5099 NP_705833 S301L not found in SNVbox database
5612 NP_705833 C814R not found in SNVbox database
2480 NP_705833 T906N not found in SNVbox database
3307 NP_705833 L531S not found in SNVbox database
4233 NP_705833 S635R not found in SNVbox database
Sequencing variant TCGA-F2-6879-01A-11D-2154-08 chr5:38337655 C>T maps to ENST00000354891 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-6879-01A-11D-2154-08 chr1:228479740 C>T maps to NM_001098623.1 Y3494Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-6879-01A-11D-2154-08 chr17:43192470 G>A maps to NM_133373.3 F567F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-6879-01A-11D-2154-08 chr17:73229048 G>A maps to NM_024844.3 T500T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-6879-01A-11D-2154-08 chr8:94767363 A>G maps to NM_153704.5 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-6879-01A-11D-2154-08 chr21:45838382 C>T maps to ENST00000397932 R1136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-6879-01A-11D-2154-08 chr1:38079562 C>T maps to NM_001038633.2 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-6879-01A-11D-2154-08 chr1:221057766 G>A maps to NM_021958.3 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-6879-01A-11D-2154-08 chr8:106815013 C>T maps to NM_012082.3 R902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-6879-01A-11D-2154-08 chr8:15967629 T>C maps to ENST00000445506 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-6879-01A-11D-2154-08 chr19:22847685 G>T maps to NM_020855.2 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-6879-01A-11D-2154-08 chr6:45390468 G>A maps to ENST00000359524 Q134Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-6879-01A-11D-2154-08 chr8:110131288 C>T maps to NM_003301.4 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-6879-01A-11D-2154-08 chr4:140811107 C>T maps to ENST00000509479 Q494Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-6879-01A-11D-2154-08 chr3:169644397 C>T maps to NM_182610.2 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-6879-01A-11D-2154-08 chr9:138590309 C>T maps to NM_001101677.1 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-6879-01A-11D-2154-08 chr19:57286067 G>A maps to NM_001146326.1 C524C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-6879-01A-11D-2154-08 chr1:167095420 C>T maps to NM_001080426.1 Y351Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-6879-01A-11D-2154-08 chr1:1654057 C>T did not map to a codon.
Sequencing variant TCGA-F2-6879-01A-11D-2154-08 chr5:32364366 T>C maps to NM_016107.3 L950L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-6879-01A-11D-2154-08 chr6:44254102 G>A maps to NM_182539.3 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-6879-01A-11D-2154-08 chr17:18668177 T>C did not map to a codon.
Sequencing variant TCGA-F2-6880-01A-11D-2154-08 chr3:122680140 A>G did not map to a codon.
Sequencing variant TCGA-F2-7276-01A-11D-2154-08 chr12:347141 G>T maps to NM_016615.3 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-7276-01A-11D-2154-08 chr11:111780949 G>T did not map to a codon.
Sequencing variant TCGA-F2-A44G-01A-11D-A26I-08 chr5:140772667 C>T maps to NM_032088.1 C96C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-A44G-01A-11D-A26I-08 chr6:45390465 A>G maps to ENST00000359524 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-A44G-01A-11D-A26I-08 chr10:125506293 G>A maps to NM_198148.2 R753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-A44G-01A-11D-A26I-08 chr3:123411657 C>T maps to NM_053025.3 E1163E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-A44G-01A-11D-A26I-08 chr7:150716446 C>T maps to NM_173681.5 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-A44G-01A-11D-A26I-08 chr19:3980039 G>T maps to NM_001961.3 Y457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-A44G-01A-11D-A26I-08 chr4:66535409 G>A maps to NM_004439.5 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-A44G-01A-11D-A26I-08 chr6:45390462 G>A maps to ENST00000359524 Q132Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-A44G-01A-11D-A26I-08 chr1:150921868 C>G maps to NM_001145415.1 S483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-A44G-01A-11D-A26I-08 chr6:170871042 G>A maps to NM_003194.4 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-A44G-01A-11D-A26I-08 chr4:84342812 C>T maps to NM_133636.2 W951*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-A44G-01A-11D-A26I-08 chr1:165177321 C>T maps to NM_177398.3 Q265Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-A44G-01A-11D-A26I-08 chr10:103348196 C>T did not map to a codon.
Sequencing variant TCGA-F2-A44G-01A-11D-A26I-08 chr17:10432366 G>A maps to NM_017534.5 I1128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-A44G-01A-11D-A26I-08 chr17:36869291 A>G maps to ENST00000378137 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-A44G-01A-11D-A26I-08 chr12:53170615 C>A maps to NM_015848.4 G154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-A44G-01A-11D-A26I-08 chr11:102708079 C>A maps to NM_002422.3 E428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-A44G-01A-11D-A26I-08 chr19:17943472 G>A maps to NM_000215.3 G845G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-A44G-01A-11D-A26I-08 chr16:9934951 G>T maps to NM_000833.3 T446T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-A44G-01A-11D-A26I-08 chr4:119609075 A>G did not map to a codon.
Sequencing variant TCGA-F2-A44G-01A-11D-A26I-08 chr11:5364520 C>T maps to NM_001005567.1 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-A44G-01A-11D-A26I-08 chr7:57528949 A>G maps to NM_001159279.1 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-A44G-01A-11D-A26I-08 chr19:49447741 C>T maps to NM_014475.3 H291H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-A44G-01A-11D-A26I-08 chr5:14756008 G>A maps to NM_054027.4 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-A44H-01A-11D-A26I-08 chrX:47045113 G>C did not map to a codon.
Sequencing variant TCGA-F2-A44H-01A-11D-A26I-08 chr7:37354483 G>A maps to NM_014800.9 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-A44H-01A-11D-A26I-08 chr6:152651473 T>C maps to NM_182961.2 E4782E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-A44H-01A-11D-A26I-08 chr8:52321507 G>C maps to NM_144651.4 A892A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-A44H-01A-11D-A26I-08 chr19:17515192 C>A maps to NM_004335.2 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-A44H-01A-11D-A26I-08 chr18:56274645 C>T maps to NM_052947.3 W45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-A44H-01A-11D-A26I-08 chr21:47704429 C>T maps to NM_003906.3 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-A44H-01A-11D-A26I-08 chr19:54744908 G>A maps to ENST00000245620 Y251Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-A44H-01A-11D-A26I-08 chr9:95610735 T>C maps to NM_031486.1 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A4P5-01A-11D-A26I-08 chr5:9066643 G>A maps to NM_003966.2 R730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A4P5-01A-11D-A26I-08 chr11:55735161 T>G maps to NM_001005491.1 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A4P5-01A-11D-A26I-08 chr17:75398244 C>T maps to NM_001113491.1 Q61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A4P5-01A-11D-A26I-08 chr9:101900287 C>A maps to NM_004612.2 S241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A4P5-01A-11D-A26I-08 chr7:4917629 G>A maps to NM_018059.4 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A4P5-01A-11D-A26I-08 chr16:1828583 G>A maps to NM_080861.3 Y52Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A4P5-01A-11D-A26I-08 chr5:140751763 C>T maps to NM_018924.2 N601N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A4P5-01A-11D-A26I-08 chr1:22927843 C>T maps to NM_020526.3 S927S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A4P5-01A-11D-A26I-08 chr19:9721439 G>A maps to NM_152289.2 H299H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A4P5-01A-11D-A26I-08 chr3:98518460 G>A maps to ENST00000326857 Q709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A4P5-01A-11D-A26I-08 chr3:52255985 G>A maps to ENST00000494383 P935P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A4P5-01A-11D-A26I-08 chr11:59629066 G>A maps to NM_001062.3 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A4P5-01A-11D-A26I-08 chr5:149576605 C>T maps to NM_014228.3 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A4P5-01A-11D-A26I-08 chr17:37339980 C>T maps to NM_000723.3 K345K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A4P5-01A-11D-A26I-08 chr9:77386695 G>A maps to NM_017662.4 C1153C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A4P6-01A-12D-A26I-08 chr2:42996987 G>T maps to NM_012205.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A4P6-01A-12D-A26I-08 chr8:68062081 T>C maps to ENST00000389042 Y710Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A4P6-01A-12D-A26I-08 chr16:84600450 T>G maps to NM_021149.2 *143Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A545-01A-11D-A26I-08 chr11:32955743 A>G maps to NM_001076786.1 V851V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A545-01A-11D-A26I-08 chr7:72413744 C>T maps to ENST00000434423 S1071S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A545-01A-11D-A26I-08 chr12:24048944 G>A maps to NM_006940.4 R18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A545-01A-11D-A26I-08 chr4:42580333 G>A maps to NM_006095.2 I357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A545-01A-11D-A26I-08 chr4:140811107 C>T maps to ENST00000509479 Q494Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A545-01A-11D-A26I-08 chr3:49723068 G>A maps to NM_020998.3 D449D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A545-01A-11D-A26I-08 chr9:124062284 T>G did not map to a codon.
Sequencing variant TCGA-FB-A545-01A-11D-A26I-08 chrX:140785783 T>A maps to NM_145665.1 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A5VM-01A-11D-A32N-08 chr2:111556627 C>T maps to NM_001142807.1 N166N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A5VM-01A-11D-A32N-08 chr11:22281144 A>G maps to NM_213599.2 E496E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A5VM-01A-11D-A32N-08 chr11:56237569 G>C maps to NM_001004742.1 S135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A5VM-01A-11D-A32N-08 chr17:67183985 C>A maps to NM_080282.3 V722V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A5VM-01A-11D-A32N-08 chr4:1388358 T>C maps to NM_175918.3 C20C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A5VM-01A-11D-A32N-08 chr5:14610392 C>T maps to NM_019018.2 N347N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A5VM-01A-11D-A32N-08 chr19:10071227 C>T maps to NM_015719.3 R1699R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A5VM-01A-11D-A32N-08 chr10:126682485 T>C maps to NM_022802.2 Q823Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A5VM-01A-11D-A32N-08 chr13:25074497 G>A maps to NM_006437.3 C119C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A5VM-01A-11D-A32N-08 chr4:5798841 G>A maps to NM_153717.2 T660T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A5VM-01A-11D-A32N-08 chr4:88732602 C>T maps to NM_004967.3 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A5VM-01A-11D-A32N-08 chr8:26627752 G>T maps to NM_000680.2 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A5VM-01A-11D-A32N-08 chr10:126682515 G>A maps to NM_022802.2 G813G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A5VM-01A-11D-A32N-08 chr1:161953821 G>A maps to ENST00000451379 I633I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A5VM-01A-11D-A32N-08 chr8:146076504 G>A maps to NM_001081003.1 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A5VM-01A-11D-A32N-08 chr22:40807693 G>A maps to NM_020831.3 D832D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A5VM-01A-11D-A32N-08 chr21:46229015 C>T maps to ENST00000411651 Q94Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A5VM-01A-11D-A32N-08 chrX:152806982 G>T maps to NM_001001344.2 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A5VM-01A-11D-A32N-08 chr8:10470230 G>A maps to NM_178857.5 T459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A5VM-01A-11D-A32N-08 chr7:36917613 C>T did not map to a codon.
Sequencing variant TCGA-FB-A5VM-01A-11D-A32N-08 chr11:33763528 T>C maps to NM_012175.3 E447E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A5VM-01A-11D-A32N-08 chrX:79932803 G>A maps to NM_153252.4 I1571I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A5VM-01A-11D-A32N-08 chr1:186916022 C>A maps to NM_024420.2 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A5VM-01A-11D-A32N-08 chr15:93595474 C>T maps to NM_020211.2 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A5VM-01A-11D-A32N-08 chr3:9956175 C>T maps to NM_001193380.1 S438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A5VM-01A-11D-A32N-08 chr10:76797812 G>A maps to NM_001003892.1 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A5VM-01A-11D-A32N-08 chr16:67695974 C>T maps to NM_016948.2 R156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A5VM-01A-11D-A32N-08 chr22:40662849 C>T maps to ENST00000454349 P886P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A5VM-01A-11D-A32N-08 chr19:54754945 G>A maps to ENST00000450632 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A5VM-01A-11D-A32N-08 chr5:140553993 G>T maps to NM_018940.2 A526A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A5VM-01A-11D-A32N-08 chr1:71873146 C>T maps to NM_173808.2 K349K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A5VM-01A-11D-A32N-08 chr12:125397651 T>C maps to NM_021009.5 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A5VM-01A-11D-A32N-08 chr7:48315040 G>A maps to NM_152701.3 P1926P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A78T-01A-12D-A32N-08 chr13:100635061 G>C maps to NM_007129.2 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A78T-01A-12D-A32N-08 chr19:4511841 G>A maps to NM_001080400.1 V696V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A78T-01A-12D-A32N-08 chr5:140229342 C>A maps to NM_031857.1 Y421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A78T-01A-12D-A32N-08 chr20:60733999 T>C did not map to a codon.
Sequencing variant TCGA-FB-A78T-01A-12D-A32N-08 chr15:75109004 C>T maps to NM_021819.2 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A78T-01A-12D-A32N-08 chr6:29455343 G>T maps to NM_052967.1 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A78T-01A-12D-A32N-08 chr2:219507560 G>A maps to NM_001105537.1 G1226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A78T-01A-12D-A32N-08 chr7:99780443 C>T maps to NM_012447.2 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A78T-01A-12D-A32N-08 chr16:72992316 G>A maps to NM_006885.3 G576G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A78T-01A-12D-A32N-08 chr6:45390462 G>A maps to ENST00000359524 Q132Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A78T-01A-12D-A32N-08 chr17:74136134 G>A maps to NM_001454.3 Y114Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A78T-01A-12D-A32N-08 chr2:189929784 T>C did not map to a codon.
Sequencing variant TCGA-FB-A78T-01A-12D-A32N-08 chr7:106508902 C>T maps to NM_002649.2 N299N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A78T-01A-12D-A32N-08 chr19:52220298 G>A maps to NM_001523.2 R284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A78T-01A-12D-A32N-08 chrX:130222629 C>T maps to NM_144967.3 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A78T-01A-12D-A32N-08 chrX:125685937 C>T maps to NM_178470.4 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A78T-01A-12D-A32N-08 chr11:72406855 C>G maps to NM_001040118.2 V1109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A78T-01A-12D-A32N-08 chr19:40520556 T>C maps to NM_178544.3 H460H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A78T-01A-12D-A32N-08 chr19:58927190 G>A maps to ENST00000322834 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A78T-01A-12D-A32N-08 chr10:134165158 G>A maps to NM_030626.2 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A78T-01A-12D-A32N-08 chr20:42695425 A>T maps to ENST00000348077 P480P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A78T-01A-12D-A32N-08 chr2:97033077 G>A maps to NM_015341.3 L655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A78T-01A-12D-A32N-08 chr5:14369547 G>A maps to NM_007118.2 A1044A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A78T-01A-12D-A32N-08 chr11:19901514 A>C maps to ENST00000396087 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A78T-01A-12D-A32N-08 chr14:24845881 G>A maps to NM_001136022.1 P876P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A78T-01A-12D-A32N-08 chr20:60889899 G>A maps to NM_005560.3 G2717G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A78T-01A-12D-A32N-08 chr18:48604735 G>T maps to NM_005359.5 E520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A78T-01A-12D-A32N-08 chr20:33345145 G>A maps to NM_014071.2 Q469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A7DR-01A-21D-A33T-08 chr20:47733692 G>A maps to NM_017453.2 I534I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A7DR-01A-21D-A33T-08 chr1:26520379 G>A did not map to a codon.
Sequencing variant TCGA-FB-A7DR-01A-21D-A33T-08 chr16:57604381 C>T maps to ENST00000349457 Y381Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A7DR-01A-21D-A33T-08 chr12:57485471 C>T maps to NM_005967.3 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A7DR-01A-21D-A33T-08 chr1:156845429 C>T maps to NM_002529.3 I491I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A7DR-01A-21D-A33T-08 chr11:22382453 C>A maps to NM_020346.2 Y195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A7DR-01A-21D-A33T-08 chr10:15183510 C>T maps to ENST00000378143 Q52Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A7DR-01A-21D-A33T-08 chr20:10273545 C>T maps to NM_003081.2 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A7DR-01A-21D-A33T-08 chr11:73022571 C>T maps to NM_014786.3 P963P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A7DR-01A-21D-A33T-08 chr5:60241049 G>A did not map to a codon.
Sequencing variant TCGA-FB-A7DR-01A-21D-A33T-08 chr8:143614730 C>T maps to NM_001702.2 T1158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A7DR-01A-21D-A33T-08 chr19:10945732 G>T maps to NM_006858.2 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A7DR-01A-21D-A33T-08 chrX:125686252 G>A maps to NM_178470.4 C113C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A7DR-01A-21D-A33T-08 chr17:79514424 G>A maps to NM_025161.5 S561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A7DR-01A-21D-A33T-08 chr4:140811107 C>T maps to ENST00000509479 Q494Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A7DR-01A-21D-A33T-08 chrX:112058795 C>T maps to NM_001113490.1 Q394Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A7DR-01A-21D-A33T-08 chr19:17943490 G>A maps to NM_000215.3 C839C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A7DR-01A-21D-A33T-08 chr17:61607500 C>T maps to NM_030779.2 D119D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A7DR-01A-21D-A33T-08 chr21:46925284 C>T maps to ENST00000359759 P1424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A7DR-01A-21D-A33T-08 chr7:44282245 G>T maps to NM_001220.4 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A7DR-01A-21D-A33T-08 chr1:248636947 G>A maps to NM_001005495.1 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A7DR-01A-21D-A33T-08 chr12:16036494 C>T maps to ENST00000025399 Q58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A7DR-01A-21D-A33T-08 chr14:73407030 G>A maps to NM_015604.3 K99K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A7DR-01A-21D-A33T-08 chr5:13900349 G>A maps to NM_001369.2 R742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FB-A7DR-01A-21D-A33T-08 chr16:84600450 T>G maps to NM_021149.2 *143Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5919-01A-11D-1609-08 chr7:43540838 C>T maps to NM_015052.3 Y1183Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5919-01A-11D-1609-08 chr5:68669706 C>T maps to NM_133339.1 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5919-01A-11D-1609-08 chr12:15673187 G>A maps to NM_030667.1 V611V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5919-01A-11D-1609-08 chr13:46066373 A>T maps to NM_031431.2 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5919-01A-11D-1609-08 chr1:110031575 G>A maps to NM_153340.4 E297E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5919-01A-11D-1609-08 chr16:80667059 G>A maps to NM_152342.2 Y230Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5919-01A-11D-1609-08 chr20:30526968 C>T maps to NM_001008409.2 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5919-01A-11D-1609-08 chr6:146207835 C>T maps to ENST00000367503 E1685E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5919-01A-11D-1609-08 chr15:82335638 G>A maps to NM_032246.3 S524S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5919-01A-11D-1609-08 chr2:179576917 C>T maps to NM_133378.4 P7969P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5919-01A-11D-1609-08 chr12:58207946 G>A maps to NM_006576.3 Y43Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5919-01A-11D-1609-08 chr19:43411980 G>T maps to NM_002782.3 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5919-01A-11D-1609-08 chrX:39933047 G>A maps to NM_001123385.1 N517N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5919-01A-11D-1609-08 chr11:20673950 C>T maps to NM_004211.3 I729I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5919-01A-11D-1609-08 chr12:99071229 C>A maps to NM_181861.1 S607S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5919-01A-11D-1609-08 chr19:7810583 G>A maps to NM_021155.3 Q190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5919-01A-11D-1609-08 chr11:46568661 C>T did not map to a codon.
Sequencing variant TCGA-FZ-5919-01A-11D-1609-08 chr19:56133797 A>C maps to NM_203374.1 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5919-01A-11D-1609-08 chr13:58208533 C>T maps to NM_001040429.2 G618G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5919-01A-11D-1609-08 chr17:73997473 G>A did not map to a codon.
Sequencing variant TCGA-FZ-5919-01A-11D-1609-08 chr4:10080532 C>T maps to NM_017491.3 T459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5919-01A-11D-1609-08 chr13:95095780 G>T maps to NM_001129889.1 Y463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5920-01A-11D-1609-08 chr7:2020095 G>A maps to NM_003550.2 D499D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5920-01A-11D-1609-08 chr8:12957787 C>T maps to NM_182643.2 A686A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-FZ-5920-01A-11D-1609-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FZ-5920-01A-11D-1609-08 chr2:145147455 C>T maps to NM_014795.3 S1069S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5920-01A-11D-1609-08 chr11:102933111 C>T maps to NM_032299.3 W230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5920-01A-11D-1609-08 chr21:31692254 G>A maps to NM_203405.1 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5920-01A-11D-1609-08 chr7:98453721 C>T maps to NM_001134450.1 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5920-01A-11D-1609-08 chr7:38433730 C>T maps to NM_001635.3 A494A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5920-01A-11D-1609-08 chr16:57003892 G>A maps to NM_000078.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5920-01A-11D-1609-08 chr3:8607272 A>C maps to NM_014583.2 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5920-01A-11D-1609-08 chr19:30935497 C>T maps to NM_014717.1 N343N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5920-01A-11D-1609-08 chr4:17579126 C>G maps to NM_015907.2 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5920-01A-11D-1609-08 chr6:28539891 A>G maps to NM_052923.1 P1258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5920-01A-11D-1609-08 chr20:44838992 G>T maps to NM_021248.1 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5920-01A-11D-1609-08 chr5:177421250 C>T maps to NM_006261.4 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5920-01A-11D-1609-08 chr7:63726844 C>T maps to NM_153363.2 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5920-01A-11D-1609-08 chr14:52495452 C>T maps to NM_007361.3 R839R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5920-01A-11D-1609-08 chrX:3240230 C>T maps to NM_015419.3 R1165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5920-01A-11D-1609-08 chr19:47575242 T>A maps to NM_015168.1 A646A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5920-01A-11D-1609-08 chr6:147525791 C>T maps to NM_001127715.1 Q42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5920-01A-11D-1609-08 chr4:174450242 G>A maps to NM_021973.2 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5920-01A-11D-1609-08 chr22:21064272 G>A maps to NM_058004.2 D1974D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5920-01A-11D-1609-08 chr19:12059965 C>G maps to NM_144566.1 S376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5920-01A-11D-1609-08 chr2:179614363 C>A maps to ENST00000375038 E4257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5920-01A-11D-1609-08 chr15:69715495 A>T did not map to a codon.
Sequencing variant TCGA-FZ-5920-01A-11D-1609-08 chr3:433472 T>A maps to NM_006614.2 Y969*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5920-01A-11D-1609-08 chr19:16024595 G>A maps to NM_021187.3 R507R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5920-01A-11D-1609-08 chr2:63283270 C>T maps to NM_014562.3 H295H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5920-01A-11D-1609-08 chr5:178416068 C>A maps to NM_000843.3 A407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5920-01A-11D-1609-08 chr21:22658658 C>T maps to NM_004540.2 C136C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5920-01A-11D-1609-08 chr1:222716970 C>T maps to NM_024746.3 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5920-01A-11D-1609-08 chr6:26027282 C>T maps to NM_003544.2 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5920-01A-11D-1609-08 chr6:56357815 A>T maps to ENST00000361203 L6611L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5921-01A-11D-1609-08 chr19:33467437 C>T maps to NM_152266.3 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5921-01A-11D-1609-08 chr15:25924727 G>T maps to NM_024490.3 T1420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5921-01A-11D-1609-08 chr10:13234463 C>T maps to NM_182751.2 S548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5921-01A-11D-1609-08 chr3:109050852 C>T maps to NM_018189.3 E68E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5921-01A-11D-1609-08 chr16:81095233 C>G maps to NM_152337.2 V240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5921-01A-11D-1609-08 chr20:44574945 C>T maps to NM_022104.3 F512F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5921-01A-11D-1609-08 chr1:169586588 C>T maps to NM_003005.3 W53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5921-01A-11D-1609-08 chr13:23910738 G>A maps to NM_014363.4 R2426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5921-01A-11D-1609-08 chr11:93836095 T>C maps to NM_001098672.1 Y864Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5921-01A-11D-1609-08 chr4:156135405 G>A maps to NM_000910.2 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5921-01A-11D-1609-08 chr17:43194109 G>A maps to NM_133373.3 C434C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5921-01A-11D-1609-08 chr15:74636145 G>A maps to NM_000781.2 D271D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5921-01A-11D-1609-08 chr19:51411613 C>T did not map to a codon.
Sequencing variant TCGA-FZ-5921-01A-11D-1609-08 chr1:159169658 G>A maps to NM_021189.3 R391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5921-01A-11D-1609-08 chr5:156378787 C>T maps to NM_138379.2 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5921-01A-11D-1609-08 chr4:81967429 G>A maps to NM_001201.2 R285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5921-01A-11D-1609-08 chr5:113698894 C>T maps to NM_021614.2 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5921-01A-11D-1609-08 chr1:85561703 G>A did not map to a codon.
Sequencing variant TCGA-FZ-5921-01A-11D-1609-08 chr17:76455226 G>A maps to ENST00000389840 A3225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5921-01A-11D-1609-08 chr10:6557091 C>T maps to NM_006257.2 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5921-01A-11D-1609-08 chr3:142218555 C>A maps to NM_001184.3 E1765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5921-01A-11D-1609-08 chrX:125685628 G>A maps to NM_178470.4 Y321Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5921-01A-11D-1609-08 chr14:59930957 C>T maps to NM_022571.5 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5921-01A-11D-1609-08 chr3:195508187 G>A maps to NM_018406.5 H3421H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5921-01A-11D-1609-08 chr12:131621522 G>A maps to NM_198827.3 L800L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5921-01A-11D-1609-08 chr3:9036079 C>T maps to NM_014850.2 R785R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5921-01A-11D-1609-08 chr16:9017121 G>A maps to NM_003470.2 H111H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5921-01A-11D-1609-08 chr19:36050066 G>C maps to NM_000704.2 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5921-01A-11D-1609-08 chr6:76022445 C>T maps to NM_015687.2 R1034R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5921-01A-11D-1609-08 chr8:10469288 C>T maps to NM_178857.5 P773P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5921-01A-11D-1609-08 chr2:141245238 G>A maps to NM_018557.2 R3064*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5921-01A-11D-1609-08 chr6:69666613 A>C maps to NM_001704.2 R480R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5921-01A-11D-1609-08 chr9:990457 C>G maps to NM_021240.2 S291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5921-01A-11D-1609-08 chr14:105419057 G>A maps to NM_138420.2 A910A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5921-01A-11D-1609-08 chr16:81095232 G>A maps to NM_152337.2 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5921-01A-11D-1609-08 chr5:140604076 C>T maps to NM_018934.2 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5921-01A-11D-1609-08 chr22:43272925 G>A maps to NM_001184970.1 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5922-01A-11D-1609-08 chr6:75840655 C>T maps to ENST00000322507 R1993R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5922-01A-11D-1609-08 chr11:58892673 G>A maps to NM_198947.3 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5922-01A-11D-1609-08 chr3:52439311 T>G did not map to a codon.
Sequencing variant TCGA-FZ-5922-01A-11D-1609-08 chr3:47618420 C>T maps to ENST00000383738 R365R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5922-01A-11D-1609-08 chr7:64166849 G>A maps to NM_016220.3 G56G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5922-01A-11D-1609-08 chr5:140476008 C>T maps to NM_018936.2 S545S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5922-01A-11D-1609-08 chr17:47246915 C>A maps to NM_153446.2 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5922-01A-11D-1609-08 chr15:33261054 T>G maps to NM_001103184.2 P726P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5922-01A-11D-1609-08 chr12:132547140 G>A maps to ENST00000333577 Q2779Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5922-01A-11D-1609-08 chr7:123508826 C>G maps to NM_012269.2 S167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5922-01A-11D-1609-08 chr10:5808001 C>T maps to NM_001494.3 K435K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5922-01A-11D-1609-08 chr12:104682724 G>A maps to NM_001093771.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5922-01A-11D-1609-08 chr4:54231748 C>T maps to NM_152540.3 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5922-01A-11D-1609-08 chr15:42520943 C>T maps to ENST00000389834 R402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5922-01A-11D-1609-08 chr2:233351012 G>A maps to NM_004826.2 D117D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5922-01A-11D-1609-08 chr6:161529825 T>C maps to NM_005922.2 L1391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5922-01A-11D-1609-08 chr22:22049264 G>T maps to NM_148175.2 E458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5922-01A-11D-1609-08 chr7:142562187 C>T maps to NM_004445.3 Y210Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5922-01A-11D-1609-08 chr2:74184337 C>T maps to NM_080916.1 H226H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5923-01A-12D-1609-08 chr19:11304176 C>T maps to NM_015493.6 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5923-01A-12D-1609-08 chr16:12875066 G>A maps to NM_018340.2 C88C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5923-01A-12D-1609-08 chr19:1487058 G>A maps to NM_017573.3 R287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5923-01A-12D-1609-08 chr7:147914426 C>T maps to NM_014141.5 Q1020*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5923-01A-12D-1609-08 chr3:197562600 G>T maps to ENST00000425562 E387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5923-01A-12D-1609-08 chr7:31890286 G>A maps to NM_001191057.1 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5923-01A-12D-1609-08 chr2:27259446 C>T maps to NM_017727.4 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5923-01A-12D-1609-08 chr2:234182378 G>A maps to ENST00000392018 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5923-01A-12D-1609-08 chr7:98254348 C>A maps to NM_002523.2 C253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5923-01A-12D-1609-08 chr10:129536922 G>A maps to NM_207426.2 A217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5923-01A-12D-1609-08 chr19:8841410 G>A maps to NM_001004699.1 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5923-01A-12D-1609-08 chr11:373803 C>T maps to NM_178537.4 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5923-01A-12D-1609-08 chrX:118763357 C>T maps to ENST00000394612 T431T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5923-01A-12D-1609-08 chr18:909572 C>T maps to NM_001117.3 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5923-01A-12D-1609-08 chr4:99325652 T>C maps to NM_001100426.1 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5923-01A-12D-1609-08 chr1:45111154 C>T maps to ENST00000453887 I481I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5923-01A-12D-1609-08 chr22:31859947 G>A maps to NM_019843.3 R102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5923-01A-12D-1609-08 chrX:18189250 G>A maps to NM_153346.4 C685C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5923-01A-12D-1609-08 chr1:240374519 G>A maps to ENST00000406993 K1493K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5923-01A-12D-1609-08 chrX:64738236 G>A maps to NM_031206.4 G519G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5923-01A-12D-1609-08 chr8:38133931 C>T maps to NM_023034.1 Q1318Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5923-01A-12D-1609-08 chr13:29598939 G>A maps to NM_001033602.2 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5923-01A-12D-1609-08 chr4:177100633 C>T maps to NM_170710.4 D1291D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5923-01A-12D-1609-08 chr9:138683988 C>T maps to ENST00000298480 R1251R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5923-01A-12D-1609-08 chr12:1943538 C>T maps to NM_001163926.1 D255D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5923-01A-12D-1609-08 chr6:29080437 G>A maps to NM_001005216.2 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5923-01A-12D-1609-08 chr3:64085556 G>A maps to NM_198859.3 R569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5923-01A-12D-1609-08 chr21:45753012 C>T maps to ENST00000397956 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5923-01A-12D-1609-08 chr9:138516227 G>A maps to NM_182974.2 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5923-01A-12D-1609-08 chr3:101177866 G>A maps to NM_020654.3 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5924-01A-13D-1609-08 chr12:45803200 C>T maps to NM_001142679.1 R648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5924-01A-13D-1609-08 chr2:207172203 G>A maps to NM_020923.1 K984K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5924-01A-13D-1609-08 chr11:66637838 G>A maps to NM_022172.2 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5924-01A-13D-1609-08 chr5:140800913 C>T maps to NM_018914.2 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5924-01A-13D-1609-08 chr10:27324225 A>G maps to NM_014915.2 D1051D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5924-01A-13D-1609-08 chr1:212459532 A>G maps to NM_006243.3 K27K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5924-01A-13D-1609-08 chr15:41101366 C>T maps to NM_001077268.1 F110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5924-01A-13D-1609-08 chr15:80800572 G>A maps to NM_014862.3 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5924-01A-13D-1609-08 chr17:30303571 C>T maps to NM_015355.2 R286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5924-01A-13D-1609-08 chr2:29295774 C>T maps to NM_001029883.1 G451G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5924-01A-13D-1609-08 chr17:39122913 A>G maps to NM_213656.3 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5924-01A-13D-1609-08 chr8:89086967 G>A maps to NM_005941.4 Q363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5924-01A-13D-1609-08 chr12:130647816 C>T maps to NM_007197.3 C110C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5924-01A-13D-1609-08 chr2:207572063 C>T maps to NM_001093730.1 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5924-01A-13D-1609-08 chr10:27702138 G>A maps to NM_001034842.3 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5924-01A-13D-1609-08 chr5:1268675 G>A maps to NM_198253.2 G847G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5924-01A-13D-1609-08 chr5:55206447 C>A maps to NM_139017.4 T530T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5924-01A-13D-1609-08 chr21:47422161 C>T maps to NM_001848.2 G699G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5924-01A-13D-1609-08 chr8:120843972 T>C did not map to a codon.
Sequencing variant TCGA-FZ-5926-01A-11D-1609-08 chrX:47058940 T>C maps to NM_153280.2 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5926-01A-11D-1609-08 chr19:8206690 G>A maps to NM_032447.3 Q259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5926-01A-11D-1609-08 chr1:34209013 G>A maps to ENST00000373381 A640A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5926-01A-11D-1609-08 chr17:7942846 G>A maps to NM_001141.2 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5926-01A-11D-1609-08 chr11:122805735 C>T maps to NM_024806.2 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5926-01A-11D-1609-08 chr19:14854231 C>T maps to NM_013447.2 T821T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5926-01A-11D-1609-08 chr5:92923761 G>A maps to NM_005654.4 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5926-01A-11D-1609-08 chr20:33324553 G>A maps to NM_014071.2 Q1968*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5926-01A-11D-1609-08 chr20:42198156 G>T did not map to a codon.
Sequencing variant TCGA-FZ-5926-01A-11D-1609-08 chr2:179319080 G>C maps to NM_001042702.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5926-01A-11D-1609-08 chr1:19455509 G>A maps to ENST00000375267 R2989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5926-01A-11D-1609-08 chr20:33324554 C>A maps to NM_014071.2 S1967S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5926-01A-11D-1609-08 chr14:91700905 G>A maps to ENST00000238699 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5926-01A-11D-1609-08 chr1:2530109 G>A maps to NM_033467.3 I387I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5926-01A-11D-1609-08 chr18:7774243 G>A maps to NM_001105244.1 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5926-01A-11D-1609-08 chr20:30064349 C>T maps to NM_014012.4 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5926-01A-11D-1609-08 chr7:129909573 C>T maps to NM_001869.2 N73N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5926-01A-11D-1609-08 chr20:44641960 G>A maps to NM_004994.2 T466T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5926-01A-11D-1609-08 chr11:7981304 A>T maps to NM_176821.3 C618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5926-01A-11D-1609-08 chrX:44936002 A>T maps to NM_021140.2 R922*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H6-8124-01A-11D-2396-08 chr14:99641459 A>C maps to NM_138576.2 G571G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H6-8124-01A-11D-2396-08 chr9:21974781 C>T maps to NM_001195132.1 W15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H6-8124-01A-11D-2396-08 chr1:2444409 C>T maps to ENST00000425477 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H6-8124-01A-11D-2396-08 chr2:219500517 G>C did not map to a codon.
Sequencing variant TCGA-H6-8124-01A-11D-2396-08 chr12:15095521 G>A maps to NM_001175.4 D180D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H6-8124-01A-11D-2396-08 chr1:12887685 T>C maps to NM_001146344.1 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H6-8124-01A-11D-2396-08 chr3:48699137 C>T maps to NM_001407.2 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H6-8124-01A-11D-2396-08 chr13:36744856 C>T maps to ENST00000511166 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H6-8124-01A-11D-2396-08 chr19:36278841 A>C maps to ENST00000007510 S1125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H6-8124-01A-11D-2396-08 chr20:30584386 C>T maps to NM_001011718.1 D289D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H6-8124-01A-11D-2396-08 chr19:53644385 T>A maps to NM_001172674.1 G566G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H6-8124-01A-11D-2396-08 chr9:116093320 G>A maps to NM_001012361.2 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H6-8124-01A-11D-2396-08 chr11:95724866 G>A maps to NM_032427.1 G720G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H6-8124-01A-11D-2396-08 chr6:170597429 G>A maps to NM_005618.3 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H6-8124-01A-11D-2396-08 chr1:68952618 C>A did not map to a codon.
Sequencing variant TCGA-H6-8124-01A-11D-2396-08 chr4:164050123 T>G maps to NM_138386.2 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H6-8124-01A-11D-2396-08 chr5:158750143 G>A maps to NM_002187.2 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H6-8124-01A-11D-2396-08 chr4:149075975 T>G maps to ENST00000511528 P701P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H6-8124-01A-11D-2396-08 chr22:29837972 T>C maps to NM_021026.2 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H6-A45N-01A-11D-A26I-08 chr11:7618801 C>T maps to NM_003621.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H6-A45N-01A-11D-A26I-08 chr1:49208354 C>T maps to NM_024603.2 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H6-A45N-01A-11D-A26I-08 chr19:14208283 C>T maps to NM_002730.3 K218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H6-A45N-01A-11D-A26I-08 chr6:45390447 G>A maps to ENST00000359524 Q127Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H6-A45N-01A-11D-A26I-08 chr21:15858389 G>C maps to ENST00000285670 S390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H6-A45N-01A-11D-A26I-08 chr2:211179818 C>A did not map to a codon.
Sequencing variant TCGA-H6-A45N-01A-11D-A26I-08 chrX:128599616 C>T maps to NM_003069.3 L970L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H6-A45N-01A-11D-A26I-08 chr20:44856261 C>T maps to NM_021248.1 T185T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-H6-A45N-01A-11D-A26I-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-H6-A45N-01A-11D-A26I-08 chr19:8660765 C>G maps to NM_030957.2 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H6-A45N-01A-11D-A26I-08 chr2:29296605 C>T maps to NM_001029883.1 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H6-A45N-01A-11D-A26I-08 chr6:10755435 C>T maps to NM_030969.3 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H6-A45N-01A-11D-A26I-08 chr10:82036257 C>T maps to NM_000429.2 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H6-A45N-01A-11D-A26I-08 chr3:188933149 C>T maps to NM_198485.3 Q94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H6-A45N-01A-11D-A26I-08 chr20:55033727 C>T maps to NM_020356.3 A762A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H6-A45N-01A-11D-A26I-08 chr12:48131366 G>A maps to NM_001098531.2 R919*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H8-A6C1-01A-11D-A32N-08 chr12:7527077 G>A maps to ENST00000416109 H1133H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H8-A6C1-01A-11D-A32N-08 chr1:79387435 C>T maps to NM_022159.3 W373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H8-A6C1-01A-11D-A32N-08 chrX:16870946 C>T maps to NM_001198719.1 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H8-A6C1-01A-11D-A32N-08 chr21:37741699 A>T maps to ENST00000290384 I679I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H8-A6C1-01A-11D-A32N-08 chr5:140228550 G>A maps to NM_031857.1 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H8-A6C1-01A-11D-A32N-08 chr22:25280107 C>T maps to NM_001039948.2 C583C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H8-A6C1-01A-11D-A32N-08 chr3:194062234 G>A maps to NM_001080513.2 C399C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H8-A6C1-01A-11D-A32N-08 chr15:74467396 G>A maps to NM_201526.1 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H8-A6C1-01A-11D-A32N-08 chr3:50329756 C>T maps to ENST00000336089 E149E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H8-A6C1-01A-11D-A32N-08 chr19:53644385 T>A maps to NM_001172674.1 G566G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H8-A6C1-01A-11D-A32N-08 chr1:57224418 A>C maps to NM_001004303.4 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H8-A6C1-01A-11D-A32N-08 chr16:84793045 G>A maps to NM_005153.2 R454R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H8-A6C1-01A-11D-A32N-08 chr2:206610561 G>A maps to NM_201266.1 W578*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H8-A6C1-01A-11D-A32N-08 chr7:114270014 A>G maps to NM_148898.3 Q209Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H8-A6C1-01A-11D-A32N-08 chr16:75269101 G>A maps to NM_001170714.1 G611G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H8-A6C1-01A-11D-A32N-08 chr19:48800556 G>A maps to NM_144577.3 G563G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H8-A6C1-01A-11D-A32N-08 chr9:124062284 T>G did not map to a codon.
Sequencing variant TCGA-H8-A6C1-01A-11D-A32N-08 chr5:95746543 G>A maps to NM_000439.4 Y343Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H8-A6C1-01A-11D-A32N-08 chr19:55494004 G>A maps to NM_017852.3 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H8-A6C1-01A-11D-A32N-08 chr1:160201177 C>A maps to NM_015726.3 E327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H8-A6C1-01A-11D-A32N-08 chr1:94502768 C>A maps to NM_000350.2 E1249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A3-01A-11D-A26I-08 chr16:30793071 G>A maps to NM_001080417.1 L859L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A3-01A-11D-A26I-08 chr18:5398075 G>A maps to NM_012307.2 R806*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A3-01A-11D-A26I-08 chr7:143747853 C>T maps to NM_012365.1 Y120Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A3-01A-11D-A26I-08 chr19:54327404 G>A maps to ENST00000391773 D8D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A3-01A-11D-A26I-08 chr5:140604696 G>A maps to NM_018934.2 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A3-01A-11D-A26I-08 chr15:26825520 C>T maps to NM_021912.4 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A3-01A-11D-A26I-08 chr18:48603027 T>A maps to NM_005359.5 C443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A3-01A-11D-A26I-08 chr19:55711613 G>A maps to NM_002842.3 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A3-01A-11D-A26I-08 chr1:19477077 G>A maps to ENST00000375267 L2475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A3-01A-11D-A26I-08 chr19:22362993 C>A maps to NM_001001411.2 E509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A3-01A-11D-A26I-08 chr3:148563349 C>A maps to NM_001871.2 Y306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A3-01A-11D-A26I-08 chr10:17363215 C>T maps to NM_001004470.1 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A3-01A-11D-A26I-08 chr1:248366500 C>T maps to NM_001004689.1 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A3-01A-11D-A26I-08 chr12:52885508 C>T maps to NM_005554.3 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A3-01A-11D-A26I-08 chr9:124062284 T>G did not map to a codon.
Sequencing variant TCGA-HV-A5A4-01A-11D-A26I-08 chr11:6432331 C>T maps to ENST00000389906 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A4-01A-11D-A26I-08 chr5:140564032 C>A maps to NM_020957.1 R633R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A4-01A-11D-A26I-08 chr6:90660534 G>A maps to NM_001170794.1 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A4-01A-11D-A26I-08 chrX:135618241 G>A maps to NM_016267.3 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A4-01A-11D-A26I-08 chr9:95077967 C>T maps to NM_017948.5 A313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A4-01A-11D-A26I-08 chr15:67555548 C>G maps to NM_001031715.2 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A4-01A-11D-A26I-08 chrX:111697970 G>A maps to NM_001004308.2 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A4-01A-11D-A26I-08 chr19:57327379 G>A maps to NM_006210.2 F810F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A4-01A-11D-A26I-08 chr3:120673879 C>T maps to NM_014980.2 R95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A4-01A-11D-A26I-08 chr19:3740729 C>T maps to NM_014428.1 Y637Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A4-01A-11D-A26I-08 chr9:80646046 G>A maps to NM_002072.3 D35D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A4-01A-11D-A26I-08 chr2:241991877 C>T maps to NM_001080437.1 C692C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A4-01A-11D-A26I-08 chr18:48604735 G>T maps to NM_005359.5 E520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A5-01A-11D-A26I-08 chr1:26608891 G>A maps to NM_183008.2 P487P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A5-01A-11D-A26I-08 chr11:102816456 A>T maps to NM_002427.3 I411I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A5-01A-11D-A26I-08 chr1:12887685 T>C maps to NM_001146344.1 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A5-01A-11D-A26I-08 chr6:137323027 C>T maps to NM_014432.2 P443P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A5-01A-11D-A26I-08 chr4:125592598 A>G maps to NM_020337.2 G611G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A5-01A-11D-A26I-08 chrX:84560886 C>T maps to ENST00000373145 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A5-01A-11D-A26I-08 chr3:13860785 G>A maps to NM_004625.3 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A5-01A-11D-A26I-08 chr8:22473259 C>T maps to NM_021174.5 N481N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A5-01A-11D-A26I-08 chr17:4356343 C>T maps to NM_182538.4 G319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A5-01A-11D-A26I-08 chr5:95152243 C>T maps to NM_002064.2 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A5-01A-11D-A26I-08 chr17:18565372 A>G maps to NM_001145045.1 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A5-01A-11D-A26I-08 chr14:24569249 C>T maps to NM_004563.2 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A5-01A-11D-A26I-08 chr4:184368444 C>T maps to NM_017632.2 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A5-01A-11D-A26I-08 chr11:64116903 G>C maps to NM_032251.5 L906L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A6-01A-11D-A26I-08 chr5:26889953 T>C maps to NM_016279.3 K501K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A6-01A-11D-A26I-08 chr6:43251408 G>A maps to NM_032538.1 A977A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A6-01A-11D-A26I-08 chr19:14749134 G>A maps to NM_032571.3 I422I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A6-01A-11D-A26I-08 chr21:30434481 G>A maps to NM_006585.2 D393D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A6-01A-11D-A26I-08 chr6:15497189 C>T maps to NM_004973.2 R578R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A6-01A-11D-A26I-08 chr14:105420572 G>A maps to NM_138420.2 C405C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A6-01A-11D-A26I-08 chr5:434609 G>A maps to NM_020731.3 S607S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A6-01A-11D-A26I-08 chr19:8609327 G>A maps to NM_012335.3 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A6-01A-11D-A26I-08 chr1:111702112 G>T maps to NM_001007794.1 E151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A6-01A-11D-A26I-08 chr11:113675588 C>T did not map to a codon.
Sequencing variant TCGA-HV-A5A6-01A-11D-A26I-08 chr10:122626195 A>T maps to NM_018117.11 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A6-01A-11D-A26I-08 chr8:42023052 C>T maps to NM_006803.3 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A6-01A-11D-A26I-08 chr19:56135867 G>A maps to NM_203374.1 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A6-01A-11D-A26I-08 chr7:23000934 A>G maps to NM_032581.3 N250N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A6-01A-11D-A26I-08 chr6:74210400 A>G maps to NM_001123226.1 S714S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A6-01A-11D-A26I-08 chr2:27449517 G>A did not map to a codon.
Sequencing variant TCGA-HV-A5A6-01A-11D-A26I-08 chr1:16262017 C>T maps to NM_015001.2 Q3095*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A6-01A-11D-A26I-08 chr11:18763930 G>A maps to NM_032781.3 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A6-01A-11D-A26I-08 chr15:99512679 G>A maps to NM_001102612.2 D115D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A5A6-01A-11D-A26I-08 chr11:67048253 C>T maps to NM_001619.3 H185H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OL-01A-11D-A33T-08 chr15:28421857 C>T maps to NM_004667.4 A3163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OL-01A-11D-A33T-08 chr1:26608891 G>A maps to NM_183008.2 P487P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OL-01A-11D-A33T-08 chr7:94052352 C>T maps to NM_000089.3 R830*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OL-01A-11D-A33T-08 chr1:222802592 C>T maps to NM_198551.2 L677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OL-01A-11D-A33T-08 chr17:56448269 A>G did not map to a codon.
Sequencing variant TCGA-HV-A7OL-01A-11D-A33T-08 chr16:1397934 G>A maps to NM_003933.4 P1057P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OL-01A-11D-A33T-08 chr11:113078689 C>T maps to ENST00000316851 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OL-01A-11D-A33T-08 chr6:139206662 A>C maps to NM_001195037.2 A683A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OL-01A-11D-A33T-08 chr16:30616625 G>A maps to NM_138447.1 C154C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OL-01A-11D-A33T-08 chr22:29834845 C>T maps to NM_021026.2 C22C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OL-01A-11D-A33T-08 chr3:186769121 G>C maps to NM_003032.2 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OL-01A-11D-A33T-08 chr2:171818251 A>C maps to NM_015530.3 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OL-01A-11D-A33T-08 chr6:90097154 G>A maps to NM_021244.4 C101C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OL-01A-11D-A33T-08 chr16:703652 C>T maps to NM_145294.4 H454H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OL-01A-11D-A33T-08 chr16:4787892 C>A maps to NM_139170.2 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OL-01A-11D-A33T-08 chr12:76791662 T>C maps to NM_020841.4 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OL-01A-11D-A33T-08 chr3:101446385 G>A did not map to a codon.
Sequencing variant TCGA-HV-A7OL-01A-11D-A33T-08 chr13:41134022 G>A maps to NM_002015.3 N535N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OL-01A-11D-A33T-08 chr20:52198225 G>A maps to NM_006526.2 C380C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OL-01A-11D-A33T-08 chr18:9255364 T>C maps to NM_015208.3 F700F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OL-01A-11D-A33T-08 chr1:26189403 C>T maps to NM_178422.5 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OL-01A-11D-A33T-08 chrX:91090547 A>G maps to NM_032968.3 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OL-01A-11D-A33T-08 chr17:9684813 C>T maps to ENST00000330255 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OL-01A-11D-A33T-08 chr3:154056054 G>A maps to NM_001038705.1 S543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OL-01A-11D-A33T-08 chr6:71232277 C>T maps to NM_001162529.1 Y364Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OL-01A-11D-A33T-08 chr9:79438589 T>C maps to NM_015225.2 G238G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OL-01A-11D-A33T-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OL-01A-11D-A33T-08 chr19:55505648 C>T maps to NM_017852.3 C907C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OL-01A-11D-A33T-08 chr16:20976523 G>A maps to NM_017539.1 Y2894Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OL-01A-11D-A33T-08 chr12:131487821 C>T maps to NM_198827.3 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr17:60754765 G>A maps to NM_006039.3 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr2:179483530 G>T maps to NM_133378.4 G13014G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr10:73472563 C>A maps to ENST00000398860 I1126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr7:2634594 G>A maps to NM_152558.3 P475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr3:55508499 G>A maps to NM_003392.3 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr4:134073205 G>A maps to NM_032961.1 E637E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr13:31858881 T>A maps to NM_194318.3 I316I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr18:32920401 G>A maps to NM_006965.2 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr12:122285008 G>A maps to NM_002150.2 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr10:126682515 G>A maps to NM_022802.2 G813G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr6:3284090 C>G maps to ENST00000436008 V574V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr12:7241474 C>T maps to ENST00000290575 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr16:57243041 T>C maps to NM_133368.1 D153D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr8:120118315 C>T maps to NM_006438.3 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr10:91162379 T>A maps to NM_001548.3 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr1:168034904 G>A maps to ENST00000367840 R839R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr12:106826184 G>A maps to NM_018082.5 L518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr10:82331252 C>T maps to NM_207372.2 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr11:17794107 G>A maps to NM_001112741.1 P489P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr5:140256418 G>A maps to NM_018903.2 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr14:34419829 G>A maps to NM_022073.3 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr18:31241679 C>T maps to NM_030632.1 H152H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr4:151023708 G>A maps to NM_001040261.4 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr10:22862386 C>T did not map to a codon.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr1:186276563 C>T maps to NM_005807.3 T571T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr1:204170870 C>T maps to NM_198447.1 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr9:35800074 G>T maps to NM_003995.3 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr19:40580665 T>C maps to NM_001142577.1 E562E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr19:4538263 G>A maps to NM_052972.2 N244N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr11:105483021 C>T maps to NM_000829.3 N36N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chrX:138643809 C>T maps to NM_000133.3 D322D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr15:67482872 A>T maps to NM_005902.3 *426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr11:55579037 T>A maps to NM_001004738.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr10:75527671 C>T maps to NM_198597.1 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr9:33948658 T>C did not map to a codon.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr10:132915166 C>T maps to NM_174937.3 E430E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr8:68423883 G>A maps to NM_020361.4 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr1:153907308 C>T maps to NM_014856.2 Q900Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr8:116599640 G>A maps to NM_014112.2 L763L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr1:228238531 G>T maps to ENST00000366753 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr6:75884784 G>A maps to ENST00000322507 D893D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr1:158390070 G>A maps to NM_001004476.1 Q196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr1:3407101 G>A maps to ENST00000452816 S1615S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr5:1232475 T>A did not map to a codon.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr5:78264931 G>C maps to NM_000046.3 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr7:99913459 A>G maps to NM_001004351.4 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr2:234638368 A>G maps to NM_019093.2 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr5:112162890 C>T maps to NM_001127510.2 R499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr20:23029061 G>A maps to NM_000361.2 G360G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr6:71246001 A>T maps to NM_001162529.1 S1335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr13:86370130 A>T maps to NM_032229.2 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr1:247875337 C>T maps to NM_001005286.1 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr19:55494010 C>T maps to NM_017852.3 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr16:68014187 G>A maps to NM_022357.3 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HV-A7OP-01A-11D-A33T-08 chr5:33936895 C>T maps to NM_016568.3 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7289-01A-11D-2154-08 chr2:109380687 C>T maps to NM_006267.4 R1231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7289-01A-11D-2154-08 chr2:70188472 C>T maps to NM_152792.2 W116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7289-01A-11D-2154-08 chr2:234681096 C>T maps to ENST00000373460 V496V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7289-01A-11D-2154-08 chr6:123824954 A>G maps to NM_006073.2 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7289-01A-11D-2154-08 chr14:60212958 A>T maps to NM_021136.2 L161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7289-01A-11D-2154-08 chr10:127677373 A>G did not map to a codon.
Sequencing variant TCGA-HZ-7289-01A-11D-2154-08 chr13:35630160 C>T maps to ENST00000400445 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7289-01A-11D-2154-08 chr6:35050547 C>T maps to NM_015245.2 H930H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7289-01A-11D-2154-08 chr12:124825184 G>A maps to NM_006312.4 P1774P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7289-01A-11D-2154-08 chr6:56393692 G>A maps to ENST00000361203 Q5665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7289-01A-11D-2154-08 chr11:108124538 A>C did not map to a codon.
Sequencing variant TCGA-HZ-7289-01A-11D-2154-08 chr19:53209242 T>C maps to NM_001161500.1 Q355Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7289-01A-11D-2154-08 chr2:27351451 C>T maps to NM_032604.3 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7289-01A-11D-2154-08 chr22:41257515 A>G maps to NM_145174.1 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7289-01A-11D-2154-08 chr19:41931792 G>A maps to NM_198540.2 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7289-01A-11D-2154-08 chr10:133106510 C>T maps to NM_174937.3 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7289-01A-11D-2154-08 chr3:169710772 A>G maps to NM_003262.3 Q374Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7289-01A-11D-2154-08 chr12:109278889 G>A maps to NM_001917.4 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7289-01A-11D-2154-08 chr19:14274078 G>A maps to NM_001008701.2 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7289-01A-11D-2154-08 chr11:110494917 G>C maps to NM_020809.2 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7289-01A-11D-2154-08 chr12:54348805 G>T maps to NM_173860.1 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7289-01A-11D-2154-08 chr12:26580902 G>A maps to NM_002223.2 L2296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7289-01A-11D-2154-08 chr16:84797845 C>T maps to NM_005153.2 T603T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7289-01A-11D-2154-08 chr17:72943311 G>A maps to NM_178233.1 S454S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7289-01A-11D-2154-08 chr8:144776009 C>T maps to NM_173831.3 D142D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7289-01A-11D-2154-08 chr17:37842225 G>A maps to NM_033419.3 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7289-01A-11D-2154-08 chr19:50390731 G>T did not map to a codon.
Sequencing variant TCGA-HZ-7289-01A-11D-2154-08 chr19:35176006 C>T maps to ENST00000221282 H434H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7289-01A-11D-2154-08 chr4:48548199 G>A maps to NM_015030.1 S1721S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7289-01A-11D-2154-08 chr3:19575467 C>T maps to NM_144633.2 N1067N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7289-01A-11D-2154-08 chr7:102518011 G>A maps to NM_145032.3 R513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7289-01A-11D-2154-08 chr22:50657233 G>A maps to NM_020461.3 D1573D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7289-01A-11D-2154-08 chr8:131793085 G>A maps to NM_001115.2 G1102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7289-01A-11D-2154-08 chr3:48508063 C>T maps to NM_016381.3 Q59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7289-01A-11D-2154-08 chr22:27008040 C>T maps to NM_001887.3 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7289-01A-11D-2154-08 chr10:93389815 G>A maps to NM_005398.4 D274D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7918-01A-11D-2154-08 chr14:21861650 C>T maps to NM_001170629.1 E2101E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7918-01A-11D-2154-08 chr16:89764125 C>T maps to NM_152339.3 E297E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7918-01A-11D-2154-08 chr2:171323215 G>C maps to NM_138995.3 V1003V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7918-01A-11D-2154-08 chr17:26108127 G>T maps to NM_000625.4 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7918-01A-11D-2154-08 chr3:27759189 C>A maps to ENST00000449599 E497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7918-01A-11D-2154-08 chr12:2760900 G>C maps to NM_199460.2 R1395R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7918-01A-11D-2154-08 chr5:76507010 G>A maps to NM_003719.3 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7918-01A-11D-2154-08 chr17:27857471 C>T maps to NM_020791.2 I732I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7918-01A-11D-2154-08 chr9:100328233 G>A maps to NM_003275.3 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7918-01A-11D-2154-08 chr5:180056836 T>A did not map to a codon.
Sequencing variant TCGA-HZ-7918-01A-11D-2154-08 chr14:103996578 C>T maps to ENST00000299201 Y88Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7918-01A-11D-2154-08 chr21:47614457 G>T maps to NM_002340.5 A645A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7918-01A-11D-2154-08 chr17:40010102 G>A maps to NM_018143.1 Y672Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7918-01A-11D-2154-08 chr7:87178759 A>G maps to NM_000927.3 R543R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7918-01A-11D-2154-08 chr6:85457658 G>A maps to NM_001080508.1 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7918-01A-11D-2154-08 chr20:61591928 C>T maps to NM_022082.3 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7918-01A-11D-2154-08 chr9:32634850 A>G maps to NM_153809.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7918-01A-11D-2154-08 chr15:65793002 G>A maps to NM_197960.2 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7918-01A-11D-2154-08 chr11:64847202 C>T maps to ENST00000404147 E100E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7918-01A-11D-2154-08 chrX:128696368 G>A maps to NM_000276.3 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7918-01A-11D-2154-08 chr8:48744457 G>A maps to NM_006904.6 L2727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7918-01A-11D-2154-08 chr19:8661291 C>A maps to NM_030957.2 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7918-01A-11D-2154-08 chr8:133595975 A>T maps to ENST00000250173 T397T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7918-01A-11D-2154-08 chr12:6692544 C>A did not map to a codon.
Sequencing variant TCGA-HZ-7918-01A-11D-2154-08 chr10:79589221 G>A maps to NM_004747.3 I692I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7918-01A-11D-2154-08 chr10:16562658 G>A maps to NM_001010908.1 Q136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7918-01A-11D-2154-08 chr7:95818664 G>T maps to NM_001160210.1 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7918-01A-11D-2154-08 chr17:59668535 C>G maps to NM_199290.3 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7918-01A-11D-2154-08 chr1:158390122 G>A maps to NM_001004476.1 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7918-01A-11D-2154-08 chr4:128804673 A>G maps to NM_014264.4 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7918-01A-11D-2154-08 chr6:2838131 G>A maps to NM_030666.2 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7918-01A-11D-2154-08 chr6:25670277 A>T maps to NM_006998.3 K149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7918-01A-11D-2154-08 chr6:116580007 A>G did not map to a codon.
Sequencing variant TCGA-HZ-7918-01A-11D-2154-08 chr6:116579983 C>T did not map to a codon.
Sequencing variant TCGA-HZ-7918-01A-11D-2154-08 chr19:12786383 G>A maps to NM_032332.3 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7918-01A-11D-2154-08 chr19:49520321 A>C did not map to a codon.
Sequencing variant TCGA-HZ-7918-01A-11D-2154-08 chr19:51503918 G>A maps to NM_144505.1 V42V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7918-01A-11D-2154-08 chr19:56565132 C>T maps to NM_153447.4 C1086C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7918-01A-11D-2154-08 chr1:22331986 C>T maps to NM_005747.4 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7918-01A-11D-2154-08 chr11:66331558 C>T maps to NM_003793.3 K460K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7918-01A-11D-2154-08 chrX:47446053 G>C maps to NM_003254.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7919-01A-11D-2154-08 chr5:140754471 C>T maps to NM_018919.2 H274H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7919-01A-11D-2154-08 chr6:2624099 G>C did not map to a codon.
Sequencing variant TCGA-HZ-7919-01A-11D-2154-08 chr11:1268339 A>T maps to ENST00000447027 P3413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7919-01A-11D-2154-08 chr15:83926673 C>T maps to NM_001717.3 T835T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7919-01A-11D-2154-08 chrX:1508185 C>T maps to NM_001636.3 Q182Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7919-01A-11D-2154-08 chr14:23828663 T>G maps to NM_005864.2 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7919-01A-11D-2154-08 chr16:89838199 C>T maps to NM_000135.2 V679V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7919-01A-11D-2154-08 chr11:33094068 G>A maps to NM_001145541.1 Q459Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7919-01A-11D-2154-08 chr14:76330127 C>T maps to NM_015072.4 Q1149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7919-01A-11D-2154-08 chr18:34289289 G>A maps to NM_025135.2 S648S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7919-01A-11D-2154-08 chr9:131386634 C>G maps to NM_001130438.2 S1954*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7919-01A-11D-2154-08 chr1:186276215 T>C maps to NM_005807.3 T455T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7919-01A-11D-2154-08 chr10:106924112 C>T maps to NM_014978.1 S595S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7919-01A-11D-2154-08 chr19:49000673 G>A maps to NM_001080434.1 Q1247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7919-01A-11D-2154-08 chr11:1606185 A>G maps to NM_001005922.1 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7919-01A-11D-2154-08 chr9:33068869 G>A maps to NM_018225.2 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7919-01A-11D-2154-08 chr19:49129494 C>T maps to NM_020126.3 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7919-01A-11D-2154-08 chr15:86212981 T>C maps to NM_006738.4 F1678F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7919-01A-11D-2154-08 chr1:201966572 C>T maps to NM_020216.3 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7919-01A-11D-2154-08 chr9:131513436 G>A maps to NM_006336.2 R383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7919-01A-11D-2154-08 chr2:143913142 C>A maps to NM_018460.3 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7919-01A-11D-2154-08 chr6:10410433 T>G maps to ENST00000379613 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7919-01A-11D-2154-08 chr20:42694632 C>T maps to ENST00000348077 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7919-01A-11D-2154-08 chr11:124626109 T>C maps to NM_138961.2 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7919-01A-11D-2154-08 chr22:32464532 C>A maps to NM_000343.3 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7919-01A-11D-2154-08 chr4:164050123 T>G maps to NM_138386.2 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7919-01A-11D-2154-08 chr20:19981312 C>G maps to ENST00000255006 L856L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7919-01A-11D-2154-08 chr1:201966563 C>T maps to NM_020216.3 I324I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7919-01A-11D-2154-08 chr19:4364083 C>T did not map to a codon.
Sequencing variant TCGA-HZ-7919-01A-11D-2154-08 chr14:23828669 T>G maps to NM_005864.2 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7920-01A-11D-2201-08 chr1:154842332 C>T maps to NM_002249.4 Q36Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7920-01A-11D-2201-08 chrX:53231137 C>T maps to NM_004187.3 Q588Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7920-01A-11D-2201-08 chr19:56701711 T>C maps to NM_001080456.2 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7920-01A-11D-2201-08 chr5:179271227 C>T did not map to a codon.
Sequencing variant TCGA-HZ-7920-01A-11D-2201-08 chr6:33287899 C>T maps to NM_001350.4 E451E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7920-01A-11D-2201-08 chr19:3053927 G>A maps to NM_198969.1 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7920-01A-11D-2201-08 chr2:204305986 T>G maps to ENST00000374493 P694P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7922-01A-11D-2154-08 chr11:123810382 T>C maps to NM_001001965.1 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7922-01A-11D-2154-08 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7922-01A-11D-2154-08 chrX:112048282 C>T maps to NM_001113490.1 A556A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7922-01A-11D-2154-08 chr1:248039220 C>T maps to NM_015431.3 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7922-01A-11D-2154-08 chr21:45389012 C>A maps to NM_001037553.1 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7922-01A-11D-2154-08 chr10:96269881 A>G maps to NM_015188.1 E545E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7922-01A-11D-2154-08 chr19:50504079 T>C maps to NM_016440.3 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7922-01A-11D-2154-08 chr16:4702742 G>T maps to NM_015246.2 E121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7922-01A-11D-2154-08 chr16:67961229 C>G maps to NM_006742.2 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7922-01A-11D-2154-08 chr19:36633200 G>A did not map to a codon.
Sequencing variant TCGA-HZ-7922-01A-11D-2154-08 chr22:29886316 G>A maps to NM_021076.3 E896E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7922-01A-11D-2154-08 chr19:51322554 T>G maps to NM_002257.2 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7922-01A-11D-2154-08 chr13:67802227 C>A maps to NM_203487.2 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7922-01A-11D-2154-08 chr2:179579857 G>A maps to NM_133378.4 S7441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7922-01A-11D-2154-08 chr2:31625969 G>T maps to NM_000379.3 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7923-01A-12D-2154-08 chr21:45959319 A>G maps to NM_198691.2 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7923-01A-12D-2154-08 chr19:35232752 T>C maps to ENST00000392232 Y533Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7925-01A-11D-2154-08 chr16:67863788 G>C maps to NM_025082.3 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7925-01A-11D-2154-08 chr19:51133282 G>A maps to NM_001160329.1 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7925-01A-11D-2154-08 chrX:153135630 G>A maps to NM_000425.3 Q291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7925-01A-11D-2154-08 chr5:60241049 G>A did not map to a codon.
Sequencing variant TCGA-HZ-7925-01A-11D-2154-08 chr2:133542682 G>A maps to NM_207363.2 G567G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7925-01A-11D-2154-08 chr17:7578524 G>T maps to NM_001126112.1 C135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7925-01A-11D-2154-08 chr14:25043946 C>T maps to NM_001911.2 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7925-01A-11D-2154-08 chr17:56356675 G>A maps to ENST00000340482 N252N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7925-01A-11D-2154-08 chr15:62993387 G>A maps to NM_015059.2 T557T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7925-01A-11D-2154-08 chr5:115327958 C>T maps to NM_173800.4 H415H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7925-01A-11D-2154-08 chr15:79296393 C>T maps to NM_002891.4 S749S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7925-01A-11D-2154-08 chr11:111780949 G>T did not map to a codon.
Sequencing variant TCGA-HZ-7926-01A-11D-2154-08 chr5:140482065 G>A maps to NM_018937.2 E611E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7926-01A-11D-2154-08 chr16:2137907 C>T maps to NM_000548.3 Y1678Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7926-01A-11D-2154-08 chr4:100512444 G>C maps to ENST00000511045 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7926-01A-11D-2154-08 chr4:84353359 C>T maps to NM_133636.2 Q703Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7926-01A-11D-2154-08 chr19:7833837 C>A maps to NM_014257.4 I388I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7926-01A-11D-2154-08 chr14:90650873 G>T maps to NM_022054.2 E252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7926-01A-11D-2154-08 chr1:222835426 C>T maps to NM_198551.2 R1715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7926-01A-11D-2154-08 chr9:119903692 G>A maps to ENST00000313400 R360R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7926-01A-11D-2154-08 chr2:212589902 A>G maps to NM_005235.2 C213C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7926-01A-11D-2154-08 chr5:55059847 C>G maps to NM_024415.2 S97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7926-01A-11D-2154-08 chr2:71417025 C>T maps to NM_020459.1 Q88Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7926-01A-11D-2154-08 chr1:158435755 C>T maps to NM_001004473.1 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7926-01A-11D-2154-08 chr1:3415046 G>A maps to ENST00000452816 D1155D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7926-01A-11D-2154-08 chr19:58549467 C>T maps to NM_182572.3 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7926-01A-11D-2154-08 chr6:43155032 G>A maps to ENST00000354495 P479P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7926-01A-11D-2154-08 chr1:16918793 G>A did not map to a codon.
Sequencing variant TCGA-HZ-7926-01A-11D-2154-08 chr20:30432694 C>T maps to NM_004118.3 A217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7926-01A-11D-2154-08 chr1:247592988 G>A maps to NM_004895.4 L753L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7926-01A-11D-2154-08 chr14:51094835 C>T maps to ENST00000358385 R403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7926-01A-11D-2154-08 chr1:93672841 G>T maps to NM_206886.2 E484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7926-01A-11D-2154-08 chr1:155160806 G>A maps to ENST00000425082 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7926-01A-11D-2154-08 chr5:101834437 T>G maps to NM_173488.3 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7926-01A-11D-2154-08 chr12:20903756 T>C maps to NM_001145946.1 H649H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7926-01A-11D-2154-08 chr5:101576430 G>A maps to NM_180991.4 R623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8001-01A-11D-2201-08 chr12:113905136 C>T maps to NM_022363.2 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8001-01A-11D-2201-08 chr6:45390465 A>G maps to ENST00000359524 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8001-01A-11D-2201-08 chr16:75579248 C>T did not map to a codon.
Sequencing variant TCGA-HZ-8001-01A-11D-2201-08 chr13:103718455 G>A maps to NM_000452.2 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8001-01A-11D-2201-08 chr21:28338458 G>A maps to NM_007038.3 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8001-01A-11D-2201-08 chr11:17415842 G>A maps to ENST00000302539 D1506D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8001-01A-11D-2201-08 chr9:36058868 C>T maps to NM_021111.2 R69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8001-01A-11D-2201-08 chr9:8492934 G>A maps to NM_002839.3 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8001-01A-11D-2201-08 chr4:154709591 G>A maps to NM_003013.2 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8001-01A-11D-2201-08 chr3:151129292 G>A maps to NM_053002.4 Q2011Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8001-01A-11D-2201-08 chr2:179574353 G>T maps to NM_133378.4 Y8320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8001-01A-11D-2201-08 chr19:58361333 G>A did not map to a codon.
Sequencing variant TCGA-HZ-8001-01A-11D-2201-08 chr19:34868484 C>T maps to NM_000175.3 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8001-01A-11D-2201-08 chr17:36499507 C>T maps to ENST00000398597 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8001-01A-11D-2201-08 chr14:105716867 C>T maps to NM_033271.2 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8001-01A-11D-2201-08 chr3:138738750 C>T maps to NM_001013650.2 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8001-01A-11D-2201-08 chr1:204588994 C>T maps to NM_201630.1 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8001-01A-11D-2201-08 chr4:71510451 A>G maps to NM_031889.2 E1103E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8001-01A-11D-2201-08 chr6:100896020 C>T did not map to a codon.
Sequencing variant TCGA-HZ-8001-01A-11D-2201-08 chr10:71683571 C>T maps to ENST00000356340 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8001-01A-11D-2201-08 chr9:140357966 G>A maps to NM_001098537.1 Y1081Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8001-01A-11D-2201-08 chr12:56705036 G>A maps to NM_014255.5 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8001-01A-11D-2201-08 chr1:27106227 C>T maps to NM_006015.4 Q1947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8002-01A-11D-2201-08 chr1:66036154 G>T did not map to a codon.
Sequencing variant TCGA-HZ-8002-01A-11D-2201-08 chrX:38146146 C>T maps to NM_001034853.1 W702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8002-01A-11D-2201-08 chr1:99772445 C>T maps to NM_014839.4 R724R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8002-01A-11D-2201-08 chr13:111870078 C>T maps to NM_001113511.1 F195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8002-01A-11D-2201-08 chr8:77766674 A>G maps to NM_024721.4 E2506E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8002-01A-11D-2201-08 chr21:44479373 G>A maps to ENST00000398168 G395G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8002-01A-11D-2201-08 chr17:14205110 G>A maps to NM_006041.1 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8002-01A-11D-2201-08 chr12:5021747 C>T maps to NM_000217.2 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8002-01A-11D-2201-08 chr11:3380509 T>C maps to NM_001130520.1 K576K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8002-01A-11D-2201-08 chr1:24022340 C>A maps to NM_000975.3 C150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8002-01A-11D-2201-08 chrX:54987326 G>A maps to NM_002625.2 R83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8003-01A-21D-2201-08 chr3:129214428 C>T maps to NM_052985.2 L780L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8003-01A-21D-2201-08 chr8:116430659 A>T maps to NM_014112.2 V907V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8003-01A-21D-2201-08 chr2:74474202 G>A maps to NM_021196.3 F673F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8003-01A-21D-2201-08 chr11:123886736 T>C maps to NM_001004462.1 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8003-01A-21D-2201-08 chr11:62760740 G>A maps to ENST00000430500 Q542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8003-01A-21D-2201-08 chrX:70360665 C>T maps to ENST00000333646 Q2079*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8003-01A-21D-2201-08 chr21:45877294 G>T maps to NM_030891.3 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8003-01A-21D-2201-08 chr16:89346133 G>A maps to NM_013275.4 D2272D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8003-01A-21D-2201-08 chr6:32800562 C>T maps to ENST00000452392 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8003-01A-21D-2201-08 chr1:145440117 T>A maps to NM_006472.3 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8003-01A-21D-2201-08 chr6:159197481 A>G maps to NM_001111077.1 N251N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8003-01A-21D-2201-08 chr19:9090830 A>G maps to NM_024690.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8003-01A-21D-2201-08 chr6:112486439 C>T maps to NM_001105206.1 V530V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8003-01A-21D-2201-08 chr7:73011746 T>G maps to NM_032951.2 P456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8003-01A-21D-2201-08 chr16:30723228 A>G maps to NM_006662.2 A522A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8003-01A-21D-2201-08 chr11:3380509 T>C maps to NM_001130520.1 K576K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8003-01A-21D-2201-08 chr3:129695839 G>A maps to NM_007117.3 E170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8003-01A-21D-2201-08 chr11:67018095 G>A maps to NM_012308.2 E865E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8003-01A-21D-2201-08 chr19:16024637 C>T maps to NM_021187.3 P493P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8003-01A-21D-2201-08 chr12:57111704 G>A maps to NM_001113203.1 P1203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8003-01A-21D-2201-08 chr1:85279807 G>A maps to NM_012152.2 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8003-01A-21D-2201-08 chr17:40262917 G>A maps to NM_024119.2 I128I. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-HZ-8003-01A-21D-2201-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HZ-8003-01A-21D-2201-08 chr19:23926860 C>T maps to NM_138286.2 K497K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8005-01A-11D-2201-08 chrX:7812054 T>A maps to NM_013452.2 *207K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8005-01A-11D-2201-08 chr8:110348355 G>A did not map to a codon.
Sequencing variant TCGA-HZ-8005-01A-11D-2201-08 chr11:66468053 G>A maps to NM_006946.2 H1172H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8005-01A-11D-2201-08 chr12:52779006 G>C maps to NM_033045.3 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8005-01A-11D-2201-08 chr8:55541790 A>G maps to NM_006269.1 V1783V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8005-01A-11D-2201-08 chr20:30556115 C>A maps to NM_001011718.1 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8005-01A-11D-2201-08 chr17:21318767 G>A maps to NM_021012.4 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8005-01A-11D-2201-08 chr8:1497635 C>T maps to ENST00000357934 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8005-01A-11D-2201-08 chr14:69704528 C>T maps to NM_001193363.1 L510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8005-01A-11D-2201-08 chr3:147128363 G>A maps to NM_003412.3 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8005-01A-11D-2201-08 chr1:8000139 T>G did not map to a codon.
Sequencing variant TCGA-HZ-8005-01A-11D-2201-08 chr14:102552341 A>T maps to NM_001017963.2 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8005-01A-11D-2201-08 chr2:21238343 C>A maps to NM_000384.2 E1136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8005-01A-11D-2201-08 chr6:13977538 C>G maps to NM_001165033.1 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8005-01A-11D-2201-08 chr1:149908107 A>G maps to NM_001145862.1 N27N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8005-01A-11D-2201-08 chr1:1565061 C>T maps to NM_080875.2 V984V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8005-01A-11D-2201-08 chr1:177001820 G>A maps to ENST00000281881 H212H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8005-01A-11D-2201-08 chr6:44255544 C>A maps to NM_182539.3 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8005-01A-11D-2201-08 chr17:7576851 C>T did not map to a codon.
Sequencing variant TCGA-HZ-8005-01A-11D-2201-08 chr9:120475077 A>G maps to NM_138554.3 K224K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8005-01A-11D-2201-08 chr16:61935230 G>A maps to NM_001796.2 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8005-01A-11D-2201-08 chr19:11917497 G>T maps to NM_152356.3 E244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8005-01A-11D-2201-08 chr16:72923764 G>A maps to NM_006885.3 Q1105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8005-01A-11D-2201-08 chrX:101910079 C>T maps to NM_001184727.1 D413D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8315-01A-11D-2396-08 chr1:1389849 G>A maps to NM_001039211.2 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8315-01A-11D-2396-08 chr3:62535604 G>A maps to ENST00000383709 Q647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8315-01A-11D-2396-08 chr20:13260456 C>T maps to NM_080826.1 D185D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8315-01A-11D-2396-08 chr4:52779459 C>G maps to ENST00000451288 S286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8315-01A-11D-2396-08 chr19:43766195 G>A maps to NM_002784.3 D175D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8315-01A-11D-2396-08 chrX:74282183 C>T maps to NM_004299.3 S639S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8315-01A-11D-2396-08 chr1:20964417 G>C maps to NM_032409.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8315-01A-11D-2396-08 chr12:58019518 C>T maps to NM_133489.2 C561C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8315-01A-11D-2396-08 chr19:10257055 C>T maps to NM_001130823.1 V955V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8315-01A-11D-2396-08 chr17:47677786 G>A maps to NM_003563.3 Q360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8315-01A-11D-2396-08 chr13:38225419 T>C maps to NM_003306.1 E687E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8315-01A-11D-2396-08 chr8:55372341 C>T maps to NM_022454.3 D344D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8315-01A-11D-2396-08 chr3:196736600 C>T maps to NM_005929.5 R471R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8315-01A-11D-2396-08 chrX:125298662 G>A maps to NM_001013628.2 D415D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8315-01A-11D-2396-08 chr17:64225476 G>A maps to NM_000042.2 I7I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8315-01A-11D-2396-08 chr19:18420596 G>A maps to NM_012321.3 D73D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8315-01A-11D-2396-08 chr12:7061301 C>T maps to ENST00000416215 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8315-01A-11D-2396-08 chr12:53552312 C>T maps to NM_015989.4 R515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8315-01A-11D-2396-08 chr19:18255423 C>T maps to NM_015016.1 S882S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8315-01A-11D-2396-08 chrX:11157012 G>A maps to NM_013427.2 N965N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8315-01A-11D-2396-08 chr2:72362467 G>A maps to NM_019885.2 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8315-01A-11D-2396-08 chr16:50745885 C>A maps to NM_022162.1 G688G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8315-01A-11D-2396-08 chr19:34180277 C>T maps to NM_022467.3 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8315-01A-11D-2396-08 chr21:28296737 G>A maps to NM_007038.3 S809S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8317-01A-11D-2396-08 chr13:35630160 C>T maps to ENST00000400445 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8317-01A-11D-2396-08 chr17:10348216 C>A did not map to a codon.
Sequencing variant TCGA-HZ-8317-01A-11D-2396-08 chr6:158923247 G>C maps to NM_020245.3 P851P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8317-01A-11D-2396-08 chr9:125486582 C>T maps to NM_001005235.1 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8317-01A-11D-2396-08 chr11:1605915 A>G maps to NM_001005922.1 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8317-01A-11D-2396-08 chrX:152031180 C>T maps to NM_015922.2 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8317-01A-11D-2396-08 chr22:32754255 G>A maps to NM_001098535.1 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8317-01A-11D-2396-08 chr4:149075981 T>G maps to ENST00000511528 P699P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8317-01A-11D-2396-08 chr11:18467783 G>T maps to NM_017448.3 G246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8317-01A-11D-2396-08 chr15:43527882 G>A maps to NM_201631.3 R500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8317-01A-11D-2396-08 chr11:1605918 G>A maps to NM_001005922.1 C187C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8317-01A-11D-2396-08 chr11:1642984 G>A maps to ENST00000359229 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8317-01A-11D-2396-08 chr3:46307530 C>T maps to NM_178328.1 C315C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8317-01A-11D-2396-08 chr6:147703992 A>G maps to NM_001127715.1 K1091K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8317-01A-11D-2396-08 chr20:31385054 G>C maps to NM_006892.3 V480V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8317-01A-11D-2396-08 chr2:85554674 C>T maps to ENST00000409015 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8317-01A-11D-2396-08 chrX:112058795 C>T maps to NM_001113490.1 Q394Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8317-01A-11D-2396-08 chr20:33345722 C>T maps to NM_014071.2 Q276Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8317-01A-11D-2396-08 chr5:140553993 G>T maps to NM_018940.2 A526A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8317-01A-11D-2396-08 chr7:114270014 A>G maps to NM_148898.3 Q209Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8317-01A-11D-2396-08 chr17:16285496 A>G maps to NM_018955.2 E92E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8317-01A-11D-2396-08 chr1:152327954 G>A maps to NM_001014342.2 S769S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8317-01A-11D-2396-08 chr17:26961607 A>G maps to NM_014680.2 P999P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8317-01A-11D-2396-08 chr19:36278841 A>C maps to ENST00000007510 S1125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8317-01A-11D-2396-08 chr14:65260214 C>T maps to ENST00000389723 S726S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8317-01A-11D-2396-08 chr2:40656238 G>A maps to NM_021097.2 H394H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8317-01A-11D-2396-08 chr5:140712119 G>A maps to NM_018912.2 T623T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8317-01A-11D-2396-08 chr22:36702079 C>T maps to NM_002473.4 P685P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8317-01A-11D-2396-08 chr4:149075975 T>G maps to ENST00000511528 P701P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8317-01A-11D-2396-08 chr11:1643035 A>G maps to ENST00000359229 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8636-01A-21D-2396-08 chr14:31404474 G>A maps to NM_001083893.1 D294D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8636-01A-21D-2396-08 chr22:37578650 C>T maps to NM_182486.1 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8636-01A-21D-2396-08 chr14:20916116 G>A maps to NM_017807.3 R247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8636-01A-21D-2396-08 chr22:24451431 G>A maps to NM_012295.3 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8636-01A-21D-2396-08 chr3:142281391 A>G maps to NM_001184.3 D284D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8636-01A-21D-2396-08 chr19:57133443 G>A maps to NM_021216.4 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8636-01A-21D-2396-08 chr5:112770239 G>A maps to NM_032028.3 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8636-01A-21D-2396-08 chr3:38593035 C>T maps to NM_001099404.1 S1609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8636-01A-21D-2396-08 chr15:65703589 G>A maps to NM_020962.1 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8636-01A-21D-2396-08 chrX:128927069 C>A maps to ENST00000443760 R353R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8636-01A-21D-2396-08 chr18:76754689 C>A maps to NM_171999.2 S900*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8636-01A-21D-2396-08 chr2:170070365 G>A maps to NM_004525.2 N1947N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8636-01A-21D-2396-08 chr1:101379318 T>C maps to NM_133496.4 H204H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8637-01A-11D-2396-08 chr15:42147502 G>T maps to ENST00000320955 T3114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8637-01A-11D-2396-08 chrX:132351105 G>A maps to NM_016521.2 N394N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8637-01A-11D-2396-08 chr14:20851407 A>C maps to NM_007110.4 S1324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8637-01A-11D-2396-08 chr6:33287899 C>T maps to NM_001350.4 E451E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8637-01A-11D-2396-08 chr3:126736302 C>T maps to NM_032242.3 C1104C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8637-01A-11D-2396-08 chr11:120998884 C>T maps to NM_005422.2 S733S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8637-01A-11D-2396-08 chr5:145719394 G>A maps to NM_002700.2 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8637-01A-11D-2396-08 chr5:78325779 A>C maps to NM_013391.2 S587S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8637-01A-11D-2396-08 chrX:112058795 C>T maps to NM_001113490.1 Q394Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8637-01A-11D-2396-08 chr12:122669268 G>T maps to NM_001098519.1 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8637-01A-11D-2396-08 chr19:49714749 G>C did not map to a codon.
Sequencing variant TCGA-HZ-8637-01A-11D-2396-08 chr12:49164672 G>A maps to NM_015270.3 N1044N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8637-01A-11D-2396-08 chr9:21201877 G>T maps to NM_021057.2 S96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8637-01A-11D-2396-08 chr3:195022344 G>A maps to NM_012287.5 R452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8637-01A-11D-2396-08 chr2:80530476 G>T maps to NM_178839.4 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8637-01A-11D-2396-08 chr19:9090830 A>G maps to NM_024690.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8637-01A-11D-2396-08 chrX:79279654 A>G maps to NM_016954.2 K150K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8637-01A-11D-2396-08 chr11:10776659 A>G maps to NM_014633.3 E100E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8637-01A-11D-2396-08 chr20:44685056 C>A maps to NM_001134771.1 S1011S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8637-01A-11D-2396-08 chr8:36788638 C>T maps to NM_001031836.2 H969H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8637-01A-11D-2396-08 chr2:96943637 C>T maps to NM_014014.3 P1887P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8637-01A-11D-2396-08 chr19:55450704 G>A maps to ENST00000446217 A522A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8637-01A-11D-2396-08 chrX:149639650 A>G maps to NM_005491.3 Q602Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8637-01A-11D-2396-08 chr5:140559336 C>T maps to NM_019120.2 T574T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8637-01A-11D-2396-08 chr1:156914927 C>T maps to NM_198236.1 K958K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8637-01A-11D-2396-08 chr19:51629103 G>A maps to NM_014441.2 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8637-01A-11D-2396-08 chr16:89341353 G>A maps to NM_013275.4 I2527I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8637-01A-11D-2396-08 chr19:41120240 C>T maps to ENST00000308370 R968*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8637-01A-11D-2396-08 chr18:9886940 A>G maps to NM_001098529.1 K155K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8637-01A-11D-2396-08 chr12:53202185 G>A maps to NM_002272.2 I413I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8637-01A-11D-2396-08 chr1:197072158 C>T maps to NM_018136.4 Q2074Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8637-01A-11D-2396-08 chr2:227945176 T>C maps to ENST00000396625 K595K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8637-01A-11D-2396-08 chr13:25044067 G>A maps to NM_006437.3 F670F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8638-01A-11D-2396-08 chr1:47407090 C>G maps to ENST00000371904 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8638-01A-11D-2396-08 chr1:248616733 A>G maps to NM_001004136.1 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A49G-01A-11D-A26I-08 chr11:63486570 G>A maps to ENST00000377819 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A49G-01A-11D-A26I-08 chr11:35227737 C>T maps to NM_000610.3 F454F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A49G-01A-11D-A26I-08 chr11:6262837 G>A maps to NM_001037329.2 Q365Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A49G-01A-11D-A26I-08 chr1:22030752 A>G did not map to a codon.
Sequencing variant TCGA-HZ-A49G-01A-11D-A26I-08 chr2:157186341 C>T maps to NM_006186.3 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A49G-01A-11D-A26I-08 chr4:140811107 C>T maps to ENST00000509479 Q494Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A49G-01A-11D-A26I-08 chr4:2341322 C>T maps to NM_020972.2 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A49G-01A-11D-A26I-08 chr19:6718397 G>C maps to NM_000064.2 S98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A49G-01A-11D-A26I-08 chr9:5233846 C>T maps to NM_002195.1 D130D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A49G-01A-11D-A26I-08 chr12:40677756 G>A maps to NM_198578.3 A774A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A49G-01A-11D-A26I-08 chr13:103299606 A>G maps to ENST00000376052 L847L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A49G-01A-11D-A26I-08 chrX:25033683 G>A maps to NM_139058.2 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A49H-01A-11D-A26I-08 chr1:110883697 A>C maps to NM_022768.4 A557A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A49H-01A-11D-A26I-08 chr10:104170668 G>A maps to NM_002779.3 I679I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A49H-01A-11D-A26I-08 chr19:2210768 C>T maps to ENST00000221482 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A49H-01A-11D-A26I-08 chr16:20491924 C>T maps to NM_001010845.2 R438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A49H-01A-11D-A26I-08 chr5:33616037 C>T maps to NM_030955.2 W761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A49H-01A-11D-A26I-08 chr1:44680449 G>A maps to NM_019100.4 K91K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A49H-01A-11D-A26I-08 chr18:56586415 G>A maps to NM_018181.4 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A49H-01A-11D-A26I-08 chr9:124062284 T>G did not map to a codon.
Sequencing variant TCGA-HZ-A49H-01A-11D-A26I-08 chr1:151678724 C>T maps to NM_007185.4 Q367Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A49I-01A-12D-A26I-08 chr1:39950370 G>A maps to ENST00000361689 P5335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A49I-01A-12D-A26I-08 chr4:185033944 G>A maps to NM_153343.3 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A49I-01A-12D-A26I-08 chr9:127316819 G>A maps to NM_033334.2 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A49I-01A-12D-A26I-08 chr10:17026278 C>A did not map to a codon.
Sequencing variant TCGA-HZ-A49I-01A-12D-A26I-08 chr1:86372900 C>T maps to NM_152890.5 G918G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A49I-01A-12D-A26I-08 chr17:73497866 G>T maps to NM_020753.3 P1096P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A49I-01A-12D-A26I-08 chr6:90661557 C>T maps to NM_001170794.1 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A49I-01A-12D-A26I-08 chr1:112046026 G>A did not map to a codon.
Sequencing variant TCGA-HZ-A49I-01A-12D-A26I-08 chr3:45817324 C>T maps to NM_020208.3 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A49I-01A-12D-A26I-08 chr7:26883667 G>A maps to NM_003930.3 D96D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A49I-01A-12D-A26I-08 chr2:141200115 G>A maps to NM_018557.2 D3457D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A49I-01A-12D-A26I-08 chr21:40650699 G>A maps to NM_018963.3 G324G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A49I-01A-12D-A26I-08 chr10:32143119 T>C maps to NM_018287.5 E321E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A49I-01A-12D-A26I-08 chr19:7796973 C>T maps to NM_198492.3 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A49I-01A-12D-A26I-08 chr1:156128240 C>T maps to NM_022367.3 C142C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A49I-01A-12D-A26I-08 chr19:55501387 A>G did not map to a codon.
Sequencing variant TCGA-HZ-A49I-01A-12D-A26I-08 chr1:161495095 T>G maps to NM_002155.3 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A4BH-01A-11D-A26I-08 chr2:204009873 C>T maps to NM_001114132.1 L1736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A4BH-01A-11D-A26I-08 chr6:45390465 A>G maps to ENST00000359524 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A4BH-01A-11D-A26I-08 chr19:10097023 G>A maps to NM_015719.3 G773G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A4BH-01A-11D-A26I-08 chr2:1520712 C>T maps to NM_000547.5 I859I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A4BH-01A-11D-A26I-08 chr10:49457186 G>A maps to NM_001018071.3 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A4BH-01A-11D-A26I-08 chr17:57271092 C>T maps to NM_018304.3 Q215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A4BH-01A-11D-A26I-08 chr6:45390462 G>A maps to ENST00000359524 Q132Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A4BH-01A-11D-A26I-08 chr9:18941743 C>T maps to NM_153707.2 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A4BH-01A-11D-A26I-08 chr13:35735928 C>T maps to ENST00000400445 R1302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A4BH-01A-11D-A26I-08 chr4:138451226 C>T maps to NM_019035.3 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A4BH-01A-11D-A26I-08 chr1:117158747 A>G maps to NM_001542.2 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A4BH-01A-11D-A26I-08 chr17:27889842 G>A maps to NM_198147.2 F381F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A4BH-01A-11D-A26I-08 chrX:34150322 G>T maps to NM_203408.3 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A4BH-01A-11D-A26I-08 chr22:38823339 G>A maps to NM_152868.1 D266D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A4BH-01A-11D-A26I-08 chr19:40882578 C>T maps to NM_012268.2 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A4BH-01A-11D-A26I-08 chr1:75036839 G>A maps to NM_001002912.4 S1518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A4BH-01A-11D-A26I-08 chr1:242030319 C>T maps to NM_006027.4 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A4BH-01A-11D-A26I-08 chr16:67682803 G>A maps to NM_001013838.1 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A4BH-01A-11D-A26I-08 chr1:202714992 C>T maps to ENST00000367264 K808K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A4BH-01A-11D-A26I-08 chr19:36302895 C>A maps to NM_021232.1 E265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A4BH-01A-11D-A26I-08 chr17:57270936 C>T maps to NM_018304.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A4BH-01A-11D-A26I-08 chr4:25158571 G>A maps to NM_016955.3 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A4BH-01A-11D-A26I-08 chr17:2996104 G>A maps to NM_002548.2 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A4BH-01A-11D-A26I-08 chr3:123383036 C>T maps to NM_053025.3 A1300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A4BH-01A-11D-A26I-08 chr19:46506728 C>T maps to NM_001080402.1 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A4BK-01A-11D-A26I-08 chr17:39577779 G>C maps to NM_003770.4 A360A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A4BK-01A-11D-A26I-08 chr7:72413744 C>T maps to ENST00000434423 S1071S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A4BK-01A-11D-A26I-08 chr10:89419766 T>C did not map to a codon.
Sequencing variant TCGA-HZ-A4BK-01A-11D-A26I-08 chr6:158923247 G>C maps to NM_020245.3 P851P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A4BK-01A-11D-A26I-08 chr10:32740611 G>A maps to NM_001026383.1 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A4BK-01A-11D-A26I-08 chr11:5510885 C>A maps to NM_001005163.2 S317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A4BK-01A-11D-A26I-08 chr1:108023320 G>A maps to NM_001113226.1 T493T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A4BK-01A-11D-A26I-08 chr9:113261345 G>A maps to ENST00000374463 V552V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A4BK-01A-11D-A26I-08 chr17:41566829 C>T maps to NM_004941.1 I54I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A4BK-01A-11D-A26I-08 chr9:95773520 C>T maps to NM_033086.2 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A4BK-01A-11D-A26I-08 chr19:13915897 G>A maps to NM_023072.2 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A4BK-01A-11D-A26I-08 chrX:136649485 C>T maps to NM_003413.3 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A4BK-01A-11D-A26I-08 chrX:153048257 C>T maps to NM_014370.3 H169H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A4BK-01A-11D-A26I-08 chr17:43531558 G>C maps to NM_014798.2 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A4BK-01A-11D-A26I-08 chr1:1654057 C>T did not map to a codon.
Sequencing variant TCGA-HZ-A4BK-01A-11D-A26I-08 chrX:2161132 C>T maps to NM_145177.2 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A4BK-01A-11D-A26I-08 chr17:39190953 G>A maps to NM_030966.1 C40C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A4BK-01A-11D-A26I-08 chr12:130935796 G>A maps to NM_015347.4 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A77O-01A-11D-A33T-08 chr12:109654725 G>A did not map to a codon.
Sequencing variant TCGA-HZ-A77O-01A-11D-A33T-08 chr22:44237768 G>A maps to NM_014351.3 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A77O-01A-11D-A33T-08 chr17:7810227 G>A maps to NM_001005271.2 P1574P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A77O-01A-11D-A33T-08 chr16:84600450 T>G maps to NM_021149.2 *143Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A77O-01A-11D-A33T-08 chr3:170723135 G>A maps to NM_000340.1 R301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A77O-01A-11D-A33T-08 chr9:114911536 G>T maps to NM_022486.3 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A77O-01A-11D-A33T-08 chr6:146351186 C>T maps to NM_000838.3 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A77O-01A-11D-A33T-08 chr19:47725041 C>T maps to NM_001127240.1 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A77O-01A-11D-A33T-08 chr20:61444808 A>G maps to NM_007346.2 P614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A77O-01A-11D-A33T-08 chr20:47309257 G>A maps to NM_020820.3 R330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A77O-01A-11D-A33T-08 chr1:161167856 G>T maps to NM_005099.4 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A77O-01A-11D-A33T-08 chr2:99907774 G>A maps to NM_174898.2 I86I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A77O-01A-11D-A33T-08 chr17:39262014 T>C maps to ENST00000377731 C120C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A77P-01A-11D-A33T-08 chr11:31823123 G>A maps to NM_001604.4 N128N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A77P-01A-11D-A33T-08 chr11:43852524 G>T did not map to a codon.
Sequencing variant TCGA-HZ-A77P-01A-11D-A33T-08 chr8:120770368 A>G maps to NM_003184.3 Y904Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A77P-01A-11D-A33T-08 chr16:14280892 G>T did not map to a codon.
Sequencing variant TCGA-HZ-A77P-01A-11D-A33T-08 chr1:160098813 C>T maps to NM_000702.3 R421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A77P-01A-11D-A33T-08 chr6:45390462 G>A maps to ENST00000359524 Q132Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A77P-01A-11D-A33T-08 chr11:13408296 G>T maps to ENST00000403290 P625P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A77P-01A-11D-A33T-08 chr8:99045354 C>T maps to ENST00000254898 D889D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A77P-01A-11D-A33T-08 chr12:4479898 G>A maps to NM_020638.2 N122N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A77P-01A-11D-A33T-08 chr19:4219625 C>T maps to ENST00000262970 H1104H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A77P-01A-11D-A33T-08 chr11:65408964 C>T maps to NM_153253.29 N191N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A77P-01A-11D-A33T-08 chrX:299379 G>T maps to NM_013239.4 I512I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A77P-01A-11D-A33T-08 chr4:15938186 C>T maps to NM_005130.3 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A77P-01A-11D-A33T-08 chr10:103590841 G>A maps to NM_014591.4 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A77P-01A-11D-A33T-08 chr14:64727335 G>A maps to NM_001437.2 D261D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A77P-01A-11D-A33T-08 chr1:179989234 G>T maps to NM_014810.4 E776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A77P-01A-11D-A33T-08 chrX:45011190 G>A maps to NM_176819.3 S336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7644-01A-11D-2154-08 chr18:48575670 C>G maps to NM_005359.5 S144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7644-01A-11D-2154-08 chr19:13445252 C>T maps to NM_023035.2 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7644-01A-11D-2154-08 chr19:41063284 T>C maps to NM_020971.2 H1882H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7644-01A-11D-2154-08 chr12:20854385 T>C maps to NM_017435.4 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7644-01A-11D-2154-08 chr22:40802488 G>A maps to NM_015705.4 T336T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7644-01A-11D-2154-08 chr5:151045923 G>A maps to NM_003118.2 D244D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7644-01A-11D-2154-08 chr11:132307161 G>A maps to NM_002545.3 N206N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7644-01A-11D-2154-08 chr2:27601874 G>A maps to NM_144631.4 D86D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7644-01A-11D-2154-08 chr16:1842048 G>A maps to NM_001146006.1 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7645-01A-22D-2201-08 chr11:61091513 C>T maps to NM_001923.3 E286E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7645-01A-22D-2201-08 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7645-01A-22D-2201-08 chr3:52649472 C>T did not map to a codon.
Sequencing variant TCGA-IB-7645-01A-22D-2201-08 chr1:35370342 C>T maps to NM_001080418.1 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7645-01A-22D-2201-08 chr12:68051337 C>T maps to NM_006482.2 H217H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7645-01A-22D-2201-08 chr14:47343250 C>A maps to NM_001113498.2 E864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7645-01A-22D-2201-08 chr12:132446054 A>G maps to ENST00000333577 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7645-01A-22D-2201-08 chr3:195453210 C>T maps to ENST00000447234 A579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7645-01A-22D-2201-08 chr5:60241049 G>A did not map to a codon.
Sequencing variant TCGA-IB-7645-01A-22D-2201-08 chr11:67209177 A>G did not map to a codon.
Sequencing variant TCGA-IB-7645-01A-22D-2201-08 chr4:123168390 G>A maps to NM_015312.3 K1797K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7645-01A-22D-2201-08 chr1:152732687 C>T maps to NM_001025231.1 F208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7645-01A-22D-2201-08 chr19:10283846 A>C maps to NM_001130823.1 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7645-01A-22D-2201-08 chr2:170177380 C>T maps to NM_004525.2 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7645-01A-22D-2201-08 chr8:87060705 C>T maps to ENST00000276616 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7645-01A-22D-2201-08 chr9:87635239 C>A maps to NM_006180.3 T764T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7645-01A-22D-2201-08 chr1:39988770 C>T maps to NM_181809.3 H347H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7645-01A-22D-2201-08 chr7:138341225 C>T maps to NM_001139456.1 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7645-01A-22D-2201-08 chr21:43838613 C>T maps to NM_018961.2 S314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7645-01A-22D-2201-08 chr19:56538510 G>T maps to NM_153447.4 A304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7645-01A-22D-2201-08 chr17:39137357 C>A maps to NM_182497.3 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7645-01A-22D-2201-08 chr19:20044699 C>T maps to NM_031218.3 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7645-01A-22D-2201-08 chr1:17250967 C>T maps to NM_014675.3 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7645-01A-22D-2201-08 chr14:20216248 C>T maps to NM_172194.1 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7645-01A-22D-2201-08 chrX:152807148 C>T maps to NM_001001344.2 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7645-01A-22D-2201-08 chr1:248756292 G>C maps to NM_001004693.1 Y259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7645-01A-22D-2201-08 chr19:17322899 G>A maps to NM_004145.3 P2085P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7646-01A-11D-2154-08 chr17:57650475 G>A did not map to a codon.
Sequencing variant TCGA-IB-7646-01A-11D-2154-08 chr14:92628034 C>T maps to NM_017437.1 Q766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7646-01A-11D-2154-08 chr3:57282265 A>C maps to NM_012096.2 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7646-01A-11D-2154-08 chr1:173795823 G>A did not map to a codon.
Sequencing variant TCGA-IB-7646-01A-11D-2154-08 chrX:107977752 T>A maps to NM_003604.2 K608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7646-01A-11D-2154-08 chr5:140554035 G>T maps to NM_018940.2 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7646-01A-11D-2154-08 chr4:71522117 G>T maps to NM_144646.3 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7646-01A-11D-2154-08 chr7:6189800 C>T maps to ENST00000404835 N658N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7646-01A-11D-2154-08 chr7:42079806 G>T maps to NM_000168.5 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7646-01A-11D-2154-08 chr12:106461626 G>A maps to NM_014840.2 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7646-01A-11D-2154-08 chr8:27634026 C>T maps to NM_001017420.2 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7646-01A-11D-2154-08 chr7:35051047 A>G maps to NM_015283.1 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7646-01A-11D-2154-08 chr16:50813756 G>A maps to ENST00000311559 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7646-01A-11D-2154-08 chr14:23869986 G>C maps to NM_002471.3 T447T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7646-01A-11D-2154-08 chr19:45818780 C>T maps to NM_001824.3 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7646-01A-11D-2154-08 chr17:39596735 G>A maps to NM_006771.3 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7646-01A-11D-2154-08 chr4:190878626 T>C maps to NM_004477.2 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7646-01A-11D-2154-08 chr20:43933093 C>T maps to ENST00000372754 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7646-01A-11D-2154-08 chr14:45398353 G>A maps to ENST00000355081 V545V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7646-01A-11D-2154-08 chr6:36368235 G>A maps to NM_152990.3 R99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7646-01A-11D-2154-08 chr10:131959073 C>T maps to NM_006541.4 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7647-01A-11D-2154-08 chr10:16970246 C>A maps to NM_001081.3 G2060G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7647-01A-11D-2154-08 chr17:1840989 C>T maps to NM_178568.2 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7647-01A-11D-2154-08 chr19:45854887 C>G maps to NM_000400.3 *761S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7647-01A-11D-2154-08 chr13:70281774 T>C maps to NM_020866.2 Q723Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7647-01A-11D-2154-08 chr1:181732594 C>T maps to ENST00000357570 A1581A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7647-01A-11D-2154-08 chr20:21492878 C>T maps to NM_002509.2 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7647-01A-11D-2154-08 chr16:25232852 G>A maps to NM_001169.2 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7647-01A-11D-2154-08 chr16:19528370 A>T maps to NM_016641.3 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7647-01A-11D-2154-08 chr2:179641505 A>G maps to NM_133378.4 Y1695Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7647-01A-11D-2154-08 chr22:16449648 C>T maps to NM_001005239.1 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7647-01A-11D-2154-08 chr5:140176360 C>T maps to NM_018905.2 N604N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7647-01A-11D-2154-08 chr21:43999847 C>T maps to NM_018964.3 F508F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7647-01A-11D-2154-08 chr6:70428940 C>T maps to NM_018368.3 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7647-01A-11D-2154-08 chr1:16455954 G>A maps to NM_004431.3 I933I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7647-01A-11D-2154-08 chr16:21974206 G>T did not map to a codon.
Sequencing variant TCGA-IB-7647-01A-11D-2154-08 chr17:43011627 G>A maps to ENST00000438933 N286N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7647-01A-11D-2154-08 chr2:85533482 A>T maps to NM_031283.2 R382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7647-01A-11D-2154-08 chr12:49580154 G>A maps to NM_006009.2 R105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7647-01A-11D-2154-08 chr19:41928084 C>T maps to NM_000709.3 Y221Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7647-01A-11D-2154-08 chr19:36018250 T>A maps to NM_001166034.1 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7647-01A-11D-2154-08 chr20:62851190 C>T maps to NM_004535.2 D699D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7647-01A-11D-2154-08 chr19:19625657 G>A maps to NM_032037.2 Y193Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7647-01A-11D-2154-08 chr4:100205882 A>G maps to NM_000667.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7647-01A-11D-2154-08 chr19:45853602 C>G maps to NM_177417.2 S383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7647-01A-11D-2154-08 chr12:75687068 G>A maps to NM_032606.3 R394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7647-01A-11D-2154-08 chr3:197707288 C>T maps to NM_001136049.2 Y214Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7647-01A-11D-2154-08 chr11:3838587 G>A maps to NM_014489.2 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7647-01A-11D-2154-08 chr3:122422821 C>T maps to NM_017554.2 L1105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7647-01A-11D-2154-08 chr2:105858389 G>A maps to NM_007227.3 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7647-01A-11D-2154-08 chrX:35820357 C>T maps to ENST00000422348 H47H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7649-01A-11D-2154-08 chr17:7579310 C>T did not map to a codon.
Sequencing variant TCGA-IB-7649-01A-11D-2154-08 chr11:107535877 G>A maps to NM_018712.3 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7649-01A-11D-2154-08 chr2:26951300 C>T maps to NM_002246.2 G350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7649-01A-11D-2154-08 chr2:127806137 G>A maps to NM_139343.1 G582G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7649-01A-11D-2154-08 chrX:47038525 C>T maps to NM_005676.3 R230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7649-01A-11D-2154-08 chr6:78172556 A>C maps to NM_000863.1 R188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7649-01A-11D-2154-08 chr11:77937955 C>T maps to NM_080491.2 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7649-01A-11D-2154-08 chr5:140720421 G>A maps to NM_018915.2 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7649-01A-11D-2154-08 chr11:10597886 C>A maps to NM_001098579.1 E902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7649-01A-11D-2154-08 chr17:15909859 A>G maps to NM_017775.2 E339E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:1424996 G>T maps to NM_014461.2 G808*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:136087968 G>A maps to NM_005862.2 D842D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:77245231 C>T maps to ENST00000396204 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:52449882 C>T maps to ENST00000360284 R370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:127646813 G>A maps to NM_207335.2 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:51010877 G>A maps to NM_138334.2 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:30041025 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:16330044 C>T maps to NM_016113.4 R369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:206632019 C>T maps to ENST00000414359 D776D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:123753543 G>A maps to NM_001735.2 R956*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:153220228 C>A maps to NM_001101337.1 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:28934817 C>T maps to NM_001942.2 R887*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:45079891 C>A maps to ENST00000453887 C227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:39141700 C>T maps to ENST00000405018 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:46717748 G>T maps to NM_147129.3 L724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:17276771 A>G maps to NM_003380.3 R321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:220348004 G>A maps to NM_005876.4 Q1940Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:7228772 C>T maps to NM_032442.2 T462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:132631613 G>T maps to NM_001008563.3 R434R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:91083356 G>A maps to NM_022769.3 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:51142312 G>T maps to NM_001080420.1 R562R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:14634067 C>T maps to NM_018179.3 R1077*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:28218700 G>A maps to ENST00000313433 D350D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:10099400 C>T maps to NM_017491.3 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:39650343 G>A maps to NM_002687.3 Q477Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:49680443 G>A maps to NM_003458.3 P459P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:113496014 C>T maps to NM_004416.2 H6H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:32196610 G>A maps to NM_001703.2 A1390A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:219738521 G>A maps to NM_006522.3 Q351Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:156130350 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:242572458 G>A maps to NM_015963.5 G371G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:140996168 C>T maps to NM_005462.4 G993G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:17280673 C>T maps to NM_175878.3 W192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:395298 G>A maps to NM_014974.2 G1027G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:53899865 G>A maps to NM_134323.1 E345E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:21492785 C>T maps to NM_002509.2 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:34710698 C>T maps to NM_001114093.1 A351A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:23522453 C>T maps to NM_020227.2 R184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:47228869 C>T maps to NM_001039877.1 W435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:150470160 C>T maps to NM_025150.3 D392D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:139835758 C>T maps to NM_018998.2 T467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:4558382 C>T maps to NM_032108.3 E29E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:88566448 C>T maps to NM_181783.3 R376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:2055425 G>A maps to NM_152640.3 I600I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:121880186 C>T maps to ENST00000377071 P1019P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:132290260 C>A maps to NM_138770.1 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:100998652 G>A maps to NM_000926.4 P383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:94187801 G>A maps to NM_178013.3 N150N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:31355351 C>A maps to NM_004086.2 I437I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:53667725 G>A maps to NM_024733.3 R673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:19169391 G>A maps to NM_001100420.1 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:216019172 G>A maps to ENST00000366943 C3016C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:129950515 G>A maps to NM_033515.2 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:18067033 G>A maps to NM_175886.2 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:57091997 C>T maps to NM_032206.3 G1256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:89790705 C>T maps to NM_006813.2 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:124545183 C>T maps to NM_017425.3 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:188584049 C>T maps to NM_005578.3 T491T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:2160861 C>T maps to NM_003036.3 R219R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:3747907 C>T maps to NM_014428.1 G846G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:44913994 A>G maps to NM_001145107.1 C781C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:16863182 G>T maps to ENST00000448080 Y261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:122219027 G>A maps to NM_019034.2 D99D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:122825824 C>T maps to ENST00000302528 K642K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:58640735 T>C maps to NM_024620.3 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:85598229 C>T maps to NM_001135023.1 R128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:140785479 C>T maps to NM_080862.1 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:79724894 C>T maps to NM_017934.5 P476P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:52952421 G>A maps to NM_018676.3 D561D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:147108845 C>T maps to NM_001168379.1 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:51382067 G>A maps to NM_002863.4 I463I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:532616 G>A maps to NM_014700.3 V332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:48670819 G>T maps to NM_022911.2 C62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:158368953 C>T maps to NM_001004475.1 Q101Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:207195512 G>A maps to NM_023938.5 S532S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:7247317 C>T maps to NM_001003699.3 D1545D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:219525922 T>C maps to NM_004328.4 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:4525689 G>A maps to NM_001013706.2 H225H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:110835646 C>T maps to NM_139164.1 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:21233847 A>G maps to NM_000384.2 L1964L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:107790513 G>A maps to ENST00000379032 D1256D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:8578035 G>A maps to NM_001146175.1 Q65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:57133839 G>A maps to NM_021216.4 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:136260728 C>T maps to NM_153710.3 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:159084344 C>T maps to ENST00000297239 R15R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:42694623 C>T maps to ENST00000348077 H420H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:70778368 G>T maps to NM_018052.3 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:79930361 C>T maps to ENST00000376646 Q1536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:76023249 C>T maps to NM_015687.2 G766G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:184971731 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:179499527 A>G maps to NM_003940.2 T805T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:133778992 C>T maps to NM_001165881.2 Q241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:120360510 C>T maps to NM_000187.3 W268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:130587515 C>T maps to NM_001114753.1 Q270Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:38403693 G>A maps to NM_003421.2 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:125397087 G>A maps to NM_021009.5 I410I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:146107484 G>T maps to NM_021061.3 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:15791298 G>A maps to NM_023944.2 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:22268112 G>A maps to NM_013302.3 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:12709022 C>A maps to NM_000550.2 G485G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:42890843 C>T maps to NM_138296.2 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:27729395 C>A maps to NM_001486.3 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:12266842 C>T maps to NM_001066.2 I384I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:108626965 C>T maps to NM_021815.2 G464G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:237075078 G>A maps to NM_001485.2 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:12395786 G>A maps to NM_015378.2 S2818S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:118247313 C>A maps to NM_004788.2 I499I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:37498086 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:170857332 G>A maps to NM_015028.2 R449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:83362284 G>A maps to NM_005711.3 G264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:4626371 G>A maps to NM_018073.5 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:19283131 C>T maps to NM_139034.2 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:99959070 C>T maps to ENST00000437596 H19H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:167944231 T>C maps to ENST00000367840 C139C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:65988130 C>T maps to NM_018026.2 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:140719047 C>T maps to NM_018915.2 Y170Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:57577892 C>A maps to NM_002332.2 G1985G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:40681898 C>A maps to NM_000958.2 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:48149437 G>A maps to NM_002843.3 K400K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:19089408 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:44285000 G>A maps to NM_002250.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:21868398 G>A maps to NM_001170629.1 I1546I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:14154653 T>C maps to NM_144636.2 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:107309825 C>T maps to NM_152434.2 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:73462038 G>A maps to ENST00000358929 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:159653574 G>A maps to NM_032532.2 P677P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:6733611 G>A maps to NM_053285.1 D28D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:75094761 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:53674484 G>A maps to ENST00000276009 D59D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:7043402 T>C maps to NM_005559.2 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:17013580 C>T maps to ENST00000443236 P1578P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:33057851 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:54754900 T>C maps to ENST00000450632 A578A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:304438 C>T maps to NM_032039.2 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:50278992 G>A maps to NM_014838.2 S561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:58118705 C>T maps to NM_032997.2 E161E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:139097398 C>T maps to NM_015439.2 R138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:1827163 C>T maps to NM_080861.3 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:796501 G>A maps to NM_017802.3 T447T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:149906094 G>A maps to NM_001145862.1 D224D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:11711198 C>A maps to NM_001372.3 I2857I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:84353107 C>T maps to NM_021197.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:62067277 A>T maps to ENST00000404929 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:96163661 C>T maps to NM_003728.3 A342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:88677770 C>T maps to ENST00000452588 R458R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:27987088 C>T maps to NM_018091.5 R230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:99667809 G>A maps to NM_018058.4 N270N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:122642571 G>A maps to NM_001031702.2 C388C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:196746671 A>G maps to NM_018897.2 A1936A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:176778194 C>T maps to NM_006816.2 E98E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:2769006 C>T maps to NM_003021.3 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:26217585 C>T maps to NM_001164747.1 R87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:11134265 C>T maps to NM_001128849.1 R978*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:135051471 C>T maps to NM_014468.2 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:97296347 C>T maps to NM_014754.1 R95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:98086852 G>A maps to NM_021033.6 E43E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:657399 C>T maps to NM_173593.3 R264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:45309857 G>A maps to NM_138415.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:28224122 C>A maps to NM_018076.2 E771*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:9971443 G>A maps to NM_058164.2 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:157689047 G>A maps to NM_016205.2 T266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:47628602 C>T maps to NM_006420.2 Y1300Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:22417979 G>A maps to NM_001039802.1 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:532556 G>A maps to NM_018303.4 I764I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:60927303 G>A maps to NM_005560.3 N227N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:235345455 A>G maps to NM_016374.5 D926D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:163174678 G>A maps to NM_022168.2 Q47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:139226861 G>A maps to NM_001080511.2 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:185803263 A>G maps to NM_194250.1 V1047V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:153056564 G>A maps to NM_001114183.1 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:38165062 C>T maps to NM_001039141.2 L2202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:24832432 C>T maps to NM_019590.3 Q1412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:88240657 A>C maps to NM_020320.3 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:41571724 G>A maps to ENST00000415018 D583D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:135095278 C>T maps to NM_001190850.1 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:56310286 G>A maps to NM_001005245.1 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:3644082 A>G did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:86545077 C>T maps to NM_001451.2 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:40776915 A>G maps to NM_024677.4 K258K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:40494849 C>A maps to ENST00000412359 T577T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:144768442 C>T maps to NM_007124.2 R571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:168465673 G>A maps to NM_024919.3 C175C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:1805555 G>A maps to NM_000142.4 V356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:219029292 C>T maps to NM_000634.2 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:16701470 G>A maps to NM_012334.2 S1011S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:24922841 C>T maps to NM_052944.2 G672G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:148017571 C>T maps to ENST00000310701 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:112476777 G>A maps to NM_001105206.1 R650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:145112596 C>T maps to ENST00000360660 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:240256572 A>C maps to ENST00000406993 G531G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:137329756 G>A maps to NM_014432.2 Q235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:10385699 G>A maps to NM_000201.2 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:91090728 C>T maps to NM_032968.3 R76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:67050267 C>T maps to NM_001619.3 I402I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:18359772 T>G maps to NM_005316.3 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:71555658 C>T maps to NM_003558.2 Y485Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:9335892 C>T maps to NM_015012.2 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:167517319 C>T maps to NM_003851.2 Q131Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:124885185 G>A maps to NM_006312.4 N558N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:97427929 G>A maps to NM_020184.3 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:13660485 G>A maps to NM_001165035.1 P674P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:135326861 G>A maps to NM_024597.3 R116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:119988593 G>A maps to NM_182915.2 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:150403767 A>G maps to NM_152394.3 I217I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:35587998 C>T maps to NM_001145775.1 E101E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:77570261 G>T maps to NM_006493.2 G238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:81625164 G>A maps to ENST00000454937 L969L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:49255901 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:31973464 A>G maps to ENST00000357886 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:74574855 C>T maps to NM_006456.2 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:104900401 G>T maps to NM_033292.2 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:46448236 G>A maps to NM_005904.3 C262C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:51457285 C>T maps to ENST00000273612 A1046A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:28193972 C>T maps to NM_002430.2 P853P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:220162752 G>A maps to NM_002846.3 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:42356112 C>T maps to NM_152447.3 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:64006313 C>T maps to ENST00000422769 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:65332854 G>A maps to NM_002227.2 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:127459092 C>T maps to NM_147191.1 E349E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:76523299 A>G maps to ENST00000307465 D327D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:18297039 G>A maps to ENST00000401790 T517T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:11107016 C>A maps to NM_001128849.1 A574A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:143079459 G>T maps to NM_001010972.1 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:54978517 G>A maps to NM_002625.2 D222D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:29886649 T>A maps to NM_021076.3 P1007P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:19671044 G>A maps to NM_001114176.1 K502K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:64606558 C>T maps to NM_017525.2 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:64536601 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:132160908 T>C maps to NM_001172700.1 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:125447553 C>T maps to NM_153442.3 R298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:43965631 G>A maps to NM_172069.3 Q1032Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:154996995 C>T maps to NM_052917.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:147108908 G>A maps to NM_001168379.1 C309C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:48965229 C>T maps to NM_170720.1 D83D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:88229393 C>A maps to NM_020320.3 G382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:155572060 G>A maps to ENST00000456144 S1351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:49842317 C>T maps to NM_198570.3 C236C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:35580388 T>C maps to NM_024772.3 F986F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:31852263 G>A maps to ENST00000395728 P949P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:14848794 C>T maps to NM_001145029.1 Q969*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:90965919 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:39178503 C>T maps to ENST00000301819 N1078N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:82937349 G>A maps to NM_001884.3 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:580752 C>T maps to NM_004066.1 D115D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:52825412 C>T maps to NM_144684.2 R304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:53122576 C>T maps to NM_001042693.1 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:53370466 G>A maps to ENST00000371522 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:230805250 C>T maps to NM_007357.2 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:71068358 A>G maps to NM_006540.2 Y747Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:30012007 T>C maps to NM_003257.3 S992S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:43423044 C>T maps to NM_018259.5 C423C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:187000169 G>A maps to NM_003265.2 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:87498876 G>A maps to NM_153354.3 I272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:134071248 T>G did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:74524939 G>A maps to NM_012201.5 R470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:198363458 G>T maps to NM_199440.1 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:118625470 G>A maps to NM_004397.4 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:3189840 G>A maps to ENST00000380989 L721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:47753292 G>A maps to NM_001048166.1 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:44053454 G>A maps to NM_001099284.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:38323736 G>A maps to NM_033386.2 K595K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:17410235 G>A maps to NM_007365.2 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:156288796 G>A maps to NM_005998.4 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:191301735 G>A maps to NM_017694.3 Q327Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:100103349 T>A maps to NM_014820.3 G236G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:5489439 C>T maps to NM_015325.1 G2266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:26761509 C>T maps to NM_021115.4 N924N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:69922017 C>A maps to NM_007014.3 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:7045980 C>T maps to NM_001940.3 H517H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:1263599 C>A maps to ENST00000447027 C1833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:98823296 G>A maps to NM_003061.2 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:140554407 C>T maps to NM_018940.2 D664D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:1904666 C>T maps to ENST00000381758 Y253Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:52375982 T>A maps to NM_032679.2 S420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:676047 C>T maps to NM_021168.4 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:115421559 G>A maps to NM_133465.2 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:98829109 G>A maps to NM_178861.4 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:11106655 G>A maps to NM_006610.2 N123N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:98209327 T>C maps to NM_001270.2 L1180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:102818143 C>T maps to NM_003854.2 Y206Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:2282334 C>T maps to NM_014853.2 L969L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:128408686 C>T maps to NM_005291.2 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:46277852 G>A maps to NM_181659.2 Q1217Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:17723476 T>G maps to NM_001005291.2 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:157551411 G>A maps to NM_031282.2 G386G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:75851895 A>G maps to NM_003369.3 R513R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:86544231 C>T maps to NM_001451.2 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:58021500 G>A maps to NM_001478.3 G428G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:26349754 G>A maps to NM_004455.2 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:30860155 C>A maps to NM_013994.2 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:32953971 T>C maps to NM_000059.3 T3013T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:95157464 C>T maps to NM_016116.2 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:155236523 G>A maps to ENST00000368361 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:138711298 G>A maps to NM_080660.3 C298C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:95157227 C>T maps to NM_016116.2 H197H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:24884116 C>T maps to NM_025081.2 I1054I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:44692046 G>A maps to NM_020967.2 R368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:88946902 C>T maps to ENST00000298786 L821L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:46216210 C>T maps to NM_001080469.1 Q181Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:57955242 C>T maps to NM_001023561.2 Q243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:137787192 G>A maps to NM_173543.2 S544S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:15349988 G>A maps to NM_058243.2 S1221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:134686591 T>C maps to NM_138609.2 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:6213355 G>A maps to NM_005934.3 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:160109760 G>A maps to NM_000702.3 R1007R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:84132742 C>T maps to NM_003791.2 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:17073412 C>A maps to NM_014406.4 E10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:78165180 C>T maps to NM_024110.2 D383D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:44121723 A>G maps to NM_133259.3 N1315N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:70970490 C>A maps to NM_018003.2 E316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:112705590 G>A maps to ENST00000413420 P374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:131486810 C>A maps to NM_207364.2 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:42342982 G>A maps to NM_173506.4 C61C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:38924355 C>T maps to ENST00000379641 C35C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:13371501 A>G maps to NM_004249.3 *221Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:9072985 A>G maps to NM_024690.2 D4820D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:45885940 G>A maps to NM_001142502.1 Y764Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:42699998 C>T maps to NM_000163.2 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:21840242 C>T maps to ENST00000434536 P408P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:69197818 A>G did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:50230696 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:228559428 C>T maps to NM_001098623.1 R6984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:178483363 G>T maps to NM_152275.3 I22I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:78475046 C>T maps to NM_015162.4 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:38123803 C>T maps to NM_001102559.1 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:47041692 C>T maps to NM_015175.1 G1368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:26902833 C>T maps to NM_012143.2 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:58621317 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:56155446 G>A maps to NM_006213.3 R36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:25144974 G>A maps to NM_001008496.2 R450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:21909802 A>C maps to NM_173531.3 A437A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:10265483 C>T maps to NM_003802.2 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:67289056 C>T maps to NM_004594.2 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:241798699 A>C maps to NM_001821.3 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:125804219 C>T maps to NM_015892.3 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:55501542 C>T maps to NM_017852.3 C840C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:181693627 G>A maps to ENST00000357570 L699L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:73915864 C>T maps to ENST00000389570 S660S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:78277272 G>A maps to NM_024678.4 R140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:184367458 C>T maps to NM_017632.2 R208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:264665 C>A maps to NM_153269.1 E82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:26212832 G>A maps to NM_173523.2 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:9780046 C>T maps to ENST00000361110 R402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:9164308 C>T maps to NM_015213.2 S1157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:91657410 T>C maps to NM_001008495.3 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:66420803 C>T maps to NM_001795.3 D101D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:37880057 T>G maps to NM_032453.1 R369R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:25331515 G>A maps to ENST00000423535 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:48545739 C>T maps to NM_001267.2 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:98997810 G>A maps to NM_000197.1 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:73433316 G>T maps to NM_015009.1 A800A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:80646713 C>T maps to ENST00000402739 N426N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:61834647 G>A maps to NM_020987.2 I1997I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:170592485 G>A maps to NM_005618.3 A627A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:39711957 G>A maps to ENST00000395670 S1275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:21529772 G>A maps to ENST00000416669 Q3134Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:74975655 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:1466896 C>T maps to NM_005883.2 P1199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:123481100 G>A maps to NM_020845.2 V562V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:16355008 G>A maps to NM_024704.4 V1081V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:34040437 C>T maps to NM_001036.3 R2705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:85695099 C>A maps to NM_006982.2 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:48840195 C>T maps to NM_020137.3 E421E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:149006811 C>A maps to NM_001001669.2 G546G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:135277104 C>T maps to NM_007344.2 G368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:33523405 G>T maps to NM_000178.2 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:58578887 C>T maps to NM_007134.1 R370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:42546760 G>A maps to NM_002088.3 Y472Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:28890250 T>C maps to NM_015594.2 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:7654162 C>T maps to NM_003621.2 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:234407223 G>T maps to NM_018218.2 C906*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:121785596 G>A maps to ENST00000379533 Q597Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:21233265 A>G maps to NM_000384.2 I2158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:39135888 G>A maps to ENST00000405018 R493R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:5464771 C>T maps to NM_015325.1 L1775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:25008754 G>A maps to NM_006437.3 L1508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:6155596 C>T maps to NM_003636.3 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:45904114 G>A maps to NM_145255.3 Y140Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:162273382 C>T maps to NM_006593.2 N154N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:347978 G>A maps to NM_003502.3 A509A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:40309818 C>A maps to ENST00000316891 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:100911185 G>A maps to NM_177949.2 G463G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:141660726 A>G maps to NM_018557.2 C1176C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:162737130 G>A maps to NM_006182.2 W425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:212285327 A>G maps to NM_005235.2 D991D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:57767888 G>A maps to NM_178457.1 R605R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:138394540 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:79744104 T>C maps to NM_014733.3 I995I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:144764984 A>G maps to NM_001164629.2 D213D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:120692376 C>T maps to NM_002830.2 R400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:176573003 G>T maps to NM_005277.3 C174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:28596991 C>T maps to NM_138414.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:134079097 G>A maps to NM_015261.2 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:137612944 C>T maps to NM_194071.2 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:114069835 G>A maps to NM_001164342.1 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:113940350 C>A maps to NM_012455.2 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:28053578 C>A maps to NM_003447.3 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:63973862 G>A maps to NM_001177387.1 P408P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:106075311 G>T maps to NM_033397.2 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:18881118 G>A maps to NM_001039999.2 F620F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:31087863 C>T maps to NM_014699.3 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:52847503 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:124091190 C>T maps to NM_000177.4 G646G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:113588107 G>A maps to NM_000576.2 R214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:67163802 C>T maps to NM_004584.2 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:21226158 G>A maps to NM_000384.2 V4045V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:38412731 G>A maps to NM_133264.4 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:111422940 A>G maps to ENST00000428084 I1188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:101584319 C>T maps to NM_145913.3 W253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:157099042 G>A maps to NM_001167912.1 G343G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:55591074 C>A maps to NM_133180.2 C45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:51768811 C>T maps to NM_001077665.2 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:62021183 C>T maps to NM_000334.4 T1313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:211502490 C>A maps to NM_001122633.1 S924*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:122626664 C>A maps to NM_018117.11 S426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:52558575 C>T maps to NM_001134231.1 P528P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:150724343 G>A maps to NM_004079.4 C180C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:139944441 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:70892691 C>T maps to NM_004896.3 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:65409264 G>A maps to NM_002083.2 R60R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:185074809 G>T maps to NM_153343.3 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:42876136 G>A maps to NM_016248.2 V1085V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:66259195 C>T maps to NM_005700.3 R319R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:166039798 G>A maps to NM_001017961.3 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:220115517 C>T maps to NM_006000.1 Q301Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:62848446 G>A maps to NM_004535.2 E553E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:44139575 G>A maps to NM_006973.2 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:116600780 G>A maps to NM_003309.3 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:40874335 G>A maps to NM_022733.2 E83E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:182844011 C>T maps to NM_001357.4 Q580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:234085993 T>C did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:241622182 G>T maps to NM_001102467.1 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:17937569 G>A maps to NM_000215.3 H1119H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:157065338 C>T maps to NM_178424.1 Q593Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:5041990 T>C maps to NM_014692.1 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:123814974 C>T maps to NM_001167856.1 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:16258455 C>A maps to NM_015001.2 V1907V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:50483665 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:117568491 G>A maps to NM_004258.3 E930E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:2119477 C>T maps to NM_003070.3 D1235D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:66436705 C>T maps to NM_015541.2 Q496Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:33988632 C>A maps to NM_001036.3 R2025R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:266375 C>T maps to ENST00000419098 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:67578666 C>T maps to NM_001193523.1 R955*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:65371059 T>C did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:101605828 C>A maps to NM_024652.3 P1729P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:36124809 G>A maps to NM_030642.1 Q389Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:134188632 C>T maps to NM_030626.2 R494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:176859017 C>T maps to NM_002082.3 C57C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:1686705 G>A maps to NM_052928.2 H695H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:30536920 G>A maps to NM_024671.3 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:42607438 G>A maps to NM_005650.1 G1291G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:28510972 C>T maps to NM_004667.4 R582R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:41594991 C>A maps to NM_000766.3 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:54967478 G>A maps to NM_005853.5 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:1251031 C>T maps to ENST00000447027 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:50769194 G>A maps to NM_018197.2 V512V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:144885612 G>A maps to NM_182706.3 G1181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:33486989 G>A maps to NM_033103.4 Y454Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:42666182 C>T maps to NM_000322.4 E297E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:245027597 C>T maps to NM_031844.2 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:57577288 C>T maps to NM_002332.2 H1930H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:47532274 C>T maps to NM_001849.3 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:100405612 C>T maps to NM_001008707.1 G776G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:12963202 C>T maps to NM_014975.2 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:137630648 G>T maps to NM_000093.3 E497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:119122679 G>A maps to NM_000127.2 D202D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:131222945 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:184297592 C>T maps to NM_004443.3 S681S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:37416127 C>A maps to NM_017438.3 G285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:33464383 G>A maps to NM_152266.3 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:15295261 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:31499494 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:20683248 T>C maps to NM_001163941.1 C224C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:163368 A>G maps to NM_005151.3 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:152383287 G>A maps to NM_016190.2 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:54939213 C>T maps to NM_003647.2 I449I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:64803115 C>T maps to NM_013306.4 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:59560890 G>A maps to NM_004177.4 E193E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:49575495 G>A maps to NM_014484.3 Q39Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:217559273 G>T maps to NM_000599.3 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:98518305 G>A maps to ENST00000326857 D760D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:156422598 C>A maps to NM_015508.4 V551V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:145509703 G>A maps to NM_020117.9 Y835Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:41019443 C>T maps to NM_020971.2 V916V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:67068442 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:60074019 G>A maps to NM_021136.2 D652D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:8083912 C>T maps to NM_006931.2 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:92928132 G>T maps to NM_004538.5 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:160164712 C>A maps to NM_004906.3 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:27147986 C>T maps to NM_153631.2 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:36028102 G>A maps to NM_001014839.1 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:54612462 C>T maps to ENST00000404951 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:92534275 G>A maps to ENST00000298047 L2699L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:88963588 A>G maps to NM_181646.2 A431A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:10874434 C>T maps to NM_004752.3 R438R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:133337216 A>G maps to NM_007027.3 I1144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:103300641 G>A maps to NM_003048.3 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:100488796 G>A maps to NM_000665.3 S572S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:24958810 T>C maps to NM_001006634.1 R411R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:145415657 T>C maps to NM_213653.3 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:21236119 G>A maps to NM_000384.2 G1376G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:6592148 G>A maps to NM_144666.2 P4469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:208811192 C>T maps to NM_001080475.2 V530V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:58260428 G>T maps to NM_020676.5 E190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:1926558 C>A maps to ENST00000399161 E328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:155851194 C>T maps to NM_152280.4 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:67645870 C>T maps to NM_006565.3 Q267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:93089888 G>A maps to NM_005665.4 R541R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:80274663 C>A maps to NM_006137.6 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:117746756 C>T maps to NM_002944.2 W21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:72308347 C>T maps to NM_023036.4 A567A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:62164955 G>A maps to NM_005975.2 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:21729845 G>A maps to NM_145061.5 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:13247771 C>T maps to ENST00000319217 E15E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:35177498 C>T maps to NM_006097.3 H122H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:116930089 G>T maps to NM_000701.7 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:12884844 G>A maps to NM_001146344.1 G422G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:33296665 G>A maps to NM_021202.1 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:2252273 C>T maps to NM_006454.2 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:2161783 G>A maps to NM_001009944.2 S1128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:72192061 G>A maps to ENST00000424560 Q1146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:20976325 G>T maps to NM_017539.1 C2960*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:27067557 C>T maps to NM_178170.2 R499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:2717567 G>A maps to NM_145173.3 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:125255506 C>A maps to NM_022062.2 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:2092670 C>T maps to NM_003970.2 S1388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:140175910 G>A maps to NM_018905.2 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:46607054 G>A maps to NM_002144.3 R254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:19702705 C>T maps to NM_020314.5 D942D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:144695732 C>T maps to NM_003313.3 E257E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:185407234 C>T maps to NM_006548.4 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:7211109 C>T maps to NM_001003699.3 R167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:24679613 C>A maps to NM_014169.3 E227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:71536591 G>A maps to NM_203350.2 R201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:101340264 G>A maps to NM_005458.7 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:37584041 A>G maps to NM_004774.3 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:47538545 G>T maps to NM_001849.3 G379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:111385712 G>T maps to NM_207430.2 R68R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:45148814 G>A maps to ENST00000404564 R19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:85685822 C>T maps to ENST00000393343 T632T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:61989074 C>T maps to NM_002841.3 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:234586198 C>T maps to NM_005646.3 E612E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:40081483 G>A maps to NM_032221.3 S1073S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:38341379 G>A maps to ENST00000373026 V642V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:121414269 C>T maps to ENST00000393667 E1700E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:183874036 T>G maps to NM_015149.3 Y503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:1381753 C>T maps to NM_001080779.1 T415T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:124380765 G>A maps to NM_001024660.3 Q2111Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:121187675 G>A maps to NM_177478.1 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:130167729 G>A maps to NM_014580.3 W394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:45412284 C>T maps to NM_000041.2 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:1129416 C>T maps to NM_001053.3 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:89712423 G>A maps to NM_001083314.1 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:63600931 T>C maps to NM_001130003.1 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:41009864 C>T maps to NM_020971.2 A497A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:25232194 C>T maps to ENST00000354454 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:83885689 C>T maps to ENST00000416472 G401G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:59225176 T>A maps to NM_001004708.1 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:101373561 G>T maps to NM_014415.3 G765G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:3301744 C>T maps to NM_022114.3 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:37420646 C>T maps to NM_017438.3 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:152082431 C>T maps to NM_007113.2 Q1087Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:58713943 G>A maps to NM_018231.1 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:27886810 C>A maps to NM_018158.2 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:13246953 C>T maps to NM_052876.2 N311N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:154379457 C>T maps to ENST00000406326 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:151372652 G>A maps to NM_016203.3 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:51975573 C>T maps to NM_013243.3 R114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:248059535 C>A maps to NM_001001957.2 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:30038974 C>T maps to NM_025236.3 A392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:49957476 G>A maps to NM_003886.2 I629I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:95453691 G>A maps to NM_003297.2 D118D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:7796185 C>T maps to NM_198492.3 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:117248278 G>T maps to NM_173560.3 G659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:84245750 G>A maps to NM_001142699.1 D127D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:41203348 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:131821408 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:43613843 C>T maps to NM_020975.4 R770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:8153657 G>T maps to ENST00000422063 A478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:7323995 T>C maps to NM_199339.2 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:1573948 G>A maps to NM_014714.3 G1050G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:142460282 C>T maps to ENST00000486171 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:179616446 A>G maps to ENST00000375038 H3562H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:11008343 C>T maps to NM_001170754.1 T616T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:112579954 G>T maps to NM_006700.2 E236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:183962462 A>G maps to NM_005787.5 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:10360802 G>A maps to NM_017533.2 L611L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:76967885 G>A maps to NM_005567.3 G510G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:58384363 C>T maps to NM_001144989.1 K798K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:44807122 G>A maps to NM_031449.3 P888P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:113439558 C>T maps to NM_032189.3 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:42340138 G>A maps to NM_002466.2 P539P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:301611 G>A maps to NM_013239.4 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:1270820 G>A maps to ENST00000447027 T4240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:51772900 C>T maps to NM_001174116.1 L2134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:48382316 T>C maps to NM_003167.3 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:151463296 C>T maps to NM_207365.3 D144D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:21132124 C>T maps to NM_003429.4 R269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:54686880 T>C maps to NM_001136023.1 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:173744848 T>C maps to NM_014458.3 C502C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:15342603 G>A maps to NM_001142886.1 H104H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:77675937 C>T maps to NM_020859.3 A1434A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:75277366 C>T maps to NM_152586.3 E939E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:184290512 C>T maps to NM_004443.3 Y135Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:121551379 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:182846017 T>G maps to NM_001357.4 V726V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:995494 G>A maps to NM_000203.3 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:12252967 C>T maps to NM_001066.2 C200C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:64962609 C>T maps to NM_015042.1 R347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:61068385 G>A maps to NM_001923.3 T1078T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:51491840 G>A maps to NM_138694.3 R3913R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:27950336 G>A maps to NM_152570.1 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:73871061 G>A maps to NM_033452.2 G473G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:43117902 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:144996820 C>A maps to NM_201380.2 E2563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:54606930 G>A maps to NM_201546.2 D201D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:75520112 G>A maps to NM_198597.1 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:81661780 G>A maps to NM_003625.2 S1132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:9084854 G>T maps to NM_024690.2 T2320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:6452622 G>A maps to NM_139179.3 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:14474149 A>T maps to ENST00000310348 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:143857417 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:47047545 C>A maps to NM_015175.1 T2304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:24533162 C>A maps to NM_006277.2 G215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:21581774 C>T maps to NM_006157.3 N609N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:87780609 A>G maps to NM_021723.3 R552R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:22156629 A>G maps to NM_007153.3 C402C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:7170279 C>T maps to NM_014746.3 Y227Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:54966711 G>A maps to NM_133267.2 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:38639377 G>A maps to NM_001099404.1 L702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:111617061 G>A maps to NM_006686.3 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:228471426 C>T maps to NM_001098623.1 C2987C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:26620436 T>G maps to NM_031418.2 Y521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:58260583 G>A maps to NM_032582.3 D1355D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:31318430 G>A maps to NM_002420.4 F1158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:30227778 C>A maps to NM_032609.2 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:100447674 G>T maps to NM_001007565.2 G130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:105509582 C>T maps to NM_013437.4 W399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:7497588 T>C maps to NM_004860.3 E329E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:149809785 C>A maps to NM_000252.2 C191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:55719535 G>T maps to NM_001142763.1 V1031V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:54117258 A>G maps to NM_014614.2 A1426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:155234049 G>A maps to ENST00000368361 I396I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:46657716 A>G maps to NM_006071.1 G501G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:9874918 C>T maps to NM_001025930.3 G705G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:102295656 C>A maps to NM_000919.3 T328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:30686167 C>T maps to ENST00000378948 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:12541218 T>C maps to NM_005815.4 E589E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:9066781 C>T maps to NM_024690.2 A6888A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:130511770 C>T maps to NM_170600.2 E286E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:25255322 G>A maps to NM_002862.3 E208E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:117078760 G>A maps to NM_001779.2 R152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:73888880 G>A maps to NM_173547.2 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:57175849 C>T maps to NM_001005850.1 E261E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:130106854 G>A maps to ENST00000397753 F467F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:219295495 C>T maps to NM_007127.2 Q333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:24239804 G>A maps to ENST00000338315 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:140069808 G>T maps to NM_013366.3 T712T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:88643860 C>T maps to ENST00000452588 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:33288801 G>A maps to NM_001350.4 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:29033583 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:11066876 C>T maps to ENST00000409790 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:10363813 C>T maps to NM_183416.3 V857V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:10506753 G>A maps to NM_007065.3 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:176304688 C>T maps to NM_133369.2 C540C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:5566984 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:95277419 C>A maps to NM_001393.3 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:153347641 C>T maps to NM_012419.4 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:101916706 C>T maps to NM_001913.2 I442I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:46609139 A>G maps to NM_001430.4 S733S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:40902859 C>A maps to NM_181882.2 E467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:39768754 G>A maps to NM_005557.3 C62C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:78290594 G>A maps to NM_144572.1 T933T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:41814316 T>C maps to NM_015540.2 A958A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:37211113 C>T maps to ENST00000423498 H495H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:133836486 C>T maps to ENST00000452339 A516A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:77671485 C>T maps to ENST00000332191 A1221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:47727312 C>T maps to NM_000293.2 I930I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:13714487 A>C maps to NM_016649.3 G610G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:27075072 C>T maps to NM_004295.3 C113C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:43357577 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:152419184 C>T maps to NM_001164507.1 T6277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:164789357 C>T maps to NM_002585.2 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:75036988 C>A maps to NM_001002912.4 G1469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:58452629 C>A maps to NM_005773.2 E516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:31091405 C>T maps to NM_030758.3 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:61488886 G>A maps to NM_006602.2 G366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:239040165 G>T maps to NM_194312.2 T937T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:68688069 T>C maps to NM_004262.2 Q414Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:3059333 A>G maps to NM_001014437.2 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:144863414 C>T maps to NM_014644.4 Q1996Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:205156671 C>T maps to NM_015375.2 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:11865482 G>A maps to NM_001372.3 T4381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:15234931 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:24860905 C>T maps to ENST00000424834 R866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:12626107 G>T maps to ENST00000415519 R638R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:79034526 C>T maps to NM_153610.3 T3313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:234891812 G>A maps to NM_024080.4 S902S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:71797771 G>A maps to NM_001130987.1 K1043K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:144994626 C>T maps to NM_014644.4 Q35Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:1035031 C>T maps to NM_014587.3 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:66461255 C>T maps to NM_001164664.1 P2083P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:3192495 G>A maps to NM_020170.3 E71E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:71041047 A>G maps to NM_006540.2 S1164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:52357888 C>T maps to ENST00000273600 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:42795085 G>A maps to NM_015125.3 P722P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:60900581 C>T maps to NM_005560.3 E1773E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:48290600 A>G maps to NM_031490.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:80550873 C>T maps to NM_001825.2 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:38287879 G>T maps to NM_005955.2 I560I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:30680737 G>A maps to NM_014641.2 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:125286412 T>C maps to NM_022776.4 Q231Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:32542989 C>T maps to NM_005802.4 E511E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:56468990 A>G maps to ENST00000460849 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:51289962 G>A maps to NM_007347.3 V929V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:2189853 G>A maps to NM_199292.2 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:40357400 C>T maps to NM_003890.2 T5304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:140057085 G>A maps to ENST00000371546 W657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:150945632 G>A maps to NM_001447.2 L954L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:55623886 G>A maps to NM_021073.2 Y377Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:68107974 C>A maps to NM_017803.3 Y283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:29762877 G>A maps to NM_021738.2 A1806A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:83346883 G>A maps to NM_004644.3 N406N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:220088898 G>A maps to NM_024085.3 D398D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:46627246 G>T maps to NM_207393.1 C82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:53793137 C>A maps to NM_033341.3 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:7013954 G>A maps to NM_005559.2 C1074C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:153391709 C>A maps to NM_176823.3 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:1719498 C>T maps to NM_018941.3 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:45554054 G>A maps to NM_012345.2 H209H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:39233118 C>T maps to NM_144691.3 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:42705407 C>T maps to NM_145166.3 F619F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:76905707 C>T maps to NM_004452.3 D4D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:69725909 C>T maps to NM_138713.2 Q728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:150097897 G>T maps to NM_001135643.1 T344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:11597323 T>C maps to NM_198256.2 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:93611923 G>A maps to NM_000313.3 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:103440219 G>A maps to NM_024089.2 G449G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:143956691 C>T maps to NM_001005328.1 E10E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:7982117 G>A maps to NM_176821.3 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:52539193 G>T maps to NM_018728.3 Y633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:45799015 G>A maps to NM_001004297.2 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:36332623 G>A maps to NM_004646.3 V936V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:49110297 G>A maps to NM_133498.2 K21K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:57068362 G>A maps to NM_033396.2 S1708S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:21735929 A>G maps to NM_138644.1 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:55206407 C>T maps to NM_003222.3 Q66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:79514337 G>T maps to NM_025161.5 G590G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:73523281 C>T maps to NM_002314.2 I400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:12976849 C>T maps to NM_014975.2 L655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:57954767 G>A maps to NM_001023561.2 Q84Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:83704531 C>T maps to ENST00000268613 I413I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:49924979 C>T maps to NM_002447.2 Q1321Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:58232253 G>A maps to ENST00000335820 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:107393757 G>A maps to NM_004075.3 R263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:101439485 C>T maps to NM_020354.3 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:26459980 G>T maps to NM_007049.3 E119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:32537344 C>T maps to NM_003253.2 E975E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:79945253 G>A maps to NM_000791.3 R66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:4286137 C>T maps to NM_001042413.1 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:43148612 C>T maps to NM_003701.3 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:110639871 C>T maps to NM_030821.4 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:113194817 G>T maps to ENST00000374463 G1722G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:77166901 G>A maps to NM_002835.3 R13R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:150696385 C>T maps to NM_000603.4 G355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:228197204 C>T maps to NM_020194.4 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:3800139 G>A maps to NM_016320.4 N106N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:128843021 C>T maps to NM_152778.2 Q365Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:117841036 A>G maps to ENST00000338728 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:22290447 C>T maps to ENST00000397199 E150E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:113088933 C>T maps to NM_198581.2 G813G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:76012830 C>T maps to NM_006399.3 N65N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:6479364 G>T maps to NM_019089.4 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:76122447 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:123965963 C>T maps to NM_014943.3 C738C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:130251745 C>T maps to NM_001005374.2 F457F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:9075034 G>T maps to NM_024690.2 L4137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:95056471 C>T maps to NM_000624.4 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:40036946 G>A maps to NM_021096.3 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:103197550 G>A maps to ENST00000428762 I1890I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:59211132 C>T maps to NM_001004728.1 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:74491292 C>T maps to NM_021196.3 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:37617835 G>A maps to NM_005128.2 T1186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:200842740 C>T maps to NM_005298.2 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:223176547 C>T maps to NM_032890.2 H603H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:18221837 G>A maps to NM_153346.4 F230F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:56007461 C>T maps to NM_182633.1 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:92459677 G>A maps to NM_013272.3 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:74124154 G>A maps to NM_032217.3 N77N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:4872556 G>A maps to NM_015099.3 R1120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:220116406 C>T maps to NM_006000.1 Q85Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:176987567 G>A maps to NM_014213.3 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:92119134 A>G maps to NM_000466.2 L1177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:43133514 G>A maps to NM_006811.2 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:51223033 G>A maps to NM_007347.3 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:35095226 C>T maps to NM_032634.2 E112E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:84372049 C>A maps to NM_024686.4 G697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:144449154 G>A maps to NM_003601.2 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:22447814 G>A maps to NM_030761.4 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:122626576 T>C maps to NM_005328.2 G477G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:50549779 C>T maps to NM_015428.1 R694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:44521861 C>T maps to NM_000308.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:129913210 G>A maps to NM_002417.4 N487N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:150280586 C>A maps to NM_031901.4 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:140237243 C>T maps to NM_018901.2 R537R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:163003924 C>T maps to ENST00000233604 K67K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:31348031 C>T maps to NM_004086.2 N85N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:46629511 C>T maps to NM_024745.4 R472R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:62595139 A>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:53265480 G>A maps to ENST00000423516 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:170606211 T>A maps to NM_144711.5 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:12856658 C>T maps to NM_001162499.1 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:140128877 C>T maps to NM_080877.2 F368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:176526267 G>A maps to NM_020318.2 E270E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:131397200 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:30878968 A>G maps to NM_001002259.1 D612D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:108013841 C>A maps to NM_001018072.1 C844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:73767331 C>T maps to NM_004273.4 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:242062164 G>A maps to ENST00000358649 D1018D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:54433605 C>A maps to NM_052940.3 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:2263662 G>A maps to NM_006454.2 Y15Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:156203495 C>T maps to NM_007221.3 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:144732312 G>T maps to NM_014789.3 G91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:74911639 C>T maps to NM_001130028.1 R183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:130919410 G>A maps to NM_015347.4 S690S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:21492087 G>T maps to NM_021269.2 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:198570572 G>A maps to NM_138395.3 Q148Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:102684140 C>T maps to NM_001136123.1 T461T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:107048101 A>G maps to ENST00000357881 Q105Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:229738418 G>A maps to NM_014409.3 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:85750272 G>A maps to NM_014991.4 V280V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:186334293 C>T maps to ENST00000273784 Y129Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:18023550 C>T maps to NM_018125.3 L1172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:45432487 C>T maps to ENST00000361462 G288G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:67206390 G>A maps to NM_020441.2 P365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:20043353 C>T maps to NM_001002911.2 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:72080330 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:101964412 A>G maps to NM_001278.3 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:116937894 G>A maps to NM_003391.2 C208C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:56679269 C>T maps to ENST00000240361 V531V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:42935594 T>C maps to NM_001080472.1 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:126736698 C>T maps to NM_032242.3 C1208C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:46591705 G>A maps to NM_030674.3 V420V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:2747722 G>A maps to NM_033267.4 S457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:1438855 C>T maps to ENST00000476071 E89E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:50413103 G>A maps to ENST00000435965 T626T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:88400698 G>A maps to NM_004684.4 R617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:90050899 C>T maps to NM_032119.3 V3826V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:204737462 C>A maps to NM_005214.3 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:62444432 G>A maps to NM_015853.3 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:108593876 C>A maps to NM_004398.2 Y551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:6707220 C>T maps to ENST00000309577 K577K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:124333229 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:186024738 C>T maps to NM_031935.2 G2359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:42585037 C>T maps to ENST00000222339 H850H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:220336653 C>T maps to NM_005876.4 S1260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:7687517 G>A maps to NM_020196.2 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:28844111 G>A maps to NM_182898.2 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:243468020 C>T maps to NM_006642.3 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:176867756 G>A maps to NM_002082.3 K487K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:137424614 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:205238373 C>T maps to NM_014858.3 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:52740551 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:56492081 G>A maps to ENST00000361203 L1337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:129929526 C>A maps to NM_001869.2 A400A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:32995579 C>A maps to NM_005508.4 Y222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:47535605 G>A maps to NM_002517.2 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:102368103 G>T maps to NM_002719.3 E301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:33960891 C>T maps to NM_133642.3 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:35742839 T>G maps to NM_172201.1 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:149924228 C>A maps to NM_003828.2 P575P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:58538163 G>A maps to NM_001130487.1 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:83784499 C>A maps to ENST00000505472 G494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:74846977 G>A maps to NM_002619.2 C83C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:4847717 C>T maps to NM_005817.4 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:189901340 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:114264286 C>T maps to NM_001148.4 L1413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:160253412 G>A maps to NM_002857.3 F29F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:118984414 C>T maps to NM_014807.3 S494S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:79118163 C>T maps to NM_001097636.1 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:141316993 C>A maps to NM_004362.2 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:58441413 G>A maps to NM_014258.2 I1418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:214815449 G>T maps to NM_016343.3 E1257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:45246287 T>C maps to NM_020229.2 V455V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:132952823 T>C did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:7693094 G>A maps to NM_020196.2 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:50664718 G>A maps to NM_020461.3 R564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:58711300 G>A maps to NM_018231.1 Y213Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:179714775 C>T maps to NM_173648.3 K1119K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:110503217 A>G maps to ENST00000426474 S3334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:88261693 G>A maps to NM_016245.3 Q254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:74679975 C>T maps to NM_001008529.1 *178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:131189240 T>C maps to NM_001018111.2 T502T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:541500 C>T maps to NM_004359.1 A220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:71188216 G>A maps to NM_017691.3 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:87809351 C>A maps to NM_144645.3 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:75133791 C>T maps to NM_001099436.1 Q141Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:4576764 T>C did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:17750860 G>A maps to NM_003473.2 P432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:93256086 C>T maps to ENST00000446394 G550G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:91435947 C>T maps to NM_002005.3 G573G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:26923312 C>T maps to NM_001260.1 D103D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:136614333 G>A maps to NM_005915.4 F530F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:33034280 C>T maps to NM_001539.2 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:123049815 G>A maps to NM_183357.2 C522C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:40111946 A>G did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:179621174 C>T maps to NM_133437.3 T3505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:19992446 G>A maps to NM_000871.1 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:149216333 G>A maps to NM_133263.3 E772E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:150911634 G>A maps to NM_005140.1 Q220Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:32560596 G>A maps to NM_025209.2 R775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:57746273 C>T maps to NM_001015878.1 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:32199033 C>T maps to NM_005093.3 R114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:28748770 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:205312648 C>T maps to NM_018203.1 E28E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:56428845 G>T maps to NM_022465.3 E497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:204938110 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:36870076 G>T maps to NM_001029864.1 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:153315695 G>A maps to NM_019041.5 R213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:42775002 C>T maps to NM_144719.3 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:44394256 G>A maps to NM_001253.2 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:197071116 G>A maps to NM_018136.4 L2422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:2552885 C>T maps to NM_080751.2 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:54133797 G>A maps to NM_014614.2 Y960Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:12124077 C>T maps to NM_002114.2 G1350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:697443 T>G maps to NM_138418.2 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:42611245 G>A maps to NM_005650.1 H22H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:47882404 C>T maps to NM_138615.2 D135D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:51021727 G>A maps to NM_001080457.1 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:68060136 C>T maps to NM_004429.4 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:182026617 C>T maps to NM_001009992.1 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:197298116 T>C maps to NM_201253.2 C212C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:205039088 C>T maps to NM_005076.3 S777S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:1467871 G>A maps to NM_005883.2 T1524T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:62599162 G>A maps to ENST00000506720 Q430Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:140517232 C>T maps to NM_015669.2 S739S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:200137032 G>A maps to NM_001172509.1 N701N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:80530749 G>A maps to NM_178839.4 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:7861321 T>C maps to NM_024091.3 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:42863067 G>T maps to ENST00000251268 G1769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:14774876 G>A maps to NM_145175.2 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:43846889 A>G maps to NM_018961.2 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:8654932 G>A maps to NM_004225.2 R1023*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:67424127 G>A maps to NM_016140.2 Y160Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:71183493 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:212548539 G>A maps to NM_001198862.1 Q357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:50681794 C>T maps to NM_172238.3 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:23650225 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:114604697 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:77605760 G>A maps to NM_174976.2 H107H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:123072360 A>G maps to NM_014708.4 S1278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:971938 C>T maps to NM_005224.2 G552G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:240656544 C>T maps to NM_022469.3 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:987392 C>T maps to NM_001184985.1 Q1160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:47563036 G>A maps to NM_020453.3 R871R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:4436304 G>A maps to NM_001124758.1 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:38791015 C>A maps to NM_005739.3 G618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:121769555 A>G maps to NM_005763.3 D82D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:1492596 G>A maps to NM_001172223.1 Q140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:93713535 G>T maps to NM_003972.2 G203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:147128516 G>A maps to NM_003412.3 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:67006909 G>A maps to NM_024922.5 W558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:20016874 G>A maps to NM_016652.4 H837H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:16456288 G>A maps to NM_020653.2 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:74090662 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:220100034 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:108615088 G>T maps to NM_005443.4 C83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:47279221 G>A maps to NM_001099772.1 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:101747862 T>C maps to NM_001855.3 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:55533930 G>A maps to NM_006269.1 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:216211552 T>G maps to NM_004044.6 Y464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:24607693 G>A maps to NM_176783.1 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:27454441 C>T maps to NM_004341.3 S798S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:434084 T>C maps to NM_020731.3 D432D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:161133728 G>A maps to NM_012475.4 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:9225458 C>A maps to NM_000014.4 V1255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:66596564 A>G maps to NM_017565.3 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:101689295 C>A maps to NM_014503.2 C430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:60522266 C>T maps to NM_181725.3 Y293Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:179269013 G>A maps to NM_016175.3 D114D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:20248579 C>A maps to NM_001005500.1 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:84129261 C>T maps to NM_003791.2 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:37268380 A>G maps to NM_019024.1 G917G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:3026774 C>A maps to NM_004203.4 E90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:101912584 C>T maps to NM_001184727.1 S1248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:979371 C>T maps to NM_198576.2 I656I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:38396311 G>A maps to NM_000692.3 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:19378799 T>C maps to NM_001010.2 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:37453837 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:27503770 G>A maps to NM_001520.3 N1013N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:99909547 G>A maps to NM_001004351.4 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:120008616 C>T maps to NM_012101.3 K41K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:113258668 C>T maps to NM_178510.1 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:82583260 G>A maps to NM_033026.5 S2336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:91424214 C>T maps to NM_002569.2 P579P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:1483416 G>A maps to NM_017573.3 C479C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:97823013 C>T maps to NM_014916.3 G1079G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:131487620 G>A maps to NM_207364.2 W299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:4836803 G>A maps to ENST00000356617 S2286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:53854086 C>T maps to NM_138374.1 C53C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:9243823 G>T maps to NM_000014.4 V814V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:48018177 A>T maps to NM_000179.2 K125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:102766457 C>T maps to NM_032429.2 R515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:71512537 C>T maps to ENST00000354608 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:123842596 C>T maps to NM_206862.2 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:58420403 C>T maps to NM_152475.2 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:111348973 G>A maps to NM_000432.3 D136D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:14340859 C>T maps to NM_014048.3 I581I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:170585923 C>A maps to ENST00000430925 G57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:120483360 G>A maps to NM_024408.2 G1000G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:6696634 A>C maps to NM_000064.2 V944V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:52229780 T>C maps to NM_181501.1 I973I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:39262170 T>C maps to ENST00000377731 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:31818562 G>A maps to ENST00000382902 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:8354152 G>A maps to ENST00000402554 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:186370257 T>C maps to NM_022375.3 Y27Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:65678348 C>T maps to NM_020962.1 A1000A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:105643298 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:36640529 C>T maps to NM_018067.3 N257N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:165504014 C>T maps to NM_000055.2 E534E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:8284227 C>T maps to NM_053044.3 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:37440778 C>T maps to NM_198539.2 R242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:47101919 C>T maps to NM_006033.2 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:49135604 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:10224726 C>A maps to NM_001040664.2 A566A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:5991325 C>A maps to NM_015253.1 C148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:1306839 G>A maps to NM_012217.2 E99E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:405970 G>A maps to NM_021805.2 D386D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:16677434 G>A maps to NM_024881.4 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:1718507 C>T maps to NM_001012416.1 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:38229998 G>A maps to NM_001172690.1 H464H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:54173410 G>A maps to NM_014464.3 K21K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:22973780 C>T maps to NM_172369.3 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:7229594 C>T maps to NM_001003699.3 G421G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:52357822 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:27751849 C>A maps to NM_015202.2 I744I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:47274754 C>T maps to NM_020820.3 Q631Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:28542675 G>T maps to NM_052923.1 S602S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:41410594 C>T maps to NM_001843.2 R766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:102482233 G>A maps to NM_001376.4 T2428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:87968326 G>A maps to NM_015021.1 K1660K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:56923985 A>G maps to NM_017661.2 L884L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:10532982 T>C maps to NM_002470.2 E1909E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:16120587 G>A maps to NM_004278.3 W16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:26798778 C>T maps to NM_001105519.1 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:32586764 G>T maps to NM_001098527.2 A377A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:105657392 C>T maps to NM_024928.4 Q222Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:38855714 C>T maps to NM_021185.4 S857S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:110729640 T>C maps to NM_003649.2 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:58545413 C>A maps to NM_001130487.1 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:74017769 C>T maps to NM_001988.2 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:11163893 C>T maps to NM_015458.3 R263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:102033282 T>C maps to NM_001130145.2 N223N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:144857633 C>T maps to NM_014644.4 T2140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:38020291 G>A maps to NM_006307.4 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:62775383 C>T maps to ENST00000280377 A343A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:6214958 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:147781653 G>A maps to NM_205836.1 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:65304577 C>T maps to NM_020680.3 D646D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:48255821 G>A maps to NM_015710.4 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:73486118 G>A maps to ENST00000295133 G934G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:8386870 C>A maps to ENST00000449223 I54I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:30747152 C>T maps to NM_005204.2 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:52685243 G>T maps to NM_002281.3 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:18439940 G>A maps to NM_182757.3 Q99Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:73973060 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:36049525 G>A maps to NM_005584.4 C250C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:34395248 C>T maps to NM_152595.4 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:66700218 G>T maps to NM_033647.2 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:27255211 G>A maps to NM_006646.5 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:132812819 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:51566351 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:124177322 C>A maps to NM_145207.2 Y831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:48918253 C>T maps to NM_175575.5 G535G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:47546053 C>T maps to NM_001849.3 I775I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:110246188 G>A maps to NM_021625.4 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:82336697 T>C maps to ENST00000376537 I659I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:40558248 C>T maps to NM_175888.2 G388G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:112942916 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:75310803 G>A maps to ENST00000361900 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:45959280 G>A maps to NM_198691.2 C251C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:38048047 C>T maps to NM_015873.3 R772*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:5430200 C>T maps to NM_001080495.2 E134E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:138936757 C>A maps to NM_173569.3 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:65971919 C>T maps to ENST00000321892 R2984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:27315812 C>T maps to NM_004103.3 I939I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:21121148 G>T maps to NM_000271.4 C799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:85605149 G>A maps to NM_014991.4 N3224N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:153945233 C>T maps to NM_130898.2 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:68686695 C>T maps to NM_178011.3 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:132636134 C>T maps to NM_024078.1 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:134362214 A>G maps to NM_178554.4 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:130095371 C>A maps to ENST00000312481 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:23713496 G>T maps to NM_033266.3 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:111658330 C>T maps to NM_001134438.1 L714L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:53558603 G>A maps to NM_001160148.1 A396A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:158299848 C>A maps to NM_001764.2 G134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:119737599 G>A maps to ENST00000313400 G592G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:45213774 G>A maps to ENST00000396750 G490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:230820882 G>A maps to NM_007357.2 R427R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:167293927 G>T maps to NM_178824.3 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:35929685 G>A maps to NM_031866.2 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:30350181 G>A maps to NM_020805.1 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:87011305 G>A maps to NM_001143935.1 W381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:60720792 T>G maps to NM_024611.4 A885A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:95353718 G>A maps to NM_006744.3 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:134123497 C>T maps to NM_014384.2 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:121702387 G>A maps to NM_018699.2 V451V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:88329151 G>A maps to NM_015567.1 P503P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:46739360 C>T maps to NM_003579.3 L518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:157816010 G>A maps to NM_003030.4 H291H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:30771463 C>T maps to NM_001172432.1 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:21928253 G>A maps to NM_001145658.1 S589S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:92353549 G>A maps to ENST00000267620 G339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:111508078 C>T maps to ENST00000428084 S747S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:77460046 G>A maps to NM_138444.3 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:111621260 C>T maps to NM_002912.3 L3117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:7226811 C>T maps to NM_032442.2 W803*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:125299094 G>A maps to NM_001013628.2 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:51493562 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:12837594 G>A maps to NM_001080830.1 E435E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:113599089 G>A maps to NM_001111322.1 R800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:144991598 C>T maps to NM_201380.2 T4267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:102509560 C>T maps to NM_003987.3 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:150076138 G>A maps to NM_018047.2 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:130648443 C>T maps to NM_007197.3 F319F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:127572609 C>T maps to NM_182487.2 I626I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:52568641 C>A maps to NM_022908.2 E10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:93487187 C>T maps to ENST00000354421 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:138837381 G>A maps to NM_001077693.2 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:94935808 A>G maps to NM_175739.3 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:90179145 C>A maps to NM_032270.4 Y339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:41077049 G>A maps to NM_005297.3 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:155264394 G>A maps to ENST00000423816 D306D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:112479989 G>A maps to NM_001105206.1 V587V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:70841707 A>G maps to NM_032821.2 Y5046Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:72822079 C>T maps to NM_006885.3 Q3365Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:14774696 C>T maps to NM_145175.2 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:71604255 G>T maps to NM_000353.2 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:73730978 C>T maps to ENST00000427855 G974G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:182850545 C>T maps to NM_001357.4 A924A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:31869269 G>T maps to NM_181610.1 C53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:71553219 G>A maps to NM_016027.2 R220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:100472709 C>T maps to ENST00000370153 Q197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:8936987 C>T maps to NM_020738.2 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:38817901 G>A maps to NM_004823.1 E267E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:79671414 C>T maps to NM_017934.5 R1216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:23821155 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:140856828 C>T maps to NM_002588.2 G382G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:8997160 C>T maps to NM_003470.2 S601S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:164781363 G>A maps to NM_002585.2 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:14080948 G>A maps to NM_002918.4 G451G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:113199286 G>A maps to NM_052864.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:137998691 C>T maps to NM_014279.4 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:95054178 C>T maps to NM_000624.4 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:54554919 C>A maps to NM_153228.2 L618L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:107979103 G>A maps to NM_003604.2 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:27849348 C>T maps to NM_020791.2 R654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:149871986 A>G maps to NM_016074.3 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:33468759 C>T maps to NM_022917.4 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:74357692 C>T maps to NM_001133.2 N316N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:37390265 C>T maps to NM_170675.2 Q49Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:29963697 C>A maps to NM_001145514.1 E394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:13988310 C>T maps to NM_001098622.1 N83N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:47979830 C>T maps to NM_007059.2 Q380Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:1807391 G>A maps to NM_000142.4 Q547Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:151493069 A>G did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:5069021 C>T maps to NM_004972.3 R443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:2143019 G>A maps to NM_001009944.2 H3697H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:158669908 A>G maps to NM_001005279.1 C178C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:45105087 G>A maps to NM_001145107.1 C442C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:32673996 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:11650326 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:28841993 C>T maps to NM_148414.1 R365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:160099108 C>A maps to NM_000702.3 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:166388931 C>T maps to NM_001873.2 Y199Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:47398551 G>T maps to NM_001080467.2 A1196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:52475297 G>A maps to NM_020163.1 R265R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:17122371 C>T maps to NM_144997.5 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:39799003 C>T maps to ENST00000289893 N688N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:91449449 G>A maps to NM_007035.3 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:73994860 G>A maps to NM_001024736.1 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:66981211 T>C maps to NM_080283.3 S1422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:9380031 C>T maps to NM_003966.2 W9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:109796946 C>T maps to NM_153015.1 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:72897827 T>C maps to NM_004885.2 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:10746124 C>T maps to NM_020428.3 N389N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:10045079 C>A maps to NM_005680.2 C300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:102286191 G>T maps to NM_005004.2 C144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:125267822 C>T maps to NM_022062.2 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:46834845 C>T maps to NM_015234.4 K550K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:127608108 C>T maps to ENST00000368314 Y117Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:27207786 G>A maps to ENST00000394906 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:48317421 T>C did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:152323364 T>C maps to NM_001014342.2 G2299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:71142485 G>A maps to ENST00000439900 T538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:70248345 C>T maps to NM_152707.2 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:78351652 G>A maps to NM_013391.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:100006172 G>A maps to NM_017984.3 Y326Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:36262088 C>T maps to ENST00000457797 H210H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:48618172 G>A maps to NM_017957.2 E333E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:150460413 G>A maps to NM_005067.5 Y163Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:78120715 C>T maps to NM_014740.3 K15K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:136533887 T>G maps to NM_014607.3 A340A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:45849994 C>T maps to ENST00000471951 T1130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:160721348 G>A maps to NM_021911.2 D426D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:142227288 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:128622691 C>T maps to NM_031445.2 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:21674238 C>T maps to NM_153270.1 P556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:109294502 G>T maps to NM_207645.3 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:219000156 A>G maps to NM_001168298.1 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:168112784 G>A maps to NM_003062.2 C1154C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:2223365 C>T maps to NM_032271.2 I326I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:40832535 G>A maps to NM_004307.1 R530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:35675755 A>G did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:45175634 G>A maps to NM_003681.4 Q272Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:3697445 G>A maps to NM_016320.4 D1782D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:147488387 A>G maps to NM_001127698.1 R560R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:67376921 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:152757164 C>T maps to NM_182961.2 P1407P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:36054426 C>T maps to NM_000704.2 E5E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:94877556 C>T maps to NM_014639.3 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:74762765 G>A maps to NM_032603.2 A455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:144808549 C>T maps to NM_198488.3 T1027T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:127791942 C>T maps to NM_173690.4 W125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:207823080 C>T maps to NM_173077.2 H108H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:29287141 A>G maps to NM_001135919.1 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:150417217 C>A maps to NM_130759.3 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:3293599 C>T maps to NM_000243.2 L629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:27803686 G>A maps to NM_032266.3 T1416T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:48844690 G>T maps to NM_001168254.1 G65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:78316860 C>T maps to NM_144572.1 Q369Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:98750320 G>T maps to NM_144992.4 E303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:65540682 G>A maps to NM_181784.2 C403C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:56614363 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:47194998 G>T maps to ENST00000449438 V565V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:76475585 C>T maps to ENST00000389840 Q2613Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:17959281 C>T maps to NM_001130009.1 R406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:26251331 T>C maps to NM_016587.2 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:36926742 C>T maps to NM_003559.4 T372T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:114429224 A>G maps to NM_001010922.2 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:49657294 C>T maps to NM_002152.2 K400K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:73541461 T>C maps to NM_002499.3 T556T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:232263042 C>T maps to NM_145236.2 Q205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:42476825 G>A maps to NM_001002909.2 S873S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:42788610 G>A maps to NM_020433.4 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:78719256 G>A maps to NM_002941.3 R513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:121362758 C>T maps to NM_152546.2 R410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:74961669 C>T maps to NM_194279.2 C144C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:23910801 C>A maps to NM_014363.4 E2405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:41633863 C>T maps to NM_000774.3 T451T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:39799705 G>A maps to ENST00000289893 Q922Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:66254052 C>T maps to NM_005700.3 Q135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:126710387 G>A maps to NM_032242.3 T452T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:33926917 A>G maps to NM_001036.3 P1053P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:18135839 C>T maps to NM_004140.3 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:120353796 G>A maps to NM_004248.2 C320C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:129160442 G>A maps to ENST00000398025 Q1178Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:2795338 G>A maps to NM_199460.2 R1979R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:216251445 C>T maps to NM_212482.1 E1526E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:72875700 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:38305725 G>A maps to NM_005955.2 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:158636272 C>A maps to NM_003126.2 E685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:8590438 C>T maps to NM_014583.2 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:111639199 G>A maps to NM_001134438.1 E645E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:73447447 C>T maps to ENST00000398860 F682F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:33406321 A>G maps to NM_024787.2 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:45774950 C>T maps to NM_031417.3 D257D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:70815787 G>A maps to NM_018052.3 Y310Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:58945595 G>A maps to NM_003433.3 C405C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:103347011 C>A maps to NM_013274.3 E36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:93606404 C>A maps to NM_003177.5 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:125437015 G>A maps to NM_032656.3 G932G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:21238317 G>A maps to NM_000384.2 A1144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:55995124 G>A maps to NM_033113.2 Q851Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:86266458 G>T maps to NM_015425.3 C1289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:40184961 G>A maps to NM_005239.4 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:7974946 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:118428590 G>A maps to NM_020153.3 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:11664625 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:79841407 C>T maps to ENST00000376646 Y417Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:162622161 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:48495697 A>C did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:9782361 C>T maps to ENST00000361110 N789N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:77618746 T>C maps to NM_024721.4 N808N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:86916301 C>T maps to NM_001025616.2 R499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:59217361 C>T maps to NM_031891.2 D600D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:56344804 A>G maps to NM_001004741.1 H131H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:132792627 G>A maps to NM_003569.2 R121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:22225377 C>T maps to NM_213599.2 Y23Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:140735708 C>T maps to NM_018917.2 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:110509384 G>T maps to ENST00000426474 E3495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:49332009 G>A maps to NM_003363.3 S571S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:56348962 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:45111148 C>T maps to ENST00000453887 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:35466169 C>T maps to NM_003322.3 P521P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:12161697 C>T maps to NM_002114.2 R2172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:13054418 C>T maps to NM_004343.3 G343G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:16101141 C>T maps to NM_017556.2 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:17973030 C>A maps to NM_000980.2 C109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:49508535 G>A maps to NM_181442.1 N905N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:52991254 G>A maps to NM_016075.2 G309G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:58500014 C>T maps to NM_025027.3 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:12884805 G>A maps to NM_001146344.1 C435C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:59271326 C>A maps to NM_001004706.1 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:64382993 T>G maps to NM_199451.2 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:99012700 C>A maps to NM_001298.2 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:79990866 C>T maps to NM_005052.2 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:156747678 C>T maps to ENST00000442283 R514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:34953056 T>G did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:24523714 C>T maps to NM_138360.3 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:134942097 C>T maps to ENST00000368577 L796L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:48809667 A>G maps to NM_172311.2 V632V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:72582591 G>A maps to NM_052840.4 D133D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:50546816 C>T maps to NM_002112.3 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:59558001 G>A maps to NM_004177.4 K100K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:108496125 C>T maps to ENST00000368983 D123D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:71437416 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:80045872 G>A maps to NM_004104.4 S941S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:184039151 G>A maps to NM_001194947.1 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:22696558 A>G maps to NM_005256.3 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:9960031 G>A maps to NM_153461.2 E169E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:191064771 A>G maps to NM_032321.2 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:10996533 G>A maps to NM_000246.3 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:91347507 G>T maps to NM_000057.2 E1224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:11898393 C>T maps to ENST00000376496 S766S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:42683163 C>T maps to ENST00000348077 Q302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:44929288 T>C did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:88405902 C>T maps to NM_198274.3 N347N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:73434831 G>A maps to NM_015009.1 S541S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:155253942 C>T maps to NM_017639.3 T640T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:39629476 G>A maps to NM_002608.2 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:136913495 C>T maps to NM_007371.3 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:1466479 G>A maps to NM_005883.2 A1060A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:212148513 G>T maps to NM_015434.3 S603S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:187534418 C>A maps to ENST00000260147 G3106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:78804037 C>T maps to NM_001190482.1 C803C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:203395673 C>T maps to NM_001204.6 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:79403571 C>T maps to NM_025074.6 Q2879*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:85610411 G>A maps to NM_002605.2 Q137Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:206592643 G>A maps to NM_201266.1 T340T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:126883687 C>T maps to ENST00000442138 F401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:96706371 G>T maps to NM_001080448.2 E217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:56271323 G>A maps to NM_000502.4 K155K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:53304224 C>T maps to NM_006969.3 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:74154527 C>T maps to ENST00000443185 E161E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:64604533 C>T maps to NM_182914.2 H4892H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:148797775 C>T maps to NM_005366.4 D210D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:3121334 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:173931057 G>A maps to NM_172071.2 H669H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:219494328 G>A maps to ENST00000432688 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:60271184 C>T maps to NM_017716.2 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:28269796 G>A maps to NM_032507.3 Q722Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:39955443 C>T maps to NM_003169.3 Q211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:77699591 A>G maps to NM_015057.4 S2632S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:126132861 G>A maps to NM_173689.5 P510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:20559395 G>T maps to NM_182617.3 G362G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:179454804 G>T maps to NM_133378.4 I17981I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:90438203 C>T maps to NM_001198829.1 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:156047473 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:149462849 C>T maps to NM_207336.1 A247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:13884824 G>T maps to NM_000529.2 C231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:34263155 G>A maps to NM_194313.2 I486I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:17256516 G>A maps to NM_014675.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:89034472 G>A maps to NM_004827.2 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:35045016 C>T maps to NM_203299.2 S797S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:51918849 C>T maps to NM_138694.3 R650R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:9317761 G>T maps to NM_002864.2 V820V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:111398942 C>A maps to NM_004336.3 V908V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:92730813 G>A maps to NM_017654.3 R1533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:21993138 G>T maps to NM_005407.1 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:56333197 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:1391219 G>A maps to NM_001452.1 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:90504401 C>A maps to NM_014611.1 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:6730345 G>A maps to ENST00000435659 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:77660199 C>T maps to NM_020859.3 R292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:31768628 C>A maps to NM_181599.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:160047705 G>A maps to NM_025153.2 G688G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:47730389 C>T maps to NM_000293.2 I998I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:25281486 C>T maps to NM_001185085.1 C809C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:81974599 C>A maps to NM_001201.2 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:106858268 G>A maps to ENST00000503451 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:40245059 C>A maps to NM_004310.3 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:179465821 C>T maps to NM_133378.4 P16035P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:12022778 C>T maps to NM_001987.4 D295D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:6042116 G>A maps to NM_000635.3 H66H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:40747105 C>A maps to NM_005857.3 Y287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:51944772 G>A maps to NM_138694.3 Y105Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:16688234 G>A maps to NM_004831.3 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:58190147 G>T maps to NM_152677.2 E393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:18507050 G>A maps to NM_145256.2 D241D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:61650906 G>A maps to NM_198833.1 E173E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:153903513 A>G maps to NM_014856.2 D1341D. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-IB-7651-01A-11D-2154-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:35792965 C>A maps to NM_003995.3 V187V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:170108125 G>A maps to NM_005414.3 P515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:99754542 C>T maps to NM_018275.3 P306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:48073290 C>T maps to NM_024604.2 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:140604405 C>T maps to NM_018934.2 D443D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:25046191 T>C maps to NM_004036.3 G923G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:140203603 G>A maps to NM_018908.2 S748S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:79181032 C>T maps to ENST00000269392 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:40583385 T>C did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:58562650 G>A maps to NM_177980.2 S327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:8975301 G>T maps to NM_144670.3 E19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:103339446 G>A maps to NM_013274.3 S497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:105407192 G>A maps to NM_138420.2 F4865F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:23080092 C>T maps to NM_020718.3 S1111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:72416265 G>T maps to ENST00000389376 E392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:55817494 T>C maps to NM_152231.1 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:76435167 G>A maps to ENST00000389840 R3923*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:127225161 C>T maps to NM_024523.5 K25K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:64573854 G>A maps to NM_001136178.1 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:120072118 C>T maps to NM_016599.3 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:157804530 C>T maps to NM_005894.2 E128E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:10620603 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:51686259 G>A maps to NM_003927.3 R375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:23495219 G>A maps to NM_004914.2 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:138522641 C>T maps to ENST00000413208 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:25390498 C>T maps to ENST00000510092 D170D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:228109545 G>T maps to NM_003395.2 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:33502411 G>A maps to NM_003873.5 R506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:30890673 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:170058136 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:169548368 C>A maps to NM_001080460.1 C428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:5463616 C>T maps to NM_015325.1 A1390A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:3380551 G>A maps to NM_001130520.1 F562F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:49510576 C>T maps to NM_006666.1 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:213186642 T>C maps to NM_144567.3 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:95945718 C>T maps to NM_144707.2 G467G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:141461130 C>T maps to NM_031466.5 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:140785539 C>T maps to NM_080862.1 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:67610093 C>T maps to NM_020806.4 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:12812935 G>A maps to NM_001136196.1 Y787Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:229568760 C>T maps to NM_001100.3 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:151687213 G>A maps to NM_020861.1 I329I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:41585305 C>T maps to NM_004941.1 L747L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:34499505 C>T maps to NM_020804.3 R389R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:130919323 G>A maps to NM_015347.4 G719G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:4732889 C>T maps to NM_015246.2 D475D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:7814232 G>A maps to NM_001005271.2 G2000G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:53837448 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:115088667 G>A maps to NM_014333.3 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:59970601 A>C maps to ENST00000356057 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:62187885 G>A maps to NM_024059.2 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:149248115 G>T maps to ENST00000404807 E1639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:79253163 G>A maps to NM_015225.2 A2923A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:132626411 C>T maps to NM_175066.3 E326E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:173316693 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:73480439 G>A maps to NM_004770.2 E157E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:186423603 C>T maps to NM_014476.4 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:170181440 C>A maps to NM_018341.1 I623I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:15807131 A>G maps to NM_004447.5 N399N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:204016308 C>T maps to NM_001114132.1 L1833L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:17405186 G>A maps to NM_024527.4 V353V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:142396961 C>T maps to NM_002511.2 R332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:125659638 A>G maps to NM_001100588.1 C50C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:23931895 G>A maps to NM_002487.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:179401006 A>G maps to NM_133378.4 S30921S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:42342045 A>T maps to NM_173506.4 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:43152467 C>T maps to ENST00000354495 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:47931369 C>T maps to ENST00000318711 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:57529400 G>T maps to NM_001159279.1 E412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:7834370 G>A maps to NM_001166621.1 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:77171306 C>A maps to NM_172387.1 P331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:23614612 G>T maps to NM_000099.2 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:73844720 G>A maps to NM_012478.3 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:46083794 T>C maps to NM_002482.3 V783V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:154727607 C>T maps to NM_173515.2 T516T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:88688649 G>A maps to ENST00000452588 P531P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:7244458 G>A maps to NM_001018039.1 V490V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:118434864 G>A maps to NM_025015.2 A485A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:11170508 C>T maps to NM_001128849.1 G1604G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:51983671 C>T maps to NM_001080405.1 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:77398215 G>A maps to NM_199355.2 R281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:75428009 C>T maps to NM_014979.1 C145C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:58537859 C>T maps to ENST00000358584 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:158900853 C>T maps to NM_020245.3 Y366Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:81932581 G>T maps to NM_145869.1 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:14105440 G>A maps to NM_145287.3 H366H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:32722002 T>G maps to NM_023037.2 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:156296173 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:135374873 G>A maps to NM_207417.1 E173E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:125576017 G>A maps to NM_023928.3 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:21800713 C>T maps to NM_015094.2 C510C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:72184055 C>T maps to NM_000503.4 G301G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:9452957 C>T maps to NM_032497.1 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:69006381 T>C did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:197541786 C>T maps to ENST00000425562 R91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:39471737 C>T maps to NM_031964.1 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:100420109 G>A maps to NM_004444.4 C197C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:101194699 G>A maps to NM_001078.3 R322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:60585188 C>T maps to NM_003185.3 T558T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:187387998 C>T maps to NM_001048.3 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:2202762 C>T maps to NM_017575.4 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:99909056 G>A maps to NM_174898.2 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:121743936 C>T maps to NM_005270.4 G680G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:25880491 G>A maps to NM_015627.2 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:44101343 C>T maps to NM_024327.2 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:15096341 G>A maps to NM_000728.3 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:15532138 G>A maps to NM_006470.3 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:38768405 C>T maps to NM_006514.2 Q926Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:144940359 G>A maps to NM_031308.1 S2354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:128389838 C>A maps to ENST00000389524 G1731G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:23117747 T>C maps to NM_152272.3 N404N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:66307146 G>T maps to NM_207340.1 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:9546845 C>T maps to NM_177990.2 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:23243279 G>A maps to NM_001126106.1 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:35563507 G>A maps to NM_015474.3 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:4790159 C>T maps to NM_139170.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:2139201 G>A maps to NM_145177.2 G291G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:31835922 G>A maps to NM_019843.3 P967P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:65962263 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:27238238 G>A maps to NM_001033561.1 P702P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:90399637 C>T maps to NM_001134479.1 H337H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:84257441 C>T maps to ENST00000434347 R261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:97928575 C>T maps to ENST00000376673 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:27222470 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:58132056 A>G maps to NM_003435.3 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:137289149 G>A maps to NM_016603.2 R553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:150864193 G>A maps to NM_001098834.1 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:95590926 C>A maps to NM_177438.2 E328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:73085531 G>A maps to NM_001077621.1 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:18144853 G>A maps to NM_004140.3 T864T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:31771684 G>A maps to ENST00000389961 I1754I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:60741866 T>G maps to NM_024611.4 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:61042027 G>A maps to NM_152718.2 Y508Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:72838585 C>T maps to NM_000835.3 E1230E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:33415413 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:75959523 C>T maps to NM_012479.3 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:43088960 A>G maps to NM_006955.1 C479C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:50945278 G>A maps to NM_033200.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:489662 C>T maps to NM_030783.1 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:103141227 G>T maps to ENST00000428762 Y2877*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:38572966 C>T maps to NM_015073.1 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:102028102 C>T maps to NM_001362.3 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:11561810 G>A maps to NM_020780.1 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:30951866 G>A maps to NM_004861.1 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:89349136 C>T maps to NM_013275.4 S1271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:176863859 C>T maps to ENST00000281881 A934A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:30186500 C>A maps to NM_032204.3 E687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:13256125 G>A maps to NM_003765.1 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:151129809 G>A maps to NM_004961.3 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:177546610 C>T maps to NM_015111.1 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:152484303 C>A maps to NM_178438.4 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:179192981 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:204409449 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:140530485 C>T maps to NM_018939.2 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:46657568 C>T maps to NM_001010870.2 F568F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:166902390 C>T maps to ENST00000510118 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:4028839 C>T maps to NM_015897.2 Y265Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:16047045 C>T maps to ENST00000025399 Q170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:46206617 G>A maps to NM_005897.2 R227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:32498115 G>A maps to NM_000343.3 T519T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:10168305 C>A maps to NM_001129998.1 G220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:118738811 G>A maps to NM_001127211.1 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:172411147 G>A maps to NM_024843.3 W224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:117037382 T>C maps to NM_002269.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:175636705 A>C maps to NM_006529.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:177569659 G>A maps to NM_022762.3 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:3205978 C>T maps to ENST00000380989 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:25268580 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:18552634 C>T maps to NM_004570.4 F682F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:54782895 G>A maps to ENST00000391747 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:45668401 G>A maps to NM_024108.1 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:47471176 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:12958424 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:59964894 G>A maps to NM_004330.2 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:79059867 G>A maps to ENST00000258883 A904A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:41467267 C>T maps to NM_178819.3 F110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:234299128 G>A maps to NM_152879.2 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:135073904 C>T maps to NM_032536.2 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:57175213 G>A maps to NM_001005850.1 C473C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:76592576 C>T maps to NM_033401.3 F1307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:22926591 C>T maps to NM_006043.1 F271F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:66914272 T>C maps to NM_007168.2 Q614Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:54219399 C>T maps to NM_014464.3 R406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:150395 G>A maps to ENST00000399953 A247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:89657064 G>A maps to NM_052941.4 D265D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:139325492 C>T maps to NM_019892.3 T542T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:31560587 G>A maps to NM_000379.3 N1290N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:204985537 C>T maps to ENST00000367172 G1305G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:134071913 G>T maps to NM_032961.1 G207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:11317061 G>A maps to NM_004958.3 Y144Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:179458928 C>T maps to NM_133378.4 T16829T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:129566324 C>T maps to NM_133448.2 E634E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:59027843 C>T maps to NM_032792.2 E399E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:72345378 C>T maps to NM_153209.3 I368I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:205275354 C>T maps to ENST00000441520 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:136700898 T>C maps to NM_001006628.1 C429C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:67018038 G>A maps to NM_012308.2 Q846Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:23812377 T>C maps to NM_005664.3 D483D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:23300345 G>A maps to ENST00000435486 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:16593732 G>T maps to NM_014695.1 E7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:50905843 C>A maps to ENST00000337034 E168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:27071172 T>C maps to NM_021219.2 N193N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:76482323 G>T maps to ENST00000389840 G2347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:58477895 A>G did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:10225212 C>T maps to NM_001040664.2 G728G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:701861 G>A maps to NM_145294.4 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:43033295 C>T maps to ENST00000458501 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:144892213 C>A maps to NM_001002812.1 *970Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:117187660 G>A maps to NM_001109903.1 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:27382724 C>T maps to NM_014915.2 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:154174797 T>C maps to ENST00000377643 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:119961569 C>T maps to NM_178499.3 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:121980655 G>A maps to NM_001178065.1 V258V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:132554068 C>T maps to ENST00000333577 G3004G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:53907061 C>T maps to NM_022899.4 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:12955493 G>A maps to NM_001013437.1 W65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:3660907 G>A maps to ENST00000418971 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:114968226 C>T maps to NM_015906.3 Q513Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:120989207 A>G maps to NM_005422.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:55668951 C>T maps to ENST00000344887 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:63525707 C>T maps to NM_173554.2 N188N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:84104309 T>C maps to NM_003791.2 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:39448646 C>T maps to NM_207361.4 I2735I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:5323022 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:56417656 G>A maps to ENST00000361203 Y5100Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:93529576 C>T maps to NM_004268.4 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:96909107 C>T maps to NM_152327.2 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:18305799 C>T maps to NM_032683.2 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:52338702 C>T maps to NM_002748.3 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:17910774 C>T maps to NM_001166139.1 E208E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:14798937 G>A maps to NM_032137.4 P667P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:39264039 C>T maps to NM_207361.4 H853H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:46628301 C>T maps to NM_002146.4 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:181767891 C>T maps to ENST00000357570 R2288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:46443144 G>A maps to NM_002516.2 A485A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:22439019 G>A maps to NM_021630.5 S324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:1396175 C>T maps to NM_003933.4 C804C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:166805949 A>G maps to NM_024753.3 C72C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:32560064 G>T maps to NM_001030055.1 G64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:42956440 G>A maps to NM_001134656.1 T318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:25815741 G>A maps to NM_018202.4 K525K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:67215737 C>A maps to NM_080282.3 G160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:65461484 G>A maps to NM_007191.4 H208H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:16343173 G>A maps to NM_138381.3 E158E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:72916087 G>A maps to NM_173477.2 D281D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:113075179 C>T maps to ENST00000316851 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:111559250 G>A maps to NM_001142807.1 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:70486760 C>T maps to NM_020794.2 A460A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:8209803 G>A maps to NM_032447.3 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:12598478 G>A maps to NM_152271.3 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:27789046 C>T maps to NM_015202.2 T1556T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:205983692 G>A maps to ENST00000406610 K243K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:102514984 C>T maps to NM_001376.4 L4451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:112017852 C>T maps to NM_019114.3 T369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:3146886 C>T maps to NM_002111.6 C1025C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:103667817 G>A maps to NM_005655.2 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:77850826 C>T maps to NM_020927.1 N81N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:116856513 C>T maps to ENST00000259410 Q415Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:29935581 T>C maps to NM_014271.3 G260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:131669895 G>A maps to NM_001127244.1 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:140208857 T>C maps to NM_018909.2 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:33588746 C>T maps to NM_018025.2 D313D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:141163404 G>A maps to NM_001080412.2 S725S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:21830443 G>A maps to NM_007192.3 R569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:233122220 G>A maps to NM_014801.3 L1953L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:50685800 C>T maps to NM_005311.4 Q271Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:183911152 C>T maps to NM_018358.2 C628C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:127714630 C>T maps to NM_014390.2 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:101125089 G>A maps to NM_005458.7 I600I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:19707734 C>T maps to NM_002688.5 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:40571781 C>T maps to NM_001098414.1 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:110884175 C>T maps to NM_022768.4 R717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:56389919 G>A maps to NM_004758.2 S754S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:5498208 C>T maps to NM_001047160.1 R453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:50385984 G>A maps to NM_006545.4 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:103174848 G>A maps to NM_015156.2 W233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:101047325 G>A maps to NM_020654.3 R954*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:69148646 C>A maps to NM_005329.2 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:29999165 C>T maps to NM_016151.2 P1191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:178427267 C>T maps to ENST00000263528 N936N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:114279142 C>T maps to NM_001148.4 S3123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:160128805 T>C maps to NM_144699.3 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:109964293 C>T maps to NM_001099289.1 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:48718061 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:181687257 G>A maps to ENST00000357570 G531G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:67710850 T>G maps to NM_013257.3 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:114288233 C>T maps to NM_007111.4 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:31082530 G>A maps to NM_015194.1 H482H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:4841115 G>A maps to NM_003562.4 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:52496963 G>A maps to ENST00000354939 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:42626569 C>A maps to NM_006095.2 E116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:75444878 A>C maps to NM_139137.2 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:12863438 C>T maps to NM_017682.2 N11N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:30316880 C>T maps to NM_020848.2 T732T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:152673221 A>G maps to NM_182961.2 H3840H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:168108245 C>T maps to NM_152381.5 G3448G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:100813092 G>A maps to NM_173701.1 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:98376417 C>T maps to NM_152309.2 K664K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:24527938 C>A maps to NM_138360.3 T481T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:3446678 C>T maps to ENST00000511533 G325G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:9002320 T>C maps to NM_144670.3 S695S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:10582263 C>A maps to NM_006691.3 E161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:32784834 C>T maps to NM_212558.2 Y218Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:72239557 C>T maps to NM_032646.5 C227C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:120182659 C>T maps to NM_012084.3 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:39770547 C>T maps to NM_004711.4 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:63544451 G>A maps to NM_000706.3 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:65243636 C>T maps to NM_003038.4 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:105836071 G>T maps to NM_000494.3 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:113813024 C>T maps to ENST00000342783 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:20215652 C>T maps to NM_172194.1 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:158223400 G>A maps to NM_024007.3 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:20215097 G>A maps to NM_007138.1 W18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:1264985 C>A maps to ENST00000447027 R2295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:9623248 A>G maps to NM_003747.2 R1165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:201337289 C>A maps to ENST00000421663 E55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:35068237 C>T maps to ENST00000339266 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:127417663 G>A maps to ENST00000356792 E295E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:69719829 C>T maps to ENST00000194900 I724I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:43533873 T>C maps to NM_006451.4 T406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:34935090 C>T maps to NM_015245.2 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:142176354 G>A maps to NM_014957.2 S460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:36205966 G>T maps to NM_014383.1 E147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:144940248 C>T maps to NM_031308.1 T2391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:57766262 C>T maps to NM_178457.1 Y63Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:2811513 C>T maps to NM_014878.4 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:53518625 C>T maps to NM_001160148.1 S819S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:11180275 C>T maps to NM_015458.3 D543D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:13941764 C>T maps to NM_023072.2 P957P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:111999343 T>G maps to NM_001688.4 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:138824679 C>T maps to NM_024926.2 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:133919107 C>A maps to NM_003235.4 R1270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:35680004 C>T maps to NM_001003681.2 R422R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:113518957 G>A maps to NM_198123.1 T1619T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:65706098 T>C maps to NM_003596.3 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:180308081 G>T maps to NM_152520.4 P437P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:18901371 G>A maps to NM_000095.2 C72C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:150930354 G>T maps to NM_001447.2 P1458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:54416251 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:131859758 G>A maps to NM_001115.2 L805L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:74228448 C>T maps to NM_001402.5 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:139890401 G>A maps to NM_152888.1 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:118039320 G>A maps to NM_004588.4 C72C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:70644061 G>A maps to NM_001130161.2 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:26107045 C>A maps to NM_005160.3 P469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:101017622 G>A maps to NM_018421.3 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:42136769 C>T maps to NM_005090.3 C558C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:233244472 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:656305 C>T maps to NM_148959.3 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:52658886 T>C maps to NM_001102657.1 K683K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:10073914 T>C maps to NM_005680.2 Y523Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:179743449 A>C maps to NM_005110.2 V388V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:121757498 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:228459770 C>T maps to ENST00000359599 D456D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:94732005 C>A maps to NM_018039.2 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:4099232 C>T maps to NM_030662.3 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:845592 C>T maps to NM_005255.2 S1151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:58605362 A>C maps to ENST00000438670 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:40884076 C>A maps to NM_012268.2 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:6647792 C>T maps to NM_003737.2 Q2118Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:75511174 C>T maps to NM_001040456.1 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:27071138 C>T maps to NM_004295.3 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:48621003 C>T maps to NM_000094.3 G1462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:23693420 T>G maps to NM_005030.3 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:17611249 A>G maps to NM_001001924.2 T689T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:32475212 C>A maps to NM_021209.4 E574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:154216604 C>T maps to NM_015271.3 N309N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:53855358 T>C maps to NM_138374.1 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:138968548 T>C maps to NM_173569.3 C966C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:145151979 C>A maps to NM_001916.3 T272T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-IB-7651-01A-11D-2154-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:20404103 C>A maps to NM_001004063.2 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:45489786 C>T maps to NM_001294.2 D249D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:121031010 C>T maps to NM_005422.2 C1619C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:65682503 G>T maps to NM_020962.1 T799T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:93978385 G>A maps to NM_001698.2 V299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:77580102 G>A maps to NM_033426.2 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:98513912 C>T maps to NM_183376.2 C380C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:147381089 G>A maps to NM_005267.4 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:32827616 A>G maps to ENST00000357033 D214D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:198540074 G>A maps to NM_144629.2 Y36Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:127622436 G>A maps to NM_001999.3 R2329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:86934770 C>T maps to NM_001285.3 I39I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:112154760 T>C maps to NM_001127510.2 C344C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:4835935 C>T maps to NM_017417.1 N150N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:86010636 G>A maps to NM_153184.3 W263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:13639486 G>A maps to NM_003675.3 E32E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:156468457 C>T maps to NM_001184997.1 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:65129423 T>G maps to ENST00000371073 Y666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:233274416 G>A maps to NM_031313.2 A478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:35578669 T>C maps to NM_024772.3 S413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:114070552 G>A maps to NM_001164342.1 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:113328754 C>T maps to NM_001143854.1 C574C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:47373546 G>A maps to NM_001080467.2 D1476D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:166848891 G>T maps to NM_001165963.1 S1631S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:113522120 T>C maps to NM_002711.3 E313E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:70852661 C>T maps to NM_001858.4 Q526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:71863049 C>T maps to NM_004817.3 G930G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:43783484 C>T maps to NM_003225.2 Q39Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:113822070 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:36984337 C>T maps to NM_001130010.1 N146N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:107145729 G>T maps to NM_004093.2 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:39886549 C>T maps to NM_003246.2 I1138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:210415324 G>A maps to NM_019605.3 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:41040187 C>T maps to NM_020971.2 L1433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:19882712 G>T maps to ENST00000334363 I320I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:93768636 C>T maps to NM_003972.2 L1289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:86800202 G>A maps to NM_152336.2 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:89016715 G>A maps to NM_004827.2 L565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:40827958 G>A maps to ENST00000373198 A826A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:181701984 C>T maps to ENST00000357570 S921S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:45713015 G>A maps to NM_000383.2 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:31096483 G>A maps to NM_001039503.2 G327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:63823666 G>A maps to NM_025075.2 R113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:180837940 C>T maps to NM_020943.2 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:1956824 C>A maps to NM_000815.4 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:126369631 G>A maps to NM_024582.4 A2487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:148801588 G>A maps to NM_001001661.2 R458R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:160112843 C>T maps to NM_001128212.1 W332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:9781552 C>T maps to ENST00000361110 Y645Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:187386921 C>T maps to NM_001048.3 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:190728550 C>T maps to NM_000534.4 L647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:173316987 A>G maps to NM_030627.2 Q84Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:116353675 C>T maps to NM_144488.4 L1027L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:59344624 C>T maps to ENST00000434298 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:130992361 A>C maps to NM_024800.4 P554P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:50548035 C>T maps to NM_015428.1 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:64607740 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:58596627 C>T maps to NM_001145542.1 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:135615145 A>C maps to NM_020863.3 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:30863425 G>A maps to ENST00000417045 N945N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:17937566 G>T maps to NM_000215.3 S1120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:11895999 G>T maps to NM_144680.2 Y49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:75949348 C>T maps to NM_153271.1 G506G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:32165081 G>T maps to NM_004557.3 V1682V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:1519140 G>A maps to ENST00000389470 G1622G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:120568521 G>A maps to NM_006836.1 G2533G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:108169234 C>T maps to NM_203436.2 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:139752882 C>T maps to ENST00000392881 G985G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:186330802 T>C maps to NM_003292.2 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:67472758 G>A maps to NM_004691.4 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:89708989 T>C maps to NM_014883.2 G395G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:43442564 C>T maps to NM_012263.4 P331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:53224075 C>T maps to NM_175834.2 K233K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:39855320 G>A maps to ENST00000398904 S671S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:57913874 C>T maps to NM_001018090.3 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:28602222 C>T maps to NM_138414.2 F244F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:139907733 G>A maps to ENST00000355090 L1559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:39872829 C>T maps to NM_194294.2 I324I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:26300999 C>T maps to NM_000437.3 Q300Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:22864732 A>G maps to NM_001160036.1 Q347Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:33630417 G>A maps to ENST00000374316 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:43482415 G>A maps to ENST00000428638 D374D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:233136191 G>A maps to NM_014801.3 H1729H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:155556567 G>A maps to NM_053043.2 P1014P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:33623337 A>G maps to ENST00000359576 S775S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:183532663 C>T maps to NM_001127651.2 T361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:38724746 G>A maps to NM_175060.1 R161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:20890163 T>C maps to NM_017435.4 C502C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:43305786 T>C maps to NM_014345.2 Q1983Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:109689672 C>T maps to NM_021224.4 V1160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:50479663 G>T maps to NM_001080447.1 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:153598819 G>A maps to NM_001024210.1 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:6181168 C>T maps to NM_015557.2 P1636P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:141283539 G>A maps to NM_018557.2 F2633F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:64641902 C>T maps to NM_006795.2 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:16232604 C>A maps to NM_005370.4 Y77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:140640599 G>A maps to ENST00000509479 G1098G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:66937402 C>T maps to NM_000044.2 R753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:67306217 C>T maps to NM_024763.4 W476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:129793150 G>A maps to NM_020228.2 Q680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:42343376 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:201786358 C>T maps to ENST00000367296 P1828P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:39361853 G>A maps to NM_001195833.1 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:115601595 G>A maps to NM_005725.4 R118*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-IB-7651-01A-11D-2154-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:31289170 G>A maps to NM_030758.3 W644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:89758864 C>T maps to NM_052988.4 C142C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:3175984 C>T maps to NM_023935.1 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:41621207 C>T maps to NM_005586.3 C212C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:24455728 T>C maps to NM_012295.3 F434F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:158548723 A>G maps to NM_001004477.1 V322V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:149128929 G>A maps to ENST00000440594 C812C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:78477490 G>A maps to ENST00000377211 R291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:101295516 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:130027776 G>A maps to NM_001868.2 Q395Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:8871625 G>A maps to NM_020738.2 L1514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:2042718 G>A maps to NM_004209.5 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:40316645 C>T maps to NM_004714.1 S533S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:128839217 G>A maps to NM_001142685.1 R1950*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:71364627 G>T maps to NM_001144952.1 A1695A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:23354090 G>T maps to NM_173527.2 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:6017314 G>A maps to NM_000535.5 V783V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:69348990 C>T maps to NM_024505.3 G751G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:62856944 G>A maps to NM_199340.2 Q1107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:54556522 G>A maps to ENST00000260323 Q1202Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:94643258 C>T maps to NM_004815.3 E938E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:66359859 G>T maps to NM_018219.2 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:11400936 G>A maps to NM_005114.2 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:57111860 C>T maps to NM_032206.3 G1670G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:46717606 G>A maps to NM_004308.2 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:99456413 C>T maps to NM_000875.3 Y577Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:77427276 C>A maps to NM_017662.4 E461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:85473689 G>A maps to NM_001080508.1 D70D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:56667669 C>A maps to NM_176870.2 C34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:43623455 G>A maps to NM_173050.2 C377C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:99226446 C>T maps to ENST00000409347 D92D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:42403027 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:45918172 C>T maps to NM_202001.2 E216E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:156639790 G>A maps to NM_006617.1 L1397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:111936362 A>G maps to NM_021994.2 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:582312 C>T maps to NM_001728.2 D359D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:27326380 C>A maps to ENST00000396636 E621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:45260656 C>T maps to NM_005178.4 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:59065516 G>A maps to NM_014453.2 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:241829556 C>T maps to NM_001085437.1 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:19789532 A>C did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:134090666 T>C maps to ENST00000451030 S1888S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:15780057 C>T maps to NM_001775.2 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:79077822 G>A maps to NM_017451.2 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:152737754 G>A maps to NM_182961.2 I1939I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:34923063 G>A maps to NM_138927.1 T509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:76936002 T>C maps to NM_144660.2 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:62366959 G>A maps to NM_176877.2 E1070E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:8197810 G>A maps to NM_201520.1 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:200824038 T>C maps to NM_024520.2 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:892378 C>T maps to NM_015658.3 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:191797506 G>A maps to ENST00000338435 W572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:123794272 A>G maps to NM_001167856.1 Y1142Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:100170651 A>G maps to ENST00000489752 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:32852675 C>T maps to NM_023037.2 S2820S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:5153585 G>A maps to NM_002234.2 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:16351369 C>A maps to NM_004070.3 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:23028929 G>T maps to NM_000361.2 C404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:178785486 C>T maps to NM_022470.3 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:64664488 A>G maps to NM_001170633.1 T530T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:137814818 G>A maps to NM_175747.2 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:112770311 G>A maps to NM_032028.3 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:1459849 C>T maps to NM_000547.5 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:56230076 C>T maps to NM_001004743.1 E267E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:62285754 A>G maps to NM_001620.1 G5378G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:79175615 G>A maps to NM_004796.4 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:41125324 C>A maps to ENST00000308370 L1114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:15212015 C>T maps to NM_031898.2 P407P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:55524377 C>T maps to NM_001005243.1 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:144240262 G>A maps to NM_001130478.1 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:85637249 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:9970067 G>A maps to NM_153461.2 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:47560057 G>A maps to NM_020453.3 V734V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:92838006 C>A maps to ENST00000453812 E323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:103565853 A>C maps to NM_012215.3 Y233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:46679084 G>A maps to NM_001872.3 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:216249592 G>A maps to NM_212482.1 Y1573Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:61729059 G>A maps to NM_017780.2 E871E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:27372992 C>T maps to NM_175769.2 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:39880298 G>T maps to NM_019088.2 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:94619985 G>A maps to NM_024717.4 N98N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:2760912 G>A maps to NM_199460.2 W1399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:4382439 C>G maps to NM_032575.2 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:19076974 C>T maps to NM_005137.2 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:17764837 G>A maps to NM_001082968.1 V410V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:124457632 G>A maps to NM_001010912.1 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:56811477 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:94965136 C>T maps to ENST00000454898 D593D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:99797351 A>G maps to NM_138798.1 Y31Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:28980977 C>T maps to NM_015254.3 A1128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:207222955 G>A maps to NM_018566.3 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:74313255 G>A maps to NM_001134.1 T307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:3209044 C>A maps to NM_001174090.1 R849R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:71726973 C>T maps to ENST00000393695 K531K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:56276416 G>A maps to NM_000502.4 T379T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:52198923 T>G maps to NM_006526.2 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:44599952 C>A maps to NM_022095.3 E33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:619546 C>T maps to NM_000283.3 C44C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:140785570 C>T maps to NM_080862.1 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:53348187 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:139341760 G>A maps to NM_014866.1 S2205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:122620103 G>A maps to NM_014938.3 P641P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:40062788 G>A maps to ENST00000401700 V340V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:93814405 G>A maps to NM_182971.2 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:7640252 G>A maps to NM_004244.4 R584R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:131107823 C>A maps to NM_005094.3 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:40433215 T>C maps to NM_003890.2 V351V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:96163598 A>C maps to NM_003728.3 T363T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:143085747 C>T maps to NM_001010972.1 Y437Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:488248 C>T maps to NM_030783.1 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:53716508 A>G maps to NM_004631.3 S843S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:21487719 A>C did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:49119336 G>A maps to NM_000979.2 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:3025458 C>T maps to NM_001501.1 R97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:216465664 A>C maps to ENST00000366943 G564G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:14819311 G>A maps to ENST00000380880 H825H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:42824841 C>T maps to NM_145663.2 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:106875686 G>T maps to NM_001042550.1 E449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:814918 C>T maps to NM_013404.4 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:52181053 C>T maps to NM_015426.4 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:56172410 T>C maps to NM_007279.2 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:48503734 G>A maps to NM_015030.1 R2833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:101731891 T>G maps to NM_014503.2 V1235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:42196271 G>A maps to NM_033502.2 P1138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:148768237 G>A maps to NM_152411.3 C542C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:64081399 C>T maps to NM_005869.2 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:16673838 G>A maps to NM_012334.2 G1708G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:43353496 G>A maps to NM_003881.2 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:117556223 T>C maps to NM_004258.3 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:12613661 G>A maps to NM_014160.3 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:171177941 A>G maps to NM_001460.2 E422E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:39847483 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:140724706 C>T maps to NM_018916.3 I369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:14862335 G>A maps to NM_152536.3 S586S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:41657700 G>A maps to NM_016359.3 R254R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:32947694 C>T maps to ENST00000395289 Y679Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:132561977 G>A maps to ENST00000333577 A3080A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:9862344 C>T maps to NM_001025930.3 I358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:32133783 C>A maps to NM_001856.3 T1095T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:62007650 G>A maps to NM_001039933.1 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:4945600 C>T maps to NM_002705.4 E363E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:85901276 G>A maps to ENST00000436406 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:2717684 G>A maps to NM_145173.3 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:42647385 C>T maps to NM_012105.3 S464S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:3129400 C>T maps to NM_004332.2 Y167Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:665886 C>T maps to NM_173593.3 V745V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:24650999 G>A maps to ENST00000458132 R953*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:8197102 G>A maps to NM_001080826.1 S735S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:114282485 G>A maps to NM_016196.3 A924A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:23282280 C>T maps to NM_001126106.1 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:71490171 G>A maps to NM_005909.3 E330E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:72301398 C>A maps to NM_023036.4 I343I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:83992883 C>A maps to NM_013370.3 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:10212990 G>A maps to NM_003802.2 L1605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:219602419 G>A maps to NM_014640.4 Q7Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:36037430 C>T maps to NM_032635.2 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:51390674 C>T maps to NM_001174125.1 Q281Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:309974 C>A maps to NM_032039.2 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:42042629 G>A maps to ENST00000219905 L2324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:74435775 C>T maps to NM_006636.3 R164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:29754581 G>T maps to NM_021738.2 P2025P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:60696111 C>T maps to NM_017870.3 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:72138494 T>C maps to NM_014003.3 R707R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:98744053 C>T maps to NM_015652.2 G969G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:125530374 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:6637889 A>G did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:67768122 C>A maps to NM_001031715.2 I922I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:22902011 G>A maps to NM_015461.2 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:107126801 G>A maps to ENST00000357881 V533V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:24056619 G>A maps to NM_001142730.1 I664I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:139243185 G>A maps to NM_001145638.1 E415E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:30315767 G>A maps to NM_020848.2 I1103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:58117675 C>T maps to NM_020880.3 H261H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:189349339 G>A maps to NM_003722.4 Q12Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:132848733 T>C maps to NM_001136557.1 N200N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:20800759 G>A maps to NM_032775.3 N503N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:153627921 G>A maps to NM_006013.3 Q59Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:110501444 G>A maps to NM_020809.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:140728841 C>T maps to NM_024757.4 N1194N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:174254338 C>T maps to NM_002129.3 K59K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:12298498 C>T maps to NM_003437.3 R436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:50796919 C>T maps to NM_001145809.1 D1815D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:164735362 G>A maps to NM_001041.3 D1244D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:226413511 G>A maps to NM_031944.1 *233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:650571 G>A maps to NM_015721.2 C237C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:55194080 T>C maps to NM_004623.4 N219N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:143792475 C>A maps to NM_001004135.1 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:2139875 G>A maps to NM_017575.4 L927L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:72889424 G>T maps to NM_014989.4 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:66472169 G>A maps to NM_006946.2 S859S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:56505029 C>A maps to NM_006191.2 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:38047332 C>T maps to NM_015873.3 A667A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:6958343 G>A maps to NM_031299.4 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:35842554 G>A maps to ENST00000360192 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:64120044 C>T maps to NM_002633.2 R503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:61511391 G>A maps to NM_033081.2 V1972V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:136513181 T>G maps to NM_014607.3 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:75975289 C>T maps to NM_001897.4 E1514E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:100965572 G>A maps to NM_018421.3 S756S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:119699911 C>A maps to NM_006770.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:720169 G>A maps to NM_138769.1 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:153947166 G>A maps to NM_006694.3 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:24243245 C>T maps to NM_018647.2 R419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:3432401 C>A maps to NM_198229.2 A1278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:34001296 C>T maps to NM_001030006.1 L761L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:167096290 G>A maps to NM_001080426.1 Q641Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:10927524 C>T maps to NM_001040274.2 D455D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:37605151 G>A maps to ENST00000297153 Q957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:40275427 G>T maps to NM_015460.2 G662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:5340231 C>T maps to NM_153247.2 F463F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:101536358 G>A maps to ENST00000375018 R541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:50904431 C>T maps to ENST00000337034 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:56094324 T>C maps to NM_001039349.1 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:113416787 G>A maps to NM_005415.3 V352V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:36905733 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:39541020 G>A maps to NM_145286.2 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:7256608 C>T maps to NM_001002914.2 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:153800601 G>A maps to NM_020699.2 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:156639368 G>T maps to NM_006617.1 G1537G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:49690579 G>A maps to NM_003458.3 L1197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:154702680 G>A maps to NM_003013.2 I270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:89348196 T>G maps to NM_013275.4 R1585R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:52887624 A>G maps to NM_001145434.1 G264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:207620180 G>A maps to NM_001039845.1 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:37679423 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:15534372 A>G maps to NM_015909.2 L1079L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:33298083 G>A maps to NM_021202.1 Q212Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:49168979 G>T maps to NM_002292.3 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:31324317 C>T maps to NM_030632.1 G1502G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:174940558 C>T maps to NM_022754.5 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:216270487 A>G maps to ENST00000366943 N1565N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:130185004 C>T maps to NM_133448.2 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:12371469 G>A maps to NM_032867.2 S605S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:96392275 G>A maps to NM_005392.3 E41E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:33806673 G>T maps to ENST00000361112 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:141012422 G>T maps to ENST00000277549 E1936*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:128204708 G>A maps to NM_032638.4 H244H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:33259940 C>A maps to NM_004761.3 G758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:8998462 G>T maps to NM_024607.2 I233I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:1629123 G>A maps to ENST00000435392 C113C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:1265996 G>A maps to ENST00000447027 T2632T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:1240705 C>T maps to NM_182632.2 Y302Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:61513635 G>A maps to NM_033081.2 D1224D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:42781272 C>T maps to NM_144719.3 Q339Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:143175312 C>T maps to NM_176883.2 H116H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:72913910 G>A maps to NM_175907.4 C198C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:36049966 G>A maps to NM_005584.4 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:33797019 G>T maps to ENST00000419414 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:9639634 C>T maps to NM_024106.1 K362K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:93730243 G>A maps to NM_001002860.2 R420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:57929365 C>T maps to NM_006959.2 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:47195736 G>A maps to NM_030790.3 R529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:44636173 G>A maps to NM_013362.2 S469S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:204320200 G>A maps to ENST00000374493 R473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:52497299 A>C maps to ENST00000354939 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:227945156 A>G did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:94257603 C>T maps to NM_001099401.1 W100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:212251573 T>G maps to NM_016448.2 S365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:156641101 C>A maps to NM_006617.1 E960*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:89861730 G>A maps to NM_152999.3 E422E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:51021715 G>A maps to NM_001080457.1 D418D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:7169899 G>T maps to NM_001734.3 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:154142945 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:179612428 C>A maps to ENST00000375038 E4902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:109765459 G>A maps to NM_022765.3 A1046A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:40739055 G>A maps to ENST00000373198 C1079C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:108923969 G>A maps to NM_001013031.1 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:47228836 G>A maps to NM_001039877.1 D446D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:178425860 C>T maps to ENST00000263528 T728T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:73145310 G>A maps to NM_004097.2 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:205027765 C>A maps to NM_005076.3 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:5475515 G>A maps to NM_001004754.2 K266K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:138603903 C>T maps to NM_001164665.1 E156E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:42874460 T>C maps to ENST00000251268 L2319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:4449012 C>T maps to NM_001105538.1 L655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:21134136 G>A maps to NM_000185.3 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:17277376 C>A maps to NM_003380.3 G406G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:9416402 C>T maps to NM_025106.3 H151H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:155219555 A>C maps to NM_017639.3 Y1515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:47686900 G>A maps to NM_003906.3 S928S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:64027453 C>T maps to NM_032437.2 R475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:85840344 G>A maps to NM_001861.2 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:19868150 G>A maps to NM_006440.3 Y392Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:107040249 C>T maps to ENST00000304514 K1391K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:44845468 C>T maps to NM_021248.1 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:21084354 T>C maps to NM_013326.3 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:66192583 G>A maps to NM_178864.3 S741S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:9605703 G>A maps to NM_003747.2 T938T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:136481789 T>C maps to ENST00000409606 V1077V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:70698335 G>T maps to NM_138383.2 C496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:42162666 A>G maps to ENST00000320955 L1847L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:47042767 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:89167208 G>A maps to NM_174917.2 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:207669656 G>A maps to NM_000651.4 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:17113892 A>G maps to NM_001081.3 S793S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:98535412 C>T maps to ENST00000359863 S1458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:63852704 C>T maps to NM_032199.2 S1161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:2347330 G>A maps to NM_001089.2 Y754Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:131749133 C>T maps to NM_015354.1 H748H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:71236359 G>A maps to NM_001162529.1 S1191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:81192457 G>A maps to NM_153367.3 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:52470605 C>T maps to NM_021934.4 Q97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:1805954 G>A maps to NM_138813.2 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:177073090 C>A maps to NM_170710.4 Y835*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:73753261 G>A maps to NM_003388.4 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:50088030 C>A maps to NM_002408.3 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:84056479 G>A maps to NM_001080442.1 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:141312860 C>T maps to NM_014773.3 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:130275524 G>T maps to NM_007037.4 A866A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:2256399 T>C maps to NM_022372.4 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:56585788 T>C maps to NM_018181.4 H90H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:103441550 G>A maps to NM_024089.2 I368I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:36029469 C>T maps to NM_001014839.1 T571T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:18054175 G>A maps to ENST00000205890 T2474T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:11361632 C>A maps to ENST00000319867 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:123337591 C>T maps to NM_053025.3 E1798E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:31905858 C>T maps to NM_178865.4 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:7615444 G>A maps to NM_001166111.1 G672G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:179201460 C>T maps to NM_014757.4 S878S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:151996393 G>A maps to NM_004344.1 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:94731921 T>G maps to NM_018039.2 A462A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:15990670 G>T maps to NM_001082.3 C384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:44582470 G>A maps to NM_022095.3 G853G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:66459842 C>T maps to NM_001164664.1 S1612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:27021477 G>A maps to NM_001886.2 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:113970913 C>T maps to NM_001148.4 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:784811 G>A maps to NM_022493.1 R167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:144991208 G>A maps to NM_201380.2 P4397P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:7950053 G>A maps to NM_001004461.1 D52D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:41749443 G>A maps to NM_003924.3 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:231339670 G>A maps to NM_001004342.3 T531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:156640643 G>A maps to NM_006617.1 G1112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:1820032 G>T maps to NM_020695.3 A850A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:74009399 C>T maps to NM_000521.3 R281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:77287541 C>T maps to NM_172387.1 R920*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:5248008 C>T maps to NM_000518.4 W38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:15260580 C>T maps to NM_001031853.3 R499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:101370677 G>A maps to NM_031212.3 I341I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:48506303 C>T maps to NM_130384.1 T710T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:75653520 G>A maps to NM_006715.2 T442T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:10419698 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:3133502 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:6790158 G>A maps to NM_001004490.1 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:41600273 C>T maps to NM_000766.3 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:150776914 C>T maps to NM_006712.3 Q59Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:196678896 C>T maps to NM_025163.2 Q2Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:45992144 C>T maps to NM_005619.3 R447R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:115099860 C>T maps to NM_014333.3 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:124483017 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:222818936 T>C maps to NM_198551.2 D1173D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:38678030 C>T maps to ENST00000379931 D423D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:21861743 G>A maps to NM_001170629.1 D2070D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:52439823 G>T maps to NM_031290.2 E104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:51094993 C>T maps to ENST00000358385 I455I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:84228382 G>A maps to NM_005077.3 S324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:11805263 C>T maps to NM_024693.4 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:43504287 C>T maps to NM_173568.3 D138D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:80064768 C>T maps to NM_002439.3 R734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:24831544 G>A maps to NM_014494.2 L1722L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:7230593 C>T maps to NM_001018039.1 L600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:8062712 G>A maps to NM_001130083.1 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:1346028 C>T maps to NM_178040.2 R816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:183212465 G>A maps to NM_005562.2 K1171K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:1624782 C>T maps to ENST00000357934 R705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:23894564 G>A maps to NM_000257.2 R783R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:122631762 C>T maps to NM_001031702.2 E884E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:54805334 C>A maps to NM_001010872.1 G522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:1291224 G>A maps to NM_178040.2 E670E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:97823514 C>T maps to NM_014916.3 S1246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:118645866 G>A maps to NM_001127211.1 S628S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:44472352 G>A maps to NM_005469.3 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:11990583 T>G maps to NM_002094.3 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:9089903 G>A maps to NM_024690.2 S637S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:17055913 T>C maps to NM_016353.4 H156H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:45459687 G>A maps to ENST00000359524 Q300Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:40889977 C>T maps to NM_144685.3 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:179076765 A>G maps to NM_033540.2 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:52622688 G>A maps to NM_000846.4 I19I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:8953038 C>T maps to NM_014316.2 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:180480218 C>A maps to NM_152547.4 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:41000308 A>G maps to NM_001039590.2 E287E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:232030715 C>T maps to NM_002807.3 Y900Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:47601356 C>T maps to NM_006420.2 Q684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:55587929 C>T maps to ENST00000395203 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:17773499 G>A maps to NM_003385.4 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:14517706 C>T maps to NM_078481.2 T714T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:6924843 G>A maps to ENST00000381407 K651K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:25887905 C>T maps to NM_020752.2 S1117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:149310692 A>C maps to NM_000440.2 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:27263358 A>G maps to NM_017727.4 A646A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:38463500 C>T maps to NM_004468.3 W181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:162834230 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:56144917 G>A maps to NM_001039349.1 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:111936883 C>A maps to NM_019114.3 E885*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:45132742 C>T maps to NM_001198721.1 N284N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:9197372 G>A maps to NM_003966.2 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:198361909 G>A maps to NM_199440.1 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:9090170 G>T maps to NM_024690.2 P548P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:109768372 G>T maps to NM_022765.3 L710L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:51279108 G>T maps to NM_182559.2 G245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:56778459 G>A maps to NM_001017992.2 D25D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:75004463 C>T maps to NM_138703.4 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:114163361 T>C maps to NM_001148.4 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:31766668 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:27170304 C>T maps to NM_002141.4 K16K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:187004175 G>T maps to NM_003265.2 E446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:43262375 G>T maps to NM_007163.3 P885P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:15601858 C>T maps to NM_015909.2 K718K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:143974005 G>A maps to NM_018460.3 K96K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:124464051 C>T maps to NM_015450.2 Q623Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:79094039 C>T maps to NM_001080395.2 V1232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:53590574 G>A maps to NM_000889.1 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:39159265 G>T maps to NM_003740.3 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:7737764 C>A maps to NM_015215.2 S962S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:21116662 G>A maps to NM_000271.4 G1073G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:21224636 C>T maps to NM_004782.3 Q84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:50216320 G>A maps to NM_152359.2 T742T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:76623952 C>T maps to ENST00000428345 Q1215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:131761747 C>T maps to ENST00000355311 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:25183049 G>A maps to NM_024940.6 K630K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:9166621 G>T maps to NM_015213.2 G1014G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:4385274 C>T maps to NM_001759.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:13140661 G>A maps to NM_018327.2 R476R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:54674995 G>T maps to NM_015360.4 V675V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:24905929 C>T maps to NM_003743.4 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:4421789 A>G maps to NM_016930.2 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:176005097 T>C did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:238632192 G>A maps to ENST00000391999 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:88415480 G>T maps to NM_004684.4 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:63084883 C>A maps to NM_015059.2 G1927G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:88485521 G>A maps to NM_018271.3 E445E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:96430576 G>A maps to NM_153234.4 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:120650125 G>A maps to NM_001080855.1 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:103564275 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:42360545 C>T maps to NM_152447.3 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:45867625 C>T maps to ENST00000471951 T848T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:128890614 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:77513681 C>T maps to NM_004715.3 D926D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:57176449 G>A maps to NM_001005850.1 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:2226884 G>A maps to ENST00000221482 A1455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:81571982 C>T maps to NM_172217.3 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:121426281 G>A maps to NM_014078.5 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:148925404 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:220356956 C>T maps to NM_005876.4 R3196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:34861514 G>T maps to NM_001040192.1 C62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:119158837 G>A maps to NM_002581.3 R1609R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:24952419 G>A maps to NM_003743.4 T979T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:160225116 C>T maps to NM_173516.1 N112N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:153998020 G>A maps to NM_207308.2 V1373V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:670815 C>T maps to NM_001071.2 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:71098867 C>T maps to NM_021965.3 G461G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:247014213 A>C maps to ENST00000428671 P1736P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:43694615 G>A maps to ENST00000374459 R300R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:21494151 G>A maps to NM_002509.2 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:77613622 A>G maps to NM_152420.1 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:177034311 G>A maps to NM_007255.2 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:86225398 C>A maps to NM_006738.4 P1708P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:187178450 C>T maps to ENST00000511608 Q600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:118949920 C>T maps to NM_021729.4 S782S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:43738920 C>A maps to NM_144626.2 C176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:66460374 C>T maps to NM_001164664.1 L1790L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:239234547 G>A maps to NM_015650.3 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:44278572 G>A maps to NM_002250.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:111493991 C>A maps to NM_018593.4 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:100006217 G>T maps to NM_017984.3 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:80197364 G>A maps to NM_181714.3 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:33625356 G>A maps to NM_018207.2 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:133827071 T>G maps to ENST00000395386 L375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:24289406 G>A maps to NM_203282.2 W72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:70605706 C>T maps to NM_012426.4 Y1215Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:1563836 C>T maps to NM_006445.3 T1558T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:21561401 C>T maps to NM_001102454.1 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:43634901 G>A maps to NM_173050.2 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:41333653 G>A maps to NM_022567.2 V316V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:176785033 G>T maps to ENST00000398128 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:9631499 C>T maps to NM_153210.3 G855G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:21771699 C>T maps to NM_032264.2 R41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:26216589 C>T maps to NM_003518.3 E94E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:54932492 T>C maps to ENST00000391739 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:26380399 T>G maps to NM_032588.2 T345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:9236903 G>A maps to NM_001001958.1 C241C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:202150029 C>T maps to NM_001080125.1 R491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:4841498 G>A maps to NM_003562.4 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:5016924 C>A maps to NM_018659.2 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:47865892 C>T maps to NM_014681.5 F512F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:47787441 C>T maps to NM_145020.3 Q155Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:18112761 C>T maps to NM_002252.3 R163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:25917917 C>T maps to ENST00000268763 C299C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:902749 A>G did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:74049646 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:2606515 G>A maps to NM_000218.2 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:42744439 C>T maps to NM_020433.4 K625K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:56155657 T>C maps to NM_005921.1 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:70226018 C>T maps to NM_020794.2 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:42837895 G>A maps to ENST00000251268 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:56283998 G>A maps to NM_018475.3 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:1154013 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:2097345 C>T maps to NM_080836.3 C309C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:36295808 C>T maps to NM_032352.3 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:66448535 C>T maps to NM_001164664.1 R1123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:48238711 G>A maps to NM_001017535.1 I367I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:112963455 C>T maps to NM_001012993.2 Q164Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:152468846 G>A maps to NM_001164507.1 G3886G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:46509479 C>T maps to NM_001114172.1 E417E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:33113456 C>T maps to ENST00000375025 R372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:6309845 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:5941724 G>A maps to ENST00000356134 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:4798397 C>T maps to NM_153827.4 L982L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:184079202 A>G did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:139371881 G>A maps to NM_014866.1 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:22618433 C>A maps to NM_005180.6 S315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:5539455 T>C maps to NM_019593.3 Q514Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:228230945 T>G maps to NM_024795.3 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:180055886 G>A maps to NM_182925.4 F366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:103696337 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:10934553 C>T maps to NM_001005361.2 G624G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:60588554 G>A maps to NM_001080512.1 S943S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:119915675 G>A maps to NM_012281.2 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:47556925 T>A maps to ENST00000397748 G527G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:49938139 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:85967451 T>C maps to ENST00000351625 C150C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:107225186 G>A maps to NM_031273.2 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:80282650 G>A maps to NM_003004.2 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:101518813 C>T maps to ENST00000375018 T739T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:160654833 G>A maps to NM_001778.2 Y76Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:111622993 G>A maps to NM_181699.2 I409I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:44943360 G>A maps to NM_003241.3 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:42828512 C>A maps to NM_145663.2 S580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:56658504 C>T maps to NM_018337.2 D75D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:17296825 C>T maps to NM_014675.3 Q1844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:67969888 G>A maps to NM_002801.2 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:33036231 C>T maps to NM_017735.4 L714L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:1109543 C>T maps to NM_014963.2 A1059A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:43344701 G>T maps to NM_017719.4 G3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:16977333 C>T maps to NM_015260.1 S623S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:105151190 C>T maps to NM_018413.5 N223N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:73990975 C>T maps to NM_032217.3 E1096E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:31576880 G>A maps to NM_015382.2 G2170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:41306815 G>T maps to NM_053046.2 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:43484459 C>T maps to NM_015052.3 I563I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:56539008 G>A maps to NM_153447.4 V470V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:89400744 C>A maps to NM_013227.3 P1643P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:69971089 C>T maps to NM_007014.3 N729N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:129906353 G>T maps to NM_002417.4 P1250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:118919075 G>A maps to NM_001130991.1 L754L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:152321119 G>T maps to NM_018151.4 E1696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:6222533 G>A maps to NM_005934.3 G236G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:2749011 G>A maps to NM_033267.4 D270D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:147486673 T>C maps to NM_001127698.1 R518R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:217526594 G>A maps to NM_000597.2 Q229Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:7027153 C>T maps to NM_080657.4 N199N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:61781024 G>A maps to NM_001003787.2 D410D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:10912015 C>T maps to NM_001039362.1 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:48537059 C>T maps to NM_000338.2 R471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:65302804 C>T maps to NM_020680.3 C446C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:19428112 G>T maps to ENST00000375267 A4308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:160466067 C>T maps to NM_001184714.1 W55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:54127091 G>A maps to NM_014614.2 N1116N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:8931979 G>A maps to NM_144693.1 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:57588275 C>T maps to NM_002332.2 R2686R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:78585183 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:32127555 G>T maps to NM_181619.1 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:100617846 C>A maps to NM_033132.3 G592G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:12483764 G>A maps to NM_018050.2 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:77631356 C>T maps to NM_020859.3 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:95363357 G>A maps to NM_001839.3 G310G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:50386979 G>A maps to NM_024682.2 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:160651019 C>T maps to NM_001778.2 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:150915037 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:89587544 C>T maps to NM_004120.3 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:18925280 C>T maps to NM_006613.3 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:26941523 A>C did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:61846504 T>C maps to NM_020987.2 S1226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:677876 C>T maps to NM_005860.2 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:42429450 T>C maps to NM_002087.2 C416C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:111966236 G>A maps to ENST00000369728 D201D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:147807241 A>G maps to NM_205836.1 E795E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:40939315 T>C maps to NM_032387.4 C499C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:10893744 G>A maps to NM_001005361.2 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:111366615 C>T maps to NM_198219.1 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:45805760 C>A maps to ENST00000262891 A684A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:71184617 G>A maps to NM_018161.4 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:46365516 C>T maps to NM_001161841.1 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:105517441 G>A maps to NM_013345.2 T344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:24566203 C>T maps to NM_004563.2 R45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:67233634 G>A maps to NM_024712.3 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:137243501 G>A maps to ENST00000230643 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:52354936 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:119084169 C>T maps to NM_020754.2 Y36Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:120602180 C>A maps to NM_006836.1 G603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:137261572 C>T maps to ENST00000230643 S542S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:34993427 G>A maps to NM_001135005.1 Q138Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:84215020 G>T maps to NM_005679.2 S385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:88449352 C>T maps to NM_025114.3 Q2320Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:143607952 C>T maps to NM_001702.2 D1121D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:50724825 G>A maps to ENST00000404971 L882L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:2749889 G>A maps to NM_033267.4 Y87Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:30361958 C>T maps to ENST00000327564 V696V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:39411912 C>T maps to ENST00000431129 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:213032417 C>T maps to NM_014053.2 C208C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:109088535 A>G maps to NM_181453.3 E917E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:32956757 C>A maps to NM_001076786.1 P1189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:20781392 C>T maps to NM_017774.3 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:52658721 C>T maps to NM_001102657.1 T738T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:68517672 G>A maps to NM_004923.3 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:46663543 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:61986599 G>A maps to NM_022843.3 I544I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:87000469 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:47058958 G>A maps to NM_153280.2 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:128841802 A>C maps to NM_152778.2 Y513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:183503950 C>T maps to NM_018023.4 S925S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:39229561 G>A maps to NM_194293.2 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:10672383 C>T maps to NM_023008.3 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:100482891 C>T maps to NM_015908.5 D406D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:70165301 C>T maps to NM_002357.2 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:145536893 C>T maps to NM_003637.3 T758T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:20279024 C>T maps to ENST00000389655 L1142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:56132912 G>A maps to ENST00000508342 T1036T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:49940298 T>C maps to NM_002447.2 E248E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:132082000 A>G maps to NM_001144058.1 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:4927464 G>A maps to NM_016936.3 Q1115Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:119054469 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:50835751 C>T maps to NM_020549.4 D344D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:113980392 C>T maps to NM_024719.2 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:46704965 C>T maps to NM_002298.4 E578E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:62871222 C>T maps to NM_004535.2 I1068I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:67190431 A>G maps to NM_003789.3 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:79347940 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:217285058 G>A maps to NM_014140.3 Q300Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:147845484 G>A maps to NM_199453.3 G360G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:51012061 G>A maps to NM_152245.2 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:7976503 G>A maps to NM_001139.2 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:35210975 C>A maps to ENST00000394681 S640S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:11845624 G>A maps to NM_001372.3 K4222K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:71174953 G>A maps to NM_020147.3 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:91873533 G>A maps to NM_032968.3 P1213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:32198192 G>A maps to NM_001703.2 C1215C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:104003288 G>A maps to NM_020139.3 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:186039889 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:154932250 G>A maps to NM_138300.3 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:8358147 T>C maps to ENST00000402554 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:73280625 C>T maps to NM_014243.1 Q189Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:118179149 G>T maps to NM_000733.3 E27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:141384673 G>A maps to NM_005471.4 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:184930593 C>T maps to NM_020225.1 C201C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:240070918 C>T maps to NM_000740.2 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:144671273 C>T maps to NM_032378.4 E326E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:99669524 G>A maps to NM_032924.3 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:103008359 C>T maps to NM_002803.2 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:25418145 C>A maps to ENST00000510092 V668V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:100177446 G>A maps to NM_000195.2 T659T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:104015878 C>T maps to NM_017564.9 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:248263565 C>T maps to NM_175911.2 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:23886419 G>T maps to NM_000257.2 A1487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:54377235 C>T maps to NM_001020818.1 Y151Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:195267 C>T maps to NM_001080478.1 Q449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:197631300 T>C maps to NM_012086.2 P842P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:111785781 C>T maps to NM_015267.3 R1372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:16668424 G>A maps to NM_012334.2 I2012I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:22974233 C>T maps to NM_172369.3 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:73045190 G>A maps to NM_031284.4 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:131561383 C>T maps to NM_198827.3 N504N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:233321074 G>A maps to NM_001631.3 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:67020490 C>T maps to NM_080283.3 L715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:89167346 C>T maps to NM_174917.2 C86C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:239159220 G>A maps to NM_022817.2 S1146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:171686049 C>T maps to NM_000817.2 Q71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:47996702 G>T maps to NM_003827.2 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:42911419 G>A maps to NM_005357.2 I681I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:117848401 G>T maps to NM_002160.2 C536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:60427937 C>T maps to NM_001794.2 D287D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:1397297 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:25915984 G>A maps to NM_005835.2 R348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:6334662 G>A maps to NM_001769.2 E46E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:2933299 C>A maps to NM_001011719.1 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:17700275 G>A maps to ENST00000395776 S1338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:26838422 A>G did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:836177 G>A maps to NM_058192.2 C237C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:110784226 C>A maps to NM_170665.3 I1027I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:31329912 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:64084843 G>A maps to NM_198859.3 S806S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:79320448 G>A maps to NM_015225.2 D2247D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:90122336 G>T maps to NM_001031709.2 V224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:78611995 G>T maps to NM_152405.4 E945*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:17166809 G>A maps to NM_033417.1 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:279105 C>A maps to NM_033089.6 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:35890399 C>T maps to NM_004414.5 T247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:64691243 C>T maps to NM_182914.2 S6816S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:158696031 G>T maps to NM_145049.3 G37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:159091909 C>T maps to NM_001128424.1 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:237054560 C>T maps to NM_000254.2 L1046L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:140741633 C>T maps to NM_018923.2 V644V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:70949648 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:95204433 C>A maps to NM_001128429.1 C965*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:74418378 G>A maps to NM_020872.1 R303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:3249837 G>A maps to ENST00000328215 D64D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:10225275 C>T maps to NM_001040664.2 G749G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:105258974 G>A maps to NM_001014432.1 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:10505908 C>A maps to NM_007065.3 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:231927222 G>A maps to NM_002807.3 E46E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:65260265 C>T maps to ENST00000389723 A709A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:247463871 G>A maps to NM_032752.1 H571H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:24419479 C>T maps to ENST00000330966 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:48056060 C>T maps to NM_153618.1 R254R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:23893857 G>T maps to NM_006940.4 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:89815012 G>A maps to NM_172240.2 R452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:19437202 C>T maps to NM_020774.2 I926I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:152770356 T>C maps to NM_178352.2 C29C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:43897592 G>A maps to NM_153700.2 Q1267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:147131178 G>A maps to NM_003412.3 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:147744091 C>T maps to NM_002025.3 Q282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:118984607 A>G maps to NM_014807.3 T512T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:33218737 G>T maps to NM_022553.4 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:116718255 C>T maps to ENST00000445177 S1289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:67940505 C>T maps to NM_182526.2 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:84363221 T>C maps to NM_001012980.2 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:185993441 C>T maps to NM_001346.2 G268G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:18194248 G>A maps to NM_004618.3 I458I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:125301266 A>G maps to NM_022062.2 E466E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:92122334 G>A maps to NM_000466.2 L1047L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:121702401 A>G maps to NM_018699.2 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:86047130 C>T maps to NM_001554.4 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:49019190 G>A maps to ENST00000425661 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:64695587 C>A maps to NM_006244.3 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:87549947 C>A maps to NM_012262.3 Y145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:118671333 G>A maps to NM_001127211.1 C442C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:64137087 G>A maps to NM_003942.2 P533P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:165353552 A>G maps to NM_004490.2 A449A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:16314367 G>A maps to NM_001130524.1 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:7846812 G>A maps to NM_001037144.4 R472R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:37723011 C>T maps to NM_018034.2 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:142681854 G>A maps to NM_198504.2 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:21141284 C>T maps to NM_000185.3 F477F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:105463554 G>A maps to NM_001385.2 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:52080880 G>A maps to NM_014191.2 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:180397252 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:52778893 C>T maps to NM_013409.1 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:66436912 C>T maps to NM_001795.3 G732G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:11415429 G>A maps to ENST00000423059 A1655A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:62705619 G>A maps to NM_005873.2 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:154544330 C>A maps to NM_000748.2 P344P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:25937131 C>T maps to ENST00000268763 C700C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:57876528 G>A maps to NM_000938.1 V469V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:129781470 T>C did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:17496470 G>A maps to ENST00000302539 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:49621898 G>A maps to NM_018111.2 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:96076503 C>T maps to ENST00000371380 T2111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:102509501 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:15063765 C>T maps to NM_005071.1 T491T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:138768565 G>A maps to ENST00000464606 C219C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:55237335 G>A maps to NM_002184.3 F777F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:10974868 C>A maps to NM_014229.1 S468S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:23364328 C>A maps to ENST00000307331 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:113683094 G>T maps to NM_020886.2 S625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:103238179 G>T maps to NM_000277.1 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:11303795 C>T maps to NM_015493.6 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:4900559 C>T maps to NM_020144.4 R294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:25042947 G>A maps to NM_004036.3 Y1096Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:2328416 G>A maps to NM_001089.2 I1530I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:139189207 G>A maps to NM_032289.2 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:50592986 T>C maps to NM_005254.5 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:19209671 C>T maps to NM_003748.3 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:134322951 G>A maps to NM_178554.4 S485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:30536779 C>T maps to NM_024671.3 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:35741770 G>A maps to NM_020944.2 Y228Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:97217024 G>A maps to ENST00000370197 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:111310253 T>C maps to NM_032194.1 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:117828430 G>T maps to NM_016200.4 G58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:37537004 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:45530204 C>T maps to NM_015340.3 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:39087083 G>A maps to NM_001042600.1 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:7762889 C>T maps to NM_002216.2 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:99051674 G>A maps to NM_006693.2 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:19283699 C>T maps to NM_138340.4 Q57Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:63884480 C>T maps to NM_013280.4 Q248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:50209129 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:39228902 C>T maps to NM_194293.2 R678R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:206225108 C>T maps to NM_000707.3 C223C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:197316583 C>T maps to NM_201253.2 D321D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:129019922 G>A maps to NM_133638.3 W919*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:55890183 T>C maps to NM_001005201.1 C112C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:131329136 C>T maps to NM_001130438.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:31749479 G>T maps to NM_006295.2 G802G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:4892302 C>A maps to ENST00000328908 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:110882329 C>T maps to NM_022768.4 D101D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:61917620 C>T maps to NM_001040694.1 S828S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:54754888 T>C maps to ENST00000450632 R582R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:45109510 G>A maps to NM_001029835.2 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:73957905 T>G maps to NM_032217.3 S1813S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:143701394 C>T maps to NM_001005281.1 Y102Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:75116789 T>C maps to NM_021819.2 T474T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:10973776 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:36642392 G>A maps to NM_018067.3 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:31555448 C>T maps to NM_007161.3 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:50728053 G>A maps to NM_012401.2 H320H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:160240288 G>A maps to NM_173516.1 A468A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:34949739 G>A maps to NM_194283.3 E426E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:64422752 G>T maps to NM_015153.2 G1757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:55086035 G>A maps to NM_001130917.1 E113E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:37899532 C>T maps to ENST00000445327 Y211Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:100232702 G>A maps to NM_000668.4 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:6816483 G>A maps to NM_003696.2 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:131708325 G>T maps to NM_014908.3 I419I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:16847917 C>T maps to ENST00000448080 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:105174223 C>T maps to ENST00000252520 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:62301543 G>A maps to NM_001620.1 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:54802688 G>A maps to NM_002205.2 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:121652805 C>T maps to NM_002851.2 L1236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:30107903 G>A maps to NM_002742.2 C301C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:64054337 C>T maps to NM_001170726.1 N172N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:61512141 G>A maps to NM_033081.2 D1722D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:40257176 C>T maps to NM_024119.2 Q420Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:156803023 G>A maps to NM_005515.3 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:39667297 C>T maps to NM_005884.3 V476V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:151504453 C>T maps to NM_006439.4 D91D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:63585406 C>T maps to NM_138471.1 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:39966943 C>T maps to NM_021096.3 R63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:89885780 T>C maps to NM_172240.2 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:73126650 G>A maps to NM_014595.1 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:47049627 C>T maps to NM_015175.1 S2557S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:150551720 G>A maps to NM_021960.4 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:46032697 C>A maps to NM_198695.2 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:118495212 G>A maps to NM_006784.2 S693S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:149866863 C>T maps to NM_004522.1 I922I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:27939444 C>T maps to NM_152345.4 N428N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:15161457 G>A maps to ENST00000378143 R383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:168260461 C>T maps to NM_005149.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:6026721 G>A maps to NM_000535.5 T558T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:40853832 C>T maps to NM_020783.3 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:75643078 G>A maps to NM_006827.5 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:11676484 G>A maps to ENST00000423059 N98N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:109367805 C>T maps to NM_006267.4 R454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:90128424 G>A maps to NM_001098173.1 N262N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:72191129 G>A maps to ENST00000424560 A1238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:166908315 C>A maps to NM_001165963.1 E293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:47193446 G>A maps to NM_014346.2 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:118453976 C>T maps to ENST00000359415 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:6244423 T>C maps to NM_032127.3 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:57564341 G>A maps to NM_001085458.1 E278E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:80039891 G>A maps to NM_004104.4 G2052G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:48621979 C>A maps to NM_000094.3 G1353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:91406462 C>A maps to NM_201269.1 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:99893883 A>G maps to NM_001080481.1 C588C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:64085152 G>A maps to NM_198859.3 S703S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:41723230 G>T maps to ENST00000351589 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:47459948 G>A maps to NM_012235.2 R731R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:77147264 G>A maps to ENST00000332191 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:2290152 G>A maps to NM_024848.1 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:57176545 G>A maps to NM_001005850.1 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:18652784 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:121132068 C>T maps to NM_014980.2 R1029*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:42208674 C>T maps to NM_016276.3 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:99207042 G>A maps to NM_024759.1 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:64573869 G>T maps to NM_001136178.1 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:1313189 G>A maps to NM_018702.2 H384H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:65225410 C>T maps to NM_032776.1 E4E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:53741427 C>T maps to NM_182609.2 V184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:179598614 A>G maps to NM_133378.4 P3923P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:32971375 C>T maps to NM_001172774.1 Y634Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:17380438 G>A maps to NM_018019.2 K28K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:4202023 T>C maps to ENST00000262970 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:43805723 C>T maps to ENST00000330266 Q248Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:133779546 G>T maps to NM_001145106.1 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:54496844 G>A maps to NM_004463.2 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:55455900 G>T maps to NM_007086.3 C457*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-IB-7651-01A-11D-2154-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:24465976 C>T maps to NM_001135816.1 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:247835701 G>T maps to NM_001005487.1 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:75204372 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:99672986 C>T maps to ENST00000336292 S1473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:56151034 G>A maps to NM_006213.3 N161N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:67513639 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:133540636 T>C maps to NM_207363.2 R1249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:152960075 G>A maps to NM_005629.3 P528P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:420736 G>A maps to NM_001012302.2 F538F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:56977192 C>T maps to NM_014685.2 I389I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:1497598 C>T maps to NM_000547.5 C598C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:108290634 T>C did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:100201160 G>A maps to NM_002593.3 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:41194881 G>A maps to NM_020857.2 L755L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:91338561 C>T maps to NM_004755.2 T755T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:44153428 C>T maps to NM_001129.3 R1016*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:29445737 C>T maps to NM_032173.2 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:31548599 G>A maps to NM_002341.1 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:128302183 C>T maps to NM_001017372.1 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:100029192 C>T maps to NM_019606.5 R518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:95818950 C>T maps to NM_032788.1 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:74771151 G>T maps to NM_024311.2 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:102595603 G>A maps to NM_173200.1 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:160019848 G>A maps to NM_033394.2 W246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:55183679 G>A maps to ENST00000427138 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:52788202 C>T maps to NM_000782.4 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:152192829 G>A maps to NM_001009931.1 G425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:23002958 G>A maps to NM_014608.2 K1227K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:13699467 G>A maps to NM_018027.3 H707H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:24782745 C>T maps to NM_020448.4 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:35068879 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:3008915 G>A maps to NM_003260.4 R401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:173916386 T>C maps to NM_007023.3 A976A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:42458802 G>A maps to ENST00000348544 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:21997707 G>A maps to NM_025232.2 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:38369970 G>A maps to NM_207412.1 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:16892236 A>G maps to NM_017940.3 C986C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:13378324 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:53262443 C>T maps to NM_024646.2 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:148801987 G>A maps to NM_001001661.2 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:124416567 C>A maps to NM_207437.3 I4285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:22381042 C>A maps to NM_020346.2 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:140711974 C>T maps to NM_024757.4 C1153C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:70926318 C>T maps to NM_003813.2 V701V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:23833185 C>T maps to NM_013261.3 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:1386074 C>T maps to NM_001039211.2 D4D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:43013725 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:23226068 C>T maps to NM_001039.3 D510D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:179782951 C>T maps to NM_173509.2 D44D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:19578928 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:228881438 G>A maps to NM_001142644.1 T1377T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:40751772 G>T maps to NM_014952.3 G370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:158549278 G>A maps to NM_032861.3 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:7563013 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:98527810 C>T maps to ENST00000359863 I1125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:91643632 T>C maps to NM_005751.4 Y1201Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:75263525 G>A maps to NM_001170714.1 A878A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:128528545 C>A maps to NM_018383.4 E4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:47075175 G>A maps to NM_006546.3 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:110116529 G>A maps to NM_006496.2 E58E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:3628545 C>A maps to NM_031965.2 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:240370367 C>T maps to ENST00000406993 G895G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:122763230 C>T maps to NM_022444.3 W433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:127497401 T>C maps to NM_001046.2 Y842Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:110716644 C>A maps to NM_001010898.2 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:91631642 T>C maps to NM_005751.4 I804I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:49965960 A>G maps to NM_153329.3 A349A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:8175942 G>T maps to NM_001080826.1 I1314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:3569997 A>G maps to NM_015041.1 E225E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:114655943 C>A maps to NM_199072.4 C341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:220338458 G>T maps to NM_005876.4 G1427G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:90513084 C>T maps to NM_014611.1 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:67432783 T>C maps to NM_013304.2 T198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:84391389 G>A maps to NM_139076.2 R148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:37138819 A>G did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:121980529 C>T maps to NM_001178065.1 D216D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:55240760 C>T maps to NM_005228.3 R669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:240070909 C>T maps to NM_000740.2 D53D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:112326327 C>T maps to NM_139078.1 Q336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:26217492 T>G maps to NM_021052.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:83793167 C>T maps to ENST00000505472 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:42135892 C>T maps to NM_005090.3 R486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:247051760 G>A maps to ENST00000428671 R773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:140720707 C>T maps to NM_018915.2 L724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:42568883 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:14308062 G>A maps to NM_198391.2 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:54448913 G>A maps to NM_153633.2 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:144061096 C>T maps to NM_005435.3 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:167921567 G>A maps to NM_016950.2 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:7531633 G>A maps to ENST00000416109 R781*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:202900482 C>T maps to NM_003507.1 H371H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:105905012 C>T maps to NM_004689.3 Y11Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:177133623 C>T maps to ENST00000281881 E63E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:100464904 G>T maps to ENST00000370153 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:103921394 T>C maps to ENST00000405356 P618P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:228547312 C>T maps to NM_052843.2 T6240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:151100467 C>T maps to NM_053002.4 R1504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:118983573 C>T maps to NM_014807.3 D459D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:117826321 G>A maps to NM_002160.2 V1171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:41282488 A>C maps to NM_022098.2 R254R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:38959658 C>T maps to NM_000540.2 G1145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:33255180 C>T maps to NM_000362.4 Y151Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:128628467 G>T maps to NM_031445.2 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:123813398 C>T maps to NM_002006.4 R239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:74104603 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:23649186 C>T maps to NM_024675.3 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:11557938 C>T maps to ENST00000436195 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:5232599 T>A maps to NM_139056.2 S607S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:22849625 C>T maps to NM_004540.2 D637D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:144997697 C>T maps to NM_201380.2 A2270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:100870519 T>C maps to NM_002106.3 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:41173717 C>T maps to NM_004756.3 P495P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:74417567 C>T maps to NM_015424.3 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:61777909 G>A maps to NM_017780.2 A2804A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:27064754 G>A maps to ENST00000449198 D64D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:120438761 C>T maps to NM_021794.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:119559877 C>T maps to NM_194286.2 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:33626893 G>T maps to ENST00000374316 E209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:140731023 G>A maps to NM_018922.2 K399K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:131107478 C>T maps to NM_005094.3 C69C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:56420277 G>T maps to NM_001080433.1 E315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:168139346 G>T maps to NM_003062.2 G832G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:68500696 G>A maps to NM_017882.2 F239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:119592128 G>A maps to NM_194286.2 S491S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:75683557 A>G maps to NM_152697.4 R539R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:33330453 C>T maps to NM_014071.2 A1202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:105950318 G>A maps to NM_015423.2 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:50071219 G>A maps to NM_012340.3 R572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:3801338 C>T maps to NM_002558.2 K366K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:80669238 C>T maps to NM_001007023.2 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:105036933 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:2717903 C>T maps to NM_133497.2 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:4400335 G>A maps to NM_003025.2 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:50060161 G>A maps to NM_015953.3 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:156876546 C>T maps to NM_001080471.1 N173N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:173368844 C>T maps to ENST00000264106 Y1086Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:100021970 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:27634226 G>A maps to NM_001017420.2 K134K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:31079553 G>A maps to NM_014070.2 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:22038098 G>A maps to NM_001005465.1 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:74655330 G>T maps to NM_000859.2 G803*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:119003515 G>A maps to NM_003054.4 K52K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:31851171 G>A maps to ENST00000395728 C1044C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:41437685 G>A maps to ENST00000378163 G470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:25656918 G>A maps to NM_015655.2 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:56035926 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:35202043 C>T maps to NM_003024.2 L1116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:46000958 G>A maps to NM_024513.2 L1171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:142409765 C>T maps to NM_002511.2 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:100591810 G>A maps to NM_139057.2 S807S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:90097792 C>A maps to NM_001481.2 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:151497152 C>T maps to NM_020770.2 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:210415339 G>A maps to NM_019605.3 Q243Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:5699532 C>T maps to NM_033034.2 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:1585097 G>A maps to NM_178129.4 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:24190109 C>T maps to NM_018647.2 C95C. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-IB-7651-01A-11D-2154-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:37988648 C>A maps to NM_017549.3 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:10318881 G>A maps to NM_002472.2 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:38997549 G>A maps to NM_002240.2 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:20832994 C>T maps to NM_000921.3 Y1072Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:49391398 C>T maps to NM_015086.1 E420E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:51458119 A>G maps to ENST00000273612 S768S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:123339641 C>T maps to NM_003959.1 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:25068830 G>A maps to NM_006437.3 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:21309117 C>T maps to NM_213569.2 K59K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:156641405 C>T maps to NM_006617.1 G858G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:56437030 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:17998309 C>T maps to NM_001105569.1 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:39904949 C>A maps to ENST00000361689 I4016I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:6477725 G>A maps to NM_033278.2 R410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:35896131 G>A maps to NM_007247.4 I1205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:139695018 G>A maps to NM_006079.3 H21H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:150171652 G>A maps to NM_175571.2 A412A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:24261217 C>A maps to NM_025203.2 E383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:11082188 G>A maps to NM_007375.3 Q241Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:142651022 G>A maps to NM_000420.2 D315D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:230391081 C>A maps to NM_004481.3 V376V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:32253480 G>A maps to NM_175858.2 C121C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:70300474 C>A maps to NM_020794.2 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:57167743 C>T maps to NM_003725.2 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:156746870 C>T maps to ENST00000442283 F486F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:11756778 C>T maps to NM_014668.3 S1115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:132169691 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:48945464 C>T maps to NM_000836.2 I833I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:19168364 C>T maps to ENST00000392336 A478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:24940293 C>T maps to ENST00000376835 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:46497061 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:21965775 C>A maps to NM_024815.3 E82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:133795813 C>T maps to NM_014987.1 P618P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:21383303 G>A maps to NM_022459.4 R471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:34827138 G>A maps to NM_017754.3 V1002V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:61554263 G>A maps to ENST00000395341 H399H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:25750767 G>A maps to NM_001135772.1 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:24783452 A>G maps to NM_019590.3 K568K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:123152118 C>T maps to NM_178827.4 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:146278524 G>A maps to ENST00000444534 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:112321681 T>C maps to NM_152624.4 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:136766 G>A maps to ENST00000399953 S548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:131298699 A>G maps to NM_001003722.1 S571S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:226349292 G>A maps to NM_022735.3 R223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:33256730 C>T maps to NM_005452.5 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:36298365 G>A maps to NM_001010903.4 C34C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:13767602 C>T maps to NM_003611.2 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:31785395 C>T maps to NM_005345.5 G621G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:45010478 G>A maps to NM_033054.2 G342G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:180666194 C>T maps to NM_005087.3 R111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:6472626 G>A maps to NM_033278.2 V525V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:75190001 T>C maps to NM_002435.1 N401N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:95922697 A>C maps to NM_032147.2 Y503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:56866493 G>A maps to NM_013267.2 G497G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:140754631 C>T maps to NM_018919.2 R328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:23391008 G>A maps to NM_006547.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:3910848 C>T maps to NM_033064.4 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:68664141 G>A maps to NM_181514.1 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:116747898 C>T maps to NM_013352.2 Y193Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:103499509 G>A maps to NM_153448.3 Y7Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:65296584 C>T maps to NM_015147.2 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:65249187 G>A maps to ENST00000389723 D1366D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:19786639 G>A maps to NM_020344.2 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:137783592 C>T maps to NM_173543.2 S673S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:49762717 C>T maps to NM_001079673.1 G631G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:18215341 G>T maps to ENST00000388870 R739R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:35406990 C>T maps to ENST00000416672 N95N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:15484042 G>A maps to NM_005858.2 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:236212172 G>A maps to NM_002508.2 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:160020016 C>A maps to NM_033394.2 G302G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:32561797 G>A maps to NM_001030055.1 S641S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:8089917 C>T maps to NM_001130083.1 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:79226463 G>A maps to NM_001037984.1 G492G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:100135183 C>T maps to NM_032425.4 S582S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:206166413 C>T maps to ENST00000406610 G873G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:3784219 G>A maps to NM_002378.3 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:49929220 G>A maps to NM_002447.2 R1108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:110778496 C>T maps to NM_170665.3 L599L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:30915872 C>T maps to NM_020869.2 Q842Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:75042450 C>A maps to NM_000761.3 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:1230811 G>A maps to NM_018702.2 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:39406329 G>A maps to ENST00000395035 Q309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:212791501 C>T maps to NM_001674.2 R92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:64055661 C>T maps to NM_001170726.1 Y311Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:150925760 G>A maps to NM_001447.2 L1643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:22840986 A>G maps to NM_004540.2 E593E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:122405934 G>A maps to NM_017554.2 K110K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:113955418 G>A maps to NM_012455.2 T851T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:45307686 G>T maps to NM_020826.2 C24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:94750763 C>T maps to NM_005172.1 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:36435680 C>A maps to NM_024509.1 A549A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:721945 C>T maps to NM_138769.1 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:23217626 G>A maps to NM_002318.2 D169D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:52513389 G>A maps to NM_018728.3 I1230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:3869813 C>T maps to NM_153638.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:40660600 C>T maps to NM_001130021.1 D708D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:10226165 G>A maps to NM_003755.3 V312V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:6925372 C>A maps to NM_000616.4 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:94419707 C>T maps to ENST00000434324 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:27429186 G>A maps to NM_003047.3 Y541Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:27737092 G>A maps to NM_173833.5 F448F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:4060751 C>T maps to NM_003913.4 L976L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:11024704 C>T maps to NM_199141.1 H274H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:179516865 C>T maps to NM_133378.4 V10650V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:52656852 G>A maps to ENST00000358212 L1069L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:4652984 G>T maps to NM_001130862.1 E42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:29674082 T>G maps to NM_013986.3 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:3814266 G>A maps to NM_004746.2 Q322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:101877432 C>T maps to ENST00000360264 R1190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:18981408 T>C maps to NM_001130914.1 K18K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:20795189 G>A maps to NM_001163941.1 E1239E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:57036218 C>A maps to NM_020813.2 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:99690410 T>G maps to NM_014361.2 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:38043328 C>T maps to NM_018957.3 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:102040564 C>T maps to NM_002465.2 C330C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:154624430 T>A maps to NM_003264.3 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:94354715 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:84695390 C>T maps to NM_024731.2 S501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:8950932 G>T maps to NM_020643.2 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:29708457 C>T maps to NM_152236.1 R673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:39826612 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:99514880 C>T maps to ENST00000429802 D713D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:12059624 T>C maps to NM_144566.1 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:20432252 C>T maps to NM_032812.7 R191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:147561476 C>T maps to NM_004575.2 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:99662629 C>T maps to NM_001184880.1 G322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:93826708 C>T maps to NM_001098672.1 G779G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:52521949 G>A maps to NM_007184.3 Q814Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:2749023 G>A maps to NM_033267.4 D266D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:100055035 G>A maps to ENST00000359773 E42E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:114340179 C>T maps to NM_018364.3 E394E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:97858363 G>A maps to ENST00000379795 G800G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:140746122 C>T maps to NM_018918.2 G742G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:99961620 C>A maps to ENST00000457907 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:71008430 G>A maps to NM_032682.4 Y667Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:60689495 C>T maps to NM_024092.2 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:367132 C>T maps to NM_003441.2 R303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:47776029 G>A maps to ENST00000489301 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:7232025 C>T maps to NM_001003699.3 L1232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:221913077 C>T maps to NM_007207.3 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:88601209 G>A maps to NM_153813.2 A948A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:75567811 G>A maps to NM_033116.4 L629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:201382200 G>A maps to ENST00000367312 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:30655228 G>A maps to NM_001009552.1 H118H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:26923285 G>A maps to NM_001260.1 W94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:97868309 G>A maps to NM_001005514.1 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:134133230 T>C maps to NM_001628.2 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:70333166 G>T maps to ENST00000338508 P1071P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:130405109 C>T maps to NM_014602.2 K1140K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:60581568 C>T maps to NM_003185.3 P740P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:100187647 G>A maps to NM_006668.1 Q351Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:44855411 C>T maps to NM_025137.3 K2413K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:82714672 G>A maps to NM_152836.2 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:7506796 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:30594072 G>A maps to NM_152458.6 C342C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:101905196 A>G maps to NM_138325.2 V636V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:136531865 G>A maps to NM_007101.3 S874S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:36424910 G>A maps to ENST00000379892 D346D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:43017877 C>T maps to NM_001168370.1 W548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:20928927 G>A maps to NM_001100814.1 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:205034325 G>A maps to NM_005076.3 W544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:29809752 C>T maps to NM_007317.1 Q109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:40529530 C>T maps to NM_001145082.2 C550C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:127230184 G>A maps to NM_001662.3 Q108Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:228444433 C>T maps to NM_001098623.1 C1464C. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-IB-7651-01A-11D-2154-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:75526269 C>T maps to NM_198597.1 N590N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:20216180 C>T maps to NM_172194.1 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:74003512 T>C did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:24034357 C>T maps to ENST00000382833 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:42301743 C>T maps to NM_001815.2 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:51736375 G>A maps to NM_001971.5 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:79219814 G>A maps to NM_001037984.1 G967G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:35691297 G>T maps to NM_024867.3 G562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:141248691 G>A maps to NM_032420.2 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:35773689 C>T maps to NM_182548.3 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:45268515 G>A maps to NM_004073.2 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:27313377 A>C maps to NM_014915.2 T1361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:21998295 C>T maps to NM_022044.2 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:161470911 G>A maps to NM_005922.2 Q536Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:10621488 C>T maps to NM_000214.2 S1047S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:26031955 G>A maps to NM_003537.3 C111C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:65178815 C>A maps to NM_032160.2 T1020T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:48381425 G>A maps to NM_031490.2 Q649Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:30951197 G>A maps to NM_004861.1 N338N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:775562 G>A maps to NM_001031737.2 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:179033099 C>T maps to NM_014864.3 R205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:144919855 G>A maps to NM_178564.3 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:17917111 G>A maps to NM_004315.4 R312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:10689806 C>T maps to NM_004565.2 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:132290276 C>T maps to NM_138770.1 R267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:49244307 G>A maps to ENST00000393198 K179K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:22475261 G>T maps to NM_021174.5 E682*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-IB-7651-01A-11D-2154-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:116747781 C>T maps to NM_013352.2 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:220473435 C>T maps to NM_052902.2 R590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:92923923 C>A maps to NM_005654.4 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:25246650 G>A maps to NM_024940.6 E1392E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:236157029 G>A maps to NM_002508.2 H890H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:90872840 A>G maps to NM_007351.2 R1068R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:102611283 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:51378883 C>T maps to NM_002863.4 T586T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:77709050 C>T maps to NM_178543.3 H203H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:64895880 C>T maps to NM_172230.2 Q609Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:62064996 C>T maps to NM_206998.1 K63K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:17516299 G>A maps to NM_004335.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:100964691 C>T maps to NM_033312.2 N543N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:152058969 A>T maps to NM_001008536.1 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:2920374 A>G maps to NM_014646.2 N869N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:6598924 C>T maps to NM_015274.1 A381A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:15654980 C>T maps to NM_030667.1 I363I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:143708592 G>A maps to NM_173552.3 E401E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:71232127 T>C maps to NM_017941.4 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:39822802 C>T maps to NM_006116.2 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:1267145 G>A maps to ENST00000447027 P3015P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:248112728 C>T maps to NM_001001963.1 D190D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:38858389 C>A maps to NM_021185.4 I968I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:3435983 C>T maps to ENST00000381913 P344P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:124856629 G>A maps to NM_006312.4 S915S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:4796847 C>T maps to NM_153827.4 G840G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:240969774 C>T maps to NM_001005853.1 Q24Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:123026645 A>G maps to NM_014708.4 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:102584188 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:90494753 G>A maps to NM_014611.1 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:42285033 G>A maps to NM_001080490.1 R428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:77711049 C>T maps to NM_178543.3 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:74648413 G>A maps to NM_001105659.1 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:7545674 G>A maps to NM_001037763.2 D332D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:103559126 G>A maps to NM_012215.3 T427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:32978375 C>T maps to NM_001079691.1 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:84115362 C>T maps to NM_003791.2 K479K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:55995118 G>A maps to NM_033113.2 T849T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:74424518 G>T maps to NM_015424.3 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:30514928 G>T maps to NM_005275.3 P467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:50635948 C>T maps to NM_025204.2 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:93712551 G>A maps to NM_001002860.2 R734R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:49281381 C>T maps to NM_020377.2 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:45292981 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:111617185 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:59730275 G>A maps to NM_014992.1 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:97967626 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:125590746 G>A maps to NM_020337.2 R1229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:36109544 G>A maps to NM_015302.1 Q320Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:59059134 C>T maps to NM_147189.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:122288312 C>T maps to NM_138287.3 G459G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:25277121 C>T maps to NM_002862.3 D832D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:67577554 G>A maps to NM_025054.4 R547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:139836665 G>A maps to NM_018998.2 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:7008408 C>T maps to NM_001113361.1 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:17124911 G>A maps to NM_144997.5 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:112048242 G>A maps to NM_001113490.1 R570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:243480089 C>T maps to NM_006642.3 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:50815322 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:30805261 C>T maps to NM_012429.2 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:47693795 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:179275063 A>C maps to NM_016175.3 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:57036569 T>C maps to NM_020813.2 I378I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:245850355 C>T maps to NM_018012.3 I1357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:14806442 G>T maps to NM_032433.2 E65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:140590473 C>A maps to NM_018932.3 G665G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:38003438 G>A maps to NM_024700.2 Y367Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:234603361 A>G maps to NM_005646.3 C378C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:58048597 G>T maps to ENST00000376233 E76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:91714145 C>T maps to NM_005751.4 D2908D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:67196454 C>T maps to NM_003952.2 D27D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:20841722 C>T maps to NM_007110.4 E2208E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:37368904 C>T maps to NM_003419.3 I391I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:169292908 G>T maps to NM_001012967.1 I1594I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:220496995 C>T maps to NM_201574.2 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:42090466 G>A maps to NM_032376.2 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:7984224 C>T maps to NM_001139.2 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:154395476 G>A maps to NM_001099293.1 L686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:23382618 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:44586500 C>T maps to NM_001137606.1 D153D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:1479047 C>T maps to ENST00000382147 G524G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:72024410 T>C maps to NM_144982.4 T1231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:22301229 C>T maps to NM_213599.2 N887N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:13345817 G>A maps to NM_023035.2 D1726D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:3253869 C>T maps to NM_033225.5 E813E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:7962939 G>T maps to NM_021156.2 S336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:55994230 C>T maps to NM_033113.2 R553R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:24581478 A>G maps to NM_006910.4 V1156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:141461344 G>A maps to NM_153702.3 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:49377869 C>A maps to NM_014330.3 A460A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:27333951 G>A maps to NM_005288.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:131909733 G>A maps to NM_178001.2 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:118724024 G>A maps to NM_001173487.1 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:133540012 G>A maps to NM_207363.2 T1457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:126062614 C>T maps to NM_014079.3 V402V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:201994683 G>A maps to NM_001127183.1 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:170051307 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:16026092 T>C maps to ENST00000445506 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:44139541 G>A maps to NM_006973.2 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:11596298 C>T maps to NM_006395.2 S698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:186319456 C>A maps to NM_003292.2 E892*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:69325508 C>T maps to NM_024505.3 H249H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:88359521 G>A maps to NM_024047.3 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:39264501 G>A maps to NM_207361.4 R1007R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:37028070 C>T maps to NM_001013736.2 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:8228995 G>A maps to NM_018986.3 W525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:165404218 A>G maps to NM_004490.2 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:140517106 G>A maps to NM_015669.2 S697S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:37310732 T>C maps to NM_206894.2 E171E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:478424 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:50746020 G>A maps to NM_022162.1 V733V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:73414461 C>T maps to NM_014243.1 Q79Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:24194190 A>G maps to NM_181713.3 Q29Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:123664000 C>T maps to NM_152618.2 C318C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:39885649 C>T maps to NM_003246.2 T1016T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:150525687 C>T maps to ENST00000369039 H131H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:10471562 G>A maps to ENST00000423585 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:69168086 C>T maps to NM_198271.3 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:78933942 C>T maps to NM_020761.2 I1181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:183387082 C>T maps to NM_005019.3 E7E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:71522186 G>T maps to NM_144646.3 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:44684366 T>C maps to NM_019100.4 A220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:85658678 C>T maps to NM_002605.2 R454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:206331210 C>T maps to NM_148964.2 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:155104108 C>A maps to NM_004428.2 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:198950754 C>T maps to NM_006226.3 H838H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:102114261 C>T maps to NM_005063.4 R174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:65026807 G>A maps to NM_014405.3 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:74654383 G>A maps to NM_001015055.1 C424C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:64669562 G>A maps to ENST00000421419 V1332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:41141437 T>C maps to NM_173079.2 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:71039252 C>T maps to NM_006540.2 Q1237Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:53045632 G>T maps to NM_000423.2 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:4118508 C>T maps to NM_001042413.1 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:18219846 C>T maps to NM_144775.2 D248D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:38120146 A>G maps to NM_001039141.2 T528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:2139897 G>A maps to NM_017575.4 V919V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:31144231 C>T maps to ENST00000311943 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:139563818 T>C maps to ENST00000358430 P633P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:6601499 G>A maps to NM_016497.3 H108H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:146678706 C>T maps to NM_000838.3 D493D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:156339201 C>T maps to NM_020407.3 D54D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:100284963 G>A maps to NM_022574.4 R147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:98928392 C>T maps to NM_144992.4 P1211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:84442093 C>T maps to ENST00000416219 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:30039013 G>A maps to NM_025236.3 Y379Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:27964175 C>T maps to NM_173576.2 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:150307597 C>T maps to NM_004698.2 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:36229025 C>T maps to NM_001128227.2 Q385Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:64216738 C>T maps to NM_000042.2 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:133955528 C>T maps to NM_001105521.2 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:38768101 C>A maps to NM_006514.2 G1028*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:58152483 G>A maps to NM_006385.3 E223E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:49656970 G>A maps to NM_002152.2 G508G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:87970600 A>C maps to NM_015021.1 S2418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:137525387 G>A maps to NM_004661.3 Y519Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:144995927 G>A maps to NM_201380.2 D2824D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:22079168 C>T maps to NM_014759.3 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:52524498 G>A maps to NM_000053.2 G828G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:200173512 G>A maps to NM_001172509.1 H570H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:64085190 G>A maps to NM_198859.3 R691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:41021216 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:231256916 C>T maps to NM_138402.4 G360G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:27455959 C>T maps to NM_004341.3 T981T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:65671659 T>C did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:57077331 C>T maps to NM_033396.2 E951E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:126242164 C>T maps to NM_024582.4 N1533N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:42356730 A>G maps to NM_152447.3 G301G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:123258034 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:19744543 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:6534896 G>A maps to NM_003811.3 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:737186 G>A maps to ENST00000248142 R427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:80718806 G>A maps to NM_152342.2 R82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:44932977 C>A maps to NM_014518.2 E660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:113312281 G>A maps to ENST00000374463 R212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:195593779 G>A maps to NM_001010938.1 S1078S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:111776114 C>T maps to NM_015267.3 I1074I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:100161556 G>A maps to NM_006076.4 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:66879089 A>G maps to NM_203487.2 G1137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:83378595 G>T maps to ENST00000268613 E256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:122646796 G>T maps to NM_001031702.2 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:126332477 G>A maps to NM_001031712.2 E280E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:113513897 G>A maps to NM_152515.3 N350N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:120022127 C>A maps to NM_016644.1 Y190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:202025275 C>T maps to NM_001127183.1 Y305Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:80021380 G>T maps to NM_022156.3 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:72775353 C>T maps to NM_017757.2 L1893L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:25515949 C>A maps to NM_017640.5 V560V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:59283899 G>A maps to NM_153377.3 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:46332592 G>A maps to ENST00000288400 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:117718172 A>G maps to NM_002944.2 Y228Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:195022899 G>A maps to NM_012287.5 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:193166085 C>T maps to NM_032279.2 G687G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:1074170 C>T maps to NM_012292.2 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:33382061 C>T maps to NM_024165.2 C265C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:179701838 G>A maps to NM_173648.3 F1369F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:105677561 G>A maps to NM_001519.2 S631S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:85488367 G>A maps to NM_004213.3 E629E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:78640309 C>T maps to NM_004378.2 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:177016489 C>T maps to NM_014621.2 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:94395236 C>A maps to NM_138344.3 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:74492595 G>T maps to NM_001105659.1 A592A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:16486700 G>T maps to NM_024704.4 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:43950754 G>A maps to NM_022785.3 D1214D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:126100553 C>A maps to NM_000274.3 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:56500404 G>A maps to ENST00000361203 D845D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:27680844 T>C did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:1801213 C>T maps to NM_000142.4 Q115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:62166297 G>A maps to NM_005975.2 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:155891296 C>A maps to NM_014949.2 G379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:31535980 C>T maps to NM_015715.3 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:176964669 C>T maps to NM_021193.3 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:39998188 T>C maps to NM_152467.3 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:74649257 G>A maps to NM_001105659.1 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:161277071 G>A maps to ENST00000360451 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:6213121 G>A maps to NM_005934.3 F537F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:116381003 C>T maps to NM_001127500.1 H542H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:213872293 G>T maps to ENST00000342002 I463I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:132516652 G>A maps to ENST00000333577 W2006*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:141543375 G>A maps to NM_015130.2 D1258D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:110442243 C>A maps to ENST00000426474 V1069V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:44561835 C>T maps to NM_013389.2 S881S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:1893189 C>T maps to ENST00000399161 R781R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:101747665 C>T maps to ENST00000360264 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:12429835 G>A maps to NM_145276.2 R335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:156046583 C>T maps to NM_001093725.1 P448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:30544312 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:4934368 C>T maps to NM_002705.4 A1429A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:21335304 G>A maps to NM_144704.2 T601T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:38678961 G>A maps to NM_001049.2 W123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:149786470 C>T maps to NM_001025159.1 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:52182141 C>T maps to ENST00000344768 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:174363156 G>A maps to NM_014857.3 P528P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:240033254 G>A maps to NM_006037.3 Q644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:44056763 G>A maps to NM_002840.3 A357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:48677207 C>T maps to NM_018896.3 D1226D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:17316891 C>T maps to ENST00000458064 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:8875869 T>C maps to NM_153332.3 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:176722103 C>T maps to NM_022455.4 Q2579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:37382696 G>T maps to NM_001171979.1 A413A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:46627924 C>T maps to NM_001001928.2 A316A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:26937350 C>T maps to NM_003595.3 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:136602207 G>T maps to NM_005915.4 Y752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:54925318 C>T maps to NM_003647.2 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:248512484 C>T maps to NM_001001918.1 R137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:107937886 G>A maps to NM_001018072.1 E487E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:27464906 C>T maps to NM_004341.3 G2004G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:186067968 C>T maps to NM_001151.3 A247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:26350741 G>A maps to NM_016131.4 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:99103949 C>T maps to NM_014569.3 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:121440887 G>A maps to NM_003105.5 Q1082Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:45059909 G>A maps to NM_176819.3 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:50195629 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:149467527 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:47337512 C>T maps to NM_020528.2 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:33517273 G>A maps to NM_000178.2 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:166019219 G>A maps to NM_006922.3 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:122677356 C>T maps to NM_001098519.1 D385D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:8612994 G>A maps to NM_012335.3 F398F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:123665935 T>C maps to NM_022757.4 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:70679737 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:5568998 G>T maps to NM_001101.3 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:9188912 C>T maps to NM_024980.4 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:11687883 G>A maps to NM_004462.3 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:7810794 C>T maps to NM_021155.3 K119K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:10200692 C>A maps to NM_018381.2 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:139264219 G>A maps to NM_052813.4 V353V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:28472206 G>A maps to NM_182701.1 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:39262206 C>A maps to ENST00000377731 C184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:73721303 G>A maps to ENST00000427855 A462A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:41388042 G>A maps to NM_000764.2 Q25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:54343146 A>G maps to NM_001126328.1 G555G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:24543645 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:48787771 G>A maps to NM_000138.4 C811C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:153907338 G>T maps to NM_014856.2 P890P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:21549148 G>A maps to NM_014572.2 R1043*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:39095427 G>A maps to NM_198963.1 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:58506769 C>T maps to NM_181707.2 D159D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:156819221 C>T maps to NM_014215.2 Q420Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:629761 C>T maps to NM_005035.3 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:61564440 G>A maps to NM_001143818.1 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:120277276 C>T maps to NM_006623.3 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:237801715 C>T maps to NM_001035.2 G2284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:228459902 C>A maps to ENST00000359599 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:122829988 T>C maps to NM_001081550.1 K161K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:100842057 G>A maps to NM_178176.2 H114H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:212285273 A>G maps to NM_005235.2 D1009D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:135073360 C>T maps to NM_032536.2 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:129961312 G>A maps to NM_014636.2 E405E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:6578435 C>T maps to NM_015274.1 D90D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:70231304 G>A maps to NM_015570.2 T558T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:96412578 C>A maps to NM_000895.1 E272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:14482806 C>T maps to NM_007118.2 I2194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:32768362 C>T maps to NM_023037.2 D1225D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:50701281 G>T maps to NM_199427.2 T584T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:36704167 C>T maps to NM_016441.2 C376C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:39133094 G>A maps to NM_033655.3 P638P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:14266185 G>A maps to NM_001008701.2 C1098C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:89938473 G>A maps to NM_032119.3 V754V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:34803133 C>T maps to NM_017754.3 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:15174859 G>A maps to ENST00000378143 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:121726194 G>A maps to NM_005763.3 A685A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:122671894 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:176959575 G>A maps to ENST00000442143 C381C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:117914324 G>A maps to ENST00000339824 P842P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:61512120 G>A maps to NM_033081.2 P1729P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:85255610 C>A maps to NM_182767.4 E665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:46407333 C>A maps to NM_000741.2 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:49954800 G>A maps to NM_017916.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:239056535 C>T maps to NM_198582.3 P404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:148998538 C>T maps to NM_001001669.2 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:63990441 C>T maps to NM_016571.2 T338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:113780107 A>G maps to NM_006028.3 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:3413806 G>T maps to ENST00000452816 G1232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:87339251 T>G maps to NM_006180.3 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:20169001 G>A maps to NM_003884.4 E570E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:226573297 G>A maps to NM_001618.3 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:124765425 G>A maps to NM_019055.5 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:111551243 G>A maps to NM_001142807.1 W59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:2124211 C>A maps to NM_000548.3 V789V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:60229916 C>T maps to NM_152866.2 Q24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:96435917 C>T maps to NM_005392.3 S800S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:64863942 G>A maps to NM_014755.2 I21I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:93118416 C>T maps to NM_024832.3 C341C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:23504174 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:15989757 T>G did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:57754063 A>C maps to NM_032866.3 R793R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:28446600 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:77423631 C>T maps to NM_203394.2 P621P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:135095824 A>G maps to NM_006659.2 L771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:186645083 C>T maps to NM_000963.2 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:48343133 G>A maps to NM_000554.4 K270K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:230415071 C>T maps to NM_004481.3 N528N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:124413186 G>T maps to NM_001024660.3 E2472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:138727815 G>A maps to ENST00000370578 Q133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:140256685 G>A maps to NM_018903.2 P543P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:114541117 G>A maps to ENST00000357389 C171C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:24123082 C>T maps to NM_005940.3 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:17055100 C>A maps to NM_016353.4 Y128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:82131893 G>A maps to NM_002153.2 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:30107918 C>T maps to NM_002742.2 R296R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:8926328 G>A maps to NM_020734.2 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:75763910 C>T maps to ENST00000378695 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:47856539 C>T maps to NM_014681.5 Q85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:33260973 G>A maps to NM_001103184.2 I753I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:25007191 G>A maps to NM_005265.2 K48K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:7620617 G>A maps to NM_181874.2 T675T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:41884212 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:150931241 C>T maps to NM_019015.1 R49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:17570599 C>T maps to NM_013358.2 S618S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:73566150 C>A maps to NM_001031803.1 R563R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:73814403 C>T maps to ENST00000334126 T784T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:70585409 G>A maps to NM_030958.2 F747F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:11860308 G>A maps to ENST00000376585 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:6751207 G>A maps to NM_006999.4 A389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:37239785 C>T maps to NM_020405.4 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:39292727 G>A maps to NM_006149.3 N243N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:150715330 C>T maps to NM_203395.2 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:87446178 C>T maps to NM_015144.2 S579S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:89764194 C>T maps to NM_152339.3 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:140109117 C>A maps to NM_001144026.1 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:145635401 C>T maps to NM_022475.1 F483F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:234743035 G>A maps to NM_182972.2 S537S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:32352161 C>T maps to NM_003405.3 R42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:96781655 C>T maps to NM_000682.5 W78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:76803496 C>T maps to NM_025090.3 Q543Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:124332578 C>T maps to NM_207437.3 D1844D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:180817220 T>C maps to NM_020943.2 K598K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:11792004 G>A maps to ENST00000356957 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:79743883 G>T maps to NM_014733.3 E922*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:231077539 C>T maps to NM_080424.2 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:49088332 G>A maps to NM_005183.2 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:170883634 C>T maps to NM_003862.2 Y150Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:142443463 C>A maps to ENST00000476941 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:22078011 C>A maps to NM_032236.5 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:71354233 G>A maps to NM_001144952.1 I1859I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:18729429 G>A maps to NM_173588.3 R1067R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:72413258 G>A maps to ENST00000434423 T909T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:76354663 G>A maps to NM_003955.3 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:32095234 G>A maps to NM_004381.4 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:33527364 A>G maps to NM_030955.2 C1571C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:101139426 A>C maps to NM_001011657.3 T324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:23311684 C>T maps to NM_004995.2 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:241737163 G>A maps to ENST00000373308 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:153484902 C>T maps to NM_052905.3 Y752Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:151021075 A>G maps to NM_017860.3 Q251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:34033453 G>A maps to NM_181435.4 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:62601978 T>C maps to NM_018093.2 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:107040936 C>T maps to ENST00000304514 Q1162Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:99422665 C>T maps to ENST00000416867 R279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:32171926 C>T maps to NM_004557.3 L1035L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:82606166 A>G maps to NM_001010893.2 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:161487865 G>A maps to NM_001136219.1 R294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:25913549 G>A maps to NM_005835.2 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:72064646 G>A maps to NM_001163.3 S678S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:37454763 G>T maps to NM_005760.2 V524V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:42178257 C>T maps to NM_001556.2 N528N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:104133247 T>C did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:38710826 G>A maps to NM_001013620.3 Q44Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:46245531 G>A maps to NM_001295.2 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:205210943 C>T maps to NM_014858.3 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:57431698 G>A maps to NM_005379.2 R639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:15826525 G>T maps to NM_001040114.1 A1189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:101912013 G>A maps to NM_001100626.1 F307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:42356346 G>A maps to NM_152447.3 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:55304312 G>A maps to NM_019036.2 G310G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:62082713 G>A maps to NM_001099789.1 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:112480016 G>A maps to NM_001105206.1 N578N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:26816641 C>T maps to NM_002223.2 S563S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:31084128 G>A maps to NM_001264.4 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:138643991 T>C maps to ENST00000394800 C296C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:70190410 C>T maps to NM_017990.3 Q757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:64485151 C>T maps to NM_020762.2 F511F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:202900638 C>T maps to NM_003507.1 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:120190844 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:38933649 G>A maps to NM_007068.2 N261N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:249142225 C>T maps to NM_024836.1 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:50204564 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:79699096 G>A maps to NM_001170574.1 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:65253541 C>T maps to ENST00000389723 Q1051Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:140175955 G>A maps to NM_018905.2 P469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:136907019 C>T maps to NM_007371.3 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:21562823 G>T maps to NM_014572.2 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:118950318 C>T maps to NM_002581.3 G434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:43161894 G>A maps to ENST00000352483 V534V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:39033739 A>G maps to NM_198963.1 D1259D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:50471770 C>T maps to NM_001080447.1 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:67984389 G>A maps to NM_005072.4 G487G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:89807274 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:43329595 C>T maps to NM_015500.1 Q330Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:105614747 G>A maps to NM_002226.3 C683C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:151672726 G>A maps to NM_005100.3 Q1067Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:75876436 G>T maps to ENST00000431480 S952S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:66043693 C>T maps to NM_030981.2 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:126128620 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:142241617 C>T maps to NM_001184.3 A1406A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:1115462 G>A maps to NM_001130045.1 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:128582341 C>A maps to NM_003069.3 E1037*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:2436265 C>T maps to ENST00000452833 P499P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:11384843 C>T maps to NM_001332.2 E370E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:144508030 C>T maps to NM_003764.3 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:189702354 G>A maps to NM_018192.3 R405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:35761741 T>C maps to NM_002791.1 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:141774406 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:244006482 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:48965136 C>T maps to NM_170720.1 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:72371288 C>T maps to NM_019885.2 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:122774740 G>A maps to NM_024806.2 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:39034061 G>A maps to NM_002062.3 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:180904328 C>T maps to NM_020950.1 S428S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:2264198 G>A maps to NM_001042371.2 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:143781977 C>T maps to ENST00000292430 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:86124898 G>A maps to NM_006738.4 E1200E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:113333195 C>T maps to NM_019014.4 L1100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:132636672 C>T maps to NM_024078.1 S454S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:26951009 C>T maps to NM_002246.2 D253D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:145719316 C>T maps to NM_002700.2 H109H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:21986449 G>A maps to NM_005144.4 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:136575092 C>A maps to NM_002299.2 G509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:135287025 A>G maps to NM_002302.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:189599452 G>A maps to NM_052952.2 C65C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:75875789 G>A maps to NM_006851.2 W117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:32164145 G>A maps to NM_004557.3 R1751R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:271137 C>A maps to NM_001170738.1 I830I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:177249378 T>G maps to NM_021928.3 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:179201851 T>C maps to NM_014757.4 L1009L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:130766993 C>T maps to ENST00000514667 S1391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:42967183 C>T maps to NM_014509.3 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:153694276 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:56042644 G>A maps to NM_001101401.2 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:24254939 C>T maps to NM_014479.3 R200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:57802169 C>A maps to NM_006635.3 Y87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:36004915 G>A maps to NM_032594.3 E486E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:139563095 C>T maps to NM_201446.1 C56C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:75599928 T>C maps to NM_003369.3 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:50356511 A>G maps to NM_001001852.3 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:67200474 C>T maps to NM_003952.2 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:126733349 C>T maps to NM_032242.3 G878G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:120436419 G>A maps to NM_207311.2 K175K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:99454484 C>T maps to NM_022820.3 I276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:155156623 G>A maps to NM_017639.3 N2605N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:166864716 A>C maps to ENST00000510118 S385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:60348320 A>C maps to ENST00000267215 G1107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:174979109 T>C maps to NM_014412.2 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:128366288 C>T maps to ENST00000389524 L884L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:148311387 C>T maps to NM_145304.2 N153N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:20248848 G>T maps to NM_014589.1 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:46685355 C>T maps to NM_017931.2 C380C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:123843829 G>A maps to NM_206862.2 K605K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:147861050 G>A maps to ENST00000513335 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:155752005 G>A maps to NM_015718.2 R288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:116840414 C>T maps to NM_001633.3 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:12368617 C>A maps to NM_015378.2 S2190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:47173813 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:48055279 C>T maps to NM_153618.1 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:154217081 G>A maps to NM_015271.3 P468P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:12262854 C>T maps to ENST00000342845 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:218520114 C>T maps to NM_001135599.2 C24C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:130877872 G>A maps to NM_001099771.2 C72C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:40417899 C>T maps to NM_138435.2 T462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:57466829 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:24900667 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:40368525 G>A maps to NM_003890.2 Y4274Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:49348050 A>G did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:42352906 G>A maps to ENST00000427618 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:103496746 G>T maps to NM_080629.2 Y235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:154420625 C>T maps to NM_000565.2 N325N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:95555145 T>G did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:35254111 T>C maps to NM_003427.3 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:79064171 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:34004314 G>A maps to NM_000841.1 C524C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:27645270 G>A maps to NM_182488.3 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:70714874 G>A maps to NM_138383.2 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:54575784 A>G did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:50393094 C>T maps to NM_172374.1 S534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:30411331 G>A maps to NM_033118.3 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:100140354 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:30666167 C>T maps to NM_024031.2 Q293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:44497023 C>T maps to NM_181489.5 W6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:26370751 C>T maps to NM_001197246.1 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:50941255 G>A maps to NM_007051.2 G583G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:159654114 C>A maps to NM_032532.2 A857A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:48255599 C>T maps to NM_002747.3 R380R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:85570250 C>T maps to NM_145172.3 C508C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:68479977 G>A maps to NM_016166.1 Q587Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:42373812 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:159163288 G>A maps to NM_021189.3 Q187Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:228195438 C>T maps to NM_020194.4 R46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:14593527 G>A maps to NM_202470.1 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:156555862 C>T maps to ENST00000354505 W186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:42986628 G>A maps to NM_057161.2 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:11727881 G>A maps to NM_145295.3 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:28302266 G>A maps to NM_007038.3 C721C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:140249980 G>A maps to NM_018902.3 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:95582074 T>C maps to NM_177438.2 P612P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:94486405 C>T maps to NM_004560.2 K790K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:7830518 C>T maps to NM_001144907.1 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:145878171 C>T maps to NM_006706.3 R769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:43451466 G>A maps to NM_006887.4 S492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:38923315 T>A maps to NM_003999.2 A610A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:81979813 C>T maps to NM_002661.2 S1172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:97007617 C>T maps to NM_015341.3 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:219099091 C>T maps to NM_005731.2 Y80Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:77976530 G>A maps to NM_006835.2 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:18031739 G>A maps to ENST00000400579 S1413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:87027679 C>T maps to NM_016206.2 W133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:176317668 G>A maps to NM_002115.2 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:30433571 A>G did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:55511078 C>A maps to NM_199421.1 C440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:62286942 A>G maps to NM_001620.1 F4982F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:109523651 G>A maps to NM_032663.3 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:134073690 C>T maps to NM_015261.2 K442K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:46827245 C>T maps to NM_015234.4 T798T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:157494129 G>T maps to NM_031281.2 S726S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:40191547 C>T maps to NM_005239.4 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:4583160 C>T maps to NM_004170.5 V439V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:101377771 T>C maps to NM_133496.4 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:1052540 G>A maps to NM_006598.2 T1062T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:104041483 G>A maps to NM_001813.2 R2384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:32460280 G>A maps to NM_001190455.1 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:113123 T>C maps to NM_022450.3 E173E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:12977512 C>T maps to NM_014975.2 D692D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:107743564 C>T maps to NM_007356.2 G368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:77907930 G>A maps to NM_032808.5 I106I. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-IB-7651-01A-11D-2154-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:35550661 C>T maps to NM_182983.2 N82N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:26110095 C>T maps to NM_000625.4 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:792040 C>T maps to NM_001191061.1 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:11160377 G>A maps to NM_013427.2 S744S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:29769595 G>A maps to NM_021738.2 I1749I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:197665543 C>T maps to NM_001134435.1 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:121753176 C>A maps to NM_005763.3 E425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:74621579 G>A maps to NM_018414.3 G545G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:3703685 G>A maps to NM_020710.2 G268G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:99347218 T>C maps to NM_012160.3 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:12954532 G>A maps to NM_001039361.3 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:2788896 C>T maps to NM_199460.2 G1841G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:188590547 C>T maps to NM_005578.3 C569C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:11643739 G>A maps to NM_145043.2 Q319Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:127306127 C>A maps to NM_033334.2 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:49052676 G>T maps to NM_032785.3 A422A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:46800053 G>A maps to ENST00000415402 D843D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:85890796 G>A maps to NM_198843.2 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:10823294 C>T maps to ENST00000429377 Q515Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:44035935 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:16456083 G>A maps to NM_004431.3 R890R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:81964504 T>C maps to NM_000722.2 E80E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:78604209 C>A maps to NM_014903.4 A2335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:152528984 G>A maps to NM_001164507.1 V1399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:82335560 G>A maps to NM_032246.3 S550S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:56647085 G>A maps to NM_173595.3 G362G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:23758361 C>T maps to NM_017707.3 E791E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:16141918 G>A maps to NM_013262.3 E114E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:105174178 C>T maps to ENST00000252520 T525T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:38470345 C>T maps to NM_012407.3 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:61542496 G>A maps to NM_033081.2 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:166039939 A>G maps to NM_001017961.3 D108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:9054330 C>A maps to NM_024690.2 E10431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:147131304 G>A maps to NM_003412.3 A437A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:18538217 G>A maps to NM_032627.3 Q39Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:179051597 C>T maps to NM_016331.1 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:125432717 G>A maps to NM_032656.3 P1100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:30689794 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:94731618 G>A maps to NM_018039.2 Q361Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:96022416 T>C maps to ENST00000371380 L1327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:72775295 C>T maps to NM_017757.2 D1873D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:46201905 G>A maps to NM_017659.3 Q245Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:129914032 G>A maps to NM_002417.4 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:39797611 T>C maps to ENST00000289893 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:46052878 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:6618916 G>A maps to NM_014865.3 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:178506422 C>T maps to NM_014594.1 C330C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:3660156 G>A maps to NM_025220.2 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:167550299 C>T maps to NM_004367.5 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:91477380 G>A maps to ENST00000416354 Q391Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:22658709 G>A maps to NM_004540.2 E153E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:87482308 C>T maps to NM_006180.3 Y532Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:75980459 A>G maps to NM_001897.4 D982D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:79692680 C>T maps to NM_017934.5 K897K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:143780342 C>T maps to NM_003630.2 C65C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:160086400 C>T maps to NM_033394.2 I1488I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:13190141 C>A maps to ENST00000319217 G709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:47164396 C>A maps to NM_014159.6 E577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:76248891 G>T maps to NM_015072.4 E860*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:69990400 C>T maps to ENST00000448226 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:1041387 C>T maps to NM_019112.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:8390957 G>A maps to NM_003501.2 P493P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:19816892 T>C did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:1592090 G>A maps to NM_001135844.1 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:17945946 C>T maps to NM_000215.3 P664P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:123848883 T>C maps to NM_145207.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:170103013 C>T maps to ENST00000439249 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:124509616 C>T maps to NM_170601.3 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:50412725 G>T maps to NM_012346.4 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:71152457 G>A maps to NM_001360.2 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:140475756 C>T maps to NM_018936.2 F461F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:44893043 C>T maps to NM_032287.2 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:66807940 C>T maps to NM_017975.3 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:52526254 G>A maps to NM_007184.3 Q1424Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:46744799 C>T maps to NM_000506.3 C129C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:35438415 T>A maps to NM_007104.4 Y181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:120348236 T>C did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:55563333 G>A maps to NM_015306.2 H1884H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:106509466 G>A maps to NM_001004720.2 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:3735095 G>A maps to NM_001039140.1 C149C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:13438715 G>A maps to NM_032320.5 R226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:146214433 A>G maps to ENST00000367503 T1601T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:159546029 C>T maps to NM_001130864.1 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:44815311 G>A maps to NM_021248.1 D526D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:14518804 C>T maps to NM_001134367.1 F434F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:60688594 G>A maps to NM_022893.3 D484D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:6477405 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:38610229 C>T maps to NM_001552.2 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:33783326 C>A maps to NM_170672.2 A543A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:123751957 G>A maps to NM_001735.2 S1014S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:21690004 A>G maps to NM_021957.3 D665D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:32902713 C>T maps to NM_004274.4 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:59028773 G>A maps to NM_032792.2 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:130067742 G>A maps to NM_021978.3 P454P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:46995360 C>T maps to NM_000809.2 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:49060384 C>T maps to NM_199069.1 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:77423892 C>T maps to NM_003664.3 A643A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:140553894 C>T maps to NM_018940.2 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:35609357 C>A maps to NM_006285.2 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:44060850 C>A maps to NM_001123066.3 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:74201962 C>T maps to NM_001123226.1 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:152506867 C>T maps to NM_001164507.1 W2418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:104387964 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:64082497 C>T maps to NM_004451.3 D256D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:157522257 C>T maps to ENST00000367148 S1550S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:122677156 C>A maps to NM_032873.4 S545S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:247492621 G>A maps to NM_032752.1 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:152476173 G>A maps to NM_182961.2 I7994I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:13716562 G>A maps to NM_000834.3 N1203N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:290821 C>T maps to ENST00000409479 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:53254331 G>A maps to ENST00000398339 R108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:34802045 C>T maps to NM_020776.1 R530R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:56212806 C>T maps to NM_014182.4 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:44052678 G>A maps to NM_001099284.1 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:131520709 G>A maps to ENST00000431975 K227K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:48371056 G>A maps to NM_153034.2 E175E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:12699158 C>T maps to NM_024899.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:228145241 T>C maps to NM_000091.4 I770I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:142655465 C>T maps to NM_000420.2 Q150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:30553099 C>T maps to NM_001025091.1 N485N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:40653290 C>T maps to NM_198578.3 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:92534059 C>T maps to ENST00000298047 P2627P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:58811414 T>G maps to NM_002892.3 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:158526366 G>A maps to NM_024007.3 N40N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:17836831 C>T maps to NM_018174.4 Y213Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:71026838 G>A maps to NM_032682.4 N461N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:9204615 C>T maps to ENST00000305465 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:70589060 G>A maps to NM_012426.4 V554V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:47429161 C>T maps to NM_001080467.2 V871V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:54496517 G>A maps to NM_004463.2 D344D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:30537046 C>T maps to NM_024671.3 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:219497007 G>A maps to ENST00000432688 Q474Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:4864470 G>A maps to NM_002448.3 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:159537008 G>A maps to NM_003628.3 L1133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:148035154 C>T maps to NM_002025.3 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:54544246 C>A maps to NM_198481.3 G227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:88474332 G>A maps to NM_018271.3 K133K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:102822113 C>T maps to NM_001177611.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:126319742 G>A maps to NM_001031712.2 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:10134656 G>A maps to ENST00000355690 W199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:62357997 C>T maps to NM_018008.3 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:58949752 G>A maps to NM_015177.1 K251K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:211749593 T>C maps to NM_021194.2 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:153296624 A>G maps to NM_012177.3 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:158299256 G>A maps to NM_001764.2 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:151458615 G>A maps to NM_207365.3 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:42244299 C>T maps to ENST00000449246 S526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:125445238 T>C maps to ENST00000278903 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:5443516 C>T maps to NM_001004757.2 I29I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:91996225 G>A maps to NM_006378.3 G494G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:75101333 G>A maps to NM_145170.3 D205D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:9416644 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:58038646 G>A maps to NM_005912.2 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:118521154 C>A maps to NM_015157.2 C1259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:91203588 G>A maps to NM_213606.3 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:63283198 C>A maps to NM_014562.3 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:54377220 C>T maps to NM_001020818.1 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:96904234 T>C maps to NM_152327.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:211449612 G>A maps to NM_001136223.1 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:44425976 G>A maps to NM_014652.3 W695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:19315992 A>G maps to NM_018371.4 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:58126673 C>T maps to NM_001122772.1 E546E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:184859343 C>A maps to NM_052966.2 G111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:248202495 A>G maps to NM_001004686.2 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:24646360 G>A maps to NM_005132.2 E212E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:56586898 G>A maps to NM_018181.4 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:28193582 G>A maps to NM_002430.2 G983G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:78032407 C>T maps to NM_017950.2 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:140985425 G>A maps to NM_138702.1 R580R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:9359998 C>T maps to NM_020648.5 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:57188213 G>A maps to NM_024946.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:30666367 G>A maps to NM_024031.2 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:61542331 G>A maps to NM_033081.2 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:53108558 C>T maps to NM_001042693.1 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:159672508 C>T maps to NM_032532.2 C1670C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:39931784 G>T maps to NM_001123385.1 T938T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:22222459 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:35737267 C>T maps to NM_020944.2 Q894Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:38151280 C>T maps to NM_002809.2 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:45605402 T>C maps to NM_020937.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:43936060 G>A maps to NM_022785.3 L1275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:28995174 G>A maps to NM_032038.2 S463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:10051374 G>A maps to NM_030962.3 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:12858053 C>A maps to NM_001162499.1 A541A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:126213269 G>A maps to NM_014026.3 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:2168026 C>T maps to NM_001009944.2 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:962265 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:51411930 C>T maps to NM_001005272.3 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:220424001 G>A maps to NM_015311.2 G1057G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:27893615 G>T maps to NM_198147.2 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:80478527 C>T maps to NM_000137.1 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:134583013 A>C did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:9404499 C>T maps to NM_001172646.1 R809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:46580535 G>A maps to NM_024512.3 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:212151703 C>T maps to NM_015434.3 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:104464826 T>C maps to NM_031274.3 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:77576197 C>T maps to NM_033426.2 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:6686218 C>T maps to NM_000064.2 Q1242Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:67016647 A>G maps to NM_080283.3 S827S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:31538307 G>A maps to NM_012131.2 R210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:111984011 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:41765517 G>A maps to NM_021913.3 E798E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:23765065 G>A maps to ENST00000359598 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:12292727 G>A maps to NM_001955.4 W73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:32495259 G>A maps to NM_000343.3 Q457Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:34500718 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:51274700 C>T maps to NM_001506.1 R282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:3544818 G>A maps to NM_001080524.1 Y35Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:27204770 C>T maps to NM_152739.3 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:117120302 G>A maps to NM_030767.4 S879S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:47427968 C>T maps to NM_000812.3 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:18779808 G>A maps to NM_018316.1 P534P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:29755642 G>A maps to NM_175900.3 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:122848533 T>C maps to NM_001098169.1 E175E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:28081320 C>T maps to NM_022128.1 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:236141259 G>A maps to NM_002508.2 G1217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:34194835 C>T maps to NM_145804.2 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:154179550 G>A maps to ENST00000377643 E555E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:138440527 G>A maps to ENST00000340780 W143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:140475111 G>A maps to NM_018936.2 K246K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:111603010 C>T maps to NM_001134438.1 N29N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:60913185 C>A maps to NM_005560.3 G593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:34147405 C>T maps to NM_139215.1 N85N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:135080488 G>A maps to NM_001190850.1 R342R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:17722392 G>A maps to NM_001005291.2 R364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:43490508 C>T maps to NM_015052.3 I827I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:17988835 C>T maps to NM_000453.2 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:54074946 C>T maps to NM_001079907.1 D33D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:51092832 G>A maps to ENST00000395542 S1329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:53607994 G>A maps to NM_000966.4 Q221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:63356267 C>T maps to ENST00000380364 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:124149505 C>T maps to NM_001024660.3 L903L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:64542661 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:124979497 G>A maps to NM_014368.3 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:28009580 T>C maps to NM_002097.2 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:87968169 G>A maps to NM_001166693.1 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:4011158 G>A maps to NM_152744.3 T592T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:72849500 C>A maps to NM_003508.2 C388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:21998635 G>A maps to NM_005691.2 F999F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:69949054 C>T maps to NM_001704.2 F917F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:68725451 G>A maps to NM_015686.2 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:2790602 G>A maps to NM_003249.3 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:118068806 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:173722354 C>T maps to NM_014458.3 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:130675021 A>C maps to NM_001001486.1 I277I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:23977639 A>C maps to NM_017552.1 A1361A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:71267540 C>T maps to NM_033141.2 E221E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:10064429 G>A maps to NM_030962.3 C80C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:97220649 C>T maps to NM_032558.2 G391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:89345737 C>T maps to NM_013275.4 T2404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:105929590 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:90402592 G>A maps to NM_014611.1 L3386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:79073802 G>T maps to NM_017451.2 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:73470187 G>A maps to NM_006429.3 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:7707365 C>T maps to ENST00000441779 D293D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:33591413 G>A maps to NM_015638.2 N685N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:122361663 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:98340825 G>A maps to NM_001079.3 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:40331284 G>A maps to NM_001436.3 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:2834612 C>T maps to NM_001102651.1 G460G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:227660981 G>A maps to NM_005544.2 L825L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:32387722 G>A maps to NM_016107.3 L811L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:40317622 A>G maps to NM_012285.2 S643S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:133779300 C>T maps to NM_001165881.2 F343F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:37005585 G>T maps to NM_001166038.1 I185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:148868427 A>G maps to NM_032383.3 A402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:139743980 C>T maps to NM_014172.4 S33S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-IB-7651-01A-11D-2154-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:67183521 G>A maps to NM_033309.2 G289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:152322114 C>T maps to NM_018151.4 G2027G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:65417743 C>T maps to NM_198686.2 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:16770132 G>A maps to NM_018090.4 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:40528414 C>T maps to NM_001145082.2 D178D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:118583135 C>T maps to NM_006773.3 V494V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:148687145 G>A maps to NM_152406.2 Q239Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:67574549 G>A maps to NM_001193523.1 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:6432328 G>A maps to ENST00000389906 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:86352067 C>A maps to NM_005181.3 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:42974253 G>A maps to NM_006245.2 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:3678682 G>A maps to NM_023068.3 S628S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:135285643 G>A maps to NM_015135.2 E767E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:62760993 G>T maps to ENST00000430500 I477I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:16192998 G>T maps to NM_153365.2 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:41895196 C>T maps to NM_004053.3 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:5428404 G>A maps to NM_012307.2 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:96140198 T>C maps to NM_003728.3 L522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:25470534 G>A maps to NM_025176.4 D524D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:72477914 G>A maps to NM_007261.2 W239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:11194520 G>A maps to NM_004958.3 I1711I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:4680519 C>T maps to NM_001080123.1 Y218Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:204588891 G>A maps to NM_201630.1 Q77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:26696369 C>T maps to NM_000638.3 E203E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:28386586 C>T maps to NM_198529.3 R869*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:73432935 G>A maps to NM_015009.1 S927S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:43359720 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:73462396 G>A maps to ENST00000398860 L898L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:37578257 G>A maps to NM_182486.1 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:125872143 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:24561581 C>T maps to NM_012295.3 S1665S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:259965 C>T maps to NM_153269.1 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:34635838 G>A maps to NM_005866.2 H154H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:207648340 C>T maps to NM_001006658.2 S832S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:183873533 G>A maps to NM_004423.3 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:49320694 C>T maps to NM_001193489.1 Q283Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:199011667 G>A maps to NM_006226.3 E1090E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:187084634 G>A maps to ENST00000356371 P588P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:71418552 G>A maps to NM_001144952.1 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:129903572 G>A maps to NM_002417.4 S2177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:44141642 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:85724405 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:43766204 C>T maps to NM_002784.3 E172E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:155850385 G>A maps to NM_152280.4 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:23066661 G>A maps to NM_012072.3 N56N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:23932600 G>A maps to NM_014363.4 Y159Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:154574526 G>A maps to ENST00000292205 I240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:81599495 G>A maps to NM_001033723.2 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:32126344 C>T maps to NM_022130.3 W290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:134591330 C>T maps to ENST00000368593 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:100705716 G>T maps to NM_003403.3 E46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:8381679 T>C maps to ENST00000360416 R1894R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:185992271 A>G maps to NM_031935.2 Q1912Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:150094567 C>T maps to NM_173680.3 G333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:237013810 A>G maps to NM_000254.2 T561T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:14995975 G>A maps to NM_021071.2 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:137328345 G>A maps to NM_002957.4 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:130785192 G>A maps to NM_014758.2 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:10557845 G>T maps to NM_001040032.1 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:66607509 C>T maps to NM_001143688.1 D317D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:169446392 C>T maps to NM_006996.2 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:90774379 C>A maps to NM_006384.3 E138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:25003611 C>T maps to NM_032501.2 Q308Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:92963454 T>C maps to NM_017667.2 S668S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:2130328 G>A maps to NM_000548.3 V1187V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:67939171 G>A maps to NM_017635.3 R220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:235647765 G>A maps to ENST00000366599 R184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:76442237 G>A maps to NM_139207.2 Q383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:22206737 C>T maps to ENST00000344041 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:87445749 C>T maps to NM_015144.2 T722T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:42139008 C>T maps to NM_005090.3 D872D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:100155440 A>G did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:153744852 C>T maps to ENST00000428986 L921L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:64818835 G>A maps to NM_007235.3 R442R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:161135182 C>T maps to NM_012475.4 S548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:129373834 G>A maps to NM_001017395.3 S541S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:51485162 A>G maps to NM_005046.2 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:56098048 G>A maps to NM_001039349.1 R376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:113281505 G>T maps to ENST00000355319 I427I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:32215143 C>T maps to NM_001136029.1 F601F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:90485728 C>T maps to NM_018319.3 Y537Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:38752373 G>A maps to NM_006514.2 G1368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:152327348 G>A maps to NM_001014342.2 S971S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:134055267 G>A maps to NM_015261.2 D733D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:9629924 C>A maps to NM_019599.2 E74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:71972656 G>T maps to NM_003667.2 G452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:51021886 G>T maps to NM_001080457.1 C361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:219528784 G>T maps to NM_022453.2 G425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:12910730 G>A maps to NM_005809.4 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:36596003 G>T maps to NM_000448.2 E384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:51068305 A>G maps to NM_173602.2 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:134322978 G>A maps to NM_178554.4 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:111895131 C>T maps to NM_002973.3 A1134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:76060854 T>C maps to NM_001142640.1 S813S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:26225339 A>C maps to NM_004289.6 I674I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:53645098 G>A maps to NM_001172674.1 R329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:31682384 C>T maps to NM_194300.2 D467D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:43669670 G>A maps to NM_001001937.1 R171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:115269645 G>A maps to NM_001130523.1 A489A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:150775932 C>T maps to NM_006712.3 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:186423588 G>A maps to NM_014476.4 F318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:147128792 C>T maps to NM_003412.3 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:43693985 C>T maps to ENST00000399460 R558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:33017509 C>T maps to NM_033111.3 W388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:116710907 G>A maps to NM_139169.4 K147K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:104577397 C>A maps to NM_001059.2 G281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:42949836 C>T maps to NM_001099858.1 Q279Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:87229944 C>T maps to NM_138817.2 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:45811194 C>T maps to NM_013351.1 Y125Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:28459811 G>A maps to NM_018318.3 Q135Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:65113212 C>T maps to NM_006268.3 G238G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:22363696 A>G maps to NM_001001411.2 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:89868814 T>C maps to NM_005467.3 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:122380799 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:43005623 C>T maps to NM_001168370.1 T1717T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:10689965 C>T maps to NM_004565.2 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:110719340 C>T maps to NM_001010898.2 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:123909486 G>A maps to NM_001004463.1 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:19883044 G>A maps to NM_006440.3 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:27728601 C>T maps to NM_001486.3 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:197875014 T>C maps to NM_001024594.2 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:179264405 G>A maps to NM_016175.3 F339F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:8871068 G>A maps to NM_020738.2 F1699F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:177421241 C>T maps to NM_006261.4 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:21057189 C>T maps to NM_003831.3 H434H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:4037767 G>A maps to NM_015897.2 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:58511690 G>A maps to NM_001104631.1 R187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:62291231 G>A maps to NM_018469.3 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:34839168 C>T maps to NM_020180.3 E436E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:16077435 G>A maps to NM_001145819.1 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:42609954 A>G maps to NM_005650.1 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:28604765 C>A maps to NM_001054.3 E166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:57232918 G>A maps to NM_003865.2 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:33752177 G>A maps to NM_181336.3 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:151175109 A>C maps to NM_198395.1 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:183209998 G>A maps to NM_130446.2 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:137772717 C>A maps to NM_004108.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:137630614 C>T maps to NM_000093.3 T485T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:44776674 C>A maps to NM_145044.2 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:734754 G>A maps to ENST00000248142 G914G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:207424740 G>A maps to NM_003812.2 K356K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:140792996 C>T maps to NM_018913.2 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:100730928 C>T maps to NM_030961.1 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:14517875 G>A maps to NM_078481.2 A737A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:4855239 C>T maps to NM_203327.1 Q309Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:115965246 C>T maps to ENST00000446284 E156E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:22664524 G>T maps to NM_004540.2 E195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:19770457 G>A maps to NM_005992.1 G344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:94834669 C>T maps to NM_000783.3 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:100681005 A>G maps to NM_001040105.1 L2103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:119668402 C>T maps to NM_003588.3 L751L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:3559852 C>T maps to NM_001031681.2 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:89341272 G>T maps to NM_013275.4 A2554A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:39381709 G>A maps to NM_001343.2 A450A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:169116330 C>A maps to NM_004946.2 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:105189034 G>T maps to NM_021930.4 E292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:90025580 C>T maps to NM_017702.2 R178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:8083843 G>T maps to NM_006931.2 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:50719910 G>A maps to NM_012401.2 R1180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:44057695 C>T maps to NM_005313.4 D217D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:21720669 C>T maps to NM_001001415.2 S605S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:143091948 A>G maps to NM_005232.4 F768F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:45287577 C>T maps to NM_012116.3 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:46605084 G>A maps to NM_001430.4 P434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:107556054 C>T maps to NM_000108.3 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:48370879 C>T maps to NM_203475.1 V180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:155348094 G>A maps to ENST00000368346 G2108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:26305806 G>A maps to NM_017433.4 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:111678314 C>T maps to NM_002912.3 Q2362Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:79933429 C>T maps to ENST00000376646 L1746L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:145007510 C>A maps to NM_201380.2 R561R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:74676923 G>A maps to NM_001130105.1 L702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:48779353 G>A maps to NM_000138.4 G1169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:36757012 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:86042164 C>A maps to NM_033402.4 I546I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:100569528 A>G maps to ENST00000471714 T474T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:42137857 C>T maps to NM_005090.3 Y691Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:18881886 G>T maps to NM_001039999.2 S364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:94668168 G>A maps to NM_004815.3 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:168352002 C>A maps to ENST00000400822 T1315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:149495412 G>T maps to NM_002609.3 L1078L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:20550137 G>A maps to ENST00000273739 T795T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:112919957 C>T maps to ENST00000392596 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:37050664 C>T maps to NM_014360.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:95131561 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:63029240 C>T maps to NM_015059.2 L1175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:33795561 G>A maps to NM_017947.2 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:55237233 C>T maps to NM_002184.3 R811R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:52268421 G>A maps to ENST00000361841 E142E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:42116131 C>T maps to NM_001128608.1 P1368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:3765498 A>G maps to NM_001810.5 F544F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:49718040 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:1563231 G>A maps to NM_006445.3 R1617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:37132271 C>T maps to NM_006194.3 R59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:45470285 C>A maps to NM_024602.5 E710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:98552884 G>A maps to ENST00000359863 P1958P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:38273868 G>A maps to ENST00000262832 S465S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:145095868 A>G maps to NM_198572.2 P389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:44815473 C>T maps to NM_021248.1 K512K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:139395285 C>T maps to NM_017617.3 P1884P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:9471723 T>C maps to NM_004853.2 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:130942770 G>A maps to NM_012127.2 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:2297999 G>A maps to NM_003245.3 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:14747317 C>A maps to ENST00000380880 E1988*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:140995615 C>T maps to ENST00000413253 G125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:45255623 C>T maps to ENST00000352766 S507S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:237272536 G>T maps to ENST00000457693 V593V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:73712498 C>T maps to NM_003356.3 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:44605037 C>T maps to NM_013398.2 R34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:90771367 C>T maps to NM_198925.2 S669S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:50295143 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:56423640 A>G maps to NM_176810.2 D514D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:31255887 C>T maps to NM_030653.3 G797G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:100730865 T>C maps to NM_030961.1 C91C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:142186835 C>T maps to NM_001184.3 E2209E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:55537453 C>T maps to NM_006269.1 R338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:80159682 C>T maps to ENST00000445854 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:107216797 G>A maps to NM_001163315.2 A635A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:10258613 C>T maps to NM_012073.3 Y280Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:70353109 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:42748844 C>A maps to NM_002463.1 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:53005078 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:41601663 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:21333706 T>G maps to NM_018847.2 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:62407097 G>A maps to NM_025224.2 A385A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:80412493 G>A maps to NM_002072.3 R183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:3909543 C>T maps to NM_033064.4 N236N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:26230289 C>A maps to NM_203399.1 E10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:88677774 C>T maps to ENST00000452588 R460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:139333310 G>A maps to NM_019892.3 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:38840487 C>T maps to ENST00000327475 D2377D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:77305390 G>A maps to NM_001042784.1 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:54313949 C>T maps to ENST00000391773 E321E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:171303753 C>A maps to NM_002022.1 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:62482811 G>T maps to NM_001079559.1 R735R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:160011434 C>T maps to NM_002241.4 V296V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:182783535 C>T maps to NM_001130445.1 Q974*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:106903306 C>T maps to NM_018082.5 L1128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:43837020 A>G maps to NM_016142.2 E142E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:46758264 G>T maps to NM_018976.4 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:135741935 C>T maps to NM_181897.2 R9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:60330859 G>T maps to NM_015888.4 E563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:77805795 G>A maps to NM_005779.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:186425702 C>T maps to NM_014476.4 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:94554836 G>A maps to NM_130847.2 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:7606276 C>T maps to NM_152551.3 R274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:116403138 T>C maps to NM_001127500.1 C818C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:53873225 G>A maps to NM_005016.5 *367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:3170127 G>A maps to NM_001042428.1 S489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:23556037 G>A maps to NM_013293.3 R94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:36691751 C>T maps to NM_016441.2 G315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:41756937 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:47363954 G>A maps to NM_001080467.2 N1690N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:140035277 C>T maps to NM_207113.1 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:127542553 G>A maps to NM_018180.2 I356I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:7177354 C>T maps to NM_001734.3 S489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:100806633 G>T maps to NM_139319.2 G425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:33385651 G>A maps to NM_001170.1 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:44839358 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:52908947 G>A maps to NM_000424.3 G517G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:130698901 C>T maps to ENST00000373110 K42K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:38138653 A>G did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:18622251 C>T maps to NM_001040272.4 C162C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:12070778 G>A maps to NM_015542.2 D370D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:43224099 C>T maps to NM_007163.3 S442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:179647623 G>T maps to NM_133378.4 R1003R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:48698702 C>T maps to NM_001407.2 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:123082325 G>A maps to NM_014708.4 T1468T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:6427419 G>A maps to NM_173637.3 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:3212029 C>T maps to NM_001174090.1 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:107288997 G>A maps to NM_001001919.1 R165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:57193570 G>A maps to ENST00000428603 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:45271005 G>A maps to NM_004073.2 K568K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:230911292 G>A maps to NM_152527.4 C183C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:153032911 G>A maps to NM_005393.2 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:39910395 A>G maps to ENST00000361689 R4439R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:70866245 A>G maps to NM_001858.4 G741G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:105208311 C>T maps to NM_199165.1 I350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:72862342 C>T maps to ENST00000442102 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:167163470 T>C maps to ENST00000303354 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:38709238 T>G maps to NM_001135155.1 R191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:166231250 T>G maps to NM_001040142.1 V1343V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:27829419 C>T maps to NM_000982.3 Y57Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:50733612 T>C maps to NM_022162.1 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:71082517 G>A maps to NM_006540.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:30316751 C>T maps to NM_020848.2 P775P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:25068787 G>A maps to NM_006437.3 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:140431090 G>A maps to NM_013340.2 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:36686020 C>T maps to NM_004734.4 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:39780088 C>T maps to NM_002164.4 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:119568491 C>T maps to NM_194286.2 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:72756149 G>A maps to NM_005098.3 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:148637958 C>T maps to NM_014945.2 L682L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:44470900 G>A maps to NM_004671.2 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:51378994 G>A maps to NM_002863.4 F549F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:44528124 C>T maps to NM_006227.2 V445V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:134158065 C>T maps to NM_030626.2 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:94180660 C>T maps to NM_022900.4 H609H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:131199339 A>G maps to NM_001431.3 S649S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:23240498 G>A maps to NM_005015.3 T435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:175110874 C>A maps to NM_001131055.1 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:133053836 G>A maps to ENST00000262283 D289D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:122097216 G>A maps to NM_173855.4 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:202934625 G>T maps to NM_016243.2 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:66857031 G>A maps to NM_207338.2 D88D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:49094858 G>A maps to NM_198880.1 Y258Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:238688108 C>T maps to ENST00000391999 N609N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:46252621 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:63473111 G>T maps to NM_139318.3 C92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:49089911 C>T maps to NM_001194998.1 E69E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:43530458 C>T maps to NM_139323.2 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:183200177 C>T maps to NM_005562.2 G599G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:53073597 G>A maps to NM_006121.3 R179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:29250055 C>T maps to ENST00000394782 R65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:19379652 G>A maps to NM_001001671.3 D1246D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:2717234 G>A maps to NM_145173.3 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:43692415 C>T maps to ENST00000399460 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:145740379 G>A maps to ENST00000428558 S520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:49312056 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:96932183 C>A maps to NM_004804.2 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:124951717 C>T maps to NM_198277.2 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:41720867 G>T maps to NM_004527.3 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:219527251 C>T maps to NM_004328.4 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:5268463 G>A maps to NM_004703.4 E572E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:446343 C>T maps to ENST00000315013 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:113560615 C>T maps to NM_030770.2 V410V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:159178307 G>A maps to ENST00000297239 T401T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:15936763 C>T maps to NM_012304.3 G315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:39907595 C>T maps to NM_022835.2 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:9949193 C>T maps to NM_006221.2 N47N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:177247922 T>C did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:79348757 C>A maps to NM_002909.4 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:70286689 G>A maps to ENST00000418685 C971C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:176951654 G>A maps to ENST00000442143 S689S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:178310194 T>C maps to NM_058230.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:26905792 G>A maps to NM_001031689.2 L702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:202744819 C>A maps to ENST00000450471 V376V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:138557548 C>T maps to ENST00000277526 C156C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:155487036 G>A maps to NM_005141.4 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:16688460 G>A maps to NM_004831.3 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:150114740 C>T maps to NM_005389.2 D176D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:24587622 C>T maps to NM_025230.4 R202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:159738894 G>A maps to NM_024565.5 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:69990948 C>T maps to NM_006431.2 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:81111234 C>T maps to NM_005593.2 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:43917060 C>T maps to NM_001077663.1 T667T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:48429255 G>A maps to NM_004962.2 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:5626733 G>A maps to NM_001003819.3 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:55589551 C>T maps to ENST00000436346 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:125273895 C>A maps to NM_054107.1 V272V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-IB-7651-01A-11D-2154-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:27185072 C>T maps to NM_000810.3 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:18662596 C>A maps to NM_000330.3 E159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:179336306 A>G maps to NM_002492.2 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:3179635 C>T maps to NM_003775.3 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:36878744 A>G maps to NM_001142294.1 A586A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:54137908 G>A maps to NM_001012728.1 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:242650890 C>T maps to NM_032329.4 R126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:100637317 C>T maps to NM_007129.2 C398C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:220347983 C>T maps to NM_005876.4 P1933P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:3842923 G>A maps to NM_020746.3 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:30749383 G>T maps to NM_006662.2 E2675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:136917481 G>A maps to NM_007371.3 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:36662453 G>A maps to NM_021215.3 K35K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:217543755 G>A maps to NM_000599.3 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:94140363 G>T maps to NM_003567.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:93011173 C>T maps to NM_032373.3 Q151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:56565461 G>A maps to NM_001080439.1 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:57415517 C>T maps to NM_016592.2 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:22162126 G>T maps to NM_005529.5 I3453I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:106037861 G>A maps to NM_183239.1 E118E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:68572462 C>T maps to NM_001799.3 Q320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:119171295 C>A maps to NM_018266.1 E140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:23391063 C>T maps to NM_006547.2 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:202065192 G>T maps to ENST00000374650 G238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:214557226 C>T maps to NM_005401.4 T657T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:23705054 G>A maps to ENST00000359598 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:19682422 C>T maps to NM_018142.2 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:207170779 C>T maps to NM_020923.1 Q510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:236902765 G>A maps to NM_001103.2 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:721081 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:69323948 C>A maps to NM_024505.3 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:98562312 C>T maps to ENST00000359863 I2290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:67360623 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:27797739 C>T maps to ENST00000409980 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:45762365 C>T maps to NM_031417.3 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:57689822 C>T maps to NM_005682.5 V312V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:228205076 C>T maps to NM_020194.4 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:88853706 C>T maps to NM_016083.4 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:62941520 G>A maps to ENST00000371140 R1940*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:179442497 C>T maps to NM_133378.4 S20317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:137814749 G>A maps to NM_175747.2 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:62373564 C>T maps to ENST00000278845 G543G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:45713670 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:116579729 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:9154664 G>A maps to NM_003966.2 F472F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:72119295 G>A maps to ENST00000424560 D2495D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:19737612 G>A maps to NM_004720.5 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:230805178 C>T maps to NM_007357.2 V224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:127771253 T>A maps to NM_014702.4 K127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:129373888 G>A maps to NM_001017395.3 I523I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:20987418 C>A maps to NM_005216.4 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:103292172 T>C maps to ENST00000428762 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:51014507 G>A maps to NM_152245.2 R245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:50921211 C>A maps to NM_024866.4 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:22059427 C>T maps to NM_006129.4 H740H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:88272488 T>C maps to NM_020320.3 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:93390550 G>A maps to NM_001275.3 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:47460251 G>A maps to NM_012235.2 D674D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:6903263 C>T maps to NM_181874.2 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:70589012 C>T maps to NM_012426.4 T538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:131755934 G>A maps to NM_015354.1 Q993Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:95802018 C>T maps to NM_181787.2 R685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:18245403 G>A maps to NM_015016.1 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:24942725 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:36644855 C>T maps to NM_001031836.2 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:60767313 C>T maps to NM_006039.3 D1211D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:24538791 T>C maps to NM_001358.2 P597P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:97823691 C>T maps to NM_014916.3 S1305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:99823031 C>T maps to NM_001130679.1 Q40Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:39170681 G>A maps to ENST00000301819 A680A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:132502100 C>T maps to ENST00000333577 S1351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:194118726 A>G maps to NM_004488.2 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:105372694 G>A maps to ENST00000369774 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:15330413 A>C maps to NM_015909.2 A2182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:16987344 C>T maps to NM_015260.1 L971L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:174919198 A>C maps to NM_022754.5 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:74114694 C>T maps to NM_032999.2 N164N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:48717611 C>T maps to NM_016453.2 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:139262244 G>A maps to NM_052813.4 H371H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:1390838 G>A maps to NM_001452.1 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:144995860 G>A maps to NM_201380.2 L2847L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:145075929 C>A maps to NM_007124.2 L2810L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:107084365 T>C maps to NM_012216.3 C157C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:36220437 C>T maps to ENST00000400445 Q2554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:8421824 G>A maps to NM_012102.3 Q672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:67292263 C>T maps to NM_004594.2 R514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:111386403 G>A maps to ENST00000428084 L1555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:15271772 C>T maps to NM_000435.2 P2222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:43944879 C>T maps to NM_014276.2 C358C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:4902974 G>A maps to NM_016936.3 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:155289472 G>A maps to NM_001135821.1 Q306Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:140329482 C>T maps to NM_001033113.1 P457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:74169838 G>A maps to NM_052916.2 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:49759355 C>T maps to NM_013334.2 E331E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:100060988 C>T maps to ENST00000426357 W210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:90814846 C>T maps to NM_001033088.1 Q235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:31570486 G>A maps to NM_000379.3 T1059T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:45188795 C>T maps to NM_022829.5 L558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:167833205 C>T maps to NM_001161661.1 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:39905983 C>A maps to NM_022835.2 Y128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:17298325 A>G maps to NM_017738.2 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:17281988 G>T maps to NM_014675.3 R1216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:55606349 G>A maps to NM_001005496.1 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:117864871 A>G maps to NM_006265.2 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:37059078 G>A maps to NM_133433.3 R2499R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:125047561 C>T maps to NM_001039112.2 V777V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:34181855 G>T maps to NM_145804.2 C814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:107979286 G>A maps to NM_003604.2 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:16450990 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:27427124 G>T maps to NM_003047.3 A707A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:176885541 G>A maps to ENST00000393565 V477V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:220033555 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:52684546 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:49794907 C>T maps to NM_001507.1 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:55752390 C>T maps to NM_138962.2 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:51255297 G>A maps to ENST00000404971 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:100365038 G>T maps to NM_139246.4 Y421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:97655718 G>A maps to ENST00000182096 W876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:39382968 C>T maps to NM_001343.2 W364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:157161740 C>T maps to NM_017872.3 R176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:88940024 C>T maps to ENST00000298786 S788S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:461407 C>T maps to NM_020664.3 Q237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:2049590 G>A maps to ENST00000431526 L653L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:15807726 C>T maps to NM_023944.2 I469I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:92588067 G>A maps to NM_004545.3 V18V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:56292169 G>A maps to NM_017777.3 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:12901215 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:12125781 G>A maps to NM_001080411.1 R634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:72131055 G>A maps to NM_001163.3 I357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:47330913 C>T maps to NM_020528.2 C190C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:12694289 G>A maps to NM_020714.2 I81I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:10107140 G>A maps to NM_033084.3 Q744Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:115805120 C>T maps to NM_000684.2 R410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:9965431 C>T maps to NM_058164.2 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:183899751 C>T maps to ENST00000411763 R319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:42117589 C>T maps to NM_001128608.1 L1501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:51897379 C>T maps to NM_203424.1 N163N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:100465481 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:33641985 T>C maps to NM_030955.2 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:66270341 C>T maps to ENST00000451741 R563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:64855531 C>T maps to NM_006782.3 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:40902344 C>T maps to NM_181882.2 E638E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:57802418 C>A maps to NM_006635.3 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:140867052 C>A maps to NM_018928.2 G771G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:48508596 C>T maps to NM_016381.3 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:117013977 G>A maps to NM_001085481.1 Q77Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:89861713 C>T maps to NM_152999.3 R417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:54652175 C>T maps to NM_014516.3 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:79367897 T>C maps to NM_025074.6 P1958P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:50102775 G>T maps to NM_182922.2 E133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:85955301 C>T maps to NM_033100.2 N36N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:12725604 G>A maps to ENST00000429478 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:86281382 G>T maps to NM_015425.3 I696I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:124740118 G>A maps to NM_022370.3 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:5364598 A>G maps to NM_001005567.1 N52N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:2384146 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:108913101 C>T maps to NM_007076.2 G409G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:12014289 C>T maps to NM_014214.1 C136C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:35223536 C>T maps to NM_005268.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:39062894 C>T maps to NM_000540.2 G4661G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:150078091 G>A maps to NM_018047.2 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:25288316 G>A maps to NM_014178.6 R179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:15756163 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:49214248 T>G did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:195013053 G>A maps to NM_012287.5 D631D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:126661535 T>C maps to ENST00000368325 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:73616568 C>T maps to NM_005477.2 R668R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:36623482 G>T maps to ENST00000451256 I439I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:47262060 C>T maps to NM_001164211.1 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:78571063 A>G maps to NM_014903.4 A1756A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:20483063 C>A maps to NM_001004712.1 G97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:20405116 G>A maps to NM_001006946.1 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:95888857 G>A maps to NM_004148.3 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:105280710 C>T maps to NM_000354.5 Q113Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:89371698 G>A maps to NM_013275.4 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:91182140 G>A maps to NM_020063.1 D204D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:150868559 C>T maps to NM_024082.3 R34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:115884934 C>T maps to NM_018017.2 Q888Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:135866286 C>T maps to NM_004188.4 C281C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:75898233 C>T maps to NM_031461.5 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:79350004 C>A maps to NM_002909.4 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:35783580 C>T maps to NM_002791.1 C201C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:113697719 G>A maps to NM_020817.1 I815I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:116938419 C>T maps to NM_001010892.2 Q212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:49753835 C>T maps to NM_022064.2 S1142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:58058795 C>T maps to NM_001039654.1 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:71715828 C>A maps to ENST00000393695 E1961*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:78947379 C>A maps to NM_001190482.1 G1507G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:78796054 C>A maps to NM_020761.2 I315I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:131243903 C>T maps to NM_153435.1 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:92762814 C>A maps to NM_152703.2 E824*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:36507082 G>A maps to NM_015526.2 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:57646918 C>T maps to NM_052882.1 W262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:6022591 C>T maps to NM_152611.3 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:145111081 G>A maps to ENST00000360660 L688L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:24039886 G>A maps to NM_001142730.1 D712D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:58953762 G>A maps to ENST00000354386 T1114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:124765467 G>A maps to NM_019055.5 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:67233303 C>T maps to NM_024712.3 D78D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:130474154 C>T maps to NM_001012502.2 A304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:47495762 C>T maps to NM_178033.1 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:113704333 C>A maps to NM_057159.2 G54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:5786850 G>A maps to NM_020175.2 H465H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:55949766 T>C maps to NM_001015885.1 T310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:58920676 C>T maps to NM_198847.2 V512V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:148808757 A>G maps to NM_015278.3 E212E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:140969365 G>A maps to NM_138702.1 E231E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:10027630 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:204948556 C>T maps to ENST00000367172 P682P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:78921374 C>T maps to NM_000750.3 V424V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:116101423 G>A maps to NM_020868.3 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:25678181 G>A maps to NM_006424.2 A628A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:58383342 T>C maps to NM_017771.3 S332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:100847800 A>G maps to NM_001161476.1 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:67199721 G>A maps to NM_001040667.2 E111E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:8636734 G>A maps to NM_002839.3 N58N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:2220180 C>T maps to ENST00000221482 A922A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:50444450 C>T maps to NM_006060.3 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:5339000 C>T maps to NM_153247.2 G384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:192900 C>T maps to NM_001042416.1 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:108227664 C>T maps to NM_007214.4 E316E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:104157271 G>A maps to NM_017564.9 S2497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:147230479 G>T maps to NM_005266.5 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:123047579 G>A maps to NM_183357.2 C572C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:129458651 C>T maps to NM_001174147.1 D377D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:52617717 T>C maps to NM_000846.4 E116E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:29853244 C>T maps to NM_017458.3 F482F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:154437669 G>A maps to NM_000565.2 P407P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:249108781 G>A maps to NM_030645.1 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:212251628 C>A maps to NM_005235.2 E1144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:42822002 C>T maps to NM_003825.2 R186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:108335410 G>A maps to NM_014648.3 Q94Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:145741443 G>A maps to ENST00000428558 Y353Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:78583833 C>A maps to NM_014903.4 Y2020*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:26224920 C>T maps to ENST00000407587 Q991*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:33696341 G>A maps to NM_002333.3 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:1089930 G>A maps to NM_002695.3 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:6867248 A>G maps to ENST00000379831 E116E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:63789346 G>A maps to NM_012183.2 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:7081410 G>A maps to NM_024341.2 E96E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:39067159 C>A maps to NM_015373.3 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:10256190 C>T maps to NM_012073.3 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:49064761 T>C maps to NM_001194998.1 Q568Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:28963773 G>A maps to NM_001010877.2 D335D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:197767388 C>A maps to NM_024989.3 G243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:23900199 C>A maps to NM_000257.2 E269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:74892093 C>T maps to NM_016218.2 Q526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:44418336 C>T maps to NM_003425.3 Q417Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:90417164 C>T maps to NM_014611.1 R2643R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:51011410 G>A maps to NM_152245.2 A415A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:128908592 C>T maps to ENST00000398025 V845V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:14369490 C>T maps to NM_007118.2 S1025S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:128815032 C>A maps to NM_014264.4 P853P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:42683123 C>T maps to ENST00000348077 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:11447892 G>A maps to NM_004283.3 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:75642132 G>A maps to NM_012091.3 S426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:1080690 G>A maps to NM_012292.2 K641K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:47911723 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:134115477 G>A maps to NM_052875.3 R335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:89171222 G>A maps to ENST00000380664 R678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:216390746 G>A maps to ENST00000366943 L1047L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:107616322 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:71249544 C>A maps to NM_021046.2 C148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:146601531 G>A maps to NM_001080531.1 K59K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:139617730 G>A maps to NM_152421.3 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:169951978 G>A maps to NM_014970.2 I512I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:16731588 G>A maps to NM_198546.1 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:20199173 G>A maps to NM_182762.3 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:4199912 C>T maps to ENST00000262970 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:48252914 G>A maps to NM_004776.3 Y367Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:45800610 G>A maps to NM_020208.3 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:73790431 C>T maps to NM_003388.4 Y567Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:43181222 C>T maps to NM_021079.3 D437D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:16216892 C>T maps to NM_004278.3 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:43480030 G>T maps to ENST00000506469 G315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:4576048 C>T maps to NM_004170.5 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:86324727 C>A maps to NM_006372.4 G540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:28093344 C>T maps to NM_025231.1 Q42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:151165608 G>A maps to NM_178822.4 N720N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:23066550 G>A maps to NM_012072.3 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:89346637 G>A maps to NM_013275.4 D2104D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:372083 C>T maps to ENST00000422053 R176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:201751923 G>T maps to ENST00000367296 E762*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:130285741 C>A maps to NM_001102608.1 Y493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:16729633 G>T maps to NM_020157.2 E80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:118501531 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:55597496 C>T maps to NM_000222.2 S715S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:38016119 C>T maps to NM_001195296.1 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:15937604 A>C maps to NM_005130.3 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:123352061 C>T maps to NM_024667.2 R153R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:18840937 C>T maps to ENST00000389467 R3091R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:9776550 C>T maps to ENST00000361110 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:16461041 A>G maps to NM_004431.3 L535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:201757710 C>T maps to ENST00000367296 A1037A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:56128999 G>A maps to NM_001142763.1 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:38298131 G>A maps to NM_000104.3 D455D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:53686653 G>A maps to NM_015272.2 R649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:52239986 G>A maps to ENST00000441729 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:13246274 C>A maps to NM_182751.2 Y804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:3030395 G>A maps to NM_004042.3 E524E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:22039066 G>A maps to NM_148175.2 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:78338188 A>T maps to NM_013391.2 G370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:150071372 G>A maps to NM_018047.2 H401H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:84566959 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:136594898 G>A maps to NM_007101.3 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:2062756 C>T maps to ENST00000423729 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:208994238 G>A maps to NM_020989.3 R60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:113246692 G>A maps to NM_198123.1 S3547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:39229726 G>A maps to NM_194293.2 R404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:89873446 C>T maps to NM_002693.2 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:77228782 C>T maps to NM_014940.2 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:152276039 G>A maps to NM_002016.1 H3774H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:47279185 G>A maps to NM_001099772.1 K176K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:18911731 G>T maps to NM_000292.2 A1193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:50881935 C>T maps to NM_007121.4 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:44583712 C>T maps to NM_001137606.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:39650730 T>C maps to NM_002687.3 S606S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:138395462 C>T maps to NM_016034.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:38229914 A>G maps to NM_001172690.1 H492H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:3844771 C>T maps to NM_174953.1 E574E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:50575757 C>T maps to NM_001113546.1 E402E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:6006978 C>A maps to NM_016588.2 G2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:17988624 G>A maps to NM_000453.2 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:110036047 G>A maps to NM_001099289.1 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:46399101 C>T maps to NM_001123041.2 Y28Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:88292494 C>A maps to ENST00000395847 G98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:81613866 C>T maps to NM_001017971.1 C141C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:86047629 C>A maps to NM_001554.4 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:45886508 G>T maps to NM_145798.2 L701L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:32895631 G>T maps to ENST00000381000 E715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:38082216 G>A maps to NM_001038633.2 C75C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:6684415 G>T maps to NM_000064.2 I1385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:17522688 G>T maps to NM_153676.3 S763S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:32016158 G>A maps to ENST00000375244 V3342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:1615575 C>T maps to ENST00000395423 T514T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:131797659 C>T maps to NM_015320.2 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:95131482 C>T maps to NM_001129889.1 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:1580535 G>A maps to ENST00000340677 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:15555768 C>T maps to NM_015909.2 S946S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:131329876 C>T maps to NM_001009185.1 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:52323861 C>T maps to NM_144651.4 Q670Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:47851774 C>T maps to NM_006031.5 S2799S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:149212985 G>A maps to NM_133263.3 E450E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:134219224 C>T maps to NM_138499.3 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:62285817 G>A maps to NM_001620.1 N5357N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:31080048 G>A maps to NM_014070.2 I29I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:98828992 G>A maps to NM_178861.4 N166N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:109637281 G>A maps to NM_001093.3 S901S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:41874827 C>T maps to NM_004275.3 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:62953074 G>T maps to ENST00000371140 G1834G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:204587773 G>A maps to NM_201630.1 A449A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:9790628 G>A maps to NM_001009566.1 G961G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:17211830 G>A maps to NM_022166.3 G743G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:14341057 C>A maps to NM_014048.3 C647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:77323305 G>A maps to NM_199355.2 C1135C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:19675131 G>A maps to NM_018142.2 W28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:91660881 A>G maps to NM_005751.4 K1434K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:104343601 C>A maps to NM_003506.3 G662G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:185678323 A>C maps to NM_001995.2 Y684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:36360567 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:24874242 G>A maps to NM_015550.2 I536I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:7249061 G>A maps to NM_016546.2 G463G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:121262976 C>T maps to NM_021110.1 S908S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:48414087 G>A maps to NM_205850.2 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:114178626 A>G maps to NM_001080398.1 S741S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:58587640 C>T maps to NM_177980.2 S785S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:34791677 C>A maps to NM_014686.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:41746755 A>G maps to NM_017886.2 D892D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:18145221 G>T maps to NM_004140.3 E931*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:134080623 C>T maps to ENST00000514516 E493E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:20230562 G>A maps to ENST00000425986 C116C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:191840587 G>A maps to NM_007315.3 G695G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:113519451 C>T maps to NM_002711.3 L565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:1718681 C>A maps to NM_001012416.1 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:6479369 G>A maps to NM_033278.2 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:32138369 T>C maps to NM_001856.3 G977G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:65688349 G>A maps to NM_020962.1 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:57358277 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:47297372 A>C maps to NM_001164211.1 R593R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:33355628 C>T maps to NM_014270.4 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:239059486 C>T maps to NM_198582.3 G506G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:158448051 C>T maps to NM_017760.5 L828L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:45888925 C>T maps to NM_001142502.1 Q714Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:46060234 C>T maps to NM_173536.3 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:11684428 G>T maps to NM_001372.3 V2552V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:139904271 C>T maps to ENST00000355090 R2223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:99123454 T>C maps to NM_014569.3 N264N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:92762926 G>T maps to NM_152703.2 T786T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:27258868 C>T maps to NM_017727.4 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:71756348 C>T maps to NM_152625.1 K325K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:6239850 C>A maps to NM_032127.3 E472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:136231829 C>T maps to NM_033161.2 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:68191126 C>T maps to NM_002335.2 R1066R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:33444366 G>A maps to NM_001128161.1 A319A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:21739635 C>T maps to ENST00000286149 I711I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:117069982 C>A maps to NM_032888.2 S1714S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:29236592 C>T maps to NM_005249.3 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:108145245 G>A maps to NM_012406.3 Q358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:178139060 C>A maps to NM_005649.2 *606Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:131666129 C>T maps to ENST00000355311 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:148679099 C>T maps to NM_152406.2 T15T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:44519144 G>A maps to NM_080749.2 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:61344640 C>A maps to NM_001129993.1 S635S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:3128609 G>A maps to NM_020896.3 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:9089849 C>T maps to ENST00000433083 R947R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:197072922 G>A maps to NM_018136.4 L1820L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:22283828 G>A maps to NM_213599.2 E595E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:39937185 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:92577128 T>G maps to ENST00000298047 V3532V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:35478604 C>T maps to NM_001008494.1 D108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:105510182 G>T maps to NM_013437.4 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:40005737 T>G maps to NM_152597.4 G365G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:165715501 C>T maps to NM_144980.3 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:84454640 G>T maps to NM_052910.1 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:27147791 T>C maps to NM_153631.2 P358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:52793858 G>A maps to NM_033033.3 D284D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:109954797 C>T maps to NM_002790.3 W100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:81037007 C>T maps to NM_020338.3 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:151687587 C>A maps to NM_020861.1 E205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:69987316 G>A maps to NM_006431.2 Q302Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:33527430 G>A maps to NM_030955.2 C1549C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:75967643 C>T maps to NM_006633.2 V968V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:96639211 G>A maps to NM_005222.3 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:47657111 C>T maps to NM_014342.3 E97E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:7866894 G>A maps to NM_024091.3 N434N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:68524105 A>G maps to NM_033281.5 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:37215951 A>G maps to NM_019024.1 N1916N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:167863126 G>T maps to NM_018417.4 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:57487214 G>A maps to NM_005967.3 T434T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:46419226 G>A maps to ENST00000458649 R1224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:89028500 G>A maps to NM_000372.4 E519E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:186272089 C>T maps to NM_001134415.1 Q499Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:81372117 C>T maps to NM_001093770.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:26301076 C>A maps to NM_000437.3 G275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:14307408 C>T maps to ENST00000397581 K47K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:101085607 T>C maps to NM_020654.3 K328K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:92508675 A>G maps to NM_019859.3 N405N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:23350347 C>T maps to NM_022482.3 T585T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:52425295 C>T maps to ENST00000273600 N3345N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:72763081 G>A maps to NM_004252.3 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:13356067 G>A maps to NM_023035.2 R1630R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:71008236 C>T maps to NM_025130.3 R441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:7639263 T>A maps to NM_004244.4 G763G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:57175555 G>A maps to NM_001005850.1 G359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:721659 G>A maps to NM_022772.3 K288K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:91162577 G>A maps to NM_001548.3 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:5042847 G>A maps to NM_004505.2 T459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:227771550 A>G maps to NM_001167608.1 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:41758364 T>C maps to NM_015138.4 R268R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:45867703 G>T maps to NM_000400.3 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:84600450 T>G maps to NM_021149.2 *143Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:37734148 C>T maps to NM_152604.1 P337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:2264202 G>A maps to NM_001042371.2 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:131813236 G>A maps to NM_001009993.2 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:74310809 G>T maps to NM_001134.1 G272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:152080721 G>A maps to NM_007113.2 R1657R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:16899860 C>T maps to ENST00000438489 L934L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:210415303 C>A maps to NM_019605.3 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:21659633 C>T maps to NM_003777.3 R1485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:29707994 C>T maps to NM_152236.1 S518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:56552388 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:101090472 C>T maps to NM_020348.2 R443R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:131820174 C>T maps to NM_002198.2 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:11532778 G>T maps to NM_001372.3 E466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:72890249 C>T maps to NM_018130.2 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:40557265 G>A maps to NM_012232.5 D204D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:234529404 C>T maps to NM_005646.3 P1474P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:150903145 G>A maps to NM_053002.4 T508T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:79031202 G>A maps to NM_153610.3 Q2205Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:69395343 C>T maps to NM_005652.3 E421E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:17699002 G>A maps to ENST00000395776 W914*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:20841223 A>G maps to NM_007110.4 N2299N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:94935882 G>A maps to NM_001161778.1 A591A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:135940535 C>T maps to NM_001807.3 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:61187475 G>A maps to NM_024811.3 D199D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:15342654 C>T maps to NM_001142886.1 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:25450685 G>A maps to NM_025176.4 N1098N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:34137127 C>T maps to NM_001036.3 D4454D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:11384996 G>A maps to NM_001332.2 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:56600159 G>A maps to NM_001002836.2 C127C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:104124865 G>T maps to NM_001701.3 P367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:34648389 C>A maps to NM_000155.2 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:133225889 A>G did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:136570076 C>T maps to NM_002299.2 Q719Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:30794889 C>T maps to NM_001080417.1 Q253Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:87056074 G>A maps to NM_018849.2 T685T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:27462672 C>T maps to NM_001831.2 E251E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:36141207 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:60685439 A>G maps to ENST00000326270 Q692Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:36185694 C>T maps to NM_015695.2 G997G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:84390189 T>C maps to NM_139076.2 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:115985895 C>T maps to NM_198795.1 T1032T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:142168271 C>T maps to NM_001184.3 *2645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:29004679 G>T maps to NM_002709.2 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:140724568 T>C maps to NM_018916.3 D323D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:14883248 A>G maps to NM_152633.2 Y128Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:40269003 C>T maps to NM_001013703.2 D736D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:65408967 G>A maps to NM_153253.29 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:57102122 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:66460173 G>A maps to NM_006946.2 L1675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:130635040 G>A maps to ENST00000223836 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:41711060 G>A maps to NM_001389.3 R498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:159890320 C>T maps to ENST00000368096 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:91735054 A>G maps to NM_005751.4 R3798R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:110954907 G>A maps to NM_001099922.2 V280V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:54080542 C>T maps to NM_001079907.1 Y243Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:52899736 C>A maps to NM_000232.4 E35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:82453618 G>A maps to NM_033026.5 S4843S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:29635427 C>T maps to NM_002433.4 R187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:15728716 T>C maps to NM_014647.3 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:126154400 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:52429071 C>T maps to ENST00000273600 P3719P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:4896835 A>G maps to NM_001080523.1 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:2347393 G>A maps to NM_001089.2 I733I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:59277342 T>C maps to NM_153377.3 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:27497258 G>A maps to ENST00000375888 I449I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:181741351 C>T maps to ENST00000357570 F1708F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:139763702 G>A maps to NM_152888.1 R695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:73198788 G>A maps to NM_144579.2 V217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:47841425 G>A maps to NM_030802.3 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:8551213 C>T maps to NM_005968.3 F634F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:32014361 C>T maps to NM_001007467.1 A1229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:45173521 C>T maps to NM_003681.4 D227D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:145155992 G>A maps to NM_014795.3 R921*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:37691267 G>A maps to NM_032777.9 E453E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:167085265 G>A maps to ENST00000303354 R1382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:70744218 C>T maps to NM_030958.2 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:65144075 G>A maps to NM_182556.2 D223D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:79343149 C>T maps to NM_025074.6 F1558F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:118475772 C>T maps to NM_001029858.3 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:96846892 C>T maps to ENST00000434261 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:63551872 C>T maps to NM_016530.2 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:169511288 C>T maps to ENST00000367796 Q1018Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:179564778 G>A maps to ENST00000444136 Q219Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:100470362 C>T maps to NM_003302.2 C432C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:48905246 A>G maps to NM_000138.4 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:35657205 C>T maps to NM_001164605.1 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:209965772 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:55708506 C>T maps to NM_002842.3 T656T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:122003167 C>T maps to NM_001178065.1 F799F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:619198 G>A maps to NM_018140.3 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:4085523 C>T maps to NM_016376.3 P692P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:47168915 C>T maps to NM_018018.4 V405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:32712325 G>A maps to ENST00000265074 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:17208309 G>T maps to NM_001134381.1 G703G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:35072835 G>A maps to NM_000949.4 D128D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:49573469 G>A maps to NM_031886.2 G407G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:122459626 G>T maps to NM_024610.4 I344I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:37441318 C>T maps to NM_014872.2 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:156746840 G>A maps to ENST00000442283 R476R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:126240892 C>T maps to NM_024582.4 F1109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:1064239 G>A maps to NM_006598.2 G855G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:48263815 G>A maps to NM_000088.3 V1289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:63935241 G>A maps to ENST00000261887 Q3783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:51870293 C>T maps to NM_173485.5 C99C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:18557950 A>G did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:144942171 G>A maps to NM_031308.1 P1750P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:47364608 C>T maps to ENST00000399249 V438V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:14041753 C>T maps to NM_005236.2 F767F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:134884440 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:169312747 G>A maps to NM_001012967.1 C1286C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:37769657 G>A maps to NM_052906.3 S639S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:170027154 G>A maps to NM_004525.2 S3762S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:16450938 G>A maps to NM_015150.1 C128C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:79175756 G>A maps to NM_006237.3 N351N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:103991720 G>A maps to NM_005029.3 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:81685953 G>A maps to NM_198390.2 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:48437339 C>T maps to NM_022167.2 S762S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:5950747 G>A maps to ENST00000381093 D172D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:132887780 G>A maps to NM_001164617.1 R254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:84651734 G>A maps to NM_152754.2 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:100378675 G>A maps to NM_032787.2 Q656Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:7565650 G>A maps to NM_004415.2 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:4228392 G>A maps to NM_177998.1 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:127954832 G>A maps to NM_018077.2 R677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:19755998 A>G maps to NM_002772.2 N147N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:42058208 C>T maps to ENST00000219905 D2692D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:163130397 G>A maps to NM_022168.2 I787I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:131102013 C>T maps to NM_152395.2 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:99691793 A>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:3813947 G>A maps to NM_015174.1 T704T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:150698687 C>A maps to NM_000603.4 T495T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:140516821 G>A maps to NM_015669.2 S602S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:195516520 G>A maps to NM_018406.5 Q644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:40486617 T>C maps to NM_006503.2 C379C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:43763285 C>T maps to NM_002784.3 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:36050048 G>A maps to NM_000704.2 C367C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:51618010 C>A maps to NM_138694.3 E2980*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:52598189 C>T maps to NM_001004127.2 N108N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:49655300 G>A maps to NM_002152.2 C662C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:36194637 A>G maps to NM_030636.2 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:120803659 A>G maps to NM_003184.3 H439H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:7417441 C>A maps to NM_000937.4 T1953T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:1438813 T>C did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:18456683 G>A maps to ENST00000332610 H188H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:99030294 C>T maps to ENST00000254898 C590C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:165634285 C>A maps to NM_000696.3 V477V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:102749182 C>T maps to NM_021830.4 R406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:9032471 G>A maps to NM_014850.2 G870G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:137019648 C>T maps to NM_052821.3 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:130108396 G>T maps to ENST00000397753 T403T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:21991200 G>A maps to NM_005407.1 S887S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:45391365 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:139741016 C>T maps to NM_001080482.2 S717S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:12858267 C>T maps to NM_153498.2 N258N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:33579113 T>C maps to NM_198992.3 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:140156609 G>A maps to NM_013446.3 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:72631634 T>C maps to NM_003901.3 C317C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:127671237 G>T maps to NM_001999.3 G1252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:140995884 G>T maps to NM_005462.4 E899*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:77762533 C>A maps to NM_024721.4 A1300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:274979 C>T maps to NM_001170738.1 D965D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:62417471 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:39517623 G>A maps to NM_178820.3 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:2399064 C>T maps to NM_182973.1 R96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:115272968 G>A maps to NM_001130523.1 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:117848461 G>A maps to NM_002160.2 C516C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:108356976 C>T maps to NM_153705.4 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:60062373 C>T maps to NM_005121.2 P821P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:32087336 G>A maps to NM_178140.2 R1261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:26943181 G>A maps to NM_014680.2 R2108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:197184557 G>A maps to NM_020760.1 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:6733015 G>T maps to NM_001080452.1 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:2511087 G>A maps to NM_025108.2 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:126294876 C>T maps to NM_032531.3 E645E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:41574501 C>T maps to NM_001429.3 R2263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:47450719 C>T maps to NM_015466.2 R570R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:15852561 C>T maps to NM_013938.1 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:61834988 G>A maps to NM_017798.3 H101H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:1457547 C>T maps to NM_000547.5 R189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:9325387 G>A maps to NM_001005191.2 N42N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:179647027 C>A maps to NM_133378.4 G1097G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:18208415 C>T maps to ENST00000388870 G616G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:53422633 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:169821052 A>G maps to NM_018186.2 E780E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:2717588 C>T maps to NM_145173.3 Q72Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:15370384 C>A maps to NM_032918.2 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:79296435 G>A maps to NM_002891.4 R735R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:78416174 G>A maps to NM_001713.2 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:189067985 G>A maps to NM_178556.3 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:18703914 G>A maps to NM_032880.4 E441E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:24291176 C>T maps to NM_016356.3 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:23016593 G>A maps to NM_001052.2 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:4874573 C>T maps to NM_018059.4 Q360Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:152732645 G>A maps to NM_001025231.1 Q194Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:52824023 C>T maps to NM_032449.2 P480P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:106155473 C>T maps to ENST00000513237 F146F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:220804391 C>T maps to NM_018650.3 R309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:197614 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:178358718 T>C maps to NM_030613.2 C135C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:167262857 A>C maps to NM_002976.2 L1427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:37769716 A>G maps to NM_005441.2 Q162Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:119914428 G>A maps to NM_182528.3 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:3800134 G>T maps to ENST00000430539 E307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:87838717 G>A maps to NM_003130.2 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:65308384 G>T maps to NM_001130144.2 T978T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:138602175 C>T maps to NM_001164665.1 A732A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:33144230 G>T maps to NM_080680.2 Y716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:146631221 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:50786281 G>A maps to NM_005154.3 G821G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:132475997 T>C maps to ENST00000333577 S928S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:6732320 G>A maps to NM_001080452.1 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:119799768 G>A maps to ENST00000369199 R221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:168949821 T>C maps to NM_022138.2 R203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:34394944 C>A maps to NM_152595.4 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:105726036 G>A maps to NM_002726.4 N705N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:78215618 C>T maps to NM_173626.3 I345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:55917296 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:124827722 C>T maps to NM_006312.4 T1595T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:77736066 C>A maps to NM_015057.4 E2191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:94800074 C>T maps to NM_153704.5 V472V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:175304877 G>A maps to NM_003285.2 G1200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:46859643 G>A maps to NM_014246.1 R1381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:80790045 G>T maps to NM_024702.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:50493028 A>C maps to NM_001080447.1 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:2812143 C>T maps to NM_016333.3 R539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:161487823 C>T maps to NM_001136219.1 D280D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:144589968 C>T maps to NM_015117.2 P554P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:33464115 C>A maps to NM_018096.3 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:98541109 A>C maps to ENST00000326857 Y264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:52864411 G>A maps to NM_173086.4 Y360Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:57248757 G>A maps to NM_001001433.1 Q288Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:118425963 T>G maps to NM_020153.3 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:45490527 C>T maps to NM_001294.2 N295N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:44191255 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:111866131 C>T maps to NM_001037954.2 S510S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:166580184 G>A maps to NM_003181.2 C122C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:53668077 C>T maps to NM_024733.3 S555S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:7045788 C>A maps to NM_001940.3 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:10755725 G>A maps to NM_173683.3 L554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:66793364 C>T maps to NM_000968.2 W252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:83793158 C>T maps to ENST00000505472 V240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:51898888 A>G maps to ENST00000382911 Q460Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:9887883 C>T maps to NM_001098529.1 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:60685484 G>A maps to ENST00000326270 K707K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:226128786 G>A maps to NM_003240.3 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:171821593 G>A maps to NM_001017995.2 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:114069697 G>A maps to NM_001164342.1 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:27449825 C>T maps to NM_004341.3 S761S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:96493195 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:130505262 C>T maps to ENST00000457563 E237E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:110248207 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:88066766 G>A maps to NM_001173543.1 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:52779403 C>T maps to NM_013409.1 C116C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:30750366 A>G maps to NM_006662.2 P3002P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:23345401 G>A maps to NM_014045.3 T415T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:86325796 C>T maps to NM_015425.3 Q123Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:187503185 C>T maps to NM_002210.3 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:18888080 C>T maps to NM_001098482.1 D614D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:24045123 G>A maps to NM_032452.2 G307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:1624760 G>A maps to NM_001500.2 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:75840676 C>T maps to ENST00000322507 T1986T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:79454461 T>C maps to NM_004796.4 Y707Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:1741886 C>T maps to NM_032642.2 C48C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:30114886 G>A maps to ENST00000376724 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:155783529 C>T maps to ENST00000368331 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:24991145 C>T maps to NM_003743.4 G1404G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:80655778 G>A maps to NM_130767.2 R147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:89520418 G>A maps to NM_002053.2 N537N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:409725 C>T maps to NM_031229.2 R480R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:63782724 G>A maps to NM_014067.3 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:79945475 G>A maps to NM_153252.4 R1240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:113825590 C>A maps to NM_173542.3 A494A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:215793741 G>T maps to NM_016121.3 E744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:130454717 C>A maps to NM_014602.2 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:41561606 G>A maps to ENST00000415018 I749I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:176760571 A>G maps to NM_020318.2 S1658S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:17873638 G>A maps to NM_015122.2 E32E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:23912281 C>T maps to NM_014363.4 T1911T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:35293165 C>T maps to NM_001077653.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:135073990 C>T maps to NM_032536.2 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:142920106 C>T maps to NM_176882.1 H312H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:44561071 C>T maps to NM_016427.2 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:192778278 C>T maps to NM_002923.3 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:42672058 C>T maps to NM_005385.3 H132H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:2907876 G>A maps to NM_002014.3 E133E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:25672225 T>G maps to NM_030979.2 T630T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:65855061 C>T maps to ENST00000371069 C439C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:59739461 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:90102048 C>T maps to NM_001481.2 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:44671915 C>A maps to NM_001134771.1 T420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:47644303 G>T maps to NM_014342.3 Y258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:78149013 C>T maps to NM_016373.1 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:12726628 G>A maps to NM_001013630.1 W369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:37702376 G>A maps to NM_018310.3 I297I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:37415633 G>T maps to NM_001032377.1 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:152127263 G>A maps to NM_001122965.1 R771*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:38192844 G>A maps to NM_001099439.1 V567V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:36108726 A>C maps to NM_001007527.1 R602R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:119212584 C>T maps to NM_031433.2 E499E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:14336785 C>T maps to NM_007118.2 R666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:32031381 C>T maps to NM_001137674.1 R271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:40317999 C>T maps to NM_004714.1 A340A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:118462853 G>A maps to NM_017686.3 R43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:13828723 C>T maps to NM_000834.3 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:56848295 C>T maps to NM_012064.3 W34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:136594307 G>A maps to NM_002299.2 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:151787890 G>A maps to ENST00000392697 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:70832203 C>T maps to ENST00000432224 R113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:60922053 G>A maps to NM_005560.3 C329C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:11170475 G>A maps to NM_001128849.1 R1593R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:17837218 C>T maps to NM_018174.4 C342C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:46989794 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:7667263 C>T maps to NM_020877.2 Q1032*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:124664938 C>T maps to NM_001081675.2 Q76Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:38463410 G>A maps to NM_004468.3 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:12123222 C>T maps to NM_002114.2 G1065G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:134032916 T>G maps to NM_021982.1 Y696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:20073695 C>T maps to NM_022720.6 Y70Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:94452254 G>A maps to NM_002729.4 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:81427609 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:48413907 G>A maps to NM_016204.1 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:1487860 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:54306704 G>A maps to ENST00000260323 W535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:44116248 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:177913770 C>T maps to NM_033127.2 E602E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:39008035 C>T maps to NM_000540.2 P3241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:115582017 T>G maps to NM_012252.2 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:44336396 G>A maps to NM_013305.4 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:127224651 C>T maps to NM_024523.5 Q195Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:18631229 T>C maps to NM_178425.2 N169N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:34029337 C>T maps to NM_001164749.1 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:151775045 G>T maps to NM_001004432.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:176016536 C>T maps to NM_001171976.1 T1042T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:86491741 G>A maps to NM_001025616.2 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:7811276 C>T maps to NM_001005271.2 R1757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:55825940 G>A maps to NM_001122964.1 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:59947319 C>T maps to NM_020748.2 E944E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:155581998 C>T maps to NM_018116.2 H235H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:100454750 G>A maps to NM_017890.3 P1111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:191905835 C>T maps to NM_003151.2 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:99947757 G>T maps to NM_004951.4 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:54795225 G>A maps to NM_002205.2 S808S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:250374 C>T maps to NM_001170738.1 R693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:49167893 G>A maps to NM_145807.1 C254C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:41860619 G>A maps to NM_030578.3 Y171Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:50958824 A>G maps to NM_004533.3 T754T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:50944250 C>T maps to NM_004533.3 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:58395339 C>T maps to NM_017771.3 R464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:134711278 C>T maps to NM_182540.4 G645G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:106739524 A>G maps to ENST00000283148 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:103908143 C>A maps to NM_015062.3 S1472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:47766793 C>T maps to NM_006031.5 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:61442418 C>T maps to NM_020810.2 Q406Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:125889981 G>A maps to NM_001182.3 G399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:42605785 G>T maps to NM_005650.1 I1842I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:186395414 C>T maps to NM_000412.2 R441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:102766921 C>A maps to NM_032429.2 I669I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:163836317 G>A maps to ENST00000361752 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:75839890 C>T maps to ENST00000322507 S2042S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:26413463 G>A maps to NM_007048.5 V362V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:11090931 G>A maps to NM_006610.2 D365D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:32917606 G>A maps to NM_006965.2 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:104432574 C>T maps to NM_015420.6 R204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:62598529 C>T maps to ENST00000506720 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:19965027 C>A maps to NM_001670.2 E594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:129993588 C>T maps to NM_001642.2 C335C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:219870945 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:32036329 G>A maps to ENST00000375244 V2019V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:50583466 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:38910675 G>A maps to NM_181534.3 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:56653484 C>T maps to NM_001141947.1 I855I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:175375802 G>A maps to NM_003285.2 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:55361563 A>G maps to NM_024335.2 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:155028285 G>A maps to NM_207197.1 E211E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:151775193 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:60042452 C>T maps to NM_005121.2 G1586G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:216292950 C>A maps to NM_212482.1 G266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:41939936 T>C maps to NM_017886.2 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:46345745 G>A maps to NM_004819.2 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:179474552 T>C maps to NM_133378.4 E14631E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:27876901 T>C maps to NM_001029882.2 A575A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:44405741 G>A maps to NM_080614.1 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:11152113 C>T maps to NM_001128849.1 D1466D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:85750254 A>C maps to NM_014991.4 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:187074870 C>T maps to ENST00000356371 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:53419602 G>A maps to NM_002590.2 S932S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:4876932 G>A maps to NM_015099.3 H716H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:78944631 T>C maps to NM_001161352.1 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:25251354 C>T maps to NM_001039948.2 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:88205715 A>G maps to NM_173824.3 V307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:96324144 A>G maps to ENST00000449279 D45D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:55589225 C>T maps to NM_015306.2 A1390A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:57340668 C>T maps to NM_000562.2 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:72055167 G>A maps to NM_001361.3 R221R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:19655591 C>T maps to NM_153221.2 N746N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:71043854 C>A maps to NM_173535.2 E220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:179193072 C>A maps to NM_014757.4 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:144945009 C>T maps to NM_031308.1 P804P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:43161677 G>A maps to ENST00000352483 R607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:173830409 C>T maps to NM_007023.3 H273H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:113478722 C>T maps to NM_032189.3 R286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:158631185 A>G maps to NM_003126.2 I826I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:14720321 G>A maps to NM_005454.2 C190C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:20043982 A>G maps to NM_001002911.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:103530352 G>A maps to NM_033163.3 C156C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:81592490 C>T maps to NM_172217.3 L942L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:4213927 C>T maps to NM_152744.3 A1625A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:10406085 C>T maps to NM_003259.3 F765F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:53746292 G>A maps to NM_004631.3 C154C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:74154149 C>T maps to ENST00000443185 E287E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:2282759 G>A maps to NM_014853.2 L1034L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:129030536 A>C maps to NM_133638.3 P975P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:59323800 C>T maps to ENST00000434298 D260D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:14568858 G>A maps to NM_213560.1 V400V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:14720267 G>A maps to NM_005454.2 H208H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:4479907 C>T maps to NM_020638.2 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:107535878 C>T maps to NM_018712.3 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:66033167 C>T maps to NM_022822.2 Y459Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:50277249 A>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:145838886 G>A maps to NM_006706.3 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:50548626 G>A maps to NM_015428.1 E309E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:119668404 G>A maps to NM_003588.3 L751L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:126371042 C>T maps to NM_024582.4 R2958*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:90400676 C>T maps to NM_001134479.1 R684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:128723009 T>A maps to ENST00000373487 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:51293262 T>C maps to NM_007347.3 L1046L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:9621565 C>T maps to NM_001039613.1 C145C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:111782370 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:194942 A>G maps to NM_001080478.1 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:128688338 C>T maps to NM_031291.2 Y199Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:113333705 G>T maps to NM_207440.1 E5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:30577644 C>T maps to NM_025159.2 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:57864505 C>A maps to NM_005269.2 G661G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:63283060 C>T maps to NM_014562.3 Y225Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:149512484 G>A maps to NM_002609.3 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:50402679 G>A maps to NM_001173984.2 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:92789301 C>T maps to NM_024813.2 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:45299201 G>A maps to NM_002476.2 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:138738248 C>T maps to ENST00000464606 S921S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:91526691 C>T maps to NM_004755.2 K29K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:64766793 G>T maps to NM_197941.2 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:114795309 G>A maps to ENST00000389544 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:26860620 G>A maps to NM_022081.4 N325N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:114282576 C>A maps to NM_148898.3 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:8390804 G>A maps to ENST00000360416 I1664I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:153219958 G>A maps to ENST00000369984 H1297H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:10323445 C>T maps to NM_002472.2 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:35821671 C>T maps to NM_000219.3 W87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:36710161 C>T maps to NM_020939.1 V555V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:10756175 G>A maps to NM_173683.3 G404G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:158835848 C>T maps to ENST00000402066 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:31641141 A>G maps to NM_015382.2 G419G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:25655515 C>T maps to ENST00000357542 V451V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:2043156 G>A maps to NM_199054.2 D153D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:128747249 C>T maps to NM_001145928.1 Q582Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:6903437 T>G maps to NM_181874.2 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:180886165 C>T maps to NM_020950.1 N309N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:37479969 G>T maps to NM_018034.2 G241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:240921627 G>T maps to ENST00000404554 I336I. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-IB-7651-01A-11D-2154-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:51411540 C>T maps to NM_001005272.3 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:127503678 G>A maps to NM_000375.2 Y56Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:3785571 C>T maps to NM_021873.2 S569S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:70541909 C>A maps to NM_020794.2 R1423R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:48264895 G>T maps to NM_000088.3 G1124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:2717700 C>A maps to NM_199460.2 S1147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:156279037 G>A maps to NM_005998.4 G530G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:39667312 G>A maps to NM_005884.3 W481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:6250582 G>A maps to NM_033439.3 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:94924735 A>G maps to NM_144665.2 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:31077196 C>T maps to NM_017769.3 C474C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:178413730 G>A maps to NM_000843.3 G508G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:235359343 A>G did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:2636274 C>T maps to NM_006392.2 I264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:51174869 G>T maps to ENST00000251020 A421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:125563012 C>T maps to NM_080859.1 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:124111571 G>A maps to NM_004099.4 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:235359426 G>A maps to NM_016374.5 Y615Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:44867539 C>T maps to NM_020242.2 N853N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:88799240 C>T maps to NM_001012338.1 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:88706263 C>T maps to NM_013278.3 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:3021849 G>A maps to NM_152341.3 Q241Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:60169242 C>T maps to NM_004731.3 G389G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:1043393 G>A maps to NM_019112.3 W284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:150598173 G>A maps to NM_207042.1 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:2280861 C>T maps to NM_198532.2 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:40814827 C>T maps to NM_020831.3 T538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:77458775 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:11091356 G>A maps to NM_023922.1 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:123624776 G>A maps to NM_001005188.1 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:197408179 G>A maps to NM_014687.1 C750C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:21859666 C>T maps to NM_001170629.1 W2340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:155198761 G>A maps to ENST00000340059 L1693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:140023462 G>T maps to ENST00000252100 V345V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:18536311 C>T maps to NM_006292.2 K90K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:166900412 G>A maps to NM_001165963.1 S603S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:160277033 C>T maps to NM_001098398.1 A407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:41646931 C>T maps to NM_007187.3 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:73768229 C>T maps to NM_003388.4 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:10748581 C>T maps to NM_020428.3 F582F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:76003125 C>T maps to NM_006633.2 F1572F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:72997451 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:45504623 G>T maps to NM_020883.1 G626G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:241808765 C>T maps to NM_000030.2 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:24859586 C>T maps to NM_013441.2 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:37546927 C>T maps to NM_015568.2 N441N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:151079023 C>T maps to ENST00000426624 A417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:81608454 T>C maps to NM_001017971.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:144991544 C>T maps to NM_201380.2 T4285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:127014936 A>G maps to NM_176814.3 D151D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:114398496 C>A maps to ENST00000409875 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:44234873 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:25932779 G>A maps to ENST00000268763 E590E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:75114201 C>T maps to NM_021819.2 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:8616131 G>A maps to NM_001014447.2 T470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:36686203 C>T maps to NM_004734.4 E175E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:61891125 G>A maps to NM_001796.2 N188N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:70256067 T>C did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:64573593 G>T maps to NM_001136178.1 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:76895228 C>T maps to NM_018115.2 K212K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:4720349 G>A maps to NM_002663.3 K567K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:151316354 C>A maps to NM_000449.3 E187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:93076495 G>A maps to NM_153216.1 F258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:176795176 C>T maps to ENST00000398128 N253N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:63453897 C>T maps to NM_139318.3 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:37741528 G>A maps to ENST00000290384 Q622Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:76395670 T>C maps to ENST00000357063 L786L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:42988050 G>A maps to ENST00000415122 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:121341874 A>G maps to NM_016298.3 K533K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:4460468 C>T maps to NM_020375.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:22927924 C>T maps to NM_020526.3 G954G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:102117040 G>A maps to NM_020244.2 K292K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:98043609 A>G maps to ENST00000376673 E343E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:74757546 G>A maps to NM_013247.4 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:60861649 C>T maps to NM_144498.1 S336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:2938528 C>A maps to NM_080431.4 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:41518230 G>A maps to NM_000767.4 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:71648855 C>T maps to NM_001037442.2 R315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:123538496 G>A maps to NM_012164.3 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:41790199 C>T maps to ENST00000417325 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:6213742 G>A maps to NM_005934.3 Y491Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:174937165 C>T maps to NM_022754.5 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:145057667 C>A maps to NM_032789.3 E697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:14504588 G>A maps to NM_001144061.1 R316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:174241550 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:44132885 G>A maps to NM_133259.3 N1103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:24076436 C>T maps to NM_003198.2 R106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:16689991 G>A maps to NM_012334.2 I1279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:47120891 C>T maps to NM_080746.2 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:8390437 G>A maps to ENST00000377479 P329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:67333396 C>T maps to NM_001100915.1 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:237729907 C>A maps to NM_001035.2 R1086R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:1680760 G>A maps to NM_012293.1 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:78893897 G>A maps to NM_000743.4 N362N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:139229122 G>A maps to NM_001145638.1 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:34985587 A>G maps to NM_018453.3 C262C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:36694366 C>T maps to NM_001031836.2 C474C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:99548173 C>A maps to NM_181670.2 G33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:3778861 G>A maps to NM_004380.2 I2062I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:81732973 G>A maps to NM_003625.2 R845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:156501020 G>A maps to NM_178229.4 A1374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:65415780 A>C maps to NM_001033057.1 V527V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:14863236 G>T maps to NM_013447.2 I564I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:41599413 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:185200168 C>T maps to NM_004721.3 D942D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:66729128 A>C maps to NM_002755.3 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:52913903 G>A maps to NM_000424.3 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:5926443 G>A maps to NM_015102.2 V1211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:27092736 C>T maps to NM_006015.4 Q920*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:51239167 G>A maps to NM_020921.3 R278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:15508539 C>T maps to NM_014371.2 T428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:22817138 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:164906548 G>A maps to NM_014926.2 S690S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:129642451 C>T maps to ENST00000319119 D258D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:99327680 G>A maps to NM_024954.3 E27E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:145641571 A>G maps to NM_017767.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:26854525 A>C maps to NM_022081.4 A577A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:644758 G>A maps to NM_033129.3 C160C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:136567504 G>A maps to NM_002299.2 G804G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:148951065 G>T maps to NM_012256.3 E350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:8168670 G>A maps to NM_012393.2 A782A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:50405477 G>A maps to NM_020436.3 H888H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:82336391 C>T maps to NM_032246.3 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:167882443 C>A maps to NM_001161661.1 S914S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:206647702 C>A maps to NM_014002.3 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:17353280 G>A maps to NM_022166.3 D159D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:70170551 G>A maps to NM_003626.2 Q103Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:123724799 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:11832602 C>T maps to NM_001080493.2 L582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:179425925 G>A maps to NM_133378.4 Y25743Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:16455433 T>C maps to NM_020653.2 K674K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:183867734 A>G maps to NM_205842.1 N118N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:33420309 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:51063695 G>A maps to ENST00000395624 D469D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:44700998 C>T maps to NM_003420.3 R382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:6303312 C>T maps to NM_006005.3 I597I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:4432088 C>T maps to NM_005483.2 C696C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:7012169 G>A maps to NM_080912.2 C54C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:127262887 G>A maps to NM_004959.4 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:90348374 C>T maps to NM_001150.2 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:87912324 A>C maps to NM_024636.2 Y205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:144899947 G>A maps to NM_078480.1 Y274Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:47619041 G>A maps to ENST00000383738 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:6238931 A>G maps to NM_032127.3 G642G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:136913345 G>A maps to NM_007371.3 C315C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:24886378 G>A maps to NM_025081.2 A1808A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:2697970 G>A maps to NM_025250.2 A434A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:50819142 C>T maps to NM_003055.2 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:125426093 G>A maps to NM_153442.3 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:162865070 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:9726290 C>T maps to NM_001077525.2 H329H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:85186745 G>T maps to NM_032856.2 A364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:233136142 G>A maps to NM_014801.3 L1746L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:1255908 G>A maps to NM_017871.4 R43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:128699596 G>A maps to NM_001145928.1 R1079*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:37916863 G>T maps to NM_152484.2 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:119394073 G>A maps to ENST00000484810 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:102117165 G>A maps to NM_000944.4 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:3380641 G>A maps to NM_001130520.1 T532T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:26638888 T>C maps to NM_018317.2 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:151773617 G>A maps to NM_001004432.2 I521I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:4325510 C>T maps to ENST00000314714 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:63283033 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:201749584 C>T maps to ENST00000367296 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:43716282 C>T maps to NM_004915.3 F606F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:7083364 C>T maps to NM_024341.2 F301F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:103901018 C>T maps to NM_015062.3 A918A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:141578909 G>A maps to NM_015130.2 L660L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:38292918 A>G maps to NM_005109.2 E467E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:21624420 T>C maps to NM_032941.2 T536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:72152160 C>T maps to NM_015556.1 R1063*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:40695694 C>A maps to NM_000263.3 R557R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:201477378 G>A maps to NM_001159.3 A437A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:46691796 C>T maps to NM_024016.3 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:91929100 G>A maps to ENST00000417249 Q651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:117222547 C>T maps to NM_014956.4 N79N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:20808151 T>C maps to NM_001076675.2 E177E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:55589479 C>T maps to NM_133180.2 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:78086952 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:19839448 C>T maps to NM_024627.5 W112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:67266799 C>T maps to NM_005478.3 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:18250689 C>T maps to NM_001145195.1 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:78111991 G>A maps to NM_014740.3 Y272Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:19698236 G>A maps to NM_020689.3 T595T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:79924944 G>A maps to NM_000791.3 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:5602223 C>T maps to NM_001005162.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:77659146 C>T maps to NM_012283.1 C244C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:56369007 G>A maps to ENST00000419009 W8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:78531041 C>T maps to NM_014903.4 F1509F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:58457163 A>C maps to NM_014258.2 T862T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:49934770 G>A maps to NM_002447.2 L709L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:37745575 G>T maps to NM_014907.2 G1183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:93967928 G>A maps to NM_004440.3 T666T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:13246050 G>A maps to NM_052876.2 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:84353100 C>T maps to NM_021197.2 C162C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:53901207 G>A maps to NM_003717.2 D17D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:18544111 A>G maps to NM_004570.4 R643R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:90463338 A>G maps to NM_014611.1 G989G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:58033914 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:26620466 G>A maps to NM_031418.2 T531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:78130967 G>A maps to NM_012301.3 D297D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:43372369 C>A maps to NM_006905.2 G376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:96992434 T>C maps to ENST00000420728 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:53042883 G>A maps to NM_000423.2 D288D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:69143879 C>T maps to NM_005329.2 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:73108696 T>C maps to NM_014989.4 C1587C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:30094744 C>A maps to NM_002720.1 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:41805285 C>A maps to NM_002344.5 E26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:17545007 G>A maps to NM_153676.3 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:57587034 C>T maps to NM_002332.2 C2544C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:26965067 A>G maps to NM_014680.2 D519D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:7810693 A>G maps to NM_001005271.2 P1663P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:141665572 A>G maps to NM_018557.2 C1131C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:76912631 C>T maps to NM_000260.3 T1664T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:64456833 C>T maps to NM_020762.2 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:5000851 T>C maps to NM_006638.2 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:10578269 C>T maps to NM_001111307.1 G878G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:120930755 T>C maps to NM_152715.3 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:7582958 C>T maps to NM_004415.2 L1822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:62296059 C>T maps to NM_001620.1 S1943S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:18843867 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:63967219 C>T maps to ENST00000261887 T2389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:170359669 T>G maps to ENST00000419050 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:20681259 C>T maps to NM_052956.2 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:45977935 G>T maps to NM_198696.2 C221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:133760701 C>T maps to NM_007313.2 R1028*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:51749342 C>T maps to NM_000839.3 C518C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:81666400 T>C maps to ENST00000454937 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:26919982 A>G maps to NM_006461.3 C93C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:129907025 C>T maps to NM_002417.4 K1026K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:35403835 C>T maps to ENST00000396787 L1559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:40440178 G>A maps to NM_001098634.1 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:114070336 G>A maps to NM_001164342.1 N196N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:39149957 G>A maps to NM_033655.3 S498S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:248005129 C>T maps to NM_001001959.1 W23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:95390543 G>A maps to NM_012415.2 V793V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:35065451 C>T maps to NM_000949.4 K536K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:109768628 G>A maps to NM_022765.3 T667T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:51851232 A>G maps to NM_139171.1 Y164Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:52302110 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:30581383 C>T maps to NM_145271.3 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:55319793 G>A maps to NM_014762.3 Y378Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:41620064 G>A maps to NM_031488.4 R328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:49942828 G>A maps to NM_012284.1 S447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:114269969 G>A maps to NM_148898.3 Q194Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:73519154 G>A maps to NM_001965.3 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:65631318 C>T maps to NM_025128.4 R336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:74971731 G>A maps to NM_000428.2 G1441G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:91964706 C>T maps to NM_024077.3 D585D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:101905442 C>T maps to NM_173647.3 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:7806615 C>T maps to NM_001005271.2 G1233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:10261799 C>T maps to NM_012073.3 I374I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:48389869 G>T maps to NM_002900.2 V336V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:145533579 G>A maps to NM_005526.2 K162K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:103597431 C>T maps to NM_006291.2 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:8244160 C>T maps to NM_001105244.1 C802C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:130581936 C>T maps to NM_001114753.1 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:151785742 G>A maps to ENST00000392697 Y436Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:31832661 G>A maps to NM_025257.2 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:17414676 T>G did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:118772711 C>T maps to NM_182557.2 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:235955383 A>G maps to NM_000081.2 D1386D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:29275056 G>A maps to NM_030946.1 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:193171891 C>T maps to NM_032279.2 T675T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:113120490 A>G maps to NM_001164496.1 N422N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:2502384 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:60977960 C>T maps to ENST00000381716 C303C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:123676619 G>T maps to NM_001005325.1 C146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:46911058 G>A maps to ENST00000256991 N751N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:90650749 C>A maps to NM_022054.2 C210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:129958827 C>T maps to NM_014636.2 D371D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:12836042 G>A maps to NM_001080830.1 E215E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:26417217 G>T maps to NM_005349.2 G106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:139256577 G>A maps to NM_001080849.1 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:108687501 C>T maps to NM_145315.3 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:150645881 C>T maps to NM_001195794.1 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:13489311 G>A maps to ENST00000396900 I396I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:68707096 C>A maps to NM_002180.2 S960S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:53818958 C>A maps to NM_020547.2 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:76909558 C>T maps to NM_000260.3 N1487N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:109843752 C>A maps to NM_001101421.3 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:172351690 G>A maps to NM_001146276.1 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:57598458 C>T maps to NM_002332.2 R3707R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:59073456 G>A maps to NM_198055.1 R729R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:139297772 G>A maps to ENST00000296202 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:36353332 G>T maps to NM_016135.2 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:134113075 G>A maps to NM_052875.3 K203K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:73921318 C>T maps to NM_001198800.1 Q201Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:131276457 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:64138975 G>A maps to NM_198859.3 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:18648446 C>T maps to NM_012181.3 Q303Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:21131955 C>T maps to NM_003429.4 N212N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:116101462 C>T maps to NM_020868.3 H82H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:33247070 C>A maps to NM_005452.5 L605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:91709391 C>T maps to NM_005751.4 L2649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:114196596 T>C maps to NM_001142782.1 F862F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:157504524 G>T maps to NM_031281.2 P520P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:47454449 G>A maps to NM_015466.2 P1562P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:1112467 G>A maps to NM_014963.2 N816N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:40735470 G>A maps to ENST00000373198 C1137C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:52895863 G>A maps to NM_016513.4 H119H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:42658800 C>T maps to NM_015255.2 R1720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:36895161 A>G maps to NM_014800.9 C726C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:623820 G>T maps to NM_207332.1 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:19389272 G>A maps to NM_144633.2 K209K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:107955829 C>T maps to NM_018013.3 S594S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:1946352 C>A maps to NM_080822.2 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:41385242 G>A maps to NM_001389.3 S1919S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:1088603 G>A maps to NM_004508.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:102028264 C>T maps to NM_001362.3 D144D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:85382962 G>A maps to NM_020778.4 Q353Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:15291786 C>T maps to NM_000435.2 T993T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:181021608 G>A maps to NM_001531.2 E281E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:52995598 A>G did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:33202820 C>T maps to NM_001105570.1 H362H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:99907720 G>A maps to NM_174898.2 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:127177698 C>T maps to NM_002799.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:112899986 C>T maps to NM_007203.4 T721T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:66031061 A>G maps to ENST00000443035 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:62356928 G>A maps to NM_018008.3 F361F. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-IB-7651-01A-11D-2154-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:159558113 A>G maps to NM_001639.3 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:186307227 T>C maps to NM_003292.2 Q1433Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:65855013 G>A maps to ENST00000371069 Q423Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:47772825 G>A maps to NM_015308.2 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:53191041 T>C maps to ENST00000219084 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:60504701 C>T maps to NM_001794.2 L681L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:176019738 C>T maps to NM_001171976.1 D1250D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:134635160 C>T maps to NM_033138.3 R611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:77288497 A>G maps to NM_001042784.1 A593A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:112509714 G>A maps to NM_024953.3 N340N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:109697951 A>G maps to ENST00000390027 *859W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:101136956 C>T maps to NM_020348.2 S774S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:42729325 C>T maps to NM_133444.1 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:53010164 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:242572743 G>A maps to NM_015963.5 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:2112581 C>T maps to NM_000548.3 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:37286130 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:25811865 C>A maps to NM_005074.3 G344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:119536007 C>T maps to NM_022002.2 H457H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:50439630 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:8032509 G>A maps to ENST00000351593 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:217341854 C>T maps to NM_014140.3 R817R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:96641196 C>T maps to NM_005230.2 N229N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:16339684 C>T maps to NM_001130524.1 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:183777673 C>T maps to NM_130770.2 F328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:78337096 C>T maps to NM_020914.4 L3900L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:100152290 G>A maps to NM_032709.2 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:59966088 C>T maps to NM_020854.3 Q1176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:678079 C>T maps to NM_007030.2 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:4934821 G>A maps to NM_002705.4 A1278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:43258659 C>T maps to NM_182707.2 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:134144148 G>A maps to NM_003235.4 S2652S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:20167395 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:99697787 C>T maps to NM_138576.2 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:55508451 G>T maps to NM_003392.3 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:15497081 C>T maps to NM_004973.2 A542A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:203192261 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:57345959 C>T maps to NM_003708.3 E269E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:100210479 G>A maps to NM_023948.4 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:135279293 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:2822077 G>A maps to NM_207013.1 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:37454708 G>A maps to NM_005760.2 R543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:53040534 G>A maps to NM_000423.2 G486G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:1862726 C>T maps to ENST00000381906 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:170493762 C>T maps to NM_004792.2 Y665Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:167416733 C>T maps to NM_007045.2 D70D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:74671482 G>T maps to NM_152635.1 G226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:85617953 C>T maps to NM_014991.4 K2873K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:112720689 C>T maps to NM_001085377.1 W130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:95182634 A>G maps to NM_001144663.1 N352N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:140331020 G>A maps to NM_001033113.1 C246C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:52258211 G>A maps to ENST00000494383 H193H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:127786983 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:156670842 C>T maps to NM_001878.3 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:126887436 G>A maps to ENST00000330542 W389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:15364969 G>A maps to NM_058243.2 S717S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:37618210 T>G maps to NM_144689.3 Y106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:31815765 C>T maps to NM_001174096.1 Y984Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:176964900 C>T maps to NM_021193.3 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:68821504 C>T maps to NM_139075.3 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:151668055 G>T maps to NM_145292.3 E92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:58490208 T>C maps to NM_025027.3 K613K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:56171052 C>A maps to NM_005921.1 I627I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:140995997 G>A maps to NM_005462.4 T936T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:23433310 G>A maps to NM_130794.1 D46D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:107546609 C>A maps to NM_005502.3 E2258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:20110762 G>A maps to NM_021020.2 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:8248571 C>T maps to ENST00000428101 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:29709920 G>T maps to NM_001193451.1 R515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:67299779 T>C maps to NM_024763.4 E595E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:72371141 G>A maps to NM_019885.2 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:32747542 C>T maps to NM_023037.2 R731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:46264734 T>G maps to NM_181659.2 T535T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:115395284 G>A maps to NM_001130064.1 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:140056960 G>A maps to NM_002109.3 G258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:118492396 A>G maps to NM_006784.2 A516A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:28602454 C>T maps to NM_001941.3 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:47449833 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:5691598 C>T maps to NM_015414.3 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:31523031 C>T maps to NM_003787.4 Q513Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:124742333 A>C maps to NM_022370.3 R406R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:71119776 C>T maps to ENST00000439900 N152N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:167747013 C>A maps to NM_014498.3 G504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:2048484 C>T maps to ENST00000431526 T821T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:32860297 G>A maps to NM_001039111.1 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:175049458 C>T maps to NM_022093.1 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:6730699 G>A maps to ENST00000330442 R682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:72551960 T>C maps to NM_020214.2 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:49446032 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:33179291 G>A maps to NM_002931.3 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:197431563 G>A maps to NM_014687.1 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:7580631 G>A maps to NM_004415.2 R1403R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:78189606 T>C maps to NM_012245.2 A349A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:18187134 G>A maps to NM_005535.1 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:24033199 C>A maps to NM_017552.1 E814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:5247766 C>T maps to NM_001818.2 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:7015723 G>A maps to NM_005559.2 C1041C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:130269378 C>T maps to NM_022833.2 R662R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:34289190 A>G maps to NM_025135.2 A615A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:40936548 G>A maps to NM_032387.4 P374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:74420530 G>A maps to NM_020872.1 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:215844618 G>A maps to ENST00000366943 Q4610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:127456126 A>G maps to NM_147191.1 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:35782422 C>T maps to NM_182548.3 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:5284790 G>A maps to NM_004703.4 Q826Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:120295297 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:14501838 G>A maps to NM_078481.2 E98E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:123699238 C>T maps to NM_017578.2 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:49772215 C>T maps to NM_001079673.1 S863S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:100453986 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:71232061 T>C maps to NM_017941.4 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:88600852 C>T maps to NM_153813.2 L829L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:46930510 G>A maps to NM_000809.2 R466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:49075896 C>T maps to ENST00000376407 T582T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:170428254 A>G maps to NM_024622.3 H95H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:77078193 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:107955418 G>A maps to NM_018013.3 S457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:61926467 C>T maps to ENST00000326996 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:30313365 C>T maps to NM_001238.1 C322C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:125746834 C>T maps to NM_012197.3 D74D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:123845302 G>A maps to NM_206862.2 P1096P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:20077417 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:9324694 G>A maps to NM_001005191.2 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:11362938 C>A maps to NM_005425.4 G61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:57389923 C>T maps to NM_007264.3 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:164906515 G>T maps to NM_014926.2 I701I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:26443676 C>T maps to NM_017433.4 G906G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:46691676 C>T maps to NM_024016.3 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:105420292 C>A maps to NM_138420.2 E499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:54420802 T>C did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:107831701 A>C maps to ENST00000379032 V643V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:40266507 G>A maps to NM_021078.2 R712*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:44144434 G>A maps to NM_001129.3 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:104183779 C>T maps to NM_024040.2 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:98592298 C>T maps to ENST00000359863 P3365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:91090958 G>A maps to NM_032968.3 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:207824431 T>C maps to NM_173077.2 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:71948166 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:9089522 C>T maps to NM_024690.2 K764K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:33385584 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:113662140 C>T maps to NM_014813.1 S989S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:7717275 G>A maps to NM_020546.2 K543K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:116381318 A>G maps to NM_002031.2 D52D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:24471131 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:48701607 A>G maps to NM_006904.6 D3586D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:75981044 C>T maps to NM_001897.4 L787L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:141524155 G>T maps to NM_030571.3 G195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:118239008 T>C maps to NM_020721.1 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:64863672 C>T maps to NM_014755.2 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:99641018 C>T maps to NM_138576.2 S718S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:85445198 C>T maps to NM_001162953.1 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:49878128 C>T maps to NM_014419.3 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:67283810 C>A maps to NM_002547.2 G681G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:76939223 G>A maps to NM_000489.3 N508N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:157069138 G>A maps to NM_001004341.2 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:153716400 C>A maps to ENST00000440701 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:37732466 C>T maps to NM_001002814.2 P396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:161144911 C>T maps to NM_003779.3 E120E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:139829449 G>A maps to NM_030647.1 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:1926670 C>T maps to ENST00000399161 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:33235787 G>A maps to NM_020888.2 E336E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:47685562 C>T maps to ENST00000371883 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:62705214 G>A maps to NM_005873.2 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:77659485 C>T maps to NM_012283.1 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:56647940 G>A maps to NM_173595.3 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:61537392 T>C maps to NM_033081.2 T478T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:176940010 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:72821413 C>T maps to NM_006885.3 S3587S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:45150591 G>A maps to NM_006505.3 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:15697375 G>A maps to NM_003638.1 V326V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:135203374 T>G maps to ENST00000372169 R1204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:36349718 C>T maps to NM_199180.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:158495691 C>T maps to NM_003898.3 V738V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:54824795 C>T maps to ENST00000371389 Y336Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:68293397 C>T maps to NM_012320.3 G359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:235377307 A>G maps to NM_016374.5 D539D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:63010503 C>T maps to NM_006572.4 R335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:140307055 C>T maps to NM_018898.3 R193R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-IB-7651-01A-11D-2154-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:33233557 G>T maps to NM_020888.2 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:202339473 C>T maps to NM_018571.5 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:56128915 A>T maps to NM_001142763.1 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:10444959 G>A maps to NM_002162.3 G439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:18710411 G>A maps to NM_004750.4 D120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:56423952 C>T maps to NM_176810.2 Q410Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:40104535 G>A maps to NM_018177.3 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:118008 G>A maps to NM_207305.3 D37D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:32955887 G>A maps to NM_001076786.1 V899V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:132498064 G>A maps to ENST00000333577 P1250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:148786100 G>A maps to NM_024605.3 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:134927582 C>A maps to NM_182489.1 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:99661459 G>A maps to NM_001184880.1 T712T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:90766792 C>T maps to NM_198925.2 G288G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:50218424 C>T maps to NM_172193.2 R386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:96051634 G>A maps to ENST00000297954 S1570S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:37537895 G>A maps to NM_012166.2 N210N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:39328260 G>A maps to NM_145027.4 I664I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:57115221 G>A maps to NM_133459.3 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:12957128 G>A maps to ENST00000429247 Q709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:3317941 G>A maps to NM_198229.2 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:28878778 A>C maps to NM_016628.3 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:94602522 C>T maps to NM_130847.2 A883A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:238726959 G>A maps to NM_001080504.2 Q467Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:73512856 G>A maps to NM_207346.2 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:20134916 G>A maps to NM_001168465.1 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:154863211 C>T maps to NM_024012.2 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:55824301 G>T maps to NM_001085488.1 C209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:152697631 G>A maps to NM_182961.2 R3070*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:130656829 C>T maps to NM_013443.3 W86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:95537599 C>T maps to NM_144705.2 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:114443915 G>A maps to NM_006594.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:100802425 C>A maps to NM_001283.3 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:58565025 C>T maps to NM_182572.3 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:90651172 C>T maps to NM_022054.2 D351D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:33183174 G>A maps to NM_001105570.1 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:5592848 G>A maps to NM_014649.2 R753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:178415759 G>A maps to NM_152517.2 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:144672377 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:34635601 C>T maps to NM_207585.1 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:92200438 G>T maps to NM_003243.4 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:65392408 G>A maps to NM_032223.2 P947P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:138192393 C>T maps to NM_031913.3 R752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:168461612 G>A maps to NM_024919.3 A390A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:56104154 G>A maps to NM_032836.2 G384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:11401428 C>T maps to NM_005114.2 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:38647543 G>A maps to NM_001099404.1 V412V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:179666972 A>T maps to NM_002752.4 I337I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:32369564 G>A maps to ENST00000468270 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:33926884 C>T maps to NM_001036.3 R1042R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:60688135 C>T maps to NM_022893.3 K637K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:104170226 T>C maps to NM_003452.2 D59D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:126746696 G>A maps to NM_001127323.1 R194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:68117024 G>A maps to NM_006421.3 L1617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:150255694 C>T maps to NM_144697.2 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:44071036 G>A maps to NM_002840.3 P1104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:179395507 C>T maps to NM_133378.4 Q32710Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:47451948 C>A maps to NM_015466.2 I887I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:126093972 G>A maps to ENST00000377985 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:33245201 G>A maps to NM_003782.3 Q2Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:2752046 G>A maps to NM_133463.1 P344P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:197074012 C>T maps to NM_018136.4 W1456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:77239491 C>T maps to NM_015336.2 R445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:75618847 T>C did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:88904552 C>T maps to NM_018418.4 D529D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:102266351 C>A maps to NM_021956.4 T437T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:151511916 G>A maps to NM_006726.3 G2058G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:132625244 C>T maps to NM_175066.3 P492P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:27659650 G>A maps to ENST00000379863 K239K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:154393592 T>C maps to NM_001099293.1 C58C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:11157551 C>A maps to NM_015458.3 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:147381176 C>T maps to NM_005267.4 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:100624920 A>C maps to NM_144620.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:25384072 G>T maps to NM_001035256.1 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:836309 G>A maps to NM_058192.2 Y193Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:75563055 C>T maps to NM_024533.3 S409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:10236628 C>T maps to NM_199133.2 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:248004961 G>T maps to NM_001001959.1 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:89015811 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:58381794 C>T maps to NM_053023.4 R361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:48953962 C>A maps to NM_031485.3 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:74719129 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:20249044 C>A maps to NM_001005500.1 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:49314775 C>T maps to NM_033124.4 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:125451138 G>T maps to ENST00000278903 E253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:107211877 G>A maps to NM_018011.3 R159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:145161566 A>G maps to NM_014795.3 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:60906107 G>A maps to NM_005560.3 H1210H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:30708464 G>A maps to NM_005803.2 H155H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:53612070 C>T maps to NM_001164309.1 E409E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:56831838 C>T maps to NM_025009.3 D286D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:32262199 C>T maps to NM_144569.4 E754E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:40351186 C>T maps to NM_017581.2 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:132375526 G>A maps to NM_199350.3 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:73519669 G>A maps to NM_001965.3 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:167929033 C>T maps to NM_002887.3 D327D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:64825601 G>A maps to ENST00000340252 Y102Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:114215987 C>T maps to NM_001142782.1 G1030G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:39450467 C>T maps to NM_207361.4 T2831T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:43638646 C>T maps to NM_152732.4 G264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:17449815 G>A maps to NM_133644.3 E215E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:124522507 C>T maps to ENST00000408936 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:53422136 G>A maps to NM_002590.2 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:121509062 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:32956036 C>T maps to NM_207313.1 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:36324350 C>T maps to NM_030636.2 D366D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:31374729 G>T maps to NM_001083893.1 G641G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:3912990 G>A maps to NM_015113.3 Y2880Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:7111475 C>T maps to NM_014469.4 G375G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:21494441 C>T maps to ENST00000416669 D2468D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:107682518 G>A maps to NM_017515.4 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:81739150 C>T maps to NM_198390.2 L713L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:111916598 C>T maps to NM_001931.4 R435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:104971327 A>G maps to NM_001007232.1 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:79650541 A>G maps to NM_017934.5 Y1778Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:100341935 G>T maps to NM_000673.4 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:23509691 G>A maps to NM_020227.2 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:61988201 G>T maps to NM_022579.1 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:169941688 G>A maps to NM_014970.2 R650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:65408724 T>C maps to NM_153253.29 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:10720072 C>T maps to NM_001079843.1 E342E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:639259 G>A maps to NM_018140.3 A421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:32903415 G>T maps to NM_002118.4 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:38208973 C>T maps to NM_001171690.1 D162D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:41745190 C>A maps to NM_015138.4 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:31434491 G>A maps to NM_012325.2 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:56440680 G>A maps to NM_017763.4 N179N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:33261569 G>A maps to NM_001103184.2 R555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:137593566 G>A maps to NM_001496.3 Y182Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:22140960 G>A maps to NM_001013693.2 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:48151571 A>G did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:33495094 C>A maps to NM_173167.2 P389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:3599697 C>T maps to NM_024337.3 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:7326105 G>A maps to NM_001018039.1 R178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:37702271 C>T maps to NM_018310.3 G332G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:115814374 C>A maps to ENST00000257414 G430G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:144102803 C>T maps to NM_002346.2 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:152658134 G>A maps to NM_182961.2 V4123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:2186912 G>T maps to NM_199292.2 S426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:117077054 G>A maps to NM_004716.2 G672G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:171083224 C>T maps to NM_006894.5 N302N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:137154341 C>T maps to NM_004717.2 R817R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:61303133 C>T maps to NM_016354.3 C686C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:89403629 C>T maps to NM_013227.3 C2302C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:170592875 G>A maps to NM_005618.3 H497H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:168107753 G>A maps to NM_152381.5 V3284V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:44687258 C>T maps to ENST00000444676 R140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:31768178 G>A maps to NM_020856.2 R840R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:90399280 C>T maps to NM_001134479.1 C218C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:55021768 C>T maps to NM_018398.2 G893G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:48888049 G>T maps to ENST00000336239 S449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:46811542 C>T maps to NM_152795.2 D143D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:6091158 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:73729382 C>A maps to ENST00000427855 L857L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:246922334 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:5221324 T>C maps to NM_001004760.2 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:186052022 C>T maps to NM_031935.2 I2938I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:41509925 C>T maps to NM_000767.4 D64D. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-IB-7651-01A-11D-2154-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:36168459 A>G maps to NM_005983.2 E194E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:242079415 G>A maps to ENST00000358649 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:242441006 C>T maps to NM_006374.3 K49K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:676653 G>A maps to ENST00000404286 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:53419068 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:27076399 G>A maps to NM_004295.3 E406E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:47487032 G>A maps to NM_002621.2 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:145393590 G>A maps to NM_152550.3 E342E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:46320234 G>A maps to NM_000211.3 F299F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:26695590 C>A maps to NM_000638.3 R310R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:23191451 C>T maps to ENST00000400191 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:123494406 G>A maps to NM_020845.2 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:236157146 G>A maps to NM_002508.2 H851H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:233715096 C>T maps to ENST00000373566 V1292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:62384602 G>A maps to NM_012200.2 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:166912073 G>A maps to ENST00000510118 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:101436159 G>A maps to ENST00000392977 W356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:45169608 C>T maps to NM_005413.3 C122C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:42602498 T>C maps to NM_198141.2 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:107423655 G>A maps to NM_000111.2 G371G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:121400547 C>T maps to ENST00000393667 E2953E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:203033017 G>A maps to ENST00000367238 G958G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:17841236 G>A maps to ENST00000417048 R806*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:78403608 C>T maps to NM_006383.2 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:153592425 G>T maps to NM_001110556.1 S748S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:121188105 C>T maps to NM_177478.1 Q150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:112736399 C>T maps to NM_015412.3 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:110323435 C>A maps to ENST00000356688 G255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:53975653 G>A maps to NM_147193.2 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:13102916 A>G maps to NM_018654.1 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:79190434 C>T maps to NM_024546.3 T487T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:2964854 C>T maps to NM_003703.1 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:60646153 C>T maps to NM_194449.2 D1548D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:79655977 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:30737857 G>T maps to NM_005877.4 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:5009470 C>A maps to NM_021801.3 I10I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:128481263 T>C maps to NM_001458.4 C618C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:116442729 A>G maps to NM_000493.3 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:132193049 G>A maps to NM_020911.1 Q135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:8006789 C>T maps to NM_031923.2 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:17612545 A>G maps to NM_001001924.2 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:175564990 G>A maps to NM_006529.2 Y447Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:7063706 C>T maps to NM_176822.3 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:12968257 G>A maps to NM_182643.2 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:24679566 C>T maps to NM_014169.3 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:119535963 G>A maps to NM_002855.4 A349A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:11995993 G>A maps to NM_201402.2 N92N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:83742225 A>G maps to ENST00000505472 R1180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:51585521 C>T maps to NM_002702.3 E139E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:14676646 G>A maps to ENST00000436007 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:48026621 A>C maps to NM_000179.2 A500A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:190531601 G>A maps to NM_019048.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:112898708 C>A maps to NM_007203.4 C295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:30212054 G>T maps to NM_032204.3 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:32800499 C>T maps to ENST00000452392 E349E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:131931289 C>A maps to ENST00000403834 G331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:91637979 G>A maps to NM_001008495.3 G354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:42154489 G>A maps to NM_152513.3 Q691Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:35929025 G>A maps to NM_031866.2 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:12903499 C>T maps to NM_002229.2 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:17488857 C>T maps to NM_001037814.1 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:31378243 G>A maps to NM_022728.2 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:33543126 G>A maps to ENST00000360661 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:46703410 G>A maps to NM_133635.4 Y138Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:68382675 G>A maps to NM_145119.3 R136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:58290545 G>A maps to NM_017652.2 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:122958718 G>A maps to NM_017612.2 V483V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:158450302 A>C maps to NM_001004472.1 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:82561516 C>A maps to NM_199418.2 E169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:128514201 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:48746711 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:41414235 C>T maps to NM_001843.2 S839S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:48876805 G>A maps to NM_012451.3 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:202700143 G>A maps to ENST00000367264 Q1393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:135114494 C>T maps to NM_032536.2 C353C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:38228670 G>A maps to NM_138797.2 R267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:100198521 A>C maps to NM_012172.4 *619Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:179430077 G>A maps to NM_133378.4 N24359N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:43882501 G>A maps to NM_001098204.1 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:43687178 G>A maps to NM_173050.2 D119D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:4164630 C>T maps to NM_001116.3 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:152770416 C>A maps to NM_178352.2 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:74124187 C>T maps to NM_032217.3 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:58864688 G>A maps to NM_130786.3 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:50357047 G>A maps to NM_033158.4 Y291Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:179044892 G>A maps to NM_005520.2 Y276Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:89925334 T>C maps to NM_032119.3 N606N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:140040341 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:99957137 C>T maps to ENST00000413850 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:128786589 G>A maps to NM_000890.3 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:6651035 G>A maps to NM_003737.2 V1634V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:45269690 A>C did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:75006443 A>G did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:14105606 C>T maps to NM_012231.4 N439N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:105412760 C>T maps to NM_138420.2 E3009E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:149248120 C>T maps to ENST00000404807 D1640D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:38823875 C>A maps to NM_152868.1 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:72821371 C>T maps to NM_006885.3 S3601S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:39030002 G>A maps to NM_198963.1 R1291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:35154345 C>T maps to ENST00000339266 F899F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:20763276 G>A maps to NM_004004.5 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:16905359 C>T maps to ENST00000438489 A1100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:169343746 G>A maps to NM_001012967.1 G724G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:88419687 C>T maps to NM_001030015.2 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:24342813 G>A maps to ENST00000380789 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:31766155 G>A maps to ENST00000446633 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:107016607 C>T maps to NM_014978.1 S1123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:5620297 G>A maps to NM_147127.4 I871I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:206657009 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:78398175 G>A maps to NM_006383.2 C149C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:156421356 A>G maps to NM_015508.4 Q464Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:94713674 C>T maps to ENST00000452913 R84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:3191913 C>T maps to ENST00000380989 Q590Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:17674449 C>T maps to NM_012387.2 I354I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:21476282 C>T maps to NM_021269.2 K495K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:38524753 G>A maps to NM_001106.3 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:37410519 C>T maps to NM_017438.3 E372E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:8844346 C>T maps to NM_001127448.1 D89D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:1165095 G>A maps to NM_012445.3 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:119093521 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:155222375 G>A maps to ENST00000340059 R546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:43527083 C>T maps to NM_201631.3 Q586Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:57021053 G>A maps to NM_001010862.2 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:83848713 C>T maps to NM_015018.2 H1651H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:55636178 G>A maps to NM_014750.4 R496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:18305856 G>A maps to NM_032683.2 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:33236216 G>A maps to NM_020888.2 R479R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:78647146 C>T maps to NM_001161352.1 S1196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:99185039 C>T maps to NM_001134224.1 G814G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:61958145 C>T maps to ENST00000326996 R1206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:56114113 G>A maps to NM_153219.2 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:108308204 G>T maps to NM_020890.2 C6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:135028023 G>A maps to NM_002410.3 K103K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:57170115 C>T maps to NM_006252.3 R421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:96603170 C>T maps to NM_006729.4 N967N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:100859507 G>A maps to NM_001084.4 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:48501641 G>A maps to NM_015030.1 L2947L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:18057689 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:74209427 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:47259279 C>T maps to NM_024301.4 C191C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:242080136 T>C maps to ENST00000358649 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:170917645 C>T maps to ENST00000442603 L1644L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:61781938 G>A maps to NM_001003787.2 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:56113510 G>A maps to NM_153219.2 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:175165071 C>A maps to NM_207015.2 I382I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:66062460 C>A maps to NM_153266.3 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:68703960 G>A maps to NM_002180.2 T671T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:103534583 C>A maps to NM_003998.3 V865V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:53497947 G>A maps to NM_003578.3 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:156717527 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:41149376 G>T maps to NM_001115131.1 G863G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:202128651 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:33167832 C>T maps to NM_207391.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:3245111 G>A maps to NM_001009984.1 R949*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:130288971 G>A maps to NM_007037.4 D312D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:8741936 G>A maps to NM_001010855.2 R45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:128680720 C>T maps to NM_002017.3 N399N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:53007819 C>A maps to NM_016075.2 E169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:28995105 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:150884172 C>T maps to ENST00000422024 E60E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:113824777 G>A maps to NM_173542.3 Q441Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:138712705 C>T maps to ENST00000409386 P1278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:46320303 G>A maps to NM_000211.3 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:106772099 G>A maps to NM_018082.5 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:192234333 C>T maps to NM_001130158.1 R367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:6261611 C>T maps to NM_001037329.2 F196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:56704379 G>T maps to NM_001080456.2 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:140176177 G>A maps to NM_018905.2 P543P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:48994108 T>C did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:139943435 G>A maps to ENST00000354402 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:50534864 C>T maps to NM_002112.3 Q527Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:187009413 A>G did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:61068394 G>T maps to NM_001923.3 S1075S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:88300354 G>A maps to NM_001143831.2 N832N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:112998845 C>T maps to NM_018704.2 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:139357392 C>T maps to NM_014866.1 S1613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:56204383 G>A maps to NM_001130071.1 P501P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:101760366 C>T maps to NM_014503.2 L2053L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:140328736 C>T maps to NM_006647.1 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:58550528 C>A maps to NM_001160305.1 R208R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:92702920 C>T maps to NM_005959.3 C10C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:37331825 T>C maps to NM_153485.1 G530G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:977108 C>T maps to NM_021240.2 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:53454542 G>A maps to NM_170754.2 Q951Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:115580985 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:178553084 C>T maps to NM_014244.4 K888K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:14209880 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:57132155 C>T maps to NM_017563.3 T525T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:168299001 G>T maps to ENST00000400822 E478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:151751710 G>A maps to NM_001083965.1 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:50385990 G>T maps to NM_006545.4 Y229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:202149923 G>A maps to NM_001080125.1 E455E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:644641 C>T maps to NM_024792.1 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:44070973 C>T maps to NM_002840.3 S1083S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:30309621 C>T maps to NM_021253.3 C381C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:6687286 C>T maps to ENST00000309577 W1740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:8993577 G>A maps to NM_003470.2 T782T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:67266819 A>G maps to ENST00000392677 S989S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:164468185 G>A maps to NM_018086.2 Y52Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:35381662 T>C maps to ENST00000396787 I797I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:21936610 A>G did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:159163240 T>G maps to NM_021189.3 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:21131670 C>A maps to NM_003429.4 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:93375521 G>A maps to NM_017594.3 C196C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:153964127 G>T maps to NM_001030.4 G68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:17447086 G>A maps to NM_001037814.1 G397G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:73720626 C>T maps to ENST00000427855 N420N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:126219701 G>A maps to NM_020946.1 R371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:61417466 T>G maps to ENST00000389520 V453V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:43113119 C>T maps to NM_002821.3 L864L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:233134990 G>A maps to NM_014801.3 C1821C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:113858409 C>A maps to NM_000796.3 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:140755254 C>T maps to NM_018919.2 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:2867429 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:72039243 C>T maps to NM_024817.2 L702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:143742744 C>A maps to NM_003937.2 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:48418516 C>T maps to NM_002536.2 Y407Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:152652460 G>A maps to NM_182961.2 S4453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:22069240 A>G maps to NM_006129.4 *987W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:76757123 C>T maps to NM_171999.2 N1235N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:41650461 T>C maps to NM_002883.2 E370E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:46628043 G>A maps to NM_002146.4 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:9661305 G>A maps to NM_001130924.2 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:202932820 G>A maps to NM_016243.2 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:30980610 G>A maps to NM_014303.2 H154H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:104119160 C>T maps to NM_004193.2 G382G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:38937110 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:176915201 C>T maps to ENST00000281881 T711T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:96639181 C>T maps to NM_005222.3 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:56310932 A>C maps to NM_004898.2 L520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:107041053 G>T maps to ENST00000304514 L1123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:52268952 C>T maps to ENST00000361841 R319R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:47284644 G>T maps to NM_182902.3 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:228553838 C>T maps to NM_001098623.1 F6376F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:88747820 C>T maps to NM_178310.3 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:103013309 C>T maps to NM_003855.2 D530D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:89038500 C>T maps to NM_024824.4 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:21467001 C>T maps to NM_024697.2 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:197654004 A>G maps to NM_012086.2 D272D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:44589367 C>T maps to NM_000394.2 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:84539608 C>T maps to NM_207517.2 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:63651 G>A maps to NM_006987.3 C313C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:90647961 A>G maps to NM_001170794.1 H648H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:60518111 A>G maps to NM_181725.3 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:40440379 G>A maps to NM_001098634.1 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:103138290 G>A maps to ENST00000428762 L2976L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:12790296 C>A maps to NM_001930.2 E218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:3011122 G>T maps to NM_003260.4 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:228437820 C>A maps to NM_001098623.1 R1397R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:407554 G>A maps to NM_021805.2 Y165Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:69519974 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:24880895 G>A maps to NM_020824.3 R1308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:46271481 G>A maps to NM_175875.4 C207C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:862728 C>A maps to ENST00000409531 C100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:33855180 A>G maps to NM_001036.3 K372K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:27247043 C>T maps to NM_012326.2 D116D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:107546685 G>A maps to NM_005502.3 D2232D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:37592369 G>A maps to NM_018302.2 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:132785209 G>A maps to NM_003569.2 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:40259625 G>A maps to NM_024119.2 F331F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:50125568 T>C maps to NM_018191.3 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:96412998 A>G maps to NM_000895.1 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:21519245 C>A maps to ENST00000416669 C2976*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:27664443 C>T maps to ENST00000379863 I494I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:40581424 C>T maps to NM_001142577.1 K309K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:43531234 G>A maps to NM_014798.2 L661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:120315331 G>A maps to NM_004547.5 Q42Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:8159876 T>C maps to ENST00000309737 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:127440423 C>T maps to ENST00000368317 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:146703541 G>A maps to NM_001112724.1 Q114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:48125030 C>T maps to NM_033226.2 S1095S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:51900372 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:223408410 A>C maps to NM_001037175.2 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:105179211 C>T maps to ENST00000252520 I886I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:76200767 C>T maps to NM_001145526.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:35191584 C>T maps to NM_003024.2 R992*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:44778192 C>T maps to NM_181756.1 G460G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:57133899 C>T maps to NM_021216.4 C415C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:2749547 G>A maps to NM_033267.4 D201D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:128457909 C>T maps to NM_022742.3 S1154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:88452317 C>T maps to NM_001171610.1 R364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:43345050 G>A maps to NM_001142930.1 Q205Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:21476147 G>T maps to NM_021269.2 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:143081625 T>C maps to NM_006734.3 S1933S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:153433215 A>G maps to NM_005927.4 G344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:140301471 G>T maps to NM_015689.3 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:88968015 C>T maps to NM_000297.2 I514I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:45429865 C>T maps to NM_001004329.2 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:18731267 C>A maps to NM_012109.2 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:48172855 C>T maps to NM_002611.3 Y19Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:72071980 G>A maps to NM_001163.3 N530N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:29118724 C>T maps to NM_001943.3 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:75673486 C>T maps to NM_002658.3 C217C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:60645586 C>T maps to NM_194449.2 S1359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:2995639 G>T maps to NM_002548.2 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:65408898 C>T maps to NM_153253.29 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:109768324 G>T maps to NM_022765.3 T726T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:38800422 G>T maps to NM_003263.3 I10I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:30065560 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:73571042 C>T maps to NM_016055.5 R155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:47786807 C>T maps to NM_006031.5 S973S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:160251583 T>G maps to NM_014247.2 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:11556084 C>T maps to NM_001372.3 C787C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:129783238 G>A maps to NM_199320.2 W454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:49042590 C>T maps to NM_177938.2 H395H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:143079467 G>A maps to NM_001010972.1 E112E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:239147803 C>T maps to NM_018645.4 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:125971723 C>T maps to NM_207408.1 Q66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:42725168 G>T maps to NM_030954.3 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:7606951 A>G maps to NM_001166111.1 S426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:26108108 G>A maps to NM_005323.3 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:56227285 C>A maps to NM_020182.3 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:160757955 G>A maps to NM_021911.2 R337R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:62850259 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:10874602 C>A maps to NM_004752.3 V382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:108862041 A>C maps to NM_001098268.1 Y525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:138860411 C>T maps to NM_198282.2 W161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:79064007 C>A maps to ENST00000258883 G765G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:39851458 G>A maps to ENST00000361689 E2672E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:40318318 G>T maps to NM_012285.2 I612I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:32754255 G>A maps to NM_001098535.1 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:118458250 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:209935960 T>G maps to NM_025228.2 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:45009399 G>A maps to NM_033054.2 D469D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:54670847 G>A maps to NM_016491.3 E168E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:3595694 C>T maps to NM_001060.5 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:89341251 G>A maps to NM_013275.4 S2561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:1943816 C>T maps to NM_001383.3 R314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:131369982 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:137765647 C>A maps to NM_016604.3 L1629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:61981706 C>T maps to NM_000744.5 V352V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:247040287 G>T maps to ENST00000428671 A1005A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:98422055 T>C maps to NM_015348.1 L722L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:73470640 C>T maps to ENST00000358929 Y397Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:42226280 C>T maps to NM_001042646.1 H156H. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-IB-7651-01A-11D-2154-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:4903512 C>T maps to NM_001004759.1 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:139727112 G>A maps to NM_022750.2 R531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:80159510 G>A maps to ENST00000445854 Q104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:103805667 C>T maps to NM_183004.3 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:21380773 A>G maps to NM_005446.3 R398R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:135942551 C>T maps to NM_001807.3 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:33937493 C>T maps to NM_016568.3 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:100723036 C>T maps to NM_017988.4 A567A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:24885463 C>T maps to NM_025081.2 G1503G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:160858178 C>T maps to ENST00000392145 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:96351994 G>T maps to NM_018063.3 E593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:144086911 T>C maps to NM_001100164.1 S403S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:44845787 C>T maps to NM_030753.3 R322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:47886655 G>A maps to NM_138295.3 G1658G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:35685747 G>A maps to ENST00000329305 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:95092162 C>A maps to NM_001129889.1 E550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:6970733 C>T maps to NM_001098536.1 V542V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:180022123 A>G maps to NM_014810.4 T1604T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:32138807 G>A maps to NM_032741.4 Y80Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:130023755 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:29287291 A>G maps to NM_001135919.1 G195G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:68128330 C>T maps to NM_018658.1 R35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:30735151 G>A maps to NM_005877.4 I488I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:47692707 C>T maps to NM_003906.3 T744T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:46784531 G>A maps to ENST00000415402 V1295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:88211753 T>C maps to ENST00000342368 G1113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:12353088 C>T maps to NM_006796.2 A411A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:81430433 G>A maps to ENST00000458088 Q159Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:6913005 G>A maps to NM_003700.1 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:36824410 G>A maps to NM_016059.4 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:3586948 C>T maps to NM_133261.2 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:45192139 G>A maps to NM_022829.5 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:30747902 C>T maps to NM_014742.3 L560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:206870180 G>A maps to NM_017759.4 L665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:149243446 G>A maps to ENST00000404807 A1227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:3215923 C>A maps to NM_016302.3 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:35245536 G>A maps to NM_013448.2 R807R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:57753327 G>A maps to NM_006622.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:8808658 G>A maps to NM_178525.3 H131H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:80866839 A>G maps to NM_001098802.1 K363K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:40920866 C>T maps to NM_170589.3 S1884S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:1455927 G>A maps to NM_018188.3 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:60053434 A>G maps to NM_024930.2 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:35748538 C>T maps to ENST00000458225 R254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:123046318 G>A maps to ENST00000368446 K81K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:30033810 T>G maps to NM_002233.2 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:100210307 G>A maps to NM_001025108.1 P630P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:103908399 C>T maps to NM_001001711.2 R284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:113975903 C>T maps to NM_005561.3 R326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:89999001 G>A maps to ENST00000304984 E374E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:40817020 C>T maps to NM_020831.3 K237K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:68045258 G>A maps to NM_020715.2 Q920Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:101921317 G>A maps to NM_001913.2 L554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:109794809 C>T maps to NM_001408.2 T703T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:32346404 C>T maps to ENST00000397492 C66C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:50188801 G>A maps to NM_001037806.3 G947G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:155582080 C>T maps to NM_018116.2 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:215815604 C>A maps to NM_173076.2 E2284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:171305025 A>G maps to NM_012300.2 D299D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:109696077 C>T maps to NM_020769.2 Q745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:22926573 G>A maps to NM_006043.1 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:4881756 C>T maps to NM_017417.1 S636S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:156552182 T>G maps to NM_001105669.2 Y289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:209564 C>T maps to NM_021932.4 D97D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:22067081 C>T maps to NM_006129.4 Y900Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:44486458 G>A maps to ENST00000398168 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:79979291 T>C maps to NM_153252.4 G535G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:77810117 G>A maps to NM_213601.1 Q126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:14489096 C>A maps to NM_001134367.1 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:44685095 G>A maps to ENST00000444676 Q131Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:249151670 A>G maps to NM_001136036.2 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:235961351 C>T maps to NM_014521.2 Y875Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:50161055 G>A maps to NM_021228.2 E1219E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:146536845 G>A maps to NM_014141.5 W84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:90097099 C>A maps to NM_021244.4 G120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:152298468 A>G maps to NM_018151.4 S566S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:76969224 G>T maps to NM_005567.3 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:204156989 C>T maps to ENST00000429815 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:51361377 C>A maps to NM_001648.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:72343145 G>A maps to NM_017757.2 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:24909749 G>A maps to NM_020824.3 I358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:42219575 G>A maps to NM_004363.2 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:19288433 T>C maps to NM_001198695.1 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:34030739 G>A maps to NM_001036.3 L2535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:108366668 C>T maps to NM_006731.2 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:27313398 A>G maps to NM_014915.2 V1354V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:48141336 G>A maps to NM_001098531.2 R516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:109283322 G>A maps to NM_032131.4 Q715Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:24524298 G>A maps to NM_031422.4 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:17462276 C>A maps to NM_002594.2 A493A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:44621143 C>T maps to NM_182547.2 E97E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:180307982 C>T maps to NM_152520.4 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:47584826 G>A maps to NM_015168.1 D461D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:120769287 C>A maps to NM_014619.2 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:72945947 C>T maps to NM_176071.1 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:50358291 C>T maps to NM_017432.3 C172C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:38407153 C>A maps to ENST00000354891 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:13971164 G>A maps to NM_025229.1 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:55253302 A>G maps to NM_020532.4 V644V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:34017071 C>T maps to NM_018449.2 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:2035968 C>T maps to NM_005262.2 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:25784912 G>A maps to NM_018202.4 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:167508214 C>T maps to NM_005025.4 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:111724394 G>A maps to ENST00000428306 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:106513207 C>T maps to NM_002649.2 A704A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:67012740 T>C maps to NM_012308.2 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:42800926 C>T maps to NM_001093726.1 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:5803762 C>T maps to NM_153717.2 I797I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:1045209 G>A maps to NM_019112.3 R475R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:74420162 G>A maps to NM_007249.4 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:228481231 G>A maps to NM_001098623.1 Q3682Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:42128306 G>A maps to NM_152513.3 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:71146495 G>A maps to NM_001360.2 C451C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:31537444 G>A maps to NM_003787.4 R425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:71490540 G>A maps to NM_005909.3 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:140214936 C>T maps to NM_018910.2 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:47423623 C>T maps to NM_001848.2 R928R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:140729347 G>A maps to NM_024757.4 E1280E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:121810498 T>C did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:31202335 C>T maps to NM_004960.3 G482G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:53747045 G>A maps to NM_182609.2 N40N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:115252228 G>A maps to NM_002524.3 Y137Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:107973465 G>A maps to NM_001113226.1 Q394Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:63312261 G>A maps to NM_004585.3 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:22363310 C>T maps to NM_020346.2 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:24480695 C>T maps to NM_012295.3 S1025S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:45152452 G>A maps to ENST00000327574 K65K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:52825102 A>G maps to NM_144684.2 E200E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:1657647 C>T maps to NM_000934.3 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:51220125 G>A maps to ENST00000391814 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:36122988 G>A maps to NM_001007527.1 I299I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:129784703 C>T maps to NM_020228.2 T916T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:1046402 C>T maps to NM_019112.3 D540D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:7863169 G>A maps to ENST00000377532 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:60392253 G>A maps to NM_000775.2 N55N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:64536229 G>A maps to NM_020762.2 L1012L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:433367 G>A maps to NM_006614.2 Q934Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:18419792 C>A maps to ENST00000332610 E484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:33468867 G>A maps to NM_022917.4 G343G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:56484400 A>G maps to ENST00000281662 N2041N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:21702190 G>A maps to NM_031314.2 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:101821937 G>A maps to NM_003090.2 N253N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:21330995 C>T maps to NM_144704.2 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:10116273 C>T maps to NM_033084.3 R926*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:1666218 A>G maps to NM_182838.2 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:49312111 C>T maps to NM_033124.4 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:158641180 C>T maps to NM_003126.2 K517K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:111216302 G>A maps to NM_002232.3 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:131945021 C>T maps to NM_005732.3 C990C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:29055871 C>A maps to NM_001944.2 S883S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:88036156 C>T maps to NM_001166693.1 S724S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:102364642 C>A maps to NM_000919.3 G933G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:144776462 C>T maps to NM_173831.3 C293C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:74689271 G>T maps to NM_006302.2 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:136573456 G>A maps to NM_007101.3 H474H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:20716896 C>T maps to NM_021954.3 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:77632490 G>A maps to NM_015057.4 C4397C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:99863269 G>A maps to NM_175735.3 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:96761414 A>G maps to NM_005390.4 K38K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:43319444 A>G maps to NM_015500.1 A529A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:39998251 C>T maps to NM_152467.3 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:139617865 G>A maps to NM_152421.3 K312K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:65420448 G>A maps to NM_138737.3 W698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:47570755 C>T maps to NM_015168.1 T923T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:6263997 C>T maps to NM_173464.3 W56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:30376269 C>T maps to ENST00000327564 R872*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:109967769 C>T maps to NM_183415.1 S901S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:128489607 C>T maps to NM_001458.4 I1725I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:18777493 C>T maps to NM_001040272.4 P1089P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:37486233 C>T maps to ENST00000374660 F943F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:77208930 A>G maps to NM_015336.2 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:35044416 C>A maps to NM_203299.2 S597S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:108363437 G>A maps to NM_014648.3 E523E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:814758 C>T maps to NM_017802.3 G733G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:48158696 C>A maps to NM_002204.2 V948V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:120114474 C>T maps to NM_006253.4 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:132358436 G>A maps to NM_032169.4 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:148921303 C>T maps to NM_003575.2 F527F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:60886790 T>C maps to NM_014207.3 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:139318377 C>T maps to NM_001001664.2 R240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:27222561 G>A maps to NM_005523.5 Y265Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:15366168 G>A maps to NM_058243.2 S662S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:179820357 C>A maps to NM_145034.4 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:52004876 G>A maps to NM_053003.2 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:20599955 C>A maps to ENST00000273739 L1223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:226925066 G>A maps to NM_002221.3 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:40039419 G>A maps to ENST00000401700 I784I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:118498784 C>T maps to NM_015157.2 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:169632083 G>A maps to NM_003247.2 H714H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:94417570 C>T maps to ENST00000434324 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:1086425 C>T maps to ENST00000441003 S1045S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:107160955 C>T maps to NM_012216.3 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:10400485 G>A maps to NM_001001331.2 A675A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:120233930 G>A maps to ENST00000276681 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:51750947 G>T maps to NM_001174116.1 I2657I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:17487908 G>A maps to NM_031310.1 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:10250487 T>C maps to NM_012073.3 Y12Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:14267879 C>T maps to NM_001008701.2 V946V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:101047521 C>T maps to NM_020654.3 S921S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:46125439 G>A maps to NM_013236.3 K288K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:5966867 C>T maps to ENST00000324058 Q154Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:105813870 G>A maps to NM_000494.3 R584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:29284865 G>A maps to ENST00000394782 E381E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:4817506 C>A maps to NM_182919.2 E295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:107501172 C>A maps to NM_018712.3 Y16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:36340236 C>T maps to NM_004646.3 W247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:29469870 C>T maps to NM_018099.3 Y351Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:115652541 C>T maps to NM_033051.3 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:76696914 G>A maps to ENST00000324767 A1139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:52550104 A>G did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:89537565 G>A maps to NM_020358.2 D24D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:51022051 C>T maps to NM_001080457.1 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:15060082 C>T maps to NM_001177382.1 Q834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:19287867 G>A maps to NM_001198695.1 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:55075381 C>T maps to NM_176782.2 W439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:53680261 C>T maps to NM_012291.4 Q1248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:90041500 C>T maps to NM_032119.3 F3621F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:46341983 C>T maps to ENST00000288400 H476H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:52447541 C>T maps to NM_001031721.3 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:5754710 G>T maps to NM_207111.2 A602A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:15522550 G>A maps to ENST00000261644 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:9237059 A>G maps to NM_001001958.1 C189C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:75756307 C>T maps to NM_015886.3 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:102747326 G>A maps to NM_015051.1 F347F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:47569241 C>T maps to NM_014346.2 A509A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:31040059 C>T maps to NM_014717.1 N1178N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:37603572 G>A maps to NM_001051.2 D90D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:33169571 C>T maps to NM_006979.2 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:141310388 G>A maps to NM_004362.2 R608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:196788366 G>A maps to NM_018897.2 S1259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:21758016 C>A maps to NM_080597.2 E685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:10192540 C>A maps to NM_003597.4 I482I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:228511296 C>T maps to NM_001098623.1 L5214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:26524883 C>A maps to NM_198137.1 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:66356254 G>A maps to NM_004439.5 Y414Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:20296206 C>A maps to NM_001004723.1 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:113810479 G>A maps to NM_173542.3 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:95657488 C>A maps to NM_004411.4 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:114156188 T>C maps to NM_017905.4 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:24729005 C>T maps to NM_000359.2 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:36673442 G>A maps to ENST00000355114 Y496Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:80549082 C>T maps to NM_007029.3 C22C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:24820879 C>T maps to NM_019590.3 G1068G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:147040936 C>T maps to NM_014790.3 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:99013654 C>T maps to NM_001298.2 D674D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:6926384 C>T maps to ENST00000381407 C667C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:146044704 C>T maps to NM_002940.2 R531R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:2463856 G>A maps to NM_024325.4 R584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:151092438 C>T maps to ENST00000427663 D129D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:40863936 C>T maps to NM_152260.1 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:31083900 G>A maps to NM_001264.4 R497R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:169168 G>A maps to ENST00000399953 R92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:217234860 G>T maps to NM_020814.2 R41R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:77937522 G>A maps to NM_080491.2 R399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:34824488 G>T maps to NM_001145521.1 E848*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:88690389 G>A maps to ENST00000452588 P630P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:57798999 G>A maps to NM_001005186.2 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:41275117 G>A maps to NM_017553.1 A1465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:114430831 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:158735143 G>A maps to NM_020245.3 E32E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:6372624 C>T maps to NM_032286.2 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:143098599 G>A maps to NM_005232.4 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:118812090 G>A maps to NM_000127.2 R701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:7978973 C>A maps to NM_001139.2 P531P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-IB-7651-01A-11D-2154-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:94711934 T>A maps to NM_058237.1 A452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:130287197 C>T maps to NM_001102608.1 G717G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:45667952 C>T maps to NM_020937.2 T1941T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:219374751 C>T maps to NM_020935.2 W325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:140793470 G>A maps to NM_018913.2 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:108136979 C>T maps to NM_080546.3 I532I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:33355999 C>T maps to NM_032509.3 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:1275967 C>T maps to ENST00000447027 N5177N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:73184316 G>A maps to NM_001306.3 I21I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:71674596 C>T maps to NM_001017967.2 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:23419833 C>T maps to NM_001142546.1 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:108383191 T>C maps to NM_015065.2 E1014E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:138007891 C>T maps to ENST00000469044 G608G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:103138681 G>A maps to ENST00000428762 R2895R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:228559431 C>T maps to NM_001098623.1 L6985L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:58490961 A>G maps to NM_025027.3 H362H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:234041355 G>T maps to NM_173508.2 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:19838352 C>T maps to NM_153208.1 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:86905862 C>T maps to NM_006536.5 G412G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:122420073 G>A maps to NM_017554.2 P891P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:78264846 C>A maps to NM_000046.3 G161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:46812849 C>T maps to NM_017653.3 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:157188104 G>A maps to NM_001167912.1 Q118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:25769378 G>A maps to NM_005495.2 Q86Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:28366050 G>T maps to ENST00000396827 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:130865958 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:33614341 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:24732734 G>A maps to ENST00000379068 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:130270428 C>T maps to NM_022833.2 A495A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:98350015 C>T maps to NM_001079.3 R283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:44272507 G>A maps to NM_020745.2 D542D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:1580997 C>T maps to ENST00000357934 S474S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:70939653 C>T maps to NM_022132.4 R361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:46117424 C>A maps to NM_198699.1 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:10547727 C>T maps to NM_002470.2 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:75978999 C>T maps to NM_006633.2 L1241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:21958191 A>G maps to NM_005691.2 G1522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:2570853 G>A maps to NM_001145815.1 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:54974225 C>T maps to NM_001033522.1 D283D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:1606275 G>A maps to NM_001005922.1 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:29629166 G>A maps to NM_183378.2 Y481Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:2308988 G>A maps to NM_003245.3 T437T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:36245051 C>T maps to NM_019104.1 D193D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:19144198 C>A maps to NM_052911.2 E596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:22964202 A>T maps to NM_015991.2 K32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:73205354 C>T maps to NM_014243.1 Q239Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:101190357 T>C maps to NM_001078.3 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:36912756 C>T maps to NM_003753.3 A357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:33649744 C>T maps to NM_030955.2 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:67863821 C>T maps to NM_173630.3 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:96040137 G>A maps to NM_013434.4 E92E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:34372077 G>A maps to NM_020702.3 D288D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:245849752 G>A maps to NM_018012.3 Q1156Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:57794322 G>T maps to NM_005550.3 S746S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:180651775 C>T maps to NM_033549.3 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:87677921 C>T maps to NM_020655.2 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:41990568 G>A maps to NM_024503.3 N1740N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:84870535 G>A maps to NM_014895.2 R926*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:603717 C>T maps to NM_001194.3 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:8619389 G>A maps to NM_012335.3 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:57499294 C>T maps to NM_003153.4 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:62080178 C>T maps to NM_001099789.1 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:373495 C>A maps to NM_178537.4 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:114186023 G>A maps to NM_198123.1 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:138749733 C>T maps to ENST00000464606 R750R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:95728749 G>A maps to NM_000439.4 D739D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:109605786 G>A maps to NM_001093.3 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:331764 G>A maps to NM_001176.3 E31E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:77675850 C>T maps to NM_020859.3 G1405G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:1576443 C>T maps to NM_006445.3 E1235E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:68691349 C>T maps to NM_001024680.1 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:62070949 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:114290827 A>G maps to NM_198123.1 Y169Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:33453161 C>A maps to NM_001128161.1 G156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:73609629 C>T maps to NM_022170.1 Q247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:92647575 C>T maps to NM_013272.3 C271C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:51860755 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:18296805 G>A maps to ENST00000401790 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:102510213 T>C maps to NM_001376.4 S4172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:100178002 G>A maps to NM_000195.2 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:62293899 G>A maps to NM_001620.1 P2663P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:75981566 C>T maps to NM_001897.4 A613A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:100779050 C>T maps to NM_000602.3 N352N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:8595094 G>A maps to NM_012335.3 Y771Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:148718165 G>A maps to NM_004911.4 D54D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:26265550 C>T maps to NM_004331.2 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:4804098 C>T maps to NM_000080.3 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:105915064 C>T maps to NM_004257.4 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:225639793 G>A maps to NM_014689.2 I1947I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:161821542 C>T maps to NM_007348.2 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:59940638 C>T maps to NM_018369.2 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:6303909 C>T maps to NM_006005.3 D796D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:51128445 G>A maps to NM_001160329.1 P560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:45104189 C>T maps to NM_001029835.2 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:64679653 C>T maps to NM_182914.2 L6329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:45270981 G>A maps to NM_004073.2 P560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:25672427 G>A maps to NM_006424.2 K300K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:67214519 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:189020150 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:32453475 G>A maps to NM_013956.3 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:155451438 G>A maps to ENST00000368346 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:2073273 C>T maps to NM_003070.3 G603G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:56599356 G>A maps to NM_004574.3 C256C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:34269618 C>T maps to NM_001164749.1 G702G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:105218205 G>T maps to NM_001001412.3 C101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:54966208 C>T maps to ENST00000431846 N253N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:36517066 G>A maps to NM_015526.2 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:54403723 C>T maps to NM_002739.3 G475G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:207636968 G>A maps to NM_014929.3 Q393Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:21982905 C>T maps to NM_005144.4 K556K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:35967780 G>A maps to NM_052961.3 Q145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:196214436 G>A maps to NM_152617.3 R131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:79082065 C>T maps to ENST00000258883 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:38050074 G>A maps to NM_001130964.1 R613R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:66043576 C>T maps to NM_030981.2 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:25189342 A>G maps to ENST00000380963 *339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:30530250 C>T maps to NM_025263.3 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:55972410 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:100615113 G>A maps to NM_000061.2 N267N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:4285373 C>T maps to NM_152744.3 N2106N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:42880263 C>T maps to ENST00000251268 P2625P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:3854898 G>A maps to NM_174953.1 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:220419271 G>A maps to NM_015311.2 G1600G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:30313163 C>A maps to NM_001238.1 V286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:101782699 A>G maps to NM_001855.3 G559G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:169503007 C>T maps to NM_004946.2 R1596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:34925771 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:24642110 G>A maps to NM_005132.2 E43E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:170815034 T>G maps to ENST00000442603 V1211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:89389500 C>T maps to NM_016323.2 S354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:35593372 C>T maps to NM_014672.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:126202641 T>C maps to NM_020946.1 G495G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:20442830 C>T maps to ENST00000442610 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:91863866 G>A maps to NM_194456.1 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:38103325 G>A maps to NM_001164232.1 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:76108228 A>G maps to NM_017791.2 E499E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:24683241 T>C maps to NM_138476.3 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:203186202 G>T maps to NM_003465.2 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:4722726 G>A maps to NM_003845.1 T457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:390526 G>T maps to NM_031229.2 E9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:62284884 G>A maps to NM_001620.1 F5668F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:187535438 G>T maps to ENST00000260147 I3048I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:196921408 G>A maps to NM_004087.2 Q124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:38595863 G>A maps to NM_001099404.1 G1573G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:111097130 G>T maps to NM_012471.2 I368I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:6241744 G>A maps to NM_033439.3 W17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:1034965 C>T maps to NM_033120.2 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:109241960 T>C maps to NM_018061.2 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:56103174 A>G maps to NM_001079521.1 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:15654734 C>T maps to NM_030667.1 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:52863464 G>A maps to NM_173086.4 G471G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:33345485 C>T maps to NM_014071.2 Q355Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:140202724 G>A maps to NM_018908.2 A455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:160494320 G>A maps to NM_000876.2 Q1589Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:3249342 G>A maps to ENST00000328215 C229C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:140516479 G>A maps to NM_015669.2 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:47769051 C>T maps to NM_006031.5 Q387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:5079957 G>T maps to NM_001005164.2 I300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:49079531 G>T maps to NM_005183.2 S658S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:14816458 G>A maps to NM_031453.2 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:118530096 G>A maps to ENST00000264029 Q472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:6077577 G>A maps to NM_017671.4 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:120458177 C>T maps to NM_024408.2 Q2389Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:21797188 G>A maps to NM_032264.2 E136E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:126079530 G>A maps to NM_032795.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:33463340 G>T maps to NM_022917.4 A1031A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:180424255 C>T maps to NM_197975.2 D147D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:180622207 G>A maps to NM_203293.1 F498F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:77812772 C>T maps to NM_213601.1 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:94342257 G>A maps to NM_014597.4 D411D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:219366592 G>T maps to NM_138794.3 G121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:49293688 C>T maps to NM_178173.3 V253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:228565677 C>A maps to NM_001098623.1 I7850I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:52493937 G>A maps to NM_007361.3 G885G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:203839003 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:159456923 G>A maps to NM_054114.3 R711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:88387539 G>A maps to NM_198274.3 W158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:15755180 G>A maps to NM_024329.5 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:839553 G>T maps to ENST00000317063 E346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:25229077 G>A maps to NM_001031680.2 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:95090072 C>A maps to ENST00000393080 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:203743397 T>G maps to NM_017773.3 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:140784351 C>A maps to NM_018921.2 A611A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:147030053 C>T maps to NM_014790.3 E228E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:42974286 G>T maps to NM_006245.2 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:32778623 C>T maps to NM_139241.2 R558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:42139602 C>T maps to NM_005090.3 P903P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:131622773 C>T maps to NM_198827.3 L843L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:113471840 G>A maps to NM_003051.3 I30I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:42693956 G>A maps to NM_000070.2 K491K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:897247 C>T maps to NM_198317.2 R178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:122622745 G>A maps to NM_014938.3 R720R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:105177985 C>T maps to ENST00000252520 P813P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr18:77246677 G>A maps to NM_172387.1 S828S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:169327214 C>T maps to NM_001012967.1 E1033E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:50788094 C>T maps to NM_005154.3 D903D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:144780065 G>A maps to NM_007124.2 K815K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:159277658 G>A maps to ENST00000368115 K240K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:120469704 G>A maps to NM_005513.2 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:136399205 A>G maps to ENST00000409606 A440A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:96789072 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:58022909 T>G maps to NM_001478.3 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:142228403 G>A maps to NM_001080431.1 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:119379150 G>T maps to NM_022135.2 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:118896083 C>A maps to NM_001112704.1 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:169632236 C>T maps to NM_003247.2 A663A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:236744594 A>C maps to NM_018072.5 L894L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:80845036 C>T maps to NM_014862.3 F337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:43417777 G>A maps to NM_033450.2 Q1448Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:34395758 T>C maps to NM_152595.4 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:54377421 C>T maps to NM_001020818.1 C213C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:115361773 C>T maps to NM_173800.4 L978L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:39340390 T>C maps to NM_030772.4 G460G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:176046211 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:55768824 G>A maps to ENST00000460849 R896*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:65008034 C>T maps to NM_021979.3 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:40714636 C>T maps to NM_001042532.2 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:109793138 G>A maps to NM_001408.2 Q146Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:81614778 G>A maps to NM_181900.2 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:4714098 C>T maps to NM_003845.1 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:30349742 C>T maps to ENST00000327564 C553C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:152283913 G>A maps to NM_002016.1 R1150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:51728522 G>A maps to NM_001772.3 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:59512419 C>A maps to NM_001144772.1 E479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:114615392 A>G maps to NM_001040440.2 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:137767232 T>C maps to NM_016604.3 H1730H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:110007428 C>T maps to NM_033390.1 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:19308953 C>T maps to NM_003721.2 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:70904001 G>A maps to NM_001185054.1 R507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:6619864 C>T maps to NM_014865.3 N111N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:59668385 C>T maps to NM_199290.3 W52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:26056410 A>G maps to NM_005319.3 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:10132383 C>T maps to NM_015725.2 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:18638415 C>T maps to NM_001037330.1 C230C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:161168078 G>A maps to NM_005099.4 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:47394316 G>A maps to NM_014897.2 R257R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:104156689 C>T maps to NM_001077494.1 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:132405896 C>A maps to NM_003565.2 I1048I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:46743902 C>T maps to NM_003579.3 I731I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:88643731 C>T maps to ENST00000452588 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:200969088 G>A maps to NM_017596.2 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:78837252 G>A maps to NM_002789.4 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:33744825 G>T maps to NM_181336.3 V422V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:2515061 C>T maps to NM_052847.2 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:155851244 C>A maps to NM_152280.4 V414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:47001551 G>A maps to NM_005880.3 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:88482593 T>G did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:38175488 G>A maps to NM_001607.3 Q93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:97832995 C>T maps to NM_014916.3 S1406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:48953706 C>T maps to NM_031485.3 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:70972946 T>C maps to NM_001851.4 P465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:75532150 A>G maps to NM_173540.2 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:150839252 C>T maps to NM_031946.4 R655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:99097578 G>A maps to NM_032164.2 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:86115388 T>C maps to ENST00000256117 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:135102388 C>T maps to NM_032536.2 P337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:149771735 C>T maps to ENST00000451292 L1209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:56716321 A>C maps to ENST00000370754 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:32052334 G>A maps to ENST00000375244 D1100D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:5920790 A>G maps to NM_001017969.2 C1735C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:107379987 C>T maps to NM_001001956.1 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:93011073 G>A maps to NM_032373.3 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:51736945 C>T maps to NM_014372.4 C139C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:6588954 G>A maps to NM_144666.2 T4072T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:31117929 G>A maps to NM_001105564.1 R425R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:76928311 C>T maps to ENST00000372690 R293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:196613101 C>A maps to NM_152699.4 G350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:18901410 G>A maps to NM_000095.2 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:15936592 G>T maps to NM_012304.3 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:226566901 G>A maps to NM_001618.3 I562I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:651780 G>A maps to ENST00000340092 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:33170374 G>T maps to NM_006979.2 E280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:65316128 G>A maps to NM_139242.3 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7652-01A-11D-2154-08 chrX:148579703 C>A maps to NM_000202.5 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7652-01A-11D-2154-08 chr11:56468063 T>C maps to NM_001013358.1 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7652-01A-11D-2154-08 chr10:24762713 C>A maps to NM_019590.3 S468S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7652-01A-11D-2154-08 chr10:75399730 G>A maps to NM_021245.2 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7652-01A-11D-2154-08 chr3:58134059 T>A maps to NM_001164317.1 C1983*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7652-01A-11D-2154-08 chr9:125140772 G>T maps to NM_000962.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7652-01A-11D-2154-08 chr4:87684336 A>T maps to NM_080685.2 P1337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7652-01A-11D-2154-08 chr1:52740257 T>C did not map to a codon.
Sequencing variant TCGA-IB-7652-01A-11D-2154-08 chr8:1497383 C>T maps to ENST00000357934 N197N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7652-01A-11D-2154-08 chr5:156608098 C>T maps to NM_005546.3 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7652-01A-11D-2154-08 chrX:65409670 C>T maps to NM_138737.3 H372H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7652-01A-11D-2154-08 chr20:30662500 C>T maps to NM_002110.3 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7652-01A-11D-2154-08 chrX:18845403 C>T maps to NM_006240.2 S587S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7652-01A-11D-2154-08 chr11:86131063 C>T maps to NM_001156474.1 Q596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7652-01A-11D-2154-08 chr17:76571031 G>A maps to ENST00000389840 N36N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7652-01A-11D-2154-08 chr2:239342282 C>G maps to NM_001040445.1 Y46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7652-01A-11D-2154-08 chr1:171254563 C>T maps to NM_002021.1 R494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7652-01A-11D-2154-08 chr2:166848438 G>A maps to NM_001165963.1 I1782I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7652-01A-11D-2154-08 chr9:138675925 C>T maps to ENST00000298480 A966A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7652-01A-11D-2154-08 chrX:102529239 T>A maps to NM_001012979.2 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7652-01A-11D-2154-08 chr19:4555519 G>A maps to NM_032108.3 Y176Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7652-01A-11D-2154-08 chr5:132535362 G>A maps to NM_015082.1 H651H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7652-01A-11D-2154-08 chr5:149001459 C>T maps to NM_001001669.2 A390A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7652-01A-11D-2154-08 chr11:111749419 G>A maps to ENST00000428306 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7652-01A-11D-2154-08 chr14:53110324 A>T maps to NM_014584.1 L457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7652-01A-11D-2154-08 chr1:197071381 C>T maps to NM_018136.4 E2333E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7652-01A-11D-2154-08 chr3:137849963 G>C maps to NM_016161.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7652-01A-11D-2154-08 chr3:195517058 C>A maps to NM_018406.5 R464R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7652-01A-11D-2154-08 chr13:33332727 A>G maps to ENST00000400481 T1082T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7652-01A-11D-2154-08 chr17:15532399 G>A maps to ENST00000455584 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7652-01A-11D-2154-08 chrX:149826496 A>C maps to NM_000252.2 A419A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7654-01A-11D-2154-08 chr9:77416899 C>T maps to NM_017662.4 A641A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7654-01A-11D-2154-08 chr5:145609321 T>A maps to NM_018989.1 Y146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7654-01A-11D-2154-08 chr19:58596648 G>A maps to NM_001145542.1 D368D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7654-01A-11D-2154-08 chr2:121747767 G>A maps to NM_005270.4 S1426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7654-01A-11D-2154-08 chr16:10032399 C>T maps to NM_000833.3 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7654-01A-11D-2154-08 chr1:38171169 C>T maps to NM_018101.2 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7654-01A-11D-2154-08 chr19:49253827 G>A maps to NM_000148.3 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7654-01A-11D-2154-08 chr3:150421568 T>C maps to NM_152394.3 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7654-01A-11D-2154-08 chr11:34162109 G>A maps to NM_024662.2 A861A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7654-01A-11D-2154-08 chr3:138762802 A>G maps to NM_001134657.1 H220H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7654-01A-11D-2154-08 chr8:99101494 C>T maps to NM_173549.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7654-01A-11D-2154-08 chr19:57868931 G>A maps to ENST00000391705 G612G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7654-01A-11D-2154-08 chr19:8160956 G>A maps to NM_032447.3 D1849D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7654-01A-11D-2154-08 chr12:347141 G>T maps to NM_016615.3 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7654-01A-11D-2154-08 chr4:144826670 C>T did not map to a codon.
Sequencing variant TCGA-IB-7654-01A-11D-2154-08 chr17:39776924 C>T maps to NM_000422.2 E389E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7654-01A-11D-2154-08 chr19:49564657 G>A maps to NM_006179.4 C199C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7654-01A-11D-2154-08 chr19:57765431 A>G maps to NM_001023563.3 K415K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7654-01A-11D-2154-08 chr1:43826617 C>T maps to NM_001255.2 Q355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7654-01A-11D-2154-08 chr7:16298588 G>A maps to NM_001101426.3 Q328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7654-01A-11D-2154-08 chr7:143657410 G>A maps to NM_012369.2 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7885-01A-11D-2154-08 chr19:55247490 C>T maps to NM_153443.3 C387C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7885-01A-11D-2154-08 chr5:176025335 C>T maps to NM_052899.2 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7885-01A-11D-2154-08 chr1:159273850 T>A maps to ENST00000368115 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7885-01A-11D-2154-08 chr11:113126680 C>T maps to ENST00000316851 D636D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7885-01A-11D-2154-08 chr8:21985132 C>T maps to NM_005144.4 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7885-01A-11D-2154-08 chr11:76918416 A>G maps to NM_000260.3 G1942G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7885-01A-11D-2154-08 chr15:89386781 C>T maps to NM_013227.3 C318C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7885-01A-11D-2154-08 chr20:62292775 G>A maps to ENST00000482936 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7885-01A-11D-2154-08 chr5:140763116 C>T maps to NM_018920.2 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7885-01A-11D-2154-08 chr5:180475167 C>T maps to NM_152547.4 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7885-01A-11D-2154-08 chr2:48873883 C>T maps to NM_172311.2 I931I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7885-01A-11D-2154-08 chr11:10645394 G>T maps to NM_001098579.1 I450I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7885-01A-11D-2154-08 chr9:35699040 C>T maps to NM_006289.3 R2329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7885-01A-11D-2154-08 chr14:51288699 T>G maps to NM_020921.3 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7885-01A-11D-2154-08 chr1:52249969 C>T maps to ENST00000428468 Y553Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7885-01A-11D-2154-08 chr9:79325845 G>A maps to NM_015225.2 D448D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7885-01A-11D-2154-08 chr17:79673937 G>A maps to NM_002949.3 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7885-01A-11D-2154-08 chr11:94862205 G>A maps to NM_015036.2 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7885-01A-11D-2154-08 chr6:128134639 G>A maps to NM_001164685.1 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7885-01A-11D-2154-08 chr22:21213613 G>A maps to NM_004782.3 K72K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7885-01A-11D-2154-08 chr7:102996159 T>C maps to NM_002803.2 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7885-01A-11D-2154-08 chr2:130921949 G>C maps to NM_017951.4 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7885-01A-11D-2154-08 chr7:43447239 A>G maps to NM_015052.3 K237K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7886-01A-11D-2154-08 chr1:176759113 G>C did not map to a codon.
Sequencing variant TCGA-IB-7886-01A-11D-2154-08 chr5:139918628 A>G maps to ENST00000253810 K2527K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7886-01A-11D-2154-08 chr2:179368598 A>T maps to NM_019091.3 P296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7886-01A-11D-2154-08 chr2:179537143 G>A maps to NM_133378.4 P10339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7886-01A-11D-2154-08 chr11:129735830 C>T maps to NM_006165.3 Q1218Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7886-01A-11D-2154-08 chr7:87195526 A>G maps to NM_000927.3 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7886-01A-11D-2154-08 chr5:162901192 A>T maps to NM_001142556.1 S345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7886-01A-11D-2154-08 chr19:42797189 C>A maps to NM_015125.3 I1184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7886-01A-11D-2154-08 chr19:11242043 G>A did not map to a codon.
Sequencing variant TCGA-IB-7886-01A-11D-2154-08 chr16:31200484 C>T maps to NM_004960.3 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7886-01A-11D-2154-08 chr5:89971102 C>T maps to NM_032119.3 D1718D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7886-01A-11D-2154-08 chr5:39383070 C>T maps to NM_001343.2 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7886-01A-11D-2154-08 chr14:99640769 G>A maps to NM_138576.2 C801C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7886-01A-11D-2154-08 chr7:90356125 G>C maps to NM_012395.2 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7886-01A-11D-2154-08 chr4:49019291 T>C maps to NM_025087.2 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7886-01A-11D-2154-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7886-01A-11D-2154-08 chr16:19883255 C>T maps to NM_016235.1 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7887-01A-11D-2154-08 chr1:158390038 G>A maps to NM_001004476.1 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7887-01A-11D-2154-08 chrX:130408063 G>A maps to NM_001170961.1 R1295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7887-01A-11D-2154-08 chr13:23906193 G>A maps to NM_014363.4 Q3941*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7887-01A-11D-2154-08 chr19:8130858 G>A maps to NM_032447.3 Q2792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7887-01A-11D-2154-08 chr8:62212793 C>T maps to NM_173519.2 Y136Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7887-01A-11D-2154-08 chr11:6662160 A>C maps to NM_003737.2 Y228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7887-01A-11D-2154-08 chr19:54691117 G>A maps to NM_024298.3 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7887-01A-11D-2154-08 chr7:42004926 G>A maps to NM_000168.5 P1248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7887-01A-11D-2154-08 chr19:17760371 G>A maps to ENST00000428389 I576I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7887-01A-11D-2154-08 chr16:70726806 G>A maps to NM_018052.3 L701L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7888-01A-11D-2154-08 chr19:36398351 C>T maps to NM_003332.3 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7888-01A-11D-2154-08 chr4:55956203 C>T maps to NM_002253.2 S1037S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7888-01A-11D-2154-08 chr6:133138133 C>G maps to NM_001016.3 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7888-01A-11D-2154-08 chr12:57111377 A>G maps to NM_001113203.1 P1312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7888-01A-11D-2154-08 chr17:39883348 C>T maps to ENST00000310778 T493T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7888-01A-11D-2154-08 chr8:27288475 C>T maps to NM_004103.3 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7888-01A-11D-2154-08 chr7:123270138 A>G maps to NM_080928.3 V520V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7888-01A-11D-2154-08 chr3:54798356 C>T maps to NM_018398.2 T453T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7888-01A-11D-2154-08 chr14:23828663 T>G maps to NM_005864.2 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7888-01A-11D-2154-08 chrX:14708829 A>T did not map to a codon.
Sequencing variant TCGA-IB-7888-01A-11D-2154-08 chr11:62519603 C>T maps to NM_024784.3 G561G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7888-01A-11D-2154-08 chr12:12629994 G>A maps to NM_030640.2 C590C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7888-01A-11D-2154-08 chr11:55927157 C>T maps to NM_001004058.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7888-01A-11D-2154-08 chr10:106207499 C>T maps to NM_001008723.1 R767R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7888-01A-11D-2154-08 chr5:177419754 A>G maps to NM_006261.4 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7888-01A-11D-2154-08 chr6:108214764 A>T maps to NM_007214.4 L532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7888-01A-11D-2154-08 chr19:19655204 G>A maps to NM_153221.2 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7888-01A-11D-2154-08 chr1:240371087 T>A maps to ENST00000406993 L1135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7888-01A-11D-2154-08 chr5:140209349 G>A maps to NM_018909.2 E558E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7888-01A-11D-2154-08 chr17:1386152 A>C did not map to a codon.
Sequencing variant TCGA-IB-7888-01A-11D-2154-08 chr17:7578274 G>A maps to NM_001126112.1 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7888-01A-11D-2154-08 chr16:1306310 C>T maps to NM_012217.2 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7888-01A-11D-2154-08 chr9:328113 G>A maps to NM_203447.3 A329A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-IB-7888-01A-11D-2154-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-IB-7888-01A-11D-2154-08 chr7:154862764 G>A maps to NM_024012.2 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7888-01A-11D-2154-08 chrX:48209005 G>A maps to NM_175711.1 Y161Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7888-01A-11D-2154-08 chr3:125648196 A>G maps to NM_001195223.1 *208R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7888-01A-11D-2154-08 chr11:45671351 G>A maps to NM_003654.4 N374N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7888-01A-11D-2154-08 chr1:152327756 C>T maps to NM_001014342.2 Q835Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7888-01A-11D-2154-08 chr6:7229367 G>T maps to NM_001003699.3 E346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7888-01A-11D-2154-08 chr17:7680921 G>A maps to NM_020877.2 W1739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7888-01A-11D-2154-08 chr1:144815945 C>T maps to NM_001037675.2 N438N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7888-01A-11D-2154-08 chrX:152845617 G>C maps to NM_001001344.2 P1175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7888-01A-11D-2154-08 chr1:149783725 G>A maps to ENST00000427880 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7888-01A-11D-2154-08 chr9:20414312 G>A maps to NM_004529.2 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7888-01A-11D-2154-08 chrX:48209017 G>C maps to NM_175711.1 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7888-01A-11D-2154-08 chr9:131295933 G>T maps to NM_001003722.1 V485V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7888-01A-11D-2154-08 chr15:55838322 T>C maps to NM_015617.1 A386A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7888-01A-11D-2154-08 chr4:164050123 T>G maps to NM_138386.2 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7888-01A-11D-2154-08 chr11:57982248 C>T maps to NM_001004458.1 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7888-01A-11D-2154-08 chr3:195515979 G>T maps to NM_018406.5 S824*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7888-01A-11D-2154-08 chr19:41633863 C>T maps to NM_000774.3 T451T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7888-01A-11D-2154-08 chr19:42873052 C>T maps to ENST00000251268 D2180D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7889-01A-11D-2154-08 chr17:7577045 C>A maps to NM_001126112.1 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7889-01A-11D-2154-08 chr2:136564939 G>A maps to NM_002299.2 R1311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7889-01A-11D-2154-08 chr16:58010413 G>A maps to NM_199046.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7889-01A-11D-2154-08 chr19:9071236 C>T maps to NM_024690.2 P5403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7889-01A-11D-2154-08 chr1:155880295 G>T maps to ENST00000368322 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7889-01A-11D-2154-08 chr9:131477727 C>T maps to NM_013355.3 D599D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7889-01A-11D-2154-08 chr17:29576088 C>T maps to NM_001042492.2 S1354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7889-01A-11D-2154-08 chr19:48919317 C>T maps to NM_000836.2 S547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7889-01A-11D-2154-08 chr15:42276760 G>A maps to NM_001080490.1 Y724Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7889-01A-11D-2154-08 chr22:25023842 G>A maps to NM_005265.2 P411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7889-01A-11D-2154-08 chr21:22656720 G>A did not map to a codon.
Sequencing variant TCGA-IB-7889-01A-11D-2154-08 chr17:65850549 C>T maps to ENST00000321892 Q370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7889-01A-11D-2154-08 chr4:139966042 C>T maps to NM_012118.2 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7889-01A-11D-2154-08 chr17:18003680 C>T maps to NM_001388.3 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7889-01A-11D-2154-08 chr15:85461804 C>T maps to NM_004213.3 H282H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7889-01A-11D-2154-08 chr2:7160799 C>G maps to NM_014746.3 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7889-01A-11D-2154-08 chr15:92981636 A>G maps to NM_006011.3 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7889-01A-11D-2154-08 chr3:50405101 G>A maps to ENST00000435965 D763D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7889-01A-11D-2154-08 chr7:123599603 C>T maps to NM_001174046.1 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7889-01A-11D-2154-08 chr7:720279 C>T maps to NM_002735.2 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7889-01A-11D-2154-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7889-01A-11D-2154-08 chr12:57389415 C>T maps to NM_007264.3 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7889-01A-11D-2154-08 chr7:33407474 G>A did not map to a codon.
Sequencing variant TCGA-IB-7890-01A-12D-2201-08 chr1:240370124 A>G maps to ENST00000406993 G814G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7890-01A-12D-2201-08 chr16:57790797 G>A maps to NM_005886.2 L636L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7890-01A-12D-2201-08 chr12:110390956 G>A maps to NM_057169.3 S394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7890-01A-12D-2201-08 chr19:5210703 G>T maps to NM_002850.3 R1783R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7890-01A-12D-2201-08 chr10:99350209 C>A maps to NM_001009997.2 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7890-01A-12D-2201-08 chr2:185801328 A>G maps to NM_194250.1 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7890-01A-12D-2201-08 chr17:7578253 C>A maps to NM_001126112.1 G199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7890-01A-12D-2201-08 chr17:7106622 G>A maps to NM_001365.3 G220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7890-01A-12D-2201-08 chr6:24146059 C>T maps to NM_080723.4 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7890-01A-12D-2201-08 chr2:73675915 T>C maps to NM_015120.4 T753T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7890-01A-12D-2201-08 chr19:9090830 A>G maps to NM_024690.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7890-01A-12D-2201-08 chrX:112058795 C>T maps to NM_001113490.1 Q394Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7890-01A-12D-2201-08 chr13:101289836 G>A maps to NM_032813.2 T318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7890-01A-12D-2201-08 chr8:144808659 G>A maps to NM_198488.3 Q991*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7890-01A-12D-2201-08 chr17:48435626 G>A maps to NM_022167.2 G667G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7890-01A-12D-2201-08 chr19:36053402 G>A maps to NM_000704.2 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7890-01A-12D-2201-08 chr17:16285490 C>T maps to NM_018955.2 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7890-01A-12D-2201-08 chr11:63472338 C>T maps to ENST00000377819 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7890-01A-12D-2201-08 chr1:120056676 C>T maps to ENST00000235547 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7890-01A-12D-2201-08 chr18:5415858 G>A maps to NM_012307.2 S675S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7890-01A-12D-2201-08 chr19:547331 G>A maps to NM_005317.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7890-01A-12D-2201-08 chr20:57769547 G>A maps to NM_178457.1 T1158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7890-01A-12D-2201-08 chr5:89977222 T>C maps to NM_032119.3 F1872F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7890-01A-12D-2201-08 chr17:43174522 C>A maps to NM_021079.3 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7890-01A-12D-2201-08 chr6:10882007 G>A maps to NM_004752.3 Q7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7890-01A-12D-2201-08 chr2:96933170 C>T maps to NM_004804.2 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7891-01A-11D-2201-08 chr2:202131314 G>T maps to NM_001080125.1 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7891-01A-11D-2201-08 chr7:4185417 C>T maps to NM_152744.3 G1431G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7891-01A-11D-2201-08 chr12:13717015 G>A maps to NM_000834.3 H1052H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7891-01A-11D-2201-08 chr5:140431927 G>A maps to NM_013340.2 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7891-01A-11D-2201-08 chr9:79319817 G>A maps to NM_015225.2 L2458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7891-01A-11D-2201-08 chrX:18797153 G>A maps to NM_006240.2 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7891-01A-11D-2201-08 chr6:40399610 G>A maps to NM_020737.1 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7891-01A-11D-2201-08 chr2:176959380 C>T maps to NM_000523.3 Q319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7891-01A-11D-2201-08 chr1:29630478 G>A maps to NM_005704.4 A873A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7891-01A-11D-2201-08 chr19:9090830 A>G maps to NM_024690.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7891-01A-11D-2201-08 chrX:112058795 C>T maps to NM_001113490.1 Q394Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7891-01A-11D-2201-08 chr9:135946985 G>C maps to NM_001807.3 G702G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7891-01A-11D-2201-08 chr15:101593293 G>T did not map to a codon.
Sequencing variant TCGA-IB-7891-01A-11D-2201-08 chr5:180622633 G>T maps to NM_203293.1 I356I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7891-01A-11D-2201-08 chr3:129695839 G>A maps to NM_007117.3 E170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7891-01A-11D-2201-08 chr5:167881062 C>T maps to NM_001161661.1 T872T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7891-01A-11D-2201-08 chr12:62715326 C>T maps to ENST00000280377 N186N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7891-01A-11D-2201-08 chr1:214556938 G>A maps to NM_005401.4 P753P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7891-01A-11D-2201-08 chr17:36486064 C>T maps to ENST00000398597 S1130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7891-01A-11D-2201-08 chr6:152763320 C>T maps to NM_182961.2 A1299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7891-01A-11D-2201-08 chr12:20903756 T>C maps to NM_001145946.1 H649H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7891-01A-11D-2201-08 chr17:48151551 C>T maps to NM_002204.2 F430F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7893-01A-11D-2201-08 chr20:1592048 G>A maps to NM_001135844.1 D129D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7893-01A-11D-2201-08 chr11:10518391 C>T maps to NM_000480.2 N497N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7893-01A-11D-2201-08 chr3:127387408 G>A maps to NM_015720.2 Q444Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7893-01A-11D-2201-08 chr14:99968672 G>A maps to ENST00000437596 W235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7893-01A-11D-2201-08 chr22:25023538 C>G maps to NM_005265.2 V387V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7893-01A-11D-2201-08 chr6:150164251 T>C maps to NM_032832.5 Q260Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7893-01A-11D-2201-08 chr9:130207139 A>G maps to NM_007135.2 K387K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7893-01A-11D-2201-08 chr16:4920916 A>G maps to NM_016936.3 K501K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7893-01A-11D-2201-08 chr16:70500120 C>A maps to NM_145059.2 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7893-01A-11D-2201-08 chr14:105609112 C>A maps to NM_002226.3 P1212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7893-01A-11D-2201-08 chr1:70486727 G>A maps to NM_020794.2 W449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7893-01A-11D-2201-08 chr1:1447652 C>A maps to NM_018188.3 S2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7893-01A-11D-2201-08 chr2:219545332 C>A maps to NM_015690.3 R382R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7893-01A-11D-2201-08 chr11:47684619 T>A maps to ENST00000357610 S833S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7893-01A-11D-2201-08 chr2:108917366 G>A maps to ENST00000437390 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7893-01A-11D-2201-08 chr20:33345722 C>T maps to NM_014071.2 Q276Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7893-01A-11D-2201-08 chr19:879934 A>G did not map to a codon.
Sequencing variant TCGA-IB-7893-01A-11D-2201-08 chr6:36368245 A>G maps to NM_152990.3 H95H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7893-01A-11D-2201-08 chr19:21606441 C>T maps to NM_001076678.2 G327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7893-01A-11D-2201-08 chr7:6465642 G>A maps to NM_139179.3 F344F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7893-01A-11D-2201-08 chr10:118315572 C>T maps to NM_000936.2 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7893-01A-11D-2201-08 chr7:44146352 A>G maps to NM_001129.3 K154K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7893-01A-11D-2201-08 chr14:105639420 G>A maps to NM_177533.3 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7893-01A-11D-2201-08 chr19:19016395 C>A maps to NM_007263.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7897-01A-21D-2201-08 chr21:43796647 A>T did not map to a codon.
Sequencing variant TCGA-IB-7897-01A-21D-2201-08 chr11:8123099 G>A maps to NM_003320.4 P540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7897-01A-21D-2201-08 chr19:33699841 T>G maps to NM_019849.2 P509P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7897-01A-21D-2201-08 chr6:32917502 G>A maps to NM_006120.3 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7897-01A-21D-2201-08 chr13:101755618 G>A maps to NM_052867.2 V987V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7897-01A-21D-2201-08 chr15:55731754 G>A maps to NM_130810.2 R270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7897-01A-21D-2201-08 chr19:57955949 T>C maps to NM_001023561.2 I478I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7897-01A-21D-2201-08 chr19:4793863 C>A maps to NM_018708.2 I666I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7897-01A-21D-2201-08 chr9:125148755 C>T maps to NM_000962.2 Y347Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7897-01A-21D-2201-08 chr2:220162726 C>A maps to NM_002846.3 G589G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7897-01A-21D-2201-08 chr2:29295747 C>T maps to NM_001029883.1 G460G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7897-01A-21D-2201-08 chr5:60241049 G>A did not map to a codon.
Sequencing variant TCGA-IB-7897-01A-21D-2201-08 chr7:114298279 C>T maps to NM_148898.3 R501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7897-01A-21D-2201-08 chr21:45877294 G>T maps to NM_030891.3 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7897-01A-21D-2201-08 chr5:37044450 G>T maps to NM_133433.3 T2037T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7897-01A-21D-2201-08 chr19:40398009 G>A maps to NM_003890.2 A2319A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7897-01A-21D-2201-08 chr3:50005373 A>T maps to NM_005777.2 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7897-01A-21D-2201-08 chrX:151935608 G>A maps to NM_005362.3 Y186Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7897-01A-21D-2201-08 chr8:105502936 G>A maps to NM_013437.4 N848N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7897-01A-21D-2201-08 chr16:87790045 C>A maps to NM_017566.3 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7897-01A-21D-2201-08 chr1:28807087 C>A maps to NM_023923.3 R588R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7897-01A-21D-2201-08 chr11:64005047 A>C maps to NM_003377.3 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7897-01A-21D-2201-08 chr12:6686949 C>T did not map to a codon.
Sequencing variant TCGA-IB-7897-01A-21D-2201-08 chr1:207787830 G>T maps to NM_000651.4 E2220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7897-01A-21D-2201-08 chr17:38928254 C>T maps to NM_181539.4 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7897-01A-21D-2201-08 chr6:30892255 C>G maps to NM_001167734.1 L894L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8126-01A-11D-2396-08 chr2:224758989 G>A maps to NM_020830.3 G264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8126-01A-11D-2396-08 chr11:72422095 G>A maps to NM_001040118.2 R395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8126-01A-11D-2396-08 chr3:24231772 G>A maps to NM_001128177.1 H25H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8126-01A-11D-2396-08 chr4:77661902 C>G maps to NM_020859.3 S859S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8126-01A-11D-2396-08 chr16:28331734 G>A maps to NM_001024401.2 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8126-01A-11D-2396-08 chr22:28194182 A>C maps to NM_002430.2 G783G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8126-01A-11D-2396-08 chr7:114269972 A>G maps to NM_148898.3 Q195Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8126-01A-11D-2396-08 chr12:8211545 A>C maps to NM_004054.2 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8126-01A-11D-2396-08 chr1:186277097 C>T maps to NM_005807.3 P749P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8126-01A-11D-2396-08 chr12:104327987 C>A maps to NM_003299.1 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8126-01A-11D-2396-08 chr10:50827782 C>T maps to NM_020549.4 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8126-01A-11D-2396-08 chr22:29695793 G>A maps to NM_013986.3 Q633Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8126-01A-11D-2396-08 chr1:185931764 C>T maps to NM_031935.2 N648N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8126-01A-11D-2396-08 chr19:53644385 T>A maps to NM_001172674.1 G566G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8126-01A-11D-2396-08 chr11:55587726 G>T maps to ENST00000395203 E210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8126-01A-11D-2396-08 chr4:140811107 C>T maps to ENST00000509479 Q494Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8126-01A-11D-2396-08 chr1:186276026 T>C maps to NM_005807.3 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8126-01A-11D-2396-08 chr3:169539978 G>T maps to NM_001080460.1 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8126-01A-11D-2396-08 chr17:27613832 T>C maps to NM_020772.2 Q393Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8126-01A-11D-2396-08 chr11:1606185 A>G maps to NM_001005922.1 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8126-01A-11D-2396-08 chr19:53855283 G>A maps to NM_138374.1 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8126-01A-11D-2396-08 chr19:36278841 A>C maps to ENST00000007510 S1125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8126-01A-11D-2396-08 chr11:9225318 A>G maps to NM_015213.2 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8126-01A-11D-2396-08 chr4:106157129 T>A maps to ENST00000513237 C698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8126-01A-11D-2396-08 chrX:49957302 A>G maps to NM_003886.2 S687S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8126-01A-11D-2396-08 chr7:55872989 G>A maps to NM_207366.2 V360V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8126-01A-11D-2396-08 chr1:7796574 C>T maps to NM_015215.2 L1080L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8126-01A-11D-2396-08 chr7:144380018 G>T maps to NM_022445.3 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8126-01A-11D-2396-08 chr1:175086324 C>T maps to NM_022093.1 D790D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr5:140783646 C>T maps to NM_018921.2 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr5:160721243 C>T maps to NM_021911.2 A461A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr2:166911146 C>T did not map to a codon.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr2:71036947 G>A maps to NM_173535.2 I527I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr19:54754888 T>C maps to ENST00000450632 R582R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr3:15731727 C>T did not map to a codon.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr9:96080242 G>A maps to ENST00000297954 P2276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr1:31899618 C>T maps to NM_178865.4 N243N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr9:21971095 C>A maps to NM_001195132.1 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr7:113518726 A>C maps to NM_002711.3 L807*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr12:57112307 A>G maps to NM_001113203.1 T1002T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr1:1374491 G>A maps to NM_022834.4 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr4:145038027 G>A maps to NM_002099.6 Y112Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr6:401643 C>T maps to NM_002460.3 D322D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr13:66879139 C>A maps to NM_203487.2 G1121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr19:55086975 C>T maps to NM_001130917.1 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr16:67876807 G>A maps to NM_020457.2 Q117Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr1:186276662 T>C maps to NM_005807.3 T604T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr2:141457899 G>A maps to NM_018557.2 R2240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr5:179044052 G>A maps to NM_005520.2 Y372Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr22:25011026 C>T maps to NM_005265.2 N105N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr9:131584645 C>A maps to NM_004435.2 V217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr1:147131791 G>A maps to NM_016361.3 Y106Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr14:103915253 A>T did not map to a codon.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr2:71740933 T>C maps to NM_001130987.1 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr5:140712338 G>A maps to NM_018912.2 A696A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr1:1961125 C>T maps to NM_000815.4 Y328Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr14:80328015 G>A maps to NM_004796.4 T965T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr9:139739951 C>T maps to NM_001080482.2 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr19:53644385 T>A maps to NM_001172674.1 G566G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr17:39389178 C>A maps to NM_031962.2 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr3:38627421 G>A maps to NM_001099404.1 I849I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr19:20026132 G>A maps to NM_031218.3 E16E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr19:42480633 G>A maps to ENST00000441343 T676T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr9:27949235 G>A maps to NM_152570.1 S478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr12:54379387 C>T maps to NM_017409.3 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr4:90872775 C>A maps to NM_007351.2 R1047R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr17:8656710 G>A maps to NM_001128076.1 F194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr11:123908880 G>A maps to NM_001004463.1 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr7:71252798 C>T maps to NM_031468.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr9:132640645 G>A maps to NM_001008563.3 S813S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr1:22925389 C>T maps to NM_020526.3 A746A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr5:825359 T>C maps to NM_024786.2 K314K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr4:164050123 T>G maps to NM_138386.2 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr16:19621688 G>A maps to NM_020314.5 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr3:174815005 C>A maps to NM_207015.2 S157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr16:67876777 A>G maps to NM_020457.2 Q107Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr4:149075975 T>G maps to ENST00000511528 P701P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SO-01A-11D-A32N-08 chr20:62729804 C>A maps to NM_000913.3 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SO-01A-11D-A32N-08 chr2:201724928 G>T maps to NM_001162407.1 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SO-01A-11D-A32N-08 chr17:74309082 G>A maps to NM_002766.2 D289D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SO-01A-11D-A32N-08 chr16:1814145 C>A maps to NM_015133.3 R685R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SO-01A-11D-A32N-08 chr3:30715707 G>T maps to NM_001024847.2 E481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SO-01A-11D-A32N-08 chr2:25505559 T>C maps to NM_175629.1 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SO-01A-11D-A32N-08 chr5:156590198 C>T maps to NM_130899.2 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SO-01A-11D-A32N-08 chr2:219735844 G>A maps to NM_006522.3 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SO-01A-11D-A32N-08 chr5:35954468 C>T maps to NM_152404.3 T469T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SO-01A-11D-A32N-08 chr14:33015217 C>T maps to NM_004274.4 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SO-01A-11D-A32N-08 chr6:132649631 G>A maps to NM_015529.2 H255H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SO-01A-11D-A32N-08 chr15:48063189 G>A maps to NM_153618.1 P810P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SO-01A-11D-A32N-08 chr6:45390462 G>A maps to ENST00000359524 Q132Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SO-01A-11D-A32N-08 chr6:45390465 A>G maps to ENST00000359524 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SO-01A-11D-A32N-08 chr11:722405 C>T maps to NM_022772.3 V355V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SO-01A-11D-A32N-08 chr4:7716915 C>T maps to NM_020777.2 Y710Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SO-01A-11D-A32N-08 chr4:164050410 G>A maps to NM_138386.2 R375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SO-01A-11D-A32N-08 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SO-01A-11D-A32N-08 chr17:16285559 T>C maps to NM_018955.2 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SO-01A-11D-A32N-08 chr3:100365496 C>T maps to NM_032787.2 Q399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SO-01A-11D-A32N-08 chr6:152457815 G>A maps to NM_182961.2 D8532D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SO-01A-11D-A32N-08 chr1:152327954 G>A maps to NM_001014342.2 S769S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SO-01A-11D-A32N-08 chr22:19707653 G>A maps to NM_002688.5 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SO-01A-11D-A32N-08 chr17:80828121 G>A maps to NM_005993.4 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SO-01A-11D-A32N-08 chr1:153907308 C>T maps to NM_014856.2 Q900Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SO-01A-11D-A32N-08 chr10:3143179 G>A maps to ENST00000381075 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SO-01A-11D-A32N-08 chr9:139908434 G>A maps to ENST00000355090 G1462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SO-01A-11D-A32N-08 chr21:38269179 T>C maps to NM_000411.5 T477T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SO-01A-11D-A32N-08 chr12:125397651 T>C maps to NM_021009.5 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SO-01A-11D-A32N-08 chr18:2937702 C>T maps to NM_014646.2 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SO-01A-11D-A32N-08 chr10:102748966 C>T maps to NM_021830.4 R334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SP-01A-11D-A32N-08 chr12:3126692 G>A did not map to a codon.
Sequencing variant TCGA-IB-A5SP-01A-11D-A32N-08 chr13:114773064 C>T maps to ENST00000389544 S569S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SP-01A-11D-A32N-08 chr1:186276473 T>C maps to NM_005807.3 T541T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SP-01A-11D-A32N-08 chr16:5053462 G>A maps to NM_014692.1 G397G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SP-01A-11D-A32N-08 chr11:19077763 G>A maps to NM_054030.2 N62N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SP-01A-11D-A32N-08 chr5:140553993 G>T maps to NM_018940.2 A526A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SP-01A-11D-A32N-08 chr20:1902131 A>T maps to ENST00000400068 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SP-01A-11D-A32N-08 chr12:44782361 C>T maps to NM_032256.1 T484T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SP-01A-11D-A32N-08 chr1:25687171 C>T maps to NM_014313.2 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SP-01A-11D-A32N-08 chr3:195965645 G>A maps to NM_005017.2 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SP-01A-11D-A32N-08 chr12:123472783 C>A maps to NM_020845.2 L998L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SP-01A-11D-A32N-08 chr2:237103688 C>T maps to NM_212556.2 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SP-01A-11D-A32N-08 chr12:124428831 C>T maps to NM_025140.1 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SP-01A-11D-A32N-08 chr1:243456472 C>T maps to NM_006642.3 D209D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SP-01A-11D-A32N-08 chr11:82645016 A>C maps to NM_145018.3 G879G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SP-01A-11D-A32N-08 chr1:215933090 T>C maps to ENST00000366943 Q3714Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SP-01A-11D-A32N-08 chr10:88704019 G>A maps to NM_024756.2 H218H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SP-01A-11D-A32N-08 chr19:9090830 A>G maps to NM_024690.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SP-01A-11D-A32N-08 chr9:79118079 C>T maps to NM_001097636.1 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SP-01A-11D-A32N-08 chr17:72846359 G>A maps to NM_000835.3 N492N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SP-01A-11D-A32N-08 chr2:25387629 C>T maps to NM_001035256.1 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SP-01A-11D-A32N-08 chrX:34150173 G>A maps to NM_203408.3 D74D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SP-01A-11D-A32N-08 chr1:152327954 G>A maps to NM_001014342.2 S769S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SP-01A-11D-A32N-08 chr3:183027560 G>A maps to NM_015078.2 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SP-01A-11D-A32N-08 chr20:51871856 C>T maps to NM_173485.5 H620H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SP-01A-11D-A32N-08 chr16:14014214 C>T maps to NM_005236.2 Q65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SP-01A-11D-A32N-08 chr5:140166588 C>T maps to NM_018900.2 N238N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SP-01A-11D-A32N-08 chr22:26849246 G>A maps to NM_022081.4 S693S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SP-01A-11D-A32N-08 chr1:153907308 C>T maps to NM_014856.2 Q900Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SP-01A-11D-A32N-08 chr1:152128185 A>G maps to NM_001122965.1 Y463Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SP-01A-11D-A32N-08 chr16:27448835 C>T maps to NM_181079.4 D82D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SP-01A-11D-A32N-08 chr15:43827456 G>A maps to NM_001130858.2 S1239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SP-01A-11D-A32N-08 chr1:27687468 C>T maps to NM_004672.3 T621T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SP-01A-11D-A32N-08 chr11:45307686 G>A maps to NM_020826.2 C24C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SP-01A-11D-A32N-08 chr18:21512192 G>A maps to ENST00000416669 R2884R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SP-01A-11D-A32N-08 chr7:18668997 G>A maps to NM_178425.2 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SQ-01A-11D-A32N-08 chr11:110108326 G>A maps to ENST00000405097 R381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SQ-01A-11D-A32N-08 chr1:145325996 A>G maps to NM_001039703.4 Q1290Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SQ-01A-11D-A32N-08 chr12:89745478 G>T maps to NM_001946.2 S113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SQ-01A-11D-A32N-08 chr5:176562808 A>G maps to NM_022455.4 T235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SQ-01A-11D-A32N-08 chr3:121097632 C>T maps to NM_014980.2 A773A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SQ-01A-11D-A32N-08 chr15:77907603 G>A maps to NM_032808.5 H215H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SQ-01A-11D-A32N-08 chr11:85468695 G>A maps to NM_001162953.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SQ-01A-11D-A32N-08 chr7:148511206 G>A maps to NM_004456.3 C565C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SQ-01A-11D-A32N-08 chr12:6933843 G>A maps to NM_019858.1 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SQ-01A-11D-A32N-08 chr22:39222606 G>A maps to NM_014293.2 T332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SQ-01A-11D-A32N-08 chr14:24885052 C>T maps to NM_025081.2 G1366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SQ-01A-11D-A32N-08 chr4:17488810 G>A maps to NM_000320.2 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SQ-01A-11D-A32N-08 chr19:14581659 C>T maps to NM_213560.1 F880F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SQ-01A-11D-A32N-08 chr21:15882756 A>G maps to ENST00000285670 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SQ-01A-11D-A32N-08 chr8:88885062 T>C maps to NM_152418.3 P379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SQ-01A-11D-A32N-08 chr6:44144380 C>T maps to NM_007058.3 D355D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SQ-01A-11D-A32N-08 chrX:54957326 G>A maps to NM_001039705.1 P1390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SQ-01A-11D-A32N-08 chr3:13377061 G>A maps to NM_024923.2 G1245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SQ-01A-11D-A32N-08 chr6:136589448 G>A maps to NM_014739.2 R750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SQ-01A-11D-A32N-08 chr21:41496169 G>A maps to NM_001389.3 N1216N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SS-01A-11D-A32N-08 chr14:24114077 C>A maps to NM_182908.4 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SS-01A-11D-A32N-08 chr5:141243879 G>A maps to NM_032420.2 S672S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SS-01A-11D-A32N-08 chr9:21971185 G>A maps to NM_001195132.1 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SS-01A-11D-A32N-08 chr3:74351866 G>T maps to NM_020872.1 S587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SS-01A-11D-A32N-08 chr1:152382519 G>A maps to NM_016190.2 H346H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SS-01A-11D-A32N-08 chr5:179538478 G>A maps to NM_175062.3 T427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SS-01A-11D-A32N-08 chr6:43039978 C>A maps to NM_201523.1 R510R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SS-01A-11D-A32N-08 chr3:30875344 A>T maps to NM_207359.2 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SS-01A-11D-A32N-08 chr5:33984520 C>G maps to NM_016180.3 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SS-01A-11D-A32N-08 chr17:40832278 G>C maps to NM_016602.2 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SS-01A-11D-A32N-08 chr1:248685732 G>A maps to NM_001013355.1 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SS-01A-11D-A32N-08 chr9:138557548 C>T maps to ENST00000277526 C156C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SS-01A-11D-A32N-08 chr1:154705583 C>A maps to NM_002249.4 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SS-01A-11D-A32N-08 chr7:21657265 C>A maps to NM_003777.3 R1380R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SS-01A-11D-A32N-08 chr10:100155146 C>A did not map to a codon.
Sequencing variant TCGA-IB-A5SS-01A-11D-A32N-08 chr1:204588727 C>T maps to NM_201630.1 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SS-01A-11D-A32N-08 chr8:13947957 C>T maps to NM_139167.2 W311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SS-01A-11D-A32N-08 chrX:10427779 G>A maps to NM_001193277.1 H451H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5ST-01A-11D-A32N-08 chr6:63990011 G>A maps to NM_016571.2 R482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5ST-01A-11D-A32N-08 chr4:25674739 G>A maps to NM_006424.2 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5ST-01A-11D-A32N-08 chr14:31827865 G>A maps to ENST00000389961 C790C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5ST-01A-11D-A32N-08 chr17:21204187 G>A maps to NM_145109.2 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5ST-01A-11D-A32N-08 chr9:136310875 G>A maps to NM_139025.3 T889T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5ST-01A-11D-A32N-08 chr10:124273730 C>A maps to NM_002775.4 V433V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5ST-01A-11D-A32N-08 chr8:2823354 G>A maps to NM_033225.5 S3074S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5ST-01A-11D-A32N-08 chr10:7679230 C>T maps to ENST00000256861 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5ST-01A-11D-A32N-08 chr1:94543308 G>A maps to NM_000350.2 F497F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5ST-01A-11D-A32N-08 chr1:29630478 G>A maps to NM_005704.4 A873A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5ST-01A-11D-A32N-08 chr11:55541692 T>C maps to NM_001001967.1 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5ST-01A-11D-A32N-08 chr17:21204217 G>A maps to NM_145109.2 Q104Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5ST-01A-11D-A32N-08 chr5:9629466 C>T maps to NM_019599.2 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5ST-01A-11D-A32N-08 chr5:147019205 G>A maps to NM_014790.3 R507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5ST-01A-11D-A32N-08 chr21:31852477 G>A maps to NM_181607.1 Y53Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5ST-01A-11D-A32N-08 chr11:111428362 A>G maps to ENST00000375615 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5ST-01A-11D-A32N-08 chr6:157528496 G>A maps to ENST00000367148 S2114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5ST-01A-11D-A32N-08 chr5:140553993 G>T maps to NM_018940.2 A526A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5ST-01A-11D-A32N-08 chr7:43484702 G>A maps to NM_015052.3 A644A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5ST-01A-11D-A32N-08 chr11:88911585 C>A maps to NM_000372.4 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5ST-01A-11D-A32N-08 chr17:7644310 G>A did not map to a codon.
Sequencing variant TCGA-IB-A6UF-01A-23D-A33T-08 chr13:19751420 G>A maps to NM_006001.1 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UF-01A-23D-A33T-08 chr10:12811798 G>A did not map to a codon.
Sequencing variant TCGA-IB-A6UF-01A-23D-A33T-08 chr10:104117902 G>T maps to NM_004193.2 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UF-01A-23D-A33T-08 chr20:46279832 G>A maps to NM_181659.2 Q1253Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UF-01A-23D-A33T-08 chr15:40659677 G>A maps to NM_033510.1 R455R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UF-01A-23D-A33T-08 chr19:20044612 A>G maps to NM_031218.3 K283K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UF-01A-23D-A33T-08 chr9:125486582 C>T maps to NM_001005235.1 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UF-01A-23D-A33T-08 chr5:37725120 G>A maps to NM_018034.2 S561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UF-01A-23D-A33T-08 chr7:137269963 G>A maps to NM_004717.2 G518G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UF-01A-23D-A33T-08 chr14:34269654 G>A maps to NM_001164749.1 S714S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UF-01A-23D-A33T-08 chr16:84600450 T>G maps to NM_021149.2 *143Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UF-01A-23D-A33T-08 chr16:18896964 A>T maps to ENST00000389467 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UF-01A-23D-A33T-08 chr10:98764502 G>C maps to NM_003061.2 G1219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UF-01A-23D-A33T-08 chr5:132098217 G>A maps to NM_001098811.1 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UF-01A-23D-A33T-08 chr1:204170870 C>T maps to NM_198447.1 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UF-01A-23D-A33T-08 chr21:28210356 G>A maps to NM_006988.3 S815S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UF-01A-23D-A33T-08 chr13:30002978 G>A did not map to a codon.
Sequencing variant TCGA-IB-A6UF-01A-23D-A33T-08 chr1:114308997 G>A maps to NM_018364.3 C671C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UF-01A-23D-A33T-08 chr1:11345758 G>A maps to NM_013319.2 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UF-01A-23D-A33T-08 chr1:45307636 G>A maps to NM_003738.4 C49C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UF-01A-23D-A33T-08 chr5:140730508 C>T maps to NM_018922.2 R228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UF-01A-23D-A33T-08 chr20:9546989 C>G maps to NM_177990.2 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UF-01A-23D-A33T-08 chrX:73960071 G>A maps to NM_001008537.2 N1440N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UF-01A-23D-A33T-08 chr9:37708408 C>T maps to NM_014907.2 H91H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UF-01A-23D-A33T-08 chr16:1812980 C>T maps to NM_015133.3 S623S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UF-01A-23D-A33T-08 chr12:56082735 G>A maps to ENST00000347027 C994C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UF-01A-23D-A33T-08 chr9:130145777 T>G maps to NM_032293.4 S741S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-IB-A6UF-01A-23D-A33T-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-IB-A6UF-01A-23D-A33T-08 chr20:50769917 G>A maps to NM_018197.2 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UF-01A-23D-A33T-08 chr22:25124283 G>A maps to NM_001008496.2 L598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UF-01A-23D-A33T-08 chr2:176981812 G>A maps to NM_002148.3 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UF-01A-23D-A33T-08 chr5:150930180 C>T maps to NM_001447.2 S1516S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UF-01A-23D-A33T-08 chr12:39735382 C>T maps to ENST00000395670 E615E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UF-01A-23D-A33T-08 chr1:226924703 C>T maps to NM_002221.3 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UF-01A-23D-A33T-08 chr6:32362626 G>A maps to ENST00000468270 H418H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UF-01A-23D-A33T-08 chr1:240371195 G>A maps to ENST00000406993 A1171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UF-01A-23D-A33T-08 chr16:3293587 C>T maps to NM_000243.2 P633P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UF-01A-23D-A33T-08 chr7:98997951 C>T maps to NM_014891.6 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UF-01A-23D-A33T-08 chr9:140671242 C>T maps to NM_024757.4 P655P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UF-01A-23D-A33T-08 chr4:186544638 A>G maps to ENST00000355634 H744H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UG-01A-32D-A33T-08 chr5:1083956 G>A maps to NM_006598.2 N344N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UG-01A-32D-A33T-08 chr5:140236910 G>A maps to NM_018901.2 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UG-01A-32D-A33T-08 chr6:39513397 C>T maps to NM_145027.4 A416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UG-01A-32D-A33T-08 chr11:6789726 C>A maps to NM_001004490.1 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UG-01A-32D-A33T-08 chr5:153174276 C>T maps to NM_000827.3 S789S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UG-01A-32D-A33T-08 chr19:50548806 C>T maps to NM_015428.1 H369H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UG-01A-32D-A33T-08 chr2:241679771 C>T maps to ENST00000373308 P1253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UG-01A-32D-A33T-08 chr11:20968880 G>T did not map to a codon.
Sequencing variant TCGA-IB-A6UG-01A-32D-A33T-08 chr1:154543679 C>T maps to NM_000748.2 Y127Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UG-01A-32D-A33T-08 chr5:15928365 C>T maps to NM_012304.3 N165N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UG-01A-32D-A33T-08 chr21:47423407 C>T maps to NM_001848.2 A856A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UG-01A-32D-A33T-08 chr19:547337 G>A maps to NM_005317.2 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UG-01A-32D-A33T-08 chr9:5765690 C>T maps to ENST00000414202 F1010F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UG-01A-32D-A33T-08 chr7:66479412 T>C maps to NM_018264.2 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UG-01A-32D-A33T-08 chr19:10428270 T>A maps to NM_133452.2 P710P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UG-01A-32D-A33T-08 chr2:228996773 G>A maps to NM_001142644.1 D20D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UG-01A-32D-A33T-08 chr1:223465928 G>A maps to NM_017982.3 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UG-01A-32D-A33T-08 chr12:21733404 T>C maps to NM_021957.3 E58E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UG-01A-32D-A33T-08 chr11:65820520 G>A maps to NM_006842.2 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UG-01A-32D-A33T-08 chr11:123893817 C>T maps to NM_001001953.1 Y33Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UG-01A-32D-A33T-08 chr11:46890545 C>T maps to ENST00000256991 R1655R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UG-01A-32D-A33T-08 chr2:208461779 T>G maps to NM_134442.3 *342E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UG-01A-32D-A33T-08 chr8:139737641 C>T maps to NM_152888.1 P727P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UG-01A-32D-A33T-08 chr18:28723622 A>T maps to NM_024421.2 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UG-01A-32D-A33T-08 chr15:33822868 T>C did not map to a codon.
Sequencing variant TCGA-IB-A6UG-01A-32D-A33T-08 chr2:166245631 C>T maps to NM_001040142.1 I1772I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UG-01A-32D-A33T-08 chr18:31685088 C>T maps to NM_003787.4 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UG-01A-32D-A33T-08 chr3:73433514 G>A maps to NM_015009.1 D734D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UG-01A-32D-A33T-08 chr9:117029788 G>A maps to NM_032888.2 P1151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UG-01A-32D-A33T-08 chr8:55049225 G>A did not map to a codon.
Sequencing variant TCGA-IB-A6UG-01A-32D-A33T-08 chr16:55361531 C>T maps to NM_024335.2 R150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UG-01A-32D-A33T-08 chr5:13776707 G>A maps to NM_001369.2 H3071H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UG-01A-32D-A33T-08 chr21:41648060 G>A maps to NM_001389.3 G773G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UG-01A-32D-A33T-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UG-01A-32D-A33T-08 chr22:23438121 G>A maps to NM_002073.2 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UG-01A-32D-A33T-08 chr7:99913459 A>G maps to NM_001004351.4 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UG-01A-32D-A33T-08 chr6:27419353 G>A maps to NM_007149.2 R662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UG-01A-32D-A33T-08 chr7:133979788 G>A maps to NM_032826.4 C264C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UG-01A-32D-A33T-08 chr16:84600450 T>G maps to NM_021149.2 *143Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UG-01A-32D-A33T-08 chr11:62414589 G>A maps to NM_030628.1 L988L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr8:88885209 C>A maps to NM_152418.3 A330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr5:837563 G>T maps to NM_024786.2 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr15:88524481 C>A maps to NM_001007156.1 G565G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr4:146073751 T>A maps to ENST00000447906 A303A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr4:108641320 C>T maps to NM_005443.4 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr18:641457 G>T maps to NM_199167.1 E376*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-LB-A7SX-01A-11D-A33T-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr11:119206986 C>T maps to NM_032015.3 D385D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr12:57642584 G>A maps to NM_145064.1 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr3:33425650 C>T maps to NM_012157.3 Y374Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr21:47686067 C>T maps to NM_003906.3 L934L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr7:42018282 G>T maps to NM_000168.5 S521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr1:180793902 G>T maps to NM_004736.3 E260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr2:206166501 G>A did not map to a codon.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chrX:54956405 C>T maps to NM_001039705.1 V1083V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr21:41032647 G>A maps to NM_033172.1 Q54Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr3:142142484 C>T did not map to a codon.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr11:129321168 C>T maps to NM_003658.4 Q238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr10:116331053 A>C did not map to a codon.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chrX:109697312 A>G maps to NM_020769.2 E1156E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr4:104640520 G>C maps to NM_001059.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr8:95538656 C>T maps to NM_015496.3 V605V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr19:33699874 G>A maps to NM_019849.2 D498D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr3:123010064 G>A maps to NM_183357.2 F1074F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr6:27833263 C>T maps to NM_003511.2 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr11:58605741 G>A maps to NM_145016.3 Q60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr14:103372119 G>A maps to NM_145725.2 *569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr17:37571340 G>A maps to NM_004774.3 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr6:105609436 G>A maps to NM_022361.4 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr15:66210373 G>A maps to NM_032445.2 N672N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr2:219204547 C>T maps to NM_015488.4 Y93Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr13:70681815 G>A maps to NM_020866.2 R6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr5:44815300 C>T maps to NM_016640.3 N439N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr17:34641447 A>G did not map to a codon.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr16:5141881 G>A maps to NM_201400.2 H85H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr14:20215849 G>A maps to NM_172194.1 Q88Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr3:119962535 G>A maps to NM_153002.2 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr22:50279763 C>T maps to NM_014838.2 N818N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr1:22416479 C>T maps to NM_044472.2 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr14:52507534 G>A maps to NM_007361.3 F620F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr8:143958529 G>A maps to ENST00000377675 F239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr1:112033385 T>C did not map to a codon.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr4:6107247 G>A maps to NM_001099433.1 D192D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr11:123625214 G>A maps to NM_001005188.1 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr16:67865087 C>G did not map to a codon.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr19:44129316 G>A maps to NM_145296.1 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr16:476686 C>T maps to NM_014700.3 F227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr8:101153415 G>A maps to NM_001029860.3 Q356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr11:65413983 C>T maps to NM_153253.29 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr21:19666603 G>A maps to NM_002772.2 A823A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr14:23945485 C>T maps to NM_001042635.1 R195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr22:47087588 G>T maps to NM_022766.5 P404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr1:248487099 G>A maps to NM_001004691.1 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr2:109367777 G>A maps to NM_006267.4 W444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr11:116631624 C>T maps to NM_032725.3 R360R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr4:157689124 G>A maps to NM_016205.2 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr8:145066089 G>C maps to NM_001009184.1 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr13:46287489 C>T maps to NM_152719.1 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr17:36940504 C>T maps to NM_003559.4 Q115Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr3:196304577 T>C maps to NM_001105573.1 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr16:88706380 C>T maps to NM_013278.3 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr1:149916370 G>A maps to NM_020205.2 F639F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chrX:50377158 A>G maps to NM_020717.3 S638S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr10:32310005 G>A maps to NM_004521.2 I716I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr20:52192920 C>T maps to NM_006526.2 Q794Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr10:71164770 G>C maps to NM_001057.2 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr11:12316360 T>C maps to NM_032867.2 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M8-A5N4-01A-11D-A26I-08 chr15:82551446 G>A maps to NM_024580.5 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M8-A5N4-01A-11D-A26I-08 chr15:43044233 C>T maps to ENST00000263802 S1475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M8-A5N4-01A-11D-A26I-08 chr2:187559052 A>G maps to NM_177454.3 Q51Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M8-A5N4-01A-11D-A26I-08 chr1:214170478 C>T maps to NM_002763.3 R201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M8-A5N4-01A-11D-A26I-08 chr7:148288175 C>T maps to NM_145304.2 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M8-A5N4-01A-11D-A26I-08 chr5:135692811 G>A maps to NM_020389.2 N88N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M8-A5N4-01A-11D-A26I-08 chrX:69478724 C>A maps to NM_002565.3 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M8-A5N4-01A-11D-A26I-08 chr2:130897919 G>A maps to NM_207310.1 N236N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M8-A5N4-01A-11D-A26I-08 chr17:34062238 G>A maps to NM_033315.3 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M8-A5N4-01A-11D-A26I-08 chr14:53235555 A>T did not map to a codon.
Sequencing variant TCGA-M8-A5N4-01A-11D-A26I-08 chr1:158517226 G>A maps to NM_001005189.1 Y223Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M8-A5N4-01A-11D-A26I-08 chr11:55563780 C>T maps to NM_001004735.1 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M8-A5N4-01A-11D-A26I-08 chr9:124062284 T>G did not map to a codon.
Sequencing variant TCGA-M8-A5N4-01A-11D-A26I-08 chr7:123593722 C>T maps to NM_001174046.1 C33C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M8-A5N4-01A-11D-A26I-08 chr7:5330779 C>T maps to NM_153247.2 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M8-A5N4-01A-11D-A26I-08 chr4:47682233 G>A maps to NM_006587.2 D352D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M8-A5N4-01A-11D-A26I-08 chr12:21968726 G>A maps to NM_005691.2 H1331H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M8-A5N4-01A-11D-A26I-08 chr22:32756680 C>T maps to NM_001098535.1 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr2:241496632 C>T maps to ENST00000401804 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr13:29855976 G>A maps to NM_001033602.2 A937A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr9:103340637 C>T maps to NM_001018116.1 D71D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr4:142150723 G>T did not map to a codon.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr8:134233082 C>T maps to NM_003882.2 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr17:7577021 G>A maps to NM_001126112.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr5:78586969 C>T maps to NM_152405.4 R459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr11:125548082 A>G maps to NM_001612.5 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr19:4652051 G>A maps to NM_152362.2 Q57Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr15:41192856 G>A maps to NM_020857.2 W614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr10:96802652 G>T maps to NM_000770.3 I381I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr19:501738 G>A maps to NM_130760.2 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr1:153271679 C>A maps to NM_052891.1 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr1:228285698 C>T maps to NM_001024228.1 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr1:22186349 G>A maps to NM_005529.5 S1720S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr3:168845678 C>T maps to NM_004991.3 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr11:70333391 G>A maps to ENST00000338508 V996V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr3:93783282 G>A maps to NM_022072.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr2:80529762 G>A maps to NM_178839.4 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr9:125486387 G>A maps to NM_001005235.1 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr12:123470863 G>A maps to NM_020845.2 Q1254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr6:88773872 C>T maps to NM_030960.2 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr16:55862731 C>T maps to NM_001025195.1 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr5:137518868 C>T maps to NM_005733.2 R282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr19:38682811 C>T maps to NM_015073.1 V1486V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr2:165997337 C>T maps to NM_006922.3 P614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr5:63509711 C>T maps to NM_001113561.1 R187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chrX:149639143 C>A maps to NM_005491.3 S433S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr19:15271826 C>T maps to NM_000435.2 P2204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr18:21426311 C>A maps to ENST00000416669 A1259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr17:29665117 T>G maps to NM_001042492.2 S2260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr7:155604783 G>A maps to NM_000193.2 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr4:154318478 G>T maps to NM_032117.2 E154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr5:158596041 C>T maps to NM_144726.2 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr22:20785507 G>T maps to NM_153334.4 C217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr12:121698197 G>A did not map to a codon.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr22:41625556 G>A maps to NM_031488.4 P634P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr22:24086055 G>A maps to NM_021916.2 C424C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr19:56243921 G>A maps to NM_176820.2 G425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr16:67006385 C>T maps to NM_024922.5 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr14:72055190 C>G maps to NM_015556.1 S201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr7:4089013 A>G maps to NM_152744.3 E879E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr14:20019959 G>A maps to ENST00000439503 D87D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr15:49776571 A>C maps to NM_002009.3 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr19:16006352 G>A maps to NM_001082.3 C102C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr5:110097038 G>T maps to NM_138773.1 G272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr19:36043992 C>T maps to NM_000704.2 A899A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr1:46491368 C>T maps to NM_015112.2 L601L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr9:139412297 G>A maps to NM_017617.3 C449C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr19:44131874 G>A maps to NM_145296.1 C44C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr1:169823494 C>A maps to NM_181093.2 L695L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr16:57714439 G>A maps to NM_170776.4 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr9:127644233 C>T did not map to a codon.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr11:71249544 C>T maps to NM_021046.2 C148C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr3:52523639 C>T maps to NM_007184.3 V1134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr2:128412101 G>A maps to NM_017980.4 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr12:59267906 T>A maps to NM_153377.3 L1015L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr17:78184613 C>T maps to NM_000199.3 R382R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr7:4839089 G>A maps to NM_018059.4 G1049G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PZ-A5RE-01A-11D-A32N-08 chrX:50378664 G>A maps to NM_020717.3 D136D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PZ-A5RE-01A-11D-A32N-08 chr19:22574740 C>T maps to NM_001098626.1 K432K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PZ-A5RE-01A-11D-A32N-08 chrX:140993256 C>T maps to NM_005462.4 Q23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PZ-A5RE-01A-11D-A32N-08 chrX:152808543 C>T maps to NM_001001344.2 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PZ-A5RE-01A-11D-A32N-08 chr19:8808040 G>A maps to NM_178525.3 N337N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PZ-A5RE-01A-11D-A32N-08 chr12:25380271 C>T maps to NM_033360.2 E62E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q3-A5QY-01A-12D-A32N-08 chr22:38120996 C>T maps to NM_001039141.2 Q812*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q3-A5QY-01A-12D-A32N-08 chr11:55541017 C>T maps to NM_001001967.1 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q3-A5QY-01A-12D-A32N-08 chr16:67578686 C>T maps to NM_001193523.1 C961C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q3-A5QY-01A-12D-A32N-08 chr1:52285520 G>A maps to NM_002525.2 G482G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q3-A5QY-01A-12D-A32N-08 chr1:211263993 G>A maps to NM_172362.2 R117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q3-A5QY-01A-12D-A32N-08 chr2:51254958 G>A maps to ENST00000404971 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q3-A5QY-01A-12D-A32N-08 chr17:46926636 G>A maps to ENST00000448105 Q171Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q3-A5QY-01A-12D-A32N-08 chr9:125681304 G>A maps to NM_020924.2 C303C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q3-A5QY-01A-12D-A32N-08 chr21:40630428 T>C maps to NM_018963.3 E685E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q3-A5QY-01A-12D-A32N-08 chr5:115148956 T>A did not map to a codon.
Sequencing variant TCGA-Q3-A5QY-01A-12D-A32N-08 chr19:40581259 G>T maps to NM_001142577.1 C364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q3-A5QY-01A-12D-A32N-08 chr15:38234405 G>T maps to NM_152453.2 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q3-A5QY-01A-12D-A32N-08 chr20:36954738 C>T maps to NM_001725.2 Q360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q3-A5QY-01A-12D-A32N-08 chr9:33068869 G>A maps to NM_018225.2 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q3-A5QY-01A-12D-A32N-08 chr2:27887290 C>T maps to NM_018158.2 C224C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q3-A5QY-01A-12D-A32N-08 chr9:133499055 G>A maps to NM_003934.1 Q311Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q3-A5QY-01A-12D-A32N-08 chrX:31222080 T>C maps to ENST00000357033 Q3268Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q3-A5QY-01A-12D-A32N-08 chr15:63632564 C>A maps to NM_001218.3 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q3-A5QY-01A-12D-A32N-08 chr1:161206280 C>T maps to NM_001077482.1 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q3-A5QY-01A-12D-A32N-08 chr16:68732254 C>T maps to NM_001793.4 S814S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q3-A5QY-01A-12D-A32N-08 chrX:140994914 G>A maps to NM_005462.4 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q3-A5QY-01A-12D-A32N-08 chr7:99913459 A>G maps to NM_001004351.4 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RB-A7B8-01A-12D-A33T-08 chr1:44468617 A>G maps to NM_201649.2 F283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RB-A7B8-01A-12D-A33T-08 chr12:43860591 A>G maps to ENST00000389420 G410G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RB-A7B8-01A-12D-A33T-08 chr9:107620843 G>A maps to NM_005502.3 R227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RB-A7B8-01A-12D-A33T-08 chr2:182360533 C>T maps to NM_000885.4 D470D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RB-A7B8-01A-12D-A33T-08 chr4:8582936 C>T maps to NM_080819.2 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RB-A7B8-01A-12D-A33T-08 chr12:129558548 G>A maps to NM_133448.2 D1057D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RB-A7B8-01A-12D-A33T-08 chr7:114269972 A>G maps to NM_148898.3 Q195Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RB-A7B8-01A-12D-A33T-08 chr20:10621877 C>T maps to NM_000214.2 E977E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RB-A7B8-01A-12D-A33T-08 chr1:151372580 C>T maps to NM_002796.2 R89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RB-A7B8-01A-12D-A33T-08 chr8:66988978 C>T maps to NM_033105.4 H68H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RB-A7B8-01A-12D-A33T-08 chr5:140257258 G>A maps to NM_018903.2 P734P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RB-A7B8-01A-12D-A33T-08 chr13:58208305 C>T maps to NM_001040429.2 F542F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RB-A7B8-01A-12D-A33T-08 chr11:64120218 C>T maps to NM_032251.5 H1120H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RB-A7B8-01A-12D-A33T-08 chr6:147680319 G>A maps to NM_001127715.1 T802T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RB-A7B8-01A-12D-A33T-08 chr4:41984153 C>T maps to NM_001029955.3 Y115Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RB-A7B8-01A-12D-A33T-08 chr11:70282507 C>T maps to NM_001184740.1 C633C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RB-A7B8-01A-12D-A33T-08 chr5:9054316 G>A maps to NM_003966.2 C857C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RB-A7B8-01A-12D-A33T-08 chrX:141291653 G>T maps to NM_016249.3 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RB-A7B8-01A-12D-A33T-08 chr15:39544773 C>T maps to NM_207445.2 C146C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RB-A7B8-01A-12D-A33T-08 chr1:228646126 T>G maps to NM_175055.2 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RB-A7B8-01A-12D-A33T-08 chr6:101073181 A>G maps to NM_006828.2 P1557P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RB-A7B8-01A-12D-A33T-08 chr12:31577540 C>T maps to NM_144973.3 E773E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RB-A7B8-01A-12D-A33T-08 chr4:53773692 G>A maps to NM_152540.3 S591S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RB-A7B8-01A-12D-A33T-08 chr19:41597725 C>A maps to NM_000766.3 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RB-A7B8-01A-12D-A33T-08 chr3:141163338 C>T maps to NM_001080412.2 A703A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RB-A7B8-01A-12D-A33T-08 chr11:123516309 G>A maps to NM_018400.3 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RB-A7B8-01A-12D-A33T-08 chr8:87423765 G>T did not map to a codon.
Sequencing variant TCGA-RB-A7B8-01A-12D-A33T-08 chr14:91760539 G>A maps to NM_001080414.2 Y1363Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RB-A7B8-01A-12D-A33T-08 chr12:346452 C>T maps to NM_016615.3 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RB-A7B8-01A-12D-A33T-08 chr11:6261425 G>A maps to NM_001037329.2 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RB-A7B8-01A-12D-A33T-08 chr6:6318800 G>A maps to NM_000129.3 Q33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RB-A7B8-01A-12D-A33T-08 chr7:6210908 C>T maps to ENST00000396741 A162A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-RB-A7B8-01A-12D-A33T-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-RB-A7B8-01A-12D-A33T-08 chr1:205307703 G>A maps to NM_018203.1 R260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RB-A7B8-01A-12D-A33T-08 chr3:9100156 C>T did not map to a codon.
Sequencing variant TCGA-RB-A7B8-01A-12D-A33T-08 chr20:50071157 G>A maps to NM_012340.3 G592G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A774-01A-21D-A32N-08 chr16:24104166 C>T maps to NM_002738.6 Y195Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A774-01A-21D-A32N-08 chr4:70146856 C>T maps to NM_053039.1 N213N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A774-01A-21D-A32N-08 chr1:152382519 G>A maps to NM_016190.2 H346H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A774-01A-21D-A32N-08 chr1:7724799 C>T maps to NM_015215.2 G731G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A774-01A-21D-A32N-08 chr11:43429012 A>T maps to NM_018259.5 P650P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A774-01A-21D-A32N-08 chr1:12887685 T>C maps to NM_001146344.1 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A774-01A-21D-A32N-08 chr2:182358061 C>T maps to NM_000885.4 I388I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A774-01A-21D-A32N-08 chr6:108214764 A>T maps to NM_007214.4 L532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A774-01A-21D-A32N-08 chrX:18234680 G>A maps to NM_153346.4 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A774-01A-21D-A32N-08 chr5:35793391 G>A maps to NM_024867.3 K1562K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A774-01A-21D-A32N-08 chr13:24242947 C>T maps to NM_018647.2 N319N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A774-01A-21D-A32N-08 chr19:9090830 A>G maps to NM_024690.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A774-01A-21D-A32N-08 chr11:7111052 G>A maps to NM_014469.4 S234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A774-01A-21D-A32N-08 chr1:45307636 G>A maps to NM_003738.4 C49C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A774-01A-21D-A32N-08 chr2:162875263 C>T maps to NM_001935.3 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A774-01A-21D-A32N-08 chr9:117756 C>T maps to NM_207305.3 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A774-01A-21D-A32N-08 chr2:63283270 C>T maps to NM_014562.3 H295H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A774-01A-21D-A32N-08 chr1:154841842 C>A maps to NM_002249.4 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A774-01A-21D-A32N-08 chr2:148657442 C>A maps to NM_001616.3 Y168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A774-01A-21D-A32N-08 chr22:26693011 C>T maps to NM_021115.4 D376D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A774-01A-21D-A32N-08 chr4:110756590 C>T maps to NM_006583.2 R123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A774-01A-21D-A32N-08 chr1:186024699 C>T maps to NM_031935.2 H2346H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A774-01A-21D-A32N-08 chr7:111926928 C>T maps to NM_021994.2 D31D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A774-01A-21D-A32N-08 chr1:242451662 C>T did not map to a codon.
Sequencing variant TCGA-US-A774-01A-21D-A32N-08 chr17:65051325 C>T maps to NM_000727.3 R138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A774-01A-21D-A32N-08 chr17:16285637 G>A maps to NM_018955.2 K139K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A774-01A-21D-A32N-08 chr1:240371420 C>T maps to ENST00000406993 P1246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A774-01A-21D-A32N-08 chr2:25467116 G>A maps to NM_175629.1 C586C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A776-01A-13D-A33T-08 chr11:108158372 T>G maps to NM_000051.3 L1347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A776-01A-13D-A33T-08 chr19:1068621 G>A maps to NM_012292.2 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A776-01A-13D-A33T-08 chr15:52667656 G>A maps to ENST00000358212 C807C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A776-01A-13D-A33T-08 chr10:6264819 C>T maps to NM_004566.3 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A776-01A-13D-A33T-08 chr7:100773786 G>A maps to NM_000602.3 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A776-01A-13D-A33T-08 chr2:189859046 C>T maps to NM_000090.3 R428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A776-01A-13D-A33T-08 chr14:72939636 C>T maps to NM_004296.4 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A776-01A-13D-A33T-08 chrX:10094324 G>A maps to NM_015691.3 P695P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A776-01A-13D-A33T-08 chr2:96049769 C>T maps to NM_013434.4 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A776-01A-13D-A33T-08 chr3:12858159 C>T maps to NM_001162499.1 R577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A776-01A-13D-A33T-08 chr19:43922331 C>A maps to NM_031451.4 S196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A776-01A-13D-A33T-08 chr2:136680483 G>A maps to NM_001349.2 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A776-01A-13D-A33T-08 chr1:55223793 G>A maps to NM_152268.3 I347I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A776-01A-13D-A33T-08 chr16:84600450 T>G maps to NM_021149.2 *143Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A776-01A-13D-A33T-08 chr12:95926775 G>A maps to NM_032147.2 Y419Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A776-01A-13D-A33T-08 chr16:58562471 C>T maps to NM_016284.3 V2120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A776-01A-13D-A33T-08 chr12:121867910 G>A did not map to a codon.
Sequencing variant TCGA-US-A776-01A-13D-A33T-08 chr4:100208112 G>A maps to NM_000667.3 D51D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A776-01A-13D-A33T-08 chr12:122213528 G>A maps to NM_001080825.2 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A776-01A-13D-A33T-08 chr19:48981401 G>A maps to NM_017457.4 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A776-01A-13D-A33T-08 chrX:100547880 G>A maps to NM_024885.3 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A776-01A-13D-A33T-08 chr10:103907023 C>T maps to NM_015062.3 R1425R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A776-01A-13D-A33T-08 chr22:21332001 C>T maps to NM_144704.2 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A776-01A-13D-A33T-08 chr5:127673719 G>A maps to NM_001999.3 H1189H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A776-01A-13D-A33T-08 chr9:113169443 C>T maps to ENST00000374463 R2815R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A776-01A-13D-A33T-08 chr11:5905893 C>A maps to NM_001005165.1 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A776-01A-13D-A33T-08 chr1:218609474 G>A maps to NM_001135599.2 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A776-01A-13D-A33T-08 chr8:99961404 G>A maps to ENST00000457907 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A776-01A-13D-A33T-08 chr6:45390444 A>G maps to ENST00000359524 Q126Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A776-01A-13D-A33T-08 chr6:42620379 A>G maps to NM_015255.2 Q922Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A776-01A-13D-A33T-08 chr12:101336204 G>A maps to ENST00000392977 K116K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A776-01A-13D-A33T-08 chr20:60963366 T>G maps to NM_001024.3 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A776-01A-13D-A33T-08 chr19:51021943 C>T maps to NM_001080457.1 A342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A776-01A-13D-A33T-08 chr19:51135877 G>A maps to NM_001160329.1 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A776-01A-13D-A33T-08 chr12:81205273 C>T maps to NM_004664.2 Q224Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A776-01A-13D-A33T-08 chr7:99913459 A>G maps to NM_001004351.4 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A776-01A-13D-A33T-08 chr1:57333281 G>A maps to NM_000562.2 Q26Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A776-01A-13D-A33T-08 chrX:119509335 C>T maps to NM_001142447.2 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A779-01A-11D-A32N-08 chr2:234580747 T>C maps to ENST00000373460 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A779-01A-11D-A32N-08 chr3:16475455 C>T maps to NM_015150.1 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A779-01A-11D-A32N-08 chr12:41419065 G>T maps to NM_001843.2 E880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A779-01A-11D-A32N-08 chr3:11643422 G>A maps to NM_014667.2 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A779-01A-11D-A32N-08 chr19:17417118 G>T maps to NM_023937.3 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A779-01A-11D-A32N-08 chr3:195965645 G>A maps to NM_005017.2 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A779-01A-11D-A32N-08 chr20:2464181 A>G maps to NM_024325.4 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A779-01A-11D-A32N-08 chr20:40979317 C>T maps to ENST00000373198 T605T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A779-01A-11D-A32N-08 chr22:41742052 C>T maps to ENST00000351589 F518F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A779-01A-11D-A32N-08 chr10:75457348 G>A maps to NM_001144000.1 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A779-01A-11D-A32N-08 chr14:105412406 C>A maps to NM_138420.2 G3127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A779-01A-11D-A32N-08 chr19:9965170 C>T maps to NM_058164.2 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A779-01A-11D-A32N-08 chr4:90872801 G>A maps to NM_007351.2 T1055T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A779-01A-11D-A32N-08 chr8:135614833 C>T maps to NM_020863.3 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A779-01A-11D-A32N-08 chr14:29237468 C>T maps to NM_005249.3 N328N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A779-01A-11D-A32N-08 chr1:156914960 G>A maps to NM_198236.1 C947C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A779-01A-11D-A32N-08 chr4:3526685 G>A maps to NM_002337.2 D99D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A779-01A-11D-A32N-08 chr3:72428209 C>A maps to ENST00000477973 E227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A779-01A-11D-A32N-08 chr4:6082003 C>T maps to NM_001099433.1 R379R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A779-01A-11D-A32N-08 chr9:35074978 G>A maps to NM_004629.1 S527S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A779-01A-11D-A32N-08 chr1:196714956 A>C maps to NM_000186.3 G1107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A779-01A-11D-A32N-08 chr16:18858859 G>A maps to ENST00000389467 L1971L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A779-01A-11D-A32N-08 chr1:153907308 C>T maps to NM_014856.2 Q900Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A779-01A-11D-A32N-08 chr7:120991268 A>T maps to NM_014888.2 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A779-01A-11D-A32N-08 chr3:73440201 G>A maps to NM_015009.1 D440D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A779-01A-11D-A32N-08 chr4:6380233 C>T maps to NM_181876.2 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77E-01A-11D-A32N-08 chr7:154667693 C>T maps to NM_130797.2 G654G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77E-01A-11D-A32N-08 chr15:89399991 C>T maps to NM_013227.3 S1392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77E-01A-11D-A32N-08 chr3:93611911 G>A maps to NM_000313.3 Y340Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77E-01A-11D-A32N-08 chr6:56492886 C>T maps to ENST00000361203 W1305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77E-01A-11D-A32N-08 chr19:31769987 C>T maps to NM_020856.2 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77E-01A-11D-A32N-08 chr3:132175222 C>A maps to NM_015268.3 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77E-01A-11D-A32N-08 chr10:26457783 C>T maps to NM_017433.4 S1085S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77E-01A-11D-A32N-08 chr2:189929336 T>C maps to NM_000393.3 K554K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77E-01A-11D-A32N-08 chr17:39538354 A>G maps to NM_021013.3 C90C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77E-01A-11D-A32N-08 chr14:93709083 G>A maps to NM_001002860.2 Y978Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77E-01A-11D-A32N-08 chr16:65032558 C>T maps to NM_001797.2 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77E-01A-11D-A32N-08 chr3:148599356 C>T maps to NM_001870.2 R209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77E-01A-11D-A32N-08 chr19:41096642 C>T maps to NM_138392.3 G592G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77E-01A-11D-A32N-08 chr12:52994909 C>T maps to NM_080747.2 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77E-01A-11D-A32N-08 chr5:169533242 G>A maps to NM_012188.4 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77E-01A-11D-A32N-08 chr16:2763622 G>A maps to NM_031948.3 Y195Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77E-01A-11D-A32N-08 chr17:39643659 G>A maps to NM_003771.4 I310I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77E-01A-11D-A32N-08 chr11:63680165 G>A maps to NM_173587.3 Q337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77E-01A-11D-A32N-08 chr17:78085869 C>T maps to NM_001079804.1 Y575Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77E-01A-11D-A32N-08 chr2:241827789 G>A maps to NM_001085437.1 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77E-01A-11D-A32N-08 chr12:113266104 G>A did not map to a codon.
Sequencing variant TCGA-US-A77E-01A-11D-A32N-08 chr10:21074741 G>A maps to ENST00000430741 Y995Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77E-01A-11D-A32N-08 chr19:868429 C>T maps to NM_005481.2 W823*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77E-01A-11D-A32N-08 chr1:153907308 C>T maps to NM_014856.2 Q900Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77E-01A-11D-A32N-08 chr2:25384177 G>A maps to NM_001035256.1 D192D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77E-01A-11D-A32N-08 chr6:123539784 A>G maps to NM_006073.2 G717G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77E-01A-11D-A32N-08 chr16:81942077 A>T maps to NM_002661.2 K539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77E-01A-11D-A32N-08 chr9:117844147 C>T maps to NM_002160.2 R769R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77G-01A-11D-A32N-08 chr5:140503631 T>C maps to NM_018938.2 S684S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77G-01A-11D-A32N-08 chrX:140985097 C>T maps to NM_138702.1 P518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77G-01A-11D-A32N-08 chr19:40902611 C>G maps to NM_181882.2 P549P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77G-01A-11D-A32N-08 chr2:176959245 C>A maps to NM_000523.3 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77G-01A-11D-A32N-08 chr4:38799731 G>A maps to NM_003263.3 Q241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77G-01A-11D-A32N-08 chr17:79478120 G>A maps to NM_001614.2 C272C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77G-01A-11D-A32N-08 chr5:176520429 C>T maps to NM_213647.1 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77G-01A-11D-A32N-08 chr5:140773876 G>A maps to NM_032088.1 A499A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77G-01A-11D-A32N-08 chr6:33690691 G>A maps to NM_054111.4 H346H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77G-01A-11D-A32N-08 chr10:102056025 G>A maps to NM_016112.2 F403F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77G-01A-11D-A32N-08 chr13:36744910 G>A maps to ENST00000511166 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77G-01A-11D-A32N-08 chr17:31082527 G>A maps to NM_015194.1 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77G-01A-11D-A32N-08 chr12:101760467 C>T maps to NM_014503.2 S2086S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77G-01A-11D-A32N-08 chr14:68249560 G>A maps to NM_015346.3 Y1436Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77G-01A-11D-A32N-08 chr12:7030923 C>A maps to NM_001975.2 S349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77G-01A-11D-A32N-08 chr22:31740472 C>T maps to NM_014323.2 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77G-01A-11D-A32N-08 chr12:667678 G>A maps to NM_173593.3 P871P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77G-01A-11D-A32N-08 chr1:153907308 C>T maps to NM_014856.2 Q900Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77G-01A-11D-A32N-08 chr10:116100475 G>A maps to NM_001001936.1 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77G-01A-11D-A32N-08 chr2:166165304 G>A did not map to a codon.
Sequencing variant TCGA-US-A77G-01A-11D-A32N-08 chr5:79974873 G>A maps to NM_002439.3 E434E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77G-01A-11D-A32N-08 chr9:21974678 G>A maps to NM_001195132.1 Q50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77G-01A-11D-A32N-08 chr3:52383088 C>T maps to ENST00000273600 S764S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77G-01A-11D-A32N-08 chr5:140221028 C>T maps to NM_018911.2 H41H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77G-01A-11D-A32N-08 chr11:5730862 C>T maps to NM_006074.4 C494C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77G-01A-11D-A32N-08 chr4:140811491 G>A maps to ENST00000509479 F366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77G-01A-11D-A32N-08 chrX:150869405 G>A maps to NM_024082.3 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77G-01A-11D-A32N-08 chr2:48809301 C>T maps to NM_172311.2 C510C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77G-01A-11D-A32N-08 chr10:134165158 G>A maps to NM_030626.2 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77G-01A-11D-A32N-08 chr1:231339742 C>T maps to NM_001004342.3 A555A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77G-01A-11D-A32N-08 chr5:140216007 G>A maps to NM_018910.2 S680S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77G-01A-11D-A32N-08 chr13:60557993 C>T maps to NM_001042517.1 E463E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77G-01A-11D-A32N-08 chr5:140255215 G>A maps to NM_018903.2 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77G-01A-11D-A32N-08 chr3:10417284 G>A maps to NM_001001331.2 Y415Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77G-01A-11D-A32N-08 chr16:84600450 T>G maps to NM_021149.2 *143Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77J-01A-11D-A32N-08 chr12:132466656 G>A maps to ENST00000333577 P557P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77J-01A-11D-A32N-08 chr16:67913802 C>T maps to NM_014329.3 S624S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77J-01A-11D-A32N-08 chr12:112843028 T>C maps to NM_001024662.1 *289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77J-01A-11D-A32N-08 chr9:140361882 G>A maps to NM_001098537.1 C975C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77J-01A-11D-A32N-08 chr5:52779373 C>T maps to NM_013409.1 C106C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77J-01A-11D-A32N-08 chr16:780575 G>A maps to NM_022493.1 Y424Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77J-01A-11D-A32N-08 chr4:146563587 G>A maps to NM_172250.2 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77J-01A-11D-A32N-08 chr16:56918047 G>A maps to NM_000339.2 W586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77J-01A-11D-A32N-08 chr19:39009887 G>A maps to NM_000540.2 P3351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77J-01A-11D-A32N-08 chr17:27031790 G>A maps to ENST00000415329 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77J-01A-11D-A32N-08 chr6:71012701 C>T did not map to a codon.
Sequencing variant TCGA-US-A77J-01A-11D-A32N-08 chr20:25056995 C>T maps to NM_014588.4 R333R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77J-01A-11D-A32N-08 chr22:45133063 C>T maps to NM_001198721.1 G391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77J-01A-11D-A32N-08 chr10:24908579 C>T maps to NM_020824.3 P748P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77J-01A-11D-A32N-08 chr4:22390724 C>T maps to NM_145290.2 R903R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77J-01A-11D-A32N-08 chrX:54978520 G>A maps to NM_002625.2 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77J-01A-11D-A32N-08 chr14:78285425 C>T maps to NM_020421.3 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77J-01A-11D-A32N-08 chr5:16794819 G>A maps to NM_012334.2 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77J-01A-11D-A32N-08 chr19:43763168 G>A maps to NM_002784.3 N276N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77J-01A-11D-A32N-08 chr19:5664053 G>A maps to ENST00000433404 P725P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-6879-01A-11D-2154-08 chr17:263344 C>T maps to NM_001013672.4 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F2-7276-01A-11D-2154-08 chr12:11420474 A>G maps to NM_006249.4 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5919-01A-11D-1609-08 chr12:100559709 T>G did not map to a codon.
Sequencing variant TCGA-FZ-5920-01A-11D-1609-08 chr11:66330621 C>T maps to NM_001104.1 Y888Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FZ-5920-01A-11D-1609-08 chr8:43197469 C>T maps to NM_001005365.2 N453N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H6-8124-01A-11D-2396-08 chr3:50311107 A>G did not map to a codon.
Sequencing variant TCGA-HZ-7919-01A-11D-2154-08 chr6:132859637 G>C maps to NM_175057.3 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-7924-01A-11D-2154-08 chr17:79609409 G>T did not map to a codon.
Sequencing variant TCGA-HZ-8003-01A-21D-2201-08 chr11:89395332 A>G did not map to a codon.
Sequencing variant TCGA-HZ-8003-01A-21D-2201-08 chr11:89395321 C>T did not map to a codon.
Sequencing variant TCGA-HZ-8003-01A-21D-2201-08 chr2:87140986 G>A maps to NM_001078170.2 K5K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-8317-01A-11D-2396-08 chr19:43439886 T>A maps to NM_002783.2 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HZ-A49H-01A-11D-A26I-08 chr19:53945836 T>C did not map to a codon.
Sequencing variant TCGA-HZ-A49I-01A-12D-A26I-08 chr16:3607670 C>T maps to ENST00000448023 A721A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7646-01A-11D-2154-08 chr21:11058352 T>C did not map to a codon.
Sequencing variant TCGA-IB-7647-01A-11D-2154-08 chr19:45853628 C>T maps to NM_177417.2 Q392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7649-01A-11D-2154-08 chr21:11098909 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:100352879 C>T maps to ENST00000349350 S1052S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:186672573 G>T maps to NM_173651.2 E6270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:16823312 G>A maps to ENST00000448080 R737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:57493471 T>G maps to NM_178504.4 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:99146024 A>G maps to NM_145111.3 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:79934590 T>C did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:43342619 G>A maps to ENST00000344686 V862V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:102733743 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:102467347 C>T maps to NM_001376.4 R1378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:90576759 G>T maps to NM_012115.3 E1251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:53945279 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:32574557 C>A maps to NM_016141.3 G334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:57494904 C>T maps to NM_178504.4 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:14284445 C>T maps to NM_006108.2 L728L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:72146771 G>A maps to ENST00000424560 R2169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:136132862 C>T maps to NM_020469.2 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:88768261 C>T maps to NM_133447.1 Q85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:34937944 T>C did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:18030103 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:79421053 C>T maps to NM_025074.6 R3099*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:3144043 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:42577716 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:52819144 G>A maps to NM_144684.2 W86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:149481007 C>T maps to NM_198455.2 G830G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:118380474 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:81181858 A>C maps to NM_052892.3 R1619R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:186673514 A>G maps to NM_173651.2 E6583E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:149499026 G>A maps to NM_198455.2 S2494S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:16321162 C>T maps to NM_016113.4 R61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:97711700 C>A maps to NM_001105580.1 G367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:32476154 C>A maps to NM_021209.4 E260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:70608838 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:15733063 C>T maps to NM_007253.3 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:11420870 T>C maps to NM_006249.4 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:227963475 C>A maps to ENST00000396625 E380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:100369521 C>T maps to ENST00000349350 C1768C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:171678657 C>T maps to NM_000817.2 C48C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:220100256 C>T maps to NM_001042410.1 R585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:40068745 G>A maps to NM_032221.3 R1301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:109383226 G>T maps to NM_006267.4 E2078*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:41747607 G>A maps to ENST00000351589 W680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:101560321 T>C did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:44148559 G>T maps to NM_001129.3 E335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:24567496 C>T maps to NM_004563.2 Q121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:58470037 C>A maps to NM_152474.4 E194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:66329612 C>T maps to NM_001104.1 R766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr22:17265005 C>A maps to NM_175878.3 E295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:89385739 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:11039049 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:31806018 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:200524582 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:85652282 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:28734550 G>A maps to NM_003752.3 K281K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:144930581 A>G did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:57496519 A>G maps to NM_178504.4 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:158627400 G>A maps to NM_003126.2 R891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:189929382 T>G did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:179568945 G>A maps to NM_133378.4 R8807*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:24813504 C>T maps to ENST00000221169 Q175Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:43858419 C>T maps to NM_020406.2 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:9009782 C>T maps to NM_144670.3 Q958*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:46252653 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:170858288 G>A maps to NM_015028.2 R411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:1252651 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:42581868 G>A maps to NM_006095.2 R321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:2795330 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:201010661 G>A maps to NM_000069.2 R1702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:31805970 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:30919784 A>C maps to NM_080870.3 R1182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:113242366 C>T maps to NM_020963.3 R882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:77377221 C>T maps to NM_017662.4 W1455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:48033395 G>T maps to NM_000179.2 E1234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:132160427 C>A maps to NM_001172700.1 E374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:182847246 C>T maps to NM_001357.4 R764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:50255259 G>A maps to NM_006841.4 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:149479933 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr8:67576840 G>A maps to NM_025054.4 R785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:37187944 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:42866637 C>T maps to ENST00000251268 R1983*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:32983847 C>T maps to ENST00000375025 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:128890569 G>A maps to NM_001127192.1 R11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:118385551 G>A maps to NM_005396.4 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr20:44699119 G>A maps to NM_020967.2 R32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:11039271 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:64599087 G>A maps to NM_017525.2 Q1065*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:33936602 C>A maps to NM_001036.3 C1216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:34166515 G>A maps to NM_019596.5 R73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr16:14029330 T>G maps to NM_005236.2 Y514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:66767871 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:128471361 G>A maps to NM_018383.4 R1035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:58049122 G>T maps to ENST00000376233 E251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:228525845 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr13:25264556 G>T maps to NM_001185085.1 G210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:100550599 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:100797875 C>T maps to NM_139319.2 Q372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:128099864 G>T maps to NM_015635.2 G985*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:2334701 G>A maps to NM_152988.2 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:9071208 C>A maps to NM_024690.2 E5413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:100364867 C>T maps to ENST00000349350 G1616G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:55922468 C>A maps to NM_030820.3 G954*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:41452250 G>T maps to NM_001389.3 Y1416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:11039075 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:21805044 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:64519118 G>T maps to NM_182914.2 E2830*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:90578292 T>C maps to NM_012115.3 L1762L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:149509002 G>A maps to NM_198455.2 E3186E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:52825079 G>T maps to NM_144684.2 E193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:150877747 G>T maps to NM_053002.4 G323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:120941849 C>T maps to NM_014980.2 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:149514987 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:66063453 G>T maps to ENST00000370616 Y452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:34166105 G>A maps to NM_019596.5 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:160084455 C>T maps to NM_033394.2 R1344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:118455299 G>A maps to NM_017686.3 R108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:103215992 A>G did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:155443 C>A maps to NM_001039127.3 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:43364232 C>T maps to ENST00000344686 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:53684804 G>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:89424666 C>T maps to NM_153696.2 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:27670789 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr10:118404617 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:43858440 C>A maps to NM_020406.2 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:189975160 C>A maps to NM_000393.3 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:1414155 G>T maps to NM_014461.2 G556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:179434670 G>T maps to NM_133378.4 Y22828*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:247654998 G>A maps to NM_001004698.2 E190E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:126138555 G>T maps to ENST00000505024 E271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:78546357 G>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:64532311 G>T maps to NM_182914.2 E3459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:141200073 G>A maps to NM_018557.2 C3471C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:66053984 G>A maps to ENST00000370616 N515N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:9048836 C>A maps to NM_024690.2 G10932*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr21:11058352 T>C did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:7721939 G>T maps to NM_198185.2 G268G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:93540696 C>T maps to NM_004268.4 Q494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:43324961 C>A maps to NM_014345.2 G364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr19:6848024 G>T maps to NM_005428.2 E677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:75616719 C>T maps to NM_031925.2 T292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:152352789 C>T maps to NM_001164507.1 S8162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr6:38691110 A>G did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:52543324 C>T maps to NM_015136.2 Q779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chrX:50144086 G>A maps to NM_001013742.1 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:179454839 C>A maps to NM_133378.4 E17970*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:211533007 G>A maps to NM_001122633.1 Q1373Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:187538355 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:89020600 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:80050686 G>A maps to NM_004104.4 G260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:92732940 G>A maps to NM_017654.3 R824*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr11:6478036 G>A maps to NM_033278.2 R307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr3:38763850 C>T maps to NM_006514.2 W1135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:72176077 C>T did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:145156910 G>A maps to NM_014795.3 Q615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:16464552 G>T maps to NM_004431.3 C369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr9:128099771 C>T maps to NM_015635.2 R954*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr15:27188449 G>A maps to NM_000810.3 W322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:19748551 C>A maps to NM_001002926.1 E30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr17:65924473 C>T maps to ENST00000321892 R2045*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr5:14387900 C>T maps to NM_007118.2 R1276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr1:115263336 G>A maps to NM_001130523.1 G640G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr7:107416976 C>A maps to NM_000111.2 E533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr12:48134178 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr14:51224356 G>A maps to NM_020921.3 R1131*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-IB-7651-01A-11D-2154-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr4:155278476 C>A did not map to a codon.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:179616304 C>A maps to ENST00000375038 E3610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7651-01A-11D-2154-08 chr2:24484037 C>T maps to NM_006277.2 W873*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7654-01A-11D-2154-08 chr21:11058339 A>C did not map to a codon.
Sequencing variant TCGA-IB-7885-01A-11D-2154-08 chr7:149524950 G>A maps to NM_198455.2 Q4959Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7888-01A-11D-2154-08 chr21:11058326 A>T did not map to a codon.
Sequencing variant TCGA-IB-7888-01A-11D-2154-08 chr21:11098755 C>A did not map to a codon.
Sequencing variant TCGA-IB-7888-01A-11D-2154-08 chr6:7229364 C>T maps to NM_001003699.3 Q345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-7889-01A-11D-2154-08 chr19:53950473 C>T did not map to a codon.
Sequencing variant TCGA-IB-7893-01A-11D-2201-08 chr12:100559709 T>G did not map to a codon.
Sequencing variant TCGA-IB-7897-01A-21D-2201-08 chr11:89395332 A>G did not map to a codon.
Sequencing variant TCGA-IB-7897-01A-21D-2201-08 chr11:89395321 C>T did not map to a codon.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr3:50311107 A>G did not map to a codon.
Sequencing variant TCGA-IB-8127-01A-11D-2396-08 chr19:43859721 T>C maps to ENST00000378012 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SO-01A-11D-A32N-08 chr9:70871888 C>T maps to NM_201453.2 Y161Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SO-01A-11D-A32N-08 chr19:43441293 C>T did not map to a codon.
Sequencing variant TCGA-IB-A5SO-01A-11D-A32N-08 chr21:11058229 C>T maps to NM_182482.2 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A5SQ-01A-11D-A32N-08 chr19:53958819 T>C maps to NM_001008401.3 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UF-01A-23D-A33T-08 chr7:100383687 G>A maps to ENST00000349350 A2301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IB-A6UG-01A-32D-A33T-08 chr7:149500901 G>T did not map to a codon.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr21:11058339 A>C did not map to a codon.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr21:11058352 T>C did not map to a codon.
Sequencing variant TCGA-LB-A7SX-01A-11D-A33T-08 chr21:11039052 C>T did not map to a codon.
Sequencing variant TCGA-OE-A75W-01A-12D-A32N-08 chr14:72055520 C>A maps to NM_015556.1 S311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A776-01A-13D-A33T-08 chr9:70871888 C>T maps to NM_201453.2 Y161Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A779-01A-11D-A32N-08 chr6:31964273 C>T maps to NM_007293.2 H1191H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-US-A77E-01A-11D-A32N-08 chr21:11039065 A>G did not map to a codon.
