8763 NP_109597 G229D not found in SNVbox database
9750 NP_109597 T543I not found in SNVbox database
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr10:52573772 G>T maps to NM_138932.2 G397G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr22:43089054 G>C maps to NM_017436.4 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LD-01A-11D-A29I-10 chr12:125561104 A>C maps to NM_023928.3 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr2:69746289 A>G maps to NM_014911.3 T431T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LA-01A-11D-A29I-10 chr6:44268370 T>C maps to NM_020745.2 S957S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr7:121769437 A>G maps to NM_005763.3 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JX-01A-11D-A29I-10 chr17:79096343 G>A maps to NM_001080395.2 D464D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JQ-01A-11D-A29I-10 chr9:107568701 G>C maps to NM_005502.3 P1428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr2:215866332 C>A maps to NM_173076.2 E938*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr7:48314044 C>G maps to NM_152701.3 G1594G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr7:48327568 G>A maps to NM_152701.3 W2950*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr7:48311656 C>T maps to NM_152701.3 N798N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr7:48311464 A>G maps to NM_152701.3 L734L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L1-01A-11D-A30A-10 chr17:67081275 G>T maps to NM_080284.2 C1359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J3-01A-11D-A29I-10 chr19:1065043 C>T maps to NM_019112.3 G2053G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J7-01A-11D-A29I-10 chr19:1065043 C>T maps to NM_019112.3 G2053G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr19:1065043 C>T maps to NM_019112.3 G2053G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr19:1047283 C>A maps to NM_019112.3 A658A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JI-01A-11D-A29I-10 chr19:1065043 C>T maps to NM_019112.3 G2053G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr19:1065043 C>T maps to NM_019112.3 G2053G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr19:1049412 C>T maps to NM_019112.3 N843N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr19:1046950 C>T maps to NM_019112.3 L591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr19:1065043 C>T maps to NM_019112.3 G2053G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KV-01A-11D-A29I-10 chr19:1065043 C>T maps to NM_019112.3 G2053G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KW-01A-11D-A29I-10 chr19:1065043 C>T maps to NM_019112.3 G2053G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr19:1065043 C>T maps to NM_019112.3 G2053G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LP-01A-11D-A29I-10 chr19:1065043 C>T maps to NM_019112.3 G2053G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr19:1065043 C>T maps to NM_019112.3 G2053G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr17:67028259 T>C maps to NM_080283.3 K478K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:87138731 C>A maps to NM_000927.3 V1116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J3-01A-11D-A29I-10 chr12:123414622 C>A maps to NM_203444.2 V712V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr16:48261749 G>C maps to NM_032583.3 S121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LD-01A-11D-A29I-10 chr16:48245092 C>T maps to NM_032583.3 E458E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr16:48155703 G>A maps to NM_033226.2 Y545Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr16:48173121 G>T maps to NM_033226.2 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr17:48741342 G>A maps to NM_003786.3 A403A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr13:95840745 G>A maps to NM_005845.3 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr13:95830010 G>A maps to NM_005845.3 D559D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr3:183679296 A>T did not map to a codon.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr3:183732093 C>T maps to NM_005688.2 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr11:17452491 G>A maps to ENST00000302539 H562H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr12:21962828 A>G maps to NM_005691.2 I1424I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr12:22069966 G>A maps to NM_005691.2 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr23:152994691 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr6:30552278 G>T maps to NM_001025091.1 E443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr9:133760172 C>T maps to NM_007313.2 H851H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L4-01A-11D-A29I-10 chr10:116225544 C>T maps to ENST00000277895 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr17:970424 T>C maps to NM_021962.2 P358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr17:35609865 C>T maps to NM_198834.1 Q641Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5H8-01A-11D-A29I-10 chr3:128614184 A>C maps to NM_014049.4 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L3-01A-11D-A29I-10 chr10:124800852 C>T maps to NM_001609.3 H213H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr15:89386841 C>A maps to NM_013227.3 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr3:195022704 C>A maps to NM_012287.5 G439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:1230155 G>A maps to NM_030649.2 G618G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr1:226342402 G>A maps to NM_022735.3 S345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr1:180471344 C>G maps to NM_032360.3 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:180471389 T>C maps to NM_032360.3 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr12:50471032 C>A maps to NM_020039.2 S199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:220379238 G>T maps to NM_018674.4 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr7:100490016 C>A maps to NM_000665.3 T497T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr17:40054038 C>A maps to ENST00000401700 V518V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KZ-01A-11D-A29I-10 chr22:41903812 A>C maps to ENST00000396512 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr14:74040290 C>T maps to NM_006821.4 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr23:23754091 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr15:78466040 G>A maps to NM_015162.4 I661I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr2:223773829 G>T maps to NM_203372.1 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr16:20476934 C>T maps to NM_001010845.2 Q92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:236902765 G>C maps to NM_001103.2 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JX-01A-11D-A29I-10 chr19:39214252 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5JL-01A-11D-A29I-10 chr20:37377138 C>T maps to NM_024855.3 F6F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JT-01A-11D-A29I-10 chr20:37377138 C>T maps to NM_024855.3 F6F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr20:37377138 C>T maps to NM_024855.3 F6F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr20:37377138 C>T maps to NM_024855.3 F6F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K8-01A-11D-A29I-10 chr20:37377138 C>T maps to NM_024855.3 F6F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr20:37377138 C>T maps to NM_024855.3 F6F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr20:37377138 C>T maps to NM_024855.3 F6F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L4-01A-11D-A29I-10 chr20:37377138 C>T maps to NM_024855.3 F6F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr20:37377138 C>T maps to NM_024855.3 F6F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr20:37377138 C>T maps to NM_024855.3 F6F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr3:53911366 G>A maps to NM_022899.4 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:127185765 A>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:127186026 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5JV-01A-11D-A29I-10 chr1:2938568 C>T maps to NM_080431.4 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JW-01A-11D-A29I-10 chr3:38519420 C>T maps to NM_001106.3 N110N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr20:43251245 C>T maps to NM_000022.2 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr17:42847370 C>G maps to NM_002390.4 Y112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:156997965 G>A maps to ENST00000430702 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LL-01A-11D-A29I-10 chr14:70926007 A>C maps to NM_003813.2 R598R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr20:3654432 C>T maps to NM_025220.2 G288G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L6-01A-11D-A29I-10 chr20:3654432 C>T maps to NM_025220.2 G288G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr10:135086883 G>A maps to NM_001109.4 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr8:38880769 G>T maps to NM_003816.2 V280V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:33576157 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:33576500 C>T maps to NM_030955.2 W1210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr10:72489934 C>G maps to NM_139155.2 R344R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LR-01A-11D-A29I-10 chr10:72498689 T>A maps to NM_139155.2 C567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr10:72434450 C>T maps to NM_139155.2 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr5:5140631 T>C maps to NM_139056.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr5:5140631 T>C maps to NM_139056.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr5:5140631 T>C maps to NM_139056.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr5:129037113 A>T maps to NM_133638.3 R990R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr5:178567009 C>T maps to NM_014244.4 W552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr4:73280550 G>C maps to NM_014243.1 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr4:73148984 T>C maps to NM_014243.1 S1162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LR-01A-11D-A29I-10 chr1:161160927 T>C maps to NM_005099.4 *838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:64747375 G>C maps to NM_197941.2 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:64755997 C>A maps to NM_197941.2 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr15:79063944 C>T maps to ENST00000258883 K786K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JL-01A-11D-A29I-10 chr15:79066580 G>A maps to ENST00000258883 D646D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr15:79068600 G>A maps to ENST00000258883 S545S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KW-01A-11D-A29I-10 chr15:79059159 T>G maps to ENST00000258883 S1031S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr11:130275862 C>A maps to NM_007037.4 E754*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr10:1284297 C>T maps to NM_018702.2 E419E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr6:143749779 T>C maps to NM_182503.2 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr19:1912816 C>T maps to NM_138422.1 Y241Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr19:1912162 G>A maps to NM_138422.1 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:45753293 G>T maps to NM_021116.2 V1020V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JL-01A-11D-A29I-10 chr2:25046089 T>C maps to NM_004036.3 S957S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr14:24800999 C>T maps to NM_139247.3 K221K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JR-01A-11D-A29I-10 chr3:123167248 G>A maps to NM_183357.2 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr16:50326733 C>T maps to NM_001114.3 Q229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr16:4164588 C>A maps to NM_001116.3 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PA-A5YG-01A-11D-A29I-10 chr4:100203571 C>T maps to NM_000667.3 E253E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr4:100235235 G>A maps to NM_000668.4 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr4:100237111 G>T maps to NM_000668.4 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr4:100131301 C>T maps to NM_001102470.1 E168E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:202915738 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr5:159344847 C>T maps to NM_000679.3 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr10:112838011 C>T maps to NM_000681.3 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr10:112838128 G>T maps to NM_000681.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr10:112839103 C>T maps to NM_000681.3 R450R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr10:115804007 C>T maps to NM_000684.2 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr11:67046986 G>A maps to NM_001619.3 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:148049221 G>T did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr4:74303977 G>A maps to NM_001134.1 E75E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr15:86791010 G>T maps to NM_152336.2 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr15:86790915 A>T maps to NM_152336.2 R135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr11:47701523 C>T did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr7:141333739 C>T maps to NM_018238.3 R210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J3-01A-11D-A29I-10 chr1:15911348 G>A maps to NM_024758.3 D38D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr1:15911348 G>A maps to NM_024758.3 D38D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr1:15911348 G>A maps to NM_024758.3 D38D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr1:15911348 G>A maps to NM_024758.3 D38D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:15911348 G>A maps to NM_024758.3 D38D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr9:88162050 A>T maps to ENST00000395847 S1218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr9:88248283 A>G maps to ENST00000395847 Y436Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr5:34998916 C>T maps to NM_031900.3 A484A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OF-01A-11D-A29I-10 chr5:177659518 C>G maps to NM_153373.2 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr6:135726086 A>C did not map to a codon.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr14:105412334 C>T maps to NM_138420.2 P3151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr14:105415286 G>C maps to NM_138420.2 A2167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr14:105416411 G>A maps to NM_138420.2 D1792D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr14:105412334 C>T maps to NM_138420.2 P3151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr14:105416009 T>C maps to NM_138420.2 T1926T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chr14:105407447 T>C maps to NM_138420.2 E4780E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr14:105409901 C>T maps to NM_138420.2 T3962T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr12:8759523 G>A maps to NM_020661.2 Y31Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:129289210 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr6:106975231 G>T maps to NM_001624.2 E1081*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr6:106968169 C>T maps to NM_001624.2 V621V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr6:106968203 C>T maps to NM_001624.2 Q633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr17:6329049 C>T maps to NM_014336.3 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr6:151647015 C>A maps to NM_144497.2 I7I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JI-01A-11D-A29I-10 chr15:86124622 A>C maps to NM_006738.4 I1108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:119048831 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5JR-01A-11D-A29I-10 chr12:4737041 G>A maps to NM_006422.2 H342H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr23:49955728 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:49957835 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5LL-01A-11D-A29I-10 chr23:49957051 T>C did not map to a codon.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr14:33014536 A>G maps to NM_004274.4 E226E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr14:33291761 C>A maps to NM_004274.4 G1581G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr19:15482784 G>T maps to NM_005858.2 S339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr10:5139658 C>T maps to NM_003739.4 R96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chr1:19600385 C>T maps to NM_201252.3 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L4-01A-11D-A29I-10 chr1:19595158 C>T maps to NM_201252.3 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J7-01A-11D-A29I-10 chr19:50376387 C>T maps to ENST00000391835 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr10:97393406 C>G did not map to a codon.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr12:105464484 G>A maps to NM_001034173.3 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr6:24533861 C>T maps to NM_170740.1 S523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr16:30081475 C>T maps to ENST00000395248 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KV-01A-11D-A29I-10 chr16:5132635 C>T maps to NM_019109.4 F383F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:110980044 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr23:110973751 G>C did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:110964939 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr9:101984047 G>C maps to NM_033087.3 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KT-01A-11D-A29I-10 chr9:101980797 C>T maps to NM_033087.3 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr2:29445208 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr2:29754830 G>A maps to NM_004304.3 H368H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:29497977 G>T maps to NM_004304.3 I676I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:30143450 G>T maps to NM_004304.3 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:73679620 A>T maps to NM_015120.4 S1988S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JX-01A-11D-A29I-10 chr17:4536240 T>C maps to NM_001140.3 T485T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr10:45869759 C>T maps to NM_000698.2 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr17:8013789 G>T maps to ENST00000380149 C494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr17:8017850 G>A maps to ENST00000380149 R367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr18:56171295 C>A maps to NM_052947.3 V2038V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr15:85401391 G>A maps to NM_020778.4 E1343E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:233245384 G>C maps to NM_001632.3 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:233273465 G>C maps to NM_031313.2 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr17:33520492 G>A maps to NM_152462.2 H278H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr9:116840417 C>A maps to NM_001633.3 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr11:46419410 G>A maps to ENST00000458649 A1162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr12:96337224 C>T maps to NM_152435.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr12:96337224 C>T maps to NM_152435.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr12:96337224 C>T maps to NM_152435.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JW-01A-11D-A29I-10 chr12:96337224 C>T maps to NM_152435.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr12:96337224 C>T maps to NM_152435.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KV-01A-11D-A29I-10 chr12:96337224 C>T maps to NM_152435.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L6-01A-11D-A29I-10 chr12:96337224 C>T maps to NM_152435.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr12:96337224 C>T maps to NM_152435.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr12:96337224 C>T maps to NM_152435.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:11316881 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5JD-01A-11D-A29I-10 chr3:49755683 T>G maps to NM_198722.2 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr3:49755683 T>G maps to NM_198722.2 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:109507775 G>C did not map to a codon.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr2:128631583 G>T maps to NM_031445.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L1-01A-11D-A30A-10 chr1:110170895 T>C maps to ENST00000393689 H478H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KT-01A-11D-A29I-10 chr7:38431435 C>T maps to NM_001635.3 T597T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr3:49459641 C>T maps to NM_000481.3 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr7:2752256 C>A maps to NM_133463.1 C414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr4:25419943 C>T maps to ENST00000510092 A790A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr8:108334172 C>T maps to NM_001146.3 E253E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr20:854939 T>C maps to NM_015985.2 Q446Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr8:41561585 G>A maps to ENST00000415018 N756N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr4:114257868 C>A maps to NM_001148.4 S1243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr10:61847903 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5JX-01A-11D-A29I-10 chr5:14769102 G>A maps to NM_054027.4 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KT-01A-11D-A29I-10 chr7:91974335 G>A maps to NM_019004.1 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L3-01A-11D-A29I-10 chr2:241465260 G>A maps to ENST00000401804 H392H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr2:241463345 G>A maps to ENST00000401804 S596S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr7:16649290 G>A maps to NM_020319.2 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr16:89352531 C>T maps to NM_013275.4 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr16:89346958 C>T maps to NM_013275.4 A1997A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr4:73956552 A>G maps to NM_032217.3 S2264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr10:99338086 A>T maps to NM_020349.2 K121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J1-01A-11D-A29I-10 chr19:4210318 C>T maps to ENST00000262970 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J3-01A-11D-A29I-10 chr19:4217955 A>G maps to ENST00000262970 A1023A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr19:4217955 A>G maps to ENST00000262970 A1023A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr19:4217955 A>G maps to ENST00000262970 A1023A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr19:4217955 A>G maps to ENST00000262970 A1023A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr18:14748543 C>A maps to NM_001145029.1 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr18:14748438 C>A maps to NM_001145029.1 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr18:14851980 G>A maps to NM_001145029.1 E1227E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:94027836 C>A maps to NM_032290.3 V857V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr2:97519167 C>T maps to NM_016466.5 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JW-01A-11D-A29I-10 chr2:198001318 A>G maps to NM_001195144.1 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr2:197865168 G>A maps to NM_001195144.1 I831I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr4:125591275 T>A maps to NM_020337.2 A1052A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr12:56638933 C>G maps to NM_173595.3 P815P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J7-01A-11D-A29I-10 chr5:55439736 C>T maps to NM_024669.2 W168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JD-01A-11D-A29I-10 chr4:77818201 T>C maps to NM_001029870.1 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K8-01A-11D-A29I-10 chr4:77818201 T>C maps to NM_001029870.1 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr4:77818201 T>C maps to NM_001029870.1 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KV-01A-11D-A29I-10 chr4:77818201 T>C maps to NM_001029870.1 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KZ-01A-11D-A29I-10 chr4:77818201 T>C maps to NM_001029870.1 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr4:77818201 T>C maps to NM_001029870.1 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr4:77818201 T>C maps to NM_001029870.1 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J2-01A-11D-A29I-10 chr2:110372191 A>G maps to NM_023016.3 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J3-01A-11D-A29I-10 chr2:110372191 A>G maps to NM_023016.3 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J7-01A-11D-A29I-10 chr2:110372191 A>G maps to NM_023016.3 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr2:110372191 A>G maps to NM_023016.3 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr2:110372191 A>G maps to NM_023016.3 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr2:110372191 A>G maps to NM_023016.3 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JL-01A-11D-A29I-10 chr2:110372191 A>G maps to NM_023016.3 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr2:110372191 A>G maps to NM_023016.3 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr2:110372191 A>G maps to NM_023016.3 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr2:110372191 A>G maps to NM_023016.3 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr2:110372191 A>G maps to NM_023016.3 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L1-01A-11D-A30A-10 chr2:110372191 A>G maps to NM_023016.3 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr2:110372191 A>G maps to NM_023016.3 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LD-01A-11D-A29I-10 chr2:110372191 A>G maps to NM_023016.3 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr2:110372191 A>G maps to NM_023016.3 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr23:118892887 G>C did not map to a codon.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr12:45833606 C>G maps to NM_001142679.1 L892L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr2:242157227 G>C maps to NM_001001891.3 P754P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr19:17435646 G>A maps to NM_020959.2 G1070G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr19:17441306 G>A maps to NM_020959.2 R334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L1-01A-11D-A30A-10 chr4:80898807 C>T maps to NM_001145794.1 R465R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr4:122607509 C>A maps to NM_001154.3 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr4:122593693 T>A maps to NM_001154.3 R207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JX-01A-11D-A29I-10 chr5:150503871 C>T maps to NM_001155.4 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr15:90378788 G>A maps to ENST00000398333 G381G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr12:99061320 C>T maps to NM_181861.1 Q465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr9:72131952 C>T maps to NM_001163.3 E58E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr9:72131952 C>T maps to NM_001163.3 E58E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr15:29400510 C>T maps to NM_005503.3 V652V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr15:29393974 C>T maps to NM_005503.3 F504F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr15:29393974 C>T maps to NM_005503.3 F504F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr20:57042376 G>A maps to NM_153360.1 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr14:20924073 G>A maps to NM_080649.1 E20E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:68805009 G>T maps to NM_173545.2 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr1:161192811 C>T maps to NM_001643.1 E27E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:21228417 C>A maps to NM_000384.2 L3774L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr16:28508068 C>T maps to NM_018690.2 G560G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr16:28509448 C>T maps to NM_018690.2 R992R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr17:58525007 G>A maps to NM_006380.2 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:66765160 A>T did not map to a codon.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr23:66765163 A>T did not map to a codon.
Sequencing variant TCGA-OR-A5LD-01A-11D-A29I-10 chr23:66765160 A>T did not map to a codon.
Sequencing variant TCGA-OR-A5JT-01A-11D-A29I-10 chr11:72412757 G>A maps to NM_001040118.2 H746H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr4:36214031 A>G maps to NM_015230.2 F373F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr8:143694447 G>T maps to NM_015193.3 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr22:43203136 C>T maps to NM_014570.4 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr20:62333491 C>T maps to NM_003224.3 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr11:46703668 G>A maps to NM_004308.2 H127H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr4:148968041 G>T did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr6:129950581 T>A maps to NM_033515.2 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr10:49658872 C>G maps to ENST00000417912 R449R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KW-01A-11D-A29I-10 chr18:6890433 A>G maps to ENST00000400091 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr1:161017555 C>T maps to NM_001025598.1 R1085R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:130222737 C>G did not map to a codon.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:153184647 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr23:153187250 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KZ-01A-11D-A29I-10 chr23:153176253 A>G did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:11682851 G>T did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr17:79827659 T>C maps to NM_004309.4 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:156926235 T>A maps to NM_198236.1 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L1-01A-11D-A30A-10 chr1:3395038 G>A maps to NM_014448.3 V559V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr1:3395173 C>A maps to NM_014448.3 S604S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:3380094 G>A maps to NM_014448.3 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr11:73020057 C>T maps to NM_014786.3 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr19:7516147 G>A maps to NM_001130955.1 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr4:106534598 C>A maps to ENST00000420470 S148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr13:111938537 G>A maps to NM_001113511.1 K686K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L9-01A-11D-A29I-10 chr13:111870036 T>C maps to NM_001113511.1 D181D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5H8-01A-11D-A29I-10 chr13:111870036 T>C maps to NM_001113511.1 D181D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr6:157505499 G>T maps to ENST00000367148 E1201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J2-01A-11D-A29I-10 chr19:929677 G>A maps to NM_005224.2 E50E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J2-01A-11D-A29I-10 chr19:929752 A>G maps to NM_005224.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr19:929740 C>T maps to NM_005224.2 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JQ-01A-11D-A29I-10 chr19:929752 A>G maps to NM_005224.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K8-01A-11D-A29I-10 chr19:929740 C>T maps to NM_005224.2 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K8-01A-11D-A29I-10 chr19:929752 A>G maps to NM_005224.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr19:929677 G>A maps to NM_005224.2 E50E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr19:929677 G>A maps to NM_005224.2 E50E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr19:929752 A>G maps to NM_005224.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr19:929752 A>G maps to NM_005224.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr19:929752 A>G maps to NM_005224.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr19:929752 A>G maps to NM_005224.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr19:929752 A>G maps to NM_005224.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OF-01A-11D-A29I-10 chr19:929752 A>G maps to NM_005224.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr19:929677 G>A maps to NM_005224.2 E50E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr19:929677 G>A maps to NM_005224.2 E50E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr19:929752 A>G maps to NM_005224.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr9:34627864 C>A maps to NM_001017363.1 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JV-01A-11D-A29I-10 chr1:235377220 G>T maps to NM_016374.5 C568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr1:235345011 A>C maps to NM_016374.5 V1074V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:235357436 T>G maps to NM_016374.5 T672T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr10:63845626 G>T maps to NM_032199.2 E456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr5:175792604 G>C maps to NM_173664.4 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JH-01A-11D-A30A-10 chr5:175792604 G>C maps to NM_173664.4 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JI-01A-11D-A29I-10 chr5:175792604 G>C maps to NM_173664.4 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr5:175792604 G>C maps to NM_173664.4 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JW-01A-11D-A29I-10 chr5:175792604 G>C maps to NM_173664.4 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:175792604 G>C maps to NM_173664.4 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr5:175792604 G>C maps to NM_173664.4 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr5:175792604 G>C maps to NM_173664.4 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr5:175792604 G>C maps to NM_173664.4 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5H8-01A-11D-A29I-10 chr5:175792604 G>C maps to NM_173664.4 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr13:50204723 C>T maps to NM_138450.5 N47N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr23:100229149 T>C did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:100243237 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5LL-01A-11D-A29I-10 chr8:66525547 T>C maps to NM_018120.4 Q132Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr6:109249376 G>A maps to NM_032131.4 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr16:31476185 C>G maps to ENST00000408912 L709L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JD-01A-11D-A29I-10 chr23:100808268 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:100911670 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:100880256 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr15:80800575 G>A maps to NM_014862.3 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr15:80869291 C>A maps to NM_014862.3 S533S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr3:9839432 C>A maps to NM_001198793.1 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr3:35730809 G>T maps to ENST00000458225 E140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr19:18119373 C>T maps to NM_015683.1 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr15:98511296 T>C maps to NM_183376.2 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr5:78076459 C>T maps to NM_000046.3 P454P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr23:2825436 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5L6-01A-11D-A29I-10 chr23:2836036 G>C did not map to a codon.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr23:2856154 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr17:66391297 C>T maps to NM_014960.3 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:2942060 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr23:2945476 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:94901700 G>T did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:23763444 G>A maps to NM_017707.3 Q479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr7:150873648 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5L6-01A-11D-A29I-10 chr23:15332558 C>G did not map to a codon.
Sequencing variant TCGA-OR-A5JD-01A-11D-A29I-10 chr23:63444867 T>G did not map to a codon.
Multiple mappings detected for codon TCGA-OR-A5JQ-01A-11D-A29I-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-OR-A5JQ-01A-11D-A29I-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-OR-A5K4-01A-11D-A29I-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-OR-A5L1-01A-11D-A30A-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-OR-A5LO-01A-11D-A29I-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr2:237123103 G>C maps to NM_212556.2 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr14:94420822 C>T maps to ENST00000434324 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr7:95157437 C>G maps to NM_016116.2 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:155452084 C>T maps to ENST00000368346 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr23:1538000 A>G did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:1571719 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr23:1546766 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr14:104561947 C>T maps to NM_001080464.1 F128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr1:197112532 G>A maps to NM_018136.4 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:197059994 T>A maps to NM_018136.4 G3207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:197113116 T>A maps to NM_018136.4 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr9:95233049 G>T maps to NM_017680.4 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr2:70188112 C>A maps to NM_152792.2 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr9:133342122 C>T maps to NM_000050.4 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr1:176852119 C>T maps to ENST00000281881 L1087L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr9:120053670 G>C maps to ENST00000313400 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr9:119488070 G>A maps to ENST00000313400 L929L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr18:31323337 C>A maps to NM_030632.1 R1176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:117062372 G>A maps to NM_130768.2 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr2:24086376 G>C maps to NM_017552.1 A451A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J3-01A-11D-A29I-10 chr1:1447692 C>T maps to NM_018188.3 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr12:51207829 T>C maps to NM_005171.4 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr12:53946409 G>A maps to NM_001130059.1 N20N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr12:14578094 G>T maps to NM_018179.3 E416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr11:64665393 T>C maps to ENST00000421419 E1639E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:242606246 G>T maps to ENST00000337606 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr11:108098417 C>T maps to NM_000051.3 R23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr11:108138055 C>T maps to NM_000051.3 S875S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr12:7045905 G>A maps to NM_001940.3 Q492Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JH-01A-11D-A30A-10 chr12:7045911 G>A maps to NM_001940.3 Q494Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JT-01A-11D-A29I-10 chr12:7045911 G>A maps to NM_001940.3 Q494Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr12:7045911 G>A maps to NM_001940.3 Q494Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PA-A5YG-01A-11D-A29I-10 chr12:7045899 G>A maps to NM_001940.3 Q490Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PA-A5YG-01A-11D-A29I-10 chr12:7045905 G>A maps to NM_001940.3 Q492Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LP-01A-11D-A29I-10 chr15:25926185 G>A maps to NM_024490.3 A1176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L4-01A-11D-A29I-10 chr5:160025959 G>A maps to NM_025153.2 L1127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr13:113508733 G>C maps to NM_032189.3 L711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr3:182538052 T>C maps to NM_014616.1 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JD-01A-11D-A29I-10 chr23:138901555 G>C did not map to a codon.
Sequencing variant TCGA-OR-A5KT-01A-11D-A29I-10 chr23:138886676 T>C did not map to a codon.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr13:25262635 C>T maps to NM_001185085.1 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:17313429 T>C maps to NM_022089.2 T1035T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chr1:17326539 G>A maps to NM_022089.2 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr3:194162114 A>T maps to NM_024524.3 C545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr3:193174876 T>C maps to NM_032279.2 T609T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr3:193032829 A>G maps to NM_198505.2 L697L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr1:160100010 C>T maps to NM_000702.3 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:160124893 C>T maps to NM_144699.3 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr23:119512612 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr12:90018031 A>T maps to ENST00000428670 V424V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr3:10491212 G>C maps to NM_001001331.2 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr23:152807869 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:152827695 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:152807876 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:152823604 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr23:152815530 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr1:203682342 G>A maps to NM_001001396.1 A754A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr10:7841034 G>C maps to NM_001001973.1 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J3-01A-11D-A29I-10 chr12:124239084 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr7:138417705 G>A maps to NM_130840.2 H608H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr4:42580309 A>C maps to NM_006095.2 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr13:26411329 G>T maps to NM_016529.4 L928L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr13:26138138 C>A maps to NM_016529.4 P481P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr15:50212565 G>A maps to NM_024837.2 Y600Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr20:3624814 C>T maps to NM_139321.2 P1355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr10:116853706 C>A maps to NM_207303.2 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:76918897 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr23:76875872 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KT-01A-11D-A29I-10 chr23:76939321 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr6:16306907 G>A maps to NM_000332.3 P700P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr12:112036796 C>T maps to NM_002973.3 Q174Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KT-01A-11D-A29I-10 chr12:112036796 C>T maps to NM_002973.3 Q174Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KZ-01A-11D-A29I-10 chr12:112036796 C>T maps to NM_002973.3 Q174Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L6-01A-11D-A29I-10 chr12:112036796 C>T maps to NM_002973.3 Q174Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L9-01A-11D-A29I-10 chr12:112036796 C>T maps to NM_002973.3 Q174Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr16:28844675 G>T did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr16:28841941 G>A maps to NM_148414.1 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr16:28848084 C>T maps to NM_145714.1 P1051P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr7:105255169 G>A maps to NM_020725.1 N537N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:74756547 G>C maps to ENST00000258081 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr7:70255627 G>A maps to NM_015570.2 E1142E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr13:31843386 C>A maps to NM_194318.3 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr11:134253804 G>A maps to NM_054025.2 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr6:71665730 C>T maps to NM_080742.2 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr19:41931792 G>A maps to NM_198540.2 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L1-01A-11D-A30A-10 chr17:81009621 C>T maps to NM_001009905.1 Q17Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr5:177034386 G>A maps to NM_007255.2 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr11:117186505 G>A maps to NM_012104.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr11:117186505 G>A maps to NM_012104.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr17:79428054 C>T maps to ENST00000436173 L2122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr17:79424536 C>T maps to ENST00000436173 L1654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:32196919 C>A maps to NM_001703.2 V1287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr17:79031711 C>T maps to NM_017451.2 D54D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr16:1393393 G>A maps to NM_003933.4 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr3:52438536 G>A maps to NM_004656.2 Y394Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr6:31590580 G>T maps to NM_080686.2 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr9:134340406 C>A maps to NM_013318.3 P554P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr1:171506484 C>T maps to ENST00000392078 R793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JH-01A-11D-A30A-10 chr6:31630240 C>T maps to NM_033177.3 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr12:57005764 G>A maps to NM_013449.3 V469V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-OR-A5KB-01A-11D-A30A-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr14:99641146 G>A maps to NM_138576.2 L676L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr14:99640940 C>A maps to NM_138576.2 S744S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr14:99641024 C>T maps to NM_138576.2 A716A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr2:111921763 C>T maps to NM_138621.3 R185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr1:147092111 G>A maps to NM_004326.2 K717K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr6:136599765 C>A maps to NM_014739.2 G85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J2-01A-11D-A29I-10 chr23:39913283 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr23:129190050 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:129148843 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:129154971 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:129173156 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr23:129155103 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr22:23655083 C>T maps to NM_004327.3 D1111D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr22:23637230 G>A maps to NM_004327.3 E967E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr14:101011365 G>A maps to NM_020836.3 Q72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:102317892 T>C did not map to a codon.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr23:102564586 A>G did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:102471391 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5J1-01A-11D-A29I-10 chr23:101409173 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:101409038 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr12:26275826 C>G maps to NM_030762.2 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OF-01A-11D-A29I-10 chr12:26275862 G>A maps to NM_030762.2 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr10:60273077 G>T maps to NM_001080512.1 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr10:60562965 C>T maps to NM_001080512.1 A715A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:32673861 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr20:61869819 G>T maps to NM_139317.1 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr17:28601154 G>A maps to NM_000386.2 R236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J3-01A-11D-A29I-10 chr19:45682697 C>A maps to NM_212550.3 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:69092924 A>G maps to NM_014482.1 I371I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr4:79832493 A>T maps to NM_198892.1 V931V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr20:55777573 C>T maps to NM_001719.2 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr10:43285923 C>T maps to NM_014753.3 R201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr10:43292519 G>T maps to NM_014753.3 E610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr9:16437423 G>T maps to NM_017637.5 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr9:16418992 T>A maps to NM_017637.5 V1098V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JX-01A-11D-A29I-10 chr3:112991311 C>T maps to ENST00000273395 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr4:13615255 C>A maps to NM_148894.2 G402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr1:149871944 C>T maps to NM_016074.3 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LD-01A-11D-A29I-10 chr6:3118991 C>T maps to NM_004332.2 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J7-01A-11D-A29I-10 chr17:41234469 A>G maps to ENST00000471181 S1436S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr22:50198008 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr19:15355538 G>A maps to NM_058243.2 P731P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr1:92446706 T>A maps to ENST00000347608 C586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chr8:37702541 C>T maps to NM_018310.3 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr8:37702688 G>A maps to NM_018310.3 Y193Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr6:36179102 G>T maps to NM_015695.2 E750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr11:1464774 G>T maps to NM_003957.2 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr11:1471881 G>A maps to NM_003957.2 T451T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:79971693 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr10:93726391 A>G did not map to a codon.
Multiple mappings detected for codon TCGA-OR-A5JD-01A-11D-A29I-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-OR-A5JD-01A-11D-A29I-10 chr17:72356325 C>T maps to ENST00000440684 T831T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr19:1993162 C>T maps to NM_017797.3 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr6:38561777 C>A maps to NM_052893.1 E171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:100615076 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5JX-01A-11D-A29I-10 chr6:26408131 A>T maps to NM_007048.5 R223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr6:26451900 A>T did not map to a codon.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr5:180432367 G>T maps to NM_197975.2 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr5:180432415 C>T maps to NM_197975.2 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr5:180477227 G>T maps to NM_152547.4 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JH-01A-11D-A30A-10 chr11:116633824 C>T maps to NM_032725.3 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr17:56388997 G>T maps to NM_004758.2 I1005I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr10:77542775 A>T maps to NM_032024.3 K15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr10:115891095 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr10:21805479 T>C maps to NM_207371.3 E424E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr10:5773062 C>T maps to NM_017782.4 C367C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr10:11912143 C>T maps to NM_153256.3 H349H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr10:11912143 C>T maps to NM_153256.3 H349H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr10:50533415 G>A maps to NM_001135196.1 S942S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr10:50531425 C>A maps to NM_001135196.1 S279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr10:50534258 C>A maps to NM_001135196.1 C1223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr10:103716387 G>A maps to NM_024541.2 R557R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KW-01A-11D-A29I-10 chr10:115526176 A>G maps to NM_182601.1 Q6Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr10:128193342 G>A maps to NM_001004298.2 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr11:76169376 G>A maps to ENST00000393457 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr11:556371 C>T maps to NM_173573.2 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr11:33564461 A>T maps to ENST00000389726 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr11:122817235 G>T maps to NM_024806.2 T555T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr11:61249382 C>A maps to NM_145017.2 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr11:63594409 G>A maps to NM_138471.1 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr11:109294763 C>G maps to NM_207645.3 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr12:27066420 C>A maps to NM_018164.2 E592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr12:32135055 A>G maps to NM_018169.3 A389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr12:32134533 A>T maps to NM_018169.3 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr12:32136906 A>T maps to NM_018169.3 T1006T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JR-01A-11D-A29I-10 chr12:49075304 G>A maps to NM_017822.3 H37H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr12:112690233 G>T maps to NM_001109662.2 R1010R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr12:112600906 A>C maps to NM_001109662.2 G4181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr12:6805619 G>T maps to NM_153685.2 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr13:42032571 T>C maps to NM_014059.2 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr14:50100682 C>G maps to NM_018139.2 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr14:50100682 C>G maps to NM_018139.2 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr14:50100682 C>G maps to NM_018139.2 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr14:50100682 C>G maps to NM_018139.2 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr14:50100682 C>G maps to NM_018139.2 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr14:81259322 C>A maps to NM_152446.3 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr14:81209476 G>C maps to NM_152446.3 L916L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JL-01A-11D-A29I-10 chr14:105054933 A>G maps to NM_001008404.1 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JV-01A-11D-A29I-10 chr14:77493646 A>G maps to NM_024496.2 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr14:77493808 C>T maps to NM_024496.2 Q109Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr14:95916423 C>T maps to NM_152592.3 A431A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr14:95932516 G>A maps to NM_152592.3 Y126Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr14:103568728 A>G maps to NM_001077594.1 E223E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr14:103568728 A>G maps to NM_001077594.1 E223E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr14:103568728 A>G maps to NM_001077594.1 E223E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr15:24921175 C>T maps to NM_018958.2 N54N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JW-01A-11D-A29I-10 chr15:34648578 G>T maps to ENST00000438749 L780L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr16:684528 G>C maps to NM_001040160.1 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr16:19628039 G>T maps to NM_020314.5 V467V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr16:85743809 G>T maps to NM_206967.2 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JW-01A-11D-A29I-10 chr16:5115840 C>T maps to ENST00000350219 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr16:3544635 A>C maps to NM_001080524.1 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr17:80361860 C>T maps to NM_175902.4 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr17:8092693 T>G maps to NM_017622.2 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr17:34190105 G>T maps to NM_152781.2 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr17:8140716 G>T maps to NM_025099.5 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr17:7329039 A>G maps to NM_175734.4 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr17:260181 T>C maps to NM_001013672.4 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr17:260181 T>C maps to NM_001013672.4 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr17:260181 T>C maps to NM_001013672.4 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr17:260181 T>C maps to NM_001013672.4 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KZ-01A-11D-A29I-10 chr17:260181 T>C maps to NM_001013672.4 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr17:260181 T>C maps to NM_001013672.4 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LP-01A-11D-A29I-10 chr17:260181 T>C maps to NM_001013672.4 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr19:30199200 G>A maps to NM_001031726.2 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L6-01A-11D-A29I-10 chr19:30433555 C>G maps to NM_003796.2 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr19:519017 C>T maps to NM_033513.2 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr19:756984 T>G maps to NM_173481.2 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr19:899443 C>T maps to NM_138774.3 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr19:3547500 G>T maps to NM_021731.2 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr19:3547980 T>G maps to NM_021731.2 L234L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-OR-A5JP-01A-11D-A29I-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr19:1010672 G>A maps to NM_001033026.1 P513P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KZ-01A-11D-A29I-10 chr12:49730134 G>C maps to NM_001008223.1 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr12:49729768 G>A maps to NM_001008223.1 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr5:34043080 G>A maps to NM_181435.4 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr12:7187964 C>T maps to ENST00000290575 P677P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr12:7260846 T>C maps to NM_016546.2 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KW-01A-11D-A29I-10 chr1:11008484 C>A maps to NM_001170754.1 G569G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr1:67591496 G>C maps to NM_001013674.1 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JH-01A-11D-A30A-10 chr1:75037844 A>G maps to NM_001002912.4 S1183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:156316634 C>T maps to NM_144627.3 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr1:60456487 G>A maps to NM_152377.2 R500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr20:34568457 C>T maps to ENST00000373973 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr20:31671497 G>A maps to NM_182519.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LD-01A-11D-A29I-10 chr20:55059238 C>T maps to ENST00000357348 C187C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr22:37397949 G>T maps to NM_001163857.1 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr22:32547006 C>G did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr15:62359892 C>A maps to NM_207322.2 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr2:106682225 T>C maps to NM_032411.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr2:106682234 C>G maps to NM_032411.2 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr2:106682225 T>C maps to NM_032411.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr2:106682234 C>G maps to NM_032411.2 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr2:106682234 C>G maps to NM_032411.2 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr2:106682234 C>G maps to NM_032411.2 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J3-01A-11D-A29I-10 chr2:241827804 C>A maps to NM_001085437.1 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr2:241828011 T>C maps to NM_001085437.1 E316E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KZ-01A-11D-A29I-10 chr2:219221845 G>A maps to NM_198559.1 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L3-01A-11D-A29I-10 chr2:29295882 T>A maps to NM_001029883.1 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr2:25013383 G>A maps to NM_001013663.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L6-01A-11D-A29I-10 chr2:228477730 G>T maps to NM_001162483.1 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chr19:6710781 G>T maps to NM_000064.2 P518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L3-01A-11D-A29I-10 chr19:6677988 G>A maps to NM_000064.2 P1632P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr19:6684637 C>T maps to NM_000064.2 K1351K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr3:112730186 T>C maps to NM_015412.3 Q206Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L6-01A-11D-A29I-10 chr3:49842191 C>T maps to NM_203370.1 D212D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr4:113505162 T>C maps to NM_018392.4 P1423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LR-01A-11D-A29I-10 chr4:130032885 T>A maps to NM_001099783.1 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JL-01A-11D-A29I-10 chr4:3250963 C>A maps to NM_001042690.1 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr5:56207217 A>G maps to NM_153706.3 Q107Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:93805737 G>A maps to ENST00000513200 V600V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr5:2752392 G>C maps to NM_178569.2 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr6:30615259 C>T maps to NM_001161376.1 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr6:74161346 C>A maps to NM_138441.2 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr6:31627652 C>A maps to NM_021184.3 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr7:25208035 G>A maps to NM_138811.3 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:120770180 C>A maps to NM_024913.4 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr8:144653154 G>A maps to NM_001100878.1 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr8:144649600 A>G maps to NM_001100878.1 A656A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr8:144649624 T>C maps to NM_001100878.1 R648R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr8:144649624 T>C maps to NM_001100878.1 R648R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L1-01A-11D-A30A-10 chr8:144649600 A>G maps to NM_001100878.1 A656A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr8:144649624 T>C maps to NM_001100878.1 R648R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JR-01A-11D-A29I-10 chr5:39341263 G>A maps to NM_001737.3 R154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr9:96097702 A>G maps to NM_001098808.1 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr9:89771510 G>T maps to NM_001001709.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr9:139739045 C>T maps to NM_001080482.2 D60D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr9:103204597 G>A maps to NM_001198812.1 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr9:111909468 T>C maps to NM_014334.2 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr9:214718 C>T maps to NM_152569.2 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr9:26842343 C>T maps to NM_024828.3 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr8:86162996 T>A maps to NM_198584.2 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr1:150232558 G>T maps to NM_012113.1 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L9-01A-11D-A29I-10 chr9:35675851 C>G maps to NM_001216.2 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr19:13319692 A>G maps to NM_023035.2 H2223H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr19:13319692 A>G maps to NM_023035.2 H2223H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr19:13319692 A>G maps to NM_023035.2 H2223H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr19:13319692 A>G maps to NM_023035.2 H2223H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr19:13319692 A>G maps to NM_023035.2 H2223H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr9:141015260 G>A maps to ENST00000277549 P2140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr3:53844132 G>C maps to NM_001128840.1 L2000L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr1:181702848 C>T maps to ENST00000357570 P1075P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:181702836 C>T maps to ENST00000357570 T1071T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr23:49083513 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:49074373 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5KV-01A-11D-A29I-10 chr23:49067891 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr17:48703751 T>C maps to NM_018896.3 P2258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JT-01A-11D-A29I-10 chr16:1254106 C>A maps to NM_021098.2 C700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr16:1252123 G>A maps to NM_021098.2 S558S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr1:201058469 G>T maps to NM_000069.2 I272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr12:1906597 G>A maps to NM_172364.4 C1033C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr16:24268164 G>A maps to NM_006539.3 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr11:115111111 G>A maps to NM_014333.3 D51D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:188245196 C>T maps to NM_005795.4 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr7:134644846 A>G maps to NM_033138.3 A728A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr10:105215372 C>T maps to NM_001001412.3 K229K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr15:68491885 G>A maps to NM_033429.2 H99H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:71571249 G>T maps to NM_031468.3 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr5:110819980 C>A maps to NM_001744.4 A413A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr3:49898694 C>T maps to NM_024046.3 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:7721840 G>C maps to NM_015215.2 V240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr12:67696265 G>A maps to NM_018448.3 E388E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:85625896 G>T maps to NM_001747.2 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr2:85628744 C>T maps to NM_001747.2 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr2:85628350 G>A maps to NM_001747.2 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr2:85628768 G>A maps to NM_001747.2 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JQ-01A-11D-A29I-10 chr11:64950969 C>T maps to NM_005186.3 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr6:44144036 C>A maps to NM_007058.3 P321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J3-01A-11D-A29I-10 chr1:223933078 C>T maps to NM_001748.4 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:110490729 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr23:110497632 T>C did not map to a codon.
Sequencing variant TCGA-PA-A5YG-01A-11D-A29I-10 chr23:110494840 C>G did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:230921738 A>T maps to NM_006615.2 G498G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5H8-01A-11D-A29I-10 chr11:34104424 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr7:116557778 A>G did not map to a codon.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr22:37915144 C>T maps to NM_014550.3 E21E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr22:37915144 C>T maps to NM_014550.3 E21E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr15:40914771 C>T maps to NM_170589.3 V796V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JW-01A-11D-A29I-10 chr15:40915044 T>G maps to NM_170589.3 T887T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr23:41437769 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr16:2235144 A>C maps to NM_020764.3 G402G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr1:15820440 G>A maps to NM_001229.3 D368D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr3:121976120 G>T maps to NM_001178065.1 E127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:10719928 C>T maps to NM_001079843.1 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr19:38845374 C>T maps to NM_021185.4 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr16:88968047 T>C maps to NM_005187.5 K56K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr18:70209320 C>A maps to NM_182511.3 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr18:70209320 C>A maps to NM_182511.3 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KT-01A-11D-A29I-10 chr18:70209320 C>A maps to NM_182511.3 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KV-01A-11D-A29I-10 chr18:70209320 C>A maps to NM_182511.3 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L1-01A-11D-A30A-10 chr18:70209320 C>A maps to NM_182511.3 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LP-01A-11D-A29I-10 chr18:70209320 C>A maps to NM_182511.3 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr18:70209320 C>A maps to NM_182511.3 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr17:77808132 G>A maps to NM_003655.2 P436P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr10:70496801 A>G maps to NM_018237.2 Q81Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr18:66721362 C>T maps to NM_024781.2 Q511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KT-01A-11D-A29I-10 chr10:74451962 C>G maps to NM_138357.1 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr22:21989305 C>T maps to NM_152612.2 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr23:48921958 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr23:48925014 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5JQ-01A-11D-A29I-10 chr19:18047282 T>G maps to NM_001136203.1 R18R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr3:42799654 G>A maps to NM_144719.3 H61H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr16:57732902 C>A maps to NM_032269.5 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr16:57732899 C>A maps to NM_032269.5 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr16:57735915 G>C maps to NM_032269.5 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr3:123650269 C>T maps to NM_022757.4 V517V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr2:179721021 G>A maps to NM_173648.3 Q943*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr17:20799303 T>C maps to NM_001004306.1 G10G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:197511081 A>G maps to NM_001080539.1 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LA-01A-11D-A29I-10 chr22:30767636 A>G did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr4:77244562 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5JX-01A-11D-A29I-10 chr23:49099774 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr23:49093666 T>A did not map to a codon.
Sequencing variant TCGA-OR-A5LP-01A-11D-A29I-10 chr1:43047056 A>G maps to NM_001080850.2 E364E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr3:180369188 C>T maps to NM_181426.1 K389K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr3:191107353 C>T maps to NM_178335.2 S464S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr12:119926593 C>A maps to NM_178499.3 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr11:93088642 C>T maps to NM_181645.3 R46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr14:91883083 T>C maps to NM_001080414.2 Q53Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JR-01A-11D-A29I-10 chr4:7044356 A>G maps to NM_153376.2 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KV-01A-11D-A29I-10 chr4:7044356 A>G maps to NM_153376.2 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KW-01A-11D-A29I-10 chr4:7044356 A>G maps to NM_153376.2 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr4:7044356 A>G maps to NM_153376.2 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr4:7044356 A>G maps to NM_153376.2 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr9:36170695 G>C maps to NM_005893.2 R399R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:50052071 G>T did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr16:2487127 A>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:162869513 G>A maps to NM_199246.1 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:1334032 G>A maps to NM_030937.4 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr1:1334590 C>A maps to NM_030937.4 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr12:49086935 A>G maps to NM_001240.2 Y687Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr3:46400061 G>A maps to NM_001123396.1 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr3:46307365 G>C maps to NM_178328.1 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr11:66366692 G>T maps to NM_005125.1 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr11:66361153 C>T maps to NM_005125.1 D27D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr1:156303392 A>T maps to NM_005998.4 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr5:10258586 C>A maps to NM_012073.3 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr22:17072882 G>A maps to NM_014406.4 H186H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J2-01A-11D-A29I-10 chr1:158224500 T>G maps to NM_001763.2 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr1:158261042 G>T maps to NM_001765.2 E61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:158325659 T>A maps to NM_030893.3 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K8-01A-11D-A29I-10 chr3:112068595 T>C maps to NM_001004196.2 V269V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JV-01A-11D-A29I-10 chr17:41930364 C>T maps to NM_145273.3 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr1:157805631 C>T maps to NM_005894.2 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:157803261 G>A maps to NM_005894.2 C253C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JL-01A-11D-A29I-10 chr2:87088949 C>T maps to NM_172213.3 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr2:87088963 A>G maps to NM_172213.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L4-01A-11D-A29I-10 chr2:87088963 A>G maps to NM_172213.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr2:87088963 A>G maps to NM_172213.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr20:23065617 A>G maps to NM_012072.3 D404D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:2637736 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5L1-01A-11D-A30A-10 chr23:2644301 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr23:149999703 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5K8-01A-11D-A29I-10 chr15:43017425 T>G maps to NM_138477.2 L1158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr19:10503779 G>T maps to NM_007065.3 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L6-01A-11D-A29I-10 chr9:4685142 G>A maps to NM_017913.2 K133K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr14:103430939 C>A maps to NM_006035.3 A875A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LD-01A-11D-A29I-10 chr11:64601932 T>C maps to NM_017525.2 T764T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr8:25365208 G>T maps to ENST00000434814 L1010L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:21755940 C>G maps to NM_004061.3 A548A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:21854884 G>A maps to NM_004061.3 Q181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr16:83378567 G>T maps to ENST00000268613 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L6-01A-11D-A29I-10 chr16:83378513 G>T maps to ENST00000268613 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr16:66946626 G>A maps to NM_004062.2 R408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr18:59221762 G>T maps to NM_031891.2 T747T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr10:73447456 G>T maps to ENST00000398860 V685V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr10:73553113 G>A maps to ENST00000398860 T2148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LR-01A-11D-A29I-10 chr14:23518917 T>C maps to NM_022478.3 R543R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr20:60448950 C>A maps to NM_001794.2 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr20:60509118 C>T maps to NM_001794.2 Y795Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LL-01A-11D-A29I-10 chr20:60348207 G>A maps to NM_001794.2 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JX-01A-11D-A29I-10 chr16:66432423 C>T maps to NM_001795.3 I517I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr18:63511175 T>C maps to NM_004361.2 D370D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr10:85978990 C>T maps to NM_001171971.1 L733L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr5:176016114 C>A maps to NM_001171976.1 T980T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JQ-01A-11D-A29I-10 chr5:176011888 G>A maps to NM_001171976.1 A869A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L6-01A-11D-A29I-10 chr11:621633 G>A maps to NM_021924.4 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr7:39990354 C>T maps to NM_003718.4 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:47086025 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr20:31967332 G>C maps to ENST00000357886 V361V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr6:21000541 G>T maps to NM_017774.3 E332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr4:76522168 G>T maps to ENST00000307465 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr23:18631387 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr23:18525232 T>G did not map to a codon.
Sequencing variant TCGA-OR-A5LR-01A-11D-A29I-10 chr23:18622932 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5K8-01A-11D-A29I-10 chr23:139865765 T>C did not map to a codon.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr20:5170813 C>T maps to NM_003818.2 I424I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L3-01A-11D-A29I-10 chr16:88872510 T>C maps to NM_030928.3 H305H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:72667506 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr23:72674261 C>G did not map to a codon.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr23:72667190 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr6:4954181 G>T maps to ENST00000328908 L563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr19:43031406 C>G maps to NM_001712.4 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J7-01A-11D-A29I-10 chr22:17983976 C>T maps to ENST00000400579 R226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr22:18003340 G>A maps to ENST00000400579 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr22:17640021 G>C maps to NM_033070.2 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr18:34853087 C>G maps to NM_020180.3 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L3-01A-11D-A29I-10 chr19:3224895 G>C maps to NM_021938.3 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr22:46835093 G>A maps to NM_014246.1 I1466I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr22:46931003 C>T maps to NM_014246.1 T688T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr3:48693262 G>A maps to NM_001407.2 S1549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr20:3765725 C>A maps to NM_001810.5 E469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr4:68380316 C>A maps to NM_001812.2 E307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr4:104082565 C>A maps to NM_001813.2 E631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr4:104102531 T>A maps to NM_001813.2 R349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KV-01A-11D-A29I-10 chr1:214816609 C>G maps to NM_016343.3 L1643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr1:214816432 C>T maps to NM_016343.3 L1584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr5:68485475 C>G maps to NM_022909.3 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr23:100400094 G>A did not map to a codon.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr6:49456157 G>T maps to NM_018132.3 E191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr9:123888003 A>G maps to NM_007018.4 A605A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr20:34063417 G>T maps to NM_007186.3 E555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr20:34090550 G>T maps to NM_007186.3 E1452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JV-01A-11D-A29I-10 chr9:80851433 G>T maps to NM_001098802.1 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr1:111725482 C>A maps to NM_001007794.1 I303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chr16:67006837 G>A maps to NM_024922.5 R534R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr5:89703514 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr1:196659280 C>T maps to NM_000186.3 C416C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JX-01A-11D-A29I-10 chr1:196801041 G>T maps to NM_002113.2 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JX-01A-11D-A29I-10 chr1:196801077 A>T maps to NM_002113.2 R314R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr1:196883673 C>A maps to NM_006684.2 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr2:201994605 C>A maps to NM_001127183.1 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr7:117232326 C>G maps to NM_000492.3 L702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JQ-01A-11D-A29I-10 chr7:117242877 A>T did not map to a codon.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr15:57731628 G>T maps to NM_032866.3 E478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:6196855 G>A maps to NM_015557.2 L836L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr20:40074317 G>A maps to NM_032221.3 G1288G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr14:21859129 T>C maps to NM_001170629.1 T2386T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr22:29130426 G>A maps to NM_001005735.1 R95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr14:93401177 A>G maps to NM_001275.3 E441E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr1:203186949 C>T maps to NM_003465.2 W358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr1:203186949 C>T maps to NM_003465.2 W358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr3:87294943 G>A maps to NM_014043.3 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr7:29407599 G>T maps to NM_004067.2 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr15:41523642 C>A maps to NM_007236.4 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr11:74413871 A>G maps to NM_015424.3 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr15:30659680 C>T maps to NM_139320.1 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JL-01A-11D-A29I-10 chr11:62677219 G>A maps to NM_000738.2 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr4:40339331 A>C maps to NM_017581.2 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr15:78921761 G>A maps to NM_000750.3 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr3:126260994 C>T maps to NM_152889.1 Y200Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr16:75513042 G>T maps to NM_021615.4 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:46433692 C>A did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr19:34263133 C>T maps to NM_022467.3 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr16:840345 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr18:12277151 C>A maps to ENST00000342845 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KW-01A-11D-A29I-10 chr19:19651139 A>G maps to NM_153221.2 E97E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr11:46784696 A>C maps to ENST00000415402 G1240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr14:103988179 G>T maps to NM_001823.3 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JH-01A-11D-A30A-10 chr14:103988179 G>T maps to NM_001823.3 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JL-01A-11D-A29I-10 chr14:103988179 G>T maps to NM_001823.3 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr14:103988179 G>T maps to NM_001823.3 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JW-01A-11D-A29I-10 chr14:103988179 G>T maps to NM_001823.3 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr14:103988179 G>T maps to NM_001823.3 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr14:103988179 G>T maps to NM_001823.3 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr14:103988179 G>T maps to NM_001823.3 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L6-01A-11D-A29I-10 chr5:80550828 C>T maps to NM_001825.2 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr2:122216418 A>G maps to NM_015282.2 I437I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LD-01A-11D-A29I-10 chr1:87033201 T>C maps to ENST00000263723 D350D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:49851056 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chr16:1500500 C>T maps to ENST00000382745 A538A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chr16:1502863 A>G maps to ENST00000382745 I415I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr16:1503878 T>A maps to ENST00000382745 A390A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr3:190039776 C>A maps to NM_021101.4 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:106172102 C>A did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr16:3063791 C>T maps to NM_020982.3 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J2-01A-11D-A29I-10 chr16:11272459 C>T maps to ENST00000409790 P1025P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J3-01A-11D-A29I-10 chr21:36042583 G>A maps to ENST00000360731 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr21:36042583 G>A maps to ENST00000360731 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr21:36042583 G>A maps to ENST00000360731 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr21:36042583 G>A maps to ENST00000360731 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L3-01A-11D-A29I-10 chr21:36042583 G>A maps to ENST00000360731 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr21:36041977 A>G maps to ENST00000360731 Q97Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr21:36042583 G>A maps to ENST00000360731 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr2:29366642 C>T maps to ENST00000379543 D239D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr15:74921336 C>T maps to NM_001130028.1 D568D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OF-01A-11D-A29I-10 chr19:6364520 G>A maps to NM_006012.2 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr5:1339096 C>T maps to NM_030782.3 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr4:17524571 G>T maps to NM_001079827.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr22:19220841 C>A did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr22:19207426 C>T maps to NM_007098.3 E962E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr2:7005368 A>G maps to NM_207315.2 C153C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JR-01A-11D-A29I-10 chr2:7005368 A>G maps to NM_207315.2 C153C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr2:7005368 A>G maps to NM_207315.2 C153C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K8-01A-11D-A29I-10 chr2:7005368 A>G maps to NM_207315.2 C153C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr2:7005368 A>G maps to NM_207315.2 C153C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:7005368 A>G maps to NM_207315.2 C153C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KZ-01A-11D-A29I-10 chr2:7005368 A>G maps to NM_207315.2 C153C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr2:7005368 A>G maps to NM_207315.2 C153C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L4-01A-11D-A29I-10 chr2:7005368 A>G maps to NM_207315.2 C153C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr2:7005368 A>G maps to NM_207315.2 C153C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr2:7005368 A>G maps to NM_207315.2 C153C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KW-01A-11D-A29I-10 chr16:66600430 C>T maps to NM_052999.3 H5H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr18:72234634 C>T maps to NM_032649.5 Y241Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr18:72178160 T>C maps to NM_018235.2 Y190Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr18:72178160 T>C maps to NM_018235.2 Y190Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:150911587 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:150911920 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:150912768 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr23:150912698 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr16:57935279 C>A maps to NM_001297.4 L984L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr16:57993955 G>A maps to NM_001297.4 R199R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr6:154732088 T>A maps to NM_173515.2 R420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr10:101124241 C>T maps to NM_020348.2 G699G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr2:97475184 C>T maps to NM_020184.3 D753D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr16:58575488 G>A maps to NM_016284.3 Y1572Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr16:58577420 C>T maps to NM_206999.1 A1508A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr19:54656062 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr4:78641629 T>C maps to ENST00000512485 P548P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr5:154254926 G>A maps to NM_004779.4 K269K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KT-01A-11D-A29I-10 chr1:24201261 A>G maps to NM_001841.2 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KV-01A-11D-A29I-10 chr1:24201356 A>G maps to NM_001841.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr9:17462994 A>T maps to NM_017738.2 K1130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr3:74548829 G>A maps to NM_020872.1 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr3:3030027 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:147844679 G>T maps to NM_014141.5 R884R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr9:39109178 C>T maps to NM_033655.3 G781G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr16:76486500 G>T maps to NM_033401.3 E389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr2:125660459 G>A maps to NM_130773.2 E1145E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:125284868 C>A maps to NM_130773.2 P494P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:125405387 C>A maps to NM_130773.2 R643R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:51111285 C>A maps to ENST00000395542 S482S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LP-01A-11D-A29I-10 chr7:51111333 C>A maps to ENST00000395542 V466V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr7:51096470 G>A maps to ENST00000395542 N856N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LP-01A-11D-A29I-10 chr17:71197438 C>T maps to NM_018714.2 S491S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr16:23415032 C>T maps to NM_153603.3 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr16:23424845 T>C maps to NM_153603.3 R444R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr16:69373209 C>T maps to NM_032382.4 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:103345393 G>T maps to NM_080629.2 R1719R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:103363704 G>T maps to NM_080629.2 G1438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JD-01A-11D-A29I-10 chr6:33138676 G>A maps to NM_080680.2 P1128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr10:71658493 G>T maps to ENST00000356340 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JX-01A-11D-A29I-10 chr8:121290693 C>T maps to NM_021110.1 R1120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LL-01A-11D-A29I-10 chr8:121344901 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr9:101749610 C>A maps to NM_001855.3 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr10:105803592 G>A maps to NM_000494.3 I808I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr6:70916976 G>T maps to NM_001858.4 *1143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J2-01A-11D-A29I-10 chr6:56044577 T>C maps to NM_030820.3 K146K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr6:56033010 C>A maps to NM_030820.3 E371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr6:56044577 T>C maps to NM_030820.3 K146K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5H8-01A-11D-A29I-10 chr6:55990908 G>T maps to NM_030820.3 G527G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr8:139609189 G>T maps to NM_152888.1 T1463T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr8:139890281 G>A maps to NM_152888.1 Y123Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr8:139793208 C>A maps to NM_152888.1 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr5:177673296 G>T maps to ENST00000390654 G457G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr5:177690259 G>T maps to ENST00000390654 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr9:117053184 C>T maps to NM_032888.2 P1488P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JL-01A-11D-A29I-10 chr9:116967404 G>T maps to NM_032888.2 P716P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr9:117070018 T>C maps to NM_032888.2 H1726H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr12:48383040 A>T maps to NM_001844.4 G364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr13:110850952 A>G maps to NM_001845.4 G382G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr13:110804811 C>T maps to NM_001845.4 A1599A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr13:111111172 G>A maps to NM_001846.2 P496P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr5:74681787 G>T maps to NM_001130105.1 G580G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:107829958 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr23:107811999 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:107911570 A>T did not map to a codon.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr23:107447549 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:107420096 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5LL-01A-11D-A29I-10 chr23:107457357 C>A did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr23:107681216 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr9:137658844 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr9:137623933 C>T maps to NM_000093.3 G450G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr9:137704527 A>T maps to NM_000093.3 G1274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr2:189917494 G>T maps to NM_000393.3 R899R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr19:10077377 G>A maps to NM_015719.3 F1501F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J7-01A-11D-A29I-10 chr21:47532262 C>T maps to NM_001849.3 D162D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr2:238275810 G>A maps to NM_004369.3 G1673G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr2:238249629 C>T maps to NM_004369.3 A2643A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr3:130124437 C>T maps to ENST00000312481 R1430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr3:130098348 G>A maps to ENST00000312481 R252R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr3:48632593 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr6:70981788 G>T maps to NM_001851.4 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J2-01A-11D-A29I-10 chr20:61470084 C>T maps to NM_001853.3 D612D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr18:346781 G>A maps to NM_130386.2 N280N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr1:160265919 T>C maps to NM_001098398.1 T770T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr4:84191030 A>G maps to NM_015697.7 D298D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr4:47746503 G>T maps to NM_006587.2 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr4:47765547 C>G maps to NM_006587.2 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr11:67206162 G>A maps to NM_020441.2 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:42578412 C>A maps to NM_004718.2 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr3:148923983 G>A maps to NM_000096.3 F393F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KV-01A-11D-A29I-10 chr7:130021607 G>A maps to NM_001868.2 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr7:130021520 A>G maps to NM_001868.2 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr3:148575242 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr17:28748839 A>T maps to NM_001304.4 V432V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L6-01A-11D-A29I-10 chr18:56979928 G>T maps to NM_181654.3 Y81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L3-01A-11D-A29I-10 chr3:131268823 T>C maps to ENST00000502818 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr6:36710068 C>A maps to NM_020939.1 A586A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr14:24545619 C>T maps to NM_006032.2 F370F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr16:89661965 G>A maps to NM_014427.4 A573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr2:211456581 C>T maps to NM_001122633.1 I331I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:211457658 C>G maps to NM_001122633.1 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:211527845 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5L4-01A-11D-A29I-10 chr7:29135785 C>T maps to NM_031311.3 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr23:88008935 A>G did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:207753723 C>A maps to NM_000651.4 P1692P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:207649600 G>A maps to NM_001006658.2 P913P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LD-01A-11D-A29I-10 chr1:207643212 A>T maps to NM_001006658.2 K331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr9:126135830 T>C maps to NM_173689.5 A1007A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JI-01A-11D-A29I-10 chr9:126135830 T>C maps to NM_173689.5 A1007A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr9:126135830 T>C maps to NM_173689.5 A1007A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr9:35735311 A>G maps to NM_006368.4 K184K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr19:4168346 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:28610011 G>T maps to NM_182898.2 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr8:67089424 T>G maps to NM_000756.2 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr8:67089424 T>G maps to NM_000756.2 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JV-01A-11D-A29I-10 chr8:67089424 T>G maps to NM_000756.2 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KZ-01A-11D-A29I-10 chr8:67089424 T>G maps to NM_000756.2 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K8-01A-11D-A29I-10 chr17:43907880 G>A maps to NM_001145146.1 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr2:36740804 C>T maps to NM_016441.2 C629C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr4:1388754 C>G maps to NM_175918.3 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr4:1388973 T>C maps to NM_175918.3 D225D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr4:1388754 C>G maps to NM_175918.3 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr4:1389129 G>A maps to NM_175918.3 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr4:1388754 C>G maps to NM_175918.3 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JT-01A-11D-A29I-10 chr4:1388754 C>G maps to NM_175918.3 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JW-01A-11D-A29I-10 chr4:1389069 A>G maps to NM_175918.3 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr4:1388754 C>G maps to NM_175918.3 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr4:1388415 A>G maps to NM_175918.3 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr4:1388847 A>C maps to NM_175918.3 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr4:1388973 T>C maps to NM_175918.3 D225D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KZ-01A-11D-A29I-10 chr4:1388754 C>G maps to NM_175918.3 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L3-01A-11D-A29I-10 chr4:1388754 C>G maps to NM_175918.3 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L3-01A-11D-A29I-10 chr4:1389069 A>G maps to NM_175918.3 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L6-01A-11D-A29I-10 chr4:1388973 T>C maps to NM_175918.3 D225D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LA-01A-11D-A29I-10 chr4:1388973 T>C maps to NM_175918.3 D225D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr4:1388754 C>G maps to NM_175918.3 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LD-01A-11D-A29I-10 chr4:1388754 C>G maps to NM_175918.3 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr4:1388973 T>C maps to NM_175918.3 D225D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr4:1388754 C>G maps to NM_175918.3 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr4:1388973 T>C maps to NM_175918.3 D225D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr6:49806195 G>A maps to NM_001131.2 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr6:49701561 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr17:1359362 T>G maps to NM_016823.2 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JT-01A-11D-A29I-10 chr4:5894585 G>A maps to NM_001014809.1 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KT-01A-11D-A29I-10 chr4:5894585 G>A maps to NM_001014809.1 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr4:5894585 G>A maps to NM_001014809.1 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr1:17266513 C>T maps to NM_014675.3 D578D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr19:18879374 G>A maps to NM_001098482.1 P380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr15:91184390 G>A maps to NM_022769.3 P537P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5H8-01A-11D-A29I-10 chr22:25627603 G>A maps to NM_000496.2 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr2:209028274 C>A maps to NM_014617.3 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr7:151136988 C>T maps to NM_144727.1 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr12:10875524 G>A maps to NM_003651.4 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr1:110467420 G>A maps to NM_000757.4 A531A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr1:110466337 C>A maps to NM_000757.4 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr23:1413335 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chr8:19263440 G>A maps to NM_018371.4 D483D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr8:3047596 G>A maps to NM_033225.5 P1745P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JV-01A-11D-A29I-10 chr8:3889600 C>A maps to NM_033225.5 G146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr8:2857495 T>C maps to NM_033225.5 Q2729Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr8:2800004 G>T maps to NM_033225.5 L3508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr8:2909996 C>T maps to NM_033225.5 P2549P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr1:34291360 C>A maps to ENST00000373381 E310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:34006179 C>G maps to ENST00000373381 A3152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LL-01A-11D-A29I-10 chr1:34276427 G>A maps to ENST00000373381 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr8:113323219 G>T maps to NM_198123.1 V2624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr8:114111073 C>A maps to NM_198123.1 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr8:114326846 G>T maps to NM_198123.1 Y118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr8:114110995 T>A maps to NM_198123.1 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr17:80206822 G>T maps to NM_001893.3 R375R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JD-01A-11D-A29I-10 chr16:58200518 G>A maps to NM_001896.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr15:75969501 A>T maps to NM_001897.4 Y1786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr15:75979766 G>A maps to NM_001897.4 F1213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr20:23805917 G>A maps to NM_001322.2 R91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LP-01A-11D-A29I-10 chr20:23618487 G>A maps to NM_000099.2 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J7-01A-11D-A29I-10 chr11:65779589 C>T maps to NM_001323.2 D25D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JH-01A-11D-A30A-10 chr11:65779589 C>T maps to NM_001323.2 D25D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr11:65779589 C>T maps to NM_001323.2 D25D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KV-01A-11D-A29I-10 chr11:65779589 C>T maps to NM_001323.2 D25D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L4-01A-11D-A29I-10 chr11:65779589 C>T maps to NM_001323.2 D25D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L9-01A-11D-A29I-10 chr11:65779589 C>T maps to NM_001323.2 D25D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LP-01A-11D-A29I-10 chr11:65779589 C>T maps to NM_001323.2 D25D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr20:23472360 G>T maps to NM_005492.2 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr23:100075446 T>G did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:100093268 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KZ-01A-11D-A29I-10 chr23:134948033 A>G did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:120009188 G>C did not map to a codon.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr23:120009055 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr23:153881524 G>C did not map to a codon.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr10:126715074 T>C maps to NM_022802.2 A418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr1:85040023 C>T maps to NM_004388.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JI-01A-11D-A29I-10 chr18:77473085 G>A maps to NM_004715.3 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr6:132271958 T>G maps to NM_001901.2 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr6:132271979 T>G maps to NM_001901.2 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr6:132271979 T>G maps to NM_001901.2 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr6:132271958 T>G maps to NM_001901.2 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr6:132271979 T>G maps to NM_001901.2 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr6:132271958 T>G maps to NM_001901.2 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr6:132271979 T>G maps to NM_001901.2 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:11364814 C>G maps to NM_001332.2 T455T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:11397216 G>A maps to NM_001332.2 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr16:67963837 C>G maps to NM_001907.2 *265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr11:88045698 C>G maps to NM_001814.4 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr10:16994284 C>T maps to NM_001081.3 A1653A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr13:113909352 G>T maps to NM_001008895.1 E649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JH-01A-11D-A30A-10 chr6:43188510 T>C maps to ENST00000354495 Y2150Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr6:33385289 G>A maps to NM_001014433.2 C94C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr6:33385454 A>G maps to NM_001014433.2 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr12:111760253 C>T maps to NM_015267.3 S932S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr10:101995431 C>T maps to NM_018294.4 Q488Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr3:39307472 A>T maps to NM_001171174.1 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr4:74735402 G>T maps to NM_001511.2 E40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:70837422 T>C did not map to a codon.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr23:70836819 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr23:30577887 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr23:30577889 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr23:35993874 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:35971804 T>G did not map to a codon.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr23:45017130 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr23:40496394 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:115593995 C>T did not map to a codon.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr16:88709868 C>T maps to NM_000101.2 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr5:156753260 G>T maps to ENST00000442283 E714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr8:145678756 G>A maps to NM_138496.1 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr23:83124905 C>T did not map to a codon.
Sequencing variant TCGA-PK-A5H8-01A-11D-A29I-10 chr23:83128177 A>G did not map to a codon.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr15:74632007 C>T maps to NM_000781.2 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr8:143960581 G>C maps to ENST00000377675 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr8:143994278 A>G maps to NM_000498.3 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr15:51514615 G>A maps to NM_031226.2 D186D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr6:32007864 T>C maps to NM_000500.5 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr6:32006982 C>T maps to NM_000500.5 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr19:41596012 A>G maps to NM_000766.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr10:96802823 C>T maps to NM_000770.3 Q324Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr7:1027031 C>G maps to NM_017781.2 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J7-01A-11D-A29I-10 chr7:99441807 C>T maps to NM_022820.3 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr19:15789192 C>A maps to NM_023944.2 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr19:15740062 G>A maps to NM_007253.3 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr2:242674749 C>T maps to NM_152783.3 C37C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr6:39867947 C>A maps to ENST00000398904 S925S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J3-01A-11D-A29I-10 chr9:124535155 C>T maps to ENST00000408936 A783A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr9:124519405 C>T maps to ENST00000408936 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr23:85950070 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:85404067 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5KT-01A-11D-A29I-10 chr12:109293173 C>T maps to NM_001917.4 R279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr9:90318056 G>T maps to NM_004938.2 V995V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr9:90321153 G>A maps to NM_004938.2 A1056A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:159175763 C>T maps to NM_001122951.2 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K8-01A-11D-A29I-10 chr6:33288623 G>A maps to NM_001350.4 Q310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr9:121929613 C>T maps to NM_014618.2 Q678Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr9:136501744 C>T maps to NM_000787.3 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr5:176900501 G>A maps to ENST00000393565 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:125686225 C>G did not map to a codon.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr23:125685582 C>T did not map to a codon.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr23:125685621 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:125299534 C>A did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr23:125298568 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr2:172330393 G>T maps to NM_025000.3 E334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr4:41984384 C>G maps to NM_001029955.3 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr8:88885851 C>T maps to NM_152418.3 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:27998832 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr23:27765407 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr23:27765555 C>A did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr23:27765446 A>G did not map to a codon.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr18:50976873 G>A maps to NM_005215.3 P1078P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr18:50278478 C>G maps to NM_005215.3 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr11:31349746 T>C maps to NM_181807.2 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr4:155411952 G>T maps to NM_001142552.1 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L3-01A-11D-A29I-10 chr4:155410821 G>A maps to NM_001142552.1 S562S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr13:36384972 C>A maps to NM_004734.4 G563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LL-01A-11D-A29I-10 chr2:74588718 C>T maps to NM_004082.4 V1248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr3:182681739 C>T maps to NM_020640.2 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:110653543 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chr20:3181068 C>T maps to NM_023935.1 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr12:31254783 C>T maps to NM_030653.3 R690R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr2:118575132 G>T maps to NM_006773.3 E67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr1:112298828 T>C maps to NM_007204.4 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:134679346 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:134707986 G>C did not map to a codon.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr17:61895427 C>T maps to NM_203499.1 S829S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr10:70672927 T>A maps to NM_024045.1 L217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:23019099 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr23:23018849 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr11:118635946 G>A maps to NM_004397.4 R206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr11:686973 G>A maps to NM_021008.2 Q230*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-OR-A5J7-01A-11D-A29I-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr1:40981322 C>G maps to NM_022774.1 V369V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:140246646 C>A maps to NM_015689.3 L710L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr15:65995234 C>T maps to ENST00000443035 L733L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr9:19300260 G>T maps to NM_017925.4 E179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:24789189 C>A maps to NM_001127453.1 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr7:24738663 A>C maps to NM_001127453.1 L491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr9:117166244 C>T maps to NM_015404.3 V783V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr23:69424884 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr22:20080377 G>T maps to NM_022720.6 V551V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:14775768 G>T maps to NM_004080.2 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr3:185985479 G>T maps to NM_001346.2 I401I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr23:50213273 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:50121626 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr12:49483719 G>A maps to NM_021044.2 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J7-01A-11D-A29I-10 chr1:12640649 C>T maps to NM_004753.4 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr14:24424288 T>C maps to NM_021004.2 H58H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr23:2184932 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr10:12148304 G>T maps to NM_018706.5 E653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr10:127555707 C>T maps to NM_018180.2 Q109Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr12:125448958 C>A maps to NM_032656.3 E676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:96724707 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr20:61512593 C>A maps to NM_033081.2 E1572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KW-01A-11D-A29I-10 chr20:61512423 C>T maps to NM_033081.2 G1628G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr14:102028261 C>G maps to NM_001362.3 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr1:223116578 G>A maps to NM_032890.2 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr15:40660191 C>T maps to NM_033510.1 L627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr15:40660191 C>T maps to NM_033510.1 L627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L3-01A-11D-A29I-10 chr15:40660191 C>T maps to NM_033510.1 L627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:154001498 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr23:154004461 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr4:107956685 C>A maps to NM_014421.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JQ-01A-11D-A29I-10 chr10:79566631 G>A maps to NM_004747.3 D1617D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr10:79581400 C>T maps to NM_004747.3 W947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr10:79613276 G>A maps to NM_004747.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J2-01A-11D-A29I-10 chr8:1645389 C>T maps to ENST00000357934 D900D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr1:44685800 G>T maps to NM_019100.4 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:31697545 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:32407760 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5JX-01A-11D-A29I-10 chr23:31792219 A>G did not map to a codon.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr23:31196847 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:31222118 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:31514987 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5L6-01A-11D-A29I-10 chr23:32407769 T>G did not map to a codon.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr19:35991470 C>T maps to NM_033317.4 A417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:50885263 C>T maps to NM_032110.1 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr1:53930344 C>A maps to NM_033067.1 Y262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr3:52402786 G>T maps to ENST00000273600 R1932R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr12:124317839 G>T maps to NM_207437.3 L1457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr12:124399086 G>T maps to NM_207437.3 E3404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr7:21932248 C>T maps to NM_003777.3 L4245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr3:57458293 G>T maps to NM_178504.4 P585P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr17:76424719 G>A maps to ENST00000389840 N4152N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JV-01A-11D-A29I-10 chr16:21042561 G>C maps to NM_017539.1 P1748P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JW-01A-11D-A29I-10 chr16:21061228 A>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:13753343 G>A maps to NM_001369.2 Q3624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:13841986 G>C maps to NM_001369.2 S1766S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr5:13792258 T>C maps to NM_001369.2 T2764T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L6-01A-11D-A29I-10 chr5:13913968 G>A maps to NM_001369.2 F473F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr5:13701413 T>C maps to NM_001369.2 G4490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr5:13809181 G>A maps to NM_001369.2 L2575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr5:13830254 C>T maps to NM_001369.2 S2043S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JW-01A-11D-A29I-10 chr2:84945468 G>A maps to NM_001370.1 L3251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr2:84899457 G>A maps to NM_001370.1 P2154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr2:84771404 C>T maps to NM_001370.1 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr2:196799350 A>T maps to NM_018897.2 V1145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr6:38800208 T>C maps to ENST00000327475 L1422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr6:38840859 G>A maps to ENST00000327475 T2460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr17:11532834 A>G maps to NM_001372.3 E484E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr17:11738037 C>A maps to NM_001372.3 V3110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr17:11607686 G>A maps to NM_001372.3 R1773R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr9:34993361 G>A maps to NM_001135005.1 K116K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J1-01A-11D-A29I-10 chr7:108212352 G>A maps to NM_012328.2 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L1-01A-11D-A30A-10 chr10:69571290 T>G maps to NM_021800.2 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr3:132166265 T>G maps to NM_015268.3 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LL-01A-11D-A29I-10 chr1:65858144 G>A maps to ENST00000371069 E500E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr9:130984507 G>A maps to ENST00000372923 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JW-01A-11D-A29I-10 chr19:10939896 A>C maps to NM_001005361.2 V748V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LD-01A-11D-A29I-10 chr19:10259654 G>A maps to NM_001130823.1 D875D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J1-01A-11D-A29I-10 chr2:25505394 T>A maps to NM_175629.1 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JD-01A-11D-A29I-10 chr2:25469925 G>A maps to NM_175629.1 V372V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr21:45666372 C>T maps to NM_013369.2 A357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J2-01A-11D-A29I-10 chr20:44420681 T>C maps to NM_052951.2 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr20:44420681 T>C maps to NM_052951.2 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr20:44420681 T>C maps to NM_052951.2 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr20:44420681 T>C maps to NM_052951.2 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr20:44420681 T>C maps to NM_052951.2 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr20:44420681 T>C maps to NM_052951.2 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr20:44420681 T>C maps to NM_052951.2 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr20:44420681 T>C maps to NM_052951.2 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr1:94342200 C>T maps to NM_014597.4 A430A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KW-01A-11D-A29I-10 chr2:225702541 C>G maps to NM_014689.2 L929L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:117700597 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr8:25101269 G>T maps to NM_024940.6 E42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr1:62940938 G>A maps to ENST00000371140 P2015P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JD-01A-11D-A29I-10 chr19:3492317 G>C maps to NM_001145165.1 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr19:3492317 G>C maps to NM_001145165.1 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LD-01A-11D-A29I-10 chr5:176936589 T>C maps to NM_024872.2 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr16:57507531 G>A maps to NM_018110.3 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JH-01A-11D-A30A-10 chr4:3494663 A>C maps to ENST00000389653 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr4:3494663 A>C maps to ENST00000389653 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr19:38713188 C>T maps to NM_001135155.1 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr2:116447466 C>T maps to NM_020868.3 Y182Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JL-01A-11D-A29I-10 chr7:153750018 C>T maps to NM_130797.2 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:153584819 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:154561205 C>T maps to NM_130797.2 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr3:109027034 T>A maps to NM_138815.3 R168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr19:54140160 C>G maps to NM_001012728.1 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr2:27121384 C>T maps to NM_020134.3 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr11:113283458 G>A maps to ENST00000355319 P321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr11:637462 G>A maps to NM_000797.3 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:100500029 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:100509495 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr18:28672246 G>T maps to ENST00000438199 C57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr21:38390296 C>T maps to NM_018962.2 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J7-01A-11D-A29I-10 chr18:28918352 A>G maps to NM_001942.2 K447K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KW-01A-11D-A29I-10 chr18:29102112 C>G maps to NM_001943.3 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr6:7579563 C>A maps to NM_004415.2 A1047A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr6:7585738 A>G maps to NM_004415.2 E2748E. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-OR-A5J2-01A-11D-A29I-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-OR-A5J3-01A-11D-A29I-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-OR-A5J4-01A-11D-A29I-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-OR-A5JF-01A-11D-A29I-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-OR-A5JI-01A-11D-A29I-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-OR-A5JQ-01A-11D-A29I-10 chr4:88536519 T>C maps to NM_014208.3 D902D. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-OR-A5JY-01A-31D-A29I-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-OR-A5K2-01A-11D-A29I-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-OR-A5K5-01A-11D-A29I-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-OR-A5K5-01A-11D-A29I-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-OR-A5K5-01A-11D-A29I-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-OR-A5K5-01A-11D-A29I-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-OR-A5K9-01A-11D-A29I-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-OR-A5K9-01A-11D-A29I-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-OR-A5K9-01A-11D-A29I-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-OR-A5K9-01A-11D-A29I-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-OR-A5KS-01A-11D-A30A-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-OR-A5KW-01A-11D-A29I-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-OR-A5L3-01A-11D-A29I-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-OR-A5L3-01A-11D-A29I-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-OR-A5L6-01A-11D-A29I-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-OR-A5L6-01A-11D-A29I-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-OR-A5L9-01A-11D-A29I-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-OR-A5L9-01A-11D-A29I-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-OR-A5LC-01A-11D-A29I-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-OR-A5LD-01A-11D-A29I-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-OR-A5LL-01A-11D-A29I-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-OR-A5LO-01A-11D-A29I-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-OR-A5LO-01A-11D-A29I-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-OR-A5LR-01A-11D-A29I-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-PK-A5HB-01A-11D-A29I-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr6:56480709 G>A maps to ENST00000281662 Q3083*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr6:56495105 C>A maps to ENST00000361203 L1195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr6:56484757 C>T maps to ENST00000281662 K1922K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr6:56391194 C>A maps to ENST00000361203 V5820V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr1:212245551 G>A maps to NM_016448.2 W344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr12:113533149 C>T maps to NM_004416.2 P523P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr12:113496053 G>A maps to NM_004416.2 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:167086596 G>T maps to NM_001080426.1 E80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J3-01A-11D-A29I-10 chr11:1578740 C>T maps to NM_004420.2 E295E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr19:57672058 G>T maps to NM_001012729.1 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J3-01A-11D-A29I-10 chr1:1273447 C>T maps to ENST00000378888 Q541Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LA-01A-11D-A29I-10 chr17:7129839 T>C maps to NM_004422.2 Q554Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr14:102484793 G>A maps to NM_001376.4 L2728L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JT-01A-11D-A29I-10 chr12:68051421 C>T maps to NM_006482.2 H245H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JD-01A-11D-A29I-10 chr2:71780214 T>C maps to NM_001130987.1 D627D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JQ-01A-11D-A29I-10 chr2:71740957 T>C maps to NM_001130987.1 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr20:32266083 G>A maps to NM_005225.2 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr6:20483016 G>T maps to NM_001949.3 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J3-01A-11D-A29I-10 chr8:86089786 C>G maps to ENST00000256117 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr8:86089786 C>G maps to ENST00000256117 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr8:86089786 C>G maps to ENST00000256117 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr14:35005308 G>A maps to NM_018453.3 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr16:23555851 C>T maps to NM_001083614.1 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:158139313 G>T maps to NM_024007.3 S466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr5:158140041 G>A maps to NM_024007.3 G435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr8:25708131 G>A maps to NM_022659.2 S558S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr10:131639126 G>A maps to ENST00000355311 S514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr10:11805248 T>C maps to NM_024693.4 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LL-01A-11D-A29I-10 chr10:11805374 G>A maps to NM_024693.4 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr10:135179539 C>A maps to NM_004092.3 E227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LP-01A-11D-A29I-10 chr5:83259161 T>C maps to NM_005711.3 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LR-01A-11D-A29I-10 chr4:148461036 T>C maps to NM_001957.3 H323H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LR-01A-11D-A29I-10 chr4:148461072 G>A maps to NM_001957.3 E335E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JW-01A-11D-A29I-10 chr12:93226500 T>C maps to NM_003566.3 Q347Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KT-01A-11D-A29I-10 chr6:74228256 G>A maps to NM_001402.5 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JD-01A-11D-A29I-10 chr3:127872601 A>G maps to NM_021937.3 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr3:127872493 G>T maps to NM_021937.3 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr17:28407845 C>T maps to NM_198529.3 N1091N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr22:44161246 T>A maps to NM_022785.3 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:63999138 T>C maps to NM_032437.2 Y167Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JD-01A-11D-A29I-10 chr13:22178257 C>T maps to NM_152726.2 R10R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr13:22178257 C>T maps to NM_152726.2 R10R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K8-01A-11D-A29I-10 chr13:22178257 C>T maps to NM_152726.2 R10R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KV-01A-11D-A29I-10 chr13:22178257 C>T maps to NM_152726.2 R10R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr8:16944543 G>T maps to NM_181723.2 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr3:19961330 T>C maps to NM_144715.3 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr2:233527634 C>T maps to NM_025202.3 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr14:23828978 G>A maps to NM_005864.2 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr14:23834216 C>T maps to NM_005864.2 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr15:82512115 G>T maps to NM_024580.5 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr5:38435282 C>T maps to ENST00000354891 G737G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L9-01A-11D-A29I-10 chr7:55249062 G>A maps to NM_005228.3 Q787Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr11:65351073 G>A maps to NM_001099409.1 A977A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr9:140676777 C>T maps to NM_024757.4 Q771*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr6:31856280 C>A maps to ENST00000395728 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr6:31854776 G>A maps to ENST00000395728 L762L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr6:31860336 T>C maps to ENST00000395728 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:36437740 G>A maps to NM_024852.2 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr7:2394990 C>T maps to ENST00000314800 N145N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LR-01A-11D-A29I-10 chr7:2394990 C>T maps to ENST00000314800 N145N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KZ-01A-11D-A29I-10 chr22:31838084 G>A maps to NM_019843.3 S742S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr3:184049833 C>T maps to NM_001194947.1 Y1533Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr1:21276547 G>A maps to NM_001198801.1 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chr17:12905889 C>G maps to NM_018127.6 G362G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr9:23701603 T>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:50610816 C>T maps to NM_021952.3 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:129205091 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr7:37272768 C>T maps to NM_014800.9 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr20:45023109 C>T maps to ENST00000439931 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr5:60067795 T>C maps to NM_024930.2 E63E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KW-01A-11D-A29I-10 chr19:48525475 T>C maps to NM_022142.4 Y188Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:79403805 G>T maps to NM_022159.3 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J3-01A-11D-A29I-10 chr16:1823443 C>G maps to NM_001010865.1 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr16:1823443 C>G maps to NM_001010865.1 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JR-01A-11D-A29I-10 chr16:1823443 C>G maps to NM_001010865.1 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JT-01A-11D-A29I-10 chr16:1823443 C>G maps to NM_001010865.1 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr16:1823443 C>G maps to NM_001010865.1 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr16:1823443 C>G maps to NM_001010865.1 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KV-01A-11D-A29I-10 chr16:1823443 C>G maps to NM_001010865.1 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L1-01A-11D-A30A-10 chr16:1823443 C>G maps to NM_001010865.1 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L4-01A-11D-A29I-10 chr16:1823443 C>G maps to NM_001010865.1 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr16:1823443 C>G maps to NM_001010865.1 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr16:1823443 C>G maps to NM_001010865.1 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr16:1823443 C>G maps to NM_001010865.1 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JT-01A-11D-A29I-10 chr18:2892374 G>A maps to NM_032048.2 S750S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr18:2885117 C>T maps to NM_032048.2 N138N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr14:100404173 C>T maps to NM_001008707.1 Q725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr12:13367529 C>T maps to NM_001423.2 Q127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:73151564 C>T maps to NM_004097.2 Y216Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr10:119305182 G>T maps to NM_004098.3 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JV-01A-11D-A29I-10 chr7:155251182 G>A maps to NM_001427.3 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr13:43896518 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:129843244 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KV-01A-11D-A29I-10 chr6:132014710 C>T maps to NM_005021.3 N453N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr17:77709338 C>G maps to NM_178543.3 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr22:40140105 G>A maps to NM_152512.3 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JW-01A-11D-A29I-10 chr22:41551038 T>A maps to NM_001429.3 T1061T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr12:132504662 G>A maps to ENST00000333577 P1485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr20:34776285 C>T maps to NM_012156.2 D297D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr18:5410573 A>G maps to NM_012307.2 T704T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr9:111956667 G>A maps to NM_019114.3 D685D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J7-01A-11D-A29I-10 chr7:37960576 C>A maps to NM_017549.3 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr7:37960576 C>A maps to NM_017549.3 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr7:143098539 C>A maps to NM_005232.4 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr4:66197803 C>T maps to NM_004439.5 G965G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr3:96706664 C>A maps to NM_001080448.2 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr3:97466265 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr3:134911553 C>T maps to NM_004441.4 G673G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr1:23222939 G>A maps to ENST00000400191 T578T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr3:184297349 C>T maps to NM_004443.3 D629D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr7:100417181 C>A maps to NM_004444.4 E432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr7:142567580 T>C maps to NM_004445.3 C823C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr17:48619271 G>A maps to NM_017957.2 Q551Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr17:48619289 G>A maps to NM_017957.2 P557P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr19:11492755 G>A maps to NM_000121.3 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JR-01A-11D-A29I-10 chr8:144940266 G>A maps to NM_031308.1 G2385G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JT-01A-11D-A29I-10 chr8:144940731 C>T maps to NM_031308.1 L2230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr8:144940620 C>T maps to NM_031308.1 A2267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr8:144940542 G>A maps to NM_031308.1 G2293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr8:144940614 G>A maps to NM_031308.1 T2269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KW-01A-11D-A29I-10 chr8:144940449 G>C maps to NM_031308.1 A2324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KZ-01A-11D-A29I-10 chr8:144940434 G>A maps to NM_031308.1 L2329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr8:144940542 G>A maps to NM_031308.1 G2293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr1:220219730 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:220178698 C>A maps to NM_004446.2 E652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr12:15814974 G>A maps to NM_004447.5 R265R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr19:55598757 G>T maps to NM_133180.2 G680G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr11:721569 C>T maps to NM_022772.3 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:212578299 C>A maps to NM_005235.2 G319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr16:14041726 G>A maps to NM_005236.2 L758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr5:172315746 G>A maps to NM_001031711.2 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chr16:20810278 C>T maps to NM_001142725.1 K281K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:43308842 C>T maps to NM_018538.3 I456I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr9:5832727 G>C maps to NM_024896.2 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JW-01A-11D-A29I-10 chr9:5832727 G>C maps to NM_024896.2 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JX-01A-11D-A29I-10 chr9:5832727 G>C maps to NM_024896.2 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr9:5832727 G>C maps to NM_024896.2 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K8-01A-11D-A29I-10 chr9:5832727 G>C maps to NM_024896.2 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr9:5832727 G>C maps to NM_024896.2 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr9:5832727 G>C maps to NM_024896.2 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr9:5832727 G>C maps to NM_024896.2 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr9:5832727 G>C maps to NM_024896.2 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L9-01A-11D-A29I-10 chr9:5832727 G>C maps to NM_024896.2 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr16:23716289 G>C maps to NM_033266.3 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr14:53110332 C>A maps to NM_014584.1 V454V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JQ-01A-11D-A29I-10 chr2:239009335 G>A maps to NM_194312.2 E92E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L6-01A-11D-A29I-10 chr2:239009335 G>A maps to NM_194312.2 E92E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr6:152201871 C>G maps to NM_001122741.1 L242L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-OR-A5L1-01A-11D-A30A-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr8:95655595 T>C maps to NM_017697.3 D109D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr12:56536718 T>C did not map to a codon.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr21:40188948 G>T maps to NM_005239.4 E175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KV-01A-11D-A29I-10 chr12:11992167 G>A maps to NM_001987.4 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr4:5795411 C>T maps to NM_153717.2 G618G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr17:18286643 C>T maps to NM_001145127.1 D244D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr9:140243588 T>C maps to NM_017820.3 K601K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JD-01A-11D-A29I-10 chr4:56737028 C>T maps to NM_018261.3 N263N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr5:466880 C>T maps to ENST00000315013 D712D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr7:133692486 C>A maps to NM_021807.3 I862I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr7:132959895 C>T maps to NM_021807.3 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr11:108380725 C>A maps to NM_015065.2 G1836G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5H8-01A-11D-A29I-10 chr8:118817056 C>T maps to NM_000127.2 E653E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr6:66005969 G>A maps to ENST00000370616 V603V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr6:65301108 C>A maps to ENST00000370616 E1551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr6:65300986 C>A maps to ENST00000370616 A1591A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LD-01A-11D-A29I-10 chr6:65655686 G>A maps to ENST00000370616 R794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L6-01A-11D-A29I-10 chr6:159188466 T>G maps to NM_001111077.1 P474P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:160969184 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr1:197031010 G>A maps to NM_001994.2 C118C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JI-01A-11D-A29I-10 chr1:169510379 G>A maps to ENST00000367796 L1321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L1-01A-11D-A30A-10 chr13:113770067 C>T maps to NM_000131.3 H175H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J1-01A-11D-A29I-10 chr23:154157134 T>C did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:154157537 G>C did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:154158315 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:154176150 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr23:138633279 A>G did not map to a codon.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr17:72889675 G>C maps to ENST00000310226 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LR-01A-11D-A29I-10 chr17:72889684 G>A maps to ENST00000310226 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:109170820 G>T maps to NM_001010883.2 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr19:1881328 G>A maps to NM_031213.3 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr19:1881487 G>A maps to NM_031213.3 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LA-01A-11D-A29I-10 chr12:111800835 G>A maps to NM_001177996.1 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr7:143556211 G>T maps to NM_014719.1 S737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:143421821 G>T maps to NM_001130025.1 *846L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KZ-01A-11D-A29I-10 chr3:57616476 G>C maps to NM_152678.2 T494T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr13:25744554 G>A maps to NM_152704.2 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:63409905 C>A did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr2:131521961 C>T maps to NM_001105195.1 Q773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JQ-01A-11D-A29I-10 chr9:129102839 G>A maps to NM_033446.1 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr2:132241687 G>A maps to NM_001085365.1 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr19:17648323 G>T maps to ENST00000335393 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr1:16385006 C>T maps to NM_182623.2 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr2:220043232 C>T maps to NM_024293.4 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JL-01A-11D-A29I-10 chr8:139165271 T>C maps to NM_015912.3 P482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr8:139158276 G>T maps to NM_015912.3 L1155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr4:89679991 G>A maps to NM_014883.2 Q547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr10:61112191 C>A maps to ENST00000442566 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr23:68725225 G>C did not map to a codon.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr23:68749608 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:68748873 C>G did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr11:6245246 C>A maps to NM_032127.3 E124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JR-01A-11D-A29I-10 chr14:74413128 C>G maps to NM_152445.1 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr14:74402692 C>T maps to NM_152445.1 R588R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr5:118970153 C>T maps to ENST00000420106 F237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PA-A5YG-01A-11D-A29I-10 chr2:187559046 G>A maps to NM_177454.3 Q49Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JX-01A-11D-A29I-10 chr5:93111871 G>A maps to NM_032042.5 V367V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J2-01A-11D-A29I-10 chr16:771611 C>A maps to NM_023933.1 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JR-01A-11D-A29I-10 chr16:771285 C>T maps to NM_023933.1 D4D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KZ-01A-11D-A29I-10 chr2:29226497 G>A maps to NM_199280.2 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JR-01A-11D-A29I-10 chr14:45542715 A>G maps to ENST00000361462 K1758K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr6:119285912 C>A maps to NM_024581.4 L1019L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JQ-01A-11D-A29I-10 chr19:35719256 G>A maps to NM_152481.1 D109D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:155217918 C>A maps to ENST00000368370 R586R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr1:155220207 G>A maps to ENST00000368370 R458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr17:18702219 T>C maps to NM_016078.4 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr4:2641521 G>T maps to ENST00000324666 E76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr5:176951843 C>T maps to ENST00000442143 T626T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr4:159092011 C>G maps to NM_001128424.1 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:113266682 C>A maps to NM_001004440.1 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr10:47915897 A>G maps to NM_018232.1 K435K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J3-01A-11D-A29I-10 chr10:46224380 C>T maps to ENST00000399588 D66D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LA-01A-11D-A29I-10 chr6:116783562 G>A maps to NM_001010919.1 Q157Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr18:10672691 G>A maps to NM_022068.2 G2667G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr23:153740191 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5JL-01A-11D-A29I-10 chr6:82461741 G>A maps to ENST00000369756 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr23:34148841 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr23:34148843 G>C did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:34960968 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:34961914 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr23:37026573 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr23:37028028 G>C did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:37027034 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:37028108 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr23:24382524 G>C did not map to a codon.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:24382643 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr23:24382452 G>C did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:24383062 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:24383064 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr11:114453401 C>T maps to NM_001077639.1 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr1:177245454 C>T maps to NM_021165.2 C299C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:190067549 G>A maps to NM_199051.1 I633I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr9:40702724 G>T maps to NM_001083124.1 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr9:40705690 C>A maps to NM_001083124.1 P1116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:166135377 C>T maps to NM_001017961.3 E36E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr5:94764305 G>C did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:94772569 C>T maps to NM_152548.2 Q285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr8:87519274 C>A maps to NM_016033.2 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr6:54805221 G>T maps to NM_001010872.1 E485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr19:49104470 T>C maps to NM_017708.3 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr2:33811715 T>A maps to ENST00000395190 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JW-01A-11D-A29I-10 chr19:38894293 G>T maps to NM_174905.3 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J2-01A-11D-A29I-10 chr23:8763158 T>A did not map to a codon.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr23:8763191 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:8763195 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:13056582 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5KW-01A-11D-A29I-10 chr3:10091152 C>T maps to NM_033084.3 N503N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr14:45644599 C>T maps to NM_020937.2 D881D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr14:45654430 G>A maps to NM_020937.2 R1509R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr10:127693587 G>A maps to ENST00000368692 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KT-01A-11D-A29I-10 chr10:127585220 C>T maps to NM_145235.3 Q4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr10:127585220 C>T maps to NM_145235.3 Q4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr10:127585220 C>T maps to NM_145235.3 Q4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr13:99083454 G>A maps to NM_005766.2 R688R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr13:99100569 G>C maps to NM_005766.2 *1046S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5H8-01A-11D-A29I-10 chr2:242396171 G>C maps to NM_014808.2 T474T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr19:13035056 G>A maps to NM_004461.2 V432V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr17:80039480 G>A maps to NM_004104.4 I2134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr17:80043738 A>G maps to NM_004104.4 A1247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:207655352 A>G maps to NM_014929.3 R652R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr20:3127457 C>T maps to NM_021826.4 A753A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr5:150946779 C>A maps to NM_001447.2 G571G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr11:92616518 C>T maps to ENST00000298047 C4299C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr4:126329906 G>T maps to NM_024582.4 G1960*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr4:126241102 C>T maps to NM_024582.4 V1179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr4:126370694 A>T maps to NM_024582.4 R2842*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:150891193 C>G did not map to a codon.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr22:45959040 C>T maps to ENST00000402984 P687P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr15:48714178 C>A maps to NM_000138.4 G2514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:127800432 G>T maps to NM_001999.3 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J7-01A-11D-A29I-10 chr19:8156469 G>A maps to NM_032447.3 I1970I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JQ-01A-11D-A29I-10 chr19:8176918 C>T maps to NM_032447.3 P1301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr9:97355867 C>T maps to NM_003837.2 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr16:30958249 G>T maps to NM_001099784.2 L629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr3:33419632 C>T maps to NM_012157.3 C296C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:15928110 C>A maps to NM_012304.3 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LL-01A-11D-A29I-10 chr5:15937009 C>T maps to NM_012304.3 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr19:39440917 T>C maps to NM_148169.1 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JD-01A-11D-A29I-10 chr19:39440917 T>C maps to NM_148169.1 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JI-01A-11D-A29I-10 chr19:39440917 T>C maps to NM_148169.1 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr19:39440917 T>C maps to NM_148169.1 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr19:39440917 T>C maps to NM_148169.1 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JX-01A-11D-A29I-10 chr19:39440917 T>C maps to NM_148169.1 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K8-01A-11D-A29I-10 chr19:39440917 T>C maps to NM_148169.1 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr19:39440917 T>C maps to NM_148169.1 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr19:39440917 T>C maps to NM_148169.1 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KZ-01A-11D-A29I-10 chr19:39440917 T>C maps to NM_148169.1 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LP-01A-11D-A29I-10 chr19:39440917 T>C maps to NM_148169.1 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr19:39440917 T>C maps to NM_148169.1 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr19:39521936 G>A maps to NM_178820.3 Q130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JW-01A-11D-A29I-10 chr14:39901156 C>A maps to NM_203301.3 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr3:121340602 C>T maps to NM_016298.3 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chr22:32881101 C>T maps to NM_012179.3 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L1-01A-11D-A30A-10 chr3:48420010 C>T maps to NM_207102.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr4:153249472 A>G maps to NM_033632.2 I435I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr19:12805413 G>A maps to ENST00000380339 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:207139093 C>A maps to NM_001170631.1 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr19:40430565 G>A maps to NM_003890.2 G459G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KT-01A-11D-A29I-10 chr19:40406018 G>A maps to NM_003890.2 C1609C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr19:40368453 C>T maps to NM_003890.2 V4298V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr19:17885269 A>G maps to NM_015122.2 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr9:137777088 G>A maps to NM_004108.2 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:157559042 C>T maps to NM_031282.2 Q86Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr1:159778892 C>T maps to NM_001004310.2 H154H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr8:125109588 G>A maps to NM_001039112.2 R1591R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr7:19184759 C>A maps to NM_152898.2 E76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr14:53386012 C>A maps to NM_001134999.1 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JR-01A-11D-A29I-10 chr14:53341961 C>G maps to NM_001134999.1 G359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr15:91436335 G>A maps to NM_002005.3 L611L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr3:62355880 G>A maps to NM_018008.3 C419C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr19:35843173 C>A maps to NM_005303.2 Y240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr19:35941566 T>C maps to NM_005306.2 G317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr9:95738780 C>A maps to NM_033086.2 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr3:192053208 G>A maps to NM_021032.4 Q119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:137790992 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr4:123748085 C>T maps to NM_002006.4 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr11:69589555 G>A maps to NM_002007.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr12:4554550 G>C maps to NM_020996.1 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr6:167417211 T>C maps to NM_007045.2 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr10:123239111 G>A maps to NM_001144915.1 L703L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr1:59844419 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5JV-01A-11D-A29I-10 chr4:153889149 G>A maps to NM_033393.2 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:135288628 C>G did not map to a codon.
Sequencing variant TCGA-OR-A5JV-01A-11D-A29I-10 chr16:67268117 G>C maps to NM_013241.2 P496P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr18:34289244 C>T maps to NM_025135.2 N633N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr9:133799256 G>A maps to NM_001145106.1 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr6:110112597 G>T maps to NM_014845.5 E734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr2:164466943 C>T maps to NM_018086.2 T466T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr3:99643212 G>A maps to NM_001042459.1 R156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:152280068 G>T maps to NM_002016.1 T2431T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr1:152280080 G>T maps to NM_002016.1 A2427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:152323874 G>T maps to NM_001014342.2 A2129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:152326655 G>T maps to NM_001014342.2 S1202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr17:18148679 C>G maps to NM_002018.2 L1221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr8:142477497 C>T did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr8:142517207 C>T maps to NM_207414.2 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr9:84607382 C>A maps to NM_001001670.2 V666V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J2-01A-11D-A29I-10 chr23:153577796 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr23:153595113 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr23:153588003 G>A did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr23:153577326 G>A did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr23:153599553 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr3:58128390 C>G maps to NM_001164317.1 A1763A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr11:63885550 G>A maps to NM_013280.4 G604G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr13:28883024 G>A maps to NM_002019.4 I1225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr15:33192239 C>A maps to NM_001103184.2 R975R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr15:33358990 C>T maps to NM_001103184.2 S365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr1:240371150 T>A maps to ENST00000406993 P1156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr1:171227312 C>A maps to NM_002021.1 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:203317353 G>C maps to NM_002023.3 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:147030345 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr23:147090159 G>T did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr2:216244002 G>A maps to NM_212482.1 V1824V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L4-01A-11D-A29I-10 chr11:47772524 C>A maps to NM_015308.2 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr3:172070714 T>C maps to NM_022763.3 P879P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr1:109273458 C>T maps to NM_001144937.1 C596C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr5:131014836 G>A maps to NM_133372.2 R412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr11:49197415 A>G maps to NM_004476.1 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr11:49195013 G>A maps to NM_004476.1 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr11:94039683 C>T maps to NM_001080486.1 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr20:22563159 G>A maps to NM_021784.4 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr16:86601195 C>A maps to NM_005251.2 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:47904232 G>A maps to NM_004474.3 Q142Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr1:63788950 C>A maps to NM_012183.2 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr14:29237444 C>T maps to NM_005249.3 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KW-01A-11D-A29I-10 chr14:29237768 G>A maps to NM_005249.3 S428S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr17:74133973 C>T maps to NM_001454.3 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr17:74133973 C>T maps to NM_001454.3 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr17:74133973 C>T maps to NM_001454.3 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr17:74133973 C>T maps to NM_001454.3 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr1:42657322 G>T maps to NM_001198850.1 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr14:89817134 C>G maps to NM_001085471.1 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr22:36900581 G>T maps to NM_001102371.1 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr19:52249449 G>C maps to NM_002029.3 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr19:52327405 C>T maps to NM_002030.3 N135N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr9:14776239 T>C maps to NM_001177704.1 Q4Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr13:39452352 T>C maps to NM_207361.4 F2918F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr13:39264774 G>T maps to NM_207361.4 L1098L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr13:39262893 C>T maps to NM_207361.4 S471S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PA-A5YG-01A-11D-A29I-10 chr10:13699099 G>T maps to NM_018027.3 S830*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr14:52187024 C>G maps to ENST00000344768 S426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:131214282 T>C did not map to a codon.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chr23:131216402 C>G did not map to a codon.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr9:37745412 G>A maps to NM_014907.2 E1128E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LL-01A-11D-A29I-10 chr9:37731006 C>T maps to NM_014907.2 D255D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr9:37744758 G>A maps to NM_014907.2 E910E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr10:49440200 G>A maps to NM_001018071.3 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:12736869 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr23:12734327 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr23:12734820 C>T did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr23:12728520 A>G did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr12:69968572 G>A maps to NM_006654.3 T455T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JD-01A-11D-A29I-10 chr13:32810274 T>C maps to NM_023037.2 L1926L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr17:79504072 C>T maps to NM_001077182.2 D506D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JQ-01A-11D-A29I-10 chr17:79504072 C>T maps to NM_001077182.2 D506D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr5:132569151 G>A maps to NM_015082.1 S324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:31090007 G>C did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr17:61903964 G>T maps to NM_017647.3 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr16:70503128 C>T maps to NM_145059.2 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr16:70508768 C>A maps to NM_145059.2 G744G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr19:5831870 C>T maps to NM_001040701.1 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr19:50311888 C>G maps to NM_025129.4 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr3:180687982 T>A maps to NM_005087.3 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KW-01A-11D-A29I-10 chr3:180685936 C>T maps to NM_005087.3 R433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr5:39135107 G>T maps to ENST00000263405 G517G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JX-01A-11D-A29I-10 chr3:46008086 G>A maps to NM_024513.2 C913C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr8:104343685 G>A maps to NM_003506.3 P690P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr7:72848663 C>T maps to NM_003508.2 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr7:72850022 A>G maps to NM_003508.2 G562G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5H8-01A-11D-A29I-10 chr19:3527018 C>T maps to NM_001136198.1 N143N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KW-01A-11D-A29I-10 chr17:41063166 C>T maps to NM_000151.2 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:153762676 C>G did not map to a codon.
Sequencing variant TCGA-OR-A5L9-01A-11D-A29I-10 chr23:153761189 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr17:78091490 G>T maps to NM_001079804.1 P808P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KZ-01A-11D-A29I-10 chr17:78083790 C>T maps to NM_001079804.1 Y458Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:153927601 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr9:101258724 G>A maps to NM_005458.7 N234N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J1-01A-11D-A29I-10 chr5:161300196 C>T maps to NM_001127648.1 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr15:27182467 C>A maps to NM_000810.3 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr4:47322218 C>A maps to NM_000812.3 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr1:1957036 T>C maps to NM_000815.4 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr4:46060306 G>T maps to NM_173536.3 C281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr15:27216690 G>A maps to NM_033223.4 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:151821116 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr3:97744480 C>T maps to NM_001105580.1 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr9:92220392 C>T maps to NM_006705.3 Q34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J2-01A-11D-A29I-10 chr11:65810208 C>T maps to NM_033036.2 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J7-01A-11D-A29I-10 chr11:65810208 C>T maps to NM_033036.2 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JI-01A-11D-A29I-10 chr11:65810208 C>T maps to NM_033036.2 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr11:65810208 C>T maps to NM_033036.2 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr11:65810718 G>A maps to NM_033036.2 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr11:65810208 C>T maps to NM_033036.2 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr11:65810208 C>T maps to NM_033036.2 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr11:65810208 C>T maps to NM_033036.2 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KW-01A-11D-A29I-10 chr11:65810208 C>T maps to NM_033036.2 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr11:65810208 C>T maps to NM_033036.2 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L4-01A-11D-A29I-10 chr11:65810208 C>T maps to NM_033036.2 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L9-01A-11D-A29I-10 chr7:99758135 T>G maps to NM_024637.4 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:154996919 G>A maps to NM_052917.2 Q71Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr2:166611441 G>C maps to NM_004482.3 Y508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr2:166621433 C>T maps to NM_004482.3 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr2:158115853 G>A maps to NM_014568.1 T420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr4:173734868 T>C maps to NM_001034845.2 P306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr7:30634629 G>C maps to NM_002047.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JH-01A-11D-A30A-10 chr7:30634629 G>C maps to NM_002047.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr7:30634629 G>C maps to NM_002047.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr7:30634629 G>C maps to NM_002047.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr17:34072811 G>T maps to NM_139285.2 V568V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J7-01A-11D-A29I-10 chr13:114525078 G>A maps to ENST00000357389 T621T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr16:90099239 G>T maps to NM_001481.2 E135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JQ-01A-11D-A29I-10 chr16:90102834 A>G maps to NM_001481.2 E199E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr23:48652249 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr23:48649678 G>A did not map to a codon.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr1:153800735 T>A maps to NM_020699.2 K30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr3:81627175 C>A maps to ENST00000264326 L506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr3:81635290 A>G maps to ENST00000264326 G429G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr10:104136513 C>T maps to NM_004193.2 C1414C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J3-01A-11D-A29I-10 chr7:150864239 G>C maps to NM_001098834.1 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr7:150864239 G>C maps to NM_001098834.1 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr2:109087645 G>T maps to NM_181453.3 E621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr6:53409374 C>A maps to NM_001498.3 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr6:10556943 A>G maps to NM_001491.2 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr5:74325229 C>T maps to NM_016591.2 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr10:48428895 C>T maps to NM_004962.2 A330A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-PK-A5HB-01A-11D-A29I-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr5:132197394 C>T maps to NM_005260.3 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr23:153669454 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:69646559 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr16:30123476 C>A maps to NM_024307.2 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr5:154299580 A>G maps to NM_015465.3 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr17:42989104 C>A maps to NM_002055.3 E281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr16:23481454 C>T maps to NM_015044.4 R494R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr19:38875167 G>A maps to NM_152657.3 L615L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr10:85909925 G>A maps to ENST00000436406 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JD-01A-11D-A29I-10 chr7:31016897 C>A maps to NM_000823.3 G369G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr3:172166143 G>A maps to NM_198407.2 D20D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr3:172165570 C>A maps to NM_198407.2 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:147380253 C>T maps to NM_005267.4 Q58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L3-01A-11D-A29I-10 chr1:228346052 C>T maps to NM_020435.2 H198H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr1:228346052 C>T maps to NM_020435.2 H198H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr4:80327935 G>A maps to NM_033214.2 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr7:8124629 G>A maps to NM_138426.2 K427K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr16:74491778 G>A maps to NM_012201.5 R1086R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr7:42079764 G>C maps to NM_000168.5 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr8:144358301 C>T maps to NM_138465.3 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr9:36147781 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr17:9792934 C>A maps to NM_004246.1 P525P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr23:14627143 T>C did not map to a codon.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr17:4693383 T>C maps to NM_001014985.2 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr19:48204609 G>A maps to NM_015711.3 S1207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr19:48183684 C>T maps to NM_015711.3 Q420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L4-01A-11D-A29I-10 chr19:48205287 G>A maps to NM_015711.3 A1433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OF-01A-11D-A29I-10 chr19:48205287 G>A maps to NM_015711.3 A1433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr19:48258036 C>T maps to NM_015710.4 G314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr19:48258618 C>T maps to NM_015710.4 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr2:70096885 C>T maps to NM_178439.3 F418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PA-A5YG-01A-11D-A29I-10 chr9:80646046 G>A maps to NM_002072.3 D35D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr20:57430198 C>T maps to NM_080425.2 Q627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:1747195 T>G maps to NM_002074.2 R68R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr22:19808791 G>A maps to NM_053004.2 C29C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr12:6954904 A>T maps to NM_002075.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr3:52727735 A>G maps to NM_014366.4 E471E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:54586951 G>C did not map to a codon.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr2:85922476 C>T maps to NM_006433.3 Y29Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr2:85924744 C>T maps to NM_006433.3 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr3:37388681 A>T did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr14:93277939 G>A maps to NM_005113.2 Q387Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr6:117923265 G>T maps to NM_020399.3 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr8:37792695 G>A maps to NM_152413.2 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr16:20331585 C>A maps to NM_001007240.1 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr16:20335324 G>A maps to NM_001007240.1 D116D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JX-01A-11D-A29I-10 chr10:113920464 G>A maps to NM_020918.4 N552N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KT-01A-11D-A29I-10 chr10:113924346 G>A maps to NM_020918.4 Q415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LP-01A-11D-A29I-10 chr19:33579127 T>C maps to NM_018025.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr19:33579079 T>A maps to NM_018025.2 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J7-01A-11D-A29I-10 chr17:42475982 G>C maps to NM_001002909.2 T1154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr2:241401647 G>A maps to NM_002081.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr23:132437296 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5J1-01A-11D-A29I-10 chr20:5556162 T>A maps to NM_019593.3 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JD-01A-11D-A29I-10 chr6:24437407 G>A maps to NM_001503.2 S710S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr7:23296586 C>T maps to ENST00000435486 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:135427144 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr23:135431106 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:135428211 G>C did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:135430561 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:135474474 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KV-01A-11D-A29I-10 chr23:135427635 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5J3-01A-11D-A29I-10 chr2:26537396 A>G maps to NM_001145168.1 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr10:134942687 C>T maps to ENST00000368577 R992R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr8:37699515 C>T maps to NM_032777.9 G1220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr8:37698804 C>A maps to NM_032777.9 G983G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr8:37699515 C>T maps to NM_032777.9 G1220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr8:37699515 C>T maps to NM_032777.9 G1220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr8:37686784 C>T maps to NM_032777.9 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr7:1097615 G>A maps to NM_138445.2 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JT-01A-11D-A29I-10 chr2:175300996 G>A maps to NM_152529.5 N820N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr10:25839903 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr1:168059901 C>G maps to NM_153832.1 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr12:6933231 G>A maps to NM_019858.1 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr23:53106283 G>C did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:53105989 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5J3-01A-11D-A29I-10 chr23:78426660 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr15:40094025 C>A maps to NM_007223.1 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J7-01A-11D-A29I-10 chr13:99948177 C>A maps to NM_004951.4 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JL-01A-11D-A29I-10 chr8:142367098 G>A maps to NM_005293.2 R309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:41554929 G>T did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr2:241569557 G>A maps to NM_001195381.1 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr7:124404169 G>A maps to NM_005302.2 C287C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr19:46094389 C>T maps to NM_005282.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:150348567 C>G did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:150349374 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5LL-01A-11D-A29I-10 chr23:150349286 C>G did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:19046317 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr4:8583230 C>A maps to NM_080819.2 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JV-01A-11D-A29I-10 chr4:8583230 C>A maps to NM_080819.2 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KW-01A-11D-A29I-10 chr4:8583230 C>A maps to NM_080819.2 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr4:8583356 G>A maps to NM_080819.2 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr23:41586497 C>G did not map to a codon.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr23:41587120 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr3:151011992 C>T maps to NM_023915.3 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LP-01A-11D-A29I-10 chr1:101005424 G>A maps to NM_022049.2 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JQ-01A-11D-A29I-10 chr16:57722327 C>T maps to NM_170776.4 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr5:89986639 G>T maps to NM_032119.3 E2245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:101909809 T>A did not map to a codon.
Sequencing variant TCGA-OR-A5JH-01A-11D-A30A-10 chr23:101971093 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:101970727 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5L9-01A-11D-A29I-10 chr23:101971017 T>C did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr10:47000007 G>A maps to NM_014696.3 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chr17:80012448 G>A maps to NM_212492.1 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KZ-01A-11D-A29I-10 chr17:7217462 T>C maps to NM_004489.4 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr9:139252665 G>A maps to NM_001145638.1 A674A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr2:10105470 C>T maps to NM_198182.2 N357N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr23:122537276 T>C did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:122532570 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr10:87379739 G>A maps to NM_017551.2 Y748Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr10:87898578 G>A maps to NM_017551.2 N241N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr4:94376817 C>T maps to NM_001510.2 A517A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr4:94436525 G>A maps to NM_001510.2 E719E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr6:102503295 C>A maps to NM_021956.4 G801G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr19:42507537 G>A maps to NM_002088.3 F820F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr12:13761623 G>T maps to NM_000834.3 I641I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr17:72842223 G>C maps to NM_000835.3 L777L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr17:72838753 G>A maps to NM_000835.3 H1174H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr19:48945879 T>C maps to NM_000836.2 A899A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr19:48945879 T>C maps to NM_000836.2 A899A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr19:1008888 G>T maps to NM_138690.1 E889*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr19:1003373 G>A maps to NM_138690.1 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr19:1003373 G>A maps to NM_138690.1 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr3:14552685 G>A maps to ENST00000507975 D738D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:48832698 T>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:48853736 C>G did not map to a codon.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr13:114325864 C>T maps to NM_002929.2 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr13:114322345 G>T maps to NM_002929.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr6:146708063 C>A maps to NM_000838.3 C547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr11:88242035 G>A maps to NM_001143831.2 I1121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L6-01A-11D-A29I-10 chr5:178419078 G>A maps to NM_000843.3 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr3:7620788 T>C maps to NM_181874.2 Y732Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr3:6903299 G>T maps to NM_181874.2 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:16168475 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr14:95235474 C>T maps to NM_173849.2 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr17:38130529 C>T maps to NM_178171.4 D252D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chr8:130760773 C>T maps to NM_031415.2 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr17:3628701 G>T maps to NM_031965.2 G491G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LP-01A-11D-A29I-10 chr9:124083613 C>T maps to NM_000177.4 G471G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr9:124064308 G>A maps to NM_000177.4 W71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:51487048 T>A did not map to a codon.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr4:106746954 G>T maps to NM_001031720.2 G510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr4:106640416 G>T maps to NM_001031720.2 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JT-01A-11D-A29I-10 chr7:142962355 T>C maps to NM_001143679.1 N185N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr13:28367931 C>T maps to NM_145657.1 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr2:144764747 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:48872173 C>A maps to NM_172311.2 G806G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr16:27523097 C>A maps to NM_001520.3 R366R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LD-01A-11D-A29I-10 chr16:27503662 T>C maps to NM_001520.3 P1049P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KT-01A-11D-A29I-10 chr2:27560193 G>C maps to NM_001521.2 Y348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr7:89982176 C>T maps to NM_033107.3 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr12:54854182 C>A maps to NM_144594.2 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr6:42156331 G>C maps to NM_002098.5 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr4:156638324 C>T maps to NM_001130684.1 G529G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr4:156680985 C>T maps to ENST00000502959 Y17Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr23:108696980 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:108708516 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chr23:108635182 T>A did not map to a codon.
Sequencing variant TCGA-OR-A5JR-01A-11D-A29I-10 chr19:49485547 G>A maps to NM_002103.4 F342F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L9-01A-11D-A29I-10 chr19:49485547 G>A maps to NM_002103.4 F342F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr1:9307032 G>A maps to NM_004285.3 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr16:778413 C>A maps to NM_207112.1 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr1:156593356 A>G maps to NM_021817.2 Q25Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr15:89430505 C>T maps to NM_178232.2 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr5:140075330 C>T maps to NM_012208.2 D178D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr19:52223025 C>A maps to NM_001523.2 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr9:19063553 T>C maps to NM_017645.3 S467S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr23:152735949 G>A did not map to a codon.
Sequencing variant TCGA-P6-A5OF-01A-11D-A29I-10 chr5:156482500 T>G maps to NM_001173393.1 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JD-01A-11D-A29I-10 chr23:153215838 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:153220098 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:153222834 G>C did not map to a codon.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr23:153225824 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5JV-01A-11D-A29I-10 chr3:121351314 G>A maps to NM_005335.4 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr1:32792570 G>A maps to NM_004964.2 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr17:42170065 G>A maps to NM_001015053.1 D251D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:48676460 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:48678640 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5L9-01A-11D-A29I-10 chr23:48676474 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr12:48189736 T>G maps to NM_015401.3 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LD-01A-11D-A29I-10 chr7:18705996 A>G maps to NM_178425.2 G543G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JR-01A-11D-A29I-10 chr15:91475755 C>G maps to ENST00000394272 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr23:7023777 A>C did not map to a codon.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr7:780484 C>T maps to NM_017802.3 G270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr17:58151223 C>T maps to NM_022070.4 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr8:145247209 A>C did not map to a codon.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr5:41061714 C>T maps to ENST00000296803 W191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr2:197143275 C>T maps to NM_020760.1 R1037R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr3:124692688 C>T maps to NM_020733.1 P1294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr10:96353306 C>T maps to NM_018063.3 R675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:65412127 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chr23:65423291 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr23:65486455 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr15:28422656 T>C did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr15:28377251 A>G maps to NM_004667.4 P4188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr15:28473415 A>G maps to NM_004667.4 L1804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JH-01A-11D-A30A-10 chr1:6305302 C>A maps to NM_001024598.3 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr1:6305302 C>A maps to NM_001024598.3 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr1:6305302 C>A maps to NM_001024598.3 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr17:8026363 C>T maps to NM_001165967.1 E41E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr8:80677602 G>A maps to NM_001040708.1 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:91866609 A>T maps to NM_001017975.3 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr4:3446681 C>T maps to ENST00000511533 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LR-01A-11D-A29I-10 chr4:3449885 G>A maps to ENST00000511533 E563E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr3:42739084 G>T maps to NM_020707.3 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr3:42738491 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr1:222713604 C>A maps to NM_024746.3 S399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:100527405 T>C maps to NM_033055.2 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JI-01A-11D-A29I-10 chr17:1960973 C>T maps to NM_001098202.1 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr17:1960973 C>T maps to NM_001098202.1 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr22:21800326 G>A maps to NM_015094.2 G381G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:114506013 C>T maps to ENST00000426820 S774S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr6:25727447 G>A maps to NM_170610.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr6:25727333 C>T maps to NM_170610.2 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JL-01A-11D-A29I-10 chr6:27114541 C>T maps to NM_080593.2 K12K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr6:26020914 A>G maps to NM_003529.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L1-01A-11D-A30A-10 chr1:149859427 A>G maps to NM_175065.2 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr1:228612627 C>T maps to NM_003493.2 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr6:143094922 G>T maps to NM_006734.3 S318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:42047293 A>G maps to NM_024503.3 L1059L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KW-01A-11D-A29I-10 chr6:31324642 G>C maps to ENST00000428231 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L9-01A-11D-A29I-10 chr6:31324585 C>T maps to ENST00000428231 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr6:32782313 G>A maps to ENST00000452392 H749H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr6:32610519 C>A maps to NM_002122.3 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KW-01A-11D-A29I-10 chr6:32628021 A>G maps to ENST00000374943 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr6:32628021 A>G maps to ENST00000374943 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J7-01A-11D-A29I-10 chr6:32548553 G>T maps to NM_002124.2 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr11:118963199 C>T maps to NM_000190.3 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LA-01A-11D-A29I-10 chr1:186031040 C>T maps to NM_031935.2 C2457C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr6:79913319 T>A maps to NM_004242.2 K42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr16:4558129 C>T maps to NM_001127205.1 N207N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr10:124909281 C>A maps to NM_005519.1 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr23:100667307 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5J3-01A-11D-A29I-10 chr19:8551111 G>T maps to NM_005968.3 L600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr11:62494433 G>A maps to NM_001079559.1 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:60312771 C>T maps to NM_015888.4 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KZ-01A-11D-A29I-10 chr12:54394283 C>T maps to NM_006897.1 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JD-01A-11D-A29I-10 chr2:177016765 C>A maps to NM_014621.2 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr10:100202967 G>A maps to NM_000195.2 G10G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr11:18339354 C>T maps to NM_181507.1 E17E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr11:18303702 C>T maps to NM_181507.1 T1041T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr19:49657888 T>C maps to NM_002152.2 E202E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr19:49657915 T>C maps to NM_002152.2 E193E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr3:186389493 C>A maps to NM_000412.2 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J2-01A-11D-A29I-10 chr1:152189037 A>G maps to NM_001009931.1 Y1689Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JV-01A-11D-A29I-10 chr1:152189028 A>G maps to NM_001009931.1 H1692H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:152188310 G>A maps to NM_001009931.1 Q1932*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr1:152185881 G>C maps to NM_001009931.1 G2741G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr4:11401092 C>T maps to NM_005114.2 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr6:114378975 T>C maps to NM_153612.3 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr23:132090978 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr13:96743550 C>G maps to NM_153456.2 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr1:120056634 G>A maps to ENST00000235547 E165E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JH-01A-11D-A30A-10 chr6:44221292 C>T maps to NM_007355.2 L711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr1:161495884 T>C maps to NM_002155.3 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr11:122929388 C>A maps to NM_006597.3 V491V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:22179235 T>A maps to NM_005529.5 L2227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr4:70920166 T>C maps to NM_002159.2 H34H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr6:78172259 C>G maps to NM_000863.1 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr6:87725123 C>G maps to NM_000865.2 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr23:114141203 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr11:113860304 G>T maps to NM_213621.3 L457L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-OR-A5J4-01A-11D-A29I-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr4:8293290 C>T maps to NM_053044.3 N301N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr23:53616610 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:53607985 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr23:53591625 A>C did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:53561132 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:53602736 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:53634660 C>A did not map to a codon.
Sequencing variant TCGA-P6-A5OF-01A-11D-A29I-10 chr11:125770030 G>A maps to NM_001134793.1 Q256Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr19:10394442 C>A maps to NM_000201.2 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr19:10450284 G>A maps to NM_002162.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr20:30193225 C>G maps to NM_002165.2 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PA-A5YG-01A-11D-A29I-10 chr10:94268533 G>T maps to NM_004969.3 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:153055721 C>G did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:148582537 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5JD-01A-11D-A29I-10 chr4:996887 C>T maps to NM_000203.3 R489R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr1:79095481 T>A maps to NM_006820.2 L202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr10:91177054 G>A maps to NM_012420.2 E33E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr9:21141178 C>A maps to NM_002177.1 E131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr7:112090793 C>A maps to NM_001007245.2 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KZ-01A-11D-A29I-10 chr16:1642209 C>A maps to NM_014714.3 E201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr20:42264652 G>A maps to NM_016004.2 A337A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr20:42233640 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr12:110630487 C>T maps to NM_014055.3 R512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr15:65622119 G>A maps to NM_004884.3 I647I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr15:65687495 C>A maps to NM_020962.1 V504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr15:65703499 C>A maps to NM_020962.1 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr15:99250941 C>T maps to NM_000875.3 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:23390951 G>T maps to NM_006547.2 R219R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr17:38600091 G>A maps to NM_001552.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr17:38600091 G>A maps to NM_001552.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LD-01A-11D-A29I-10 chr17:38600091 G>A maps to NM_001552.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5H8-01A-11D-A29I-10 chr2:217559483 G>T maps to NM_000599.3 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr12:53494881 C>T maps to NM_002178.2 R180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr1:201184274 C>T maps to NM_001164586.1 T2996T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr11:68682295 G>A maps to NM_002180.2 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:130411108 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:130419879 G>T did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr23:130416499 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr3:151166385 T>A maps to NM_178822.4 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KZ-01A-11D-A29I-10 chr3:151155637 G>T maps to NM_178822.4 I2237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr3:118621405 G>T maps to NM_152538.2 V418V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JH-01A-11D-A30A-10 chr11:18736088 A>G maps to NM_173588.3 N538N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KV-01A-11D-A29I-10 chr9:111674680 C>T maps to NM_003640.3 W351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr1:206650064 A>G maps to NM_014002.3 Q195Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LP-01A-11D-A29I-10 chr1:206651106 G>A maps to NM_014002.3 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:50468108 G>C maps to NM_006060.3 A448A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr2:213872284 G>T maps to ENST00000342002 V466V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr17:37934012 C>A maps to NM_012481.3 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr5:158750251 G>T maps to NM_002187.2 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LA-01A-11D-A29I-10 chr1:67852334 G>A maps to NM_001559.2 T643T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr23:117925778 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5JW-01A-11D-A29I-10 chr3:9956278 G>A maps to NM_153483.2 P488P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:105011208 C>A did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr6:137329835 C>T maps to NM_014432.2 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J3-01A-11D-A29I-10 chr1:24465112 C>T maps to NM_021258.2 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr1:67724386 C>A maps to NM_144701.2 S489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr19:50404911 G>T maps to NM_172374.1 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:155235034 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:155239891 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5L6-01A-11D-A29I-10 chr23:155239803 C>G did not map to a codon.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr19:10798172 C>T maps to NM_017620.2 H741H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr2:86371957 C>T maps to NM_006839.2 W570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr8:57905817 G>A maps to NM_017813.3 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr11:61914281 G>A maps to NM_001040694.1 E704E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr13:111371921 C>T maps to NM_005537.3 N304N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr13:111368315 C>T maps to NM_005537.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr13:111368315 C>T maps to NM_005537.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JT-01A-11D-A29I-10 chr13:111368315 C>T maps to NM_005537.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr13:111368315 C>T maps to NM_005537.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr13:111368315 C>T maps to NM_005537.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr13:111368315 C>T maps to NM_005537.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chr13:111368315 C>T maps to NM_005537.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KZ-01A-11D-A29I-10 chr13:111368315 C>T maps to NM_005537.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LR-01A-11D-A29I-10 chr13:111368315 C>T maps to NM_005537.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OF-01A-11D-A29I-10 chr13:111368315 C>T maps to NM_005537.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr2:121103889 C>T maps to NM_002193.2 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr2:121103940 C>T maps to NM_002193.2 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr2:121103964 C>T maps to NM_002193.2 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr2:121106702 A>G maps to NM_002193.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr15:41313296 G>C maps to NM_017553.1 Y1025*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr15:41337218 G>T maps to NM_017553.1 R930R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr2:99155994 C>T maps to NM_001134224.1 F225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr9:139324135 G>A maps to NM_019892.3 S642S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr11:15197587 G>T maps to NM_001031853.3 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L6-01A-11D-A29I-10 chr20:20348961 C>T maps to NM_002196.2 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr14:36004657 C>A maps to NM_032594.3 G400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr14:36004657 C>A maps to NM_032594.3 G400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr4:128584579 G>A maps to NM_015693.3 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr9:102888722 C>T maps to NM_014425.2 C55C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JX-01A-11D-A29I-10 chr6:33703229 G>A maps to NM_054111.4 D8D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr6:154533921 A>T maps to NM_001130700.1 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr23:53284063 G>C did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:53278001 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:53279725 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:53279965 G>C did not map to a codon.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr12:247899 G>A maps to NM_001170738.1 E457E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JX-01A-11D-A29I-10 chr7:123105041 G>A maps to NM_178827.4 Q535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L1-01A-11D-A30A-10 chr23:153284191 A>G did not map to a codon.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr1:234744412 C>A maps to NM_182972.2 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr1:234744412 C>A maps to NM_182972.2 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr6:401668 C>T maps to NM_002460.3 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr11:615102 G>A maps to NM_004031.2 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L9-01A-11D-A29I-10 chr11:615102 G>A maps to NM_004031.2 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr14:24631380 C>T maps to NM_006084.4 R10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr19:44223765 C>T maps to NM_019612.3 D352D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr19:44223897 C>A maps to NM_019612.3 A396A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JX-01A-11D-A29I-10 chr19:44098974 T>C maps to NM_001007561.2 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr19:44097164 C>T maps to NM_001007561.2 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JL-01A-11D-A29I-10 chr13:110435727 C>G maps to NM_003749.2 T891T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr23:107979445 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:107976956 G>A did not map to a codon.
Sequencing variant TCGA-P6-A5OF-01A-11D-A29I-10 chr23:107979157 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr5:1882128 T>G maps to NM_016358.2 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K8-01A-11D-A29I-10 chr5:1882128 T>G maps to NM_016358.2 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr5:1879671 C>A maps to NM_016358.2 E228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr5:1882128 T>G maps to NM_016358.2 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr16:55360429 G>T maps to NM_024335.2 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr20:13269301 G>A maps to NM_080826.1 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JR-01A-11D-A29I-10 chr14:77965093 G>A maps to NM_199296.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr14:77965093 G>A maps to NM_199296.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JH-01A-11D-A30A-10 chr22:35480437 T>G maps to NM_001008494.1 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr3:128853774 T>A maps to ENST00000418265 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr19:18546480 G>A maps to NM_016368.4 V382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LR-01A-11D-A29I-10 chr19:18546677 T>C maps to NM_016368.4 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr16:314145 C>T maps to NM_032039.2 H440H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr2:182360585 G>T maps to NM_000885.4 E488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr2:182399022 G>T maps to NM_000885.4 E937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr2:182374440 T>A maps to NM_000885.4 G584G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr10:15761653 G>A maps to NM_003638.1 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr16:31288326 C>T maps to NM_001145808.1 I390I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5H8-01A-11D-A29I-10 chr2:187521094 G>A maps to NM_002210.3 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr16:31374305 C>T maps to NM_000887.3 D470D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JI-01A-11D-A29I-10 chr13:102227871 C>T maps to NM_004791.1 D187D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L6-01A-11D-A29I-10 chr3:52824812 C>T maps to NM_002215.2 D790D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr10:7768993 C>T maps to NM_002216.2 R356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr10:7788556 C>T maps to NM_002216.2 G861G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr10:7608356 G>A maps to ENST00000256861 N721N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:54800535 A>C did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:54817376 A>T did not map to a codon.
Sequencing variant TCGA-OR-A5LL-01A-11D-A29I-10 chr23:78616968 C>A did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr23:78616966 A>T did not map to a codon.
Sequencing variant TCGA-OR-A5K8-01A-11D-A29I-10 chr14:93408016 C>T maps to NM_014216.4 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr19:41245299 C>T maps to NM_025194.2 T629T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr3:4693829 G>T maps to ENST00000356617 R289R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr12:26732986 G>A maps to NM_002223.2 P1494P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L6-01A-11D-A29I-10 chr6:33657015 C>T maps to ENST00000374316 G2232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr21:35208766 C>T maps to NM_003024.2 Y1164Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr21:35166742 A>G maps to NM_003024.2 E641E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr1:152883055 A>G maps to NM_005547.2 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:152883313 G>A maps to NM_005547.2 E347E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J2-01A-11D-A29I-10 chr19:49245555 C>T maps to NM_182575.2 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr10:133930933 C>T maps to NM_001105521.2 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr10:133954010 C>T maps to NM_001105521.2 D467D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr20:42788358 C>T maps to NM_020433.4 Q356Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr16:87678020 C>T maps to NM_020655.2 D180D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr8:143746415 A>G maps to NM_003724.2 H354H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr23:8538723 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr23:8553423 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr9:738457 C>T maps to NM_015158.2 S1169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr9:712592 T>A maps to NM_015158.2 S609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JL-01A-11D-A29I-10 chr19:11303816 G>C maps to NM_015493.6 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr19:8399627 A>G maps to NM_198471.2 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr19:8399627 A>G maps to NM_198471.2 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr19:8399627 A>G maps to NM_198471.2 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr19:8399627 A>G maps to NM_198471.2 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KV-01A-11D-A29I-10 chr19:8400650 C>G maps to NM_198471.2 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr19:8399708 C>A maps to NM_198471.2 V334V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LD-01A-11D-A29I-10 chr1:62713266 T>A maps to NM_181712.4 A920A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr11:65479767 G>A maps to NM_182710.1 G10G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr15:65369530 G>T maps to NM_001101362.2 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JW-01A-11D-A29I-10 chr15:65369530 G>T maps to NM_001101362.2 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr15:65369530 G>T maps to NM_001101362.2 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr15:65369530 G>T maps to NM_001101362.2 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JT-01A-11D-A29I-10 chr12:5020978 C>A maps to NM_000217.2 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J3-01A-11D-A29I-10 chr1:111216298 G>T maps to NM_002232.3 S378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr12:4920364 G>A maps to NM_002235.3 G386G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr19:49573388 G>A maps to NM_031886.2 D434D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr19:49575617 A>G maps to NM_031886.2 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KV-01A-11D-A29I-10 chr19:49575617 A>G maps to NM_031886.2 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr20:47991196 G>T maps to NM_004975.2 R300R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr8:73480115 G>T maps to NM_004770.2 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:110766352 C>A maps to NM_004978.4 A482A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:48822693 C>G did not map to a codon.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr23:48826542 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:119914835 C>A maps to NM_012281.2 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr2:223917880 C>T maps to NM_080671.2 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr16:84256304 G>A maps to NM_172347.2 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr1:210856742 C>T maps to NM_172362.2 Q950Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:211264024 A>T maps to NM_172362.2 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr3:19554464 G>T maps to NM_144633.2 E695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr4:20884246 C>A maps to ENST00000382152 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr21:38997474 C>A maps to NM_002240.2 E420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr14:88652421 G>T maps to NM_138318.2 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr10:78761183 G>T maps to NM_001161352.1 C749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr3:178546025 T>C maps to NM_005832.3 N96N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr1:154842251 A>C maps to NM_002249.4 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr1:154744851 A>G maps to NM_002249.4 N349N. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-OR-A5J8-01A-11D-A29I-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr6:73332039 C>G maps to NM_001160133.1 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr6:73332039 C>G maps to NM_001160133.1 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr6:73332039 C>G maps to NM_001160133.1 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr9:138669185 C>T maps to ENST00000298480 G784G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr16:29918290 C>A maps to NM_178863.2 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr11:77885165 G>A maps to NM_001029859.1 N145N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr19:48894555 C>T maps to NM_006801.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr6:18215281 C>T maps to ENST00000388870 V719V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr5:137722267 G>A maps to NM_016604.3 V446V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr1:44134890 G>A maps to NM_014663.2 T428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr19:5143982 C>T maps to NM_015015.2 C852C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr19:5041153 T>C maps to NM_015015.2 C108C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr12:431709 G>A maps to NM_001042603.1 L767L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr17:7752794 A>C maps to NM_001080424.1 T1063T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr14:24901481 C>A maps to NM_015299.2 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr19:6416661 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5L6-01A-11D-A29I-10 chr19:6417771 G>A maps to NM_003685.2 G353G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr1:19545801 G>A maps to NM_015047.1 R993*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L6-01A-11D-A29I-10 chr16:71956528 C>T maps to NM_014761.2 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr17:73485706 G>A maps to ENST00000375248 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr6:24581183 C>A maps to NM_014809.3 E417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JW-01A-11D-A29I-10 chr19:34843760 C>A maps to NM_014686.3 P1038P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr9:114246950 T>C maps to NM_001080398.1 K25K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr9:114148673 C>T maps to NM_001080398.1 W1348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr20:36641453 G>T maps to NM_014657.1 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr16:15732946 C>G maps to NM_014647.3 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr1:43906895 A>G maps to NM_015284.2 E1553E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr16:27782956 G>A maps to NM_015202.2 P1394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr9:138377450 C>T maps to NM_014811.3 D365D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J3-01A-11D-A29I-10 chr12:55368244 G>A maps to NM_001098815.1 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr1:39880127 C>T maps to NM_015038.1 T1397T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr4:123227128 C>A maps to NM_015312.3 S3257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr15:81224295 C>A maps to NM_018689.1 T903T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr15:81218051 C>T maps to NM_018689.1 H792H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr23:118219365 T>C did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:118215374 C>G did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:118221792 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:118222704 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr23:118215301 A>T did not map to a codon.
Sequencing variant TCGA-OR-A5LP-01A-11D-A29I-10 chr23:118222405 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5JW-01A-11D-A29I-10 chr4:57181585 C>T maps to NM_020722.1 R640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chr6:138613010 C>A maps to NM_020340.4 P1063P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LR-01A-11D-A29I-10 chr14:94152958 C>T maps to ENST00000393153 N2348N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr8:95538628 C>A maps to NM_015496.3 E615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LL-01A-11D-A29I-10 chr9:5754923 A>G maps to ENST00000414202 Q562Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr10:30315256 G>A maps to NM_020848.2 L1274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr12:13232843 G>A maps to NM_020853.1 E588E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr2:226447395 C>G maps to NM_020864.1 Y421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr9:100070350 G>A maps to ENST00000375206 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr19:7682924 C>T maps to NM_001080429.2 G1271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JQ-01A-11D-A29I-10 chr16:84516308 G>A maps to NM_020947.3 N322N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr1:180914480 C>T maps to NM_020950.1 D1110D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr18:43529493 G>A maps to NM_020964.2 R485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chr19:18375607 G>A maps to NM_001145304.1 A914A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr9:20929355 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr9:115336644 G>A maps to NM_133465.2 Q95Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr9:115421991 G>A maps to NM_133465.2 T598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr23:73960664 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr23:73961523 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr23:73962656 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr23:73961528 C>G did not map to a codon.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr10:94397208 A>G maps to NM_004523.3 L689L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr8:28929233 G>A maps to NM_015254.3 V1707V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JV-01A-11D-A29I-10 chr20:16253900 C>T maps to NM_024704.4 G1317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr1:21013967 G>A maps to NM_020816.2 A617A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr1:21012574 G>A maps to NM_020816.2 P661P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr2:241737133 G>A maps to ENST00000373308 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:10364623 T>C maps to NM_183416.3 C1127C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr17:4926820 C>A maps to NM_006612.5 S896*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr12:39695355 C>A maps to ENST00000395670 V1620V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr14:104644167 C>T maps to NM_015656.1 S1681S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr14:104644098 T>C maps to NM_015656.1 S1658S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JH-01A-11D-A30A-10 chr14:104644098 T>C maps to NM_015656.1 S1658S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr14:104644098 T>C maps to NM_015656.1 S1658S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr14:104641875 C>T maps to NM_015656.1 A917A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L1-01A-11D-A30A-10 chr14:104643408 A>G maps to NM_015656.1 A1428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L1-01A-11D-A30A-10 chr14:104643420 T>C maps to NM_015656.1 L1432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L3-01A-11D-A29I-10 chr14:104644098 T>C maps to NM_015656.1 S1658S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr14:104644098 T>C maps to NM_015656.1 S1658S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr14:104644983 G>T maps to NM_015656.1 P1736P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr14:104644098 T>C maps to NM_015656.1 S1658S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr9:86504165 G>A maps to NM_017576.1 V604V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr5:61673486 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:154396952 G>T maps to NM_001099293.1 V1178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr15:90176982 A>G maps to NM_198525.2 L842L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr15:90192527 G>A maps to NM_198525.2 N200N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr1:169951996 C>T maps to NM_014970.2 G506G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr8:145697997 C>T maps to NM_145754.2 A590A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr19:1854556 A>G maps to NM_031918.3 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:56259772 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr12:27933961 C>A maps to NM_020782.1 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr1:18809304 C>T maps to NM_152375.2 D610D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KZ-01A-11D-A29I-10 chr1:205306589 G>A maps to NM_018203.1 A330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr13:70413105 A>T did not map to a codon.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr17:39998281 A>T maps to NM_152467.3 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:117043643 T>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:117043656 G>T did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr23:117033020 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr23:24006590 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr1:6659126 G>A maps to NM_014851.2 N469N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LL-01A-11D-A29I-10 chr5:137056266 C>T maps to NM_017415.2 K7K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LL-01A-11D-A29I-10 chr2:239059525 C>T maps to NM_198582.3 G519G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr6:53519455 C>A maps to NM_001003760.4 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:86890617 T>A did not map to a codon.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr7:23163400 G>A maps to NM_001031710.2 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr19:51532677 G>T maps to NM_019598.2 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr19:51485655 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chr1:241752062 T>G maps to NM_003679.3 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr10:135000147 T>C maps to ENST00000368572 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LA-01A-11D-A29I-10 chr10:135000147 T>C maps to ENST00000368572 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LD-01A-11D-A29I-10 chr10:135015371 G>T maps to ENST00000368572 A1121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr10:135000123 C>T maps to ENST00000368572 D424D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr10:135000147 T>C maps to ENST00000368572 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr17:66039349 A>G maps to NM_002266.2 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr13:50283732 G>T maps to NM_002267.3 S336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr2:88327570 G>C maps to NM_016618.1 S171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr17:39766463 G>A maps to NM_005557.3 G435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr17:39775872 G>A maps to NM_000422.2 R424R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr17:39780503 G>T maps to NM_000422.2 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr12:53044229 C>A maps to NM_000423.2 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr17:38936016 G>T maps to NM_181537.3 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr12:53189265 G>T maps to ENST00000309505 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr17:39645882 C>A maps to NM_003771.4 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr12:52841764 G>A maps to NM_005555.3 A407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr12:52863506 G>T maps to NM_173086.4 A457A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr12:52627325 C>A maps to NM_005556.3 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr12:52627214 A>G maps to NM_005556.3 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KT-01A-11D-A29I-10 chr12:52627214 A>G maps to NM_005556.3 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr12:52992833 C>A maps to NM_080747.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr12:52967317 C>A maps to NM_175053.3 G82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L6-01A-11D-A29I-10 chr12:52828025 C>T maps to ENST00000252245 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JH-01A-11D-A30A-10 chr12:52680107 G>T maps to NM_002281.3 C483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OF-01A-11D-A29I-10 chr12:52757871 G>A maps to NM_002283.3 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr17:39190722 A>G maps to NM_030966.1 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J7-01A-11D-A29I-10 chr21:46057624 T>C maps to NM_181688.1 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr21:46057633 T>C maps to NM_181688.1 C100C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr21:46057639 C>T maps to NM_181688.1 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr21:46057624 T>C maps to NM_181688.1 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr21:45971107 C>T maps to NM_198693.2 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L4-01A-11D-A29I-10 chr21:45971224 T>C maps to NM_198693.2 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J2-01A-11D-A29I-10 chr21:45993850 C>T maps to NM_198687.1 C72C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr21:45993850 C>T maps to NM_198687.1 C72C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L6-01A-11D-A29I-10 chr21:45993850 C>T maps to NM_198687.1 C72C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr21:46047798 T>G maps to NM_198690.2 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr21:32253539 G>T maps to NM_175858.2 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr21:31655214 A>T maps to NM_001085455.1 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr17:39274237 A>G maps to NM_033059.3 C110C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LR-01A-11D-A29I-10 chr17:39274237 A>G maps to NM_033059.3 C110C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr17:39324163 G>T maps to NM_033187.1 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KT-01A-11D-A29I-10 chr11:71276950 T>C maps to ENST00000422553 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr11:1629042 T>C maps to ENST00000359229 K241K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OF-01A-11D-A29I-10 chr11:1628991 G>A maps to ENST00000359229 G258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L4-01A-11D-A29I-10 chr11:1643203 G>A maps to ENST00000359229 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr11:1643257 C>T maps to ENST00000359229 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JW-01A-11D-A29I-10 chr11:1651645 C>T maps to NM_001001480.2 Y192Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr11:1651189 C>T maps to NM_001001480.2 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr17:39411753 G>A maps to NM_030975.2 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chr1:155141957 G>A maps to NM_173852.3 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KV-01A-11D-A29I-10 chr12:117993063 C>T maps to ENST00000339824 P476P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr14:56103914 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:153133824 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr23:153133281 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr20:42143399 G>T maps to NM_032107.4 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr18:7013828 C>T maps to NM_005559.2 G1116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JX-01A-11D-A29I-10 chr6:129691084 G>T maps to NM_000426.3 E1637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr18:21456301 C>T maps to ENST00000416669 T1683T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K8-01A-11D-A29I-10 chr6:112455802 G>T maps to NM_001105206.1 I1141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr20:60900599 C>A maps to NM_005560.3 G1767G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:107684338 G>T maps to NM_007356.2 I1443I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr7:107696426 G>T maps to NM_007356.2 T1135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LR-01A-11D-A29I-10 chr1:183072589 T>C maps to NM_002293.3 C182C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr4:113570693 C>T maps to ENST00000509061 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:145509682 C>T maps to NM_020117.9 G842G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr17:37070575 A>C did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr15:100996193 G>T maps to ENST00000394113 Y312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr19:8316106 C>T maps to NM_024552.2 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:169404168 G>T maps to ENST00000392687 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KW-01A-11D-A29I-10 chr1:225600345 T>A maps to NM_194442.1 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J7-01A-11D-A29I-10 chr15:68120013 C>T maps to ENST00000380035 Y616Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr15:68120013 C>T maps to ENST00000380035 Y616Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr15:68120013 C>T maps to ENST00000380035 Y616Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J1-01A-11D-A29I-10 chr1:152800121 C>T maps to NM_178348.2 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J1-01A-11D-A29I-10 chr1:152800130 C>T maps to NM_178348.2 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr1:152760074 A>G maps to ENST00000417924 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr1:152760074 A>G maps to ENST00000417924 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JI-01A-11D-A29I-10 chr1:152760101 C>A maps to ENST00000417924 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JR-01A-11D-A29I-10 chr1:152760095 A>T maps to ENST00000417924 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr1:152760074 A>G maps to ENST00000417924 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:32741015 G>T maps to ENST00000373562 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr16:25151547 G>A maps to ENST00000380963 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr9:139634003 C>T maps to NM_001001712.2 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr10:98708915 G>A maps to NM_001170765.1 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr4:18023335 G>C maps to NM_001166139.1 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr5:169685168 C>T maps to NM_005565.3 V324V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr11:18451363 C>T maps to NM_017448.3 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr19:11234003 G>C maps to NM_000527.4 V765V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr23:140271094 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5J3-01A-11D-A29I-10 chr3:189713204 T>C maps to NM_018192.3 E169E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JQ-01A-11D-A29I-10 chr1:236702373 G>A maps to NM_201545.1 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr19:35625481 T>A maps to NM_139284.2 K35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr14:93170992 C>T maps to NM_005606.6 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:180240551 C>A maps to NM_033343.3 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr9:124971943 G>T maps to NM_014368.3 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:75622717 C>A maps to NM_001001933.1 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr22:30639990 C>T maps to NM_002309.3 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr19:55105903 A>G did not map to a codon.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr19:54849246 C>T maps to NM_012276.3 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr19:54744360 A>C maps to ENST00000419410 G349G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr19:54746588 G>A maps to ENST00000407860 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JL-01A-11D-A29I-10 chr19:54725991 G>A maps to NM_001081450.1 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JW-01A-11D-A29I-10 chr19:54725991 G>A maps to NM_001081450.1 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr19:54722274 G>A maps to NM_001081450.1 A516A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr22:31667153 G>A maps to NM_001031801.1 R429R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J3-01A-11D-A29I-10 chr2:109293129 A>G maps to NM_001193484.1 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LR-01A-11D-A29I-10 chr15:58834740 G>T maps to NM_000236.2 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr19:42914842 C>T maps to NM_005357.2 A345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr21:15481358 C>T maps to NM_198996.2 E467E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JD-01A-11D-A29I-10 chr17:73565070 C>A maps to NM_001031803.1 G445G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KV-01A-11D-A29I-10 chr17:73565070 C>A maps to NM_001031803.1 G445G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr12:66517670 C>T maps to NM_032338.3 K113K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JQ-01A-11D-A29I-10 chr15:75113022 G>A maps to NM_021819.2 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr12:49491820 C>T maps to NM_018113.2 V436V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr3:197702953 C>T maps to NM_001136049.2 R135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5H8-01A-11D-A29I-10 chr1:156105771 G>A maps to NM_170707.2 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr5:126154660 T>C maps to NM_005573.3 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr7:123302044 C>T maps to NM_207163.1 D135D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr7:97821141 G>A maps to NM_014916.3 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr19:48994784 G>T maps to NM_001080434.1 T1397T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JD-01A-11D-A29I-10 chr19:49004260 C>T maps to NM_001080434.1 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr19:49002213 G>A maps to NM_001080434.1 P733P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:165322433 G>A maps to NM_177398.3 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr5:96315241 C>T maps to NM_005575.2 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:13183602 C>T maps to NM_001136561.2 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr16:48278490 T>C maps to NM_031490.2 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr16:48295432 G>A maps to NM_031490.2 E274E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JR-01A-11D-A29I-10 chr1:153233577 C>T maps to NM_000427.2 C51C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr1:153233577 C>T maps to NM_000427.2 C51C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr1:153233700 A>C maps to NM_000427.2 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KT-01A-11D-A29I-10 chr1:153233700 A>C maps to NM_000427.2 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KV-01A-11D-A29I-10 chr1:153233700 A>C maps to NM_000427.2 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KW-01A-11D-A29I-10 chr1:153233700 A>C maps to NM_000427.2 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KZ-01A-11D-A29I-10 chr1:153233700 A>C maps to NM_000427.2 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr1:153233700 A>C maps to NM_000427.2 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:153233700 A>C maps to NM_000427.2 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr8:23179794 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr2:74779680 C>T maps to NM_032603.2 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:85279732 G>T maps to NM_012152.2 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr15:34651422 G>A maps to NM_153613.2 R494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr19:14272166 C>T maps to NM_001008701.2 Q494Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr1:82409448 C>A maps to ENST00000370717 A398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr17:56326517 T>C maps to NM_006151.2 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr17:56344749 G>A maps to NM_006151.2 P578P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JW-01A-11D-A29I-10 chr19:814974 G>A maps to NM_024888.1 Y170Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr19:814547 G>A maps to NM_024888.1 F267F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:99772257 G>T maps to NM_014839.4 E662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr3:197598288 C>T maps to ENST00000425562 R696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr19:39805166 G>A maps to NM_020862.1 D270D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr19:36430695 C>T maps to NM_024509.1 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr19:36431133 C>T maps to NM_024509.1 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr14:42356829 T>A maps to NM_152447.3 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr12:59284578 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr12:59313935 T>G maps to NM_153377.3 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5H8-01A-11D-A29I-10 chr10:85992140 G>T maps to NM_015613.2 R472R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr10:85982397 C>A maps to NM_001017924.2 E311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr12:57581074 C>A maps to NM_002332.2 A2289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LL-01A-11D-A29I-10 chr14:23345362 C>T maps to NM_014045.3 G402G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:141128387 C>T maps to NM_018557.2 K3633K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:141245191 G>A maps to NM_018557.2 D3079D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr2:141259363 A>G maps to NM_018557.2 D2914D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr2:170032988 C>T maps to NM_004525.2 Q3501Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JD-01A-11D-A29I-10 chr2:170096094 C>G maps to NM_004525.2 R1412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:170088311 G>T maps to NM_004525.2 C1713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr19:33696353 C>T maps to NM_002333.3 R226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr11:46914636 G>A maps to ENST00000256991 T573T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L1-01A-11D-A30A-10 chr11:68174121 G>A maps to NM_002335.2 E644E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr8:145745150 G>A maps to NM_014665.2 Q14Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr5:191991 G>A maps to NM_001080478.1 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr5:191991 G>A maps to NM_001080478.1 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr5:194840 G>A maps to NM_001080478.1 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr5:192354 C>A maps to NM_001080478.1 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr3:194080770 C>A maps to NM_001135057.2 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr3:194080701 G>A maps to NM_001135057.2 D363D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr8:145747993 C>T maps to NM_001024678.3 E469E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr11:76370746 G>T maps to NM_001128922.1 I630I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr17:30348896 C>T maps to ENST00000327564 N271N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr3:26751492 A>T maps to NM_052953.2 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chr19:51052014 G>A maps to NM_001080457.1 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr11:40136450 C>T maps to NM_020929.1 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr3:120068021 C>G maps to NM_001099678.1 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JI-01A-11D-A29I-10 chr3:120068021 C>G maps to NM_001099678.1 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr3:120068006 C>A maps to NM_001099678.1 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr3:120068021 C>G maps to NM_001099678.1 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr19:7964189 G>T maps to NM_025061.3 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr19:7965668 C>T maps to NM_025061.3 G754G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr15:101565123 G>A maps to NM_024652.3 L728L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr1:204588337 G>A maps to NM_201630.1 P261P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-PK-A5HB-01A-11D-A29I-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr19:34710314 T>G maps to NM_001114093.1 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr19:34710314 T>G maps to NM_001114093.1 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr19:34687594 C>T maps to NM_001114093.1 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr17:7760498 G>A maps to NM_032356.3 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L3-01A-11D-A29I-10 chr21:47614442 A>G maps to NM_002340.5 H650H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr12:21196448 T>C maps to ENST00000381541 D277D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr14:75018959 G>A maps to NM_000428.2 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr11:65319518 G>A maps to NM_001130144.2 D485D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:114540823 G>C did not map to a codon.
Sequencing variant TCGA-OR-A5J1-01A-11D-A29I-10 chr19:43968549 C>T maps to NM_014400.2 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr10:102766681 T>G maps to NM_032429.2 G589G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr1:39852988 A>G maps to ENST00000361689 K2763K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chr19:35800807 C>T maps to NM_002361.3 C421C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LR-01A-11D-A29I-10 chr19:35786867 C>T maps to NM_002361.3 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:152482813 G>T did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr23:152482235 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:148797321 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr23:148797591 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr23:151900356 A>G did not map to a codon.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr23:151900372 A>C did not map to a codon.
Sequencing variant TCGA-OR-A5KW-01A-11D-A29I-10 chr23:151900365 G>A did not map to a codon.
Sequencing variant TCGA-P6-A5OF-01A-11D-A29I-10 chr23:151935711 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:151092270 T>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:30268639 T>A did not map to a codon.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr23:30268990 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:27840274 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KZ-01A-11D-A29I-10 chr23:35821126 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:30237540 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr23:30261198 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr23:26212977 G>C did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:26212652 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:26212779 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5J3-01A-11D-A29I-10 chr23:140994406 C>G did not map to a codon.
Sequencing variant TCGA-OR-A5J3-01A-11D-A29I-10 chr23:140994418 T>C did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:140993232 C>G did not map to a codon.
Sequencing variant TCGA-OR-A5L1-01A-11D-A30A-10 chr23:140994912 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5L1-01A-11D-A30A-10 chr23:140994922 A>T did not map to a codon.
Sequencing variant TCGA-OR-A5L1-01A-11D-A30A-10 chr23:140994938 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr23:140994547 A>G did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:141291128 G>T did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr23:140926204 T>C did not map to a codon.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr23:75648450 C>G did not map to a codon.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr23:75003781 T>G did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr15:23889841 G>T maps to NM_019066.4 P1016P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr1:114225610 G>T maps to NM_001142782.1 E1141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JQ-01A-11D-A29I-10 chr1:114196494 A>G maps to NM_001142782.1 T828T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr23:49021300 A>T did not map to a codon.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr12:10766107 G>A maps to NM_018048.3 Y8Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LA-01A-11D-A29I-10 chr23:77111009 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr6:10796401 C>G maps to NM_005906.3 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr8:120252496 T>C maps to ENST00000276681 N132N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L4-01A-11D-A29I-10 chr2:110873263 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr5:179193192 C>A maps to NM_014757.4 S394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KZ-01A-11D-A29I-10 chr11:95825373 T>C maps to NM_032427.1 Q607Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr23:149639047 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:149639348 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr15:91450635 A>G maps to NM_006122.2 Q369Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr4:6621655 T>C maps to NM_015274.1 A939A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LP-01A-11D-A29I-10 chr20:35944721 G>A maps to NM_022077.3 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:43590511 G>T did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr19:17844086 C>T maps to NM_018174.4 S958S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr17:67515497 G>T maps to NM_002758.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr19:7975939 C>T maps to ENST00000425613 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr19:40720078 C>T maps to NM_002446.3 D831D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr23:19425346 A>T did not map to a codon.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr23:19390841 C>T did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr6:161510388 G>A maps to NM_005922.2 A953A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr6:136913612 T>C maps to NM_005923.3 G1006G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr6:91233442 T>A maps to NM_145331.1 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr19:39103251 T>G maps to NM_001042600.1 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JI-01A-11D-A29I-10 chr11:75298796 A>G maps to NM_033063.1 D583D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr3:183543008 C>A maps to NM_024871.2 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr23:20044070 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr23:135323410 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr23:135303013 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:135313957 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr23:135313872 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5JV-01A-11D-A29I-10 chr15:42115151 C>T maps to NM_001128608.1 S1116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JL-01A-11D-A29I-10 chr12:58149445 C>T maps to NM_138396.4 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr1:11105561 C>T maps to NM_006610.2 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr5:66429339 A>G did not map to a codon.
Sequencing variant TCGA-OR-A5KT-01A-11D-A29I-10 chr10:82033593 G>A maps to NM_000429.2 Y377Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5H8-01A-11D-A29I-10 chr10:82034841 A>G maps to NM_000429.2 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5H8-01A-11D-A29I-10 chr10:82034853 T>C maps to NM_000429.2 V290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr7:99725209 G>T maps to NM_203397.1 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KW-01A-11D-A29I-10 chr7:99725209 G>T maps to NM_203397.1 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr16:89986316 C>T maps to ENST00000304984 H217H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:103349891 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr3:182733293 G>A maps to NM_020166.3 Q704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LP-01A-11D-A29I-10 chr6:31497705 C>T maps to NM_001011700.2 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:138699718 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5L6-01A-11D-A29I-10 chr23:138713563 A>G did not map to a codon.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr13:113741679 C>T maps to NM_001112732.1 H892H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr13:113719263 C>T maps to NM_001112732.1 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr22:35815945 C>T maps to NM_006739.3 S591S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr7:99697289 A>T maps to NM_005916.3 I66I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OF-01A-11D-A29I-10 chr19:7589910 T>A maps to NM_020533.2 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LD-01A-11D-A29I-10 chr12:49957271 G>A maps to NM_001012300.1 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr7:114655907 T>C maps to NM_199072.4 C329C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr12:69210627 C>T maps to NM_002392.3 R71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr18:48458689 C>G maps to NM_002396.4 V459V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:70352312 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr23:70356162 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:40568697 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr23:40518764 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr6:131914267 C>T maps to ENST00000403834 W1098*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr1:156437982 C>T maps to NM_005920.2 A452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr16:3293668 G>C maps to NM_000243.2 T606T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr16:3304572 G>T maps to NM_000243.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JH-01A-11D-A30A-10 chr16:3304572 G>T maps to NM_000243.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JQ-01A-11D-A29I-10 chr16:3304572 G>T maps to NM_000243.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JV-01A-11D-A29I-10 chr16:3304572 G>T maps to NM_000243.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr16:3304572 G>T maps to NM_000243.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr16:3296526 G>A maps to NM_000243.2 H536H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr16:3304572 G>T maps to NM_000243.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr16:3304572 G>T maps to NM_000243.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KZ-01A-11D-A29I-10 chr16:3304572 G>T maps to NM_000243.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L9-01A-11D-A29I-10 chr16:3304572 G>T maps to NM_000243.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr16:3304572 G>T maps to NM_000243.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr19:42841341 G>A maps to ENST00000251268 P499P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr19:42867197 A>G did not map to a codon.
Sequencing variant TCGA-OR-A5J1-01A-11D-A29I-10 chr9:123421743 G>T maps to ENST00000426959 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr9:123367686 T>A maps to ENST00000426959 G567G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr22:42114181 G>T maps to NM_152513.3 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr22:42114183 G>A maps to NM_152513.3 E213E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr11:64574691 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KW-01A-11D-A29I-10 chr11:64573816 G>C maps to NM_130804.2 Y317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OF-01A-11D-A29I-10 chr11:64574680 C>T maps to NM_130804.2 W270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr4:99982341 T>G maps to NM_015143.2 T345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J1-01A-11D-A29I-10 chr9:132395086 C>T maps to NM_014064.2 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J7-01A-11D-A29I-10 chr18:48723210 C>G maps to NM_016626.4 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OF-01A-11D-A29I-10 chr15:44102009 A>C maps to NM_005926.2 A330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr1:17302154 G>A maps to NM_017459.2 N119N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr12:8813474 G>T maps to NM_003480.2 V26V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chr2:228195446 G>A maps to NM_020194.4 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr8:8750466 A>G maps to NM_004225.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr8:145736052 C>A maps to NM_138431.1 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr16:4731690 C>T maps to NM_015246.2 S424S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J1-01A-11D-A29I-10 chr6:31378524 C>T maps to NM_000247.1 N92N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JD-01A-11D-A29I-10 chr6:109767927 C>A maps to NM_022765.3 E759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr11:12234877 G>A maps to NM_014632.2 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr11:12265541 A>G maps to NM_014632.2 L889L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr22:38323451 G>A maps to NM_033386.2 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JL-01A-11D-A29I-10 chr7:1484571 A>G maps to NM_182924.3 G378G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr7:1484571 A>G maps to NM_182924.3 G378G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:10535273 G>T did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr5:56234784 T>A maps to ENST00000381226 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr22:24236678 A>T maps to NM_002415.1 V6V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr22:24237110 C>T maps to NM_002415.1 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr17:4793051 C>T maps to NM_153827.4 R447R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr14:37736242 G>T maps to NM_001195296.1 R40R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr10:129903548 C>T maps to NM_002417.4 K2185K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L1-01A-11D-A30A-10 chr7:131084166 A>G maps to NM_013255.4 E226E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr3:37055928 G>C maps to NM_000249.3 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr3:37083762 G>T maps to NM_000249.3 E558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr12:49420172 C>T maps to NM_003482.3 L5192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr12:49445551 T>G maps to NM_003482.3 P638P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr12:49437704 C>T maps to NM_003482.3 Q1755Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr7:151879462 C>A maps to ENST00000355193 E1828*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:151947964 C>A maps to ENST00000355193 E570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LP-01A-11D-A29I-10 chr7:151962268 C>T maps to ENST00000355193 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr19:36229229 C>T maps to NM_014727.1 D2640D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr10:21971184 C>T maps to NM_004641.3 N566N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K8-01A-11D-A29I-10 chr9:20414348 G>A maps to NM_004529.2 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr13:49796458 A>T maps to NM_001507.1 G395G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr16:2256103 C>A maps to NM_022372.4 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr12:122623074 C>A maps to NM_014938.3 I787I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr16:83933192 C>T maps to NM_012213.2 D148D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr12:110011234 G>T maps to NM_052845.3 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr1:2541268 A>G maps to NM_033467.3 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr22:24121480 C>A maps to NM_005940.3 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JW-01A-11D-A29I-10 chr11:102595541 C>A maps to NM_002424.2 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LA-01A-11D-A29I-10 chr11:102586131 G>A maps to NM_002424.2 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr4:90872783 G>A maps to NM_007351.2 P1049P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr10:88702602 G>A maps to NM_024756.2 S646S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JV-01A-11D-A29I-10 chr22:28194899 T>C maps to NM_002430.2 Q544Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:106185910 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:106242922 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr23:102931749 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr1:2316500 G>A maps to NM_024848.1 N151N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr7:100212601 T>A maps to NM_023948.4 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr22:50552816 G>T maps to NM_018995.2 G298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr9:13192143 C>A maps to ENST00000319217 E652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L6-01A-11D-A29I-10 chr15:75185138 A>G maps to NM_002435.1 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr11:3249999 G>A maps to ENST00000328215 H10H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L4-01A-11D-A29I-10 chr19:13879743 C>T maps to NM_001031727.2 Y277Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr3:131219273 C>T maps to ENST00000425847 Q150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JX-01A-11D-A29I-10 chr7:42971991 C>T maps to NM_031903.2 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J2-01A-11D-A29I-10 chr1:54678297 C>T maps to NM_016491.3 G319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L1-01A-11D-A30A-10 chr16:1822946 C>G maps to ENST00000432952 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr1:19584003 G>A maps to NM_016183.3 E110E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr2:48026604 C>T maps to NM_000179.2 R495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr16:818657 G>A maps to NM_013404.4 S606S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KT-01A-11D-A29I-10 chr8:15967635 G>C maps to ENST00000445506 A456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr4:4862087 G>A maps to NM_002448.3 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr5:174152036 G>A maps to NM_002449.4 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr8:121458715 T>C maps to NM_022045.3 I54I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:154294182 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5JX-01A-11D-A29I-10 chr1:11863056 G>A maps to ENST00000376585 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr16:86575736 C>T maps to NM_001159377.1 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:149818248 G>C did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:149905229 C>A did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr23:149931072 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr15:31269077 G>A maps to NM_017762.2 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:63579297 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5JX-01A-11D-A29I-10 chr23:63488901 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr6:153323805 A>G maps to NM_019041.5 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr6:153315692 G>C maps to NM_019041.5 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr8:125568470 A>C did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr13:29599428 A>G maps to NM_001033602.2 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr13:29600622 G>T maps to NM_001033602.2 G606G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JI-01A-11D-A29I-10 chr11:26587132 T>C maps to NM_001135091.1 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr19:9060202 G>T maps to NM_024690.2 T9081T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr19:9070333 A>T maps to NM_024690.2 T5704T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr19:9090530 T>C maps to NM_024690.2 E428E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr11:1093409 C>A maps to ENST00000441003 T1743T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr11:1093253 C>T maps to ENST00000441003 T1691T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr11:1093298 G>A maps to ENST00000441003 T1706T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JW-01A-11D-A29I-10 chr11:1093310 C>A maps to ENST00000441003 T1710T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr11:1093013 C>G maps to ENST00000441003 T1611T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr11:1093412 G>T maps to ENST00000441003 T1744T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L9-01A-11D-A29I-10 chr11:1093313 A>T maps to ENST00000441003 P1711P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr11:1269599 T>C maps to ENST00000447027 T3833T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr11:1276466 A>G maps to ENST00000447027 P5290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J7-01A-11D-A29I-10 chr11:1270601 C>A maps to ENST00000447027 A4167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr11:1262201 G>T maps to ENST00000447027 L1367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr11:1271222 C>G maps to ENST00000447027 T4374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr11:1253941 T>C maps to ENST00000447027 Y672Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5H8-01A-11D-A29I-10 chr11:1250487 C>T maps to ENST00000447027 C355C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LA-01A-11D-A29I-10 chr11:1027715 G>T maps to NM_005961.2 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr9:103348270 G>A maps to NM_001018116.1 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KW-01A-11D-A29I-10 chr6:8041502 T>A did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr6:8041438 T>C maps to NM_201280.2 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:3241450 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:3242693 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5JD-01A-11D-A29I-10 chr23:3229332 A>T did not map to a codon.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr23:3228790 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:3229121 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:3241637 C>G did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:3248113 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr23:3240297 C>G did not map to a codon.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr6:135513460 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr6:135517035 G>T maps to NM_001130173.1 E367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr20:42328525 C>T maps to NM_002466.2 R265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JV-01A-11D-A29I-10 chr20:42343868 C>T maps to NM_002466.2 P640P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr12:102043127 A>G maps to NM_002465.2 G429G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr19:50962396 C>A maps to NM_004533.3 T875T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr1:109839773 G>A maps to NM_001010985.2 D156D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr13:77780869 A>G maps to NM_015057.4 C1169C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr17:10402001 C>T maps to NM_005963.3 Q1374Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr17:10408288 G>T maps to NM_005963.3 L843L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr17:8424544 G>A maps to ENST00000360416 S672S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr17:10213063 G>A maps to NM_003802.2 V1580V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr19:50713813 G>T maps to NM_001145809.1 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr17:10432657 G>C maps to NM_017534.5 L1086L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LL-01A-11D-A29I-10 chr17:10551909 G>A maps to NM_002470.2 N233N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr17:10356510 G>T maps to NM_017533.2 T1023T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr17:10363403 C>G maps to NM_017533.2 V427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr14:23872557 C>G maps to NM_002471.3 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr17:10296485 G>A maps to NM_002472.2 D1736D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr17:10304059 C>A maps to NM_002472.2 E1128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L1-01A-11D-A30A-10 chr22:36702091 G>T maps to NM_002473.4 G681G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr18:3277812 C>A maps to NM_033546.3 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr6:16145407 C>T maps to NM_013262.3 Q370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr3:123452837 G>A maps to NM_053025.3 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr3:123357036 A>G maps to NM_053025.3 N1614N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr16:46744682 T>G maps to NM_182493.2 P711P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr3:169492100 C>T maps to NM_018657.4 H6H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr5:16701080 C>T maps to NM_012334.2 A1141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr5:16711034 C>T maps to NM_012334.2 W717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5H8-01A-11D-A29I-10 chr17:18041506 C>T maps to ENST00000205890 L1652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr22:26164758 G>T maps to ENST00000407587 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr17:1371411 C>T maps to NM_001080779.1 A922A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr11:76912589 C>T maps to NM_000260.3 N1650N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr11:76905569 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr11:76900478 C>T maps to NM_000260.3 C1198C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:128367425 C>A maps to ENST00000389524 A1009A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr17:12626173 A>G maps to NM_001146312.1 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr8:2037832 G>C maps to NM_003970.2 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr8:2054092 C>A maps to NM_003970.2 C932*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:24417404 G>A maps to ENST00000330966 V439V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr20:62839772 G>T maps to NM_004535.2 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr3:175189491 G>T maps to NM_207015.2 G533G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr3:174814614 C>T maps to NM_207015.2 Q27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr3:175165095 G>T maps to NM_207015.2 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr17:59668145 A>T maps to NM_199290.3 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr19:13246605 C>T maps to NM_052876.2 G195G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L3-01A-11D-A29I-10 chr9:138903544 G>A maps to NM_144653.3 D527D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr19:50865551 G>C maps to NM_004851.1 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JW-01A-11D-A29I-10 chr16:790925 C>T maps to NM_022493.1 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LD-01A-11D-A29I-10 chr15:60734696 A>G maps to NM_024611.4 Y781Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr8:18257899 C>A maps to NM_000015.2 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr8:18258376 T>A maps to NM_000015.2 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L6-01A-11D-A29I-10 chr11:20067063 C>T maps to ENST00000396087 D1273D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr12:78392164 C>G maps to NM_014903.4 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:15372586 C>A maps to NM_015909.2 L2065L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr2:203972653 G>A maps to NM_001114132.1 L535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:204039944 G>T maps to NM_001114132.1 G2104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr3:47036640 G>A maps to NM_015175.1 A472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JD-01A-11D-A29I-10 chr1:148004748 C>T maps to ENST00000310701 L860L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr1:148010971 A>G maps to ENST00000310701 C555C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr1:144821918 A>G did not map to a codon.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr11:113103920 C>G maps to ENST00000316851 A524A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr19:19337772 G>A maps to NM_004386.2 V517V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr12:6639951 G>A maps to NM_014865.3 Q1311Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KT-01A-11D-A29I-10 chr12:6631168 C>A maps to NM_014865.3 I640I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K8-01A-11D-A29I-10 chr9:100396171 G>A maps to NM_002486.4 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr1:36026522 C>A maps to NM_001014839.1 C257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr2:133541905 A>T maps to NM_207363.2 P826P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr19:3198894 C>T maps to NM_020170.3 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr8:71057033 C>T maps to NM_006540.2 Q885Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr12:124856617 A>G maps to NM_006312.4 A919A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr12:124819001 G>C maps to NM_006312.4 A2198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr15:23931488 G>T maps to NM_002487.2 S292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr10:75567678 C>T maps to NM_003635.3 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr4:118975229 C>A maps to NM_004784.2 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr4:115769494 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr4:115773934 C>A maps to NM_022569.1 E588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OF-01A-11D-A29I-10 chr23:119007287 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5JD-01A-11D-A29I-10 chr14:92588001 T>G maps to NM_004545.3 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:47002021 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:47002126 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:152563489 C>A maps to NM_001164507.1 E353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr20:32248097 G>T maps to NM_031232.3 S164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr18:55816790 G>A maps to NM_001144968.1 Q8Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr6:11185652 G>T maps to NM_006403.3 V749V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr22:29885593 A>T maps to NM_021076.3 P655P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr22:29885860 T>C maps to NM_021076.3 A744A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr22:29885593 A>T maps to NM_021076.3 P655P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr22:29885731 A>G maps to NM_021076.3 E701E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr22:29885734 A>C maps to NM_021076.3 A702A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JW-01A-11D-A29I-10 chr22:29885566 A>C maps to NM_021076.3 A646A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr22:29885563 A>G maps to NM_021076.3 E645E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr22:29885593 A>T maps to NM_021076.3 P655P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr22:29885731 A>G maps to NM_021076.3 E701E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr22:29885734 A>C maps to NM_021076.3 A702A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr22:29885593 A>T maps to NM_021076.3 P655P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LL-01A-11D-A29I-10 chr22:29885593 A>T maps to NM_021076.3 P655P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr8:24811263 C>T maps to ENST00000221169 V405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr8:24774958 G>T maps to NM_005382.2 E531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr17:27064882 G>A maps to NM_178170.2 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr11:21250962 C>A maps to NM_006157.3 C504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JT-01A-11D-A29I-10 chr15:73428300 G>T maps to NM_002499.3 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J3-01A-11D-A29I-10 chr1:156640502 C>T maps to NM_006617.1 G1159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr1:156640676 C>T maps to NM_006617.1 P1101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr10:105344755 T>C maps to NM_004210.4 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr10:105330701 G>T maps to NM_004210.4 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr10:105344836 C>A maps to NM_004210.4 I398I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr1:78401560 C>A maps to NM_144573.3 I435I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr17:29560114 G>T maps to NM_001042492.2 E1198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr17:29560225 C>T maps to NM_001042492.2 Q1235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr17:29533325 T>C maps to NM_001042492.2 F443F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr17:29664420 G>T maps to NM_001042492.2 E2155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr17:29662046 C>T maps to NM_001042492.2 Q2002*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr22:30057312 G>A maps to NM_181832.2 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:204937425 C>A maps to ENST00000367172 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:204966445 C>A maps to ENST00000367172 V1084V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LD-01A-11D-A29I-10 chr1:204923328 C>T maps to ENST00000367172 R77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr19:3449046 A>T maps to ENST00000269778 K332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr9:94171972 C>T maps to NM_005384.2 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J2-01A-11D-A29I-10 chr10:104159195 A>G maps to NM_001077494.1 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr10:104159195 A>G maps to NM_001077494.1 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr10:104159195 A>G maps to NM_001077494.1 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr10:104159195 A>G maps to NM_001077494.1 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr10:104159195 A>G maps to NM_001077494.1 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JT-01A-11D-A29I-10 chr10:104159195 A>G maps to NM_001077494.1 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr10:104159415 G>T maps to NM_001077494.1 A470A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr10:104159195 A>G maps to NM_001077494.1 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr10:104159195 A>G maps to NM_001077494.1 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LA-01A-11D-A29I-10 chr10:104159195 A>G maps to NM_001077494.1 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr10:104159195 A>G maps to NM_001077494.1 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr10:104159195 A>G maps to NM_001077494.1 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J2-01A-11D-A29I-10 chr6:44233371 G>A maps to NM_004556.2 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr11:129754658 G>C maps to NM_006165.3 T266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr6:41060790 A>G maps to NM_002505.4 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr17:47584003 C>T maps to NM_002507.3 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr6:18122525 A>G maps to NM_198586.2 H104H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:71354403 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chr14:52520648 G>A maps to NM_007361.3 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:37000490 T>C maps to NM_133433.3 H1107H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr5:36953862 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr3:52522396 G>T maps to NM_007184.3 R963R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:118723943 C>G did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr8:23538991 C>A maps to NM_006167.3 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr17:7318829 C>T maps to NM_020795.2 R346R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr23:5821336 G>A did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr5:65058793 G>A maps to NM_020726.4 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:32477522 C>T maps to NM_021209.4 W76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr16:57060003 G>A maps to NM_032206.3 Q383Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr17:5436274 C>A maps to NM_033004.3 E1055*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LD-01A-11D-A29I-10 chr11:7982582 G>A maps to NM_176821.3 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr19:56410248 G>T maps to NM_176810.2 L948L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr19:55494292 G>A maps to NM_017852.3 K409K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JI-01A-11D-A29I-10 chr19:56369592 T>C maps to NM_134444.4 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr19:56369428 G>T maps to NM_134444.4 E224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr19:56226563 G>C maps to NM_176820.2 V786V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr1:169292365 A>G maps to NM_013330.3 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr2:232393590 C>A maps to NM_006056.4 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:144098646 C>T maps to ENST00000467773 E112E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LD-01A-11D-A29I-10 chr12:132633390 G>C maps to NM_024078.1 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr16:50744556 G>T maps to NM_022162.1 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr9:95077070 G>A maps to NM_017948.5 S612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L3-01A-11D-A29I-10 chr16:14988884 G>T maps to ENST00000456867 G1159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr4:2948137 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chr12:6672531 G>A maps to ENST00000382421 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr17:26089866 T>C maps to NM_000625.4 T919T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr7:150706626 G>A maps to NM_000603.4 A822A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr9:139391449 C>G maps to NM_017617.3 L2247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5H8-01A-11D-A29I-10 chr9:139407931 A>G maps to NM_017617.3 N755N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr19:15292436 T>C maps to NM_000435.2 P914P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr19:15303224 G>A maps to NM_000435.2 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr19:15284880 G>A maps to NM_000435.2 I1578I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:100105368 T>C did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr15:69347713 G>T maps to NM_024505.3 L680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr14:33684462 T>C maps to NM_001164749.1 Y72Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:44579179 G>C maps to NM_013389.2 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr10:72014862 G>A maps to ENST00000277942 S381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr10:72014862 G>A maps to ENST00000277942 S381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr10:72014862 G>A maps to ENST00000277942 S381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr2:110962527 C>T maps to NM_000272.3 Q6Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr17:79577265 C>T maps to NM_017921.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KV-01A-11D-A29I-10 chr5:32712220 C>T maps to ENST00000265074 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr7:34698161 C>G maps to NM_207172.1 Y46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr7:98256609 G>A maps to NM_002523.2 W341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr4:164271439 C>T maps to NM_006174.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr6:3012809 G>T maps to NM_000904.3 G69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr19:50881824 G>A maps to NM_007121.4 Q173Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JD-01A-11D-A29I-10 chr19:50881824 G>A maps to NM_007121.4 Q173Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr19:50881824 G>A maps to NM_007121.4 Q173Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr19:50881824 G>A maps to NM_007121.4 Q173Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J7-01A-11D-A29I-10 chr11:47282858 C>T maps to NM_005693.2 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr12:95434274 C>A maps to NM_003297.2 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr3:15046087 T>C maps to NM_003298.3 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr15:72105934 C>T maps to NM_014249.2 H318H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr19:17343367 G>A maps to NM_005234.3 T336T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr5:142662180 G>A maps to NM_001024094.1 N712N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr2:157185930 G>T maps to NM_006186.3 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JQ-01A-11D-A29I-10 chr10:115375527 C>A maps to ENST00000369358 P1015P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr7:107820769 C>T maps to ENST00000379032 P916P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr8:32620756 A>T maps to NM_001160004.1 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr5:139227531 C>T maps to NM_013982.2 P849P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:105132286 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:105153824 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:105178367 C>G did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:105187992 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:105197069 A>G did not map to a codon.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr23:105142617 A>G did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr23:105132367 G>A did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr23:105153235 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr6:24145936 G>T maps to NM_080723.4 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:50574003 C>T maps to NM_138735.2 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr11:64402916 G>T maps to NM_015080.3 T1137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KW-01A-11D-A29I-10 chr11:64480640 G>A maps to NM_015080.3 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr11:64480640 G>A maps to NM_015080.3 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OF-01A-11D-A29I-10 chr11:64480640 G>A maps to NM_015080.3 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr14:79175582 C>T maps to NM_004796.4 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr5:176687120 C>T maps to NM_022455.4 R1700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JR-01A-11D-A29I-10 chr5:6633041 C>T maps to NM_017755.5 E17E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr5:6633041 C>T maps to NM_017755.5 E17E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KV-01A-11D-A29I-10 chr5:6633041 C>T maps to NM_017755.5 E17E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr17:73127682 T>C maps to NM_014595.1 Q40Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OF-01A-11D-A29I-10 chr17:73127682 T>C maps to NM_014595.1 Q40Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KZ-01A-11D-A29I-10 chr2:18766155 G>T maps to ENST00000455492 S193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr6:86195052 C>A maps to NM_002526.2 G284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr16:15131996 A>T maps to NM_173474.2 L275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J2-01A-11D-A29I-10 chr19:49164951 A>G maps to NM_145807.1 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr19:49164951 A>G maps to NM_145807.1 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J7-01A-11D-A29I-10 chr19:49164951 A>G maps to NM_145807.1 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr19:49164951 A>G maps to NM_145807.1 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr19:49164951 A>G maps to NM_145807.1 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr19:49164951 A>G maps to NM_145807.1 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KW-01A-11D-A29I-10 chr19:49164951 A>G maps to NM_145807.1 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L1-01A-11D-A30A-10 chr19:49164951 A>G maps to NM_145807.1 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr19:49164951 A>G maps to NM_145807.1 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr2:11810117 G>C maps to NM_012344.3 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KV-01A-11D-A29I-10 chr2:11809649 C>G maps to NM_012344.3 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr2:11810063 G>T maps to NM_012344.3 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J2-01A-11D-A29I-10 chr23:51076023 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5JV-01A-11D-A29I-10 chr23:51076023 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:51075871 C>A did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr23:51076023 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr19:33183315 A>G maps to NM_001105570.1 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K8-01A-11D-A29I-10 chr19:33183351 G>C maps to NM_001105570.1 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr11:71718456 G>A maps to ENST00000393695 D1753D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JR-01A-11D-A29I-10 chr11:71717105 G>A maps to ENST00000393695 A1895A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr14:73743996 G>A maps to NM_001005743.1 T415T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr14:73750813 C>T maps to NM_001005743.1 K308K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr19:41175845 G>A maps to NM_004756.3 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr19:41173870 C>T maps to NM_004756.3 Q444Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr19:41173873 T>C maps to NM_004756.3 Q443Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr19:41173882 C>T maps to NM_004756.3 Q440Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L1-01A-11D-A30A-10 chr19:41173885 C>T maps to NM_004756.3 Q439Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L1-01A-11D-A30A-10 chr19:41173897 T>C maps to NM_004756.3 Q435Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr12:69129045 C>T maps to NM_020401.2 A808A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr7:135262570 C>T maps to NM_015135.2 Q226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr3:13368891 G>A maps to NM_024923.2 C1444C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr16:56782299 C>G maps to NM_014669.3 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr11:3752721 G>T maps to NM_016320.4 V543V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:102334158 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:101096061 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5JQ-01A-11D-A29I-10 chr14:24878484 G>A maps to NM_025081.2 P495P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr23:41333839 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr12:113348874 T>G maps to NM_001032409.1 Y163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr12:113442851 C>T maps to NM_016817.2 I431I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr1:228471219 C>T maps to NM_001098623.1 F2918F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr1:228504668 G>A maps to NM_001098623.1 A4515A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr1:228504668 G>A maps to NM_001098623.1 A4515A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:228496915 G>T maps to NM_001098623.1 G4286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr1:228504668 G>A maps to NM_001098623.1 A4515A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chr1:228561681 C>T maps to NM_001098623.1 F7451F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr1:228399798 C>T maps to NM_001098623.1 C105C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr1:228563505 T>C maps to NM_001098623.1 I7589I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LP-01A-11D-A29I-10 chr1:228399798 C>T maps to NM_001098623.1 C105C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LP-01A-11D-A29I-10 chr1:228504668 G>A maps to NM_001098623.1 A4515A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:220435374 G>A maps to NM_015311.2 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr19:17337554 C>A maps to NM_024578.1 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr19:17337554 C>A maps to NM_024578.1 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OF-01A-11D-A29I-10 chr19:17337554 C>A maps to NM_024578.1 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr23:128722896 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr23:128721081 A>G did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr19:474729 G>A maps to NM_182577.2 C6C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J2-01A-11D-A29I-10 chr23:123787621 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:123657284 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:123663786 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:123680873 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:123870852 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr5:167674405 C>T maps to NM_001122679.1 F2145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr5:167617505 A>T maps to NM_001122679.1 K903*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr4:183696222 G>T maps to NM_001080477.1 E1741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr4:183659683 G>T maps to NM_001080477.1 L1122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr4:183721230 C>T maps to NM_001080477.1 Y2609Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr11:78372535 G>A maps to NM_001098816.2 L2503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr7:44714132 C>T maps to ENST00000444676 Y319Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr7:44747185 G>A maps to ENST00000444676 S949S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr20:61443812 C>T maps to NM_007346.2 C282C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:70776863 A>T did not map to a codon.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr13:53624434 C>A maps to NM_006418.3 T354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr13:53603039 G>A maps to NM_006418.3 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr9:127549289 G>T maps to NM_182487.2 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:161989831 C>A maps to ENST00000451379 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr1:59004876 T>C maps to NM_145243.3 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr3:193376762 C>T maps to NM_130837.2 L807L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:29189701 C>A maps to NM_000911.3 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr8:54147370 C>T maps to NM_000912.3 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr8:54163561 C>A maps to NM_000912.3 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L4-01A-11D-A29I-10 chr8:54163561 C>A maps to NM_000912.3 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr8:54163561 C>A maps to NM_000912.3 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LR-01A-11D-A29I-10 chr8:54163561 C>A maps to NM_000912.3 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J2-01A-11D-A29I-10 chr14:22038524 G>T maps to NM_001005465.1 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KT-01A-11D-A29I-10 chr14:22038524 G>T maps to NM_001005465.1 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr19:15905079 C>T maps to NM_001004466.1 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:158435407 C>G maps to NM_001004473.1 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:158390611 G>C maps to NM_001004476.1 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr11:58035111 C>A maps to NM_207374.3 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JD-01A-11D-A29I-10 chr11:58034970 C>T maps to NM_207374.3 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr14:20666483 T>C maps to NM_001005503.1 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr14:19378108 G>C maps to NM_001013354.1 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L1-01A-11D-A30A-10 chr14:19378495 T>C maps to NM_001013354.1 N301N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:248004442 G>T maps to NM_001001959.1 Y252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:248512582 C>A maps to NM_001001918.1 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:248844882 G>A maps to NM_001004734.1 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr17:3101228 G>T maps to NM_012352.1 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JQ-01A-11D-A29I-10 chr19:15198850 A>T maps to NM_001004713.1 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr9:125562550 C>A maps to NM_080859.1 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5H8-01A-11D-A29I-10 chr9:125330324 C>G maps to NM_001004454.1 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr9:125377150 C>T maps to NM_012364.1 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr11:57970676 C>G maps to NM_001004459.1 *326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr7:143826246 G>A maps to NM_001001659.1 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr11:6913107 G>T maps to NM_003700.1 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr11:6942957 C>A maps to NM_001004684.1 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:143657460 C>A maps to NM_012369.2 S133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LD-01A-11D-A29I-10 chr7:143657800 A>G maps to NM_012369.2 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JQ-01A-11D-A29I-10 chr6:29079939 G>A maps to NM_001005216.2 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:248263393 C>G maps to NM_175911.2 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr1:248366791 T>C maps to NM_001004689.1 C141C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:248402253 C>T maps to NM_017504.1 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:248756493 G>T maps to NM_001004693.1 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:248756526 G>T maps to NM_001004693.1 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:248790267 G>T maps to NM_001001964.1 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr1:248813279 C>T maps to NM_001001824.1 Q302Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr1:248525379 C>A maps to NM_001004696.1 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:248525751 C>A maps to NM_001004696.1 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr1:247654467 C>T maps to NM_001004698.2 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr11:55322210 A>G maps to NM_001001920.1 K143K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr11:51515988 C>T maps to NM_001004703.1 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr15:102358850 C>T maps to NM_001001674.1 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr15:22369045 C>T maps to NM_001004719.2 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr14:20295861 C>T maps to NM_001004723.1 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr14:20296518 G>A maps to NM_001004723.1 K304K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr15:22382672 C>A maps to NM_001005241.1 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr11:55405832 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr11:48267185 C>A maps to NM_001004727.1 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr11:4968177 G>T maps to NM_001005329.1 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JR-01A-11D-A29I-10 chr11:4790670 C>T maps to ENST00000380383 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JW-01A-11D-A29I-10 chr11:4903671 C>A maps to NM_001004759.1 C208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JD-01A-11D-A29I-10 chr11:4470955 C>A maps to NM_001005172.2 C129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr11:5809713 C>G maps to NM_001001913.1 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr11:5842284 C>T maps to NM_001005174.1 F240F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr11:5969055 T>C maps to NM_001003443.2 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr11:6023817 G>A maps to NM_001005179.2 Y187Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr11:58206693 C>A maps to NM_001004733.2 G311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr11:58207132 G>A maps to NM_001004733.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr11:58170453 G>A maps to NM_001005469.1 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JH-01A-11D-A30A-10 chr11:55541041 G>A maps to NM_001001967.1 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JT-01A-11D-A29I-10 chr11:55579238 G>A maps to NM_001004738.1 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr11:55595125 G>A maps to NM_001004739.1 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr11:56310505 A>G maps to NM_001005245.1 N76N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr11:56185246 C>A maps to NM_001004744.1 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr14:21109454 C>T maps to NM_001001968.1 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:142749490 T>C maps to NM_001001667.1 F18F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr7:142750330 G>A maps to NM_001001667.1 V298V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr19:14938183 A>G maps to NM_017506.1 Y290Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr19:14938189 A>G maps to NM_017506.1 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JW-01A-11D-A29I-10 chr19:9362063 C>A maps to NM_001079935.1 C115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L4-01A-11D-A29I-10 chr19:9236885 A>G maps to NM_001001958.1 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr11:56058499 G>T maps to NM_001005199.1 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr12:48921822 G>A maps to NM_001005203.2 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:142723926 G>T maps to NM_001001658.1 S98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr16:30964660 C>T maps to NM_152288.2 N128N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr3:125257452 G>A maps to NM_022776.4 N622N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K8-01A-11D-A29I-10 chr18:21752365 A>G maps to NM_080597.2 Y725Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr17:45894627 T>A maps to NM_145798.2 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr8:90937357 A>G maps to NM_001126111.1 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JT-01A-11D-A29I-10 chr23:38260573 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:26696888 G>T maps to NM_194248.2 I1126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr3:161214846 C>T maps to NM_001080440.1 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr4:4228455 G>T maps to NM_177998.1 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr4:4228471 T>C maps to NM_177998.1 E40E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr4:4228455 G>T maps to NM_177998.1 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JQ-01A-11D-A29I-10 chr4:4228471 T>C maps to NM_177998.1 E40E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K8-01A-11D-A29I-10 chr4:4228455 G>T maps to NM_177998.1 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K8-01A-11D-A29I-10 chr4:4228471 T>C maps to NM_177998.1 E40E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr4:4228455 G>T maps to NM_177998.1 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr4:4228455 G>T maps to NM_177998.1 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr4:4228455 G>T maps to NM_177998.1 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr4:4228471 T>C maps to NM_177998.1 E40E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:48814312 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:69282885 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr15:31776738 C>G maps to ENST00000382902 V520V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr1:149939225 T>C maps to NM_020205.2 E165E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr17:1945353 C>A maps to NM_080822.2 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr12:29628091 G>T maps to NM_183378.2 S501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JH-01A-11D-A30A-10 chr1:111957532 C>T maps to ENST00000369728 Q594Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L6-01A-11D-A29I-10 chr1:111957532 C>T maps to ENST00000369728 Q594Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr13:97639826 T>G maps to NM_080818.3 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr17:3592841 G>A maps to ENST00000435558 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr12:121622496 C>A maps to NM_002562.5 S560S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr11:72945488 C>T maps to NM_176071.1 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr23:69478420 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr17:79818286 C>A maps to NM_000918.3 E21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr12:56504464 G>A maps to NM_006191.2 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr20:43550236 C>T maps to NM_001124756.1 A247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr20:43559219 C>T maps to NM_001124756.1 Y364Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr13:25671121 C>T maps to NM_030979.2 Y262Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr13:25671754 G>A maps to NM_030979.2 T473T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr14:23791463 G>A maps to NM_004643.3 E142E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr4:20711304 G>C did not map to a codon.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr11:66001333 C>A maps to NM_018026.2 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr11:47202119 G>A maps to NM_016223.4 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:17575685 G>A maps to NM_016233.2 V18V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr9:138453659 C>T maps to NM_002571.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr8:81905396 A>G maps to NM_018440.3 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr12:103306613 G>T maps to NM_000277.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr5:43556099 C>T maps to NM_006451.4 E89E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KZ-01A-11D-A29I-10 chr2:71417064 G>T maps to NM_020459.1 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr23:110439737 C>T did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr23:110406820 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr20:9543656 C>A maps to NM_177990.2 R499R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LD-01A-11D-A29I-10 chr20:9546652 C>A maps to NM_177990.2 E457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr20:9538345 G>T maps to NM_177990.2 S551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr12:56716449 G>T maps to NM_001127460.2 G866G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JW-01A-11D-A29I-10 chr10:91404831 T>C maps to NM_148977.1 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:2440354 C>A maps to ENST00000425477 A759A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:2445884 C>G maps to ENST00000425477 A473A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:78944446 G>T maps to NM_173797.3 E277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J2-01A-11D-A29I-10 chr5:6753080 C>T maps to NM_006999.4 H455H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr14:73712813 G>T maps to ENST00000427855 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr14:73711366 C>A maps to ENST00000427855 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr14:73711366 C>A maps to ENST00000427855 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr14:97029217 G>C maps to NM_032632.3 L710L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr14:97027049 T>C did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr9:119097158 C>A maps to NM_002581.3 C1139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:176769204 G>T maps to NM_020318.2 V1713V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr10:89469056 C>T maps to NM_001015880.1 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr16:3021278 C>T maps to NM_152341.3 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr3:142681440 G>T maps to NM_198504.2 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr10:34663855 T>A maps to NM_019619.3 G538G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr2:206364736 T>C maps to ENST00000406610 S1054S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr10:51040917 C>A maps to NM_003631.2 E860*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr4:75938040 C>A maps to NM_015393.3 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LD-01A-11D-A29I-10 chr23:150840184 T>C did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:242066762 C>A maps to ENST00000358649 E523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr22:31740472 C>T maps to NM_014323.2 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr10:102568923 C>T maps to NM_003987.3 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:19018405 G>T maps to NM_002584.2 E249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr14:37135760 C>T maps to NM_006194.3 N242N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr7:154760665 C>A maps to NM_007349.3 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr3:52584593 T>A maps to ENST00000296302 P1580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr6:32157638 C>T maps to NM_002586.4 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L1-01A-11D-A30A-10 chr9:128724399 C>T maps to ENST00000373487 N364N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr11:66631379 G>A maps to NM_022172.2 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr5:134296369 G>A maps to NM_032151.4 *131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr4:134071921 G>A maps to NM_032961.1 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr4:134073850 C>A maps to NM_032961.1 P852P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr4:134072248 T>C maps to NM_032961.1 Y318Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr23:91090884 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5JW-01A-11D-A29I-10 chr23:91132450 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:91132645 T>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:91133491 C>G did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:91133562 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:91873457 G>C did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:91873487 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr23:91132407 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr10:55582280 G>A maps to NM_001142763.1 A1742A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr4:138442413 A>G maps to NM_019035.3 S1059S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr4:138452024 T>C maps to NM_019035.3 K406K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:99661492 G>C did not map to a codon.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr4:30725206 C>A maps to NM_001173523.1 P721P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr4:30724204 C>A maps to NM_001173523.1 A387A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:140167126 C>T maps to NM_018900.2 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr5:140237078 C>T maps to NM_018901.2 D482D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J3-01A-11D-A29I-10 chr5:140255098 G>C maps to NM_018903.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr5:140256781 C>T maps to NM_018903.2 G575G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr5:140255506 T>A maps to NM_018903.2 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:140181420 A>T maps to NM_018906.2 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L4-01A-11D-A29I-10 chr5:140182623 G>T maps to NM_018906.2 G614G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:140187137 G>A maps to NM_018907.2 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr5:140215776 C>T maps to NM_018910.2 Y603Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:140573564 G>T maps to NM_018930.3 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr5:140595248 T>G maps to NM_018933.2 S518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:140595008 C>G maps to NM_018933.2 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr5:140594582 T>C maps to NM_018933.2 N296N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr5:140595599 G>C maps to NM_018933.2 A635A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:140604120 C>A maps to NM_018934.2 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:140625196 C>A maps to NM_018935.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:140562214 C>T maps to NM_020957.1 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:140562793 A>T maps to NM_020957.1 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr5:140476410 A>C maps to NM_018936.2 A679A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr5:140476410 A>C maps to NM_018936.2 A679A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr5:140482311 A>G maps to NM_018937.2 A693A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PA-A5YG-01A-11D-A29I-10 chr5:140482341 T>C maps to NM_018937.2 F703F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JT-01A-11D-A29I-10 chr5:140503193 G>A maps to NM_018938.2 P538P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr5:140515675 G>A maps to NM_015669.2 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr5:140516393 C>T maps to NM_015669.2 R460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr5:140516905 C>T maps to NM_015669.2 S630S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr5:140531247 C>T maps to NM_018939.2 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr5:140531451 G>A maps to NM_018939.2 A538A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr5:140553993 G>T maps to NM_018940.2 A526A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr5:140559513 G>A maps to NM_019120.2 E633E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:140725477 G>T maps to NM_018916.3 V626V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr5:140725294 C>T maps to NM_018916.3 P565P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr5:140724076 C>T maps to NM_018916.3 D159D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J2-01A-11D-A29I-10 chr5:140736326 C>T maps to NM_018917.2 F520F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:140745588 C>T maps to NM_018918.2 Y564Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr5:140764325 G>T maps to NM_018920.2 G620G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:140762549 A>G maps to NM_018920.2 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr5:140774155 G>A maps to NM_032088.1 V592V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:140782719 C>T maps to NM_018921.2 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LL-01A-11D-A29I-10 chr5:140731779 C>T maps to NM_018922.2 S651S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr5:140799543 G>A maps to NM_018927.2 A706A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr5:140865108 C>T maps to NM_018928.2 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr13:113839828 C>A maps to ENST00000246505 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr20:56139390 G>T maps to NM_002591.3 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr14:24568381 C>T maps to NM_004563.2 C263C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr8:17796409 A>T maps to NM_006197.3 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr8:52744111 G>T maps to NM_052937.2 R200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L1-01A-11D-A30A-10 chr21:47851795 G>A maps to NM_006031.5 A2806A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr21:47836749 T>C maps to NM_006031.5 A2306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr21:47858132 T>C maps to NM_006031.5 N3052N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr14:71575456 G>A maps to NM_014982.2 V2146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr1:233225847 T>C maps to NM_014801.3 T1345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr11:65387377 T>A maps to NM_032223.2 A661A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr11:65386302 G>C maps to NM_032223.2 R490R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr15:101922385 C>G maps to NM_002570.3 V480V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chr15:101922322 A>G maps to NM_002570.3 C501C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JW-01A-11D-A29I-10 chr11:117077033 A>G maps to NM_004716.2 T679T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr23:24593414 C>G did not map to a codon.
Sequencing variant TCGA-OR-A5L3-01A-11D-A29I-10 chr3:33877675 C>T maps to NM_001162429.1 D330D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr2:101192891 C>T maps to NM_024065.4 D218D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KW-01A-11D-A29I-10 chr2:178762823 T>C maps to NM_016953.3 E421E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr2:183088595 C>T maps to NM_005019.3 Q273Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr12:54967208 T>C maps to NM_000924.3 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr12:20523172 G>T maps to NM_000921.3 E319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr19:10574512 C>A maps to NM_001111307.1 T596T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr19:10578110 G>A maps to NM_001111307.1 R825R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:58270493 C>A maps to NM_001104631.1 T809T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:144854655 C>A maps to NM_014644.4 G2272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:144871771 G>T maps to NM_014644.4 G1730G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:149505086 G>C maps to NM_002609.3 G576G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr4:96762413 A>G maps to NM_005390.4 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr16:335178 G>C maps to NM_006849.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr16:20376739 A>T did not map to a codon.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr23:24517000 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr4:186427747 G>T maps to NM_014476.4 R241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr5:131607852 G>A maps to NM_003687.3 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr4:95497185 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr5:176916509 C>T maps to NM_005451.3 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr4:39868539 A>G maps to NM_001100399.1 L861L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr13:33232434 A>G maps to ENST00000400481 Q124Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr20:1961121 G>T maps to NM_024411.4 Y204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr23:69508313 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5JD-01A-11D-A29I-10 chr5:32074508 G>A maps to NM_178140.2 T1099T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr11:119057342 G>T maps to ENST00000392817 G158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr23:153073941 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5JD-01A-11D-A29I-10 chr1:160182973 A>C maps to ENST00000368075 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr2:216930059 C>A maps to NM_018441.5 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr11:66243097 C>T maps to NM_145065.2 D290D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:7869981 C>A maps to ENST00000377532 Y424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr4:152638109 C>T maps to NM_004564.2 K186K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr7:92134187 G>A maps to NM_000466.2 T643T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:2341849 C>T maps to NM_153818.1 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LD-01A-11D-A29I-10 chr2:61275820 C>T maps to NM_002618.3 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr1:10596340 C>T maps to NM_004565.2 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr12:7356125 T>G maps to NM_001131023.1 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr6:42946489 C>A maps to NM_000287.3 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JI-01A-11D-A29I-10 chr6:42946489 C>A maps to NM_000287.3 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr6:42946489 C>A maps to NM_000287.3 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JW-01A-11D-A29I-10 chr6:42946489 C>A maps to NM_000287.3 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr6:42946489 C>A maps to NM_000287.3 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr6:42946489 C>A maps to NM_000287.3 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr6:42946489 C>A maps to NM_000287.3 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr6:42946489 C>A maps to NM_000287.3 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr6:42946489 C>A maps to NM_000287.3 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr4:74847661 G>A maps to NM_002619.2 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L3-01A-11D-A29I-10 chr4:74846971 G>A maps to NM_002619.2 D85D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr21:45736188 C>T maps to NM_002626.4 N270N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr11:61018641 C>T maps to ENST00000422676 N352N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr12:133294106 G>T maps to NM_001170543.1 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr2:197707447 G>C maps to NM_024989.3 S876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr1:249211952 G>C maps to NM_170725.2 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr15:34396375 C>T maps to NM_152595.4 Y548Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:230468645 C>T maps to ENST00000321327 W436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr1:230492645 T>C maps to ENST00000321327 Q281Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr6:49754246 T>C maps to NM_138733.4 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JD-01A-11D-A29I-10 chr19:17622613 C>T maps to NM_012088.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JQ-01A-11D-A29I-10 chr19:17622613 C>T maps to NM_012088.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr19:17622613 C>T maps to NM_012088.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr19:17622613 C>T maps to NM_012088.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KW-01A-11D-A29I-10 chr19:17622613 C>T maps to NM_012088.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chr19:17622613 C>T maps to NM_012088.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr19:17622613 C>T maps to NM_012088.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr19:17622613 C>T maps to NM_012088.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr19:17622613 C>T maps to NM_012088.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr19:15586649 C>G maps to NM_052890.3 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L1-01A-11D-A30A-10 chr1:153309753 G>A maps to NM_020393.2 G282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr9:70972108 C>T maps to NM_021965.3 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:118370646 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:118374360 G>C did not map to a codon.
Sequencing variant TCGA-PA-A5YG-01A-11D-A29I-10 chr23:118370383 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5LL-01A-11D-A29I-10 chr5:125939824 G>A maps to NM_032177.3 E220E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr12:9085174 C>A maps to ENST00000433083 I469I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J1-01A-11D-A29I-10 chr1:33820014 C>T maps to ENST00000419414 P515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr23:22117126 G>C did not map to a codon.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr5:133896520 T>C maps to ENST00000448712 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr5:133896568 C>T maps to ENST00000448712 C218C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr6:64395053 C>T maps to NM_015153.2 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr23:133547877 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:18911674 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:18942241 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr7:56149872 G>A maps to NM_006213.3 Y207Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr11:118495741 C>T maps to NM_015157.2 R150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OF-01A-11D-A29I-10 chr11:118509667 A>G maps to NM_015157.2 E865E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr3:111632245 C>T maps to NM_001134438.1 T472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr19:44005885 C>T maps to NM_198850.3 Q178Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JQ-01A-11D-A29I-10 chr11:71954892 G>A maps to NM_005169.3 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr11:598467 G>A maps to ENST00000264555 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr7:77579100 C>A maps to ENST00000427986 S689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L9-01A-11D-A29I-10 chr10:99410789 T>C maps to ENST00000416867 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr22:21172827 C>A maps to NM_058004.2 E209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:145579295 C>T maps to NM_006099.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr1:27121403 G>A maps to NM_017837.2 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr10:98380276 C>T maps to NM_152309.2 S591S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr12:18435176 C>T maps to NM_004570.4 Y54Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr12:18491452 C>T maps to NM_004570.4 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr18:39567810 A>G maps to ENST00000398870 K189K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:106509034 C>A maps to NM_002649.2 G343G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr7:106508800 A>G maps to NM_002649.2 Q265Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr5:67522733 T>C maps to ENST00000396611 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr17:8741936 G>T maps to NM_001010855.2 R45R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr23:71417262 C>G did not map to a codon.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr1:20960229 C>T maps to NM_032409.2 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr1:20960229 C>T maps to NM_032409.2 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr1:20960229 C>T maps to NM_032409.2 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J2-01A-11D-A29I-10 chr7:77011933 A>G maps to NM_017439.3 H161H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:142836632 C>A maps to NM_002652.2 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JI-01A-11D-A29I-10 chr17:1465836 C>T maps to ENST00000313486 E6E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LA-01A-11D-A29I-10 chr12:123471093 G>A maps to NM_020845.2 H1205H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr10:3214936 G>A maps to ENST00000380989 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr8:22147805 G>T maps to NM_001135721.1 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr11:94340768 C>T maps to NM_152431.2 C601C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr16:2140476 G>A maps to NM_001009944.2 L4085L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr16:2167873 G>A maps to NM_001009944.2 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K8-01A-11D-A29I-10 chr16:2156446 G>A maps to NM_001009944.2 L2481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr16:2156446 G>A maps to NM_001009944.2 L2481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L6-01A-11D-A29I-10 chr16:2140971 G>A maps to NM_001009944.2 R3972R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr16:2156446 G>A maps to NM_001009944.2 L2481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr16:2140911 G>C maps to NM_001009944.2 A3992A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr7:47930171 C>A maps to NM_138295.3 V881V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr7:47897370 A>G maps to NM_138295.3 H1474H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr16:81232404 A>G maps to NM_052892.3 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr16:81199552 G>T maps to NM_052892.3 R1037R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr16:81164208 G>A maps to NM_052892.3 Y1966Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr4:88996107 C>T maps to NM_000297.2 A889A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr22:46658469 C>G maps to NM_006071.1 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr6:51512886 A>G maps to NM_138694.3 P3780P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr6:51920446 G>A maps to NM_138694.3 R592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr6:51774096 C>A maps to NM_138694.3 L2222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr6:51890569 G>A maps to NM_138694.3 N1346N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr6:51695743 A>C maps to NM_138694.3 P2739P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr8:110464350 A>T did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr8:110457218 T>A maps to ENST00000426474 Y1707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr16:3024608 G>A maps to NM_004203.4 H307H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr19:14552019 C>T maps to NM_213560.1 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr19:14552086 C>T maps to NM_213560.1 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr9:131469665 A>T maps to NM_013355.3 K273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr12:32996206 G>A maps to NM_004572.3 G473G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr1:20501581 G>A maps to NM_001105572.1 R36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr19:48601408 C>T maps to NM_003706.2 E185E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr15:42364532 G>A maps to NM_178034.3 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:20416345 C>T maps to NM_000929.2 Q84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr2:160885415 G>A maps to NM_007366.4 H300H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LP-01A-11D-A29I-10 chr21:42551431 T>A maps to NM_182832.2 R42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr2:28827532 C>T maps to NM_153021.4 R956R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr12:113812651 C>A maps to NM_173542.3 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr20:8770165 G>T maps to NM_015192.2 E1094*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J1-01A-11D-A29I-10 chr15:40587140 C>T maps to NM_004573.2 T634T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr20:9353693 C>T maps to NM_001172646.1 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr20:9417683 A>G maps to NM_001172646.1 K883K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J3-01A-11D-A29I-10 chr3:38050644 G>A maps to NM_001130964.1 N558N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr2:219498431 C>T maps to ENST00000432688 Y550Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr10:96084320 G>A maps to ENST00000371380 V2239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr20:39794148 C>A maps to NM_002660.2 T523T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr16:81929526 C>G maps to NM_002661.2 T396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr8:144990527 A>G maps to NM_201380.2 A4624A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr8:144998513 C>T maps to NM_201380.2 A1998A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr8:144997022 C>T maps to NM_201380.2 A2495A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr8:144996262 G>A maps to NM_201380.2 L2713L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr8:144998513 C>T maps to NM_201380.2 A1998A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr8:144998792 C>T maps to NM_201380.2 L1905L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JH-01A-11D-A30A-10 chr8:145001783 A>G maps to NM_201380.2 L1321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JI-01A-11D-A29I-10 chr8:144998189 A>G maps to NM_201380.2 A2106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr8:144998168 C>T maps to NM_201380.2 A2113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JL-01A-11D-A29I-10 chr8:144998513 C>T maps to NM_201380.2 A1998A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JL-01A-11D-A29I-10 chr8:145001783 A>G maps to NM_201380.2 L1321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JR-01A-11D-A29I-10 chr8:144990527 A>G maps to NM_201380.2 A4624A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JV-01A-11D-A29I-10 chr8:145001783 A>G maps to NM_201380.2 L1321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JX-01A-11D-A29I-10 chr8:144999416 C>T maps to NM_201380.2 A1697A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr8:144998168 C>T maps to NM_201380.2 A2113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr8:144998189 A>G maps to NM_201380.2 A2106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr8:144990527 A>G maps to NM_201380.2 A4624A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr8:144998189 A>G maps to NM_201380.2 A2106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr8:144999416 C>T maps to NM_201380.2 A1697A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr8:145001783 A>G maps to NM_201380.2 L1321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr8:144994966 G>A maps to NM_201380.2 R3145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr8:144998168 C>T maps to NM_201380.2 A2113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr8:145001783 A>G maps to NM_201380.2 L1321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr8:144998168 C>T maps to NM_201380.2 A2113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr8:144998189 A>G maps to NM_201380.2 A2106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr8:144998368 T>A maps to NM_201380.2 K2047*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K8-01A-11D-A29I-10 chr8:144998168 C>T maps to NM_201380.2 A2113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K8-01A-11D-A29I-10 chr8:144998189 A>G maps to NM_201380.2 A2106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K8-01A-11D-A29I-10 chr8:144998867 C>T maps to NM_201380.2 A1880A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr8:144998189 A>G maps to NM_201380.2 A2106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr8:145001783 A>G maps to NM_201380.2 L1321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr8:144991253 G>A maps to NM_201380.2 S4382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr8:144998168 C>T maps to NM_201380.2 A2113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr8:144998189 A>G maps to NM_201380.2 A2106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr8:144999416 C>T maps to NM_201380.2 A1697A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr8:145001783 A>G maps to NM_201380.2 L1321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr8:144992384 G>A maps to NM_201380.2 D4005D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr8:144998189 A>G maps to NM_201380.2 A2106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KV-01A-11D-A29I-10 chr8:145001783 A>G maps to NM_201380.2 L1321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KW-01A-11D-A29I-10 chr8:144990527 A>G maps to NM_201380.2 A4624A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KW-01A-11D-A29I-10 chr8:144999416 C>T maps to NM_201380.2 A1697A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chr8:144999416 C>T maps to NM_201380.2 A1697A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr8:144998168 C>T maps to NM_201380.2 A2113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr8:144998189 A>G maps to NM_201380.2 A2106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr8:145001783 A>G maps to NM_201380.2 L1321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L3-01A-11D-A29I-10 chr8:144990527 A>G maps to NM_201380.2 A4624A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L3-01A-11D-A29I-10 chr8:144999416 C>T maps to NM_201380.2 A1697A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L4-01A-11D-A29I-10 chr8:144999416 C>T maps to NM_201380.2 A1697A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L9-01A-11D-A29I-10 chr8:144990395 G>T maps to NM_201380.2 Y4668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L9-01A-11D-A29I-10 chr8:144998513 C>T maps to NM_201380.2 A1998A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LA-01A-11D-A29I-10 chr8:144998189 A>G maps to NM_201380.2 A2106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LA-01A-11D-A29I-10 chr8:145001783 A>G maps to NM_201380.2 L1321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LD-01A-11D-A29I-10 chr8:145001783 A>G maps to NM_201380.2 L1321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LR-01A-11D-A29I-10 chr8:144992387 G>A maps to NM_201380.2 D4004D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr8:145001783 A>G maps to NM_201380.2 L1321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J2-01A-11D-A29I-10 chr14:67878764 G>A maps to NM_016445.1 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JW-01A-11D-A29I-10 chr1:204242837 A>C maps to ENST00000367191 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr19:30165468 G>A maps to ENST00000436066 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr14:65209937 C>G maps to ENST00000394691 S1059S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr1:6534210 A>G maps to NM_198681.2 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr1:6529190 C>T maps to NM_198681.2 E797E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr12:6426578 G>A maps to NM_001144856.1 Q289Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr12:6424202 G>A maps to NM_001144856.1 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L1-01A-11D-A30A-10 chr17:43552920 C>T maps to NM_014798.2 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr6:161134146 T>A maps to NM_000301.3 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KW-01A-11D-A29I-10 chr15:90209134 G>A maps to NM_002666.4 F416F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L9-01A-11D-A29I-10 chr15:90209134 G>A maps to NM_002666.4 F416F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr17:7297120 G>A maps to NM_020360.2 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr3:126733328 C>T maps to NM_032242.3 P871P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr3:126733052 C>T maps to NM_032242.3 R813R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr3:126733052 C>T maps to NM_032242.3 R813R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr3:126733052 C>T maps to NM_032242.3 R813R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KV-01A-11D-A29I-10 chr3:126733052 C>T maps to NM_032242.3 R813R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr3:126733052 C>T maps to NM_032242.3 R813R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KZ-01A-11D-A29I-10 chr1:208202215 G>C maps to NM_025179.3 L1799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KZ-01A-11D-A29I-10 chr23:153694333 C>G did not map to a codon.
Sequencing variant TCGA-OR-A5LA-01A-11D-A29I-10 chr23:153694333 C>G did not map to a codon.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr23:153689642 G>A did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr23:153689659 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:131865383 G>T maps to NM_020911.1 L1200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:131912279 C>G maps to NM_020911.1 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr22:50722600 G>A maps to NM_012401.2 Y741Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr23:153042766 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:153042777 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5JD-01A-11D-A29I-10 chr23:153035384 G>C did not map to a codon.
Sequencing variant TCGA-OR-A5JH-01A-11D-A30A-10 chr23:153032638 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr23:153032898 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:153033265 G>C did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:153035683 A>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:153036069 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:153036422 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:153042415 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr15:74315307 C>T maps to NM_033238.2 Q248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LL-01A-11D-A29I-10 chr15:74335394 C>T maps to NM_033238.2 T592T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr7:6022453 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr7:6042242 G>A maps to NM_000535.5 H126H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr7:6026766 G>A maps to NM_000535.5 D543D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:152936620 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5J7-01A-11D-A29I-10 chr19:50370407 T>C maps to NM_007254.3 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr19:50370407 T>C maps to NM_007254.3 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chr19:50370407 T>C maps to NM_007254.3 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr19:50370407 T>C maps to NM_007254.3 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LP-01A-11D-A29I-10 chr19:50370407 T>C maps to NM_007254.3 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr10:118318730 T>G maps to NM_000936.2 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:152226030 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:152226511 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:152226744 G>C did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:152159411 G>C did not map to a codon.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr19:46997222 G>A maps to NM_020709.1 N500N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LR-01A-11D-A29I-10 chr6:36260857 C>T maps to ENST00000457797 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr23:7890070 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr19:7615941 G>A maps to NM_001166111.1 L720L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr7:108112845 C>T maps to NM_015723.2 *783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LL-01A-11D-A29I-10 chr3:127379707 C>T maps to NM_015720.2 F279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr21:46707761 G>A maps to NM_133635.4 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr19:50918778 C>T maps to ENST00000391817 I909I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr12:133219830 T>C maps to ENST00000455752 A1513A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JD-01A-11D-A29I-10 chr17:7399865 G>A maps to NM_000937.4 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KT-01A-11D-A29I-10 chr17:7412402 T>C maps to NM_000937.4 F1202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JQ-01A-11D-A29I-10 chr19:622325 C>G maps to NM_005035.3 A558A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:53103414 G>A maps to NM_182595.3 K17K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:53103438 C>A maps to NM_182595.3 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr3:119379039 A>G maps to NM_022135.2 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr23:48368342 C>G did not map to a codon.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr7:124491966 G>T maps to NM_015450.2 S303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr14:19573145 T>C did not map to a codon.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr22:16287621 A>G maps to NM_001136213.1 D88D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JX-01A-11D-A29I-10 chr19:42603759 C>T maps to ENST00000342301 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr11:120180234 G>A maps to NM_014352.2 E336E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J2-01A-11D-A29I-10 chr6:99283375 T>G maps to NM_005604.2 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J3-01A-11D-A29I-10 chr6:99283375 T>G maps to NM_005604.2 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr6:99283375 T>G maps to NM_005604.2 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr6:99283375 T>G maps to NM_005604.2 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr6:99283375 T>G maps to NM_005604.2 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JR-01A-11D-A29I-10 chr6:99283375 T>G maps to NM_005604.2 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr6:99283375 T>G maps to NM_005604.2 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr6:99283375 T>G maps to NM_005604.2 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr6:99283375 T>G maps to NM_005604.2 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KT-01A-11D-A29I-10 chr6:99283375 T>G maps to NM_005604.2 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr6:99283375 T>G maps to NM_005604.2 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr2:105472054 T>C maps to NM_006236.1 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr2:105472054 T>C maps to NM_006236.1 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr2:105473179 C>A maps to NM_006236.1 G404G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr13:79176515 C>A maps to NM_006237.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr8:128428182 G>T maps to NM_001159542.1 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr8:128428588 C>T maps to NM_001159542.1 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PA-A5YG-01A-11D-A29I-10 chr8:128428620 C>A maps to NM_001159542.1 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr7:39243894 G>A maps to NM_007252.3 Q84Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr9:134183370 G>A maps to NM_032728.3 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LR-01A-11D-A29I-10 chr9:134165545 C>T maps to NM_032728.3 D54D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr6:35388051 G>T maps to NM_006238.4 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr23:18822064 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr11:70228236 G>A maps to NM_003626.2 R1198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr1:203025514 C>A maps to ENST00000367238 R686R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr6:149862717 G>T maps to NM_139126.2 C25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:102508857 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr16:4935145 C>T maps to NM_002705.4 V1170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr11:73957233 A>G maps to NM_016147.1 K316K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr12:111160002 G>A maps to NM_002710.2 C273C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J3-01A-11D-A29I-10 chr19:55628608 A>G maps to NM_017607.2 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr19:55628608 A>G maps to NM_017607.2 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KV-01A-11D-A29I-10 chr19:55628608 A>G maps to NM_017607.2 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr19:55628608 A>G maps to NM_017607.2 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr14:104205312 G>A maps to NM_015316.2 H880H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr14:104206355 G>A maps to NM_015316.2 P799P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr19:45900157 C>G maps to NM_001142502.1 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L9-01A-11D-A29I-10 chr19:49377872 G>A maps to NM_014330.3 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr7:113519564 C>A maps to NM_002711.3 E528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr23:49126713 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:49142337 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr23:299593 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:322315 G>A did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr23:299352 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr14:94741741 C>T maps to NM_058237.1 S827S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JI-01A-11D-A29I-10 chr9:127951862 G>A maps to NM_001123355.1 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LR-01A-11D-A29I-10 chr22:41997127 G>T maps to NM_015704.2 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J3-01A-11D-A29I-10 chr5:64878974 T>A maps to NM_015342.2 P487P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:48929616 C>G did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr19:8563980 A>G maps to NM_032152.4 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr22:22890509 G>T maps to NM_206954.1 C503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr22:22890728 G>T maps to NM_206954.1 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:12854330 G>C maps to NM_023013.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:12854134 G>A maps to NM_023013.2 W120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr1:12920066 C>G maps to NM_023014.1 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr12:11461595 T>G maps to NM_002723.3 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr11:45204460 C>A maps to NM_020229.2 G125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr9:133556749 G>A maps to NM_021619.2 T266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr9:133553992 C>T maps to NM_021619.2 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr9:133556767 G>A maps to NM_021619.2 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr8:70981759 C>A maps to NM_024504.2 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr8:70981594 G>A maps to NM_024504.2 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr1:3329262 C>T maps to NM_022114.3 G834G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr1:3329262 C>T maps to NM_022114.3 G834G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:3328611 G>C maps to NM_022114.3 T617T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr12:108145669 G>A maps to NM_012406.3 D216D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:23524574 C>A maps to NM_020227.2 Y361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr1:203452908 C>T maps to NM_201348.1 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:203452437 C>A maps to NM_201348.1 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:203452761 C>T maps to NM_201348.1 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr8:69069639 G>T maps to NM_024870.2 E1439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr8:69020558 G>A maps to NM_024870.2 S977S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr20:62198661 A>G maps to NM_001037335.2 Y683Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KT-01A-11D-A29I-10 chr3:64133072 G>A maps to NM_198859.3 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr3:64133283 C>T maps to NM_198859.3 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J1-01A-11D-A29I-10 chr6:57393111 T>C maps to NM_000947.2 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:84649725 A>T maps to NM_182948.2 K129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr9:71628333 T>C maps to NM_002732.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr17:66526419 G>T maps to NM_212472.1 E326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr17:66519040 G>T maps to NM_212472.1 E108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr17:66521051 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr17:64731689 C>T maps to NM_002737.2 D380D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr11:6341364 C>T maps to NM_145040.2 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr10:6521127 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5JR-01A-11D-A29I-10 chr19:11558366 G>A maps to ENST00000436195 E321E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JV-01A-11D-A29I-10 chr19:11558366 G>A maps to ENST00000436195 E321E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KT-01A-11D-A29I-10 chr19:11558366 G>A maps to ENST00000436195 E321E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr1:2103505 C>G maps to NM_002744.4 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr2:37543586 A>T maps to NM_005813.3 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr8:48790324 C>A maps to NM_006904.6 E1774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr8:48689403 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr4:82125943 C>A maps to NM_006259.1 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr6:22294739 G>T maps to ENST00000397199 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr10:120353661 G>C maps to NM_004248.2 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J7-01A-11D-A29I-10 chr4:148605039 C>T maps to NM_138364.2 E33E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr21:48068518 G>A maps to NM_206962.1 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr3:71834134 G>T maps to NM_001126128.1 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr3:71834119 G>C maps to NM_001126128.1 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr20:5283021 C>A maps to NM_144773.2 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr11:60666650 G>A maps to NM_014502.4 G318G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:150298335 A>G maps to NM_004698.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr6:4037634 C>T maps to NM_003913.4 R415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr23:106890919 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr6:166720805 G>C maps to NM_175922.3 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JX-01A-11D-A29I-10 chr6:166720805 G>C maps to NM_175922.3 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr6:166720805 G>C maps to NM_175922.3 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr6:166720805 G>C maps to NM_175922.3 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr6:166720805 G>C maps to NM_175922.3 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr19:42814035 C>T maps to NM_199285.2 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr2:240982102 A>G maps to NM_001080835.1 H99H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr3:138725071 C>A maps to NM_001134659.1 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr3:138739401 G>A maps to NM_001013650.2 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr3:138762922 G>C maps to NM_001134657.1 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr23:150869180 C>T did not map to a codon.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr3:9988096 G>A maps to NM_207351.3 R920R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr16:2903973 G>A maps to NM_022119.3 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr16:31143830 G>A maps to NM_002773.3 D208D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr15:56032849 T>A maps to NM_173814.4 K43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5H8-01A-11D-A29I-10 chr9:79318584 G>C maps to NM_015225.2 A2648A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LL-01A-11D-A29I-10 chr9:80919785 T>G maps to ENST00000421149 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JT-01A-11D-A29I-10 chr5:139197104 T>C maps to NM_032289.2 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JT-01A-11D-A29I-10 chr2:113956370 G>C maps to NM_012455.2 T893T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J3-01A-11D-A29I-10 chr1:227077808 C>T maps to ENST00000391872 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr19:43772122 C>T maps to NM_002784.3 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr8:87076708 G>T maps to ENST00000276616 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr15:78838003 G>A maps to NM_002789.4 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr17:61905532 C>A maps to NM_002805.5 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KV-01A-11D-A29I-10 chr17:38144958 G>T maps to NM_002809.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr2:54152699 G>A maps to NM_014614.2 T595T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J1-01A-11D-A29I-10 chr1:11561525 G>A maps to NM_020780.1 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr1:71512492 C>T maps to ENST00000354608 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J3-01A-11D-A29I-10 chr19:47127323 C>G maps to NM_000960.3 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J7-01A-11D-A29I-10 chr19:47127323 C>G maps to NM_000960.3 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr19:47127323 C>G maps to NM_000960.3 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr19:47127323 C>G maps to NM_000960.3 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JQ-01A-11D-A29I-10 chr19:47127323 C>G maps to NM_000960.3 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JR-01A-11D-A29I-10 chr19:47127323 C>G maps to NM_000960.3 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr19:47127323 C>G maps to NM_000960.3 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr19:47127323 C>G maps to NM_000960.3 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KW-01A-11D-A29I-10 chr19:47127323 C>G maps to NM_000960.3 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr19:47127323 C>G maps to NM_000960.3 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LP-01A-11D-A29I-10 chr19:47127323 C>G maps to NM_000960.3 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr9:125154576 G>T maps to NM_000962.2 G518G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LD-01A-11D-A29I-10 chr3:46943320 C>A maps to NM_000316.2 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr8:141749129 G>A maps to NM_005607.4 D626D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:136912823 T>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:32374452 C>T maps to NM_080391.3 *168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr3:123247280 C>T maps to NM_198402.3 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LL-01A-11D-A29I-10 chr11:47587389 C>T maps to NM_001143984.1 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LR-01A-11D-A29I-10 chr11:47587368 C>T maps to NM_001143984.1 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr4:87643505 C>T maps to NM_080685.2 I509I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr11:18765654 C>T maps to NM_032781.3 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr12:7060781 C>T maps to ENST00000416215 R9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L6-01A-11D-A29I-10 chr20:2945573 C>G maps to NM_002836.3 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr1:198711466 C>A maps to ENST00000271610 R890R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JI-01A-11D-A29I-10 chr9:8485822 C>T maps to NM_002839.3 T998T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr10:129839225 C>T maps to NM_006504.4 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr10:129871713 G>A maps to NM_006504.4 T526T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr1:44057522 G>A maps to NM_002840.3 S524S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L6-01A-11D-A29I-10 chr1:44057030 A>G maps to NM_002840.3 G446G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr11:48161170 G>A maps to NM_002843.3 A762A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:220159707 C>T maps to NM_002846.3 L888L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr19:5206811 G>A maps to NM_002850.3 L1940L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr19:5244044 G>A maps to NM_002850.3 N479N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr20:40713386 G>A maps to ENST00000373198 V1379V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:121624142 C>G maps to NM_002851.2 Y300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr12:44142371 C>A maps to NM_031292.3 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr21:45548438 G>A maps to NM_005049.2 G839G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr10:134219065 G>C maps to NM_138499.3 V354V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr10:134219044 C>T maps to NM_138499.3 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L3-01A-11D-A29I-10 chr10:134219035 G>A maps to NM_138499.3 E344E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L3-01A-11D-A29I-10 chr10:134219044 C>T maps to NM_138499.3 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr10:134219044 C>T maps to NM_138499.3 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr10:134219065 G>C maps to NM_138499.3 V354V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LP-01A-11D-A29I-10 chr10:134219044 C>T maps to NM_138499.3 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr10:134219476 G>A maps to NM_138499.3 G491G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr8:52321747 G>A maps to NM_144651.4 H812H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr12:133264331 C>T maps to NM_018663.1 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OF-01A-11D-A29I-10 chr12:133264331 C>T maps to NM_018663.1 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OF-01A-11D-A29I-10 chr20:25276296 G>A maps to NM_002862.3 Q790Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr11:64518842 G>A maps to NM_005609.2 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr20:3145552 G>A maps to NM_014731.2 P523P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L3-01A-11D-A29I-10 chr20:42966024 T>C maps to NM_178491.2 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr22:23503120 G>A maps to NM_004914.2 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LP-01A-11D-A29I-10 chr22:23503120 G>A maps to NM_004914.2 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr17:72740493 C>T maps to NM_001006638.2 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:102755187 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5JT-01A-11D-A29I-10 chr23:102192302 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr3:128840320 C>T maps to NM_198490.1 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JV-01A-11D-A29I-10 chr1:174210749 G>A maps to NM_014857.3 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JX-01A-11D-A29I-10 chr12:50400411 G>A maps to NM_013277.3 I31I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr5:34913588 G>C maps to NM_002853.3 S98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr5:68684967 A>T maps to NM_133339.1 S345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr19:13063540 G>A maps to NM_005053.2 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L3-01A-11D-A29I-10 chr5:131927721 T>C maps to NM_005732.3 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr1:46743899 C>T maps to NM_003579.3 A730A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr7:4841488 G>A maps to NM_018059.4 A879A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr7:4876099 G>A maps to NM_018059.4 N224N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr20:55931509 C>T maps to NM_001015885.1 C68C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr5:34823554 G>A maps to NM_001145521.1 K536K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr14:36191027 G>T maps to NM_194301.2 S711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JH-01A-11D-A30A-10 chr7:45197432 G>A maps to NM_005856.2 E2E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr7:45197432 G>A maps to NM_005856.2 E2E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr7:45197432 G>A maps to NM_005856.2 E2E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LP-01A-11D-A29I-10 chr7:45197432 G>A maps to NM_005856.2 E2E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OF-01A-11D-A29I-10 chr7:45197432 G>A maps to NM_005856.2 E2E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr5:170668123 C>A maps to NM_022897.3 S872*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr9:6013221 C>A maps to NM_012416.2 E796*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr12:69047920 C>T maps to NM_015646.4 Y71Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:21940489 C>T maps to NM_001145658.1 R192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:131348262 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr12:48131973 A>T did not map to a codon.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr17:38345577 C>T maps to ENST00000456989 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JX-01A-11D-A29I-10 chr11:47469438 A>G maps to NM_005055.3 Y152Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr3:158449964 T>C maps to NM_206963.1 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr5:179564922 C>A maps to NM_175062.3 E44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LL-01A-11D-A29I-10 chr5:179563434 T>C maps to NM_175062.3 E127E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr15:79307706 A>G maps to NM_002891.4 F596F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr15:79323770 G>A maps to NM_002891.4 Y411Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr15:79290535 G>A maps to NM_002891.4 N972N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:33752421 C>T maps to NM_170672.2 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr19:49227596 G>T maps to NM_017805.2 L847L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr13:27847562 C>T maps to NM_206827.1 Q221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr10:45484789 G>A maps to NM_032023.3 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr1:206681322 C>T maps to NM_182663.2 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr11:562157 C>T maps to NM_003475.3 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JI-01A-11D-A29I-10 chr18:56936394 T>C maps to NM_013435.2 Q294Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr18:56936394 T>C maps to NM_013435.2 Q294Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr18:56936394 T>C maps to NM_013435.2 Q294Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LA-01A-11D-A29I-10 chr18:56936394 T>C maps to NM_013435.2 Q294Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr8:53569633 C>A maps to NM_014781.4 E919*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr1:33134948 A>G maps to NM_005610.2 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LP-01A-11D-A29I-10 chr23:16871807 A>G did not map to a codon.
Sequencing variant TCGA-OR-A5JR-01A-11D-A29I-10 chr16:53468698 C>T maps to NM_005611.3 Y77Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr23:47039882 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:47032529 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr3:51430915 A>T maps to NM_013286.4 K696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr23:48433574 T>A did not map to a codon.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr7:155534694 G>A maps to NM_053043.2 S744S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr4:40440853 G>C maps to NM_001098634.1 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr4:40440853 G>C maps to NM_001098634.1 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr4:40440853 G>C maps to NM_001098634.1 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr4:40440853 G>C maps to NM_001098634.1 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr4:40440853 G>C maps to NM_001098634.1 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KW-01A-11D-A29I-10 chr3:50103898 T>C maps to NM_005777.2 V969V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr3:50097174 C>T maps to NM_005777.2 R742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JV-01A-11D-A29I-10 chr23:135961559 C>G did not map to a codon.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr3:139258410 G>A maps to NM_002899.3 R50R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr6:46214634 C>A maps to ENST00000405162 G141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J7-01A-11D-A29I-10 chr13:50123621 G>C maps to NM_018191.3 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr11:63679515 G>A maps to NM_173587.3 R465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:211462518 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr6:31926214 C>T maps to ENST00000375425 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr14:68191942 C>T maps to NM_152443.2 I105I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr14:68191957 G>A maps to NM_152443.2 E110E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:18736654 C>T maps to NM_020905.3 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr19:1496348 C>T maps to ENST00000395479 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr7:103180835 C>A maps to ENST00000428762 V2246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr7:103230146 G>A maps to ENST00000428762 C1347C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr7:150069547 C>G maps to NM_001099695.1 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr7:150069841 G>A maps to NM_001099695.1 S561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr12:15262052 G>A maps to NM_032918.2 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr10:43622075 C>T maps to NM_020975.4 D1031D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr2:85577298 G>A maps to NM_017750.3 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr7:73649930 G>A maps to NM_181471.1 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr16:74670455 G>T maps to NM_018124.3 S405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr19:14074019 G>A maps to NM_002918.4 L880L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr9:3263054 A>C maps to NM_134428.1 T495T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:109696334 G>C did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:109696662 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr23:109695051 G>C did not map to a codon.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr5:98109827 G>A maps to NM_001012761.2 E59E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KV-01A-11D-A29I-10 chr5:73165980 C>A maps to NM_001080479.2 S838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr9:35752651 C>A maps to ENST00000456972 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:107041064 G>A maps to ENST00000304514 L1120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JX-01A-11D-A29I-10 chr4:3388162 C>T maps to NM_198229.2 G673G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr20:62705724 C>T maps to NM_005873.2 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr9:116269608 C>T maps to NM_144488.4 V376V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr6:49574559 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr2:227729480 C>T maps to NM_001167608.1 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr22:29656388 G>T maps to NM_012265.1 A303A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr11:66834251 C>T maps to NM_014578.3 D88D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr23:119249706 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr5:38966808 C>A maps to ENST00000296782 V411V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:152320980 G>T maps to NM_018151.4 V1649V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JI-01A-11D-A29I-10 chr12:130921470 T>C maps to NM_015347.4 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr12:130921470 T>C maps to NM_015347.4 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KV-01A-11D-A29I-10 chr12:130921470 T>C maps to NM_015347.4 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr12:130921470 T>C maps to NM_015347.4 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr12:130921470 T>C maps to NM_015347.4 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr12:130921470 T>C maps to NM_015347.4 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr6:73000414 C>T maps to NM_014989.4 H1196H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr6:72968724 T>A maps to NM_014989.4 R988R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr6:73000436 C>T maps to NM_014989.4 Q1204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr5:31526975 G>A maps to NM_013235.4 R22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JV-01A-11D-A29I-10 chr18:29598846 C>T maps to NM_017831.3 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr3:149678533 C>T maps to NM_007282.4 H263H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr5:179394007 C>T maps to NM_018434.4 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr16:2018634 C>A maps to NM_174903.4 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr11:74546990 C>A maps to NM_001098638.1 S448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr13:25363493 G>T maps to ENST00000381927 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr1:185069017 C>G maps to NM_007212.3 S278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr13:79191111 C>A maps to NM_024546.3 E262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr5:175959060 G>A maps to NM_014901.4 R81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J2-01A-11D-A29I-10 chr12:117187906 T>C maps to NM_001109903.1 H115H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr12:117273984 G>C did not map to a codon.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr12:117187906 T>C maps to NM_001109903.1 H115H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KV-01A-11D-A29I-10 chr12:117187906 T>C maps to NM_001109903.1 H115H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr12:117187906 T>C maps to NM_001109903.1 H115H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L3-01A-11D-A29I-10 chr12:117187918 C>T maps to NM_001109903.1 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L9-01A-11D-A29I-10 chr12:117187906 T>C maps to NM_001109903.1 H115H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr12:117187906 T>C maps to NM_001109903.1 H115H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr12:117187918 C>T maps to NM_001109903.1 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr12:117187906 T>C maps to NM_001109903.1 H115H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr12:117273790 C>T maps to NM_001109903.1 G353G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr1:201951889 G>T maps to NM_020216.3 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr3:77147393 C>T maps to ENST00000332191 H97H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr15:60797799 C>T maps to NM_134260.2 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:151789188 G>A maps to ENST00000392697 C137C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr6:117622296 C>T maps to NM_002944.2 W2191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr8:10468988 G>A maps to NM_178857.5 T873T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr8:10465814 G>A maps to NM_178857.5 D1931D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr23:96139816 A>G did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr6:111329293 T>C maps to NM_032194.1 D149D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr14:21793412 G>T maps to NM_020366.3 G746G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr16:53692790 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr12:113304641 G>A maps to NM_001143854.1 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr14:47120738 G>A maps to NM_080746.2 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr16:89627670 C>T maps to NM_033251.1 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr16:89627670 C>T maps to NM_033251.1 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JL-01A-11D-A29I-10 chr16:89627670 C>T maps to NM_033251.1 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr16:89627670 C>T maps to NM_033251.1 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr16:89627670 C>T maps to NM_033251.1 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr23:118923903 T>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:154334872 C>A maps to NM_019845.2 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr16:2014527 G>A maps to NM_002952.3 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr16:2013251 T>C maps to NM_002952.3 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr19:8386553 G>C maps to NM_001031.4 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr19:58905868 C>A maps to NM_001009.3 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr1:26856461 T>G maps to NM_002953.3 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JD-01A-11D-A29I-10 chr1:26856461 T>G maps to NM_002953.3 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JL-01A-11D-A29I-10 chr1:26856461 T>G maps to NM_002953.3 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:26856461 T>G maps to NM_002953.3 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:26856461 T>G maps to NM_002953.3 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr6:166862232 T>C maps to ENST00000510118 T462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr6:166826303 T>C maps to ENST00000510118 S741S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr23:83372102 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr17:78599561 C>G maps to NM_020761.2 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr23:55758010 C>G did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr20:17617311 C>A maps to ENST00000377813 V749V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr20:17617259 G>T maps to ENST00000377813 R767R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr10:99145705 G>A maps to NM_015179.3 H354H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr10:99155983 G>A maps to NM_015179.3 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr10:99160151 A>G maps to NM_015179.3 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr21:45107796 G>A maps to NM_015056.2 P514P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr22:42912028 G>T maps to NM_015703.4 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr1:114354653 T>C maps to NM_018364.3 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr1:114354653 T>C maps to NM_018364.3 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr1:114354653 T>C maps to NM_018364.3 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KV-01A-11D-A29I-10 chr1:114354653 T>C maps to NM_018364.3 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L4-01A-11D-A29I-10 chr1:114354653 T>C maps to NM_018364.3 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LP-01A-11D-A29I-10 chr1:114354653 T>C maps to NM_018364.3 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr16:11940359 G>T maps to NM_015659.2 C211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr6:159401949 G>A maps to NM_031924.4 Q381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr8:108970362 A>G maps to NM_178565.4 C187C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr22:23482459 A>G maps to NM_014433.2 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr20:62309672 C>T maps to ENST00000482936 D337D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J3-01A-11D-A29I-10 chr14:101349016 A>G maps to NM_001134888.2 F703F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr14:101347632 C>A maps to NM_001134888.2 E1165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr14:101349079 G>A maps to NM_001134888.2 T682T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr14:60212794 C>A maps to NM_021136.2 E216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr8:92972687 G>T maps to NM_175634.2 R533R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr8:93023262 G>A maps to NM_175634.2 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr8:93029538 C>T maps to NM_175634.2 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JL-01A-11D-A29I-10 chr6:45390513 G>A maps to ENST00000359524 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JR-01A-11D-A29I-10 chr6:45390513 G>A maps to ENST00000359524 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KV-01A-11D-A29I-10 chr9:35546625 T>G maps to NM_001135999.1 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr3:127842495 C>A maps to NM_003707.2 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:33938185 C>T maps to NM_016568.3 Y447Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr9:137325960 C>G maps to NM_002957.4 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr6:33164381 C>A maps to ENST00000374685 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr19:38966035 C>T maps to NM_000540.2 D1413D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr19:38993358 G>A maps to NM_000540.2 S2609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr19:39019289 G>A maps to NM_000540.2 L3663L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr19:39038918 C>A maps to NM_000540.2 L4047L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr19:38931500 G>A maps to NM_000540.2 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr19:39018333 C>T maps to NM_000540.2 G3578G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:237666654 T>A maps to NM_001035.2 P821P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:237811774 G>T maps to NM_001035.2 A2458A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:237947788 C>T maps to NM_001035.2 L4259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr1:237754019 C>T maps to NM_001035.2 N1296N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr15:34111986 C>A maps to NM_001036.3 S3579S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LD-01A-11D-A29I-10 chr15:34030715 C>T maps to NM_001036.3 Y2527Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr19:10624718 G>T maps to NM_001166215.1 C323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr11:18257404 C>A maps to NM_006512.3 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr19:47673133 A>G maps to NM_005500.2 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:234229339 C>A maps to NM_000541.4 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:134992241 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr23:134994107 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5L3-01A-11D-A29I-10 chr8:119391790 T>C maps to NM_207506.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr1:84764248 A>G maps to NM_001010971.2 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr14:55203811 A>T maps to NM_015589.4 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr14:55227102 C>T maps to NM_015589.4 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KT-01A-11D-A29I-10 chr19:39871262 C>G maps to NM_018028.2 G562G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chr22:44368203 A>G maps to NM_015380.4 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr22:50845168 C>T maps to ENST00000216061 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JL-01A-11D-A29I-10 chr5:133945287 C>T maps to NM_016103.3 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JT-01A-11D-A29I-10 chr17:26723259 C>A maps to ENST00000379061 G708G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chr1:109772187 C>T maps to ENST00000369923 N147N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J2-01A-11D-A29I-10 chr6:148792616 A>G maps to NM_015278.3 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr23:23803893 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:84362767 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr23:84362925 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:84362969 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr22:50901134 C>A maps to ENST00000337034 P670P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JL-01A-11D-A29I-10 chr19:36015651 C>T maps to NM_001166034.1 S570S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr19:50157654 G>T maps to NM_021228.2 A1122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr1:155230130 C>T maps to NM_005698.2 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr8:27516982 C>T maps to NM_016240.2 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr8:27779157 C>A maps to NM_173833.5 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J1-01A-11D-A29I-10 chr17:1543261 C>T maps to NM_003693.2 G361G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr22:20780090 C>G maps to NM_153334.4 P729P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr22:20780096 G>C maps to NM_153334.4 R727R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JL-01A-11D-A29I-10 chr22:20780096 G>C maps to NM_153334.4 R727R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JR-01A-11D-A29I-10 chr22:20780096 G>C maps to NM_153334.4 R727R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr22:20780090 C>G maps to NM_153334.4 P729P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr22:20780096 G>C maps to NM_153334.4 R727R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KT-01A-11D-A29I-10 chr22:20780096 G>C maps to NM_153334.4 R727R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr22:20780090 C>G maps to NM_153334.4 P729P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L3-01A-11D-A29I-10 chr22:20780090 C>G maps to NM_153334.4 P729P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L3-01A-11D-A29I-10 chr22:20780096 G>C maps to NM_153334.4 R727R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr22:20780090 C>G maps to NM_153334.4 P729P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr22:20780096 G>C maps to NM_153334.4 R727R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr22:20780090 C>G maps to NM_153334.4 P729P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr22:20780096 G>C maps to NM_153334.4 R727R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr4:54011641 G>T maps to NM_152540.3 I473I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr2:224462284 C>G maps to NM_003469.4 G572G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:224463928 C>T maps to NM_003469.4 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr15:52011689 C>T maps to NM_013243.3 A458A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr5:147261609 G>A maps to NM_054023.4 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr4:129964622 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr6:108068043 C>T maps to NM_198081.3 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KT-01A-11D-A29I-10 chr2:166898934 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr2:166152581 C>A maps to NM_001040142.1 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:166198816 G>A maps to NM_001040142.1 G800G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr2:166153537 A>T maps to NM_001040142.1 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr3:38618242 G>A maps to NM_001099404.1 S1140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr2:167298120 G>A maps to NM_002976.2 L648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr12:52188153 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr22:50962207 T>G maps to NM_001169111.1 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr8:144874553 T>C maps to NM_182706.3 P1450P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JH-01A-11D-A30A-10 chr8:144874553 T>C maps to NM_182706.3 P1450P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JQ-01A-11D-A29I-10 chr8:144892936 C>A maps to NM_182706.3 P441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JT-01A-11D-A29I-10 chr8:144874553 T>C maps to NM_182706.3 P1450P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chr8:144874553 T>C maps to NM_182706.3 P1450P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OF-01A-11D-A29I-10 chr8:144874553 T>C maps to NM_182706.3 P1450P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:1153175 G>A maps to NM_016547.2 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr1:17380490 G>A maps to NM_003000.2 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr7:4169610 G>A maps to NM_152744.3 S1337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr15:85230911 A>G maps to NM_014300.2 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OF-01A-11D-A29I-10 chr17:75190961 C>T maps to NM_001039573.2 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JL-01A-11D-A29I-10 chr22:30891249 T>C maps to NM_174977.3 Q138Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr9:139341309 G>A maps to NM_014866.1 P2263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr4:83785612 G>A maps to ENST00000505472 Q446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chr14:81961478 A>C maps to NM_005065.4 V377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr4:25760663 G>A maps to NM_015187.3 I994I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr1:169672444 G>C maps to NM_000655.4 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:84644490 G>T maps to NM_152754.2 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr3:50211680 C>T maps to NM_004186.3 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr5:115813771 C>T maps to ENST00000257414 A502A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr5:115782362 T>C maps to ENST00000257414 K1030K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr5:115815885 C>T maps to ENST00000257414 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr20:43836225 A>G maps to NM_003007.3 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr20:43850725 T>A maps to NM_003008.2 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr3:185337190 G>T maps to ENST00000427465 G524G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr6:76423517 C>T maps to NM_015571.2 Q1036*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr6:76380282 T>C maps to NM_015571.2 I413I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr1:87369101 C>T maps to NM_004261.3 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr1:26139206 C>T maps to NM_020451.2 F437F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr1:26138261 T>C maps to NM_020451.2 P391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K8-01A-11D-A29I-10 chr22:19702146 G>A maps to NM_002688.5 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr23:118774714 C>G did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:118763332 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5JH-01A-11D-A30A-10 chr17:75483521 T>G maps to NM_001113491.1 G310G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J7-01A-11D-A29I-10 chr14:94845821 C>T maps to NM_001127707.1 E348E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KZ-01A-11D-A29I-10 chr14:94752475 G>T maps to NM_001100607.1 S371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr14:95054238 G>A maps to NM_000624.4 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:105279360 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5L3-01A-11D-A29I-10 chr23:105277574 A>T did not map to a codon.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr14:94933708 C>T maps to NM_175739.3 E231E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr18:61587035 C>T maps to NM_005024.1 D129D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr18:61390439 C>G maps to NM_080475.2 S329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr18:61564453 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr2:179979929 T>C maps to NM_178123.4 Q567Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JH-01A-11D-A30A-10 chr2:179986552 T>C maps to NM_178123.4 K462K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K8-01A-11D-A29I-10 chr16:30976944 C>T maps to NM_014712.1 D581D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J3-01A-11D-A29I-10 chr3:47163591 G>C maps to NM_014159.6 S845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr3:9516181 A>T maps to ENST00000407969 K1202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J2-01A-11D-A29I-10 chr17:27286749 G>A maps to NM_178860.4 D579D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr22:26689104 G>A maps to NM_021115.4 Q276Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr2:198257794 T>C maps to NM_012433.2 V1219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr10:7213880 C>T maps to NM_001018039.1 P797P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KV-01A-11D-A29I-10 chr1:27189834 C>G maps to NM_006142.3 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:35658608 A>G maps to NM_005066.2 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr4:154709636 G>T maps to NM_003013.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:70701182 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5JQ-01A-11D-A29I-10 chr5:64023980 C>T maps to ENST00000513458 K77K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr21:33065780 G>A maps to NM_020706.2 R447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr23:1713020 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr23:1720321 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr12:132250711 G>C maps to NM_004592.2 L667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KW-01A-11D-A29I-10 chr10:81706388 C>A maps to NM_003019.4 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr3:153970946 C>T maps to NM_015595.3 S781S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr1:67195021 G>A maps to ENST00000237247 P637P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr10:52067048 C>G maps to ENST00000361543 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr10:52103640 G>A maps to ENST00000361543 N84N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr2:223423172 T>C maps to NM_152386.2 C252C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr17:78188919 G>A maps to NM_000199.3 Y89Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr22:25240889 G>A maps to NM_001039948.2 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr17:2280077 G>T maps to NM_014853.2 L887L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JW-01A-11D-A29I-10 chr17:2275733 C>G maps to NM_014853.2 S580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr17:2265552 G>A maps to NM_014853.2 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr19:2757761 C>A maps to NM_003021.3 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr5:65000122 T>G maps to NM_019072.2 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:156779503 T>C maps to NM_001161441.1 K231K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:156779557 T>C maps to NM_001161441.1 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LR-01A-11D-A29I-10 chr6:80406275 A>G maps to NM_031469.2 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr22:38051354 G>A maps to NM_018957.3 P590P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr22:38043304 A>G maps to NM_018957.3 P356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L1-01A-11D-A30A-10 chr22:38051354 G>A maps to NM_018957.3 P590P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LA-01A-11D-A29I-10 chr22:38046717 A>G maps to NM_018957.3 A528A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr4:2826399 T>C maps to NM_001145856.1 H157H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JX-01A-11D-A29I-10 chr2:235951818 A>G maps to NM_014521.2 L802L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:235951204 G>T maps to NM_014521.2 E598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr1:249106347 G>C maps to NM_030645.1 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KT-01A-11D-A29I-10 chr1:249106347 G>C maps to NM_030645.1 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:249106287 A>G maps to NM_030645.1 D331D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr9:17795614 T>C maps to NM_003026.2 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr23:19587242 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:148407035 C>A maps to NM_024577.3 R753R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr19:51172453 G>T maps to ENST00000391814 P929P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr19:51171187 G>A maps to ENST00000391814 T1351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr11:70333394 G>A maps to ENST00000338508 Y995Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr22:51159594 C>T maps to NM_001080420.1 L1128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr8:145158502 G>T maps to NM_030974.3 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JI-01A-11D-A29I-10 chr8:145158502 G>T maps to NM_030974.3 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L1-01A-11D-A30A-10 chr8:145158502 G>T maps to NM_030974.3 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr15:49135624 C>A maps to NM_203349.3 G488G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr16:46637517 A>C maps to NM_024745.4 V382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JL-01A-11D-A29I-10 chr19:4280206 G>C maps to NM_020209.3 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:96324203 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr7:155596412 C>T maps to NM_000193.2 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr17:3518688 G>A maps to NM_013276.2 N322N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr4:77662247 G>A maps to NM_020859.3 S974S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr4:77662247 G>A maps to NM_020859.3 S974S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr4:77662308 C>T maps to NM_020859.3 L995L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:50377364 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:50377404 C>G did not map to a codon.
Sequencing variant TCGA-OR-A5KV-01A-11D-A29I-10 chr23:50376326 T>C did not map to a codon.
Sequencing variant TCGA-OR-A5LL-01A-11D-A29I-10 chr23:50377343 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr3:164786983 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr3:164764718 C>A maps to NM_001041.3 A599A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr20:3673210 G>T maps to NM_023068.3 A1329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr19:52003396 G>A maps to ENST00000441969 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr18:43417751 C>G maps to NM_213602.2 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr19:52132320 G>A maps to ENST00000222107 Q237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr6:100898138 C>A maps to NM_005068.2 E118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr14:72128142 C>A maps to NM_015556.1 I738I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr19:38591714 C>T maps to NM_015073.1 G626G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr19:38573332 C>T maps to NM_015073.1 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr19:38572783 G>T maps to NM_015073.1 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr19:38590771 G>A maps to NM_015073.1 L612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr20:1456853 T>A maps to NM_001122962.1 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr12:120750303 G>T maps to NM_012240.2 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr2:45171841 A>G maps to NM_005413.3 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr2:45171841 A>G maps to NM_005413.3 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr2:45171841 A>G maps to NM_005413.3 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr2:45171841 A>G maps to NM_005413.3 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr2:45171841 A>G maps to NM_005413.3 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LP-01A-11D-A29I-10 chr19:46269608 T>A maps to NM_175875.4 P536P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr18:47908516 G>T maps to NM_145060.3 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr6:31928994 A>G maps to NM_006929.4 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr5:54619983 C>A maps to NM_015360.4 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr8:134072519 G>C maps to NM_006748.3 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr14:70246041 G>A maps to NM_003049.3 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr13:103701771 C>T maps to NM_000452.2 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:153716004 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr8:82607083 C>A maps to NM_001010893.2 E42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr4:87769947 C>A maps to NM_197965.2 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr16:56936359 G>A maps to NM_000339.2 E941E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr18:43221303 C>A maps to NM_007163.3 I374I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr17:73096273 C>T maps to ENST00000450736 F212F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr6:74345204 C>T maps to NM_012434.4 W240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JT-01A-11D-A29I-10 chr10:119003689 G>A maps to NM_003054.4 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr10:119003662 C>A maps to NM_003054.4 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr2:65217142 C>A maps to NM_003038.4 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr11:64368344 C>T maps to NM_144585.2 A511A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr14:23821013 G>A maps to NM_020372.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr11:62886490 G>T maps to NM_001136506.1 Y241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr11:62931535 A>C maps to NM_199352.3 A468A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr6:160864676 G>A maps to ENST00000392145 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr6:43266401 G>C maps to ENST00000372585 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr11:62782277 C>T maps to ENST00000430500 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr5:138714363 G>A maps to NM_152685.3 F365F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr14:92792242 C>A maps to NM_153646.3 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L3-01A-11D-A29I-10 chr10:70243287 G>C maps to NM_152707.2 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr22:18070753 C>T maps to NM_031481.1 N213N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr19:6452331 G>A maps to NM_024103.2 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LD-01A-11D-A29I-10 chr1:108728483 T>C maps to NM_013386.3 K92K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr3:66419941 A>G maps to NM_173471.3 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr23:118587002 C>T did not map to a codon.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr12:58015618 C>T maps to NM_133489.2 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:128302150 G>T maps to NM_001017372.1 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr15:85432029 T>C maps to NM_004213.3 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr12:40422217 T>A maps to NM_052885.3 G270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr12:40499117 G>A maps to NM_052885.3 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KV-01A-11D-A29I-10 chr17:7187305 G>T maps to NM_001042.2 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KV-01A-11D-A29I-10 chr9:136340731 G>T maps to NM_017585.3 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LD-01A-11D-A29I-10 chr9:136339192 T>C maps to NM_017585.3 A315A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-OR-A5KX-01A-11D-A29I-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:27479290 C>T maps to NM_003459.4 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr2:32396390 C>T maps to NM_001193513.1 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr2:32417995 C>T maps to NM_001193513.1 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr8:118183271 G>C did not map to a codon.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr9:140130531 T>C maps to NM_080877.2 A488A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JQ-01A-11D-A29I-10 chr9:140128913 C>T maps to NM_080877.2 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr6:44222511 G>A maps to NM_178148.2 Y410Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr11:45832786 C>T maps to NM_018389.4 G332G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KT-01A-11D-A29I-10 chr5:150723805 G>A maps to NM_181776.2 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr11:92881963 G>A maps to NM_152313.2 F418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr11:92881942 G>A maps to NM_152313.2 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr12:46756129 A>T maps to NM_018976.4 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr3:50256023 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:48319043 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr23:48317385 A>G did not map to a codon.
Sequencing variant TCGA-OR-A5JW-01A-11D-A29I-10 chr16:84070499 C>G maps to NM_001080442.1 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr10:18254444 G>T maps to NM_001145195.1 G193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr18:33706546 G>A maps to NM_012319.3 R142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr2:190430179 G>A maps to NM_014585.5 Y220Y. Only missense variants will be evaluated by CHASM.
Reference base specified for sequencing variant TCGA-OR-A5JT-01A-11D-A29I-10 chr5:33954510 C>A does not match reference base at that coordinate in hg19.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chr5:33944895 G>A maps to NM_016180.3 Q484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr17:42337787 G>A maps to NM_000342.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:162820703 C>A maps to NM_001178015.1 Y974*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr2:162820667 C>T maps to NM_001178015.1 F962F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr20:3214625 G>A maps to NM_001174090.1 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr20:3218584 A>T maps to NM_001174090.1 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr7:150771568 T>C maps to NM_003040.3 Y958Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr2:220505264 T>C maps to NM_201574.2 L1158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J2-01A-11D-A29I-10 chr21:35468283 G>T maps to NM_006933.4 G263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr22:32614515 G>A maps to NM_014227.2 H655H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr19:17994714 C>A maps to NM_000453.2 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr2:108609539 G>T maps to NM_021815.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L3-01A-11D-A29I-10 chr2:108627277 C>T maps to NM_021815.2 S568S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr2:108609478 T>A maps to NM_021815.2 L115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr12:101584301 G>A maps to NM_145913.3 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr12:101603552 G>T maps to NM_145913.3 S25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KT-01A-11D-A29I-10 chr3:11072861 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KT-01A-11D-A29I-10 chr3:10967738 T>C maps to NM_014229.1 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr23:115582607 T>C did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:115568955 A>C did not map to a codon.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr12:85257274 A>T maps to NM_182767.4 A587A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr19:49793930 G>T maps to NM_014037.2 I624I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:152954054 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:152958806 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr13:30088673 C>T maps to NM_003045.4 A611A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr19:33699841 T>G maps to NM_019849.2 P509P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr23:70148708 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr23:70146474 G>C did not map to a codon.
Sequencing variant TCGA-OR-A5KT-01A-11D-A29I-10 chr19:33355068 A>G maps to NM_014270.4 C137C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr2:40657110 C>A maps to NM_021097.2 E104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr19:47951115 C>T maps to NM_015063.2 V571V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr19:47951133 C>T maps to NM_015063.2 T565T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr14:70515628 G>C maps to NM_183002.1 G754G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr1:27429000 G>A maps to NM_003047.3 G565G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LD-01A-11D-A29I-10 chr1:27436202 G>A maps to NM_003047.3 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr3:111898521 C>T maps to NM_183061.1 G925G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr2:103300744 T>C maps to NM_003048.3 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr5:480043 G>T maps to NM_004174.2 V518V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:135098853 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:135112309 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:46541865 C>A did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr5:101631818 G>A maps to NM_180991.4 Q50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J7-01A-11D-A29I-10 chr17:33586497 T>C maps to NM_144975.3 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr17:33592238 C>T maps to NM_144975.3 Q670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr5:168201334 C>T maps to NM_003062.2 Q400Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr13:84455468 G>T maps to NM_052910.1 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:144904122 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:144905092 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:144905169 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr3:164907801 G>A maps to NM_014926.2 R273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:142717516 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr23:142717896 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5J2-01A-11D-A29I-10 chr4:146435773 G>A maps to NM_001003688.1 V3V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr15:66995715 C>T maps to NM_005585.4 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr18:46447840 G>A maps to NM_005904.3 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr13:37427573 G>A maps to NM_001127217.2 I414I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:128649927 G>T did not map to a codon.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr19:11097012 C>T maps to NM_001128849.1 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr4:144442734 C>T maps to NM_003601.2 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr2:217300104 C>T maps to NM_014140.3 N510N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr2:217332760 G>T maps to NM_014140.3 E746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr2:217285233 C>T maps to NM_014140.3 Q359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JH-01A-11D-A30A-10 chr3:47712201 T>C maps to NM_003074.3 K615K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr7:150938651 G>A maps to NM_003078.3 Q276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr23:53410123 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr23:53430780 G>C did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr23:53432787 G>A did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr2:17906607 C>T maps to ENST00000381272 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LP-01A-11D-A29I-10 chr17:2203569 G>C maps to NM_017575.4 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr6:168842112 T>G maps to NM_022138.2 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr6:168842112 T>G maps to NM_022138.2 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JR-01A-11D-A29I-10 chr6:168842112 T>G maps to NM_022138.2 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KW-01A-11D-A29I-10 chr6:168842112 T>G maps to NM_022138.2 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr6:168842112 T>G maps to NM_022138.2 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J7-01A-11D-A29I-10 chr20:4163301 A>G maps to ENST00000443211 A392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr11:6413008 A>C maps to NM_000543.4 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr16:68398923 C>T maps to NM_018667.3 P465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:130911966 C>A maps to NM_017951.4 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PA-A5YG-01A-11D-A29I-10 chr22:31495742 C>T maps to ENST00000454496 Q907*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr22:21213415 A>G maps to NM_004782.3 K6K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr6:84290238 G>T maps to NM_014841.2 P743P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J1-01A-11D-A29I-10 chr9:139272546 C>T maps to NM_003086.2 Q1244Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JH-01A-11D-A30A-10 chr9:139273287 C>T maps to NM_003086.2 E997E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr20:1286661 G>A maps to ENST00000381876 P527P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr2:96948948 G>T maps to NM_014014.3 L1635L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:1094064 C>G maps to NM_018968.3 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr14:78205322 C>A maps to NM_012245.2 E138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J3-01A-11D-A29I-10 chr5:53814051 T>C maps to NM_052870.2 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr5:53814051 T>C maps to NM_052870.2 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K8-01A-11D-A29I-10 chr5:53814051 T>C maps to NM_052870.2 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr1:179312751 C>T maps to NM_003101.4 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JL-01A-11D-A29I-10 chr18:67993001 C>T maps to NM_004232.3 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr4:24801353 C>T maps to NM_003102.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JL-01A-11D-A29I-10 chr4:24801353 C>T maps to NM_003102.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JT-01A-11D-A29I-10 chr4:24801353 C>T maps to NM_003102.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr4:24801353 C>T maps to NM_003102.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr16:597407 G>C maps to NM_005632.2 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr16:602137 G>T maps to NM_005632.2 A811A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LP-01A-11D-A29I-10 chr16:597452 C>T maps to NM_005632.2 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr21:34923318 A>G maps to NM_138927.1 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr21:34924818 G>A maps to NM_138927.1 S1094S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr8:22421833 G>A maps to NM_005775.4 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr10:108589373 G>T maps to NM_001013031.1 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr4:7716055 G>A maps to NM_020777.2 A693A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JV-01A-11D-A29I-10 chr4:7725584 G>A maps to NM_020777.2 E862E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KV-01A-11D-A29I-10 chr11:121429443 G>A maps to NM_003105.5 T936T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr1:109884774 T>G maps to NM_002959.4 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr14:50616831 C>A maps to NM_006939.2 E760*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr22:38374132 G>A maps to NM_006941.3 N146N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JV-01A-11D-A29I-10 chr17:7492610 G>T maps to NM_006942.1 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr11:16256217 C>A did not map to a codon.
Sequencing variant TCGA-P6-A5OF-01A-11D-A29I-10 chr2:231174694 C>T maps to NM_007237.4 C705C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr7:21516827 C>T maps to NM_003112.3 Q604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J2-01A-11D-A29I-10 chr2:171573184 G>T maps to NM_001003845.2 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:171573184 G>T maps to NM_001003845.2 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LL-01A-11D-A29I-10 chr2:171573184 G>T maps to NM_001003845.2 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr7:20824952 G>C maps to NM_182700.4 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr7:20824952 G>C maps to NM_182700.4 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:20824577 G>A maps to NM_182700.4 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr17:26919547 G>A maps to NM_006461.3 N238N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr7:123599734 G>A maps to NM_001174046.1 K414K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr23:140336571 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:142605190 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr23:142605205 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr13:24825998 C>T maps to ENST00000424834 N758N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr3:172766821 G>A maps to NM_031955.5 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr2:201342531 C>T maps to ENST00000409151 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr2:169745768 G>T maps to NM_020675.3 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J2-01A-11D-A29I-10 chr7:99917415 G>A maps to NM_001004351.4 P525P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr7:101989089 G>A maps to NM_001146210.1 D261D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr2:220332028 C>T maps to NM_005876.4 G1005G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:16174570 G>T maps to NM_015001.2 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J3-01A-11D-A29I-10 chr13:46288016 C>A maps to NM_152719.1 S286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L4-01A-11D-A29I-10 chr13:46288016 C>A maps to NM_152719.1 S286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr15:44918705 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr16:89574944 G>A maps to NM_003119.2 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr16:89611116 C>T maps to NM_003119.2 D462D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:228883708 T>A maps to NM_001142644.1 K621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:228884764 C>A maps to NM_001142644.1 E269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:57162365 G>C did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:57146347 A>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:57146371 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chr23:57146332 C>G did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:57020872 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5JQ-01A-11D-A29I-10 chr15:41148198 C>T maps to NM_181642.2 Y425Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L9-01A-11D-A29I-10 chr17:4391131 C>T maps to NM_182538.4 N494N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L9-01A-11D-A29I-10 chr17:4391152 A>G maps to NM_182538.4 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J3-01A-11D-A29I-10 chr10:73848074 C>T maps to NM_014767.2 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr10:73848074 C>T maps to NM_014767.2 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr10:73848074 C>T maps to NM_014767.2 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L4-01A-11D-A29I-10 chr4:88902691 T>C maps to NM_001040058.1 D94D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JW-01A-11D-A29I-10 chr1:153085134 C>T maps to NM_001014450.1 E25E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr1:152975762 C>A maps to NM_005416.2 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr23:155004279 A>G did not map to a codon.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr12:53470945 T>A maps to NM_032840.2 R41R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr3:140785131 G>T maps to NM_080862.1 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr1:158641929 A>G maps to NM_003126.2 H469H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LL-01A-11D-A29I-10 chr1:158641185 G>A maps to NM_003126.2 Q516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LL-01A-11D-A29I-10 chr1:158644355 G>A maps to NM_003126.2 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JH-01A-11D-A30A-10 chr14:65242043 C>T maps to ENST00000389723 A1551A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr14:65249146 G>T maps to ENST00000389723 S1380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr2:54858732 C>G maps to NM_003128.2 A1183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JQ-01A-11D-A29I-10 chr19:41073912 G>C maps to NM_020971.2 V2227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr19:41025757 G>A maps to NM_020971.2 L1118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L3-01A-11D-A29I-10 chr19:41063158 C>T maps to NM_020971.2 F1840F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr15:42167248 T>C maps to ENST00000320955 A1431A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr9:94794821 C>T maps to NM_006415.2 T449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J7-01A-11D-A29I-10 chr5:6633778 C>G maps to NM_001047.2 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr5:6633778 C>G maps to NM_001047.2 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr5:6633778 C>G maps to NM_001047.2 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JL-01A-11D-A29I-10 chr5:6633778 C>G maps to NM_001047.2 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr5:6633778 C>G maps to NM_001047.2 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KT-01A-11D-A29I-10 chr5:6652008 G>A maps to NM_001047.2 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L6-01A-11D-A29I-10 chr5:6633778 C>G maps to NM_001047.2 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L9-01A-11D-A29I-10 chr5:6633778 C>G maps to NM_001047.2 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OF-01A-11D-A29I-10 chr5:6633778 C>G maps to NM_001047.2 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr5:6633778 C>G maps to NM_001047.2 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5H8-01A-11D-A29I-10 chr5:6633778 C>G maps to NM_001047.2 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JD-01A-11D-A29I-10 chr1:11119898 T>C maps to NM_003132.2 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JL-01A-11D-A29I-10 chr1:11119898 T>C maps to NM_003132.2 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr1:11119898 T>C maps to NM_003132.2 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:11119898 T>C maps to NM_003132.2 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KZ-01A-11D-A29I-10 chr1:11119898 T>C maps to NM_003132.2 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LD-01A-11D-A29I-10 chr1:11119898 T>C maps to NM_003132.2 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr1:11119898 T>C maps to NM_003132.2 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LL-01A-11D-A29I-10 chr23:153047593 A>C did not map to a codon.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr23:99905847 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr12:119594332 C>A maps to NM_194286.2 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr12:119583268 C>T maps to NM_194286.2 Y285Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr20:60738544 G>A maps to NM_198935.1 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr7:149518552 C>T maps to NM_198455.2 Q4212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:149486860 C>A maps to NM_198455.2 S1546S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:149518740 C>A maps to NM_198455.2 C4249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr16:1129593 G>A maps to NM_001053.3 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JI-01A-11D-A29I-10 chr23:48123216 A>T did not map to a codon.
Sequencing variant TCGA-OR-A5KV-01A-11D-A29I-10 chr23:48214669 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr23:48053646 G>T did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr8:53044609 G>A maps to NM_014682.2 S858S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr11:8724249 C>T maps to NM_005418.3 R863R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:107423333 C>A maps to NM_001142351.1 E464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:107459874 C>A maps to NM_001142351.1 E187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr2:107459761 C>T maps to NM_001142351.1 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr17:74625597 C>T maps to NM_018414.3 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr18:44260304 G>A maps to NM_013305.4 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr3:52556368 C>T maps to NM_015136.2 H2163H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr3:52554030 C>T maps to NM_015136.2 A1769A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr3:52550141 G>A maps to NM_015136.2 G1344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr12:104107545 G>T maps to NM_017564.9 E1513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chr12:104100616 C>T maps to NM_017564.9 C1348C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr23:123215365 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr23:67941901 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:67940920 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5JD-01A-11D-A29I-10 chr4:77231086 C>T maps to NM_003943.3 C337C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr5:172744903 G>A maps to NM_003714.2 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr4:27000928 G>A maps to ENST00000382009 Q282Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr19:1220639 C>T maps to NM_000455.4 Q220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr4:184931817 G>A maps to NM_020225.1 T609T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr17:61780973 G>A maps to NM_001003787.2 D427D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr23:7252143 G>C did not map to a codon.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr12:131285772 G>A maps to NM_194356.1 D200D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr19:7708094 C>T maps to ENST00000441779 F368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr12:118841233 G>T maps to NM_022491.2 E239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J2-01A-11D-A29I-10 chr13:53237235 G>T maps to NM_001130912.1 E162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr20:46385939 C>A maps to NM_001161841.1 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J7-01A-11D-A29I-10 chr19:49079308 C>T maps to NM_177973.1 D61D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr7:48068433 G>A maps to NM_152782.3 D34D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr17:27028023 G>A maps to NM_003170.3 T1624T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LL-01A-11D-A29I-10 chr1:149876664 G>A maps to NM_014849.3 I710I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr9:113169656 A>G maps to ENST00000374463 Y2744Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr10:29818652 C>A maps to NM_021738.2 E743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr10:29821522 T>C maps to NM_021738.2 K591K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chr10:29747416 C>T maps to NM_021738.2 P2168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5H8-01A-11D-A29I-10 chr10:29839863 A>C maps to NM_021738.2 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr8:110587863 C>T maps to NM_001099744.1 T421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr20:58450353 G>T maps to NM_014258.2 G1107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr9:93640008 G>A maps to NM_003177.5 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr6:152551837 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr6:152763326 C>A maps to NM_182961.2 A1297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr6:152737528 G>A maps to NM_182961.2 Q2015*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr6:152793440 G>C maps to NM_182961.2 A486A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr14:64644167 C>T maps to NM_182914.2 H5841H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr14:64596620 T>C did not map to a codon.
Sequencing variant TCGA-OR-A5K8-01A-11D-A29I-10 chr6:33408541 G>A maps to NM_006772.2 S571S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr22:39777907 C>T maps to NM_004711.4 Q231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr16:2042138 C>A maps to NM_004209.5 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KV-01A-11D-A29I-10 chr10:75407621 C>A maps to NM_001114133.1 A596A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr19:55684926 G>T maps to NM_003180.2 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:99941087 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr11:64898228 T>C maps to NM_172230.2 A336A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr6:166580286 G>T maps to NM_003181.2 Y88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L1-01A-11D-A30A-10 chr6:132910156 A>G maps to NM_003967.2 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JX-01A-11D-A29I-10 chr23:30873288 T>C did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:30849616 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr10:124008227 C>T maps to NM_206862.2 A2821A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LD-01A-11D-A29I-10 chr10:123842917 A>T maps to NM_206862.2 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JR-01A-11D-A29I-10 chr4:1729794 A>G maps to NM_006342.1 E222E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:75425973 G>C maps to NM_001058.3 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:59042423 G>A maps to NM_002353.2 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JV-01A-11D-A29I-10 chr3:9831617 A>C maps to NM_006354.2 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:70596892 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:70598292 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr23:70674671 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr23:70587375 G>T did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:222737422 G>A maps to NM_005681.2 F313F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr16:84213113 C>T maps to NM_005679.2 V681V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr10:8006162 A>G maps to NM_031923.2 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr23:100542522 T>G did not map to a codon.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr9:108425001 G>T maps to NM_005421.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr16:29994574 T>C maps to NM_016151.2 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr16:29994972 A>G maps to NM_016151.2 R470R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr16:30002193 C>T maps to NM_004783.2 S845S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr12:6562835 G>A maps to NM_018009.4 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:19181156 C>T maps to NM_152232.2 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JI-01A-11D-A29I-10 chr1:1268158 C>T maps to NM_152228.1 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J1-01A-11D-A29I-10 chr12:11150318 T>C maps to NM_176889.2 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:141672601 G>T maps to NM_176817.4 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr12:11244168 G>A maps to NM_176884.2 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr12:11244189 A>G maps to NM_176884.2 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr23:153647889 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr4:37903766 C>A maps to NM_015173.2 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr4:38138931 G>A maps to NM_015173.2 T1161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr4:38016371 G>A maps to NM_015173.2 A220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr4:38119793 A>T maps to NM_015173.2 G981G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr16:30369774 G>A maps to NM_015527.3 S639S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J7-01A-11D-A29I-10 chr10:96163038 C>G maps to NM_015188.1 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr10:96163038 C>G maps to NM_015188.1 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LP-01A-11D-A29I-10 chr10:96163038 C>G maps to NM_015188.1 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr10:96163038 C>G maps to NM_015188.1 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr9:131559409 G>T maps to NM_018201.3 E154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr17:77984097 C>A maps to NM_019020.2 E214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:48417291 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr17:15638661 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr2:101656657 G>A maps to NM_001102426.1 I339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:101670675 G>A maps to NM_001102426.1 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:106083403 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr23:9673125 G>A did not map to a codon.
Sequencing variant TCGA-P6-A5OF-01A-11D-A29I-10 chr23:9656264 A>G did not map to a codon.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr16:2025626 A>G maps to NM_006453.2 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JL-01A-11D-A29I-10 chr6:170871003 G>A maps to NM_003194.4 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JX-01A-11D-A29I-10 chr6:170871042 G>A maps to NM_003194.4 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr6:170871003 G>A maps to NM_003194.4 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr6:170871015 G>A maps to NM_003194.4 Q64Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr6:170871003 G>A maps to NM_003194.4 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr6:170871042 G>A maps to NM_003194.4 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr6:170871003 G>A maps to NM_003194.4 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr6:170871096 G>A maps to NM_003194.4 Q91Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr6:170871093 G>A maps to NM_003194.4 Q90Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr22:19752530 T>C maps to NM_080647.1 Y245Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JH-01A-11D-A30A-10 chr6:85446963 G>T maps to NM_001080508.1 A421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:79278675 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr17:59560685 C>T maps to ENST00000393853 R484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr12:114793513 G>T maps to NM_000192.3 S460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr7:139655386 A>G maps to NM_001166253.1 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:102884853 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr23:101382399 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5L6-01A-11D-A29I-10 chr23:102864219 C>A did not map to a codon.
Sequencing variant TCGA-P6-A5OF-01A-11D-A29I-10 chr23:102864349 G>A did not map to a codon.
Sequencing variant TCGA-P6-A5OF-01A-11D-A29I-10 chr23:101395945 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr18:44561325 G>A maps to NM_016427.2 Q104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KT-01A-11D-A29I-10 chr5:145838661 G>A maps to NM_006706.3 Q218Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr5:145834679 C>T maps to NM_006706.3 R41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr20:590455 A>G maps to NM_004609.3 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JR-01A-11D-A29I-10 chr20:590455 A>G maps to NM_004609.3 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JW-01A-11D-A29I-10 chr20:590455 A>G maps to NM_004609.3 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr20:590455 A>G maps to NM_004609.3 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LP-01A-11D-A29I-10 chr20:590455 A>G maps to NM_004609.3 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JD-01A-11D-A29I-10 chr19:1619338 T>C maps to NM_003200.2 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JR-01A-11D-A29I-10 chr19:1619347 G>A maps to NM_003200.2 G431G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr19:1619332 G>A maps to NM_003200.2 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr19:1619338 T>C maps to NM_003200.2 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr19:1619338 T>C maps to NM_003200.2 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr19:1619338 T>C maps to NM_003200.2 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr19:1619338 T>C maps to NM_003200.2 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KZ-01A-11D-A29I-10 chr19:1619338 T>C maps to NM_003200.2 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OF-01A-11D-A29I-10 chr19:1619332 G>A maps to NM_003200.2 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OF-01A-11D-A29I-10 chr19:1619338 T>C maps to NM_003200.2 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr10:114711349 C>A maps to NM_030756.4 S122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr10:114711347 C>G maps to NM_030756.4 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JX-01A-11D-A29I-10 chr6:167592575 G>A maps to NM_001145121.1 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KT-01A-11D-A29I-10 chr6:167592575 G>A maps to NM_001145121.1 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L1-01A-11D-A30A-10 chr11:33065393 C>T maps to NM_001145541.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr1:45271827 T>C maps to NM_001013632.2 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr1:45271827 T>C maps to NM_001013632.2 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr1:45271827 T>C maps to NM_001013632.2 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L6-01A-11D-A29I-10 chr1:45271827 T>C maps to NM_001013632.2 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OF-01A-11D-A29I-10 chr14:90450895 T>C maps to NM_018319.3 D307D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L1-01A-11D-A30A-10 chr10:115982439 C>T maps to NM_198795.1 D995D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr1:179621205 C>T maps to ENST00000444136 Y678Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr6:46657181 G>A maps to NM_001010870.2 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr9:100234689 G>T maps to NM_014290.2 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JR-01A-11D-A29I-10 chr14:104394849 C>T maps to NM_153046.2 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr14:104470599 G>T maps to NM_153046.2 G503G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr14:104481117 T>C maps to NM_153046.2 V721V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr7:97854150 C>T maps to ENST00000379795 T886T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr11:121016700 C>T maps to NM_005422.2 C1327C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LA-01A-11D-A29I-10 chr16:1547476 T>C maps to NM_016111.3 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr16:1544461 G>T maps to NM_016111.3 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr10:70450766 A>T maps to NM_030625.2 S1869S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr23:69902634 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr23:69774509 T>C did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:104464178 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:104465050 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr17:62271011 G>A maps to NM_018469.3 R695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JW-01A-11D-A29I-10 chr6:155606324 C>T maps to NM_016020.3 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:132352121 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr3:100451358 G>T maps to NM_001007565.2 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JX-01A-11D-A29I-10 chr22:26888059 G>A maps to NM_012143.2 I811I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr7:93518485 C>T maps to NM_006528.2 E107E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:218607681 A>C maps to NM_001135599.2 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr1:218609420 C>G maps to NM_001135599.2 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr14:76447101 T>G maps to NM_003239.2 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chr9:101894968 T>A maps to NM_004612.2 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:92182148 C>A maps to NM_003243.4 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J2-01A-11D-A29I-10 chr23:89177680 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr14:24731330 G>T maps to NM_000359.2 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JL-01A-11D-A29I-10 chr14:24729686 C>T maps to NM_000359.2 E242E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr14:24718578 G>A maps to NM_000359.2 D798D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr20:36767874 G>A maps to NM_004613.2 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr11:2188687 G>T maps to NM_199292.2 Y255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr20:57568154 G>A maps to NM_198976.1 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr2:242573028 G>A maps to NM_015963.5 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5H8-01A-11D-A29I-10 chr7:108205171 T>C maps to NM_001130475.1 Q217Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr6:169622342 C>T maps to NM_003247.2 T1074T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:122747367 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:122755030 G>C did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr23:122757037 C>T did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr23:122820489 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5J1-01A-11D-A29I-10 chr19:2790452 G>A maps to NM_003249.3 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr1:36767182 C>T maps to NM_005119.3 G844G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr13:52951586 C>A maps to NM_018676.3 E840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:137814533 T>A maps to ENST00000272643 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr6:155450836 A>T maps to ENST00000456144 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr6:155503405 G>T maps to ENST00000456144 R918R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr1:43784955 A>G maps to NM_005424.2 L991L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr1:43779575 C>A maps to NM_005424.2 T782T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr8:144681840 G>T maps to NM_032862.4 E590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr17:76921134 G>A maps to NM_003255.4 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr3:156413770 A>T maps to NM_015508.4 R402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr9:71861603 A>G did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr9:71831373 G>A maps to NM_004817.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr3:53269000 G>A maps to ENST00000423516 F217F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L1-01A-11D-A30A-10 chr2:171850328 T>G maps to ENST00000360843 A775A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr4:167020585 G>T maps to ENST00000507499 V961V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr9:35720205 G>A maps to NM_006289.3 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J2-01A-11D-A29I-10 chr15:63017230 G>A maps to NM_015059.2 T1061T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LA-01A-11D-A29I-10 chr23:12903658 A>T did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr5:170737205 C>T maps to NM_021025.2 Y158Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JL-01A-11D-A29I-10 chr17:4685847 C>G maps to NM_003963.2 Y103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr11:64880089 G>C maps to NM_003273.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr11:64880089 G>C maps to NM_003273.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr11:64880089 G>C maps to NM_003273.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L6-01A-11D-A29I-10 chr11:64880089 G>C maps to NM_003273.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LD-01A-11D-A29I-10 chr11:64880089 G>C maps to NM_003273.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr11:64880089 G>C maps to NM_003273.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr11:64880089 G>C maps to NM_003273.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr11:64880089 G>C maps to NM_003273.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr12:50136044 A>G maps to NM_001098576.1 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr20:2542506 A>T maps to NM_080751.2 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr20:2582893 C>T maps to NM_080751.2 R454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr15:81624990 G>T maps to ENST00000454937 P1027P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JX-01A-11D-A29I-10 chr16:19492709 G>C maps to NM_001105248.1 L762L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr16:19067932 G>A maps to NM_024847.3 T647T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr3:129373857 C>A maps to NM_001017395.3 E534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr3:129546843 G>T maps to NM_001017395.3 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr13:114154418 G>A maps to NM_017905.4 K257K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr13:114156092 C>T maps to NM_017905.4 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LP-01A-11D-A29I-10 chr13:114152754 C>T maps to NM_017905.4 D181D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JH-01A-11D-A30A-10 chr1:20009736 G>A maps to NM_181719.4 S567S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr17:72786400 C>T maps to NM_017728.3 Y104Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JR-01A-11D-A29I-10 chr12:108986111 G>C maps to NM_181724.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L4-01A-11D-A29I-10 chr12:108986111 G>C maps to NM_181724.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr14:105995323 C>T maps to NM_025268.2 C51C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr1:43738797 C>T maps to NM_144626.2 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr11:60701986 G>A maps to NM_017870.3 S530S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JD-01A-11D-A29I-10 chr11:60701986 G>A maps to NM_017870.3 S530S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr12:129558464 G>T maps to NM_133448.2 C1085*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KT-01A-11D-A29I-10 chr11:67235050 G>A maps to NM_025124.2 R84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr11:87013484 G>T did not map to a codon.
Sequencing variant TCGA-PK-A5H8-01A-11D-A29I-10 chr19:5744508 G>T maps to NM_152784.3 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JL-01A-11D-A29I-10 chr4:56262373 A>G maps to NM_018475.3 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr4:56262373 A>G maps to NM_018475.3 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr4:56283353 T>C maps to NM_018475.3 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr5:138861256 C>T maps to NM_198282.2 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr22:38620882 G>A maps to NM_012264.4 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:19765211 T>A maps to NM_152774.3 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr9:74349871 C>A maps to NM_013390.2 G415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr6:130761683 C>G maps to NM_052913.2 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr9:140099814 C>A maps to NM_053045.1 E18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L6-01A-11D-A29I-10 chr1:212560296 A>T maps to NM_001198862.1 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr7:129832630 C>T maps to NM_032842.3 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr2:27257049 G>A maps to NM_017727.4 K89K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr11:62559436 C>G maps to NM_001080501.2 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JQ-01A-11D-A29I-10 chr6:75994150 A>G maps to NM_018247.3 I68I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J1-01A-11D-A29I-10 chr3:12779633 C>G did not map to a codon.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr3:194336339 T>C maps to NM_001166305.1 Q337Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr8:92008966 G>C maps to NM_018710.2 S182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr14:77685875 T>A maps to NM_020431.2 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr14:77708803 C>T maps to NM_020431.2 D393D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr8:125339633 T>A maps to NM_194291.2 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L9-01A-11D-A29I-10 chr10:45430461 C>T maps to NM_001123376.1 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr15:42503947 C>G did not map to a codon.
Sequencing variant TCGA-OR-A5L4-01A-11D-A29I-10 chr16:426159 G>A maps to NM_021259.2 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr9:35853770 C>T maps to NM_001042590.1 N451N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr9:136379901 C>T maps to NM_001080483.2 W174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KT-01A-11D-A29I-10 chr15:52073254 G>T maps to NM_014548.3 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr12:98940139 G>T maps to NM_001032283.2 G332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr12:98940165 A>G maps to NM_001032283.2 V340V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LA-01A-11D-A29I-10 chr21:42845382 A>G maps to NM_001135099.1 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr22:37465236 C>T maps to ENST00000381792 L663L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PA-A5YG-01A-11D-A29I-10 chr22:37462260 C>T maps to ENST00000381792 P778P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr19:2425144 C>T maps to NM_182973.1 L921L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr12:29786205 C>A maps to NM_001193451.1 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr13:101287403 G>A maps to NM_032813.2 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr13:101316488 G>A maps to NM_032813.2 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr9:117797596 T>C maps to NM_002160.2 R1891R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J7-01A-11D-A29I-10 chr9:117853264 G>T maps to NM_002160.2 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr18:60036088 A>G maps to NM_003839.2 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr18:60017105 G>A maps to NM_003839.2 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr1:6521700 C>T maps to ENST00000355862 E350E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr1:6525617 C>T maps to ENST00000355862 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr20:62328452 T>C maps to NM_003823.2 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr3:170928940 G>T maps to NM_015028.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr3:170789053 A>T maps to NM_015028.2 Y1169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr3:170928928 T>A maps to NM_015028.2 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr3:195594804 A>G maps to NM_001010938.1 A851A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JW-01A-11D-A29I-10 chr3:195594804 A>G maps to NM_001010938.1 A851A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr3:195594804 A>G maps to NM_001010938.1 A851A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:99854699 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:175046898 G>T maps to NM_022093.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KT-01A-11D-A29I-10 chr1:175048703 C>T maps to NM_022093.1 G215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr19:55667610 G>A maps to ENST00000344887 C80C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr1:175335233 C>T maps to NM_003285.2 S698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:175348814 G>T maps to NM_003285.2 L612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr1:175372699 C>T maps to NM_003285.2 E184E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr7:5410915 G>C maps to NM_001080495.2 A1103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr7:5427516 G>A maps to NM_001080495.2 G646G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr7:5372405 G>T maps to NM_001080495.2 R1998R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JR-01A-11D-A29I-10 chr7:5352634 T>G maps to NM_001080495.2 S2629S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr7:5352547 T>G maps to NM_001080495.2 S2658S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:5372405 G>T maps to NM_001080495.2 R1998R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr7:5372405 G>T maps to NM_001080495.2 R1998R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L6-01A-11D-A29I-10 chr7:5372405 G>T maps to NM_001080495.2 R1998R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LA-01A-11D-A29I-10 chr7:5352664 T>G maps to NM_001080495.2 S2619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LA-01A-11D-A29I-10 chr7:5372405 G>T maps to NM_001080495.2 R1998R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LD-01A-11D-A29I-10 chr7:5372405 G>T maps to NM_001080495.2 R1998R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LP-01A-11D-A29I-10 chr7:5372498 C>T maps to NM_001080495.2 K1967K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr22:40657845 G>T maps to ENST00000454349 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr22:40666126 C>A maps to ENST00000454349 V950V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr17:76045634 G>A maps to NM_001142640.1 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr17:76067212 G>C maps to NM_001142640.1 R939R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JQ-01A-11D-A29I-10 chr17:76100841 C>T maps to NM_001142640.1 S1699S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr7:47331568 C>G maps to NM_022748.11 L1304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr6:32017976 G>A maps to ENST00000375244 S3079S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr6:32037420 C>T maps to ENST00000375244 P1832P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr22:35742924 T>G maps to ENST00000451197 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr22:35734780 G>A maps to ENST00000451197 A417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr20:42683067 C>T maps to ENST00000348077 Q270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr17:7579311 C>A maps to NM_001126112.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr17:7579520 C>A maps to NM_001126112.1 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr17:7579721 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr17:7574011 C>A maps to NM_001126112.1 E339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr17:7577017 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5K8-01A-11D-A29I-10 chr11:68851465 G>T maps to NM_139075.3 A581A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr1:154141803 G>A maps to ENST00000328159 H240H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr19:48305649 C>T maps to NM_198479.2 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JR-01A-11D-A29I-10 chr19:48305649 C>T maps to NM_198479.2 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr16:1291286 C>T maps to ENST00000461509 H72H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr21:10944669 G>T maps to NM_199261.2 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr13:20024410 G>A maps to NM_199254.2 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr20:30388861 C>T maps to ENST00000340513 F777F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr22:50636362 C>T maps to NM_025204.2 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr16:67189372 C>A maps to NM_003789.3 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr9:139818400 G>C maps to ENST00000359662 V464V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr6:111912950 G>A maps to ENST00000340026 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:209936415 C>A maps to NM_025228.2 Y185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:209936706 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr12:112590549 C>G maps to NM_006700.2 S568S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J1-01A-11D-A29I-10 chr3:42265105 C>T maps to NM_001042646.1 G913G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JT-01A-11D-A29I-10 chr4:118005440 T>A maps to NM_152402.2 *370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:152710778 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5L3-01A-11D-A29I-10 chr20:368652 A>G did not map to a codon.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr4:154216709 G>A maps to NM_015271.3 T344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr1:114948140 C>A maps to NM_015906.3 E887*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr7:99507253 G>A maps to NM_033017.3 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr3:140407266 C>T maps to NM_152616.4 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr17:73871532 G>C maps to NM_033452.2 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr11:5701023 C>T maps to NM_033034.2 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr8:67049358 C>T maps to NM_184085.1 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr1:248039250 C>T maps to NM_015431.3 T307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J7-01A-11D-A29I-10 chr11:5624520 A>C maps to NM_001003819.3 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr1:26386771 G>T maps to NM_032588.2 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:231349590 C>A maps to NM_001004342.3 T718T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:231349648 C>T maps to NM_001004342.3 Q738*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr14:51492066 G>T maps to ENST00000338969 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr4:189068072 C>A maps to NM_178556.3 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr5:14420026 A>C maps to NM_007118.2 T1700T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KZ-01A-11D-A29I-10 chr5:14387851 C>T maps to NM_007118.2 L1259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr22:38121764 C>T maps to NM_001039141.2 R1068*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:230723755 C>G maps to ENST00000389044 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JX-01A-11D-A29I-10 chr23:100297092 T>C did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr14:103999081 C>T maps to ENST00000299201 C165C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr23:54951476 A>G did not map to a codon.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr23:111195290 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:111025190 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:135692847 G>C maps to NM_020389.2 Y76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:135692904 C>A maps to NM_020389.2 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr5:135587358 C>T maps to NM_020389.2 P519P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr15:31295068 C>A maps to NM_002420.4 T1256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr21:45838382 C>T maps to ENST00000397932 R1136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr21:45795726 C>T maps to ENST00000397932 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr9:77431650 C>A maps to NM_017662.4 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr15:50941082 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KT-01A-11D-A29I-10 chr2:234858624 T>C maps to NM_024080.4 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:142606675 C>A maps to NM_019841.4 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr7:98609725 C>T maps to ENST00000359863 D3776D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr7:98581869 G>C maps to ENST00000359863 R3063R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:141955028 T>A maps to NM_001001317.2 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr9:135781059 T>A maps to NM_000368.4 T635T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr3:150128967 G>T maps to NM_014779.2 E611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr7:100064718 A>G maps to NM_030935.3 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr14:81557475 A>T maps to NM_000369.2 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JX-01A-11D-A29I-10 chr18:72998267 T>C maps to NM_005786.4 D257D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr19:50245267 C>T maps to NM_021733.1 S457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OF-01A-11D-A29I-10 chr8:143427200 C>A maps to ENST00000445818 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:99890215 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr12:3390494 G>A maps to ENST00000407263 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr23:53112256 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr6:116574988 A>T maps to ENST00000368611 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr2:54482556 G>T maps to NM_001003937.2 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr2:3196228 G>A maps to ENST00000398659 D342D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr8:144695921 G>A maps to NM_003313.3 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JQ-01A-11D-A29I-10 chr1:231042731 T>A maps to NM_024525.4 V834V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr3:180324358 C>A maps to NM_133462.3 Y380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr9:130479966 C>T maps to NM_144965.1 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr2:166773970 G>A maps to NM_024753.3 Y565Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:94852290 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5L4-01A-11D-A29I-10 chr2:47277185 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr6:80744820 A>G maps to NM_003318.4 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:1117119 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5JR-01A-11D-A29I-10 chr6:167753690 C>T maps to NM_031949.4 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr3:9870856 G>A maps to NM_001025930.3 Q587Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L3-01A-11D-A29I-10 chr14:76219244 C>T maps to NM_015072.4 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr2:179477033 C>A maps to NM_133378.4 E14172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:179422420 G>T maps to NM_133378.4 I26652I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:179429434 C>A maps to NM_133378.4 E24574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:179437247 T>C maps to NM_133378.4 T21969T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:179560964 A>T maps to NM_133378.4 A9034A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:179598047 C>T maps to NM_133378.4 E4080E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:179634823 G>T maps to NM_133378.4 V2868V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr2:179543216 C>T maps to NM_133378.4 E10034E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr2:179401240 C>A maps to NM_133378.4 V30843V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr2:179410343 A>T maps to NM_133378.4 P29263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr20:43118013 C>T maps to NM_024331.3 N287N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L6-01A-11D-A29I-10 chr13:19751261 G>A maps to NM_006001.1 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr10:95169 C>T maps to NM_177987.2 E3E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr17:40767022 G>A maps to NM_001070.4 R440R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr15:22855077 G>T maps to NM_052903.4 T513T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr12:3046801 A>G maps to NM_001160408.1 T310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr6:158870080 A>G maps to NM_020245.3 R199R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr14:53004372 T>C maps to NM_020784.2 E87E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr18:9886691 G>T maps to NM_001098529.1 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chr22:19867770 C>T maps to NM_006440.3 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr19:10476462 C>T maps to NM_003331.4 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr19:10476222 C>T maps to NM_003331.4 W327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JH-01A-11D-A30A-10 chr15:41862355 T>C did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr7:72159703 A>C maps to NM_001145440.1 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr19:34941213 A>G maps to NM_005499.2 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr4:68510475 G>T maps to NM_018227.5 G472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr16:1364364 A>G maps to NM_194259.1 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:142967265 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr8:48955656 C>T maps to NM_003350.2 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LA-01A-11D-A29I-10 chr12:109947449 G>T maps to NM_183415.1 E558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr7:157041207 C>T maps to NM_014671.2 Y876Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr20:3090888 C>A maps to NM_014948.2 E497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KV-01A-11D-A29I-10 chr2:170762565 A>T maps to ENST00000442603 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L3-01A-11D-A29I-10 chr1:19447842 C>G maps to ENST00000375267 L3327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr8:103284936 G>T maps to NM_015902.4 R2265R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr8:103297998 C>T maps to NM_015902.4 A1742A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr10:13275733 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr2:128934399 T>C maps to NM_020120.3 T1184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr2:128945078 G>A maps to NM_020120.3 P1511P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr4:69417566 C>T maps to NM_001076.2 K356K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:35968209 G>C maps to NM_152404.3 Y74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr4:115544818 A>T maps to NM_003360.3 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr6:34838841 G>A maps to NM_017754.3 P1310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr12:132401136 G>T did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr21:43510405 A>T did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr21:43531011 C>T maps to NM_173568.3 G560G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L3-01A-11D-A29I-10 chr19:17741046 A>G maps to ENST00000428389 V1280V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr15:54825157 G>T maps to ENST00000260323 E1864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr17:33513334 G>A maps to NM_173167.2 E851E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr8:35579842 C>G maps to ENST00000416672 G416G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr8:35608158 G>A maps to ENST00000416672 A670A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JH-01A-11D-A30A-10 chr11:67763106 A>G maps to NM_030930.2 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr11:67763106 A>G maps to NM_030930.2 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr11:67763106 A>G maps to NM_030930.2 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr12:109536256 C>G maps to NM_080911.2 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr22:24911293 G>T maps to NM_016327.2 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LL-01A-11D-A29I-10 chr19:18966868 C>G maps to ENST00000418384 A571A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr10:12046669 C>A maps to NM_015542.2 E455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J2-01A-11D-A29I-10 chr22:45691449 G>A maps to NM_006953.3 G238G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J3-01A-11D-A29I-10 chr19:29704001 T>C maps to NM_006003.2 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr19:29704001 T>C maps to NM_006003.2 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JI-01A-11D-A29I-10 chr19:29704001 T>C maps to NM_006003.2 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LD-01A-11D-A29I-10 chr19:29704001 T>C maps to NM_006003.2 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OF-01A-11D-A29I-10 chr19:29704001 T>C maps to NM_006003.2 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr11:17542438 T>C maps to NM_153676.3 P396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr1:216062268 T>C maps to ENST00000366943 L2574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr1:215821062 G>T maps to ENST00000366943 L4864L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:216144041 G>T maps to ENST00000366943 Y2294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:216498840 G>T maps to ENST00000366943 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:216246595 G>A maps to ENST00000366943 V1873V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr3:179437818 T>C maps to NM_003940.2 H299H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr12:62778064 A>G maps to ENST00000280377 P485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L9-01A-11D-A29I-10 chr11:119234663 G>C maps to NM_171997.2 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr9:132637738 C>T maps to NM_001008563.3 T733T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OF-01A-11D-A29I-10 chr16:23119495 C>T maps to NM_020718.3 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JH-01A-11D-A30A-10 chr2:61417513 G>T maps to NM_014709.3 A3255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr2:85872160 C>T maps to NM_006590.2 D506D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr7:6175529 C>G maps to ENST00000404835 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr17:9549359 T>G maps to NM_153210.3 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr23:55515271 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:41025465 G>C did not map to a codon.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr23:41075160 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr23:129059083 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:129053171 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr13:52604695 G>T maps to NM_021645.5 E586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr12:101723172 G>A maps to NM_014503.2 Q1121Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr16:70726794 C>A maps to NM_018052.3 P705P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:7837353 G>A maps to NM_004781.3 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:116206307 G>T maps to NM_001172412.1 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr6:31759412 G>A maps to NM_006295.2 N358N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr6:31747037 G>A maps to NM_006295.2 G1144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr6:30890884 C>T maps to NM_001167734.1 G760G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JT-01A-11D-A29I-10 chr16:4431678 G>A maps to NM_138440.2 Q267Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JQ-01A-11D-A29I-10 chr9:136650965 C>T maps to NM_001134398.1 Q488Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:108138962 C>A maps to NM_006113.4 E741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:108417588 C>A maps to NM_006113.4 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:82808021 C>A maps to NM_004385.4 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr8:67579169 C>A maps to NM_025054.4 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr23:7811811 C>G did not map to a codon.
Sequencing variant TCGA-OR-A5J7-01A-11D-A29I-10 chr23:8434366 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5JQ-01A-11D-A29I-10 chr3:38038981 T>C maps to NM_015873.3 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr3:38040536 G>A maps to NM_015873.3 G359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr9:2643346 C>T maps to NM_003383.3 C212C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr19:53762455 C>T maps to NM_173856.2 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr6:133014262 C>T maps to NM_004666.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr15:62170945 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5J1-01A-11D-A29I-10 chr1:12309383 T>G maps to NM_015378.2 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr1:12294376 C>G maps to NM_015378.2 V18V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:12339595 G>A maps to NM_015378.2 L1497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:12476831 G>T maps to NM_015378.2 G4095G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr12:122717401 G>A maps to NM_022916.4 L518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr16:46697063 C>T maps to NM_018206.4 W553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:107320375 C>A did not map to a codon.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr23:107320487 G>C did not map to a codon.
Sequencing variant TCGA-OR-A5JW-01A-11D-A29I-10 chr12:118506185 A>T maps to NM_019086.5 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr11:124618581 G>A maps to NM_014312.3 Q222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:54617624 C>G maps to ENST00000404951 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr14:68120199 C>A maps to NM_006370.2 E186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr10:116049186 C>T maps to NM_198496.1 H687H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr12:6125361 G>C maps to NM_000552.3 S1783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr12:6219642 G>A maps to NM_000552.3 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:48547808 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr1:27736228 G>A maps to NM_006990.2 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr9:14857 C>G maps to NM_182905.4 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:123329096 T>C maps to NM_003941.2 S485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr2:224809875 G>T maps to NM_020830.3 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr4:10086076 G>A maps to NM_017491.3 D343D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr17:9542006 C>A maps to NM_145054.4 I518I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr4:177098262 T>A maps to NM_170710.4 S1207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L6-01A-11D-A29I-10 chr4:177061125 G>T did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr19:985941 G>A maps to NM_024100.3 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr14:100996311 T>C maps to NM_001161476.1 Y523Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr2:128477186 G>T maps to NM_018383.4 G804G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr2:20174292 G>T maps to NM_001006657.1 C224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr21:44296861 G>C maps to NM_018669.4 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J7-01A-11D-A29I-10 chr23:117570691 G>C did not map to a codon.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr23:117532432 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:48934318 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr23:48935336 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:48935535 G>A did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr3:113145005 C>T maps to NM_001164496.1 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr16:74922198 C>A maps to NM_030581.3 R738R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr7:158738346 G>A maps to NM_018051.4 A1026A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:241846793 T>C maps to NM_144625.4 N200N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr12:122413554 C>T maps to NM_144668.4 V990V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr7:134871774 C>T maps to NM_014149.3 S676S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr2:160132120 T>C maps to NM_001128212.1 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:27627875 G>A maps to ENST00000319394 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr11:9595767 C>T maps to NM_003390.3 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr4:6302544 C>T maps to NM_006005.3 F341F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr12:65471559 G>A maps to NM_007191.4 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr20:43348734 C>A maps to NM_003881.2 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JD-01A-11D-A29I-10 chr20:43348734 C>A maps to NM_003881.2 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr20:43348734 C>A maps to NM_003881.2 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr20:43348734 C>A maps to NM_003881.2 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L9-01A-11D-A29I-10 chr20:43348734 C>A maps to NM_003881.2 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr1:68624823 G>A maps to NM_024911.6 C162C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr9:96021244 G>A maps to ENST00000297954 T805T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr9:96021292 G>A maps to ENST00000297954 P821P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr9:96025907 T>C maps to ENST00000297954 F1157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr9:96051772 C>T maps to ENST00000297954 G1616G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:54228530 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:54263788 C>G did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:54263898 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr11:75898195 G>A maps to NM_004626.2 V326V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr7:120971849 C>T maps to NM_057168.1 N155N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr17:44846088 C>T maps to NM_030753.3 W222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr12:1742039 C>T maps to NM_032642.2 N99N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr3:13896294 G>T maps to NM_004625.3 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr11:32456693 C>A maps to NM_024426.4 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JR-01A-11D-A29I-10 chr11:32456693 C>A maps to NM_024426.4 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr11:32456693 C>A maps to NM_024426.4 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr11:32456693 C>A maps to NM_024426.4 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr11:32456693 C>A maps to NM_024426.4 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr23:10035509 A>G did not map to a codon.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:10106874 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5L9-01A-11D-A29I-10 chr8:87437478 T>G maps to NM_007013.3 G363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr16:69963354 G>A maps to NM_007014.3 K413K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5H8-01A-11D-A29I-10 chr3:39230609 G>A maps to NM_194293.2 H109H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:168107714 T>G maps to NM_152381.5 Y3271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:100169961 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:128888455 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr13:21374332 A>G maps to NM_022459.4 T703T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L4-01A-11D-A29I-10 chr8:21846585 G>C maps to ENST00000434536 L629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L4-01A-11D-A29I-10 chr8:21862550 A>G maps to ENST00000434536 S1081S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:67741212 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:67751769 C>G did not map to a codon.
Sequencing variant TCGA-OR-A5JY-01A-31D-A29I-10 chr23:67718935 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr14:75265521 A>G maps to NM_019589.2 G1174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:135738653 G>C maps to NM_025052.3 T1219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr1:155630074 G>T maps to ENST00000368339 I680I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr23:21875128 T>G did not map to a codon.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr2:98354471 G>A maps to NM_001079.3 P546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr3:167033572 G>T maps to ENST00000307529 Y413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr20:56186831 G>A maps to NM_030776.2 H275H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr6:109798047 G>A maps to NM_014797.2 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:119387849 G>T did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr9:129642193 C>T maps to ENST00000319119 C172C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr3:141162486 A>T maps to NM_001080412.2 G419G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr12:57397417 G>A maps to NM_014830.2 I428I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JR-01A-11D-A29I-10 chr19:59028584 G>A maps to NM_032792.2 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L9-01A-11D-A29I-10 chr19:59028584 G>A maps to NM_032792.2 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr19:59028362 G>A maps to NM_032792.2 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr9:125673274 G>A maps to NM_006626.4 C359C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5H8-01A-11D-A29I-10 chr1:37941414 C>G maps to NM_025079.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JI-01A-11D-A29I-10 chr23:64719017 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr11:110035300 A>G maps to NM_033390.1 T497T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr14:89069361 C>T maps to NM_024824.4 L569L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr19:47575242 T>A maps to NM_015168.1 A646A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr19:47575266 C>G maps to NM_015168.1 P638P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr19:47597798 G>A maps to NM_015168.1 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:117959691 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:111698227 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:111698590 G>C did not map to a codon.
Sequencing variant TCGA-P6-A5OF-01A-11D-A29I-10 chr10:81205022 G>A maps to NM_153367.3 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J7-01A-11D-A29I-10 chr20:278514 T>C maps to NM_033089.6 D96D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JQ-01A-11D-A29I-10 chr20:278514 T>C maps to NM_033089.6 D96D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr20:278514 T>C maps to NM_033089.6 D96D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr20:278514 T>C maps to NM_033089.6 D96D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KT-01A-11D-A29I-10 chr20:278514 T>C maps to NM_033089.6 D96D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L3-01A-11D-A29I-10 chr20:278514 T>C maps to NM_033089.6 D96D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:77912639 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:207174021 T>G maps to NM_020923.1 T1590T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chr5:825359 T>C maps to NM_024786.2 K314K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr23:74649033 C>G did not map to a codon.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr23:74636937 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr22:20131120 G>C maps to NM_013373.3 P656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:128940382 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr2:145153987 C>A maps to NM_014795.3 E1020*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr9:131513409 C>A maps to NM_006336.2 R392R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr7:1195214 A>C maps to ENST00000401903 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LD-01A-11D-A29I-10 chr8:135615136 G>T maps to NM_020863.3 Y275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr16:72829227 C>T maps to NM_006885.3 K2451K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr8:77617609 G>T maps to NM_024721.4 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr8:77763362 T>C maps to NM_024721.4 C1402C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr8:77764445 G>T maps to NM_024721.4 G1763G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr19:57065767 T>C maps to NM_020828.1 C538C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr2:43452792 C>G maps to NM_006887.4 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr19:36884173 A>G maps to NM_133466.2 H356H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr11:64855516 G>T maps to NM_006782.3 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr8:106814997 G>A maps to NM_012082.3 P896P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr8:106814686 G>T maps to NM_012082.3 G793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr8:106813888 C>T maps to NM_012082.3 R527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr14:68229078 G>T maps to NM_015346.3 G2070G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JX-01A-11D-A29I-10 chr4:2275834 G>A maps to NM_020972.2 F720F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J1-01A-11D-A29I-10 chr3:147108755 C>G maps to NM_001168379.1 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr23:101139568 A>G did not map to a codon.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr23:101139312 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5LO-01A-11D-A29I-10 chr7:44802985 C>T maps to NM_031449.3 R612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L9-01A-11D-A29I-10 chr23:70467668 C>T did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr20:45865240 G>A maps to ENST00000471951 I896I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr19:58578301 G>A maps to NM_007134.1 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr4:367200 C>A maps to NM_003441.2 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JV-01A-11D-A29I-10 chr19:58213467 T>G maps to NM_001085384.1 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KW-01A-11D-A29I-10 chr23:47230122 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr19:53572916 G>A maps to NM_001102603.1 C290C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr19:53577420 C>T maps to NM_001102603.1 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr16:3454511 G>A maps to NM_003450.2 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr23:47836738 G>T did not map to a codon.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr6:28244218 T>G maps to NM_001023560.2 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr16:3169353 C>T maps to NM_001042428.1 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OF-01A-11D-A29I-10 chr19:22171651 C>T maps to NM_007153.3 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr16:3191158 C>T maps to NM_001134655.1 G397G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr14:21560705 C>G maps to NM_001102454.1 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr14:21560705 C>G maps to NM_001102454.1 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KU-01A-11D-A29I-10 chr14:21560705 C>G maps to NM_001102454.1 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JX-01A-11D-A29I-10 chr19:44680488 G>C maps to NM_001032372.1 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JQ-01A-11D-A29I-10 chr19:44739302 T>C maps to NM_182490.1 N240N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr19:24309377 C>A maps to NM_203282.2 C192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L4-01A-11D-A29I-10 chr19:57723886 C>T maps to NM_003417.4 F474F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L9-01A-11D-A29I-10 chr19:9524184 A>G maps to NM_006631.2 A472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr7:111982630 C>A maps to NM_021994.2 T400T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chr22:22869084 C>T maps to NM_080740.3 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr19:45579613 G>C maps to NM_145288.1 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr19:9271916 C>T maps to NM_020933.4 C532C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr1:90487882 G>A maps to NM_182976.2 A460A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr1:90486369 C>T maps to NM_182976.2 H398H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr4:142154999 G>T maps to NM_014487.4 E274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr19:7585010 C>T maps to NM_018083.4 Q295*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-OR-A5J8-01A-11D-A29I-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr12:6777080 C>T maps to ENST00000407384 L129L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-OR-A5L5-01A-11D-A29I-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr12:6777074 C>T maps to ENST00000407384 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr18:72775250 G>T maps to NM_017757.2 P1858P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr19:8576669 C>T maps to NM_001146175.1 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr19:8576669 C>T maps to NM_001146175.1 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr19:8576669 C>T maps to NM_001146175.1 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr19:8576669 C>T maps to NM_001146175.1 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr19:53612772 A>T maps to NM_001164309.1 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr19:58002903 C>T maps to NM_001098491.1 D47D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr19:11892030 A>G maps to NM_152355.2 V464V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr3:44488378 C>T maps to NM_181489.5 P928P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr9:109746464 A>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:149463035 C>T maps to NM_207336.1 E185E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:149466283 C>A maps to NM_207336.1 E53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L6-01A-11D-A29I-10 chr7:149462336 G>A maps to NM_207336.1 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr7:149462336 G>A maps to NM_207336.1 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr19:50548674 C>T maps to NM_015428.1 C325C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KO-01A-11D-A29I-10 chr10:44111805 G>A maps to NM_145312.3 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr19:20307779 T>C maps to NM_052852.2 C87C. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-OR-A5J4-01A-11D-A29I-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr10:77159790 G>T maps to NM_032772.4 C219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr10:135122506 G>A maps to NM_145806.2 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr10:135122506 G>A maps to NM_145806.2 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr4:10446968 T>A maps to NM_053042.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr18:22806810 C>T maps to NM_015461.2 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr19:30935330 G>T maps to NM_014717.1 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr19:57911239 G>T maps to NM_001172773.1 E541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr19:12637691 T>A maps to NM_144976.3 I410I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr19:37210810 T>C maps to ENST00000423498 C394C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr19:56090492 A>C maps to NM_152600.2 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr19:56090308 G>A maps to NM_152600.2 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JR-01A-11D-A29I-10 chr15:85333952 A>G maps to NM_014630.2 Q746Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KZ-01A-11D-A29I-10 chr16:2049848 T>C maps to ENST00000431526 T567T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr16:2049848 T>C maps to ENST00000431526 T567T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr19:58500062 G>A maps to NM_025027.3 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr19:52856954 C>T maps to NM_001161425.1 D28D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JR-01A-11D-A29I-10 chr9:116810203 G>A maps to ENST00000374126 Q426Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JH-01A-11D-A30A-10 chr19:20807299 A>G maps to NM_001076675.2 A461A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LK-01A-11D-A29I-10 chr19:55995157 G>A maps to NM_033113.2 Q862Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JV-01A-11D-A29I-10 chr23:47918423 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:47919259 A>T did not map to a codon.
Sequencing variant TCGA-OR-A5J7-01A-11D-A29I-10 chr16:31092942 T>C maps to NM_014699.3 C1766C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr19:53668191 A>G maps to NM_024733.3 N517N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr19:23844979 G>A maps to NM_138330.2 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L9-01A-11D-A29I-10 chr19:22363459 A>G maps to NM_001001411.2 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chr8:144378867 A>G maps to NM_030895.2 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr8:144378867 A>G maps to NM_030895.2 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr8:144378867 A>G maps to NM_030895.2 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JL-01A-11D-A29I-10 chr8:144378867 A>G maps to NM_030895.2 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JP-01A-11D-A29I-10 chr8:144378867 A>G maps to NM_030895.2 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JT-01A-11D-A29I-10 chr8:144378867 A>G maps to NM_030895.2 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JV-01A-11D-A29I-10 chr8:144378867 A>G maps to NM_030895.2 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr8:144378867 A>G maps to NM_030895.2 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chr8:144378867 A>G maps to NM_030895.2 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chr8:144378867 A>G maps to NM_030895.2 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr8:144378867 A>G maps to NM_030895.2 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr8:144378867 A>G maps to NM_030895.2 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr8:144378867 A>G maps to NM_030895.2 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L1-01A-11D-A30A-10 chr8:144378867 A>G maps to NM_030895.2 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L3-01A-11D-A29I-10 chr8:144378867 A>G maps to NM_030895.2 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LA-01A-11D-A29I-10 chr8:144378867 A>G maps to NM_030895.2 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr8:144378867 A>G maps to NM_030895.2 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr19:12060899 T>A maps to NM_144566.1 S687S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr19:53086055 C>T maps to NM_001172655.1 C314C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr8:81553603 G>A maps to NM_001033723.2 D412D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr19:57133638 C>T maps to NM_021216.4 C328C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr23:84519341 T>C did not map to a codon.
Sequencing variant TCGA-OR-A5KZ-01A-11D-A29I-10 chr4:289887 G>A maps to ENST00000419098 C20C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K2-01A-11D-A29I-10 chr19:53912283 A>G maps to NM_001040185.1 K492K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr15:35275400 G>A maps to NM_014106.3 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr19:56133257 C>T maps to NM_203374.1 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr16:30594018 C>T maps to NM_152458.6 W360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JB-01A-11D-A29I-10 chr19:38027959 C>T maps to NM_001013659.2 Q134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr2:185803042 G>T maps to NM_194250.1 E974*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:185800947 T>C maps to NM_194250.1 T275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KW-01A-11D-A29I-10 chr19:53058712 A>G maps to NM_001039886.3 K848K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:47705684 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr19:58384935 C>A maps to NM_001144989.1 E608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JF-01A-11D-A29I-10 chr19:58384711 A>G maps to NM_001144989.1 H682H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chr19:58384444 A>G maps to NM_001144989.1 P771P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JX-01A-11D-A29I-10 chr19:58384417 A>G maps to NM_001144989.1 S780S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JX-01A-11D-A29I-10 chr19:58384711 A>G maps to NM_001144989.1 H682H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chr19:58384738 A>G maps to NM_001144989.1 G673G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr19:58384711 A>G maps to NM_001144989.1 H682H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr19:58385032 A>G maps to NM_001144989.1 S575S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5H8-01A-11D-A29I-10 chr19:58384711 A>G maps to NM_001144989.1 H682H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr19:11832935 A>G maps to NM_001080493.2 Y471Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr20:57769217 C>A maps to NM_178457.1 P1048P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr20:57829494 T>A maps to NM_178457.1 A1577A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr19:57175987 C>A maps to NM_001005850.1 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L2-01A-11D-A30A-10 chr19:57176050 G>T maps to NM_001005850.1 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chr19:52658976 T>C maps to NM_001102657.1 L653L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chr19:52568563 C>T maps to NM_001136499.1 A857A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr19:53856027 C>T maps to NM_138374.1 F700F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K9-01A-11D-A29I-10 chr19:9869035 T>C maps to NM_001077624.1 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr19:52888416 C>A maps to NM_001145434.1 V528V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JL-01A-11D-A29I-10 chr11:64884741 C>G maps to NM_014205.2 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LA-01A-11D-A29I-10 chr19:5456614 C>T maps to NM_181710.3 D371D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JH-01A-11D-A30A-10 chr3:102171983 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr23:15841142 A>G did not map to a codon.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr19:58549353 C>T maps to NM_182572.3 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr19:58846515 C>T maps to NM_181846.2 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr20:44486487 G>A maps to NM_080752.3 K8K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chr23:57619014 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr17:3959639 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KS-01A-11D-A30A-10 chr17:3916822 G>A maps to NM_015113.3 G2833G. Only missense variants will be evaluated by CHASM.
