5183 NP_705833 T224N not found in SNVbox database
5699 NP_705833 R345T not found in SNVbox database
6511 NP_705833 L484F not found in SNVbox database
9843 NP_705833 T904K not found in SNVbox database
9875 NP_705833 R185H not found in SNVbox database
3593 NP_705833 H79Y not found in SNVbox database
3853 NP_705833 H395R not found in SNVbox database
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-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-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-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-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-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-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 chr2:25505394 T>A maps to NM_175629.1 A121A. 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-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-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-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-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-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-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-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-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-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-A5J2-01A-11D-A29I-10 chrX:89177680 C>A maps to NM_138960.3 S199S. 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-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-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-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-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-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-A5J4-01A-11D-A29I-10 chr12:55714971 G>T maps to NM_001005182.1 G197*. Only missense variants will be evaluated by CHASM.
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-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-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-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-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-A5J4-01A-11D-A29I-10 chr19:51485655 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5J4-01A-11D-A29I-10 chr19:55105903 A>G did not map to a codon.
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-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-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-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-A5J4-01A-11D-A29I-10 chr22:50198008 C>A did not map to a codon.
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-A5J4-01A-11D-A29I-10 chr2:29445208 C>T did not map to a codon.
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-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-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-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-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-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-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-A5J4-01A-11D-A29I-10 chr6:135726086 A>C did not map to a codon.
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-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-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-A5J4-01A-11D-A29I-10 chr9:78910310 G>A maps to NM_001190482.1 E1102E. 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-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-A5J4-01A-11D-A29I-10 chrX:128722896 C>A maps to NM_000276.3 L792L. 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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-OR-A5J5-01A-11D-A29I-10 chr11:113860304 G>T maps to NM_213621.3 L457L. 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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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 chr16:48155703 G>A maps to NM_033226.2 Y545Y. 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-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 chr17:37934012 C>A maps to NM_012481.3 A239A. Only missense variants will be evaluated by CHASM.
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-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-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-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 chr19:1496348 C>T maps to ENST00000395479 R138R. 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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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 chr1:110467420 G>A maps to NM_000757.4 A531A. 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-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-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-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 chr20:1961121 G>T maps to NM_024411.4 Y204*. 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-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-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-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-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-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-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-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-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-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 chr5:131014836 G>A maps to NM_133372.2 R412*. Only missense variants will be evaluated by CHASM.
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-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-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-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-A5J5-01A-11D-A29I-10 chr7:97854150 C>T maps to ENST00000379795 T886T. 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-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-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-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-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-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-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 chr8:106814997 G>A maps to NM_012082.3 P896P. 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-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-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-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-A5J5-01A-11D-A29I-10 chr9:71861603 A>G did not map to a codon.
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 chr9:117166244 C>T maps to NM_015404.3 V783V. 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-A5J5-01A-11D-A29I-10 chrX:73961523 G>A maps to NM_001008537.2 T956T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chrX:106890919 C>T maps to NM_002764.3 N263N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chrX:114141203 C>T maps to NM_000868.2 F201F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J5-01A-11D-A29I-10 chrX:119512612 C>T maps to NM_001142447.2 Y299Y. Only missense variants will be evaluated by CHASM.
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-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-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-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-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-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-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-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-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-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-A5J6-01A-31D-A29I-10 chr7:116557778 A>G did not map to a codon.
Sequencing variant TCGA-OR-A5J6-01A-31D-A29I-10 chrX:19587242 G>A maps to NM_031892.2 L454L. 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-A5J7-01A-11D-A29I-10 chr14:94845821 C>T maps to NM_001127707.1 E348E. 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-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-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-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-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-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-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-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-A5J8-01A-11D-A29I-10 chr11:18451363 C>T maps to NM_017448.3 L109L. 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.
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-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-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-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-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-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-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-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-A5J8-01A-11D-A29I-10 chr18:19053017 G>T maps to NM_001142966.1 E737*. 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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-A5J8-01A-11D-A29I-10 chr9:96025907 T>C maps to ENST00000297954 F1157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J8-01A-11D-A29I-10 chrX:20044070 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5J9-01A-11D-A29I-10 chr12:56075585 C>T maps to NM_152637.2 T16T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J9-01A-11D-A29I-10 chr15:41680714 A>T maps to NM_016013.2 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J9-01A-11D-A29I-10 chr15:45724278 A>G maps to NM_197955.1 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J9-01A-11D-A29I-10 chr16:58031920 G>A maps to NM_020807.1 H83H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J9-01A-11D-A29I-10 chr19:35551398 C>T maps to NM_182983.2 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J9-01A-11D-A29I-10 chr1:4772334 G>A maps to NM_018836.3 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5J9-01A-11D-A29I-10 chr2:24522815 G>T maps to NM_006277.2 R436R. 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-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 chr11:48267185 C>A maps to NM_001004727.1 L177L. 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-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-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-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-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-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-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-OR-A5JA-01A-11D-A29I-10 chr12:129028582 C>A maps to NM_001136103.2 G352G. 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-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-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 chr14:36191027 G>T maps to NM_194301.2 S711*. 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-A5JA-01A-11D-A29I-10 chr15:54825157 G>T maps to ENST00000260323 E1864*. 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-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-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-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-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 chr17:28601154 G>A maps to NM_000386.2 R236*. 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 chr18:43221303 C>A maps to NM_007163.3 I374I. 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-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-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-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-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-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 chr1:204588337 G>A maps to NM_201630.1 P261P. 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-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-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-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-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-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-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-A5JA-01A-11D-A29I-10 chr3:148575242 G>T did not map to a codon.
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-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-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 chr4:37903766 C>A maps to NM_015173.2 V17V. 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-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-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-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-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-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-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-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-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-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-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 chr6:30552278 G>T maps to NM_001025091.1 E443*. 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-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-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-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-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-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-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-A5JA-01A-11D-A29I-10 chr6:135513460 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr6:151647015 C>A maps to NM_144497.2 I7I. 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-A5JA-01A-11D-A29I-10 chr7:63982291 G>T maps to NM_178558.4 I280I. 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-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-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-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-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-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-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-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-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 chrX:2942060 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chrX:40568697 G>T maps to NM_004229.3 S396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chrX:67741212 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chrX:70596892 C>A maps to ENST00000449580 S188*. 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-A5JB-01A-11D-A29I-10 chr10:61847903 C>A did not map to a codon.
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-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-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-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-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-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-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-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-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-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-A5JB-01A-11D-A29I-10 chr12:48131973 A>T 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-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-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-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-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-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-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-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-A5JB-01A-11D-A29I-10 chr13:70413105 A>T did not map to a codon.
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-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-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-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-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-OR-A5JB-01A-11D-A29I-10 chr15:28422656 T>C did not map to a codon.
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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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 chr19:38027959 C>T maps to NM_001013659.2 Q134*. 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-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-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-A5JB-01A-11D-A29I-10 chr19:51890472 C>A maps to NM_030657.3 A75A. 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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-A5JB-01A-11D-A29I-10 chr4:15689682 G>A maps to NM_001145191.1 L361L. 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-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-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-A5JB-01A-11D-A29I-10 chr5:26881655 C>A maps to NM_016279.3 R653R. 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-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-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-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-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-A5JB-01A-11D-A29I-10 chr7:6022453 C>T did not map to a codon.
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-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-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-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-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-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-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-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-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-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-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-A5JB-01A-11D-A29I-10 chrX:83124905 C>T maps to NM_021118.1 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JC-01A-11D-A29I-10 chr11:1643233 G>T maps to ENST00000359229 G30G. 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-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-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-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-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-A5JC-01A-11D-A29I-10 chrX:150884635 C>A maps to NM_033085.2 S15S. 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-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-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-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-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-A5JE-01A-11D-A29I-10 chr11:72578933 C>T maps to ENST00000409314 V452V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JE-01A-11D-A29I-10 chr11:92624212 G>A maps to ENST00000298047 V4568V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JE-01A-11D-A29I-10 chr19:8370030 G>C maps to NM_016579.3 S51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JE-01A-11D-A29I-10 chr1:247875886 G>T maps to NM_001005286.1 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JE-01A-11D-A29I-10 chr1:248845365 G>A maps to NM_001004734.1 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JE-01A-11D-A29I-10 chr20:57485074 T>C maps to NM_080425.2 A946A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JE-01A-11D-A29I-10 chr2:190595327 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5JE-01A-11D-A29I-10 chr2:215847043 G>T maps to NM_173076.2 G1482G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JE-01A-11D-A29I-10 chr5:140215890 C>T maps to NM_018910.2 D641D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JE-01A-11D-A29I-10 chr7:27880466 C>T maps to NM_175061.3 E135E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JE-01A-11D-A29I-10 chr9:139990834 A>G maps to NM_016219.3 T204T. 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-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-A5JF-01A-11D-A29I-10 chr15:62170945 C>A did not map to a codon.
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 chr16:53692790 C>T did not map to a codon.
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-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-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-A5JF-01A-11D-A29I-10 chr5:66429339 A>G did not map to a codon.
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-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-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-A5JF-01A-11D-A29I-10 chrX:110973751 G>C did not map to a codon.
Sequencing variant TCGA-OR-A5JG-01A-11D-A29I-10 chr11:1643233 G>T maps to ENST00000359229 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JG-01A-11D-A29I-10 chr16:1306346 G>C maps to NM_012217.2 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JG-01A-11D-A29I-10 chr16:3304218 C>T maps to NM_000243.2 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JG-01A-11D-A29I-10 chr17:7579310 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5JG-01A-11D-A29I-10 chr19:44934457 G>A maps to NM_014518.2 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JG-01A-11D-A29I-10 chr19:58132311 A>G maps to NM_003435.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JG-01A-11D-A29I-10 chr21:42749765 C>T maps to NM_002463.1 C100C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JG-01A-11D-A29I-10 chr4:100512917 A>G maps to ENST00000511045 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JG-01A-11D-A29I-10 chr7:143175366 G>T maps to NM_176883.2 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JG-01A-11D-A29I-10 chr8:61766036 G>A maps to NM_017780.2 S2251S. 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-A5JH-01A-11D-A30A-10 chr19:55869898 T>G maps to NM_001145402.1 P779P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JH-01A-11D-A30A-10 chr19:55869901 C>T maps to NM_001145402.1 Q778Q. 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-A5JH-01A-11D-A30A-10 chr3:183959625 G>T maps to ENST00000413060 E1189*. 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-A5JJ-01A-11D-A29I-10 chr12:53663136 C>T maps to NM_012291.4 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JJ-01A-11D-A29I-10 chr12:82147976 C>T maps to NM_003625.2 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JJ-01A-11D-A29I-10 chr1:151503098 G>A maps to NM_020770.2 Q816Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JJ-01A-11D-A29I-10 chr20:34129864 C>T maps to ENST00000447986 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JJ-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-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-A5JK-01A-11D-A29I-10 chr10:102775565 G>A maps to NM_001195263.1 Q526*. 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-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-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-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-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-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-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-A5JK-01A-11D-A29I-10 chrX:27765407 G>A maps to NM_001136533.1 E132E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JK-01A-11D-A29I-10 chrX:129059083 G>A maps to NM_006649.3 K554K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JL-01A-11D-A29I-10 chr17:7750175 T>C maps to NM_001080424.1 L251L. Only missense variants will be evaluated by CHASM.
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-A5JM-01A-11D-A29I-10 chr11:56310463 G>T maps to NM_001005245.1 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JM-01A-11D-A29I-10 chr19:11598308 C>T maps to NM_138783.3 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JM-01A-11D-A29I-10 chr19:17838766 C>T maps to NM_018174.4 N858N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JM-01A-11D-A29I-10 chr19:20728339 A>G maps to NM_001159293.1 H223H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JM-01A-11D-A29I-10 chr1:181767903 G>A maps to ENST00000357570 G2292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JM-01A-11D-A29I-10 chr2:166032829 G>T maps to NM_006922.3 I25I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JM-01A-11D-A29I-10 chr3:49155467 C>T maps to ENST00000434032 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JM-01A-11D-A29I-10 chr3:123633688 C>T maps to NM_022757.4 A892A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JM-01A-11D-A29I-10 chr5:57755591 C>G maps to NM_006622.2 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JM-01A-11D-A29I-10 chr6:18459915 C>A maps to NM_182757.3 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JM-01A-11D-A29I-10 chr7:29923751 G>C maps to NM_001080529.1 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JM-01A-11D-A29I-10 chr7:100416168 C>T maps to NM_004444.4 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JM-01A-11D-A29I-10 chr8:101540155 T>C maps to NM_198401.2 E129E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JM-01A-11D-A29I-10 chrX:19428067 A>G maps to NM_001001671.3 F574F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JM-01A-11D-A29I-10 chrX:56591775 C>G maps to NM_013444.3 G490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JM-01A-11D-A29I-10 chrX:110395636 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5JO-01A-11D-A29I-10 chr10:126480360 C>G maps to NM_212554.2 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JO-01A-11D-A29I-10 chr19:4531657 G>A maps to NM_001013706.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JO-01A-11D-A29I-10 chr2:95539854 T>G did not map to a codon.
Sequencing variant TCGA-OR-A5JO-01A-11D-A29I-10 chr2:223782836 C>T maps to NM_203372.1 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JO-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-A5JO-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-A5JO-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-A5JO-01A-11D-A29I-10 chr5:64468660 G>A maps to NM_197941.2 Q1029*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JO-01A-11D-A29I-10 chr5:140222696 G>T maps to NM_018911.2 V597V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JO-01A-11D-A29I-10 chr6:82461741 G>A maps to ENST00000369756 G120G. 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-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-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-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-A5JP-01A-11D-A29I-10 chr12:52188153 G>T did not map to a codon.
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-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-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-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-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-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-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-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-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-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-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-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-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-A5JP-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-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-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 chr17:39262095 C>T maps to ENST00000377731 P147P. 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-A5JQ-01A-11D-A29I-10 chr7:117242877 A>T did not map to a codon.
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-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-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-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-A5JR-01A-11D-A29I-10 chr19:58385797 C>T maps to NM_001144989.1 G320G. 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-A5JS-01A-11D-A29I-10 chr11:95825406 C>T maps to NM_032427.1 Q596Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JS-01A-11D-A29I-10 chr12:120616699 G>A maps to NM_006836.1 H160H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JS-01A-11D-A29I-10 chr13:48934193 C>T maps to NM_000321.2 Q217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JS-01A-11D-A29I-10 chr16:20335573 A>G maps to NM_001007240.1 Y33Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JS-01A-11D-A29I-10 chr17:38561084 G>A maps to ENST00000357601 F704F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JS-01A-11D-A29I-10 chr17:77043878 C>T maps to ENST00000392445 F195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JS-01A-11D-A29I-10 chr4:15444215 C>T maps to NM_001135170.1 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JS-01A-11D-A29I-10 chr4:126367513 C>T maps to NM_024582.4 S2420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JS-01A-11D-A29I-10 chr5:16701500 G>A maps to NM_012334.2 D1001D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JS-01A-11D-A29I-10 chr6:27368445 C>T maps to NM_001076781.1 H99H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JS-01A-11D-A29I-10 chr6:82461741 G>A maps to ENST00000369756 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JS-01A-11D-A29I-10 chr6:108194051 G>T maps to NM_007214.4 S700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JS-01A-11D-A29I-10 chr6:137193358 G>A maps to NM_000288.3 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JS-01A-11D-A29I-10 chr8:72981347 G>T maps to NM_007332.2 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JS-01A-11D-A29I-10 chr9:15478494 G>A maps to NM_001128217.1 P203P. 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-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-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-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-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-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-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-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 chr5:140503193 G>A maps to NM_018938.2 P538P. 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-A5JU-01A-11D-A30A-10 chr20:43943205 G>C did not map to a codon.
Sequencing variant TCGA-OR-A5JU-01A-11D-A30A-10 chr22:19706332 C>A maps to ENST00000383045 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JU-01A-11D-A30A-10 chr2:21233523 T>A maps to NM_000384.2 P2072P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JU-01A-11D-A30A-10 chr3:173322701 C>A maps to NM_014932.2 S105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JU-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-OR-A5JU-01A-11D-A30A-10 chr4:1388973 T>C maps to NM_175918.3 D225D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JU-01A-11D-A30A-10 chr6:161015129 G>A maps to NM_005577.2 P1163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JU-01A-11D-A30A-10 chr7:11441491 C>T maps to ENST00000423059 P1447P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JU-01A-11D-A30A-10 chrX:72674419 G>T maps to NM_005193.1 *285L. 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-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-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-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-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-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-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-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-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-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-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-A5JW-01A-11D-A29I-10 chr16:21061228 A>T did not map to a codon.
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-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-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-A5JW-01A-11D-A29I-10 chrX:91132450 C>A maps to NM_032968.3 I404I. 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-A5JX-01A-11D-A29I-10 chr19:42603759 C>T maps to ENST00000342301 P135P. 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-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-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-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-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-A5JX-01A-11D-A29I-10 chrX:31792219 A>G maps to ENST00000357033 L2467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JX-01A-11D-A29I-10 chrX:49099774 C>T maps to NM_014008.3 P187P. 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-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-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-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-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-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-A5JY-01A-31D-A29I-10 chr20:30388861 C>T maps to ENST00000340513 F777F. 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-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-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-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-A5JY-01A-31D-A29I-10 chr7:127991344 A>G maps to NM_001174164.1 A755A. 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-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-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-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-OR-A5JZ-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-A5JZ-01A-11D-A29I-10 chr19:52249665 G>A maps to NM_002029.3 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JZ-01A-11D-A29I-10 chr1:16577407 C>T maps to NM_018994.1 Q637Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JZ-01A-11D-A29I-10 chr2:201437309 G>T maps to NM_152524.5 T747T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JZ-01A-11D-A29I-10 chr4:79351449 T>C maps to NM_025074.6 L1616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5JZ-01A-11D-A29I-10 chr8:12957771 A>G maps to NM_182643.2 L692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K0-01A-11D-A29I-10 chr11:63994396 G>A maps to NM_032344.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K0-01A-11D-A29I-10 chr11:117335892 G>T maps to NM_020693.2 P1070P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K0-01A-11D-A29I-10 chr13:98658493 A>G maps to NM_002271.4 P554P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K0-01A-11D-A29I-10 chr14:86089504 C>A maps to NM_013231.4 G549G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K0-01A-11D-A29I-10 chr16:23706391 G>C maps to NM_033266.3 V664V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-OR-A5K0-01A-11D-A29I-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-OR-A5K0-01A-11D-A29I-10 chr17:3195042 T>A maps to ENST00000397187 G284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K0-01A-11D-A29I-10 chr17:40342699 C>T maps to NM_032484.4 V410V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K0-01A-11D-A29I-10 chr19:964308 C>A maps to NM_005224.2 Y276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K0-01A-11D-A29I-10 chr19:15839026 C>T maps to NM_013939.2 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K0-01A-11D-A29I-10 chr19:46914645 C>T maps to NM_032040.3 Q474Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K0-01A-11D-A29I-10 chr19:56901429 G>A maps to NM_144690.1 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K0-01A-11D-A29I-10 chr1:153748354 G>T maps to ENST00000271857 G256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K0-01A-11D-A29I-10 chr1:240371483 A>T maps to ENST00000406993 L1267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K0-01A-11D-A29I-10 chr3:113655143 A>G maps to NM_017577.4 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K0-01A-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-A5K0-01A-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-A5K0-01A-11D-A29I-10 chr5:1244383 G>A maps to NM_182632.2 G464G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K0-01A-11D-A29I-10 chr6:41652374 G>T maps to ENST00000343317 R551R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K0-01A-11D-A29I-10 chr6:105526423 C>A maps to NM_001004317.2 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K0-01A-11D-A29I-10 chr6:170033153 G>A maps to NM_182552.3 L704L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K0-01A-11D-A29I-10 chr7:44151811 G>C maps to NM_001129.3 P703P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K0-01A-11D-A29I-10 chr8:6296612 C>T maps to NM_024596.3 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K0-01A-11D-A29I-10 chr8:28654145 G>A maps to NM_018250.3 N257N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K0-01A-11D-A29I-10 chrX:76939348 T>A maps to NM_000489.3 K467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K1-01A-11D-A29I-10 chr14:67578630 T>C maps to NM_020806.4 D489D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K1-01A-11D-A29I-10 chr1:55349289 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5K1-01A-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-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-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-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-A5K4-01A-11D-A29I-10 chr10:48428895 C>T maps to NM_004962.2 A330A. Only missense variants will be evaluated by CHASM.
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-A5K4-01A-11D-A29I-10 chr11:63531282 G>A maps to NM_001144936.1 D548D. 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-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-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-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-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-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-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-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-A5K4-01A-11D-A29I-10 chr12:117273984 G>C 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-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-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-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-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-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-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-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-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-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-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-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-A5K4-01A-11D-A29I-10 chr17:18286643 C>T maps to NM_001145127.1 D244D. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-OR-A5K4-01A-11D-A29I-10. Mapping will be selected arbitrarily.
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-A5K4-01A-11D-A29I-10 chr18:18981162 G>A maps to NM_001142966.1 T195T. 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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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 chr2:133541905 A>T maps to NM_207363.2 P826P. 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-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-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-A5K4-01A-11D-A29I-10 chr3:130124437 C>T maps to ENST00000312481 R1430*. 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-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-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-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 chr5:126154660 T>C maps to NM_005573.3 A329A. Only missense variants will be evaluated by CHASM.
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-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-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-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-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-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-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-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-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 chr8:145745150 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 chr9:101258724 G>A maps to NM_005458.7 N234N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chrX:54951476 A>G maps to NM_001039705.1 E487E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chrX:107811999 C>T maps to ENST00000328300 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chrX:114425209 G>A maps to NM_001145346.1 G402G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chrX:129190050 C>T maps to ENST00000303743 Y1766Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K4-01A-11D-A29I-10 chrX:153588003 G>A maps to NM_001110556.1 S1330S. 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-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-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-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-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-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-A5K5-01A-11D-A29I-10 chr17:37070575 A>C did not map to a codon.
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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-A5K5-01A-11D-A29I-10 chrX:53410123 C>T maps to NM_006306.2 Q1008Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K5-01A-11D-A29I-10 chrX:107979445 G>T maps to NM_003604.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K6-01A-11D-A29I-10 chr11:65826802 C>T maps to NM_006842.2 D438D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K6-01A-11D-A29I-10 chr17:56399728 C>T maps to NM_004758.2 E454E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K6-01A-11D-A29I-10 chr17:61787882 G>A maps to NM_001003787.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K6-01A-11D-A29I-10 chr19:45028105 G>A maps to NM_001102597.1 Q129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K6-01A-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-A5K6-01A-11D-A29I-10 chr2:133425988 C>T maps to ENST00000409034 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K6-01A-11D-A29I-10 chr2:145187557 C>A maps to NM_014795.3 E37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K6-01A-11D-A29I-10 chr3:153994064 G>T maps to NM_020865.2 S974S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5K6-01A-11D-A29I-10 chr7:99305479 G>C maps to ENST00000292414 V457V. 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-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-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 chr6:33288623 G>A maps to NM_001350.4 Q310*. 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-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-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-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-A5K9-01A-11D-A29I-10 chr11:113103920 C>G maps to ENST00000316851 A524A. 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.
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-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-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-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-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-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-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-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-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-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-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-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-A5K9-01A-11D-A29I-10 chr1:1720546 A>C maps to NM_002074.2 A287A. 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-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-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-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-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-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-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-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-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-A5K9-01A-11D-A29I-10 chr4:69817433 G>C maps to NM_024743.3 L15L. 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-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-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-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-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-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-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-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-A5K9-01A-11D-A29I-10 chrX:101139312 C>T maps to NM_001011657.3 Q362Q. 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-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-A5KB-01A-11D-A30A-10 chr10:13275733 C>A did not map to a codon.
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-A5KB-01A-11D-A30A-10 chr10:25839903 G>T did not map to a codon.
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-A5KB-01A-11D-A30A-10 chr10:49934092 C>G maps to NM_020945.1 L253L. 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-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-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 chr10:61112191 C>A maps to ENST00000442566 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr10:68139069 G>T maps to NM_013266.2 A524A. 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-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-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 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 chr10:108589373 G>T maps to NM_001013031.1 T228T. 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-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-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-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-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-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-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-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-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-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 chr11:15197587 G>T maps to NM_001031853.3 E167*. 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-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 chr11:55433022 C>A maps to NM_001004704.1 P127P. 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-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-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-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-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 chr11:64855516 G>T maps to NM_006782.3 R288R. 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-A5KB-01A-11D-A30A-10 chr11:87013484 G>T did not map to a codon.
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-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-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 chr11:103818442 G>A maps to NM_025208.4 Q174*. 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 chr12:4554550 G>C maps to NM_020996.1 R62R. 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-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-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-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-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-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-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-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-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-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-A5KB-01A-11D-A30A-10 chr12:102055035 C>A maps to NM_002465.2 I676I. Only missense variants will be evaluated by CHASM.
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-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-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-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-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-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-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-A5KB-01A-11D-A30A-10 chr13:43896518 C>A did not map to a codon.
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-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 chr13:96743550 C>G maps to NM_153456.2 R145R. 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-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-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 chr14:35005308 G>A maps to NM_018453.3 L83L. 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-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-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-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-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-A5KB-01A-11D-A30A-10 chr14:95030148 C>G maps to NM_006215.2 T110T. 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 chr14:97029217 G>C maps to NM_032632.3 L710L. 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-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-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-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-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-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 chr15:42503947 C>G did not map to a codon.
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 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 chr15:50941082 C>A 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-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 chr15:81224295 C>A maps to NM_018689.1 T903T. 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-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-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 chr16:4164588 C>A maps to NM_001116.3 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr16:10769881 C>A maps to NM_144674.1 L340L. 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-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 chr16:20331585 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 chr16:20476934 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 chr16:23716289 G>C maps to NM_033266.3 L304L. 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-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-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 chr16:55360429 G>T maps to NM_024335.2 A76A. 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-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-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-A5KB-01A-11D-A30A-10 chr16:68012505 G>T maps to NM_022357.3 C171*. 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-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-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-A5KB-01A-11D-A30A-10 chr17:3959639 C>A did not map to a codon.
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-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-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 chr17:10402001 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-A5KB-01A-11D-A30A-10 chr17:11461110 C>T maps to NM_207386.3 H382H. 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-OR-A5KB-01A-11D-A30A-10 chr17:15638661 G>A did not map to a codon.
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-A5KB-01A-11D-A30A-10 chr17:27383223 G>A maps to NM_016518.2 G358G. 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 chr17:28748839 A>T maps to NM_001304.4 V432V. 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-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-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-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-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 chr17:45894627 T>A maps to NM_145798.2 T232T. 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-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-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-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-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-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 chr18:34853087 C>G maps to NM_020180.3 A280A. 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 chr18:44561325 G>A maps to NM_016427.2 Q104*. 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-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-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 chr18:72775250 G>T maps to NM_017757.2 P1858P. 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-OR-A5KB-01A-11D-A30A-10 chr19:6416661 C>A did not map to a codon.
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 chr19:15586649 C>G maps to NM_052890.3 L277L. 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-A5KB-01A-11D-A30A-10 chr19:31769009 G>T maps to NM_020856.2 S563S. 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 chr19:39103251 T>G maps to NM_001042600.1 R222R. 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-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 chr1:1117119 G>A did not map to a codon.
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-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 chr1:6196855 G>A maps to NM_015557.2 L836L. 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-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 chr1:12854330 G>C maps to NM_023013.2 L185L. 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-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 chr1:27627875 G>A maps to ENST00000319394 P464P. Only missense variants will be evaluated by CHASM.
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-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-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-A5KB-01A-11D-A30A-10 chr1:44063548 G>A maps to NM_002840.3 A648A. Only missense variants will be evaluated by CHASM.
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-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-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-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-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-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 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 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 chr1:144854655 C>A maps to NM_014644.4 G2272*. 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-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-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 chr1:157559042 C>T maps to NM_031282.2 Q86Q. 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-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 chr1:159175763 C>T maps to NM_001122951.2 L181L. 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-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-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-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-A5KB-01A-11D-A30A-10 chr1:181767816 C>A maps to ENST00000357570 S2263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr1:182499424 C>A maps to NM_001137669.1 S724S. 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-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-A5KB-01A-11D-A30A-10 chr1:201009797 C>A maps to NM_000069.2 L1726L. 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 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-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-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 chr1:211264024 A>T maps to NM_172362.2 P106P. 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-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-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-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-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-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-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 chr1:237954769 C>A maps to NM_001035.2 A4506A. 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 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 chr1:248263393 C>G maps to NM_175911.2 T239T. 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 chr1:248512582 C>A maps to NM_001001918.1 S169S. 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 chr20:2542506 A>T maps to NM_080751.2 S135S. 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-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-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-A5KB-01A-11D-A30A-10 chr20:5904313 C>A maps to NM_001819.2 S508S. 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-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-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-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-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 chr20:23472360 G>T maps to NM_005492.2 V19V. Only missense variants will be evaluated by CHASM.
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 chr20:34090550 G>T maps to NM_007186.3 E1452*. 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-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-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-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-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-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-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-A5KB-01A-11D-A30A-10 chr21:19666953 C>T maps to NM_002772.2 Q759Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr21:31812926 C>A maps to NM_181623.1 S94S. 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 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 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 chr22:28559431 C>T maps to NM_001145418.1 V363V. 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-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-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-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-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-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-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-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 chr2:32477522 C>T maps to NM_021209.4 W76*. 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 chr2:33752421 C>T maps to NM_170672.2 S342S. 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 chr2:48872173 C>A maps to NM_172311.2 G806G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr2:74761337 G>T maps to NM_032603.2 A655A. 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-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 chr2:107041064 G>A maps to ENST00000304514 L1120L. 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 chr2:125284868 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 chr2:128367425 C>A maps to ENST00000389524 A1009A. 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-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-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-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-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-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-A5KB-01A-11D-A30A-10 chr2:165353719 C>A did not map to a codon.
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-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-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-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 chr2:179481738 A>T maps to NM_133378.4 V13391V. 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 chr2:185800947 T>C maps to NM_194250.1 T275T. Only missense variants will be evaluated by CHASM.
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-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-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-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-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-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-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 chr2:230723755 C>G maps to ENST00000389044 S253S. 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 chr2:242066762 C>A maps to ENST00000358649 E523*. 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-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-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 chr3:13896294 G>T maps to NM_004625.3 R102R. 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-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-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-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-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-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-OR-A5KB-01A-11D-A30A-10 chr3:129695710 C>A maps to NM_007117.3 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr3:149095253 C>T maps to ENST00000383054 L27L. Only missense variants will be evaluated by CHASM.
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-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-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-A5KB-01A-11D-A30A-10 chr3:164786983 C>A did not map to a codon.
Alternatively spliced codon TCGA-OR-A5KB-01A-11D-A30A-10. Mapping will be selected arbitrarily.
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-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 chr3:183679296 A>T did not map to a codon.
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-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-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 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 chr3:194080770 C>A maps to NM_001135057.2 P340P. 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-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-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-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-A5KB-01A-11D-A30A-10 chr4:77244562 C>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-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-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 chr4:95497185 G>T did not map to a codon.
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-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-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-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-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-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-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 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-OR-A5KB-01A-11D-A30A-10 chr4:148968041 G>T did not map to a codon.
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 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 chr4:167020585 G>T maps to ENST00000507499 V961V. 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-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-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-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 chr5:13753343 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-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-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-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-A5KB-01A-11D-A30A-10 chr5:33576157 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr5:33938185 C>T maps to NM_016568.3 Y447Y. 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 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-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-A5KB-01A-11D-A30A-10 chr5:93077152 C>A maps to NM_153216.1 A39A. Only missense variants will be evaluated by CHASM.
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-A5KB-01A-11D-A30A-10 chr5:94852290 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-OR-A5KB-01A-11D-A30A-10 chr5:102508857 G>T did not map to a codon.
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-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-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 chr5:140167126 C>T maps to NM_018900.2 L418L. 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-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-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-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-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-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 chr5:140745588 C>T maps to NM_018918.2 Y564Y. 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-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-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-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-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-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-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-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-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-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-A5KB-01A-11D-A30A-10 chr6:26451900 A>T did not map to a codon.
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-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-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-A5KB-01A-11D-A30A-10 chr6:49574559 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr6:49701561 C>A did not map to a codon.
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-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-A5KB-01A-11D-A30A-10 chr6:56965610 G>T maps to ENST00000370708 E133*. 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-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-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 chr6:130761683 C>G maps to NM_052913.2 P39P. 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-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-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-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-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-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-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-A5KB-01A-11D-A30A-10 chr7:6554006 T>A maps to NM_001145118.1 T474T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:6561557 G>T maps to NM_001145118.1 S317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:8258072 C>A maps to ENST00000422063 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:11419313 A>C maps to ENST00000423059 P1511P. 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-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-OR-A5KB-01A-11D-A30A-10 chr7:45697346 G>A maps to NM_021116.2 E390E. 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-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-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 chr7:63529395 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:65554140 G>A maps to NM_000048.3 K299K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:65617217 G>T maps to ENST00000450043 R289R. 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-A5KB-01A-11D-A30A-10 chr7:81359059 C>A maps to NM_000601.4 E301*. 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-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-A5KB-01A-11D-A30A-10 chr7:96324203 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chr7:100855544 C>T maps to NM_001084.4 R372R. 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-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-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-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 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-A5KB-01A-11D-A30A-10 chr7:136912823 T>A did not map to a codon.
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-A5KB-01A-11D-A30A-10 chr7:140269462 C>A maps to NM_015689.3 E508*. 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-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-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-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-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-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-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-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-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-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-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-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-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-A5KB-01A-11D-A30A-10 chr8:23179794 C>T 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-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-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 chr8:38880769 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 chr8:69069639 G>T maps to NM_024870.2 E1439*. 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 chr8:86162996 T>A maps to NM_198584.2 P22P. 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-A5KB-01A-11D-A30A-10 chr8:92145518 G>T maps to NM_001129890.1 G189*. 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-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-A5KB-01A-11D-A30A-10 chr8:110464350 A>T did not map to a codon.
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-OR-A5KB-01A-11D-A30A-10 chr8:118183271 G>C did not map to a codon.
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-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-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-A5KB-01A-11D-A30A-10 chr8:133090000 G>T maps to ENST00000262283 G123G. 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-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-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-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 chr9:19063553 T>C maps to NM_017645.3 S467S. 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 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 chr9:88162050 A>T maps to ENST00000395847 S1218S. 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-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-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-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 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 chr9:125154576 G>T maps to NM_000962.2 G518G. 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-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 chr9:131513409 C>A maps to NM_006336.2 R392R. 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-A5KB-01A-11D-A30A-10 chr9:137658844 G>T did not map to a codon.
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-OR-A5KB-01A-11D-A30A-10 chrX:3241637 C>G maps to NM_015419.3 V696V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:3248113 C>A maps to NM_015419.3 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:8763195 C>A maps to NM_174951.3 G252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:15841142 A>G maps to NM_005089.3 K409K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:16168475 G>A maps to NM_005314.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:18942241 G>A maps to NM_000292.2 G575G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:19046317 C>A maps to NM_001079858.2 E133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:26212779 G>T maps to NM_173523.2 E273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:30268639 T>A maps to NM_177404.2 R10R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:32360318 C>A maps to ENST00000357033 G1940G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:37027034 G>T maps to NM_001013736.2 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:48678640 C>A maps to ENST00000444343 G786G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:48935535 G>A maps to ENST00000322995 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:50377364 G>T maps to NM_020717.3 R570R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:50377404 C>G maps to NM_020717.3 G556G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:51487048 T>A maps to NM_018094.4 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:54586951 G>C did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:69646559 G>A maps to NM_001171192.1 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:77912639 G>T maps to NM_152694.2 I426I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:91132645 T>A maps to NM_032968.3 S469S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:91133491 C>G maps to NM_032968.3 V751V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:91133562 C>A maps to NM_032968.3 S775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:100615076 C>A maps to NM_000061.2 E280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:100880256 C>A maps to NM_016607.3 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:101909809 T>A maps to NM_001184727.1 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:101970727 G>T maps to NM_138437.5 E311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:102334158 C>A maps to NM_022052.1 V456V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:104464178 C>A maps to NM_031274.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:106083403 G>T maps to NM_017752.2 G494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:110964939 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:115568955 A>C did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:118222704 C>A maps to NM_020721.1 E830*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:118370646 C>A maps to NM_006667.3 Y107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:119048831 C>A maps to NM_178813.5 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:120009188 G>C maps to NM_001145718.1 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:122532570 C>A maps to NM_000828.4 R333R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:122755030 G>C maps to NM_001081550.1 S1398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:125686225 C>G maps to NM_178470.4 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:128888455 C>T maps to NM_003399.5 D372D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:130222737 C>G maps to NM_144967.3 G541G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:134679346 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:135313957 C>T maps to NM_024597.3 P386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:138699718 G>T maps to ENST00000370578 R463R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:141291128 G>T maps to NM_016249.3 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:144904122 C>A maps to NM_001144010.2 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:147030345 C>A maps to NM_002024.5 L627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:148049221 G>T maps to NM_002025.3 L1089L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:150911920 G>T maps to NM_005140.1 E316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:150912768 G>A maps to NM_005140.1 Q598Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:151092270 T>A maps to ENST00000427663 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:152936620 G>T maps to NM_001039582.3 Y296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:153133824 G>T maps to NM_000425.3 P545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KB-01A-11D-A30A-10 chrX:154157537 G>C maps to NM_000132.3 G1509G. 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-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-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-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-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-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-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-A5KO-01A-11D-A29I-10 chr6:106968247 C>T maps to NM_001624.2 S647S. 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-A5KO-01A-11D-A29I-10 chrX:53430780 G>C maps to NM_006306.2 R747R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr10:5436106 C>A maps to NM_024803.2 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chr10:93726391 A>G did not map to a codon.
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-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-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-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-A5KP-01A-11D-A30A-10 chr19:53856660 A>G maps to NM_138374.1 G911G. 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-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-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-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-A5KP-01A-11D-A30A-10 chr4:36345150 G>A maps to ENST00000456874 W804*. 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-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-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-A5KP-01A-11D-A30A-10 chrX:74649033 C>G did not map to a codon.
Sequencing variant TCGA-OR-A5KP-01A-11D-A30A-10 chrX:100400094 G>A maps to NM_006733.2 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KQ-01A-11D-A30A-10 chr11:71276875 A>G maps to ENST00000422553 K138K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KQ-01A-11D-A30A-10 chr12:10584763 C>T maps to NM_002260.3 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KQ-01A-11D-A30A-10 chr16:23079690 G>T maps to NM_020718.3 G1245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KQ-01A-11D-A30A-10 chr1:62675663 G>A maps to NM_019079.4 E406E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KQ-01A-11D-A30A-10 chr6:151293138 T>C maps to NM_015440.3 S690S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KQ-01A-11D-A30A-10 chrX:27765407 G>A maps to NM_001136533.1 E132E. 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-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-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-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-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-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-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-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-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-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-A5KT-01A-11D-A29I-10 chr3:11072861 G>T did not map to a codon.
Sequencing variant TCGA-OR-A5KT-01A-11D-A29I-10 chr3:64133072 G>A maps to NM_198859.3 L365L. 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-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-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-A5KT-01A-11D-A29I-10 chrX:76939321 G>A maps to NM_000489.3 Q476*. 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-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-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-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-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-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-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-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-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-A5KV-01A-11D-A29I-10 chr21:45970771 A>G maps to NM_198693.2 P190P. Only missense variants will be evaluated by CHASM.
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-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-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-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-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-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-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-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-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-A5KW-01A-11D-A29I-10 chrX:151900365 G>A maps to NM_005367.5 D145D. Only missense variants will be evaluated by CHASM.
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-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-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-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-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-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-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-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-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-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-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-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-A5KX-01A-11D-A29I-10 chrX:57619014 G>A maps to NM_007157.3 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KX-01A-11D-A29I-10 chrX:65423291 C>T maps to NM_138737.3 Q776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KY-01A-11D-A29I-10 chr10:81904034 G>C maps to NM_001012973.1 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KY-01A-11D-A29I-10 chr11:64572612 G>A maps to NM_130804.2 R420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KY-01A-11D-A29I-10 chr13:46542981 T>A maps to ENST00000242848 R1233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KY-01A-11D-A29I-10 chr14:38679310 C>A maps to NM_001049.2 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KY-01A-11D-A29I-10 chr19:2853643 G>C maps to NM_152791.4 V527V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KY-01A-11D-A29I-10 chr19:38905652 G>C maps to ENST00000405332 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KY-01A-11D-A29I-10 chr19:48965217 C>G maps to NM_170720.1 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KY-01A-11D-A29I-10 chr1:196227366 C>T maps to NM_198503.2 V1056V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5KY-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-A5KY-01A-11D-A29I-10 chr7:98988566 G>A maps to NM_005720.2 P184P. 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-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 chr4:289887 G>A maps to ENST00000419098 C20C. 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-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-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-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-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-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-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-A5L1-01A-11D-A30A-10 chr6:132910156 A>G maps to NM_003967.2 F223F. 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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-A5L2-01A-11D-A30A-10 chr20:31115668 G>A maps to ENST00000201961 V29V. 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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-A5L2-01A-11D-A30A-10 chrX:75648450 C>G maps to NM_020932.2 S43*. 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-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-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-A5L3-01A-11D-A29I-10 chr20:368652 A>G did not map to a codon.
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-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-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-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-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-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-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-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-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-A5L4-01A-11D-A29I-10 chr2:179512176 C>A maps to ENST00000429997 E197*. 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-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-A5L5-01A-11D-A29I-10 chr11:1643257 C>T maps to ENST00000359229 G22G. 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-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-A5L5-01A-11D-A29I-10 chr19:55869898 T>G maps to NM_001145402.1 P779P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L5-01A-11D-A29I-10 chr19:55869901 C>T maps to NM_001145402.1 Q778Q. 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-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-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-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-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-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-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-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-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-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-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-A5L8-01A-11D-A29I-10 chr16:72993516 G>A maps to NM_006885.3 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L8-01A-11D-A29I-10 chr19:6937658 G>A maps to ENST00000381407 T887T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L8-01A-11D-A29I-10 chr19:17296756 C>T maps to NM_004145.3 L842L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5L8-01A-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-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-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-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-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-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-A5LA-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-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-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-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-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-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-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-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-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-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-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-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-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 chr15:72105934 C>T maps to NM_014249.2 H318H. Only missense variants will be evaluated by CHASM.
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-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-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-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-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-A5LB-01A-11D-A29I-10 chr17:11461176 G>A maps to NM_207386.3 P404P. Only missense variants will be evaluated by CHASM.
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-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 chr19:5831870 C>T maps to NM_001040701.1 T236T. 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-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-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-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-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-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-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-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-A5LB-01A-11D-A29I-10 chr22:28501522 C>T maps to NM_001145418.1 L1017L. 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-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-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-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-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 chr2:190430179 G>A maps to NM_014585.5 Y220Y. 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-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-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-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-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-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-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-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-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-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-A5LB-01A-11D-A29I-10 chrX:110497632 T>C did not map to a codon.
Sequencing variant TCGA-OR-A5LB-01A-11D-A29I-10 chrX:132437296 G>A maps to NM_001448.2 S455S. 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-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-A5LC-01A-11D-A29I-10 chr16:28844675 G>T did not map to a codon.
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-A5LC-01A-11D-A29I-10 chr19:51172453 G>T maps to ENST00000391814 P929P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-01A-11D-A29I-10 chr19:53856660 A>G maps to NM_138374.1 G911G. 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-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-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-A5LC-01A-11D-A29I-10 chr20:42233640 G>T did not map to a codon.
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-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-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-OR-A5LC-01A-11D-A29I-10 chr3:195508391 T>A maps to NM_018406.5 V3353V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LC-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-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-A5LC-01A-11D-A29I-10 chr7:150873648 C>A did not map to a codon.
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-A5LC-01A-11D-A29I-10 chrX:129155103 C>T maps to ENST00000303743 R1196*. 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-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-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-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-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-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-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-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-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-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-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-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-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-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-A5LD-01A-11D-A29I-10 chr9:136339192 T>C maps to NM_017585.3 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LE-01A-11D-A29I-10 chr10:47087601 C>A maps to NM_005972.4 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LE-01A-11D-A29I-10 chr17:39240790 C>G maps to ENST00000377731 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LE-01A-11D-A29I-10 chr19:2191207 C>T maps to ENST00000221482 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LE-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-A5LE-01A-11D-A29I-10 chr2:155555817 C>T maps to NM_002239.2 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LE-01A-11D-A29I-10 chr4:88536435 C>T maps to NM_014208.3 S874S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LE-01A-11D-A29I-10 chr6:82461741 G>A maps to ENST00000369756 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LE-01A-11D-A29I-10 chr7:139164979 G>A maps to NM_198508.2 Y257Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LE-01A-11D-A29I-10 chrX:130192419 T>A did not map to a codon.
Sequencing variant TCGA-OR-A5LF-01A-11D-A30A-10 chr12:21624010 A>C maps to NM_032941.2 A563A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LF-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-A5LF-01A-11D-A30A-10 chr15:70349953 C>T maps to NM_005078.2 A368A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LF-01A-11D-A30A-10 chr16:31213957 C>T maps to NM_013258.4 E18E. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-OR-A5LF-01A-11D-A30A-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-OR-A5LF-01A-11D-A30A-10 chr3:186793512 T>C maps to NM_003032.2 H381H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LF-01A-11D-A30A-10 chr6:72945408 C>G maps to NM_014989.4 S612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LF-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-A5LF-01A-11D-A30A-10 chr9:5969126 G>C maps to NM_001017969.2 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LF-01A-11D-A30A-10 chrX:53440046 A>G maps to NM_006306.2 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LG-01A-11D-A29I-10 chr11:71276680 T>C maps to NM_001012710.1 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LG-01A-11D-A29I-10 chr12:2058257 G>C maps to NM_152640.3 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LG-01A-11D-A29I-10 chr15:74865528 C>T maps to ENST00000395077 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LG-01A-11D-A29I-10 chr16:71012909 G>T maps to NM_032821.2 A1514A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LG-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-A5LG-01A-11D-A29I-10 chr9:32630735 C>T maps to NM_153809.2 E1614E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LG-01A-11D-A29I-10 chrX:101971585 G>T maps to NM_138437.5 E597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LH-01A-11D-A29I-10 chr20:35838496 T>G maps to NM_002951.3 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LH-01A-11D-A29I-10 chr5:96232567 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5LI-01A-11D-A30A-10 chr11:1092965 C>A maps to ENST00000441003 T1595T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LI-01A-11D-A30A-10 chr14:79434570 C>T maps to NM_004796.4 L635L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LI-01A-11D-A30A-10 chr17:38289308 T>C maps to ENST00000398532 S501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LI-01A-11D-A30A-10 chr17:40322161 C>T maps to NM_012285.2 A451A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LI-01A-11D-A30A-10 chr19:19764810 G>A maps to NM_020410.2 A652A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LI-01A-11D-A30A-10 chr19:36342536 C>T maps to NM_004646.3 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LI-01A-11D-A30A-10 chr4:76926001 G>C maps to NM_002416.1 S79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LI-01A-11D-A30A-10 chr4:139966423 G>A maps to NM_012118.2 W364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LI-01A-11D-A30A-10 chr6:153323805 A>G maps to NM_019041.5 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LI-01A-11D-A30A-10 chr7:148951007 G>A maps to NM_012256.3 Q330Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr10:23729555 G>C maps to NM_001145373.2 V390V. 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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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 chr16:314145 C>T maps to NM_032039.2 H440H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr16:2854955 G>C maps to NM_001135086.1 L260L. 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-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-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-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-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-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-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-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-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-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-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-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-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-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-A5LJ-01A-11D-A29I-10 chr18:44181266 G>A maps to NM_144612.6 I349I. 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-A5LJ-01A-11D-A29I-10 chr18:61564453 G>A did not map to a codon.
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-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-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-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-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-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-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-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-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-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-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-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 chr1:67195021 G>A maps to ENST00000237247 P637P. 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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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 chr3:38618242 G>A maps to NM_001099404.1 S1140S. 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-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-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-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 chr3:140407266 C>T maps to NM_152616.4 S581S. Only missense variants will be evaluated by CHASM.
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-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-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-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-A5LJ-01A-11D-A29I-10 chr3:195516578 T>C maps to NM_018406.5 T624T. 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-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-OR-A5LJ-01A-11D-A29I-10 chr4:17711135 G>A maps to NM_015688.1 C91C. 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-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-A5LJ-01A-11D-A29I-10 chr5:115813771 C>T maps to ENST00000257414 A502A. 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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-A5LJ-01A-11D-A29I-10 chr7:56125796 G>A did not map to a codon.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chr7:63537843 T>C maps to NM_001159522.1 A139A. 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-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-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-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-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-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-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-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-A5LJ-01A-11D-A29I-10 chr9:140115250 G>A maps to NM_031297.3 G138G. 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-A5LJ-01A-11D-A29I-10 chrX:7890070 G>A maps to NM_001142389.1 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LJ-01A-11D-A29I-10 chrX:74636937 G>A maps to NM_144969.2 N317N. 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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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 chr5:140731779 C>T maps to NM_018922.2 S651S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LL-01A-11D-A29I-10 chr8:133090150 G>A maps to ENST00000262283 S73S. 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-A5LM-01A-11D-A29I-10 chr12:26774091 C>T maps to NM_002223.2 G1142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LM-01A-11D-A29I-10 chr16:70176290 G>A maps to NM_017990.3 K490K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LM-01A-11D-A29I-10 chr17:39240790 C>G maps to ENST00000377731 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LM-01A-11D-A29I-10 chr19:41173885 C>T maps to NM_004756.3 Q439Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LM-01A-11D-A29I-10 chr19:41173897 T>C maps to NM_004756.3 Q435Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LM-01A-11D-A29I-10 chr4:48139492 G>A maps to NM_003215.2 F612F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LM-01A-11D-A29I-10 chr7:103008173 A>T maps to NM_002803.2 I354I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LM-01A-11D-A29I-10 chr8:37704588 G>A maps to NM_018310.3 R107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LM-01A-11D-A29I-10 chrX:35944285 G>C did not map to a codon.
Sequencing variant TCGA-OR-A5LN-01A-11D-A29I-10 chr10:55587196 A>C maps to NM_001142763.1 P1446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LN-01A-11D-A29I-10 chr12:54778301 C>T maps to NM_001130967.1 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LN-01A-11D-A29I-10 chr17:41170155 G>C maps to NM_006373.3 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LN-01A-11D-A29I-10 chr20:46279862 G>A maps to NM_181659.2 Q1263Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LN-01A-11D-A29I-10 chr22:18347737 G>T maps to NM_015241.2 P844P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LN-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-A5LN-01A-11D-A29I-10 chr5:101816043 G>A maps to NM_173488.3 Y151Y. 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-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-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-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-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-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-OR-A5LO-01A-11D-A29I-10 chr17:66521051 G>A did not map to a codon.
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-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-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-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-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-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-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-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-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-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-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 chrX:30577887 C>T maps to NM_025159.2 E195E. 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-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-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-A5LS-01A-11D-A29I-10 chr11:1643215 C>T maps to ENST00000359229 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LS-01A-11D-A29I-10 chr12:11244813 T>C maps to NM_176884.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LS-01A-11D-A29I-10 chr16:61851432 C>G maps to NM_001796.2 V409V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LS-01A-11D-A29I-10 chr19:52941933 G>A maps to NM_001143939.1 G420G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LS-01A-11D-A29I-10 chr5:133640094 C>A did not map to a codon.
Sequencing variant TCGA-OR-A5LT-01A-11D-A29I-10 chr12:85449576 C>T maps to NM_001079910.1 R336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LT-01A-11D-A29I-10 chr16:67876795 A>G maps to NM_020457.2 Q113Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LT-01A-11D-A29I-10 chr16:67876813 G>A maps to NM_020457.2 Q119Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LT-01A-11D-A29I-10 chr17:40093012 A>G did not map to a codon.
Sequencing variant TCGA-OR-A5LT-01A-11D-A29I-10 chr17:73282383 C>T did not map to a codon.
Sequencing variant TCGA-OR-A5LT-01A-11D-A29I-10 chr9:124936829 C>G maps to NM_198469.2 Y121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LT-01A-11D-A29I-10 chrX:24844591 C>T maps to ENST00000379068 L1204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OU-A5PI-01A-12D-A29I-10 chr19:3543551 G>C did not map to a codon.
Sequencing variant TCGA-OU-A5PI-01A-12D-A29I-10 chr1:22304886 T>C maps to NM_007352.2 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OU-A5PI-01A-12D-A29I-10 chr1:155020585 A>G maps to NM_152494.3 A603A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OU-A5PI-01A-12D-A29I-10 chr20:34292407 G>T maps to NM_184234.1 R530R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OU-A5PI-01A-12D-A29I-10 chr22:29885593 A>T maps to NM_021076.3 P655P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OU-A5PI-01A-12D-A29I-10 chr3:132387705 T>C maps to NM_024818.3 N114N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OU-A5PI-01A-12D-A29I-10 chr4:1388973 T>C maps to NM_175918.3 D225D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OU-A5PI-01A-12D-A29I-10 chr5:170640670 T>A maps to NM_022897.3 V756V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OU-A5PI-01A-12D-A29I-10 chr7:146805371 A>G maps to NM_014141.5 G228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OU-A5PI-01A-12D-A29I-10 chr9:1056585 A>G maps to NM_181872.4 R333R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OU-A5PI-01A-12D-A29I-10 chrX:130218193 A>T maps to NM_144967.3 A187A. 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-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-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-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-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-P6-A5OF-01A-11D-A29I-10 chr22:29444478 G>T maps to NM_032173.2 E239*. 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-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-P6-A5OG-01A-22D-A29I-10 chr10:45799843 C>A maps to NM_001004297.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr10:70652485 C>T maps to NM_001130161.2 N988N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr10:96447543 C>T maps to NM_000772.2 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr10:134942816 C>T maps to ENST00000368577 S1035S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr11:15257155 C>G maps to NM_001031853.3 T440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr11:30435805 G>T maps to NM_001584.2 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr11:88027677 T>C did not map to a codon.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr11:89892473 G>T maps to NM_005467.3 G320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr11:92592484 G>A maps to ENST00000298047 L3885L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr11:95657076 C>T maps to NM_016156.5 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr12:8998815 C>T maps to NM_144670.3 Q561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr12:55615092 G>T maps to NM_001005280.1 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr13:23905552 T>C maps to NM_014363.4 P4154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr14:69676280 C>T maps to NM_001193363.1 R32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr14:103599181 C>T maps to NM_006291.2 F506F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr16:55725870 C>T maps to NM_001043.3 F275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr16:81232624 G>C maps to NM_052892.3 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr17:3101621 A>T maps to NM_012352.1 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr18:14748540 G>A maps to NM_001145029.1 K41K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr19:3590127 C>T maps to NM_133261.2 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr19:3834848 G>T maps to NM_015174.1 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr19:36581422 G>A did not map to a codon.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr19:36606494 G>A maps to NM_001281.2 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr19:43699272 G>T maps to NM_002780.3 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr1:6636572 C>A maps to NM_138697.3 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr1:19536670 G>A maps to ENST00000375267 D24D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr1:24435086 G>T maps to ENST00000330966 R14R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr1:24787010 G>T maps to NM_020448.4 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr1:27057915 C>T maps to NM_006015.4 Q542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr1:94640287 G>A maps to NM_004815.3 L975L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr1:151341950 C>A maps to ENST00000435071 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr1:173947731 C>T maps to NM_172071.2 Q332Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr1:216061974 C>A maps to ENST00000366943 L2672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr1:233362970 C>A did not map to a codon.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr1:237893640 G>A maps to NM_001035.2 L3640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr20:23728452 C>G maps to NM_001898.2 *142Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr20:44314619 C>T maps to NM_172006.2 Q4Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr22:29885593 A>T maps to NM_021076.3 P655P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr22:32550279 C>T maps to NM_001010859.1 W86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr2:74307672 G>T maps to ENST00000409262 T785T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr2:128757633 T>A maps to NM_001145928.1 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr2:220288497 G>A did not map to a codon.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr2:220309865 G>T maps to NM_005876.4 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr3:49694134 G>A maps to NM_003458.3 L2382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr3:111760857 C>A maps to ENST00000443106 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr3:154890001 G>T did not map to a codon.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr3:180377266 C>T maps to NM_181426.1 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr4:40245455 G>A maps to NM_004310.3 E150E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr4:46973175 C>T maps to NM_000809.2 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr4:114276889 C>A maps to NM_001148.4 S2372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr4:186423471 C>A maps to NM_014476.4 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr5:90672526 C>A maps to NM_020801.2 E141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr5:137522994 C>A maps to NM_005733.2 R856R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr5:140248775 C>T maps to NM_018902.3 Q30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr5:158743704 C>A maps to NM_002187.2 V325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr5:176824890 G>T maps to NM_003052.4 T508T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr5:178310055 A>G maps to NM_058230.2 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr6:168439394 G>A maps to NM_030615.2 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr7:70255108 G>C maps to NM_015570.2 P969P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr7:112724533 G>A maps to NM_018970.6 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr7:135287598 C>G maps to NM_015135.2 L853L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr7:148702356 C>A maps to NM_004911.4 G466G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr7:157903543 G>T maps to NM_002847.3 P540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr8:38961140 A>G maps to NM_003816.2 Q794Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr8:55542714 C>T maps to NM_006269.1 I2091I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr9:77749308 C>T maps to NM_012383.4 Q136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chr9:114145492 G>C maps to NM_001080398.1 L1445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chrX:52826337 A>G maps to NM_001009616.2 C17C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OG-01A-22D-A29I-10 chrX:149638553 A>T maps to NM_005491.3 K237*. 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-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-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-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-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-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-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-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-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-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-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-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-P6-A5OH-01A-11D-A30A-10 chr19:58385797 C>T maps to NM_001144989.1 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OH-01A-11D-A30A-10 chr1:61554104 T>A maps to NM_001145512.1 V149V. Only missense variants will be evaluated by CHASM.
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 chr1:218609420 C>G maps to NM_001135599.2 S316S. Only missense variants will be evaluated by CHASM.
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-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-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-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-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-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-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-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-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-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-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-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 chr22:31495742 C>T maps to ENST00000454496 Q907*. 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-PK-A5H8-01A-11D-A29I-10 chr11:34104424 G>T did not map to a codon.
Sequencing variant TCGA-PK-A5H8-01A-11D-A29I-10 chr19:56012010 G>A maps to NM_001144950.1 R819R. 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-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-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-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-PK-A5H9-01A-11D-A29I-10 chr14:31765135 A>G maps to ENST00000389961 T1860T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5H9-01A-11D-A29I-10 chr18:21703900 G>A maps to NM_001135993.1 V430V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5H9-01A-11D-A29I-10 chr1:12884875 A>T maps to NM_001146344.1 L412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5H9-01A-11D-A29I-10 chr7:100677144 A>G maps to NM_001040105.1 T816T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HA-01A-11D-A29I-10 chr10:106214281 G>A maps to NM_001008723.1 T871T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HA-01A-11D-A29I-10 chr11:17485035 C>G maps to ENST00000302539 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HA-01A-11D-A29I-10 chr11:55944119 C>T maps to NM_001005492.1 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HA-01A-11D-A29I-10 chr11:123893784 C>T maps to NM_001001953.1 D22D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HA-01A-11D-A29I-10 chr12:40715838 C>T maps to NM_198578.3 R1725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HA-01A-11D-A29I-10 chr12:124413962 C>T maps to NM_207437.3 Q4032*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HA-01A-11D-A29I-10 chr17:41008410 C>T maps to NM_003734.2 D712D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HA-01A-11D-A29I-10 chr18:8069960 C>T maps to NM_001105244.1 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HA-01A-11D-A29I-10 chr19:39899248 C>T maps to NM_003407.2 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HA-01A-11D-A29I-10 chr1:44685738 C>T maps to NM_019100.4 R368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HA-01A-11D-A29I-10 chr1:78958568 C>A maps to NM_000959.3 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HA-01A-11D-A29I-10 chr3:190321956 C>T maps to NM_002182.3 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HA-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-PK-A5HA-01A-11D-A29I-10 chr9:88967901 A>T maps to NM_024617.3 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HA-01A-11D-A29I-10 chr9:136338636 G>A maps to NM_017585.3 G374G. 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-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-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-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 chr10:49951057 A>T maps to NM_020945.1 R642*. 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-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-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 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-PK-A5HB-01A-11D-A29I-10 chr10:97393406 C>G did not map to a codon.
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-PK-A5HB-01A-11D-A29I-10 chr10:115891095 C>A did not map to a codon.
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-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-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-PK-A5HB-01A-11D-A29I-10 chr11:686973 G>A maps to NM_021008.2 Q230*. 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-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 chr11:56310505 A>G maps to NM_001005245.1 N76N. 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-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 chr11:72945485 C>A maps to NM_176071.1 A94A. 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-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-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-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-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 chr12:431709 G>A maps to NM_001042603.1 L767L. 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-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-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-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-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-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-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-PK-A5HB-01A-11D-A29I-10 chr12:50725577 A>G maps to NM_001145475.1 L2241L. 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-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-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-PK-A5HB-01A-11D-A29I-10 chr12:122248665 G>A maps to NM_015048.1 G605G. 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-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 chr13:28883024 G>A maps to NM_002019.4 I1225I. 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-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-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-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-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-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-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-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-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-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 chr14:24800999 C>T maps to NM_139247.3 K221K. 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 chr14:56103914 G>A did not map to a codon.
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-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-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-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-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-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-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-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-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-PK-A5HB-01A-11D-A29I-10 chr15:44918705 C>T did not map to a codon.
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-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-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-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-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 chr15:98511296 T>C maps to NM_183376.2 S192S. 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-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-PK-A5HB-01A-11D-A29I-10 chr16:2487127 A>T 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-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-PK-A5HB-01A-11D-A29I-10 chr16:20376739 A>T did not map to a codon.
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 chr16:23555851 C>T maps to NM_001083614.1 R156R. Only missense variants will be evaluated by CHASM.
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 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-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-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-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-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 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 chr16:74922198 C>A maps to NM_030581.3 R738R. 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-PK-A5HB-01A-11D-A29I-10 chr17:7577017 C>A did not map to a codon.
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-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-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-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-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-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-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-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-PK-A5HB-01A-11D-A29I-10 chr19:10394799 C>T maps to NM_000201.2 F243F. 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-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-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-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 chr19:17844086 C>T maps to NM_018174.4 S958S. 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-PK-A5HB-01A-11D-A29I-10 chr19:20307779 T>C maps to NM_052852.2 C87C. 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-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-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-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-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-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 chr19:50245267 C>T maps to NM_021733.1 S457S. 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-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 chr19:53612772 A>T maps to NM_001164309.1 V175V. 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-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-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-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-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 chr1:7837353 G>A maps to NM_004781.3 R69R. 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-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-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-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-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-PK-A5HB-01A-11D-A29I-10 chr1:44466853 G>T maps to NM_201649.2 G512G. 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-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-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-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-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-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-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-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-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-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-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-PK-A5HB-01A-11D-A29I-10 chr1:160969184 C>T did not map to a codon.
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-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-PK-A5HB-01A-11D-A29I-10 chr1:181762805 A>C maps to ENST00000357570 P1968P. 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-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-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-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-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-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-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-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-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-PK-A5HB-01A-11D-A29I-10 chr21:45970771 A>G maps to NM_198693.2 P190P. 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 chr22:21989305 C>T maps to NM_152612.2 S318S. 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-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-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-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-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 chr22:50636362 C>T maps to NM_025204.2 V261V. Only missense variants will be evaluated by CHASM.
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-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-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-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-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 chr2:97519167 C>T maps to NM_016466.5 V126V. 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-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-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 chr2:141259363 A>G maps to NM_018557.2 D2914D. 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-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-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-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 chr2:179401240 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 chr2:197143275 C>T maps to NM_020760.1 R1037R. Only missense variants will be evaluated by CHASM.
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-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 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 chr2:242573028 G>A maps to NM_015963.5 T181T. 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-PK-A5HB-01A-11D-A29I-10 chr3:42738491 C>T did not map to a codon.
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-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-PK-A5HB-01A-11D-A29I-10 chr3:81635290 A>G maps to ENST00000264326 G429G. 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-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-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-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-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-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-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-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 chr4:8583356 G>A maps to NM_080819.2 L216L. 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-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 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 chr4:68380316 C>A maps to NM_001812.2 E307*. 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-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-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-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 chr4:89679991 G>A maps to NM_014883.2 Q547*. 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-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 chr5:16711034 C>T maps to NM_012334.2 W717*. 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-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 chr5:65058793 G>A maps to NM_020726.4 R103R. 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-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 chr5:115815885 C>T maps to ENST00000257414 T394T. 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-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-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-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-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-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-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-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-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 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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-PK-A5HB-01A-11D-A29I-10 chr7:45124122 T>C maps to NM_001146334.1 E552E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr7:45124944 G>T maps to NM_001146334.1 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chr7:45125541 T>A maps to NM_001146334.1 A79A. 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-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-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-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 chr7:99507253 G>A maps to NM_033017.3 L167L. 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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-PK-A5HB-01A-11D-A29I-10 chr8:48689403 C>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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-A5HB-01A-11D-A29I-10 chr9:129642193 C>T maps to ENST00000319119 C172C. 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-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-PK-A5HB-01A-11D-A29I-10 chrX:84519341 T>C maps to ENST00000360700 D228D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chrX:130416499 G>A maps to NM_001170961.1 G388G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chrX:149931072 C>A maps to NM_003828.2 A623A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chrX:152994691 G>A maps to NM_000033.3 E302E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HB-01A-11D-A29I-10 chrX:153689659 C>T maps to NM_017514.3 F272F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HC-01A-11D-A30A-10 chr15:41853472 C>T maps to NM_006293.3 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HC-01A-11D-A30A-10 chr18:3079306 C>T maps to NM_003803.3 K1506K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HC-01A-11D-A30A-10 chr18:19780773 G>C maps to NM_005257.3 L592L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HC-01A-11D-A30A-10 chr19:46733363 G>C did not map to a codon.
Sequencing variant TCGA-PK-A5HC-01A-11D-A30A-10 chr19:58385797 C>T maps to NM_001144989.1 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HC-01A-11D-A30A-10 chr1:18691916 C>T maps to NM_032880.4 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HC-01A-11D-A30A-10 chr1:233372602 C>A maps to NM_014801.3 S782S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HC-01A-11D-A30A-10 chr2:168104661 C>T maps to NM_152381.5 L2254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HC-01A-11D-A30A-10 chr2:201440157 C>T maps to NM_152524.5 F1252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HC-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-A5HC-01A-11D-A30A-10 chr4:99996089 G>A maps to NM_000671.3 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HC-01A-11D-A30A-10 chr4:128608946 G>A maps to NM_015693.3 Q458Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HC-01A-11D-A30A-10 chr4:158256821 G>T did not map to a codon.
Sequencing variant TCGA-PK-A5HC-01A-11D-A30A-10 chr5:140223017 C>A maps to NM_018911.2 I704I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HC-01A-11D-A30A-10 chr5:176318106 C>A maps to NM_002115.2 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HC-01A-11D-A30A-10 chr5:180687439 T>C maps to NM_032765.2 E125E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HC-01A-11D-A30A-10 chr6:26271438 C>G maps to NM_003534.2 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HC-01A-11D-A30A-10 chr7:128851519 C>T maps to NM_005631.4 S615S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HC-01A-11D-A30A-10 chr8:37823624 C>A maps to NM_000025.2 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PK-A5HC-01A-11D-A30A-10 chrX:7890139 C>T did not map to a codon.
Multiple mappings detected for codon TCGA-OR-A5J4-01A-11D-A29I-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-OR-A5JA-01A-11D-A29I-10 chr17:7579721 C>A did not map to a codon.
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-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-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-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-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-A5K4-01A-11D-A29I-10 chrX:41333839 C>T maps to NM_022567.2 F378F. 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 chr14:104641875 C>T maps to NM_015656.1 A917A. Only missense variants will be evaluated by CHASM.
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-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 chr4:4862087 G>A maps to NM_002448.3 P154P. Only missense variants will be evaluated by CHASM.
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-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-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-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-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-OR-A5KB-01A-11D-A30A-10 chrX:134679497 G>T did not map to a codon.
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-A5LC-01A-11D-A29I-10 chr17:2966181 G>T maps to ENST00000333466 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OR-A5LN-01A-11D-A29I-10 chr22:28194935 C>T maps to NM_002430.2 Q532Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P6-A5OF-01A-11D-A29I-10 chr22:29444479 G>T did not map to a codon.
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 chr19:38875167 G>A maps to NM_152657.3 L615L. 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-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-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-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-A5HC-01A-11D-A30A-10 chr10:77158944 G>T maps to NM_032772.4 Y501*. Only missense variants will be evaluated by CHASM.
