2 A681A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70D-01A-11D-A35D-08 chr12:30818752 A>G maps to NM_006390.3 C416C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6GT-01A-11D-A35D-08 chr9:95418812 T>C maps to NM_022755.5 Q50Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70V-01A-11D-A35D-08 chr23:53279663 G>A did not map to a codon.
Sequencing variant TCGA-RW-A68F-01A-11D-A35D-08 chr23:53268383 C>A did not map to a codon.
Sequencing variant TCGA-PR-A5PG-01A-11D-A35D-08 chr1:145538807 G>A maps to NM_003637.3 R973R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TT-A6YN-01A-12D-A35I-08 chr3:52819187 C>T maps to NM_002215.2 A512A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A80P-01A-11D-A35I-08 chr3:52812033 G>A did not map to a codon.
Sequencing variant TCGA-WB-A81E-01A-11D-A35I-08 chr3:52840339 T>A maps to NM_002217.3 I658I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A7CZ-01A-11D-A35D-08 chr1:59248090 G>A maps to NM_002228.3 Q218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A705-01A-11D-A35D-08 chr23:8536369 A>G did not map to a codon.
Sequencing variant TCGA-WB-A81M-01A-11D-A35I-08 chr3:67054374 G>T maps to NM_032505.2 G328G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81Q-01A-11D-A35I-08 chr11:17757752 G>C maps to NM_001112741.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70D-01A-11D-A35D-08 chr12:49938148 C>T maps to NM_012284.1 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70G-01B-11D-A35D-08 chr14:63174995 G>A maps to NM_139318.3 Q733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81W-01A-11D-A35I-08 chr14:63246574 G>A maps to NM_139318.3 V630V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MT-01A-11D-A35I-08 chr17:61619702 C>T maps to NM_030779.2 Q686*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A7U0-01A-11D-A35D-08 chr17:21318659 C>T maps to NM_021012.4 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A707-01A-11D-A35D-08 chr1:196254822 C>A maps to NM_198503.2 V887V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SP-A6QK-01A-11D-A35I-08 chr16:2732746 G>A maps to NM_018992.3 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W2-A7HB-01A-11D-A35I-08 chr12:464374 G>A maps to NM_001042603.1 D273D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81V-01A-11D-A35I-08 chr1:202700149 G>A maps to ENST00000367264 L1391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6ZZ-01A-11D-A35D-08 chr23:53231142 T>C did not map to a codon.
Sequencing variant TCGA-QR-A705-01A-11D-A35D-08 chr5:141309156 A>G maps to NM_014773.3 Q141Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70G-01B-11D-A35D-08 chr6:42832766 G>T maps to NM_015349.1 R941R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A67V-01A-11D-A35D-08 chr1:43905437 C>G maps to NM_015284.2 S1448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7WL-01A-11D-A35I-08 chr16:27751696 C>A maps to NM_015202.2 S693S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A680-01A-11D-A35D-08 chr9:138376460 C>T maps to NM_014811.3 D35D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SP-A6QF-01A-12D-A35I-08 chr15:81224298 C>T maps to NM_018689.1 S904S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A684-01A-12D-A35D-08 chr10:24669919 T>C maps to NM_019590.3 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XG-A823-01A-11D-A35I-08 chr17:44248900 C>T maps to NM_015443.3 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A68G-01A-11D-A35D-08 chr20:36869017 A>G maps to NM_001029864.1 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81V-01A-11D-A35I-08 chr9:20933054 G>A maps to NM_017794.3 S1120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70P-01A-11D-A35D-08 chr3:44847334 A>G did not map to a codon.
Sequencing variant TCGA-QR-A70A-01A-11D-A35D-08 chr12:39735382 C>T maps to ENST00000395670 E615E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A67X-01A-11D-A35D-08 chr13:33635726 G>A maps to NM_004795.3 T837T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A8AZ-01A-11D-A35D-08 chr13:74339085 T>C maps to NM_007249.4 Q286Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81V-01A-11D-A35I-08 chr12:27933766 C>T maps to NM_020782.1 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A8AZ-01A-11D-A35D-08 chr16:84693463 T>A maps to NM_024731.2 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SP-A6QK-01A-11D-A35I-08 chr19:51534094 G>A maps to NM_019598.2 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A822-01A-11D-A35I-08 chr19:51563780 G>A maps to NM_015596.1 Q50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70K-01A-12D-A35D-08 chr12:10462060 G>T maps to ENST00000381908 G28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A680-01A-11D-A35D-08 chr12:52967342 G>A maps to NM_175053.3 Y73Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70X-01A-11D-A35D-08 chr12:53295658 G>A maps to NM_002273.3 D174D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6GS-01A-11D-A35D-08 chr12:52714801 G>T maps to NM_002282.3 C106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6H3-01A-11D-A35D-08 chr17:39197280 G>A maps to NM_030967.2 C123C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A68A-01A-11D-A35D-08 chr21:46117403 C>T maps to NM_198699.1 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A688-01A-11D-A35D-08 chr21:45978262 G>T maps to NM_198696.2 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70P-01A-11D-A35D-08 chr21:46077964 C>T maps to NM_198697.2 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XJ-01A-11D-A35D-08 chr21:31971175 G>A maps to NM_181604.1 Y6Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7WT-01A-12D-A35I-08 chr17:25932725 C>T maps to ENST00000268763 D572D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SP-A6QK-01A-11D-A35I-08 chr23:153134382 G>A did not map to a codon.
Sequencing variant TCGA-WB-A81G-01A-11D-A35I-08 chr18:21523935 G>A did not map to a codon.
Sequencing variant TCGA-WB-A81S-01A-11D-A35I-08 chr6:112452192 G>A maps to NM_001105206.1 V1315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7WX-01A-11D-A35I-08 chr20:60886279 C>T maps to NM_005560.3 Q3342Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81H-01A-11D-A35I-08 chr2:211302428 G>A maps to NM_001136575.1 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6GW-01A-11D-A35D-08 chr13:21555611 G>T maps to NM_014572.2 L886L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A680-01A-11D-A35D-08 chr21:40781998 G>A maps to NM_152505.3 I396I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SA-A6C2-01A-11D-A35I-08 chr2:136564699 G>A maps to NM_002299.2 Q1391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70O-01A-11D-A35D-08 chr1:226076583 G>A maps to NM_020997.2 Y61Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A706-01A-11D-A35D-08 chr3:189704594 C>A maps to NM_018192.3 G390G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A821-01A-11D-A35I-08 chr7:103969247 T>C maps to NM_199000.2 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7WV-01A-11D-A35I-08 chr1:197887021 C>T maps to NM_020204.2 H23H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TT-A6YK-01A-11D-A35I-08 chr19:54848253 G>A maps to NM_012276.3 Y371Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A7D0-01A-11D-A35D-08 chr2:128412101 G>A maps to NM_017980.4 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TT-A6YN-01A-12D-A35I-08 chr2:99778809 G>A maps to NM_015929.3 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70X-01A-11D-A35D-08 chr2:97373549 A>G maps to NM_001142292.1 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PR-A5PH-01A-11D-A35D-08 chr1:156106110 G>T maps to NM_170707.2 E422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PR-A5PG-01A-11D-A35D-08 chr23:118143094 G>T did not map to a codon.
Sequencing variant TCGA-WB-A80V-01A-12D-A35I-08 chr6:160999681 A>G maps to NM_005577.2 C1448C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6GY-01A-11D-A35D-08 chr23:78010712 C>T did not map to a codon.
Sequencing variant TCGA-S7-A7X2-01A-12D-A35I-08 chr12:7086307 T>G maps to NM_005768.5 *488Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W2-A7H7-01A-11D-A35I-08 chr8:19811697 A>G maps to NM_000237.2 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81S-01A-11D-A35I-08 chr9:104075135 G>T maps to NM_017753.2 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TT-A6YP-01A-21D-A35I-08 chr1:99772001 C>T maps to NM_014839.4 I576I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7X2-01A-12D-A35I-08 chr12:57589942 C>T maps to NM_002332.2 N2925N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6H1-01A-11D-A35D-08 chr2:141092043 T>C maps to NM_018557.2 Q4067Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A816-01A-11D-A35I-08 chr1:53728166 C>T maps to NM_004631.3 R575R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A8AZ-01A-11D-A35D-08 chr3:196387236 C>T maps to NM_198565.1 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81A-01A-11D-A35I-08 chr17:30348407 G>A maps to ENST00000327564 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81M-01A-11D-A35I-08 chr1:204587793 G>A maps to NM_201630.1 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SQ-A6I6-01A-11D-A35I-08 chr11:65314940 C>T maps to NM_001130144.2 R692R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7WN-01A-12D-A35I-08 chr1:235929421 G>T maps to NM_000081.2 Y2026*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W2-A7UY-01A-11D-A35I-08 chr23:151900044 C>T did not map to a codon.
Sequencing variant TCGA-WB-A81V-01A-11D-A35I-08 chr23:151869867 C>T did not map to a codon.
Sequencing variant TCGA-QR-A6GT-01A-11D-A35D-08 chr23:30268673 A>T did not map to a codon.
Sequencing variant TCGA-SR-A6MZ-01A-11D-A35I-08 chr23:26213092 C>T did not map to a codon.
Sequencing variant TCGA-RT-A6YA-01A-12D-A35D-08 chr23:140994472 C>T did not map to a codon.
Sequencing variant TCGA-RW-A680-01A-11D-A35D-08 chr23:140996019 G>T did not map to a codon.
Sequencing variant TCGA-SR-A6MY-01A-11D-A35I-08 chr23:140994959 G>A did not map to a codon.
Sequencing variant TCGA-W2-A7H5-01B-11D-A35I-08 chr23:140994959 G>A did not map to a codon.
Sequencing variant TCGA-P8-A5KC-01A-11D-A35D-08 chr23:51637808 C>T did not map to a codon.
Sequencing variant TCGA-P7-A5NX-01A-11D-A35D-08 chr23:75651039 G>A did not map to a codon.
Sequencing variant TCGA-WB-A815-01A-11D-A35I-08 chr3:65425584 C>T maps to NM_001033057.1 Q413Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A67X-01A-11D-A35D-08 chr1:53692716 C>T maps to NM_002370.2 *147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A68B-01A-11D-A35D-08 chr1:53692716 C>T maps to NM_002370.2 *147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81P-01A-11D-A35I-08 chr18:56411727 G>A did not map to a codon.
Sequencing variant TCGA-RW-A684-01A-12D-A35D-08 chr5:179193111 A>C maps to NM_014757.4 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MP-01A-11D-A35I-08 chr5:179193270 G>T maps to NM_014757.4 P420P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6H0-01A-11D-A35D-08 chr4:140811107 C>T maps to ENST00000509479 Q494Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A7IP-01A-11D-A35D-08 chr4:140811107 C>T maps to ENST00000509479 Q494Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7WX-01A-11D-A35I-08 chr4:140811116 C>T maps to ENST00000509479 Q491Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A80K-01A-11D-A35I-08 chr4:140811107 C>T maps to ENST00000509479 Q494Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81H-01A-11D-A35I-08 chr4:140811107 C>T maps to ENST00000509479 Q494Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A820-01A-11D-A35I-08 chr9:140001176 C>A maps to NM_016219.3 V494V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7WL-01A-11D-A35I-08 chr15:43820462 C>T maps to ENST00000382031 T2502T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81S-01A-11D-A35I-08 chr5:71492289 G>A maps to NM_005909.3 P1036P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A706-01A-11D-A35D-08 chr19:17831772 C>T maps to NM_018174.4 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RT-A6Y9-01A-12D-A35D-08 chr3:47958221 G>A maps to ENST00000426837 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RT-A6Y9-01A-12D-A35D-08 chr3:47958224 T>C maps to ENST00000426837 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A67Y-01A-11D-A35D-08 chr2:39499634 G>A maps to NM_003618.2 L615L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6H2-01A-11D-A35D-08 chr14:50904709 G>C maps to NM_198794.1 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A700-01A-11D-A35D-08 chr2:160604778 C>T maps to NM_022826.2 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A700-01A-11D-A35D-08 chr6:29454797 G>T maps to NM_052967.1 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XJ-01A-11D-A35D-08 chr20:43933258 G>A maps to ENST00000372754 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A7IN-01A-11D-A35D-08 chr6:30672357 G>T maps to NM_014641.2 A1534A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7WL-01A-11D-A35I-08 chr23:153296730 C>T did not map to a codon.
Sequencing variant TCGA-RW-A688-01A-11D-A35D-08 chr23:70350000 T>A did not map to a codon.
Sequencing variant TCGA-SP-A6QI-01A-12D-A35I-08 chr12:116413345 G>A maps to NM_015335.4 C1854C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P8-A5KD-01A-11D-A35D-08 chr16:3293587 C>T maps to NM_000243.2 P633P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XN-01A-11D-A35D-08 chr2:112686862 A>T maps to NM_006343.2 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70R-01A-11D-A35D-08 chr7:141708442 G>T maps to ENST00000475668 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81T-01A-11D-A35I-08 chr7:141730214 T>C maps to ENST00000475668 Y425Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7WX-01A-11D-A35I-08 chr11:12243219 C>T maps to NM_014632.2 A412A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W2-A7H7-01A-11D-A35I-08 chr17:73266261 A>G maps to NM_020679.2 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70E-01A-11D-A35D-08 chr10:129913861 G>A maps to NM_002417.4 Y270Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A67W-01A-11D-A35D-08 chr16:74725329 C>T maps to NM_152649.2 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A80O-01A-11D-A35I-08 chr11:118372558 G>A maps to NM_001197104.1 P2164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81S-01A-11D-A35I-08 chr11:118376686 A>C maps to NM_001197104.1 S3360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SP-A6QD-01A-12D-A35I-08 chr7:151945601 G>A maps to ENST00000355193 G639G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6GW-01A-11D-A35D-08 chr9:20414330 G>A maps to NM_004529.2 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70J-01A-11D-A35D-08 chr4:90816481 C>T maps to NM_007351.2 N120N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MX-01A-11D-A35I-08 chr9:13190214 T>C maps to ENST00000319217 T684T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MX-01A-11D-A35I-08 chr12:123706151 T>C maps to NM_022782.2 K61K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6GT-01A-11D-A35D-08 chr11:18159634 C>T maps to NM_054031.3 Q296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6H4-01A-11D-A35D-08 chr8:121432124 T>G maps to NM_014078.5 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MQ-01A-11D-A35I-08 chr2:48032101 G>T maps to NM_000179.2 V1164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W2-A7HA-01B-11D-A35I-08 chr16:816648 T>G maps to NM_013404.4 P412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SQ-A6I6-01A-11D-A35I-08 chr16:819595 C>T maps to NM_001025190.1 A998A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MQ-01A-11D-A35I-08 chr23:64951749 A>G did not map to a codon.
Sequencing variant TCGA-RW-A68F-01A-11D-A35D-08 chr6:151336056 G>A maps to NM_015440.3 K783K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A706-01A-11D-A35D-08 chr23:149807484 G>A did not map to a codon.
Sequencing variant TCGA-QT-A7U0-01A-11D-A35D-08 chr15:31251151 G>C maps to NM_017762.2 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81M-01A-11D-A35I-08 chr1:237024422 A>T did not map to a codon.
Sequencing variant TCGA-QR-A70T-01A-11D-A35D-08 chr19:9009598 G>A maps to NM_024690.2 L13043L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RM-A68W-01A-11D-A35D-08 chr19:9065746 A>G maps to NM_024690.2 T7233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PR-A5PG-01A-11D-A35D-08 chr11:1270622 C>A maps to ENST00000447027 G4174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A700-01A-11D-A35D-08 chr23:3239394 G>T did not map to a codon.
Sequencing variant TCGA-QR-A702-01A-11D-A35D-08 chr23:3238547 G>A did not map to a codon.
Sequencing variant TCGA-QR-A70C-01A-21D-A35D-08 chr17:1381196 G>A maps to NM_001080779.1 I490I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A816-01A-11D-A35I-08 chr12:109844592 G>A did not map to a codon.
Sequencing variant TCGA-S7-A7WN-01A-12D-A35I-08 chr18:47421442 C>T maps to NM_001080467.2 Q971Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XN-01A-11D-A35D-08 chr8:2046697 G>A maps to NM_003970.2 L775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SA-A6C2-01A-11D-A35I-08 chr8:41792301 A>G maps to NM_006766.3 L1146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RT-A6YC-01A-12D-A35D-08 chr20:62854520 C>T maps to NM_004535.2 H818H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6GU-01A-11D-A35D-08 chr11:64822093 G>T maps to ENST00000340252 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70U-01A-11D-A35D-08 chr4:164050123 T>C maps to NM_138386.2 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7WX-01A-11D-A35I-08 chr23:72433371 G>C did not map to a codon.
Sequencing variant TCGA-QT-A5XL-01A-11D-A35D-08 chr3:47043264 G>A maps to NM_015175.1 A1577A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A67X-01A-11D-A35D-08 chr1:148009410 G>A maps to ENST00000310701 C637C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70W-01A-12D-A35D-08 chr1:148594438 A>G maps to NM_001170755.1 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81K-01A-11D-A35I-08 chr15:29561153 C>T maps to NM_138704.2 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SP-A6QG-01A-12D-A35I-08 chr10:21158715 G>A maps to ENST00000430741 R179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A708-01A-11D-A35D-08 chr15:56142796 C>T maps to ENST00000508342 R849R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6GS-01A-11D-A35D-08 chr17:29541603 G>T did not map to a codon.
Sequencing variant TCGA-RW-A67Y-01A-11D-A35D-08 chr17:29528440 C>T maps to NM_001042492.2 Q400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A7D0-01A-11D-A35D-08 chr17:29528480 C>G maps to NM_001042492.2 S413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81V-01A-11D-A35I-08 chr17:29657337 T>A maps to NM_001042492.2 C1878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TT-A6YK-01A-11D-A35I-08 chr18:77170439 C>T maps to NM_172387.1 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RM-A68W-01A-11D-A35D-08 chr12:54686886 C>A maps to NM_001136023.1 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70C-01A-21D-A35D-08 chr2:178095650 T>C maps to NM_006164.3 L560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A820-01A-11D-A35I-08 chr19:3382110 G>A maps to ENST00000269778 E144E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7WN-01A-12D-A35I-08 chr4:103516121 T>C maps to NM_003998.3 N428N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RT-A6YC-01A-12D-A35D-08 chr12:104517192 T>C maps to NM_006166.3 K80K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P8-A5KD-01A-11D-A35D-08 chr3:52521841 G>T maps to NM_007184.3 L778L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MQ-01A-11D-A35I-08 chr23:119059272 G>T did not map to a codon.
Sequencing variant TCGA-QR-A6H0-01A-11D-A35D-08 chr3:173322723 A>G maps to NM_014932.2 Q112Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XN-01A-11D-A35D-08 chr19:56369262 G>A maps to NM_134444.4 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A7U0-01A-11D-A35D-08 chr19:56466122 C>T maps to NM_176811.2 Y233Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A67W-01A-11D-A35D-08 chr10:96112724 C>G maps to NM_022451.9 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XO-01A-11D-A35D-08 chr9:33466939 G>C maps to NM_022917.4 P640P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XJ-01A-11D-A35D-08 chr2:203155920 A>C maps to NM_015934.3 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6H4-01A-11D-A35D-08 chr9:139395285 C>T maps to NM_017617.3 P1884P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6N0-01A-11D-A35I-08 chr6:32184731 A>G maps to NM_004557.3 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XJ-01A-11D-A35D-08 chr12:100904691 C>T maps to ENST00000392986 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6GT-01A-11D-A35D-08 chr10:18840856 C>T maps to NM_182543.2 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A68F-01A-11D-A35D-08 chr1:205687521 T>C maps to NM_022731.4 K206K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70H-01A-12D-A35D-08 chr5:162886939 G>T maps to NM_145266.4 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MQ-01A-11D-A35I-08 chr23:51076023 G>A did not map to a codon.
Sequencing variant TCGA-WB-A81R-01A-11D-A35I-08 chr4:123843574 G>A maps to NM_007083.3 D51D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A69Q-01A-11D-A35D-08 chr19:41186838 G>A maps to NM_004756.3 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A707-01A-11D-A35D-08 chr23:102339402 G>A did not map to a codon.
Sequencing variant TCGA-W2-A7HC-01A-11D-A35I-08 chr23:108784842 T>C did not map to a codon.
Sequencing variant TCGA-QR-A70A-01A-11D-A35D-08 chr14:24884875 C>T maps to NM_025081.2 F1307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W2-A7HH-01A-11D-A35I-08 chr12:113442842 G>A maps to NM_016817.2 R428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W2-A7H5-01B-11D-A35I-08 chr1:228505605 G>A maps to NM_001098623.1 K4621K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6GX-01A-11D-A35D-08 chr23:123526097 T>G did not map to a codon.
Sequencing variant TCGA-QT-A5XO-01A-11D-A35D-08 chr23:123518382 T>C did not map to a codon.
Sequencing variant TCGA-WB-A81D-01A-11D-A35I-08 chr23:123663782 A>G did not map to a codon.
Sequencing variant TCGA-WB-A815-01A-11D-A35I-08 chr10:50948876 C>G maps to NM_018245.2 R673R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P8-A6RX-01A-11D-A35D-08 chr23:70767855 A>G did not map to a codon.
Sequencing variant TCGA-QR-A70C-01A-21D-A35D-08 chr23:70756121 C>T did not map to a codon.
Sequencing variant TCGA-WB-A821-01A-11D-A35I-08 chr10:74673075 G>A maps to NM_152635.1 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P8-A6RY-01A-12D-A35D-08 chr19:46032457 G>A maps to NM_001017989.2 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A7D0-01A-11D-A35D-08 chr11:7960833 C>T maps to NM_001003745.1 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6GZ-01A-11D-A35D-08 chr11:6867635 G>A maps to ENST00000379831 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XO-01A-11D-A35D-08 chr1:158369199 G>A maps to NM_001004475.1 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A706-01A-11D-A35D-08 chr9:125239395 C>T maps to NM_001004451.1 K270K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6N0-01A-11D-A35I-08 chr9:125273103 C>T maps to ENST00000444856 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W2-A7HE-01A-11D-A35I-08 chr7:143807112 G>A maps to NM_001005480.2 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70A-01A-11D-A35D-08 chr1:248202162 G>A maps to NM_001004686.2 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6ZZ-01A-11D-A35D-08 chr15:102346303 A>T maps to NM_001005326.1 K128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A706-01A-11D-A35D-08 chr14:20444561 T>G maps to NM_001005486.1 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6GY-01A-11D-A35D-08 chr11:5221717 G>A maps to NM_001004760.2 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SA-A6C2-01A-11D-A35I-08 chr11:4615552 C>A maps to ENST00000450052 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XG-A823-01A-11D-A35I-08 chr12:55688980 G>C maps to NM_001005493.1 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P8-A6RY-01A-12D-A35D-08 chr1:158687536 G>A maps to ENST00000368146 Y139Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6H6-01A-11D-A35D-08 chr11:123814296 G>A maps to NM_001005187.1 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SA-A6C2-01A-11D-A35I-08 chr19:9213130 C>T maps to NM_001005193.1 V284V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81Q-01A-11D-A35I-08 chr11:55860830 A>G maps to NM_001003750.1 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A68C-01A-11D-A35D-08 chr11:55926911 G>A maps to NM_001004058.2 N294N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A700-01A-11D-A35D-08 chr7:103807332 C>T did not map to a codon.
Sequencing variant TCGA-TT-A6YP-01A-21D-A35I-08 chr11:59382786 C>A maps to NM_002556.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XN-01A-11D-A35D-08 chr17:72937758 C>T maps to NM_178233.1 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SQ-A6I6-01A-11D-A35I-08 chr2:42990173 G>A maps to NM_148962.4 D382D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7WX-01A-11D-A35I-08 chr3:152554690 T>A maps to NM_002563.2 *374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RT-A6YA-01A-12D-A35D-08 chr1:17395637 G>A maps to NM_007365.2 D633D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70J-01A-11D-A35D-08 chr1:17597606 C>T maps to NM_016233.2 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81E-01A-11D-A35I-08 chr1:17575682 G>A maps to NM_016233.2 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RM-A68W-01A-11D-A35D-08 chr23:110435355 G>A did not map to a codon.
Sequencing variant TCGA-RW-A68F-01A-11D-A35D-08 chr23:110439690 C>G did not map to a codon.
Sequencing variant TCGA-WB-A81M-01A-11D-A35I-08 chr11:124489204 C>A maps to NM_052959.2 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RX-A8JQ-01A-11D-A35D-08 chr10:34985326 C>T maps to NM_019619.3 Q47Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MX-01A-11D-A35I-08 chr20:21689897 C>T maps to NM_006192.3 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6ZZ-01A-11D-A35D-08 chr11:66638897 C>T maps to NM_022172.2 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PR-A5PH-01A-11D-A35D-08 chr24:4968045 C>T did not map to a codon.
Sequencing variant TCGA-SR-A6MY-01A-11D-A35I-08 chr13:67802020 C>T maps to NM_203487.2 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W2-A7HE-01A-11D-A35I-08 chr5:140236811 G>A maps to NM_018901.2 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XL-01A-11D-A35D-08 chr5:140215200 C>T maps to NM_018910.2 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A7CZ-01A-11D-A35D-08 chr5:140574404 C>T maps to NM_018930.3 G760G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XK-01A-11D-A35D-08 chr5:140517244 C>T maps to NM_015669.2 T743T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70H-01A-12D-A35D-08 chr5:140553993 G>T maps to NM_018940.2 A526A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70N-01A-12D-A35D-08 chr5:140753700 C>A maps to NM_018919.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A821-01A-11D-A35I-08 chr7:82389987 T>C maps to NM_033026.5 R5085R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70V-01A-11D-A35D-08 chr8:52732911 T>G maps to NM_052937.2 *358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SP-A6QC-01A-11D-A35I-08 chr17:79862804 C>T maps to NM_001184917.1 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A80Q-01A-11D-A35I-08 chr1:144879386 G>A maps to NM_014644.4 R1355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70U-01A-11D-A35D-08 chr8:66635839 T>C maps to ENST00000401827 K393K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SP-A6QC-01A-11D-A35I-08 chr5:32058105 G>C maps to NM_178140.2 G699G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A821-01A-11D-A35I-08 chr1:7886648 G>A maps to ENST00000377532 A689A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7X1-01A-11D-A35I-08 chr4:152682118 G>A maps to NM_004564.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A67V-01A-11D-A35D-08 chr23:77224417 A>G did not map to a codon.
Sequencing variant TCGA-WB-A80K-01A-11D-A35I-08 chr17:47486439 G>A maps to NM_002634.2 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P7-A5NX-01A-11D-A35D-08 chr23:133549218 C>G did not map to a codon.
Sequencing variant TCGA-SP-A6QK-01A-11D-A35I-08 chr3:52456805 C>T maps to ENST00000454052 C277C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6GW-01A-11D-A35D-08 chr23:18915369 C>T did not map to a codon.
Sequencing variant TCGA-QR-A70W-01A-12D-A35D-08 chr20:43804500 G>A did not map to a codon.
Sequencing variant TCGA-QR-A70K-01A-12D-A35D-08 chr9:35092368 C>T maps to NM_032634.2 E505E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7WX-01A-11D-A35I-08 chr17:34894045 C>T maps to NM_178517.3 R366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A80O-01A-11D-A35I-08 chr3:178919202 C>A maps to NM_006218.2 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70D-01A-11D-A35D-08 chr3:138382750 G>A maps to NM_006219.1 G931G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XP-01A-11D-A35D-08 chr23:48776049 C>T did not map to a codon.
Sequencing variant TCGA-WB-A81S-01A-11D-A35I-08 chr16:81253678 C>A maps to NM_052892.3 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81I-01A-11D-A35I-08 chr8:110457176 C>T maps to ENST00000426474 V1693V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XJ-01A-11D-A35D-08 chr19:14574925 G>A maps to NM_213560.1 Q570Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7X2-01A-12D-A35I-08 chr8:42045067 C>T maps to NM_000930.3 E129E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A705-01A-11D-A35D-08 chr2:198948750 A>G maps to NM_006226.3 K170K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RM-A68T-01A-11D-A35D-08 chr11:16823312 G>A maps to ENST00000448080 R737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XP-01A-11D-A35D-08 chr6:151161959 T>A maps to NM_001029884.1 S1362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A80Q-01A-11D-A35I-08 chr1:16046371 C>G maps to ENST00000420314 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6H1-01A-11D-A35D-08 chr23:103040510 G>A did not map to a codon.
Sequencing variant TCGA-QR-A707-01A-11D-A35D-08 chr23:153695646 C>T did not map to a codon.
Sequencing variant TCGA-W2-A7HA-01B-11D-A35I-08 chr3:48445925 T>C maps to NM_001130082.1 A2125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A681-01A-11D-A35D-08 chr2:55900134 T>C maps to NM_033109.3 Q253Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70G-01B-11D-A35D-08 chr19:14043664 C>T maps to NM_024825.3 R464R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7X2-01A-12D-A35I-08 chr23:24761357 T>C did not map to a codon.
Sequencing variant TCGA-RW-A680-01A-11D-A35D-08 chr7:44154458 C>G maps to NM_006230.2 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7X2-01A-12D-A35I-08 chr4:2129862 T>C maps to NM_181808.2 V653V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XP-01A-11D-A35D-08 chr13:38160279 G>T maps to NM_006475.2 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6GR-01A-11D-A35D-08 chr8:43147782 C>T maps to NM_001005365.2 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6ZZ-01A-11D-A35D-08 chr14:19553784 C>T maps to NM_001005356.2 Y123Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A80L-01A-11D-A35I-08 chr4:23816226 G>T maps to NM_013261.3 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7WW-01A-11D-A35I-08 chr4:76787340 C>T did not map to a codon.
Sequencing variant TCGA-RW-A684-01A-12D-A35D-08 chr12:81741404 C>A maps to NM_003625.2 L713L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SQ-A6I6-01A-11D-A35I-08 chr19:45885940 G>A maps to NM_001142502.1 Y764Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PR-A5PG-01A-11D-A35D-08 chr11:64014016 C>G maps to NM_138689.2 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PR-A5PF-01A-11D-A35D-08 chr15:41120791 C>A maps to NM_001130143.1 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6GT-01A-11D-A35D-08 chr8:8998549 A>G maps to NM_024607.2 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A7CZ-01A-11D-A35D-08 chr23:49143520 C>T did not map to a codon.
Sequencing variant TCGA-WB-A81A-01A-11D-A35I-08 chr9:104357179 C>T maps to NM_147180.2 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6GT-01A-11D-A35D-08 chr6:32130672 C>T maps to NM_138717.1 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70A-01A-11D-A35D-08 chr23:48759213 C>A did not map to a codon.
Sequencing variant TCGA-P8-A6RX-01A-11D-A35D-08 chr12:11546414 T>C maps to NM_006248.3 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81W-01A-11D-A35I-08 chr1:3327969 C>T maps to NM_022114.3 Y403Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SP-A6QI-01A-12D-A35I-08 chr2:27355236 G>A maps to NM_013388.4 R263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A7D0-01A-11D-A35D-08 chr8:68934376 T>A did not map to a codon.
Sequencing variant TCGA-QT-A5XJ-01A-11D-A35D-08 chr11:57154991 G>A maps to NM_002728.4 R209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70E-01A-11D-A35D-08 chr23:49034505 G>A did not map to a codon.
Sequencing variant TCGA-QR-A70D-01A-11D-A35D-08 chr19:14208593 G>A maps to NM_002730.3 D176D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A8AZ-01A-11D-A35D-08 chr17:66521050 A>G did not map to a codon.
Sequencing variant TCGA-QR-A708-01A-11D-A35D-08 chr3:169993050 G>A maps to NM_002740.5 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A7D0-01A-11D-A35D-08 chr19:50185322 G>C did not map to a codon.
Sequencing variant TCGA-QR-A70K-01A-12D-A35D-08 chr4:15989291 T>A maps to NM_006017.2 G708G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81K-01A-11D-A35I-08 chr15:55965851 A>G maps to NM_173814.4 I523I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81M-01A-11D-A35I-08 chr19:40900181 C>T maps to NM_181882.2 E1359E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W2-A7HB-01A-11D-A35I-08 chr19:43439886 T>A maps to NM_002783.2 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70P-01A-11D-A35D-08 chr19:43262331 G>A maps to NM_182707.2 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XK-01A-11D-A35D-08 chr20:60715936 G>A maps to NM_002792.2 Q54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RM-A68T-01A-11D-A35D-08 chr2:54124013 G>T maps to NM_014614.2 I1205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A703-01A-11D-A35D-08 chr1:45288334 G>A maps to NM_003738.4 Q1122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MZ-01A-11D-A35I-08 chr10:27700843 T>C maps to NM_001034842.3 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P8-A5KC-01A-11D-A35D-08 chr9:112185068 C>T maps to NM_002829.3 R355R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70G-01B-11D-A35D-08 chr9:112182719 G>T maps to NM_002829.3 R433R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W2-A7HC-01A-11D-A35I-08 chr2:1652632 G>A maps to NM_012293.1 A973A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A822-01A-11D-A35I-08 chr2:1652158 G>A maps to NM_012293.1 P1131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SA-A6C2-01A-11D-A35I-08 chr20:3146604 C>T maps to NM_014731.2 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A820-01A-11D-A35I-08 chr2:37594433 G>A maps to NM_012413.3 E202E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70X-01A-11D-A35D-08 chr9:139118700 G>A maps to NM_181701.3 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A67V-01A-11D-A35D-08 chr19:8464765 A>G maps to NM_004218.3 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W2-A7HE-01A-11D-A35I-08 chr23:154493535 A>C did not map to a codon.
Sequencing variant TCGA-WB-A80Q-01A-11D-A35I-08 chr23:102755565 T>A did not map to a codon.
Sequencing variant TCGA-WB-A81T-01A-11D-A35I-08 chr11:73388972 T>C maps to NM_198896.1 Q199Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W2-A7UY-01A-11D-A35I-08 chr5:131931304 T>A maps to NM_005732.3 I670I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A688-01A-11D-A35D-08 chr3:51697225 G>C maps to NM_015106.2 A1398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6GW-01A-11D-A35D-08 chr2:109384206 G>A maps to NM_006267.4 W2404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70H-01A-12D-A35D-08 chr2:204354774 G>A maps to ENST00000374493 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6H6-01A-11D-A35D-08 chr4:53731671 C>T maps to NM_023940.2 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SP-A6QF-01A-12D-A35I-08 chr3:50369083 T>A maps to NM_170714.1 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6GX-01A-11D-A35D-08 chr6:155126574 A>C maps to NM_014892.3 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81M-01A-11D-A35I-08 chr10:6154184 G>A maps to NM_001145547.1 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7WL-01A-11D-A35I-08 chr14:23371510 G>A maps to NM_001077351.1 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A684-01A-12D-A35D-08 chr7:155503997 G>A maps to NM_053043.2 P350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A688-01A-11D-A35D-08 chr19:36124120 G>T maps to NM_024321.3 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6GS-01A-11D-A35D-08 chr4:40440292 C>T maps to NM_001098634.1 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81D-01A-11D-A35I-08 chr23:135961212 G>T did not map to a codon.
Sequencing variant TCGA-RW-A680-01A-11D-A35D-08 chr10:48390172 G>T maps to NM_002900.2 T235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81V-01A-11D-A35I-08 chr19:10132232 G>A maps to NM_015725.2 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81N-01A-11D-A35I-08 chr17:80007801 T>C maps to NM_002917.1 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A706-01A-11D-A35D-08 chr22:29837975 C>A maps to NM_021026.2 V273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MS-01A-11D-A35I-08 chr6:117203567 G>A maps to NM_173560.3 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A68F-01A-11D-A35D-08 chr23:109695455 C>T did not map to a codon.
Sequencing variant TCGA-WB-A817-01A-11D-A35I-08 chr23:46951082 G>T did not map to a codon.
Sequencing variant TCGA-WB-A81D-01A-11D-A35I-08 chr10:62648780 T>C maps to NM_014836.4 Q215Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XP-01A-11D-A35D-08 chr19:33486989 G>A maps to NM_033103.4 Y454Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A7D0-01A-11D-A35D-08 chr5:38950322 C>T maps to ENST00000296782 T1209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MS-01A-11D-A35I-08 chr19:39359958 G>C maps to NM_001195833.1 S522S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70P-01A-11D-A35D-08 chr12:121002880 C>T maps to ENST00000458409 R563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70V-01A-11D-A35D-08 chr13:25399863 T>C maps to ENST00000381927 C733C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A68C-01A-11D-A35D-08 chr14:24629073 C>T maps to NM_017999.4 G967G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70A-01A-11D-A35D-08 chr6:37328328 A>G maps to NM_003958.3 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70J-01A-11D-A35D-08 chr2:11333966 G>A maps to NM_004850.3 R1209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6H3-01A-11D-A35D-08 chr8:55541349 C>T maps to NM_006269.1 Y1636Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MP-01A-11D-A35I-08 chr8:10467863 C>A maps to NM_178857.5 G1248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A680-01A-11D-A35D-08 chr23:38156539 G>T did not map to a codon.
Sequencing variant TCGA-W2-A7HH-01A-11D-A35I-08 chr23:38146338 T>G did not map to a codon.
Sequencing variant TCGA-RW-A67V-01A-11D-A35D-08 chr6:133138154 G>A maps to NM_001016.3 E97E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A817-01A-11D-A35I-08 chr15:63447931 T>C did not map to a codon.
Sequencing variant TCGA-QR-A6GT-01A-11D-A35D-08 chr1:152128185 A>G maps to NM_001122965.1 Y463Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XK-01A-11D-A35D-08 chr1:152128185 A>G maps to NM_001122965.1 Y463Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XL-01A-11D-A35D-08 chr1:152128185 A>G maps to NM_001122965.1 Y463Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A819-01A-11D-A35I-08 chr1:152128185 A>G maps to NM_001122965.1 Y463Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70P-01A-11D-A35D-08 chr1:114354413 G>A maps to NM_018364.3 C207C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A68F-01A-11D-A35D-08 chr11:77386294 T>C maps to NM_016578.3 Q1116Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A689-01A-11D-A35D-08 chr12:122990195 G>A maps to NM_023012.5 Q395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W2-A7HD-01A-11D-A35I-08 chr5:178994548 T>C maps to NM_025158.3 N230N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7WN-01A-12D-A35I-08 chr6:45390465 A>G maps to ENST00000359524 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W2-A7HE-01A-11D-A35I-08 chr6:45390444 A>G maps to ENST00000359524 Q126Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W2-A7HA-01B-11D-A35I-08 chr4:184572390 G>A maps to ENST00000326397 N65N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A821-01A-11D-A35I-08 chr1:101705532 C>T maps to NM_001400.4 C331C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7X0-01A-12D-A35I-08 chr19:10624928 G>C maps to NM_001166215.1 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70W-01A-12D-A35D-08 chr2:234243688 C>T maps to NM_000541.4 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A80Q-01A-11D-A35I-08 chr23:23803818 G>A did not map to a codon.
Sequencing variant TCGA-SP-A6QC-01A-11D-A35I-08 chr4:77100807 G>A maps to NM_005506.2 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XN-01A-11D-A35D-08 chr3:38639330 C>T maps to NM_001099404.1 P717P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A685-01A-11D-A35D-08 chr12:52145211 C>T maps to NM_014191.2 C735C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A700-01A-11D-A35D-08 chr16:23366678 G>A maps to ENST00000307331 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MP-01A-11D-A35I-08 chr8:144891005 G>A maps to NM_182706.3 Q630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MP-01A-11D-A35I-08 chr8:144892897 G>A maps to NM_182706.3 P454P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6GS-01A-11D-A35D-08 chr22:43606946 G>T maps to NM_173050.2 T788T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70U-01A-11D-A35D-08 chr11:9068918 A>G maps to ENST00000457346 H662H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70H-01A-12D-A35D-08 chr12:100722991 T>C maps to NM_017988.4 C552C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70C-01A-21D-A35D-08 chr9:139302343 T>C maps to NM_001039707.1 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A68F-01A-11D-A35D-08 chr7:83029536 G>A maps to NM_012431.2 Y391Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81P-01A-11D-A35I-08 chr15:74706921 G>A maps to NM_003612.3 H420H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MT-01A-11D-A35I-08 chr5:132099469 G>C maps to NM_001098811.1 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A705-01A-11D-A35D-08 chr18:61565019 A>G maps to NM_001143818.1 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TT-A6YK-01A-11D-A35I-08 chr13:50055169 G>A maps to NM_031915.2 Q370Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70U-01A-11D-A35D-08 chr22:25289432 C>T maps to NM_001039948.2 T657T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SQ-A6I6-01A-11D-A35I-08 chr22:25243679 C>G maps to NM_001039948.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A8AZ-01A-11D-A35D-08 chr4:42403413 C>G maps to NM_001080505.1 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SP-A6QF-01A-12D-A35I-08 chr19:52130951 G>A maps to ENST00000222107 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6H5-01A-11D-A35D-08 chr21:44837472 G>A maps to NM_173354.3 A642A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A707-01A-11D-A35D-08 chr3:121647371 T>A maps to NM_021082.3 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7X2-01A-12D-A35I-08 chr11:22396359 A>G maps to NM_020346.2 G367G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70E-01A-11D-A35D-08 chr11:64359372 G>A maps to NM_144585.2 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70G-01B-11D-A35D-08 chr6:160645780 C>T maps to NM_003058.3 G519G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W2-A7HC-01A-11D-A35I-08 chr7:107414430 G>A maps to NM_000111.2 H647H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70O-01A-11D-A35D-08 chr9:131118064 G>A maps to NM_005094.3 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PR-A5PG-01A-11D-A35D-08 chr20:45354640 C>A maps to NM_030777.3 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A68D-01A-11D-A35D-08 chr5:139947372 G>T maps to NM_080670.2 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A68F-01A-11D-A35D-08 chr11:45827750 C>G maps to NM_018389.4 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A68F-01A-11D-A35D-08 chr12:47172478 C>T maps to NM_018018.4 T266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7WT-01A-12D-A35I-08 chr7:150768534 G>A maps to NM_003040.3 T678T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W2-A7H5-01B-11D-A35I-08 chr1:44474155 C>T maps to NM_201649.2 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A700-01A-11D-A35D-08 chr2:103120166 G>A did not map to a codon.
Sequencing variant TCGA-WB-A822-01A-11D-A35I-08 chr12:20868176 C>T maps to NM_017435.4 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A681-01A-11D-A35D-08 chr10:98808820 G>A maps to NM_003061.2 D452D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70A-01A-11D-A35D-08 chr23:142717978 C>A did not map to a codon.
Sequencing variant TCGA-QT-A5XK-01A-11D-A35D-08 chr2:130930856 A>G maps to NM_017951.4 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A7IP-01A-11D-A35D-08 chr9:33068869 G>A maps to NM_018225.2 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81N-01A-11D-A35I-08 chr17:1686378 A>G maps to NM_052928.2 S737S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7WO-01A-11D-A35I-08 chr2:1241770 G>A maps to NM_018968.3 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7WN-01A-12D-A35I-08 chr4:186544638 A>G maps to ENST00000355634 H744H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A80N-01A-11D-A35I-08 chr4:186544635 G>A maps to ENST00000355634 H745H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MP-01A-11D-A35I-08 chr17:70117788 G>A maps to NM_000346.3 W86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70P-01A-11D-A35D-08 chr1:118548120 C>T maps to NM_206996.2 E1564E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A7D0-01A-11D-A35D-08 chr20:34205715 C>T maps to NM_003116.1 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6H5-01A-11D-A35D-08 chr23:142795396 C>A did not map to a codon.
Sequencing variant TCGA-RW-A680-01A-11D-A35D-08 chr13:24858318 C>T maps to ENST00000424834 N774N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7WU-01A-11D-A35I-08 chr3:172642090 G>A maps to NM_031955.5 F415F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A69Q-01A-11D-A35D-08 chr23:155004225 C>T did not map to a codon.
Sequencing variant TCGA-QR-A70K-01A-12D-A35D-08 chr11:55653269 G>A maps to NM_032681.3 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A702-01A-11D-A35D-08 chr14:65220493 C>T maps to ENST00000389723 T2125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SP-A6QF-01A-12D-A35I-08 chr14:65260382 G>C maps to ENST00000389723 G670G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A703-01A-11D-A35D-08 chr11:66475223 C>T maps to NM_006946.2 T472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A681-01A-11D-A35D-08 chr11:66457284 C>A maps to NM_006946.2 A1980A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81I-01A-11D-A35I-08 chr22:42273264 G>A maps to NM_004599.2 A473A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A7IN-01A-11D-A35D-08 chr16:2815445 T>A maps to NM_016333.3 G1639G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P8-A5KD-01A-11D-A35D-08 chr2:182784163 C>T maps to NM_001130445.1 S1045S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A7CZ-01A-11D-A35D-08 chr11:67079324 C>T maps to NM_017857.3 S649S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W2-A7HF-01A-11D-A35I-08 chr23:48206946 C>A did not map to a codon.
Sequencing variant TCGA-SA-A6C2-01A-11D-A35I-08 chr23:48049617 C>A did not map to a codon.
Sequencing variant TCGA-WB-A816-01A-11D-A35I-08 chr11:130068266 C>T maps to NM_021978.3 C508C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MR-01A-11D-A35I-08 chr3:186793531 G>T maps to NM_003032.2 E388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TT-A6YK-01A-11D-A35I-08 chr12:57642947 T>C maps to NM_145064.1 E70E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81T-01A-11D-A35I-08 chr12:57642486 A>C did not map to a codon.
Sequencing variant TCGA-S7-A7WQ-01A-12D-A35I-08 chr1:36823839 C>T maps to ENST00000373130 Q119Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70G-01B-11D-A35D-08 chr19:47228839 G>A maps to NM_001039877.1 Y445Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6H0-01A-11D-A35D-08 chr6:152539539 T>C did not map to a codon.
Sequencing variant TCGA-W2-A7HD-01A-11D-A35I-08 chr6:152590364 G>A maps to NM_182961.2 P6210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81H-01A-11D-A35I-08 chr6:152472813 G>A maps to NM_182961.2 G8108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70E-01A-11D-A35D-08 chr14:64450465 G>A maps to NM_182914.2 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SP-A6QH-01A-21D-A35I-08 chr7:105738243 T>C maps to NM_006754.2 Q116Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81M-01A-11D-A35I-08 chr23:99945086 T>A did not map to a codon.
Sequencing variant TCGA-RT-A6YA-01A-12D-A35D-08 chr23:30877654 T>C did not map to a codon.
Sequencing variant TCGA-W2-A7HA-01B-11D-A35I-08 chr23:30872732 T>C did not map to a codon.
Sequencing variant TCGA-WB-A821-01A-11D-A35I-08 chr23:30873679 C>A did not map to a codon.
Sequencing variant TCGA-QR-A70J-01A-11D-A35D-08 chr10:123970863 C>A maps to NM_206862.2 P2308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MX-01A-11D-A35I-08 chr4:1732664 C>T maps to NM_006342.1 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70D-01A-11D-A35D-08 chr23:70603866 C>T did not map to a codon.
Sequencing variant TCGA-TT-A6YJ-01A-11D-A35I-08 chr9:32633093 A>T maps to NM_153809.2 V828V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7WQ-01A-12D-A35I-08 chr5:68661171 A>C maps to NM_001015892.1 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MX-01A-11D-A35I-08 chr7:141464341 G>A maps to NM_016943.2 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A820-01A-11D-A35I-08 chr3:10318139 A>G maps to NM_014760.3 K643K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W2-A7HA-01B-11D-A35I-08 chr4:38051408 C>T maps to NM_015173.2 F600F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XJ-01A-11D-A35D-08 chr23:106082535 A>G did not map to a codon.
Sequencing variant TCGA-SR-A6MP-01A-11D-A35I-08 chr17:37822067 G>A maps to NM_003673.3 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MP-01A-11D-A35I-08 chr17:37822169 G>A maps to NM_003673.3 E104E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6H0-01A-11D-A35D-08 chr1:152082551 C>T maps to NM_007113.2 E1047E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MQ-01A-11D-A35I-08 chr9:100258050 C>T maps to NM_014290.2 N1061N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A684-01A-12D-A35D-08 chr9:27180334 A>G maps to NM_000459.3 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A708-01A-11D-A35D-08 chr16:1551467 C>G maps to NM_016111.3 P443P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A681-01A-11D-A35D-08 chr16:69404384 C>T did not map to a codon.
Sequencing variant TCGA-TT-A6YK-01A-11D-A35I-08 chr23:69825318 T>C did not map to a codon.
Sequencing variant TCGA-QR-A70T-01A-11D-A35D-08 chr10:60146033 A>G maps to NM_003201.1 K52K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A80K-01A-11D-A35I-08 chr16:4312677 G>C maps to NM_003223.2 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A814-01A-11D-A35I-08 chr1:92174279 G>A maps to NM_003243.4 Q743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A80V-01A-12D-A35I-08 chr2:105924110 T>A maps to NM_004257.4 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W2-A7HC-01A-11D-A35I-08 chr2:85554506 C>T maps to ENST00000409015 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W2-A7HA-01B-11D-A35I-08 chr15:39885297 C>T maps to NM_003246.2 T955T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A820-01A-11D-A35I-08 chr2:138413156 C>T maps to ENST00000272643 V1347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A815-01A-11D-A35I-08 chr6:54191705 G>T maps to NM_014464.3 E206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81N-01A-11D-A35I-08 chr23:153557887 C>T did not map to a codon.
Sequencing variant TCGA-QR-A70T-01A-11D-A35D-08 chr9:84205888 A>G maps to NM_005077.3 L554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A684-01A-12D-A35D-08 chr9:84228340 A>G maps to NM_005077.3 R338R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7WT-01A-12D-A35I-08 chr20:30732973 G>T maps to NM_014742.3 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6GT-01A-11D-A35D-08 chr16:19056298 C>T maps to NM_024847.3 C477C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81H-01A-11D-A35I-08 chr4:159158778 A>G maps to NM_018342.4 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A80O-01A-11D-A35I-08 chr3:136573457 T>C maps to NM_025246.2 N52N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A8AZ-01A-11D-A35D-08 chr9:35853199 C>G maps to NM_001042590.1 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81T-01A-11D-A35I-08 chr17:31260233 G>A maps to NM_015544.2 E58E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A684-01A-12D-A35D-08 chr6:138201286 C>T maps to NM_006290.2 C662C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A80Y-01A-11D-A35I-08 chr1:175375784 C>T maps to NM_003285.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81E-01A-11D-A35I-08 chr8:59720341 C>T maps to NM_014729.2 G515G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81P-01A-11D-A35I-08 chr16:52473704 A>T maps to ENST00000407228 L388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7WN-01A-12D-A35I-08 chr15:43712933 C>G did not map to a codon.
Sequencing variant TCGA-W2-A7HA-01B-11D-A35I-08 chr21:45518254 G>A maps to NM_003274.4 K1062K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70P-01A-11D-A35D-08 chr8:110100448 T>C maps to NM_003301.4 N236N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A80V-01A-12D-A35I-08 chr3:32932861 C>T maps to NM_001039111.1 H722H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6H0-01A-11D-A35D-08 chr4:189060900 G>A maps to NM_178556.3 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SP-A6QG-01A-12D-A35I-08 chr23:100297189 G>A did not map to a codon.
Sequencing variant TCGA-RW-A67Y-01A-11D-A35D-08 chr20:5924292 C>A maps to NM_015939.3 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A706-01A-11D-A35D-08 chr23:54949633 G>A did not map to a codon.
Sequencing variant TCGA-SR-A6MQ-01A-11D-A35I-08 chr2:234891752 C>T maps to NM_024080.4 G882G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81S-01A-11D-A35I-08 chr2:99695277 T>A did not map to a codon.
Sequencing variant TCGA-P8-A6RX-01A-11D-A35D-08 chr18:72998960 C>G maps to NM_005786.4 Y488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MX-01A-11D-A35I-08 chr20:51871508 A>G maps to NM_173485.5 E504E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MS-01A-11D-A35I-08 chr17:46868937 C>T maps to NM_001130918.1 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70G-01B-11D-A35D-08 chr2:179596173 G>A maps to NM_133378.4 D4529D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A681-01A-11D-A35D-08 chr2:179455965 T>A maps to NM_133378.4 V17594V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7WT-01A-12D-A35I-08 chr2:179418226 A>T did not map to a codon.
Sequencing variant TCGA-SP-A6QJ-01A-11D-A35I-08 chr2:179650739 G>A maps to NM_133378.4 Y735Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A68B-01A-11D-A35D-08 chr2:130951511 C>T maps to NM_207312.2 Q301Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TT-A6YN-01A-12D-A35I-08 chr6:112397153 G>A maps to NM_016262.4 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A80M-01A-11D-A35I-08 chr22:50659142 G>A maps to NM_020461.3 H1215H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W2-A7UY-01A-11D-A35I-08 chr12:104713351 C>T maps to NM_001093771.1 Y326Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70E-01A-11D-A35D-08 chr7:66479412 T>C maps to NM_018264.2 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7WW-01A-11D-A35I-08 chr7:66474574 C>T maps to NM_018264.2 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A820-01A-11D-A35I-08 chr21:44521485 G>A maps to NM_001025203.1 D63D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XP-01A-11D-A35D-08 chr3:49848256 G>A maps to NM_003335.2 S413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6H5-01A-11D-A35D-08 chr17:16285490 C>T maps to NM_018955.2 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A820-01A-11D-A35I-08 chr12:125397414 G>A maps to NM_021009.5 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TT-A6YN-01A-12D-A35I-08 chr7:157060409 C>G maps to NM_014671.2 L1071L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XJ-01A-11D-A35D-08 chr1:19481548 C>G maps to ENST00000375267 A2107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XN-01A-11D-A35D-08 chr20:62571397 G>A maps to NM_017859.3 G526G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A67Y-01A-11D-A35D-08 chr4:69403498 G>C maps to NM_001076.2 V479V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A684-01A-12D-A35D-08 chr4:70346369 C>T maps to NM_021139.2 K523K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SA-A6C2-01A-11D-A35I-08 chr5:36049137 G>A maps to NM_174914.3 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81G-01A-11D-A35I-08 chr4:115544470 T>C maps to NM_003360.3 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S7-A7WU-01A-11D-A35I-08 chr1:215823954 G>A maps to ENST00000366943 S4774S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P8-A6RX-01A-11D-A35D-08 chr12:62785103 C>T maps to ENST00000280377 R710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81T-01A-11D-A35I-08 chr8:11995944 G>A maps to NM_201402.2 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70J-01A-11D-A35D-08 chr3:49151651 G>A maps to ENST00000434032 L784L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SQ-A6I6-01A-11D-A35I-08 chr16:23117809 T>A did not map to a codon.
Sequencing variant TCGA-QR-A70U-01A-11D-A35D-08 chr23:41045775 C>T did not map to a codon.
Sequencing variant TCGA-QR-A70U-01A-11D-A35D-08 chr23:41069760 G>A did not map to a codon.
Sequencing variant TCGA-WB-A818-01A-11D-A35I-08 chr23:40990707 A>G did not map to a codon.
Sequencing variant TCGA-QR-A700-01A-11D-A35D-08 chr1:7837365 G>A maps to NM_004781.3 W73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XM-01A-11D-A35D-08 chr6:30893360 C>T maps to NM_001167734.1 F972F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A68C-01A-11D-A35D-08 chr19:6821670 C>A maps to NM_005428.2 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81E-01A-11D-A35I-08 chr9:35057380 G>A maps to NM_007126.3 G769G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70I-01A-11D-A35D-08 chr8:67577498 A>G maps to NM_025054.4 S565S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SP-A6QG-01A-12D-A35I-08 chr8:100479756 C>T maps to NM_017890.3 V1187V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81Q-01A-11D-A35I-08 chr3:184689501 C>T maps to ENST00000437079 Q1128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70P-01A-11D-A35D-08 chr23:65242293 G>A did not map to a codon.
Sequencing variant TCGA-WB-A81T-01A-11D-A35I-08 chr23:65253673 T>C did not map to a codon.
Sequencing variant TCGA-QR-A70N-01A-12D-A35D-08 chr1:119575970 T>A maps to NM_015836.3 K216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A68F-01A-11D-A35D-08 chr13:27255298 C>T maps to NM_006646.5 H275H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6H6-01A-11D-A35D-08 chr7:71142221 C>A maps to NM_022479.1 V477V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A80M-01A-11D-A35I-08 chr4:85636524 C>A maps to NM_014991.4 V2629V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70J-01A-11D-A35D-08 chr19:36585022 A>T maps to NM_001083961.1 P808P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A7U0-01A-11D-A35D-08 chr19:36579970 G>T maps to NM_001083961.1 G600G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QT-A5XO-01A-11D-A35D-08 chr1:241886683 C>T maps to NM_144625.4 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A702-01A-11D-A35D-08 chr8:124146351 A>G did not map to a codon.
Sequencing variant TCGA-QR-A70N-01A-12D-A35D-08 chr8:38175552 G>T maps to NM_017778.2 S620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A821-01A-11D-A35I-08 chr1:168510201 G>A maps to NM_003175.3 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6H1-01A-11D-A35D-08 chr2:31628831 T>C did not map to a codon.
Sequencing variant TCGA-QR-A6GT-01A-11D-A35D-08 chr23:128887217 C>T did not map to a codon.
Sequencing variant TCGA-TT-A6YK-01A-11D-A35I-08 chr8:21827086 C>A maps to ENST00000434536 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A685-01A-11D-A35D-08 chr12:64818383 A>G maps to NM_007235.3 E396E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81W-01A-11D-A35I-08 chr17:7193312 C>T maps to NM_015982.3 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A8AZ-01A-11D-A35D-08 chr10:27406651 A>C maps to NM_139312.1 P581P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A816-01A-11D-A35I-08 chr10:27409415 T>C maps to NM_139312.1 K510K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MU-01A-11D-A35I-08 chr2:174085984 C>T maps to NM_133646.2 N365N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81J-01A-11D-A35I-08 chr23:2408699 C>T did not map to a codon.
Sequencing variant TCGA-QR-A70O-01A-11D-A35D-08 chr19:59028620 C>G maps to NM_032792.2 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SR-A6MU-01A-11D-A35I-08 chr10:31791357 C>T maps to NM_001174096.1 D135D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SP-A6QG-01A-12D-A35I-08 chr2:145147118 C>A maps to NM_014795.3 E1182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PR-A5PF-01A-11D-A35D-08 chr8:144332585 A>G maps to NM_173832.3 K191K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A80M-01A-11D-A35I-08 chr4:2306615 G>T maps to NM_020972.2 S484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A816-01A-11D-A35I-08 chr23:47836773 C>T did not map to a codon.
Sequencing variant TCGA-QR-A707-01A-11D-A35D-08 chr6:27419846 C>T maps to NM_007149.2 T497T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81G-01A-11D-A35I-08 chr23:152085711 C>A did not map to a codon.
Sequencing variant TCGA-SP-A6QC-01A-11D-A35I-08 chr17:18565372 A>G maps to NM_001145045.1 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6GX-01A-11D-A35D-08 chr16:58032115 T>A maps to NM_020807.1 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TT-A6YP-01A-21D-A35I-08 chr20:45130891 C>T maps to NM_018102.3 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W2-A7HA-01B-11D-A35I-08 chr20:45130414 T>C maps to NM_018102.3 E521E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A68A-01A-11D-A35D-08 chr10:64429986 T>C maps to NM_199451.2 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A6GT-01A-11D-A35D-08 chr18:72775247 G>A maps to NM_017757.2 A1857A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81H-01A-11D-A35I-08 chr10:31137680 G>A maps to NM_182755.2 S551S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P7-A5NX-01A-11D-A35D-08 chr1:247492594 G>T maps to NM_032752.1 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PR-A5PH-01A-11D-A35D-08 chr19:42584206 G>A maps to ENST00000222339 R573R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QR-A70C-01A-21D-A35D-08 chr19:42584441 C>T maps to ENST00000222339 Q652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81R-01A-11D-A35I-08 chr1:249141580 C>T maps to NM_024836.1 H36H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A67Y-01A-11D-A35D-08 chr1:26688342 G>T maps to ENST00000436292 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A67X-01A-11D-A35D-08 chr22:24087096 T>C maps to NM_021916.2 Q77Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WB-A81V-01A-11D-A35I-08 chr9:130197488 C>T maps to NM_007135.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PR-A5PF-01A-11D-A35D-08 chr3:113955351 C>T maps to NM_007136.3 K190K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RW-A67X-01A-11D-A35D-08 chr3:102196340 C>A maps to NM_175056.1 S392*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-QR-A700-01A-11D-A35D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-QR-A7IN-01A-11D-A35D-08 chr23:57935102 A>G did not map to a codon.
Sequencing variant TCGA-QR-A707-01A-11D-A35D-08 chr17:3981267 G>A maps to NM_015113.3 S966S. Only missense variants will be evaluated by CHASM.
