6680 NP_001070868 S486R not found in SNVbox database
8974 NP_705833 D991G not found in SNVbox database
531 NP_001070868 V645M not found in SNVbox database
805 NP_705833 S116G not found in SNVbox database
1358 NP_705833 W962R not found in SNVbox database
1685 NP_705833 T358K not found in SNVbox database
1696 NP_001070868 K391Q not found in SNVbox database
1836 NP_705833 E200D not found in SNVbox database
2973 NP_705833 V474L not found in SNVbox database
4826 NP_001070868 T315K not found in SNVbox database
4927 NP_001070868 R680C not found in SNVbox database
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr19:58863781 C>T maps to NM_130786.3 E160E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr10:52595832 C>A did not map to a codon.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr16:7657341 T>G did not map to a codon.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr3:151545614 C>T maps to NM_001086.2 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SR-01B-11D-A377-08 chr1:12721808 C>G maps to NM_001013630.1 Y131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr16:70303596 G>T maps to ENST00000418685 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr7:121731807 C>A maps to NM_005763.3 V655V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr7:48315046 C>T maps to NM_152701.3 V1928V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr7:48318293 T>C maps to NM_152701.3 T2501T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr7:48443342 C>A maps to NM_152701.3 G3979G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7742-01A-11D-2114-08 chr7:48352728 C>T maps to NM_152701.3 S3194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IK-01A-11D-A364-08 chr7:48318264 C>T maps to NM_152701.3 L2492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87K-01A-11D-A34U-08 chr7:48314143 T>C maps to NM_152701.3 A1627A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WH-01A-11D-A377-08 chr7:48280529 G>T maps to NM_152701.3 E377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr1:94506836 G>A maps to NM_000350.2 C1150C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr1:94502296 C>A maps to NM_000350.2 A1287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr17:67252296 C>T did not map to a codon.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr17:67300890 G>C maps to ENST00000392677 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr19:1058147 C>T maps to NM_019112.3 L1677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A872-01A-11D-A34U-08 chr19:1043360 C>T maps to NM_019112.3 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WI-01A-11D-A377-08 chr19:1050919 G>C maps to NM_019112.3 L851L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr17:66972094 G>T maps to NM_080283.3 P1612P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I6-01A-11D-A364-08 chr2:169826553 C>A did not map to a codon.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr7:87082327 A>G maps to NM_018849.2 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr7:87104730 C>T maps to NM_018849.2 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr7:20685386 C>T maps to NM_001163941.1 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr23:74318817 C>A did not map to a codon.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr6:43416687 C>A maps to NM_033450.2 P1315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr16:48226508 C>A maps to NM_032583.3 V876V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr17:48741194 G>T maps to NM_003786.3 G384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr13:95862990 G>C maps to NM_005845.3 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8469-01A-11D-2395-08 chr3:183667863 G>A maps to NM_005688.2 I998I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr1:94980699 A>G did not map to a codon.
Sequencing variant TCGA-EJ-7315-01A-31D-2114-08 chr11:119027720 T>C maps to NM_001142505.1 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr2:44040308 A>T maps to NM_022436.2 L634L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr15:89719094 C>A maps to NM_152924.4 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A725-01A-12D-A32B-08 chr19:17405641 G>A maps to NM_024527.4 C258C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7233-01A-11D-2114-08 chr7:150554544 C>T maps to ENST00000416793 R329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr3:38167372 C>A did not map to a codon.
Sequencing variant TCGA-J4-A83M-01A-11D-A34U-08 chr17:35536314 A>T maps to NM_198834.1 T1655T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AP-01A-12D-A33T-08 chr12:109703024 T>C maps to NM_001093.3 S2351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AV-01A-11D-A32B-08 chr12:112153742 C>T maps to NM_001136538.1 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I9-01A-11D-A364-08 chr12:121164961 G>A maps to NM_000017.2 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5502-01A-01D-1576-08 chr17:7240073 C>T maps to NM_014716.3 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr17:7240645 G>T maps to NM_014716.3 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr11:108017035 C>A maps to NM_000019.3 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr2:220396490 C>T maps to NM_018674.4 R325R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr11:44100334 G>T did not map to a codon.
Sequencing variant TCGA-KK-A8IL-01A-11D-A364-08 chr11:44092837 A>G maps to NM_032592.3 K107K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76W-01A-11D-A33T-08 chr23:15605909 G>C did not map to a codon.
Sequencing variant TCGA-EJ-7328-01A-31D-2114-08 chr23:70828894 T>A did not map to a codon.
Sequencing variant TCGA-KK-A8II-01A-11D-A364-08 chr15:78526788 G>A maps to NM_015162.4 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B4-01A-11D-A32B-08 chr16:20563465 C>T maps to NM_182617.3 K298K. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CH-5772-01A-11D-1576-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr12:81647349 T>C maps to NM_024560.2 A632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr1:229568582 G>A maps to NM_001100.3 D58D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A875-01A-31D-A34U-08 chr7:5568827 G>A maps to NM_001101.3 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SO-01B-31D-A377-08 chr17:79478955 G>A maps to NM_001614.2 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr19:39219697 C>A maps to NM_004924.3 T827T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr2:114709087 A>T maps to NM_005721.3 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr3:53905309 C>A maps to NM_022899.4 G506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr23:127185483 C>A did not map to a codon.
Sequencing variant TCGA-YL-A8HJ-01A-11D-A364-08 chr23:127185974 G>T did not map to a codon.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr10:127737878 G>A maps to NM_003474.4 G623G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr10:127730775 G>A maps to NM_021641.3 N714N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VL-01A-21D-A377-08 chr8:39495170 G>A maps to NM_014237.2 W259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76W-01A-11D-A33T-08 chr8:39624424 G>A maps to NM_001464.3 I483I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76W-01A-11D-A33T-08 chr8:39624554 G>C maps to NM_001464.3 S440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr4:175897498 G>T maps to NM_014269.4 E275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr4:175897857 C>T maps to NM_014269.4 I394I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr8:38880739 G>A maps to NM_003816.2 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr8:24254908 G>A maps to NM_014479.3 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr19:8670019 C>A maps to NM_030957.2 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr5:33630977 C>T maps to NM_030955.2 Q643Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr5:5303542 G>A maps to NM_139056.2 Q984Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MU-01A-11D-A377-08 chr5:128994428 A>G maps to NM_133638.3 A802A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr12:43777765 A>G maps to ENST00000389420 C1489C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67T-01A-11D-A30X-08 chr12:43944935 G>A maps to ENST00000389420 R77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87C-01A-11D-A34U-08 chr4:73186557 T>A maps to NM_014243.1 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A725-01A-12D-A32B-08 chr21:28338098 C>T maps to NM_007038.3 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr5:64629881 G>T maps to NM_197941.2 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr3:64554180 G>A maps to NM_182920.1 Q1463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FN-01A-11D-A34U-08 chr9:18504837 C>T maps to NM_001040272.4 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr21:46642108 C>A maps to NM_015833.3 P741P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8D0-01A-11D-A364-08 chr7:140373322 C>T maps to NM_052853.3 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr7:45744118 C>A maps to NM_021116.2 L907L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WN-01A-11D-A377-08 chr1:167871269 G>A maps to NM_018417.4 D92D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6333-01A-12D-1961-08 chr5:7626341 C>A maps to NM_020546.2 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr14:24799471 C>A maps to NM_139247.3 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8X3-01A-11D-A377-08 chr14:24791403 G>A maps to NM_139247.3 F818F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr12:49169814 C>T maps to NM_015270.3 G579G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr16:4163967 C>A maps to NM_001116.3 T492T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr4:2929961 C>A maps to NM_014189.2 P673P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr18:77896568 T>C maps to NM_014913.3 F1091F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65J-01A-11D-A30X-08 chr8:26628172 G>A maps to ENST00000356368 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HO-01A-11D-A364-08 chr8:26623612 A>G maps to NM_033304.2 H441H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr5:148206405 C>T maps to NM_000024.5 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr5:148207350 T>G maps to NM_000024.5 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr23:147733626 G>T did not map to a codon.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr2:100623892 C>G maps to NM_001025108.1 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QW-01A-11D-A377-08 chr18:12370899 T>C maps to NM_006796.2 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I8-01A-11D-A364-08 chr2:178386035 C>T maps to NM_003659.3 F579F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A878-01A-31D-A34U-08 chr2:178402826 A>G maps to NM_003659.3 L627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr1:970663 C>A maps to NM_198576.2 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7079-01A-11D-1961-08 chr9:88211350 G>T maps to ENST00000395847 L783L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr1:247014375 G>C maps to ENST00000428671 A1682A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7783-01A-11D-2114-08 chr1:27874813 C>T maps to NM_001029882.2 P1271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VT-01A-11D-A377-08 chr11:62284329 C>A maps to NM_001620.1 V5853V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr11:62289689 T>A maps to NM_001620.1 K4067*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr14:105418915 C>A maps to NM_138420.2 E958*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7211-01A-11D-2114-08 chr14:105420974 C>A maps to NM_138420.2 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr6:106969053 T>A maps to NM_001624.2 L916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7327-01A-11D-2114-08 chr1:159035789 A>T maps to NM_004833.1 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr7:6054934 C>A maps to NM_006303.3 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr6:131490306 A>G maps to ENST00000431975 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr7:91631336 A>G maps to NM_005751.4 L702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr7:91667794 A>G maps to NM_005751.4 G1467G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr6:109867180 C>A maps to NM_001145128.2 V1038V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7820-01A-11D-2114-08 chr1:19597013 G>T maps to NM_201252.3 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FA-01A-21D-A33T-08 chr19:40745987 G>A maps to NM_001626.3 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WL-01A-11D-A377-08 chr23:55039949 G>T did not map to a codon.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr19:49967983 C>A maps to NM_153329.3 P511P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7748-01A-11D-2114-08 chr15:101425524 A>C maps to NM_000693.2 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr9:38396791 G>A maps to NM_000692.3 G349G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7742-01A-11D-2114-08 chr3:125824674 G>A maps to ENST00000273450 V859V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CL-01A-11D-A34U-08 chr14:74537997 T>C maps to NM_005589.2 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr12:38712250 C>A maps to NM_001013620.3 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr9:101980872 G>A maps to NM_033087.3 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Y-01A-11D-A26M-08 chr14:78174326 G>A maps to NM_006020.2 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SH-01B-11D-A377-08 chr2:73717896 T>G maps to NM_015120.4 Y2936*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8468-01A-21D-2395-08 chr2:233323609 G>A maps to NM_001631.3 S447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7821-01A-12D-2114-08 chr18:56246186 C>T maps to NM_052947.3 Q607Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A48F-01A-11D-A257-08 chr15:85403129 T>G maps to NM_020778.4 P1565P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HK-01A-11D-A364-08 chr15:85402607 G>T maps to NM_020778.4 E1520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr1:21889688 G>T maps to NM_000478.4 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr2:233245441 C>A maps to NM_001632.3 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr2:233273011 C>A maps to NM_031313.2 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr3:46724744 C>A maps to NM_147129.3 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr1:110607210 G>A maps to NM_006492.2 Q198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:110603474 G>A maps to NM_006492.2 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6385-01A-11D-1786-08 chr4:71472191 C>A maps to NM_016519.4 G363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr16:56436912 C>A maps to NM_001144.4 G320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7212-01A-11D-2114-08 chr12:53819284 A>G maps to NM_020547.2 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8470-01A-11D-2395-08 chr12:47472524 C>T maps to NM_001143668.1 W87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr3:49755884 G>A maps to NM_198722.2 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WH-01A-11D-A377-08 chr23:112022740 T>C did not map to a codon.
Sequencing variant TCGA-V1-A8MF-01A-11D-A364-08 chr4:25393992 G>T maps to ENST00000510092 E247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr12:110815281 C>A maps to NM_016238.2 E459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A8O0-01A-41D-A377-08 chr8:6360775 C>T maps to NM_001147.2 W446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr20:861825 C>T maps to NM_015985.2 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88P-01A-11D-A34U-08 chr9:129870587 G>T maps to NM_012098.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr8:41572580 G>A maps to ENST00000415018 T538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr8:41559077 C>A maps to ENST00000415018 S817S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NF-01A-11D-A33T-08 chr4:114278435 A>T maps to NM_001148.4 K2888*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr4:114275161 C>T maps to NM_001148.4 D1796D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88L-01A-11D-A34U-08 chr4:114274942 A>G maps to NM_001148.4 A1723A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7785-01A-11D-2114-08 chr17:54558082 G>A maps to NM_153228.2 V668V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr5:14711383 C>T maps to NM_054027.4 G467G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr5:139887387 T>A maps to ENST00000253810 G1190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7F3-01A-21D-A33T-08 chr5:139905803 G>A maps to ENST00000253810 K1572K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr12:133311996 C>A maps to NM_015114.1 V565V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr4:74005374 T>G maps to NM_032217.3 G986G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-8200-01A-11D-A29Q-08 chr10:27381414 T>A maps to NM_014915.2 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr19:33113351 G>T maps to NM_032139.2 P601P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SA-01A-21D-A377-08 chr3:15736274 T>A maps to NM_015199.3 R548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr18:14757888 C>G maps to NM_001145029.1 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B4-01A-11D-A32B-08 chr12:56638933 C>T maps to NM_173595.3 P815P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr5:55472068 C>T maps to NM_024669.2 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr5:55422828 C>T maps to NM_024669.2 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr6:34985544 C>A maps to NM_015245.2 P573P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8470-01A-11D-2395-08 chr16:4780009 C>T maps to NM_133450.2 Q47Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr12:101493354 G>A did not map to a codon.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr11:22296149 C>A maps to NM_213599.2 P757P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr4:80954650 G>T maps to NM_001145794.1 Y257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QY-01A-11D-A377-08 chr10:46113585 G>C did not map to a codon.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr8:124705462 G>A maps to NM_001003954.1 R247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VT-01A-11D-A377-08 chr15:60641329 T>A maps to NM_001002858.2 K320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr17:41004622 C>G maps to NM_003734.2 A421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SB-01A-31D-A377-08 chr2:201499583 A>G maps to NM_001159.3 G764G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88L-01A-11D-A34U-08 chr14:24035555 C>T maps to NM_003917.2 E134E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr19:50302914 G>T maps to NM_014203.2 R388R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr15:83332551 C>A did not map to a codon.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr19:2114784 G>T maps to ENST00000355272 P795P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NH-01A-12D-A33T-08 chr9:72131100 C>T maps to NM_001163.3 K342K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FA-01A-21D-A33T-08 chr9:72131765 G>A maps to NM_001163.3 Q121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr10:26825130 C>A maps to NM_019043.3 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SB-01A-31D-A377-08 chr10:26785234 T>C maps to NM_019043.3 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr5:112154850 G>T maps to NM_001127510.2 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr5:112175855 T>G maps to NM_001127510.2 L1522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YJ-A8SW-01A-11D-A377-08 chr19:1465240 C>T maps to NM_005883.2 G647G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr3:49714354 C>A maps to ENST00000438011 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr11:43345104 A>C maps to NM_001142930.1 L223L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CH-5739-01A-11D-1576-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-VN-A88O-01A-11D-A34U-08 chr11:116692050 C>T maps to NM_000482.3 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MG-01A-11D-A364-08 chr2:21249773 A>G maps to NM_000384.2 F710F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr22:39421245 C>T maps to NM_152426.3 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87J-01A-11D-A34U-08 chr22:39439010 T>G maps to NM_145298.5 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E0-01A-11D-A30X-08 chr1:183617688 A>T maps to NM_203454.2 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7789-01A-11D-2114-08 chr19:45445566 G>T maps to NM_001646.1 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A48F-01A-11D-A257-08 chr22:36123053 C>T maps to NM_030642.1 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8468-01A-21D-2395-08 chr17:58529352 A>G maps to NM_006380.2 G464G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr17:58525051 G>A maps to NM_006380.2 Q550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A721-01A-12D-A32B-08 chr15:35207357 C>T maps to NM_014691.2 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr11:72420925 G>A maps to NM_001040118.2 Y504Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr4:36130283 T>G maps to NM_015230.2 R1171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A878-01A-31D-A34U-08 chr4:36130196 G>A maps to NM_015230.2 L1200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8S8-01A-11D-A377-08 chr1:228284841 C>T maps to NM_001024228.1 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6336-01A-11D-1786-08 chr11:110450381 C>T maps to NM_020809.2 R1096R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr1:161022537 T>C maps to NM_001025598.1 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr11:128844093 C>A maps to NM_001142685.1 E986*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr19:36278628 C>A maps to ENST00000007510 P1054P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr19:36278577 C>A maps to ENST00000007510 P1037P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SA-01A-21D-A377-08 chr23:130217749 T>A did not map to a codon.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr8:145773443 G>A maps to NM_025251.1 A342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A8O0-01A-41D-A377-08 chr14:32561296 A>G maps to NM_001030055.1 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr23:11204544 T>C did not map to a codon.
Multiple mappings detected for codon TCGA-G9-6377-01A-11D-1961-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr1:17958925 C>T maps to NM_018125.3 L565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8472-01A-11D-2395-08 chr17:8215725 G>A maps to NM_173728.3 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:16534047 G>A maps to NM_153213.3 N281N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr1:16534594 A>G maps to NM_153213.3 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8261-01A-11D-2260-08 chr23:62857908 C>T did not map to a codon.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr1:27106760 A>G maps to NM_006015.4 K2124K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr6:157150549 C>T maps to ENST00000367148 Q578*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A9DK-01A-11D-A377-08 chr6:157502128 G>A maps to ENST00000367148 G1094G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7744-01A-11D-2114-08 chr1:235338685 T>G maps to NM_016374.5 S1159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NF-01A-11D-A33T-08 chr17:79650771 C>G maps to NM_001040025.1 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7210-01A-11D-2114-08 chr2:235405079 T>A maps to ENST00000339728 K51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr6:109215668 G>T did not map to a codon.
Sequencing variant TCGA-YL-A8HL-01A-11D-A364-08 chr16:31476479 G>T maps to NM_024742.2 L712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr23:100911777 C>A did not map to a codon.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr23:100912073 G>T did not map to a codon.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr15:80866542 A>T maps to NM_014862.3 S457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr3:9845525 G>T did not map to a codon.
Sequencing variant TCGA-EJ-5505-01A-01D-1576-08 chr3:169486065 A>G maps to NM_032487.4 Y91Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87E-01A-31D-A34U-08 chr23:2838676 A>C did not map to a codon.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr23:2876455 A>G did not map to a codon.
Sequencing variant TCGA-VP-A872-01A-11D-A34U-08 chr23:2856152 G>A did not map to a codon.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr23:3002394 G>T did not map to a codon.
Sequencing variant TCGA-VP-A878-01A-31D-A34U-08 chr23:3002433 A>G did not map to a codon.
Sequencing variant TCGA-YL-A9WJ-01A-11D-A377-08 chr23:2990115 C>A did not map to a codon.
Sequencing variant TCGA-EJ-7331-01A-11D-2114-08 chr17:66364820 G>T maps to NM_014960.3 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr8:131249204 C>G maps to NM_018482.2 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A879-01A-11D-A34U-08 chr1:23782630 G>A maps to NM_017707.3 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E0-01A-11D-A30X-08 chr2:239353280 C>T maps to NM_001040445.1 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IB-01A-11D-A364-08 chr7:123269121 T>C maps to NM_080928.3 V358V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NM-01A-21D-A33T-08 chr12:48543214 G>A maps to NM_024095.3 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr22:30200814 C>A maps to NM_032204.3 E389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr6:101098515 T>C maps to NM_006828.2 V1050V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5505-01A-01D-1576-08 chr1:155451979 A>T maps to ENST00000368346 C227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FS-01A-11D-A34U-08 chr1:155429592 G>C maps to ENST00000368346 S1694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QW-01A-11D-A377-08 chr1:155348169 A>T maps to ENST00000368346 V2083V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr17:3379479 A>G maps to NM_000049.2 E9E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr1:197104364 G>C maps to NM_018136.4 P678P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A879-01A-11D-A34U-08 chr1:197111886 T>A maps to NM_018136.4 K499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CL-01A-11D-A34U-08 chr3:130743333 G>A maps to ENST00000514044 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr1:176984011 C>A did not map to a codon.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr20:31021260 C>T maps to ENST00000375687 A420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7510-01A-11D-2260-08 chr1:1389855 T>G maps to NM_001039211.2 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8258-01A-11D-2260-08 chr6:32083516 C>T maps to NM_004381.4 *704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr12:14628822 G>T did not map to a codon.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr14:96800091 G>A maps to NM_018036.5 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7328-01A-31D-2114-08 chr23:107396936 G>A did not map to a codon.
Sequencing variant TCGA-V1-A8WL-01A-11D-A377-08 chr11:108199782 T>C maps to NM_000051.3 S2375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SC-01A-11D-A377-08 chr11:108224577 C>G maps to NM_000051.3 G2919G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8S9-01A-11D-A377-08 chr15:25959330 T>G maps to NM_024490.3 R612R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr5:160114832 G>T maps to NM_025153.2 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7521-01A-11D-2260-08 chr5:160114976 T>C maps to NM_025153.2 K35K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr4:47527618 G>T maps to NM_020453.3 E246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr3:182586926 C>T maps to NM_014616.1 Q584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr3:194126842 C>T maps to NM_024524.3 E1162E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WW-A8ZI-01A-11D-A377-08 chr3:194146083 A>G maps to NM_024524.3 P1100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SR-01B-11D-A377-08 chr3:193183887 T>G maps to NM_032279.2 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr12:110765383 T>A maps to NM_170665.3 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr3:10443925 C>A maps to NM_001001331.2 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8CY-01A-11D-A364-08 chr3:130698120 G>T maps to NM_001001486.1 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr16:84473063 G>T maps to ENST00000416219 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr19:36046699 C>A maps to NM_000704.2 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr19:36046699 C>A maps to NM_000704.2 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6385-01A-11D-1786-08 chr12:57032139 T>C maps to NM_001686.3 K519K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr17:73035038 A>G maps to NM_006356.2 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-7775-01A-11D-2114-08 chr23:40457948 T>C did not map to a codon.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr7:138437473 G>A maps to NM_130840.2 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr1:44442866 G>C maps to NM_004047.3 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr8:87126082 C>A maps to NM_152565.1 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SC-01A-11D-A377-08 chr2:10915196 T>A maps to NM_001039362.1 Y275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr23:77254140 C>A did not map to a codon.
Sequencing variant TCGA-YL-A8SO-01B-31D-A377-08 chr23:77264644 G>A did not map to a codon.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr18:55319856 C>A maps to NM_005603.4 G1040G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr1:154317894 C>A maps to NM_020452.3 L889L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr15:50212486 C>A maps to NM_024837.2 E627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7788-01A-11D-2114-08 chr20:50244192 C>A maps to NM_006045.1 R597R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr3:142204016 A>T maps to NM_001184.3 G2062G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr23:76940432 A>C did not map to a codon.
Sequencing variant TCGA-VP-A878-01A-31D-A34U-08 chr23:76855226 C>A did not map to a codon.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr16:28847438 C>A maps to NM_148414.1 P1027P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr3:63898513 G>A maps to NM_001177387.1 E80E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7210-01A-11D-2114-08 chr7:70252228 C>A maps to NM_015570.2 P781P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FA-01A-21D-A33T-08 chr7:70228265 C>T maps to NM_015570.2 Q385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr7:32582772 C>A maps to NM_015060.1 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr12:63543827 A>G maps to NM_000706.3 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr23:69261785 T>C did not map to a codon.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr17:63553973 C>G maps to NM_004655.3 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr6:33246263 C>A maps to NM_003782.3 P356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr11:134253747 G>T maps to NM_054025.2 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YJ-A8SW-01A-11D-A377-08 chr11:373291 G>C did not map to a codon.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr6:90661074 G>A maps to NM_001170794.1 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IH-01A-11D-A364-08 chr8:143565393 G>A maps to NM_001702.2 E729E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr6:69703721 C>A maps to NM_001704.2 T599T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr6:69758170 C>T maps to NM_001704.2 N734N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7744-01A-11D-2114-08 chr6:69349085 T>G maps to NM_001704.2 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr22:38494423 G>A maps to NM_025045.4 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chr16:88061087 G>C did not map to a codon.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr2:215645850 G>A maps to NM_000465.2 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr14:35255347 C>T maps to NM_013448.2 W530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8266-01A-11D-2260-08 chr2:160289577 A>G maps to NM_013450.2 P530P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-8200-01A-11D-A29Q-08 chr11:27077077 T>A maps to NM_003986.2 L34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7210-01A-11D-2114-08 chr15:73029879 G>A maps to NM_033028.3 A504A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87D-01A-11D-A34U-08 chr1:156618649 C>T maps to NM_021948.3 R354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7218-01B-11D-A32B-08 chr1:115123931 A>C maps to NM_005872.2 Y58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr19:49299744 G>A maps to NM_001190.3 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr19:45262793 C>A maps to NM_005178.4 P429P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EJ-5518-01A-01D-1576-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr3:187451334 G>A maps to ENST00000449623 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr23:39914705 A>G did not map to a codon.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr23:129159053 C>A did not map to a codon.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr23:129146575 G>C did not map to a codon.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr23:129147471 G>C did not map to a codon.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr22:23524101 C>A maps to NM_004327.3 R319R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HO-01A-11D-A364-08 chr11:27679583 T>C maps to NM_001143810.1 Q258Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr11:61730038 C>A maps to NM_001139443.1 P411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr12:70072611 A>G maps to NM_032735.2 Y181Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr1:45253306 C>T maps to NM_153274.2 W24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E0-01A-11D-A30X-08 chr12:32369194 C>G maps to NM_001714.2 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IK-01A-11D-A364-08 chr15:91346838 G>A maps to NM_000057.2 L1149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A876-01A-11D-A34U-08 chr10:22615873 T>A maps to NM_005180.6 C56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76W-01A-11D-A33T-08 chr14:54417157 G>A maps to NM_130850.2 V273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr10:43288531 G>T maps to NM_014753.3 G343G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr23:15534240 G>T did not map to a codon.
Sequencing variant TCGA-VP-A87D-01A-11D-A34U-08 chr15:83935779 C>T maps to NM_001717.3 Q81Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MU-01A-11D-A377-08 chr1:151011473 G>A maps to NM_138278.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr4:13601500 G>A maps to NM_148894.2 S2341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr4:13616972 G>T maps to NM_148894.2 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr4:13604755 C>T maps to NM_148894.2 L1256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr7:140550012 C>A did not map to a codon.
Sequencing variant TCGA-J9-A8CL-01A-11D-A34U-08 chr22:50217770 G>A maps to ENST00000342989 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr16:50368806 C>A did not map to a codon.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr16:50402141 C>A maps to NM_001173984.2 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr2:28117447 C>T maps to NM_004899.3 R9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr6:36196699 C>A maps to NM_015695.2 R1101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr23:135572581 G>A did not map to a codon.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr21:40568277 C>A maps to NM_033656.2 T2239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr21:40630418 G>T maps to NM_018963.3 R689R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr23:79937585 C>A did not map to a codon.
Sequencing variant TCGA-YL-A8HJ-01A-11D-A364-08 chr23:79984394 C>A did not map to a codon.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr3:49692403 C>A maps to NM_003458.3 P1805P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr11:122850124 C>A maps to NM_001098169.1 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr11:13424826 T>A did not map to a codon.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr16:3640680 G>A maps to NM_032444.2 L986L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr14:93709032 A>T maps to NM_001002860.2 G995G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr3:15677017 C>A maps to NM_000060.2 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr23:100613414 C>A did not map to a codon.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr6:26407899 A>T maps to NM_007048.5 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr5:180432841 C>A maps to NM_197975.2 P457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A5OB-01A-11D-A29Q-08 chr15:40501920 G>A maps to ENST00000412359 L757L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IJ-01A-11D-A34U-08 chr6:41889338 G>A maps to NM_004053.3 Q13Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83I-01A-11D-A364-08 chr10:21804624 G>A maps to NM_207371.3 C709C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A9DI-01A-11D-A377-08 chr10:99968461 A>G maps to ENST00000314594 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr10:103649192 G>A maps to NM_024541.2 H612H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr10:134261402 C>A maps to NM_173541.2 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67T-01A-11D-A30X-08 chr10:134261456 C>G maps to NM_173541.2 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83M-01A-11D-A34U-08 chr11:76257109 T>C maps to ENST00000393457 T1182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr11:33564581 C>A maps to ENST00000389726 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr11:101946633 G>T maps to NM_032930.2 E156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7523-01A-11D-2260-08 chr11:63581247 G>A maps to NM_138471.1 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IK-01A-11D-A364-08 chr12:53693738 T>C did not map to a codon.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr12:107365135 C>A maps to NM_152261.2 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr12:82792602 C>A maps to NM_032230.2 Y187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I6-01A-11D-A364-08 chr12:82796856 T>C maps to NM_032230.2 S409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr12:32135814 C>T maps to NM_018169.3 G642G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SJ-01B-11D-A377-08 chr12:103700091 C>T maps to NM_001099336.1 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr12:97085089 T>A did not map to a codon.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr13:111973279 C>T maps to NM_152324.1 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8II-01A-11D-A364-08 chr13:31531141 A>T maps to NM_152325.1 R149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr13:44464252 T>C maps to NM_153218.2 I379I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SP-01B-11D-A377-08 chr13:31498490 A>T maps to NM_032849.3 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr14:81251837 G>A maps to NM_152446.3 Q538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr14:91647608 T>C maps to NM_001102368.1 C270C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A4JI-01A-11D-A257-08 chr14:24769364 C>T maps to NM_174913.1 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr15:40675137 T>C maps to NM_033286.3 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr15:81427610 G>T maps to ENST00000458088 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr15:83674444 C>A did not map to a codon.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr15:90129087 C>A maps to NM_152259.3 P442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7328-01A-31D-2114-08 chr15:65871952 C>G maps to ENST00000420799 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr15:34649646 C>T maps to ENST00000438749 D1136D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr15:44094001 T>G maps to NM_016400.3 *130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87K-01A-11D-A34U-08 chr16:67699023 C>A maps to NM_032140.1 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr16:2511085 C>A maps to NM_025108.2 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A875-01A-31D-A34U-08 chr16:2512432 C>T maps to NM_025108.2 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr16:58149202 G>C maps to NM_013242.2 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr16:30771663 G>T maps to NM_001014979.2 S137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr17:72949180 C>A maps to NM_030630.2 E658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SL-01B-21D-A377-08 chr17:10614355 C>G maps to NM_020233.4 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr17:79207798 C>T maps to NM_144679.2 K119K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr17:34191782 G>T maps to NM_152781.2 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr17:34185975 C>A maps to NM_152781.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7783-01A-11D-2114-08 chr17:8138501 A>C maps to NM_025099.5 R436R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr17:7160287 G>A maps to NM_203414.1 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B3-01A-11D-A33T-08 chr17:3716469 C>T maps to NM_001114118.1 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr18:34385448 C>A maps to NM_015476.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr18:43820010 C>A maps to NM_145055.3 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A879-01A-11D-A34U-08 chr1:22973819 G>A maps to NM_172369.3 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr12:7177942 C>T maps to NM_001734.3 P685P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:244724124 G>A maps to NM_001130957.1 E395E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr1:200880631 C>A maps to NM_018265.2 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr1:92709885 G>A maps to NM_001012425.1 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr1:75038905 C>A maps to NM_001002912.4 E830*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88L-01A-11D-A34U-08 chr1:75037028 C>T maps to NM_001002912.4 Q1455Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr1:55144481 C>A maps to ENST00000454855 P697P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr1:55280636 C>T maps to NM_001110533.1 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:154179946 T>A maps to NM_001098616.1 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr1:151020888 C>A maps to NM_017860.3 S189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr1:156702826 G>T maps to NM_015997.3 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr1:156704061 C>T maps to NM_015997.3 Q300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr1:43868960 C>A maps to ENST00000310739 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr1:156263001 T>C did not map to a codon.
Sequencing variant TCGA-G9-6333-01A-12D-1961-08 chr1:226784501 G>T did not map to a codon.
Sequencing variant TCGA-ZG-A8QZ-01A-11D-A377-08 chr20:55099932 T>G maps to NM_001012971.3 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I4-01A-11D-A364-08 chr20:20232250 T>C maps to ENST00000389655 N727N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7821-01A-12D-2114-08 chr20:56726067 T>G maps to NM_178456.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A725-01A-12D-A32B-08 chr21:33887451 C>T maps to NM_058187.3 N426N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65J-01A-11D-A30X-08 chr22:38340507 C>T maps to NM_032561.3 Q166Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr22:32794015 A>G maps to NM_014306.4 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr2:27804601 C>A maps to NM_032266.3 P1721P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr2:27804793 C>A maps to NM_032266.3 P1785P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B4-01A-11D-A32B-08 chr2:220038175 G>A maps to NM_015680.4 Q196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr2:26671661 T>C maps to NM_145038.2 C500C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr2:106690369 C>A maps to NM_032411.2 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr2:210993895 A>G maps to NM_152519.2 V363V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr2:29296095 G>T maps to NM_001029883.1 P344P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7523-01A-11D-2260-08 chr2:120078760 G>A maps to NM_001017927.2 N51N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr2:24406451 T>A maps to NM_001040710.1 C113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr3:119217640 C>A maps to NM_016589.3 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FE-01A-12D-A33T-08 chr3:49842263 G>A maps to NM_203370.1 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr3:192517392 G>T maps to NM_178496.3 Y86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr3:49313858 C>A did not map to a codon.
Sequencing variant TCGA-V1-A8WS-01A-11D-A377-08 chr4:100434270 G>A maps to NM_032149.2 Q11Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr4:99030363 T>C maps to NM_174952.2 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr9:123805396 C>T maps to NM_001735.2 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr19:47823990 C>A maps to ENST00000355085 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SU-A7E7-01A-22D-A33T-08 chr5:31534434 A>T maps to NM_018356.2 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr5:442820 C>A maps to NM_138464.2 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr5:131796341 C>A maps to NM_001013717.1 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VL-01A-21D-A377-08 chr5:41160289 G>T maps to NM_001115131.1 G546G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83K-01A-11D-A34U-08 chr5:41172405 T>A maps to NM_001115131.1 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr6:165715063 C>T maps to NM_144980.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr6:170102662 C>A maps to ENST00000439249 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7314-01A-31D-2114-08 chr6:47846329 G>A maps to NM_001013732.3 S750S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr6:118790442 T>G maps to NM_001042475.2 T682T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A879-01A-11D-A34U-08 chr6:118790274 C>T maps to NM_001042475.2 Q738Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8472-01A-11D-2395-08 chr6:170175419 G>T maps to NM_018341.1 E458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7821-01A-12D-2114-08 chr5:40958241 T>C maps to NM_000587.2 H456H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr7:86848786 G>A maps to NM_024315.2 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A876-01A-11D-A34U-08 chr7:39606041 T>C maps to NM_020192.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IG-01A-11D-A364-08 chr7:66413639 C>T maps to NM_017994.4 C185C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E0-01A-11D-A30X-08 chr7:120768458 A>C maps to NM_024913.4 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr7:112579784 G>A maps to NM_152556.2 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr8:69434116 C>A maps to NM_052958.2 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr8:67809085 C>A maps to NM_173518.4 P506P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr5:39311237 C>T did not map to a codon.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr9:35662652 A>G maps to NM_032818.2 D253D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr9:35043624 C>A maps to NM_203299.2 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr9:90501021 C>A maps to NM_178828.4 P540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr9:114468872 C>A maps to NM_173521.3 V840V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr9:15744746 A>G maps to NM_173550.2 G842G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8266-01A-11D-2260-08 chr9:136260869 C>G maps to NM_153710.3 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SK-01B-21D-A377-08 chr8:86163131 C>T maps to NM_198584.2 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr17:58236706 G>T maps to NM_000717.3 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SU-A7E7-01A-22D-A33T-08 chr8:61137093 A>C did not map to a codon.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr1:227153069 C>T maps to NM_020247.4 Q183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FU-01A-11D-A364-08 chr22:24530348 C>G maps to NM_012295.3 L1571L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6366-01A-11D-2114-08 chr22:24460517 G>A maps to NM_012295.3 L635L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr1:65142589 C>T maps to ENST00000371073 C996C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr19:13414689 C>A maps to NM_023035.2 T666T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr12:2764405 T>G did not map to a codon.
Sequencing variant TCGA-KK-A7AP-01A-12D-A33T-08 chr12:2676867 G>A maps to NM_199460.2 L601L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88N-01A-11D-A364-08 chr12:2566834 C>T maps to NM_199460.2 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IA-01A-11D-A364-08 chr3:53809969 C>T maps to NM_001128840.1 L1420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr1:181727099 C>T maps to ENST00000357570 F1449F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A875-01A-31D-A34U-08 chr1:201046059 G>A maps to NM_000069.2 I605I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A875-01A-31D-A34U-08 chr1:201046221 G>A maps to NM_000069.2 S551S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8D0-01A-11D-A364-08 chr7:81667506 G>A maps to NM_000722.2 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7328-01A-31D-2114-08 chr12:2022194 C>T maps to NM_172364.4 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76W-01A-11D-A33T-08 chr17:37341090 C>G maps to NM_000723.3 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6366-01A-11D-2114-08 chr2:152732967 C>A maps to NM_000726.3 E165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr22:36960763 G>A maps to NM_006078.3 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr17:65021030 G>T maps to NM_014405.3 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr17:64873578 C>A maps to NM_014404.1 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A4JI-01A-11D-A257-08 chr19:54444868 G>A maps to NM_031896.4 E190E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8ML-01A-11D-A377-08 chr2:27445188 A>G maps to NM_004341.3 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8258-01A-11D-2260-08 chr11:115047193 C>A maps to NM_014333.3 *443Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8213-01A-11D-A29Q-08 chr3:62535599 C>G maps to ENST00000383709 L648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr3:62570915 A>G maps to ENST00000383709 D507D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WH-01A-11D-A377-08 chr7:122111517 C>G maps to NM_001167940.1 L699L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr7:93065362 G>T maps to NM_001164737.1 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr1:7723411 G>T did not map to a codon.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr12:67700300 T>C maps to NM_018448.3 V951V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7315-01A-31D-2114-08 chr2:30961159 C>T did not map to a codon.
Sequencing variant TCGA-KK-A7AU-01A-11D-A32B-08 chr15:42681284 C>T maps to NM_000070.2 C264C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr23:110494931 C>A did not map to a codon.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr11:104971435 C>A maps to NM_001007232.1 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I6-01A-11D-A364-08 chr11:65793292 G>A maps to NM_053054.3 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88L-01A-11D-A34U-08 chr11:65789324 G>A maps to NM_053054.3 S485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr14:92102830 G>T maps to NM_024764.2 P560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr19:38858383 C>T maps to NM_021185.4 D966D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7079-01A-11D-1961-08 chr14:24897521 C>A maps to NM_001039771.2 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr17:77808662 C>A maps to NM_003655.2 G260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6329-01A-13D-1961-08 chr17:77809098 C>T maps to NM_003655.2 K114K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr12:54639978 C>A maps to NM_012117.2 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr10:97791668 C>A maps to NM_001159747.1 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr3:42906719 C>A maps to NM_001296.4 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr16:28602972 C>A maps to NM_138414.2 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XA-A8JR-01A-11D-A364-08 chr4:186392097 C>G did not map to a codon.
Sequencing variant TCGA-EJ-A7NM-01A-21D-A33T-08 chr19:48801472 C>T maps to NM_144577.3 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr2:131096731 G>C maps to NM_032357.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59X-01A-11D-A29Q-08 chr16:57738846 C>T maps to NM_032269.5 D253D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-7775-01A-11D-2114-08 chr2:179702243 C>A maps to NM_173648.3 V1234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83M-01A-11D-A34U-08 chr7:76885703 G>T maps to NM_020879.2 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr11:124857793 C>T maps to NM_025004.2 Q558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr19:11531588 C>A maps to NM_145045.4 E568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:159860403 G>C maps to NM_012337.2 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr3:49294495 C>A maps to NM_178173.3 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr12:94763728 T>C maps to NM_001042399.1 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr10:32833173 G>T did not map to a codon.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr3:49201176 C>A maps to NM_022903.3 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr19:47773662 G>A did not map to a codon.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr6:31124677 G>T maps to NM_001105564.1 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr4:26491106 C>A did not map to a codon.
Sequencing variant TCGA-G9-7523-01A-11D-2260-08 chr17:34641447 A>G did not map to a codon.
Sequencing variant TCGA-YL-A8SO-01B-31D-A377-08 chr13:37014262 T>C maps to NM_003914.3 F347F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr5:68470882 T>C maps to NM_031966.2 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr5:162868106 T>A maps to NM_199246.1 C96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr5:159680552 G>A maps to NM_024565.5 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr1:1333665 G>A maps to NM_030937.4 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr10:35854949 G>T did not map to a codon.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr3:45942585 C>T maps to NM_031200.2 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7744-01A-11D-2114-08 chr12:69986784 T>C maps to NM_006431.2 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr5:140011611 G>T maps to NM_001174105.1 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8CY-01A-11D-A364-08 chr12:7653873 G>A maps to NM_004244.4 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7519-01A-11D-2260-08 chr1:158226846 C>T maps to NM_001763.2 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VL-01A-21D-A377-08 chr1:158262072 A>T maps to NM_001765.2 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I9-01A-11D-A364-08 chr1:158151248 G>A maps to NM_001766.3 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HJ-01A-11D-A364-08 chr3:112546089 T>C did not map to a codon.
Sequencing variant TCGA-VP-A87D-01A-11D-A34U-08 chr19:35831814 A>G maps to NM_001771.3 Q427Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5515-01A-01D-1576-08 chr11:66082755 C>T maps to NM_020404.2 Q581Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7075-01A-11D-1961-08 chr11:118223126 G>A maps to NM_000073.2 K164K. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CH-5739-01A-11D-1576-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-V1-A8MF-01A-11D-A364-08 chr1:157805767 A>T maps to NM_005894.2 L78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr11:60785402 C>A maps to NM_006725.3 P585P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XA-A8JR-01A-11D-A364-08 chr12:56120994 G>A maps to NM_001780.4 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A721-01A-12D-A32B-08 chr17:7484693 A>T did not map to a codon.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr11:44626915 C>T maps to NM_002231.3 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7078-01A-11D-2114-08 chr3:121828208 A>T maps to NM_175862.3 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76X-01A-11D-A33T-08 chr13:115016140 G>A maps to NM_003903.3 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A878-01A-31D-A34U-08 chr1:43828700 G>A maps to NM_001255.2 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr22:19504129 G>T maps to NM_001178010.1 V539V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr8:25327467 C>A maps to ENST00000434814 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr8:25341515 A>C maps to ENST00000434814 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr5:21755849 G>A maps to NM_004061.3 Q579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr16:83704516 G>C maps to ENST00000268613 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr8:95183128 C>A maps to NM_001144663.1 G290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HL-01A-11D-A364-08 chr18:59166541 C>T maps to NM_031891.2 R124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr10:73472476 C>A maps to ENST00000398860 V1097V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr10:73468897 C>T maps to ENST00000398860 A1055A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr14:23522820 C>T maps to NM_022478.3 E370E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr16:66426284 G>T maps to NM_001795.3 G406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr16:66436960 C>A maps to NM_001795.3 T748T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr16:66426124 C>A maps to NM_001795.3 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr5:31323129 C>A maps to NM_004932.2 A696A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr1:1572562 C>A maps to ENST00000401097 G522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr17:37686905 C>A maps to NM_016507.2 P1270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr17:37627428 C>A maps to NM_016507.2 P448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr17:37627876 C>T maps to NM_016507.2 Q598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr17:37676289 A>G maps to NM_016507.2 L1015L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr7:40085625 T>C did not map to a codon.
Sequencing variant TCGA-HC-8261-01A-11D-2260-08 chr6:110944513 A>T maps to NM_015076.3 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87K-01A-11D-A34U-08 chr9:90585481 C>G did not map to a codon.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr7:150754242 G>C maps to NM_004935.3 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6361-01A-21D-1961-08 chr17:46048773 G>T did not map to a codon.
Sequencing variant TCGA-WW-A8ZI-01A-11D-A377-08 chr17:46054118 G>A maps to NM_176096.1 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87J-01A-11D-A34U-08 chr12:12871203 T>G maps to NM_004064.3 L144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr23:139866375 C>A did not map to a codon.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr19:42312920 G>A maps to NM_001815.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7788-01A-11D-2114-08 chr14:23587879 G>A maps to NM_001805.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A632-01A-11D-A29Q-08 chr1:109801498 C>T maps to NM_001408.2 S1252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr4:104041394 C>T maps to NM_001813.2 V2413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr1:214819711 G>T maps to NM_016343.3 E2267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VO-01A-11D-A377-08 chr4:56886919 G>A maps to NM_025009.3 R1098R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VV-01A-11D-A377-08 chr15:49059644 A>C maps to NM_001194998.1 Y678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8264-01B-11D-2395-08 chr11:117241959 T>C maps to NM_014956.4 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88R-01A-11D-A364-08 chr1:243362461 A>G maps to NM_014812.2 Y177Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr20:34092574 C>A maps to NM_007186.3 P2126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr2:65299087 C>A maps to NM_015147.2 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr18:12699202 C>A did not map to a codon.
Sequencing variant TCGA-HC-8213-01A-11D-A29Q-08 chr1:196711059 G>A maps to NM_000186.3 K1004K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y6-A8TL-01A-21D-A377-08 chr1:196928039 G>T maps to ENST00000367421 E215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr10:75542177 C>A maps to NM_203298.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A9DK-01A-11D-A377-08 chr3:126445988 C>A maps to ENST00000508789 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr5:98192173 C>T maps to NM_001270.2 Q1681Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IB-01A-11D-A364-08 chr5:98216806 T>G maps to NM_001270.2 V1011V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr1:146765329 T>C maps to NM_004284.3 N810N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7212-01A-11D-2114-08 chr17:7806621 C>T maps to NM_001005271.2 A1235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52B-01A-11D-A26M-08 chr17:7811745 G>T maps to NM_001005271.2 E1786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr12:6686949 C>T did not map to a codon.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr20:40052147 G>T maps to NM_032221.3 P1513P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr20:40161770 G>T maps to NM_032221.3 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr8:61654707 C>A maps to NM_017780.2 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A9DI-01A-11D-A377-08 chr8:61655593 C>T maps to NM_017780.2 Q535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr14:21871247 A>G maps to NM_001170629.1 L1214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8261-01A-11D-2260-08 chr14:21860704 T>A maps to NM_001170629.1 R2244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VT-01A-11D-A377-08 chr16:53190609 T>A maps to ENST00000219084 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr16:53190624 C>T maps to ENST00000219084 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr12:133428222 C>T maps to NM_001161344.1 P503P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8261-01A-11D-2260-08 chr14:93399079 C>T maps to NM_001275.3 R392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr3:367693 C>A maps to NM_006614.2 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NF-01A-11D-A33T-08 chr3:419626 T>C did not map to a codon.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr3:401997 C>A maps to NM_006614.2 P399P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr3:184102329 G>T maps to NM_003741.2 V482V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8ID-01A-11D-A364-08 chr23:109963153 C>T did not map to a codon.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr11:74421956 G>T maps to NM_015424.3 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr8:42611139 G>T maps to NM_004198.3 S401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr15:40764281 C>A maps to NM_130468.3 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7315-01A-31D-2114-08 chr3:142840956 C>G maps to NM_004267.3 V433V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr5:129520760 A>G maps to NM_175856.4 E642E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr5:129241301 C>A maps to NM_175856.4 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NG-01A-31D-A33T-08 chr10:101960456 T>C maps to NM_001278.3 G550G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr15:65502036 C>A maps to NM_003613.3 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr19:1271164 C>T maps to ENST00000413636 Q44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XA-A8JR-01A-11D-A364-08 chr16:69194304 T>C maps to NM_032830.2 N497N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr12:120166399 C>A maps to ENST00000392521 L1166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IH-01A-11D-A364-08 chr12:120214535 A>C maps to ENST00000392521 S592S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YJ-A8SW-01A-11D-A377-08 chr2:113514461 A>G maps to NM_152515.3 C162C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8264-01B-11D-2395-08 chr11:46772925 T>C maps to ENST00000415402 L1764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr1:86916414 C>T maps to NM_006536.5 N718N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I6-01A-11D-A364-08 chr1:86898057 A>G maps to NM_006536.5 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7791-01A-11D-2114-08 chr7:143013472 C>A maps to NM_000083.2 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr4:170613386 C>A maps to NM_173872.2 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7792-01A-11D-2114-08 chr23:10176201 G>A did not map to a codon.
Sequencing variant TCGA-J9-A8CK-01A-11D-A34U-08 chr23:49689924 G>T did not map to a codon.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr1:11889285 C>A maps to ENST00000376496 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr12:122825727 C>A maps to ENST00000302528 E675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6499-01A-12D-1961-08 chr1:155240636 C>T maps to ENST00000368361 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr15:74911651 C>A maps to NM_001130028.1 R187R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CP-01A-11D-A34U-08 chr4:56304466 T>G maps to NM_004898.2 P781P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CH-5739-01A-11D-1576-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr12:7295772 C>A maps to NM_014718.3 P571P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr12:7293960 C>A maps to NM_014718.3 R483R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr22:19198012 T>C maps to NM_007098.3 L1024L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr6:123319156 C>A maps to NM_001010852.2 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6361-01A-21D-1961-08 chr13:100518572 C>A maps to NM_206808.2 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IF-01A-11D-A364-08 chr16:81735395 G>A maps to NM_198390.2 L629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr16:66600559 C>T maps to NM_052999.3 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr5:79029069 A>G maps to NM_153610.3 K1494K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr5:79034559 C>A maps to NM_153610.3 P3324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7748-01A-11D-2114-08 chr4:47938767 G>C maps to NM_001142564.1 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr23:150909340 C>A did not map to a codon.
Sequencing variant TCGA-VP-A87B-01A-11D-A34U-08 chr16:58633153 G>A maps to NM_016284.3 Q30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7797-01A-11D-2260-08 chr3:32800948 G>C did not map to a codon.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr7:135106937 A>C maps to NM_001190850.1 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6366-01A-11D-2114-08 chr1:246810984 A>G maps to NM_152609.2 G494G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr19:40730406 G>A maps to NM_024877.3 C167C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8470-01A-11D-2395-08 chr12:41316216 C>A maps to NM_001843.2 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SP-01B-11D-A377-08 chr1:205033528 C>T maps to NM_005076.3 C440C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr3:74414718 C>A maps to NM_020872.1 E361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr3:2613234 C>A maps to NM_175607.1 C16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FU-01A-11D-A364-08 chr3:2944669 C>T maps to NM_175607.1 N396N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-8200-01A-11D-A29Q-08 chr3:1394065 G>T maps to NM_014461.2 G475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr17:40843414 G>T maps to NM_003632.2 G744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6M7-01A-11D-A31L-08 chr17:40843293 C>T maps to NM_003632.2 D733D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr2:125521375 C>T maps to NM_130773.2 R787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-8198-01A-11D-2260-08 chr2:125547650 G>A maps to NM_130773.2 V974V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SK-01B-21D-A377-08 chr2:125547509 A>G maps to NM_130773.2 L927L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr17:7852465 C>A maps to NM_001037144.4 P881P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SU-A7E7-01A-22D-A33T-08 chr17:7852809 G>T maps to NM_001037144.4 R920R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87J-01A-11D-A34U-08 chr17:7836489 G>T maps to NM_001037144.4 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7742-01A-11D-2114-08 chr17:40717504 G>T maps to NM_001042532.2 V497V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B4-01A-11D-A32B-08 chr17:71193479 G>T maps to NM_018714.2 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr1:230824181 C>A maps to NM_007357.2 S556S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A875-01A-31D-A34U-08 chr13:46050412 A>G maps to NM_031431.2 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr16:23417459 A>G maps to NM_153603.3 N533N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr6:116446571 G>T maps to NM_000493.3 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr1:103462680 C>A did not map to a codon.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr1:103385905 G>T maps to NM_080629.2 P1253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AV-01A-11D-A32B-08 chr1:103400615 A>T maps to NM_080629.2 A1176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XA-A8JR-01A-11D-A364-08 chr6:75884865 G>A maps to ENST00000322507 T866T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A876-01A-11D-A34U-08 chr8:121237424 A>T maps to NM_021110.1 S612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr10:105798242 G>A maps to NM_000494.3 P997P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr10:105815720 C>A maps to NM_000494.3 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88R-01A-11D-A364-08 chr10:105832988 T>A maps to NM_000494.3 R132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr7:94037157 G>A did not map to a codon.
Sequencing variant TCGA-EJ-7314-01A-31D-2114-08 chr1:86488274 C>A did not map to a codon.
Sequencing variant TCGA-J4-A67T-01A-11D-A30X-08 chr4:109767342 G>A maps to ENST00000333642 D489D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr9:116968049 A>G maps to NM_032888.2 G727G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr9:117052372 A>G maps to NM_032888.2 P1414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr2:189874961 T>C maps to NM_000090.3 C1294C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr2:189875580 A>T maps to NM_000090.3 K1407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr13:111156529 G>T maps to NM_001846.2 G1441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr2:228155517 C>A maps to NM_000091.4 G1042G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7318-01B-11D-A32B-08 chr19:10096992 T>A maps to NM_015719.3 K784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6333-01A-12D-1961-08 chr21:47423617 C>T maps to NM_001848.2 F926F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr2:238266525 C>A did not map to a codon.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr2:238274667 C>A maps to NM_004369.3 L1837L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr2:238266525 C>A did not map to a codon.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr3:130284216 C>T maps to NM_001102608.1 N347N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr2:3691605 C>T maps to ENST00000418971 D252D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chr19:18898324 C>G maps to NM_000095.2 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr1:160275313 C>A maps to NM_001098398.1 E535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr7:99686976 C>G maps to NM_006833.4 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7523-01A-11D-2260-08 chr7:99688237 C>T maps to NM_006833.4 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y6-A8TL-01A-21D-A377-08 chr12:120966915 C>T maps to NM_032314.3 W10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NH-01A-12D-A33T-08 chr6:75950897 C>T maps to NM_001865.3 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr3:148896262 A>G maps to NM_000096.3 S939S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr3:148924001 G>T maps to NM_000096.3 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8D1-01A-11D-A364-08 chr3:148903045 C>T maps to NM_000096.3 L755L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QY-01A-11D-A377-08 chr3:148916152 C>G did not map to a codon.
Sequencing variant TCGA-VP-A875-01A-31D-A34U-08 chr10:101802207 C>T maps to NM_001308.2 R451R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr8:87549806 C>A maps to NM_003909.3 S159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr6:36767796 G>T maps to NM_020939.1 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr2:211454903 G>A maps to NM_001122633.1 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr2:211421555 A>G maps to NM_001122633.1 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76X-01A-11D-A33T-08 chr2:211542609 G>A did not map to a codon.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr14:92608696 T>C did not map to a codon.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr2:9595848 C>G maps to NM_016207.2 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7075-01A-11D-1961-08 chr10:125528212 C>A maps to NM_198148.2 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr16:1718166 G>T maps to NM_020825.3 E1103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A721-01A-12D-A32B-08 chr9:131860405 G>A maps to NM_000755.3 A450A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr1:197313414 A>G maps to NM_201253.2 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7791-01A-11D-2114-08 chr7:28527794 T>C maps to NM_182898.2 I2I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr16:3786755 A>G maps to NM_004380.2 H1485H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8D0-01A-11D-A364-08 chr4:1389213 C>T maps to NM_175918.3 C305C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr6:49704220 C>A did not map to a codon.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr1:152382840 G>T maps to NM_016190.2 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr22:25627720 C>T maps to NM_000496.2 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr3:97662112 C>A maps to ENST00000182096 P1008P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr12:53567191 G>A maps to NM_015989.4 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr20:47692014 C>T maps to NM_001316.2 I431I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr1:110466550 C>A maps to NM_000757.4 P436P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr23:1407463 G>T did not map to a codon.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr17:38172079 A>G maps to NM_000759.3 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr10:43678848 C>A maps to NM_018590.3 P496P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr8:2910128 T>A maps to NM_033225.5 S2505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A6RC-01A-11D-A32B-08 chr8:3263666 C>T maps to NM_033225.5 G716G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr8:2806883 C>A maps to NM_033225.5 G3447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6DY-01A-12D-A30X-08 chr8:2832108 G>A maps to NM_033225.5 A2868A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y6-A8TL-01A-21D-A377-08 chr8:2886874 C>T maps to NM_033225.5 T2607T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr8:113657356 A>T maps to NM_198123.1 V1097V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr8:113277664 C>T maps to NM_198123.1 W3221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A725-01A-12D-A32B-08 chr8:113358323 A>G did not map to a codon.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr4:70798272 C>A did not map to a codon.
Sequencing variant TCGA-YL-A8SL-01B-21D-A377-08 chr15:64464143 G>A maps to NM_022048.3 Q419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83N-01A-11D-A34U-08 chr8:68087550 C>T maps to ENST00000389042 L1027L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NK-01A-12D-A34U-08 chr3:39185626 C>T did not map to a codon.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr1:201453912 A>G maps to NM_001193572.1 C170C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr20:18142698 A>G maps to NM_020536.4 K306K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr23:134948024 G>T did not map to a codon.
Sequencing variant TCGA-EJ-A65G-01A-21D-A29Q-08 chr23:120008935 G>A did not map to a codon.
Sequencing variant TCGA-VN-A88P-01A-11D-A34U-08 chr23:120009179 G>A did not map to a codon.
Sequencing variant TCGA-YL-A8SA-01A-21D-A377-08 chr14:39769117 A>G maps to ENST00000396158 K246K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8S8-01A-11D-A377-08 chr6:132032075 C>A maps to NM_001145659.1 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr20:56099192 C>T maps to ENST00000423479 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I9-01A-11D-A364-08 chr20:56099165 T>C maps to ENST00000423479 K32K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7079-01A-11D-1961-08 chr10:68526132 C>A maps to NM_013266.2 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QZ-01A-11D-A377-08 chr9:111734981 G>C maps to NM_003798.2 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7075-01A-11D-1961-08 chr23:16720990 G>T did not map to a codon.
Sequencing variant TCGA-KK-A6E1-01A-11D-A30X-08 chr14:25043657 C>A maps to NM_001911.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr10:17032434 C>T maps to NM_001081.3 E1416E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QW-01A-11D-A377-08 chr13:113899532 C>T maps to NM_001008895.1 I504I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr6:43188276 C>A maps to ENST00000354495 P2121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr6:43166473 C>A maps to ENST00000354495 P977P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr6:43174216 C>A maps to ENST00000354495 A1727A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65G-01A-21D-A29Q-08 chr10:101503042 T>A maps to NM_015960.2 Y109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr4:48994015 T>C maps to NM_025087.2 Y140Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TB-01A-11D-A364-08 chr4:74735479 C>T maps to NM_001511.2 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr2:237489566 C>A maps to NM_020311.2 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr5:139060932 C>A maps to NM_016463.7 C275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65J-01A-11D-A30X-08 chr23:19984248 G>A did not map to a codon.
Sequencing variant TCGA-V1-A8WS-01A-11D-A377-08 chr23:40506742 G>A did not map to a codon.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr23:23934358 T>C did not map to a codon.
Sequencing variant TCGA-YL-A8HJ-01A-11D-A364-08 chr23:36103578 T>C did not map to a codon.
Alternatively spliced codon TCGA-EJ-7125-01A-11D-1961-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-J4-A6G3-01A-11D-A30X-08 chr11:61118522 G>A maps to NM_001161454.1 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65E-01A-11D-A29Q-08 chr23:37660565 T>A did not map to a codon.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr8:145150821 G>A maps to NM_001916.3 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7078-01A-11D-2114-08 chr15:22945110 G>A maps to NM_014608.2 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7510-01A-11D-2260-08 chr8:143995678 C>T did not map to a codon.
Sequencing variant TCGA-EJ-7788-01A-11D-2114-08 chr20:52779273 C>T maps to NM_000782.4 Q324Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7788-01A-11D-2114-08 chr20:52779276 G>T maps to NM_000782.4 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr2:219677401 C>A maps to NM_000784.3 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87H-01A-11D-A34U-08 chr2:219677082 G>A maps to NM_000784.3 E195E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr19:41386417 C>A maps to NM_000764.2 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8472-01A-11D-2395-08 chr10:96827285 C>A maps to NM_000770.3 G111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6333-01A-12D-1961-08 chr10:96741066 C>A maps to NM_000771.3 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HO-01A-11D-A364-08 chr22:42525128 G>T maps to NM_000106.4 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr19:16040399 C>A maps to NM_021187.3 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr19:15662135 G>T maps to NM_173483.3 E484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83I-01A-11D-A364-08 chr19:15763395 G>A maps to NM_000896.2 K312K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr1:47514235 G>T did not map to a codon.
Sequencing variant TCGA-XJ-A9DI-01A-11D-A377-08 chr8:59412636 A>T maps to NM_000780.3 I7I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WN-01A-11D-A377-08 chr23:77529209 C>A did not map to a codon.
Sequencing variant TCGA-SU-A7E7-01A-22D-A33T-08 chr17:20109179 A>G maps to NM_001033553.1 L606L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88R-01A-11D-A364-08 chr14:59797407 T>C did not map to a codon.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr6:39828786 G>A maps to ENST00000398904 K84K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A8O0-01A-41D-A377-08 chr6:39869130 C>T maps to ENST00000398904 D955D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7075-01A-11D-1961-08 chr23:86068205 G>A did not map to a codon.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr23:85769328 A>G did not map to a codon.
Sequencing variant TCGA-2A-A8VT-01A-11D-A377-08 chr11:61110227 C>A maps to NM_015533.3 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr11:61111397 G>A maps to NM_015533.3 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7788-01A-11D-2114-08 chr9:90252884 C>T maps to NM_004938.2 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MG-01A-11D-A364-08 chr19:3964646 G>T maps to NM_001348.1 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr1:159176131 C>A maps to NM_001122951.2 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88P-01A-11D-A34U-08 chr9:121930372 G>A maps to NM_014618.2 P425P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WH-01A-11D-A377-08 chr11:20178065 G>A maps to ENST00000227256 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88L-01A-11D-A34U-08 chr9:37801315 C>G maps to NM_024345.3 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7218-01B-11D-A32B-08 chr23:125685211 G>A did not map to a codon.
Sequencing variant TCGA-J9-A52B-01A-11D-A26M-08 chr23:125685924 C>G did not map to a codon.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr4:17805632 G>T maps to NM_017741.3 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QZ-01A-11D-A377-08 chr14:73418523 C>T maps to NM_015604.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7213-01A-11D-2114-08 chr23:27766320 C>A did not map to a codon.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr3:98519474 A>C maps to ENST00000326857 V616V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr18:50848420 G>T maps to NM_005215.3 L686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SC-01A-11D-A377-08 chr1:32674909 G>A maps to NM_001099434.1 K72K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr4:155253864 G>A maps to NM_017639.3 P666P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr10:115609162 G>T maps to NM_014881.3 P567P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr5:112337353 C>A maps to NM_152624.4 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr7:50595941 C>A maps to NM_000790.3 G203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr7:50611678 G>T maps to NM_000790.3 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr10:74034534 G>A maps to NM_019058.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr2:15753346 G>T did not map to a codon.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr2:118577354 C>A maps to NM_006773.3 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr23:134709031 G>A did not map to a codon.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr20:47845306 C>T maps to NM_017895.7 R285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83I-01A-11D-A364-08 chr5:134152275 T>C maps to ENST00000452510 L865L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr10:70666555 C>A maps to NM_024045.1 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A721-01A-12D-A32B-08 chr23:23018290 G>T did not map to a codon.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr7:44612249 G>T maps to NM_019082.2 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8II-01A-11D-A364-08 chr7:44611158 T>C maps to NM_019082.2 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr9:32467790 C>A maps to NM_014314.3 V718V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr4:169227601 T>C maps to NM_017631.5 Q178Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr8:91029479 G>T maps to NM_001359.1 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B3-01A-11D-A33T-08 chr16:90027429 G>C maps to NM_207514.1 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr7:140223197 G>T maps to NM_015689.3 P858P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr1:68947727 C>A did not map to a codon.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr7:24758793 C>A maps to NM_001127453.1 G150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr2:234371287 G>T did not map to a codon.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr7:137082143 A>T maps to NM_004717.2 L987*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr2:74177855 C>A maps to NM_080916.1 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IL-01A-11D-A364-08 chr2:74154093 C>T maps to NM_080916.1 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr11:71153384 C>A maps to NM_001360.2 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8ID-01A-11D-A364-08 chr19:12790631 C>A maps to NM_001930.2 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr23:2184931 C>T did not map to a codon.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr10:127525311 C>A maps to NM_018180.2 E726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr20:37634886 C>A maps to NM_021931.3 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr16:72130067 C>T maps to NM_014003.3 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr16:72130759 G>T maps to NM_014003.3 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr14:95557423 G>T maps to NM_177438.2 P1850P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr20:61525241 G>A maps to NM_033081.2 T959T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr20:61511006 C>A maps to NM_033081.2 E2101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr20:61513278 G>T maps to NM_033081.2 P1343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr1:54360026 G>T maps to NM_000792.5 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TB-01A-11D-A364-08 chr14:102027946 C>T maps to NM_001362.3 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IL-01A-11D-A364-08 chr21:47961678 C>T maps to ENST00000318711 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8S8-01A-11D-A377-08 chr21:47987297 G>A maps to ENST00000318711 W1494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr12:51089054 A>T maps to NM_173602.2 V575V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr12:51054040 C>A maps to NM_173602.2 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7210-01A-11D-2114-08 chr10:408504 G>A maps to NM_014974.2 L907L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7737-01A-11D-2114-08 chr2:189599334 A>G maps to NM_052952.2 *105Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr1:231830154 T>C maps to NM_001164537.1 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5515-01A-01D-1576-08 chr23:153994550 G>C did not map to a codon.
Sequencing variant TCGA-XJ-A83H-01A-11D-A34U-08 chr10:54076404 C>A maps to NM_012242.2 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr3:38135138 T>C maps to NM_007335.2 G600G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr3:38139332 G>A maps to NM_007335.2 Q888Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7788-01A-11D-2114-08 chr11:83243768 T>C maps to NM_001142699.1 G725G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr17:7106237 G>T maps to NM_001365.3 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SK-01B-21D-A377-08 chr10:79571812 G>A maps to NM_004747.3 F1397F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr8:1616603 C>T maps to ENST00000357934 D582D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr1:44680395 C>A maps to NM_019100.4 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr23:32380925 T>C did not map to a codon.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr23:32536159 C>T did not map to a codon.
Sequencing variant TCGA-HC-8264-01B-11D-2395-08 chr23:31986567 C>G did not map to a codon.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr1:50885065 C>T maps to NM_032110.1 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr15:51750825 T>C did not map to a codon.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr15:51855613 C>T maps to NM_001174116.1 W177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr10:70191660 C>A maps to NM_001080449.1 V733V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MF-01A-11D-A364-08 chr10:70231684 G>A maps to NM_001080449.1 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WH-01A-11D-A377-08 chr10:70196775 T>C maps to NM_001080449.1 L632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7521-01A-11D-2260-08 chr3:52412684 C>A maps to ENST00000273600 T2422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr12:124395092 G>A maps to NM_207437.3 K3218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr3:57488128 C>T maps to NM_178504.4 V388V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr17:76496389 G>T maps to ENST00000389840 Y1865*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr17:7673933 G>A maps to NM_020877.2 K1386K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr17:7696465 C>A maps to NM_020877.2 L2504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NG-01A-31D-A33T-08 chr17:7734508 C>T maps to NM_020877.2 G4112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr17:7680785 C>G maps to NM_020877.2 S1694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8470-01A-11D-2395-08 chr16:20952768 C>A maps to NM_017539.1 E3870*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr5:13735946 T>C maps to NM_001369.2 L3850L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr6:38747768 G>T maps to ENST00000327475 L677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr6:38980408 C>A maps to ENST00000327475 P4558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SB-01A-31D-A377-08 chr6:38877388 G>T maps to ENST00000327475 L3191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BV-01A-31D-A26M-08 chr17:11687705 C>T maps to NM_001372.3 L2637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SF-01A-11D-A377-08 chr9:34490061 C>T maps to NM_012144.2 D147D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7327-01A-11D-2114-08 chr9:34997171 C>T maps to NM_001135005.1 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A71Y-01A-22D-A32B-08 chr9:34993217 T>C maps to NM_001135005.1 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7522-01A-11D-2260-08 chr3:128181920 C>G maps to NM_153330.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr2:183593381 C>A maps to NM_018981.1 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr3:132165394 G>T did not map to a codon.
Sequencing variant TCGA-EJ-A8FU-01A-11D-A364-08 chr7:102953048 T>C maps to NM_014377.1 E611E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr1:38023280 C>A maps to NM_003462.3 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr2:25467185 C>T maps to NM_175629.1 V563V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr2:25469137 C>T maps to NM_175629.1 W440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CL-01A-11D-A34U-08 chr23:117742297 A>G did not map to a codon.
Sequencing variant TCGA-KK-A6E1-01A-11D-A30X-08 chr23:117775255 T>C did not map to a codon.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr3:51101985 G>A maps to NM_004947.4 E141E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr3:51102012 G>A maps to NM_004947.4 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr3:51347718 C>T maps to NM_004947.4 F993F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83M-01A-11D-A34U-08 chr1:63048922 T>C maps to ENST00000371140 V601V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IG-01A-11D-A364-08 chr6:83850060 C>A maps to NM_015018.2 S1785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87H-01A-11D-A34U-08 chr21:37605186 G>C maps to NM_005128.2 V812V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr19:2222179 C>T maps to ENST00000221482 H1004H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr19:2210675 C>A maps to ENST00000221482 P391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr1:101479331 C>A maps to NM_015958.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr1:101487276 T>C maps to NM_015958.2 E60E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr11:66259192 C>T maps to NM_005700.3 Y318Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HK-01A-11D-A364-08 chr3:109031398 G>A maps to NM_138815.3 Y58Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67T-01A-11D-A30X-08 chr3:109050825 C>T maps to NM_018189.3 K77K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr12:63976242 T>C maps to NM_173812.4 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr2:27165566 C>A maps to NM_020134.3 P463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr2:74750267 C>T maps to NM_133637.2 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CL-01A-11D-A34U-08 chr23:100511154 G>A did not map to a codon.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr21:41684281 C>T maps to NM_001389.3 P596P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65E-01A-11D-A29Q-08 chr21:41551003 G>A maps to NM_001389.3 Q933*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-7775-01A-11D-2114-08 chr21:41719855 G>T maps to NM_001389.3 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr11:117301513 G>T maps to NM_020693.2 T1930T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr11:117310572 C>A maps to NM_020693.2 V1374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7818-01A-11D-2114-08 chr11:117332279 G>A maps to NM_020693.2 L1160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WV-01A-11D-A377-08 chr8:120865379 T>C maps to NM_024094.2 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr6:116720685 C>A maps to NM_013352.2 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr18:65179269 G>T maps to NM_032160.2 S869*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr6:56341000 T>C maps to ENST00000361203 K7059K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VT-01A-11D-A377-08 chr20:17581393 G>T maps to NM_006870.3 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr1:212274087 T>C maps to NM_016448.2 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr18:32438305 C>A maps to NM_001390.4 P503P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SF-01A-11D-A377-08 chr7:76112080 A>G maps to NM_020892.2 Q175Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BV-01A-31D-A26M-08 chr15:45433154 G>A maps to NM_175940.1 G484G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EJ-7123-01A-11D-1961-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr17:80016029 T>G maps to NM_022156.3 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83M-01A-11D-A34U-08 chr19:5790153 T>C maps to NM_020175.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr22:31059966 G>A maps to NM_152511.3 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr1:167095420 C>T maps to NM_001080426.1 Y351Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr23:152915607 G>T did not map to a codon.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr14:102474612 C>A maps to NM_001376.4 S1972S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7331-01A-11D-2114-08 chr7:95705499 T>C maps to NM_004411.4 N564N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FN-01A-11D-A34U-08 chr16:66770009 G>A maps to NM_006141.2 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr16:66770147 C>T did not map to a codon.
Sequencing variant TCGA-KK-A8IF-01A-11D-A364-08 chr11:103124074 C>G maps to NM_001080463.1 L3375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr12:68050893 C>A maps to NM_006482.2 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr2:71816721 G>T did not map to a codon.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr2:71730400 C>A maps to NM_001130987.1 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr3:137796415 G>T maps to NM_173543.2 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr3:108347995 A>G maps to NM_014648.3 E223E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CL-01A-11D-A34U-08 chr16:2284612 C>T maps to NM_004424.3 H541H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7821-01A-12D-2114-08 chr16:23555839 C>G maps to NM_001083614.1 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr8:25745378 C>A maps to NM_022659.2 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr23:48386619 A>T did not map to a codon.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr9:95263190 C>A maps to NM_001393.3 L583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr15:74948191 C>A maps to NM_025083.3 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59X-01A-11D-A29Q-08 chr14:21215867 A>G maps to NM_006683.4 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6329-01A-13D-1961-08 chr4:148407184 C>T maps to NM_001957.3 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87K-01A-11D-A34U-08 chr4:148453711 A>G maps to NM_001957.3 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83H-01A-11D-A34U-08 chr17:28380699 A>G maps to NM_198529.3 Q576Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr1:64022883 G>A maps to NM_032437.2 E438E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr6:52285246 G>A maps to NM_018100.3 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7230-01A-11D-2114-08 chr2:233546302 C>T maps to NM_025202.3 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr14:23828654 C>T maps to NM_005864.2 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr5:137803739 C>A maps to NM_001964.2 T534T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65J-01A-11D-A30X-08 chr10:64573203 G>A maps to NM_001136178.1 F398F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7078-01A-11D-2114-08 chr11:64622146 C>T maps to NM_006795.2 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr3:184922217 G>T maps to NM_001966.3 S299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7213-01A-11D-2114-08 chr11:125450014 C>A maps to ENST00000278903 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr7:6080675 G>T maps to NM_014413.3 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr15:40313179 A>G maps to NM_001013703.2 K1418K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr12:124106407 C>T maps to NM_001414.3 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr8:141567319 C>T maps to NM_012154.3 Q298Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr23:24075811 T>C did not map to a codon.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr10:120802284 C>A did not map to a codon.
Sequencing variant TCGA-H9-7775-01A-11D-2114-08 chr1:32690026 C>T maps to NM_003757.2 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr22:38258977 G>T maps to ENST00000262832 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NH-01A-12D-A33T-08 chr22:38254722 C>G maps to ENST00000262832 Y180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr7:73604628 C>T maps to NM_022170.1 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7783-01A-11D-2114-08 chr14:103807367 C>T maps to NM_183004.3 D425D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FS-01A-11D-A34U-08 chr4:139980683 G>C maps to ENST00000379550 S412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88R-01A-11D-A364-08 chr23:129208568 A>C did not map to a codon.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr23:129200818 G>A did not map to a codon.
Sequencing variant TCGA-EJ-7218-01B-11D-A32B-08 chr7:36910036 G>A maps to NM_014800.9 C622C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr16:67234422 G>A maps to NM_024712.3 W214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7789-01A-11D-2114-08 chr4:110972802 T>C maps to NM_024090.2 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr8:27957464 C>A maps to NM_018091.5 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IJ-01A-11D-A34U-08 chr14:89148372 T>C maps to ENST00000380664 G995G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr19:14887553 G>C maps to NM_013447.2 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7170-01A-11D-2114-08 chr7:155255150 G>A maps to NM_001427.3 Q257Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr1:8923005 T>C did not map to a codon.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr13:43872564 C>A maps to NM_001127615.1 E455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr6:132195476 A>G maps to NM_006208.2 Q545Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr10:101455822 C>T maps to NM_020354.3 N318N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr3:27760934 A>T maps to ENST00000449599 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr22:41527560 C>A maps to NM_001429.3 P484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr22:41551077 C>A maps to NM_001429.3 P1074P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87H-01A-11D-A34U-08 chr12:132445685 C>T maps to ENST00000333577 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr1:29314299 A>G maps to NM_001166005.1 E117E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr2:120932464 A>G maps to NM_020909.3 L728L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7318-01B-11D-A32B-08 chr3:89468540 G>T did not map to a codon.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr3:89444999 C>A maps to NM_005233.5 V440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7079-01A-11D-1961-08 chr3:96533588 C>A maps to NM_001080448.2 S41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr6:93982057 G>T maps to NM_004440.3 P469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7750-01A-11D-2114-08 chr1:22924680 C>T maps to NM_020526.3 N718N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8W1-01A-11D-A377-08 chr3:134670793 C>T maps to NM_004441.4 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr3:134911532 G>C maps to NM_004441.4 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87D-01A-11D-A34U-08 chr3:134885816 C>T maps to NM_004441.4 S576S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IK-01A-11D-A364-08 chr1:23111210 C>T maps to ENST00000400191 D151D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6G1-01A-11D-A30X-08 chr7:100320665 T>G maps to NM_000799.2 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr8:144940860 G>T maps to NM_031308.1 L2187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BL-01A-31D-A257-08 chr1:220213573 G>A maps to NM_004446.2 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr1:51826840 A>G did not map to a codon.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr1:51869092 C>A maps to NM_001981.2 E597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6366-01A-11D-2114-08 chr17:37881013 T>C maps to NM_004448.2 Y781Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6G3-01A-11D-A30X-08 chr12:56492615 C>T maps to NM_001982.2 D922D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr2:212251656 C>A maps to NM_005235.2 V1134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A721-01A-12D-A32B-08 chr23:71425374 C>G did not map to a codon.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr8:37602101 G>A maps to NM_007175.6 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6329-01A-13D-1961-08 chr16:23716454 C>T maps to NM_033266.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr1:8074379 G>T maps to NM_018948.3 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr18:19154389 T>A maps to NM_052911.2 R139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BN-01A-61D-A257-08 chr20:13695682 T>C maps to NM_016649.3 E798E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr5:54281324 C>G maps to NM_007036.4 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr12:53666574 T>G maps to NM_012291.4 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr8:95676989 C>G maps to NM_017697.3 S237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr5:137844469 G>T maps to NM_004730.2 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HM-01A-11D-A364-08 chr7:13975391 G>A maps to NM_004956.4 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr1:157105281 T>A maps to NM_001145312.1 K89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr17:41611324 G>A maps to NM_001079675.1 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7797-01A-11D-2260-08 chr4:5735119 C>T maps to NM_153717.2 D220D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8W3-01A-11D-A377-08 chr17:74006444 G>C maps to NM_001988.2 T947T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr10:99203014 C>A maps to NM_016046.3 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr8:145134857 C>A maps to NM_019037.2 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr11:44165855 C>A maps to NM_001178083.1 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr6:66205252 A>T maps to ENST00000370616 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr6:66115186 G>A maps to ENST00000370616 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8II-01A-11D-A364-08 chr6:66115237 T>G maps to ENST00000370616 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FA-01A-21D-A33T-08 chr1:197008542 T>A did not map to a codon.
Sequencing variant TCGA-HC-A76W-01A-11D-A33T-08 chr19:17000462 C>T maps to NM_003950.2 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83M-01A-11D-A34U-08 chr13:113772751 C>T maps to NM_000131.3 D277D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr23:154225298 G>T did not map to a codon.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr23:154158636 G>T did not map to a codon.
Sequencing variant TCGA-HC-7232-01A-11D-2114-08 chr23:154182173 G>A did not map to a codon.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr5:14687627 A>T did not map to a codon.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr11:58919680 A>G maps to NM_198847.2 E180E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NF-01A-11D-A33T-08 chr11:58893555 T>C maps to NM_198947.3 V662V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr12:47629814 C>A maps to NM_138371.1 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr6:170627812 C>A maps to NM_032448.1 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7314-01A-31D-2114-08 chr6:170627924 C>T maps to NM_032448.1 Q483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7519-01A-11D-2260-08 chr23:54185949 A>G did not map to a codon.
Sequencing variant TCGA-KK-A8IJ-01A-11D-A34U-08 chr13:25743972 T>C maps to NM_152704.2 P595P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr7:22985645 A>G maps to NM_032581.3 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr2:201846108 G>A maps to NM_173822.3 Q493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr23:134166692 T>A did not map to a codon.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr1:184787939 C>A maps to NM_052966.2 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6361-01A-21D-1961-08 chr8:139209801 C>T maps to NM_015912.3 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr8:139164038 G>T maps to NM_015912.3 T893T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AV-01A-11D-A32B-08 chr8:139144958 C>A maps to NM_015912.3 V1366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr4:89671666 G>C maps to NM_014883.2 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr5:137277735 T>C did not map to a codon.
Sequencing variant TCGA-V1-A8ML-01A-11D-A377-08 chr10:61011333 C>T maps to ENST00000435852 R561R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr1:55077405 C>T maps to NM_176782.2 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr13:108518236 C>A maps to NM_001080396.2 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr5:74091852 A>G did not map to a codon.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr10:15254958 C>T maps to NM_001010924.1 W876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8260-01A-11D-2260-08 chr10:15255015 G>A maps to NM_001010924.1 H857H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr5:99871329 C>T maps to NM_198507.1 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr10:102698451 C>A maps to NM_001136123.1 P871P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-7775-01A-11D-2114-08 chr2:29237324 T>C maps to NM_199280.2 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87J-01A-11D-A34U-08 chr17:15406354 C>A maps to NM_145301.2 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr4:91229662 T>C maps to NM_001145065.1 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr10:128973759 G>T maps to NM_001039762.2 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr10:128973612 G>A maps to NM_001039762.2 I349I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A4JI-01A-11D-A257-08 chr10:128973672 C>T maps to NM_001039762.2 P329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr23:34150169 A>T did not map to a codon.
Sequencing variant TCGA-KK-A8ID-01A-11D-A364-08 chr23:34148191 C>A did not map to a codon.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chr23:34961793 T>C did not map to a codon.
Sequencing variant TCGA-SU-A7E7-01A-22D-A33T-08 chr23:34960973 G>A did not map to a codon.
Sequencing variant TCGA-VP-A87D-01A-11D-A34U-08 chr23:37028159 C>T did not map to a codon.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr6:3850539 C>G maps to NM_012135.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5505-01A-01D-1576-08 chr15:59064094 T>G maps to NM_001040450.1 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr16:67576896 C>A maps to NM_001193523.1 P756P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr13:114514744 C>T maps to NM_182614.2 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MG-01A-11D-A364-08 chr5:156590507 C>G maps to NM_130899.2 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr19:50979131 G>A maps to ENST00000391816 D106D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr9:40702846 C>A maps to NM_001083124.1 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr9:90535289 T>C maps to NM_001145124.1 D156D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr8:124195407 C>A maps to NM_032899.4 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr6:54735286 T>C maps to NM_001010872.1 D81D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr19:49107167 G>A maps to NM_017708.3 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TK-A8OK-01A-22D-A364-08 chr8:144810217 G>A maps to NM_198488.3 G471G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83I-01A-11D-A364-08 chr23:14883151 C>A did not map to a codon.
Sequencing variant TCGA-V1-A8WW-01A-11D-A377-08 chr23:14863073 T>C did not map to a codon.
Sequencing variant TCGA-YL-A8S8-01A-11D-A377-08 chr3:10128871 T>A maps to NM_033084.3 C1130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr14:45639924 T>G maps to NM_020937.2 S712S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr10:90768685 C>A maps to NM_000043.3 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr20:3128063 C>T maps to NM_021826.4 K551K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr4:187541625 G>T maps to ENST00000260147 P2041P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FS-01A-11D-A34U-08 chr4:187540590 G>A maps to ENST00000260147 L2386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7328-01A-31D-2114-08 chr5:150911163 G>A maps to NM_001447.2 R3265R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6385-01A-11D-1786-08 chr5:150922323 T>C maps to NM_001447.2 G2788G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr11:92570899 C>T maps to ENST00000298047 V3432V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr11:92088334 C>A maps to ENST00000298047 V1019V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8469-01A-11D-2395-08 chr11:92086738 G>A maps to ENST00000298047 V487V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-7775-01A-11D-2114-08 chr11:92568222 C>T maps to ENST00000298047 D3353D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr11:92086236 G>A maps to ENST00000298047 W320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VT-01A-11D-A377-08 chr4:126372550 A>G maps to NM_024582.4 G3460G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr4:126371607 T>A maps to NM_024582.4 L3146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr4:126371767 T>C maps to NM_024582.4 Y3199Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr4:126372475 C>A maps to NM_024582.4 P3435P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7797-01A-11D-2260-08 chr4:126242059 C>G maps to NM_024582.4 A1498A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr4:126412061 C>A maps to NM_024582.4 P4695P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AP-01A-12D-A33T-08 chr4:126319976 A>T maps to NM_024582.4 P1738P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MJ-01A-11D-A364-08 chr4:126411434 G>C maps to NM_024582.4 G4486G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65J-01A-11D-A30X-08 chr3:13659705 C>T maps to NM_001165035.1 C620C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr15:48707833 A>G maps to NM_000138.4 N2650N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr5:127648419 G>T maps to NM_001999.3 T1595T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7210-01A-11D-2114-08 chr5:127710363 A>G maps to NM_001999.3 C684C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8D0-01A-11D-A364-08 chr19:8137033 C>T maps to NM_032447.3 P2662P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A721-01A-12D-A32B-08 chr19:8130922 A>C maps to NM_032447.3 P2770P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88K-01A-11D-A34U-08 chr7:100190515 T>C maps to NM_012172.4 C261C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr5:171299982 C>A maps to NM_012300.2 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr12:117465847 C>A maps to NM_153348.2 I556I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr1:207133069 A>G maps to NM_001170631.1 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr19:7764642 C>A maps to NM_002002.4 E2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QW-01A-11D-A377-08 chr19:40362964 C>A maps to NM_003890.2 V5035V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7708-01A-11D-2114-08 chr1:161479820 C>A maps to NM_001136219.1 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NM-01A-21D-A33T-08 chr1:161642792 G>T maps to NM_004001.4 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr5:72370578 G>T maps to NM_138782.2 R530R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr1:157558992 C>G did not map to a codon.
Sequencing variant TCGA-KK-A6DY-01A-12D-A30X-08 chr1:157559033 G>A maps to NM_031282.2 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr1:157504476 T>C maps to NM_031281.2 S536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr8:11667247 G>A maps to NM_004462.3 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A5OB-01A-11D-A29Q-08 chr17:72858968 A>C maps to ENST00000442102 P525P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A720-01A-12D-A32B-08 chr11:61563273 C>T maps to NM_004111.4 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A720-01A-12D-A32B-08 chr11:61563279 C>A maps to NM_004111.4 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr8:125078686 C>A maps to NM_001039112.2 R1192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I4-01A-11D-A364-08 chr7:121942293 G>A maps to NM_001024613.2 N395N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6G3-01A-11D-A30X-08 chr4:155509999 A>G maps to NM_000508.3 H103H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr23:54481901 C>T did not map to a codon.
Sequencing variant TCGA-Y6-A8TL-01A-21D-A377-08 chr6:36993602 A>G maps to NM_173558.3 E498E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr9:95784667 A>C maps to NM_033086.2 A518A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr12:32764088 T>C maps to NM_139241.2 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AP-01A-12D-A33T-08 chr15:49716686 A>T maps to NM_002009.3 R65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NM-01A-21D-A33T-08 chr10:123325039 G>A maps to ENST00000351936 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83K-01A-11D-A34U-08 chr10:123325039 G>A maps to ENST00000351936 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr4:155526060 C>A maps to ENST00000407946 G437G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr4:155532985 T>C maps to ENST00000407946 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr16:67264086 G>A maps to NM_013241.2 P1032P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7794-01A-11D-2114-08 chr9:133779561 G>A maps to NM_001145106.1 R425R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A876-01A-11D-A34U-08 chr23:15373391 G>A did not map to a codon.
Sequencing variant TCGA-KC-A7F3-01A-21D-A33T-08 chr2:164466568 G>C maps to NM_018086.2 L591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E5-01A-11D-A30X-08 chr3:99649663 G>C maps to NM_001042459.1 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr1:152275292 A>G maps to NM_002016.1 D4023D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr1:152281406 G>T maps to NM_002016.1 S1985S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr1:152281160 G>T maps to NM_002016.1 P2067P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HK-01A-11D-A364-08 chr1:152280683 G>C maps to NM_002016.1 G2226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SQ-01B-11D-A377-08 chr1:152277017 G>A maps to NM_002016.1 S3448S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TK-A8OK-01A-22D-A364-08 chr11:128680405 C>T maps to NM_002017.3 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7797-01A-11D-2260-08 chr9:84607229 T>C maps to NM_001001670.2 S615S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr23:153587626 G>A did not map to a codon.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr7:128481389 C>A maps to NM_001458.4 P660P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7F6-01A-11D-A33T-08 chr20:14306919 A>G maps to NM_198391.2 I411I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr13:28610091 C>T maps to NM_004119.2 K466K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6DY-01A-12D-A30X-08 chr13:28608022 C>G did not map to a codon.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr1:203316789 C>T maps to NM_002023.3 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr6:159635998 C>A maps to NM_032532.2 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QY-01A-11D-A377-08 chr5:131008039 T>C maps to NM_133372.2 L699L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr4:159790452 C>T maps to ENST00000379346 R912*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr11:71850177 G>T maps to ENST00000442948 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr11:94039856 G>A maps to NM_001080486.1 W106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr14:38060571 A>C maps to NM_004496.2 *473E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr1:42657172 G>T maps to NM_001198850.1 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr17:26851603 C>T maps to NM_003593.2 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7209-01A-11D-2114-08 chr3:71037203 G>A maps to NM_032682.4 Q363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7233-01A-11D-2114-08 chr6:1313421 G>A maps to NM_033260.3 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr23:55651013 T>G did not map to a codon.
Sequencing variant TCGA-VP-A879-01A-11D-A34U-08 chr23:55650283 C>T did not map to a codon.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr13:39262557 T>C maps to NM_207361.4 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr13:39261855 G>A maps to NM_207361.4 K125K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WJ-01A-11D-A377-08 chr13:39263437 C>T maps to NM_207361.4 L653L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QZ-01A-11D-A377-08 chr13:39438592 T>G maps to NM_207361.4 P2611P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr4:190862185 A>T maps to NM_004477.2 K8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr15:44211980 C>A maps to NM_032892.3 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr23:131219960 G>A did not map to a codon.
Sequencing variant TCGA-FC-7708-01A-11D-2114-08 chr23:131212857 G>T did not map to a codon.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr4:48551611 C>T maps to NM_015030.1 W1554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr4:162577599 A>G maps to NM_020116.3 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WJ-01A-11D-A377-08 chr4:162307015 G>T maps to NM_020116.3 Y809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr21:47570138 G>T maps to ENST00000397748 S267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8CY-01A-11D-A364-08 chr5:121187963 C>T maps to NM_177478.1 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IJ-01A-11D-A34U-08 chr16:53913759 C>G maps to NM_001080432.2 S327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7789-01A-11D-2114-08 chr6:37426393 C>T maps to NM_015050.2 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BL-01A-31D-A257-08 chr6:143828560 C>T maps to NM_032020.4 W75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7523-01A-11D-2260-08 chr15:91422744 C>T maps to NM_002569.2 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr10:75533465 C>A maps to NM_173540.2 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr19:49207193 G>T maps to NM_001097638.2 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr14:66208992 G>C maps to NM_178155.1 V531V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr14:66208944 C>A maps to NM_178155.1 P515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr6:96651186 C>T maps to NM_006581.3 N52N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr17:7495580 T>C maps to NM_004860.3 S639S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr19:35613745 G>T maps to NM_021910.2 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr17:42635478 C>T maps to NM_001466.3 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr17:42636060 C>G maps to NM_001466.3 Y335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr17:42636210 C>T maps to NM_001466.3 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr17:42636498 C>T maps to NM_001466.3 F481F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5502-01A-01D-1576-08 chr8:28385110 A>T maps to NM_017412.3 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr11:86662612 G>A maps to NM_012193.2 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr11:86662879 G>A maps to NM_012193.2 F306F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr11:86663023 G>A maps to NM_012193.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr1:209849323 C>A maps to NM_015714.3 R99R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr5:151166204 C>A maps to NM_198395.1 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8ID-01A-11D-A364-08 chr4:47405708 T>G maps to NM_000812.3 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr23:151138737 C>T did not map to a codon.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr23:151124291 C>G did not map to a codon.
Sequencing variant TCGA-KK-A8ID-01A-11D-A364-08 chr4:46067499 T>C maps to NM_173536.3 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6499-01A-12D-1961-08 chr6:89888604 T>G maps to NM_002042.3 R442R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IF-01A-11D-A364-08 chr9:101608341 T>C maps to NM_024642.3 D514D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8S8-01A-11D-A377-08 chr2:31155003 G>A maps to NM_024572.2 R330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr1:230338964 C>T maps to NM_004481.3 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7737-01A-11D-2114-08 chr3:16261010 A>G maps to NM_054110.4 P498P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr15:42641675 C>A maps to NM_198141.2 S838S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr19:36027832 C>A maps to NM_014364.4 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr9:130152978 C>A maps to NM_032293.4 R935R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr21:34903823 C>A maps to NM_001136006.1 E190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr17:34072055 C>A maps to NM_139285.2 L820L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HK-01A-11D-A364-08 chr12:101018419 C>T maps to NM_174942.1 L613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7783-01A-11D-2114-08 chr17:39871694 C>T maps to NM_000805.3 R3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7079-01A-11D-1961-08 chr23:48650527 T>C did not map to a codon.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr18:19780662 C>A maps to NM_005257.3 P555P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr18:19780662 C>A maps to NM_005257.3 P555P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VO-01A-11D-A377-08 chr1:153790535 G>A maps to NM_020699.2 Q237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8266-01A-11D-2260-08 chr1:153788812 G>C maps to NM_020699.2 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr1:89587610 G>C maps to NM_004120.3 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr1:89480251 G>A maps to NM_018284.2 Q136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr7:150846191 C>A maps to NM_001098834.1 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr21:34117168 C>A maps to NM_016631.3 V708V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8260-01A-11D-2260-08 chr2:163005634 G>A maps to ENST00000233604 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr7:44185093 A>G did not map to a codon.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr6:53010373 A>G maps to NM_003643.3 N19N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr12:120582544 G>T maps to NM_006836.1 P1750P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr12:120615276 G>A maps to NM_006836.1 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A632-01A-11D-A29Q-08 chr6:10529593 T>A maps to NM_145649.4 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WL-01A-11D-A377-08 chr6:10556755 C>T maps to NM_001491.2 Q34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8264-01B-11D-2395-08 chr5:74325283 C>T maps to NM_016591.2 E193E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr10:48426602 G>T maps to NM_004962.2 P468P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr5:132200138 C>A maps to NM_005260.3 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr17:649428 G>T maps to NM_015721.2 P618P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr5:74056730 T>C maps to NM_032380.3 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr2:69554132 G>T maps to ENST00000357308 P656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SQ-01B-11D-A377-08 chr5:179740917 G>A maps to NM_005110.2 R440R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr19:38876986 A>G maps to NM_152657.3 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr17:34934520 G>A maps to NM_024835.3 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr10:85904773 T>C did not map to a codon.
Sequencing variant TCGA-YL-A8SJ-01B-11D-A377-08 chr3:10331493 C>T maps to NM_016362.3 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr11:59608633 A>G maps to NM_005142.2 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WW-01A-11D-A377-08 chr2:233655741 G>T maps to ENST00000373566 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr17:42882006 G>T maps to NM_001080383.1 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7788-01A-11D-2114-08 chr23:30737630 G>C did not map to a codon.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr11:134181018 G>A maps to NM_001080407.2 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr15:51676021 G>A maps to NM_181789.2 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QY-01A-11D-A377-08 chr9:131296230 G>A did not map to a codon.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chr23:14627240 G>A did not map to a codon.
Sequencing variant TCGA-KK-A8II-01A-11D-A364-08 chr23:120182328 G>A did not map to a codon.
Sequencing variant TCGA-KK-A8I9-01A-11D-A364-08 chr1:182355538 T>C did not map to a codon.
Sequencing variant TCGA-EJ-A8FN-01A-11D-A34U-08 chr11:58604620 T>G maps to NM_145016.3 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr16:4882095 C>A maps to NM_032569.3 G141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr19:19748734 C>A maps to NM_016573.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr3:49759675 G>A maps to NM_013334.2 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr12:102158273 G>T maps to NM_024312.4 P807P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7521-01A-11D-2260-08 chr12:100551033 C>G maps to ENST00000266746 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr12:133351741 G>A maps to NM_005895.3 R1376R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr3:37323636 C>A maps to NM_001172713.1 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A879-01A-11D-A34U-08 chr15:74368248 G>A maps to NM_001038640.2 H214H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr3:121413150 T>C maps to ENST00000393667 E2073E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr9:88650292 A>G maps to ENST00000376023 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7327-01A-11D-2114-08 chr3:194118888 C>T maps to NM_004488.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SL-01B-21D-A377-08 chr1:167038354 C>T maps to NM_005814.1 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88R-01A-11D-A364-08 chr2:96689179 G>A maps to NM_207328.2 G635G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr19:33608947 G>A did not map to a codon.
Sequencing variant TCGA-KK-A8ID-01A-11D-A364-08 chr1:27226495 A>T maps to NM_022078.2 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65G-01A-21D-A29Q-08 chr23:132887601 G>C did not map to a codon.
Sequencing variant TCGA-KK-A8IB-01A-11D-A364-08 chr23:132437322 T>A did not map to a codon.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr12:50497832 C>A did not map to a codon.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr7:1131447 C>A maps to NM_001505.2 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr19:34887246 A>G maps to NM_000175.3 G368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr19:34857282 G>T maps to NM_000175.3 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87E-01A-31D-A34U-08 chr7:23286529 A>C maps to ENST00000435486 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WV-01A-11D-A377-08 chr9:132853234 A>C maps to NM_001136557.1 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7748-01A-11D-2114-08 chr12:123186915 G>A maps to NM_177551.3 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SL-01B-21D-A377-08 chr6:46973589 C>T maps to ENST00000283297 K853K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr6:47650244 G>A maps to NM_153839.6 K582K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr23:135431328 C>A did not map to a codon.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr23:135429591 G>A did not map to a codon.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr23:135428403 C>A did not map to a codon.
Sequencing variant TCGA-YL-A8SO-01B-31D-A377-08 chr23:135426828 T>A did not map to a codon.
Sequencing variant TCGA-KK-A8I6-01A-11D-A364-08 chr16:57608858 A>T maps to ENST00000349457 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7210-01A-11D-2114-08 chr23:129518742 C>G did not map to a codon.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr10:95326920 G>T maps to NM_181745.3 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr10:134942934 T>C maps to ENST00000368577 L1075L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr12:131487812 C>A maps to NM_198827.3 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr16:20043983 G>T maps to NM_001002911.2 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87C-01A-11D-A34U-08 chr17:72363724 T>C maps to NM_181790.1 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr1:9171451 G>A maps to NM_024980.4 D160D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr2:128408803 G>A maps to NM_005291.2 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr23:78426886 A>G did not map to a codon.
Sequencing variant TCGA-VN-A88R-01A-11D-A364-08 chr1:202092722 T>C did not map to a codon.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr23:150348253 G>A did not map to a codon.
Sequencing variant TCGA-HC-7230-01A-11D-2114-08 chr23:150348880 T>C did not map to a codon.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr16:57691385 C>A maps to NM_005682.5 A423A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr23:19031990 G>T did not map to a codon.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr23:19037718 C>T did not map to a codon.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr12:54756633 G>T maps to NM_020370.2 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7818-01A-11D-2114-08 chr12:54757586 G>A maps to NM_020370.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr16:57722300 C>A maps to NM_170776.4 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr16:57718005 C>T maps to NM_170776.4 F348F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr5:90106487 C>T maps to NM_032119.3 F5137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr5:89933654 T>C maps to NM_032119.3 F710F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr23:101972034 T>G did not map to a codon.
Sequencing variant TCGA-HC-7233-01A-11D-2114-08 chr12:13061953 G>A maps to NM_003979.3 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr17:73316459 G>T maps to NM_002086.4 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr1:24676594 C>G maps to NM_021180.3 Y564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chr23:122616695 A>C did not map to a codon.
Sequencing variant TCGA-ZG-A8QW-01A-11D-A377-08 chr11:105797469 C>T maps to NM_000829.3 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7328-01A-31D-2114-08 chr10:87407078 G>A maps to NM_017551.2 F691F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr19:42569513 C>T maps to NM_002088.3 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr16:9858033 C>A maps to NM_000833.3 E1123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr12:13717456 G>T maps to NM_000834.3 A905A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr9:104432659 C>T maps to NM_133445.2 W678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8CY-01A-11D-A364-08 chr3:14545075 C>A maps to ENST00000507975 E991*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr23:48847437 G>T did not map to a codon.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr13:114324000 G>T did not map to a codon.
Sequencing variant TCGA-VN-A88L-01A-11D-A34U-08 chr6:146350829 C>T maps to NM_000838.3 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr6:34003798 G>A maps to NM_000841.1 P696P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CL-01A-11D-A34U-08 chr7:126086369 A>T maps to NM_001127323.1 S829S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I5-01A-11D-A364-08 chr7:126746595 A>T maps to NM_001127323.1 Y227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BV-01A-31D-A26M-08 chr23:16142273 T>C did not map to a codon.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr17:38062139 C>T maps to NM_001165958.1 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7315-01A-31D-2114-08 chr17:38073350 C>T maps to NM_001165958.1 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr17:38062396 G>A maps to NM_001165958.1 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr8:144643540 C>T maps to NM_024736.6 D228D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr1:110217412 C>G maps to ENST00000369830 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SL-01B-21D-A377-08 chr4:54966543 C>A maps to NM_133267.2 I11I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7789-01A-11D-2114-08 chr1:89319012 A>T maps to NM_001514.5 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A48F-01A-11D-A257-08 chr8:30436472 G>A maps to NM_002095.4 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YJ-A8SW-01A-11D-A377-08 chr8:30472223 A>G maps to NM_002095.4 H89H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr11:18362865 A>G maps to NM_005316.3 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7075-01A-11D-1961-08 chr2:27564919 G>T maps to NM_001521.2 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FS-01A-11D-A34U-08 chr6:111288986 G>A maps to NM_138408.3 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VO-01A-11D-A377-08 chr10:1044995 G>A maps to NM_012341.2 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr20:60773004 C>T maps to NM_015666.3 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr11:106810482 C>T maps to ENST00000282249 K303K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr11:106558381 C>A maps to ENST00000282249 E729*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr4:156643198 G>T maps to NM_001130684.1 G576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IH-01A-11D-A364-08 chr12:14766077 G>A maps to NM_004963.3 T1065T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr23:108718894 G>C did not map to a codon.
Sequencing variant TCGA-HC-7075-01A-11D-1961-08 chr20:23345559 C>A maps to NM_022482.3 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7232-01A-11D-2114-08 chr14:25101105 C>T maps to ENST00000382542 E220E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr5:134705106 G>T maps to NM_138610.2 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr17:39881201 G>T maps to ENST00000310778 T589T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7075-01A-11D-1961-08 chr5:82940275 C>A maps to NM_001884.3 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr1:156593629 C>A maps to NM_021817.2 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59X-01A-11D-A29Q-08 chr18:43685266 C>T maps to NM_138443.3 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr5:156514273 C>A maps to NM_032782.3 G249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr1:154247928 C>A maps to NM_006118.3 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr11:5289794 A>T maps to NM_005330.3 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5505-01A-01D-1576-08 chr23:153224169 A>C did not map to a codon.
Sequencing variant TCGA-KK-A7AV-01A-11D-A32B-08 chr23:153216819 T>C did not map to a codon.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr12:104487294 T>G maps to NM_013320.2 A472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7078-01A-11D-2114-08 chr1:155255753 G>T maps to NM_020897.1 G492G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr6:55142194 T>C maps to NM_001526.3 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr3:13542246 C>T maps to NM_024827.3 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QZ-01A-11D-A377-08 chr5:141009252 G>C maps to NM_003883.3 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr23:48673410 C>T did not map to a codon.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr23:71787744 G>C did not map to a codon.
Sequencing variant TCGA-EJ-7331-01A-11D-2114-08 chr7:18687445 G>A maps to NM_178425.2 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr15:91475003 G>T maps to ENST00000394272 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87E-01A-31D-A34U-08 chr23:7023870 G>A did not map to a codon.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr1:236760201 C>G maps to NM_018072.5 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SA-01A-21D-A377-08 chr2:37284596 G>A maps to NM_019024.1 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B1-01A-11D-A32B-08 chr17:58143747 C>T did not map to a codon.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr10:93253265 G>A did not map to a codon.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr7:43484981 C>T maps to NM_015052.3 D737D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr12:66725337 A>G maps to NM_033647.2 V1025V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr11:124793826 T>G maps to NM_152722.4 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr15:28473496 C>A maps to NM_004667.4 L1777L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr15:28375704 C>A maps to NM_004667.4 V4202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr15:28375389 G>T maps to NM_004667.4 R4241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SQ-01B-11D-A377-08 chr10:69748521 T>G maps to NM_022079.2 V568V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr7:35674968 G>T maps to NM_022373.4 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr3:193855646 C>A maps to NM_005524.2 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr17:80382310 C>A maps to NM_173620.2 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr1:91843737 T>A maps to NM_001017975.3 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr1:91781958 C>A maps to NM_001017975.3 E963*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88I-01A-11D-A34U-08 chr1:91859786 G>A maps to NM_001017975.3 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8469-01A-11D-2395-08 chr17:79657218 C>A maps to NM_004712.4 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr1:210522366 C>T maps to NM_001170580.1 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88L-01A-11D-A34U-08 chr1:210637879 C>T maps to NM_001170580.1 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr7:27565970 G>A maps to NM_152740.3 D291D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6353-01A-11D-1961-08 chr10:102306904 C>A maps to ENST00000442724 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr11:119002675 C>G maps to NM_198971.1 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr7:75168700 C>A maps to NM_005338.4 L1001L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr7:75192342 C>A maps to NM_005338.4 E306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr1:114510460 T>C maps to ENST00000426820 L890L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7210-01A-11D-2114-08 chr7:139285233 G>A maps to NM_022740.4 A788A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8ID-01A-11D-A364-08 chr7:139416758 G>A maps to NM_022740.4 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr11:33373267 T>C maps to NM_005734.3 H974H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr11:33374936 C>A maps to NM_005734.3 P1157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr6:26217531 C>A maps to NM_021052.2 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7521-01A-11D-2260-08 chr6:27101128 G>A maps to NM_021064.4 E93E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr6:27861557 G>A maps to NM_003527.4 E106E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8W3-01A-11D-A377-08 chr6:26045769 G>A maps to NM_003531.2 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr1:149783761 G>T maps to ENST00000427880 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65G-01A-21D-A29Q-08 chr6:143092406 G>A maps to NM_006734.3 Q1157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HM-01A-11D-A364-08 chr6:32714044 G>A maps to NM_020056.4 E214E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr3:148760004 A>T maps to NM_003071.3 I715I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr1:186055462 T>G maps to NM_031935.2 G2990G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:186009010 G>A maps to NM_031935.2 Q2060Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr1:185987440 T>C maps to NM_031935.2 N1809N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6G1-01A-11D-A30X-08 chr1:186106991 C>T maps to NM_031935.2 R4604R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E0-01A-11D-A30X-08 chr1:186064438 C>T maps to NM_031935.2 T3453T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IJ-01A-11D-A34U-08 chr1:186056777 G>A did not map to a codon.
Sequencing variant TCGA-KK-A8IL-01A-11D-A364-08 chr1:186063455 C>A maps to NM_031935.2 A3415A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TK-A8OK-01A-22D-A364-08 chr1:186024594 C>T maps to NM_031935.2 S2311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr1:24129054 C>A did not map to a codon.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr5:43294963 C>A did not map to a codon.
Sequencing variant TCGA-XJ-A83H-01A-11D-A34U-08 chr5:43293007 A>T maps to NM_002130.6 G417G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8261-01A-11D-2260-08 chr12:121434122 C>T maps to NM_000545.5 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr12:121434122 C>T maps to NM_000545.5 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr4:83280637 C>A maps to NM_031370.2 E149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr19:39334539 A>G maps to ENST00000221419 N274N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr1:23650123 T>C maps to ENST00000414299 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7F3-01A-21D-A33T-08 chr1:23637360 G>C maps to ENST00000414299 G500G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr19:41778017 C>A maps to NM_007040.3 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr2:38818745 G>C maps to NM_138394.3 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FN-01A-11D-A34U-08 chr7:27204580 T>A maps to NM_152739.3 R166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr17:46622153 C>G maps to NM_002145.3 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr17:46629479 G>T maps to NM_002146.4 P119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr12:54379099 C>A maps to NM_017409.3 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr2:177034057 C>T maps to NM_006898.4 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr1:21103088 C>G did not map to a codon.
Sequencing variant TCGA-HC-7740-01A-11D-2114-08 chr11:18313151 T>C maps to NM_181507.1 G759G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr10:103826088 G>T maps to NM_024747.4 G286G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr10:103826901 C>A maps to NM_024747.4 P557P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WJ-01A-11D-A377-08 chr1:152187687 T>C maps to NM_001009931.1 R2139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr16:22926768 A>G maps to NM_006043.1 K330K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VT-01A-11D-A377-08 chr23:131762489 G>A did not map to a codon.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr1:209879154 G>C did not map to a codon.
Sequencing variant TCGA-EJ-7791-01A-11D-2114-08 chr4:88278429 C>A did not map to a codon.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr19:49339659 C>A maps to NM_016246.2 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BL-01A-31D-A257-08 chr5:118837733 A>G did not map to a codon.
Sequencing variant TCGA-YL-A8SO-01B-31D-A377-08 chr1:120056907 C>A maps to ENST00000235547 Y256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr8:145537688 C>A maps to NM_005526.2 P452P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I8-01A-11D-A364-08 chr14:102548542 A>T maps to NM_001017963.2 L787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7327-01A-11D-2114-08 chr6:44219538 C>A maps to NM_007355.2 S460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5505-01A-01D-1576-08 chr6:31797487 C>G maps to NM_005346.4 A587A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr5:137893675 C>A did not map to a codon.
Sequencing variant TCGA-XJ-A9DI-01A-11D-A377-08 chr7:75933152 C>T maps to NM_001540.3 Y133Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MU-01A-11D-A377-08 chr11:111784195 A>G maps to NM_001541.3 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr5:53752033 T>C maps to NM_006308.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr17:40275107 C>A maps to NM_033194.2 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr3:122459554 G>A maps to NM_024610.4 G368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7791-01A-11D-2114-08 chr2:198353197 A>G maps to NM_199440.1 D411D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87B-01A-11D-A34U-08 chr1:22168750 G>T maps to NM_005529.5 P3011P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QW-01A-11D-A377-08 chr13:31727070 T>G maps to NM_006644.2 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr23:135593929 T>G did not map to a codon.
Sequencing variant TCGA-YL-A8S8-01A-11D-A377-08 chr23:135593231 G>A did not map to a codon.
Sequencing variant TCGA-EJ-7791-01A-11D-2114-08 chr1:23520100 C>T maps to NM_000864.4 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr6:87725480 C>A maps to NM_000865.2 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B4-01A-11D-A32B-08 chr23:113965813 A>C did not map to a codon.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr10:124271536 A>G maps to NM_002775.4 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr23:53657924 T>C did not map to a codon.
Sequencing variant TCGA-G9-7510-01A-11D-2260-08 chr23:53618048 T>C did not map to a codon.
Sequencing variant TCGA-J4-A6G1-01A-11D-A30X-08 chr3:50340315 G>T maps to NM_153281.1 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr16:70934963 C>T maps to NM_032821.2 L2996L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88L-01A-11D-A34U-08 chr16:70902477 G>A maps to NM_032821.2 R3768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HJ-01A-11D-A364-08 chr16:70843712 T>A maps to NM_032821.2 T4951T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr11:125769838 C>A maps to NM_001134793.1 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-8198-01A-11D-2260-08 chr1:220273971 T>C maps to NM_018060.3 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr19:10394817 G>A maps to NM_000201.2 Q249Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7318-01B-11D-A32B-08 chr19:10398383 C>T maps to NM_001544.3 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83M-01A-11D-A34U-08 chr1:159002390 T>A maps to ENST00000295809 Y413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88N-01A-11D-A364-08 chr1:159021836 T>G maps to ENST00000295809 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr10:91162646 C>A maps to NM_001548.3 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7328-01A-31D-2114-08 chr10:91177945 C>T maps to NM_012420.2 A330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7519-01A-11D-2260-08 chr9:21186978 T>C maps to NM_021068.2 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76W-01A-11D-A33T-08 chr3:129185798 T>G maps to NM_052985.2 Y261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr2:27688725 C>A maps to NM_015662.1 R572R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr2:27688725 C>A maps to NM_015662.1 R572R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr3:107885799 A>G maps to ENST00000457963 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8CY-01A-11D-A364-08 chr15:65621730 G>A maps to NM_004884.3 P734P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VO-01A-11D-A377-08 chr23:130419245 C>A did not map to a codon.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr23:130407831 G>T did not map to a codon.
Sequencing variant TCGA-KK-A8IB-01A-11D-A364-08 chr3:151165278 A>G maps to NM_178822.4 D830D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SK-01B-21D-A377-08 chr3:118621498 G>A maps to NM_152538.2 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SR-01B-11D-A377-08 chr16:21658766 T>C maps to NM_005849.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr11:133790583 G>T maps to NM_014987.1 I1012I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr2:213886795 C>G maps to ENST00000342002 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr3:159711353 G>A did not map to a codon.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr3:159710860 A>G maps to NM_000882.2 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr23:117895120 A>G did not map to a codon.
Sequencing variant TCGA-V1-A8WV-01A-11D-A377-08 chr22:50437762 C>T maps to NM_001001694.2 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IB-01A-11D-A364-08 chr2:103063566 C>T maps to NM_003853.2 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WI-01A-11D-A377-08 chr2:103063626 G>A maps to NM_003853.2 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WW-A8ZI-01A-11D-A377-08 chr2:113593794 T>C maps to NM_000576.2 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr23:29972727 C>A did not map to a codon.
Sequencing variant TCGA-HC-7740-01A-11D-2114-08 chr23:104728368 T>A did not map to a codon.
Sequencing variant TCGA-VN-A88N-01A-11D-A364-08 chr23:104984611 C>A did not map to a codon.
Sequencing variant TCGA-G9-6361-01A-21D-1961-08 chr1:207040804 T>C did not map to a codon.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr22:37524300 C>T maps to ENST00000406505 G502G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6353-01A-11D-1961-08 chr22:37524347 G>A maps to ENST00000406505 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr23:1464311 C>A did not map to a codon.
Sequencing variant TCGA-HC-7209-01A-11D-2114-08 chr23:1501314 A>G did not map to a codon.
Sequencing variant TCGA-KK-A8IH-01A-11D-A364-08 chr23:1499969 C>T did not map to a codon.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr16:27372110 C>T maps to NM_000418.2 R292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A878-01A-31D-A34U-08 chr5:55248075 A>C did not map to a codon.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr18:22008831 G>A did not map to a codon.
Sequencing variant TCGA-VP-A875-01A-31D-A34U-08 chr3:101023019 T>C maps to NM_016247.2 E157E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TK-A8OK-01A-22D-A364-08 chr1:62257042 T>C maps to NM_176877.2 Y364Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr4:184431717 C>A maps to NM_001564.2 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr2:220439862 G>A maps to NM_002191.3 W239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr2:234113039 C>A maps to ENST00000359570 R1082R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr11:2182080 G>A maps to NM_001042376.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr19:7174735 C>A maps to NM_000208.2 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7079-01A-11D-1961-08 chr1:156819188 C>A maps to NM_014215.2 A431A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr8:19682475 C>T maps to NM_018142.2 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VL-01A-21D-A377-08 chr17:60003894 A>C maps to NM_020748.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr1:153735802 C>A maps to ENST00000428986 S578S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr1:153732835 C>A maps to ENST00000428986 I430I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr1:212118152 C>T maps to NM_015434.3 L858L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TB-01A-11D-A364-08 chr8:28692855 C>A maps to NM_018250.3 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr4:128626837 A>G maps to NM_015693.3 K553K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7750-01A-11D-2114-08 chr9:103055172 T>C maps to NM_014425.2 D878D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7791-01A-11D-2114-08 chr1:201821310 C>A maps to NM_018085.4 T198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88N-01A-11D-A364-08 chr2:237285744 C>A did not map to a codon.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr3:51929025 C>A maps to NM_152397.2 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr3:51864454 A>T maps to NM_001085479.1 K35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr15:91040569 C>T maps to NM_003870.3 Q1620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7079-01A-11D-1961-08 chr12:247626 C>A maps to NM_001170738.1 A366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr3:10251300 G>A maps to NM_001570.3 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr19:46388639 A>G maps to NM_015649.1 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A725-01A-12D-A32B-08 chr6:397163 G>A maps to NM_002460.3 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr16:85936701 T>C maps to NM_002163.2 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6499-01A-12D-1961-08 chr16:85936653 A>C maps to NM_002163.2 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65J-01A-11D-A30X-08 chr19:44099418 G>A maps to NM_001007561.2 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr19:44097035 C>A maps to NM_001007561.2 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6361-01A-21D-1961-08 chr5:2747710 G>T maps to NM_033267.4 T461T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr16:54966501 A>G maps to NM_005853.5 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr16:54966432 C>A maps to NM_005853.5 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-8198-01A-11D-2260-08 chr15:74467264 C>T maps to NM_201526.1 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8II-01A-11D-A364-08 chr14:77948908 G>A maps to NM_199296.2 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CP-01A-11D-A34U-08 chr20:33068459 T>A maps to ENST00000262650 R666R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr16:47189689 C>A did not map to a codon.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr16:304438 C>A maps to NM_032039.2 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7210-01A-11D-2114-08 chr16:314963 C>T maps to NM_032039.2 D534D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr5:52183670 G>T maps to NM_181501.1 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I9-01A-11D-A364-08 chr1:145532145 C>T maps to NM_003637.3 R264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr17:42455140 G>T maps to NM_000419.3 I704I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr2:182376433 T>C maps to NM_000885.4 F618F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr12:56088618 G>T maps to ENST00000347027 L757L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr16:31422455 C>A maps to ENST00000444228 T488T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CL-01A-11D-A34U-08 chr16:31409183 G>T maps to ENST00000444228 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WW-01A-11D-A377-08 chr16:30500699 C>A maps to NM_002209.2 G402G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MU-01A-11D-A377-08 chr16:31382412 G>A maps to NM_000887.3 A573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TK-A8OK-01A-22D-A364-08 chr17:73728051 C>T maps to NM_001005619.1 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VL-01A-21D-A377-08 chr23:54783700 G>T did not map to a codon.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr5:156638317 C>A maps to NM_005546.3 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr1:160850468 C>T maps to NM_017625.2 K198K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr19:41231252 C>A maps to NM_025194.2 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HL-01A-11D-A364-08 chr12:26780981 G>A maps to NM_002223.2 D1016D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8264-01B-11D-2395-08 chr21:35237514 C>T maps to NM_003024.2 D1317D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A872-01A-11D-A34U-08 chr15:40707599 G>A maps to NM_002225.3 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr1:185269160 A>G maps to NM_006469.4 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8261-01A-11D-2260-08 chr14:105618059 G>A maps to NM_002226.3 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr1:65300334 A>C maps to NM_002227.2 Y1125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr19:17950418 T>A maps to NM_000215.3 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7327-01A-11D-2114-08 chr10:133949432 G>T did not map to a codon.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr10:133976843 C>A maps to NM_001105521.2 V782V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7314-01A-31D-2114-08 chr10:64967186 T>G maps to NM_032776.1 S1414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A6RC-01A-11D-A32B-08 chr10:64936220 G>A maps to NM_032776.1 Q2413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A725-01A-12D-A32B-08 chr10:64958387 A>G maps to NM_032776.1 F1792F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr14:24040358 G>A maps to NM_032452.2 D527D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6333-01A-12D-1961-08 chr1:59248568 C>A maps to NM_002228.3 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B1-01A-11D-A32B-08 chr17:39915086 G>A maps to NM_021991.2 C511C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr23:8502427 G>T did not map to a codon.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr23:8553408 T>C did not map to a codon.
Sequencing variant TCGA-J9-A8CL-01A-11D-A34U-08 chr3:124374510 G>T maps to NM_001024660.3 V1952V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WW-A8ZI-01A-11D-A377-08 chr9:731263 A>C maps to NM_015158.2 G1001G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FD-01A-11D-A33T-08 chr1:15386728 C>T maps to NM_201628.2 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87B-01A-11D-A34U-08 chr1:111217005 C>T maps to NM_002232.3 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr3:156192554 G>T maps to NM_172159.3 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr17:7827735 G>T maps to NM_004732.2 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MG-01A-11D-A364-08 chr11:17793786 G>A maps to NM_001112741.1 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr7:120381667 C>A maps to NM_012281.2 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NM-01A-21D-A33T-08 chr1:112525242 T>A maps to ENST00000315987 K36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NF-01A-11D-A33T-08 chr18:77659467 C>T maps to NM_012283.1 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr14:63175049 G>A maps to NM_139318.3 Q715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr2:233635817 C>A maps to NM_002242.4 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6M7-01A-11D-A31L-08 chr22:38823054 C>G maps to NM_152868.1 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr11:128781512 G>T maps to NM_000890.3 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CP-01A-11D-A34U-08 chr10:118969533 C>A maps to NM_181840.1 Y293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88Q-01A-11D-A34U-08 chr11:64064396 G>A maps to ENST00000422670 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr19:38810913 T>C did not map to a codon.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr11:2549249 T>C did not map to a codon.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr1:196254843 C>T maps to NM_198503.2 L880L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr8:36767014 C>A maps to NM_001031836.2 R765R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65G-01A-21D-A29Q-08 chr12:109894045 G>C maps to NM_031954.3 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr1:23408759 G>T maps to NM_001009999.2 R782R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CL-01A-11D-A34U-08 chr11:66985326 G>A maps to NM_012308.2 K271K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr2:86693618 G>T maps to NM_001146688.1 G378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr19:5144057 C>A maps to NM_015015.2 S877S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SP-01B-11D-A377-08 chr19:5039896 C>T maps to NM_015015.2 D64D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr23:44938411 A>G did not map to a codon.
Sequencing variant TCGA-EJ-7331-01A-11D-2114-08 chr23:44969494 G>A did not map to a codon.
Sequencing variant TCGA-V1-A8ML-01A-11D-A377-08 chr23:44938584 G>T did not map to a codon.
Sequencing variant TCGA-YL-A8SQ-01B-11D-A377-08 chr23:44945221 A>G did not map to a codon.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr17:73491707 C>A maps to ENST00000375248 T982T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr14:105361069 C>A maps to ENST00000453495 P1516P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr6:24601302 G>T maps to NM_014809.3 S10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr1:35916054 G>T maps to NM_024874.4 P706P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr9:114204656 C>A maps to NM_001080398.1 V284V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr9:114199252 A>G maps to NM_001080398.1 G403G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XA-A8JR-01A-11D-A364-08 chr20:36640364 G>A maps to NM_014657.1 C618C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr1:43912678 G>A maps to NM_015284.2 V2143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr16:27585274 G>T maps to NM_015202.2 E21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8W1-01A-11D-A377-08 chr13:42273389 A>C maps to NM_015058.1 T1127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr13:42259306 G>A maps to NM_015058.1 F1401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8469-01A-11D-2395-08 chr17:6503778 C>T did not map to a codon.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr17:6513402 G>T maps to NM_014804.2 S541S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr1:39877440 G>T maps to NM_015038.1 E502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7521-01A-11D-2260-08 chr18:8824762 G>A maps to ENST00000456698 E1404E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QY-01A-11D-A377-08 chr14:55844785 A>G maps to NM_014924.3 F334F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr1:155883914 G>T maps to NM_014949.2 P614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr18:29488974 T>C did not map to a codon.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr15:79748638 C>G maps to NM_015206.2 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr9:34971619 C>A maps to NM_015297.1 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr4:123192754 G>A maps to NM_015312.3 V2692V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A6RA-01A-11D-A33T-08 chr4:123202795 A>G maps to NM_015312.3 P2968P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A879-01A-11D-A34U-08 chr4:123237981 A>G maps to NM_015312.3 E3545E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr17:44248975 C>A maps to NM_015443.3 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7212-01A-11D-2114-08 chr17:44145008 C>A maps to NM_015443.3 E520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87K-01A-11D-A34U-08 chr10:72291080 G>A maps to NM_014431.2 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr14:94004550 G>T maps to ENST00000393153 E447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WW-A8ZI-01A-11D-A377-08 chr8:95507177 G>C maps to NM_015496.3 A1517A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VO-01A-11D-A377-08 chr4:186111651 C>T maps to NM_020827.1 Q233Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A875-01A-31D-A34U-08 chr2:226447086 G>T maps to NM_020864.1 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7750-01A-11D-2114-08 chr9:100071829 G>A maps to ENST00000375206 Q251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr4:1348987 A>G maps to NM_020894.2 K377K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr19:7682253 T>C maps to NM_001080429.2 P1112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A6RC-01A-11D-A32B-08 chr6:56918133 A>G maps to NM_020931.2 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WN-01A-11D-A377-08 chr6:56917923 A>G maps to NM_020931.2 E209E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7783-01A-11D-2114-08 chr1:180885313 A>G maps to NM_020950.1 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr13:45594564 T>A did not map to a codon.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr1:233489600 G>T maps to NM_032435.2 R345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7230-01A-11D-2114-08 chr1:233518096 C>G maps to NM_032435.2 L917L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6329-01A-13D-1961-08 chr8:22472958 G>A maps to NM_021174.5 Q409Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IB-01A-11D-A364-08 chr23:73963817 T>A did not map to a codon.
Sequencing variant TCGA-M7-A721-01A-12D-A32B-08 chr9:5919990 G>C maps to NM_001017969.2 S2002*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87K-01A-11D-A34U-08 chr9:6007387 C>A maps to NM_001017969.2 G134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr9:116858373 C>A maps to ENST00000259410 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr1:200587191 G>T maps to NM_014875.2 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr20:16360551 C>A maps to NM_024704.4 E699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr20:16360453 G>A maps to NM_024704.4 D731D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chr1:21040006 C>G maps to NM_020816.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87B-01A-11D-A34U-08 chr1:21009256 G>A maps to NM_020816.2 A784A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr11:28058050 A>G maps to NM_031217.3 I703I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Z-01A-12D-A26M-08 chr17:72340363 C>A maps to NM_153209.3 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr1:10292481 C>T maps to ENST00000377086 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr5:137520548 G>A maps to NM_005733.2 Q579Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76W-01A-11D-A33T-08 chr10:91512348 C>T maps to ENST00000416354 C1446C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6333-01A-12D-1961-08 chr1:200972743 C>T maps to NM_017596.2 R394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr6:168431489 G>T maps to NM_030615.2 G44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr1:245849236 C>A maps to NM_018012.3 S984S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8264-01B-11D-2395-08 chr1:245850130 G>A maps to NM_018012.3 L1282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr20:30897747 C>G maps to NM_004798.3 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr23:69550105 G>T did not map to a codon.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr12:57962798 C>T maps to NM_004984.2 N256N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83I-01A-11D-A364-08 chr12:57957898 G>A maps to NM_004984.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr10:32337437 T>C maps to NM_004521.2 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr1:169953738 T>C maps to NM_014970.2 V459V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr6:33377449 C>T maps to NM_002263.3 Q669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7209-01A-11D-2114-08 chr8:145697576 G>A maps to NM_145754.2 E514E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IL-01A-11D-A364-08 chr19:55340906 C>T maps to NM_013289.2 C364C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B3-01A-11D-A33T-08 chr13:33635171 C>A maps to NM_004795.3 A652A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IF-01A-11D-A364-08 chr13:33628319 T>A maps to NM_004795.3 I412I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr11:66026226 G>T maps to NM_022822.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr8:103664290 T>A did not map to a codon.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr16:87782412 C>A maps to NM_017566.3 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr12:27950649 C>A maps to NM_020782.1 R357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SB-01A-31D-A377-08 chr1:18809301 G>C maps to NM_152375.2 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr23:117043608 G>T did not map to a codon.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr23:117053578 G>C did not map to a codon.
Sequencing variant TCGA-KK-A8IH-01A-11D-A364-08 chr23:24007024 A>G did not map to a codon.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr3:47376265 C>A maps to NM_025010.4 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FD-01A-11D-A33T-08 chr3:47364055 A>G did not map to a codon.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr4:166234519 T>C did not map to a codon.
Sequencing variant TCGA-G9-6333-01A-12D-1961-08 chr1:173744959 C>A maps to NM_014458.3 A539A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr5:136963995 C>T maps to NM_017415.2 R527R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr8:124663854 C>A maps to NM_001081675.2 G438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8469-01A-11D-2395-08 chr23:86887269 T>C did not map to a codon.
Sequencing variant TCGA-KC-A4BV-01A-31D-A26M-08 chr23:86919797 G>C did not map to a codon.
Sequencing variant TCGA-KK-A8I4-01A-11D-A364-08 chr19:51534118 G>T maps to NM_019598.2 C172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7519-01A-11D-2260-08 chr19:51582741 G>A maps to NM_022046.4 R160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr19:51453322 G>A maps to NM_012427.4 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr4:187175747 C>A maps to ENST00000511608 P487P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7788-01A-11D-2114-08 chr19:10670557 C>T maps to NM_023008.3 E291E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7789-01A-11D-2114-08 chr7:91870305 C>T did not map to a codon.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr17:38859678 C>A maps to NM_019016.2 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr17:38905555 G>C maps to NM_181534.3 Y399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7821-01A-12D-2114-08 chr17:38906789 C>T maps to NM_181534.3 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7821-01A-12D-2114-08 chr17:39502451 A>G maps to NM_004138.2 C378C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A8O0-01A-41D-A377-08 chr17:39635634 C>T maps to NM_002280.4 K225K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WJ-01A-11D-A377-08 chr17:39595065 A>G maps to NM_006771.3 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr12:52979801 C>A maps to NM_080747.2 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr12:52820635 C>A did not map to a codon.
Sequencing variant TCGA-KK-A8IL-01A-11D-A364-08 chr12:53242525 C>A maps to NM_173352.2 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WW-01A-11D-A377-08 chr12:53217007 G>A maps to NM_175834.2 Q387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8CY-01A-11D-A364-08 chr12:52700019 C>T maps to NM_002284.3 I401I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr21:45959619 C>T maps to NM_198691.2 Q138Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr11:71277127 C>A maps to ENST00000422553 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr11:71259903 C>T maps to ENST00000422553 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BL-01A-31D-A257-08 chr17:39383025 C>T maps to NM_031961.2 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CN-01A-11D-A34U-08 chr12:118199015 C>T maps to ENST00000339824 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr2:143790836 C>T maps to NM_003937.2 R330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FN-01A-11D-A34U-08 chr23:153137809 C>T did not map to a codon.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr23:153130076 G>C did not map to a codon.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr20:42161555 T>C maps to NM_032107.4 Y454Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr20:42162928 C>A maps to NM_032107.4 P513P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WL-01A-11D-A377-08 chr19:54872559 C>T maps to NM_002287.3 W109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr18:6943332 C>A maps to NM_005559.2 V2971V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr18:21426326 C>T maps to ENST00000416669 G1264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83M-01A-11D-A34U-08 chr18:21330979 T>C maps to ENST00000416669 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr7:107580684 C>A maps to NM_002291.2 S1170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AU-01A-11D-A32B-08 chr3:182853619 C>T maps to NM_014398.3 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr2:211336686 C>T maps to NM_001136575.1 W65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr4:17590564 C>A maps to NM_015907.2 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7218-01B-11D-A32B-08 chr1:152777720 G>A maps to NM_178351.3 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7789-01A-11D-2114-08 chr15:43620820 A>G maps to NM_014793.4 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr9:139847393 G>A maps to NM_178536.3 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr9:139847375 G>T maps to NM_178536.3 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr9:139651557 C>T maps to ENST00000371689 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IF-01A-11D-A364-08 chr13:46701743 T>C maps to NM_002298.4 K622K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AU-01A-11D-A32B-08 chr2:136570300 G>A maps to NM_002299.2 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7209-01A-11D-2114-08 chr10:88447003 C>T maps to NM_001171610.1 Q290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr19:11233931 A>T maps to NM_000527.4 T741T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr12:71898435 C>A maps to NM_003667.2 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83K-01A-11D-A34U-08 chr12:71978096 C>A maps to NM_003667.2 A769A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr1:202245637 C>T maps to NM_001017403.1 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87E-01A-31D-A34U-08 chr6:63990018 G>A maps to NM_016571.2 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr2:48915654 A>T maps to NM_000233.3 Y427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr19:48646815 C>A maps to NM_000234.1 E300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr13:108861450 C>T maps to NM_001098268.1 K722K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr19:55086231 C>A maps to NM_001130917.1 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr19:54823140 C>A maps to NM_021250.2 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SC-01A-11D-A377-08 chr19:54745450 C>A did not map to a codon.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr19:55148262 T>G maps to ENST00000427581 P680P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SK-01B-21D-A377-08 chr19:54721087 G>T maps to NM_001081450.1 S591S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr19:54760065 G>T maps to NM_001081442.1 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr4:41621298 G>A maps to NM_014988.2 E259E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-8200-01A-11D-A29Q-08 chr17:61776289 G>A maps to NM_030576.3 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr17:18137335 C>T maps to NM_004140.3 D187D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IB-01A-11D-A364-08 chr15:75114225 C>T maps to NM_021819.2 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8213-01A-11D-A29Q-08 chr13:76379698 G>A maps to ENST00000357063 E263E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr1:165175155 G>T maps to NM_177398.3 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr9:129455527 C>A maps to NM_001174147.1 R223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NM-01A-21D-A33T-08 chr16:20855294 C>T maps to NM_030941.2 Q556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6361-01A-21D-1961-08 chr15:74219534 G>C maps to NM_005576.2 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8S8-01A-11D-A377-08 chr2:74762801 G>A maps to NM_032603.2 G443G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7519-01A-11D-2260-08 chr6:161020596 A>G maps to NM_005577.2 T1074T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr23:78010845 T>C did not map to a codon.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr4:62599225 C>T maps to ENST00000506720 H451H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7748-01A-11D-2114-08 chr4:62903459 G>A maps to ENST00000506720 E1201E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr18:2925281 G>T maps to NM_014646.2 P626P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr13:47269053 G>T maps to NM_001164211.1 E383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6361-01A-21D-1961-08 chr11:803449 G>A maps to NM_145886.3 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr19:36431058 G>A maps to NM_024509.1 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7078-01A-11D-2114-08 chr19:4538287 C>T maps to NM_052972.2 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr7:133812131 C>A maps to NM_144648.1 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FA-01A-21D-A33T-08 chr3:66502032 T>C maps to NM_015541.2 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr1:113636958 A>T did not map to a codon.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr12:59283854 G>A maps to NM_153377.3 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr12:59274657 C>A maps to NM_153377.3 T502T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SK-01B-21D-A377-08 chr10:85992630 C>T maps to NM_015613.2 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr12:57574173 C>T maps to NM_002332.2 I1766I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr2:141777642 C>A maps to NM_018557.2 V606V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88Q-01A-11D-A34U-08 chr2:141108608 T>A did not map to a codon.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr2:170136032 G>A maps to NM_004525.2 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SH-01B-11D-A377-08 chr11:46924427 T>G maps to ENST00000256991 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6367-01A-11D-1786-08 chr2:44153049 T>C maps to NM_133259.3 R929R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr10:134165143 C>A maps to NM_030626.2 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr11:76371901 G>A maps to NM_001128922.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr17:30349139 A>C maps to ENST00000327564 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7232-01A-11D-2114-08 chr15:71185231 T>G did not map to a codon.
Sequencing variant TCGA-EJ-A65E-01A-11D-A29Q-08 chr11:56949993 C>T maps to NM_001005210.2 D209D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr11:550099 C>A maps to NM_198075.3 S151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IG-01A-11D-A364-08 chr4:52860764 G>C maps to NM_001024611.1 S808*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7789-01A-11D-2114-08 chr8:67922952 C>G maps to ENST00000421742 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr1:70502286 T>C maps to NM_020794.2 H718H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83N-01A-11D-A34U-08 chr1:70484493 T>C maps to NM_020794.2 G433G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6499-01A-12D-1961-08 chr1:90058586 C>A maps to NM_015350.2 C799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Z-01A-12D-A26M-08 chr2:238668783 A>G maps to NM_001137552.1 Q275Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr3:37125218 A>G maps to NM_006309.2 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr1:74575076 C>A did not map to a codon.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr15:101606926 C>A maps to NM_024652.3 R1951R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CN-01A-11D-A34U-08 chr15:101595337 G>A maps to NM_024652.3 R1414R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HO-01A-11D-A364-08 chr3:3887995 G>T maps to NM_020873.5 S557S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FS-01A-11D-A34U-08 chr1:204589108 G>A maps to NM_201630.1 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A4JI-01A-11D-A257-08 chr2:80530542 C>T maps to NM_178839.4 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chr2:76975913 G>A maps to NM_001134745.1 S560S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr3:194379703 G>T maps to NM_018385.2 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65J-01A-11D-A30X-08 chr19:35753474 C>T maps to NM_205834.2 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr11:65320671 G>T maps to NM_001130144.2 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7791-01A-11D-2114-08 chr15:41804905 G>A maps to NM_002344.5 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6361-01A-21D-1961-08 chr23:114541232 C>T did not map to a codon.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr2:160688256 C>T maps to NM_001198759.1 E1294E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr2:160709825 C>A maps to NM_001198759.1 G901*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88O-01A-11D-A34U-08 chr2:160665082 C>A did not map to a codon.
Sequencing variant TCGA-KC-A7FA-01A-21D-A33T-08 chr1:160771694 G>A maps to NM_001033667.1 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7233-01A-11D-2114-08 chr4:4281392 A>T maps to NM_017816.2 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A6RA-01A-11D-A33T-08 chr8:56860228 C>A maps to NM_002350.2 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr1:151137674 C>T maps to NM_212551.4 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52B-01A-11D-A26M-08 chr15:100269695 G>A maps to NM_152449.2 Q176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr1:235950606 A>G maps to NM_000081.2 N1585N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr22:21349316 T>G did not map to a codon.
Sequencing variant TCGA-EJ-7218-01B-11D-A32B-08 chr8:20110913 C>T maps to NM_021020.2 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr1:39798823 A>G maps to ENST00000289893 G628G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr1:39747938 C>T maps to ENST00000361689 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87H-01A-11D-A34U-08 chr1:39798763 T>C maps to ENST00000289893 F608F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr7:2041726 C>A maps to NM_003550.2 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr11:47345220 G>C did not map to a codon.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr19:35786795 C>A maps to NM_002361.3 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr19:35786681 G>A maps to NM_002361.3 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A879-01A-11D-A34U-08 chr23:151303839 G>T did not map to a codon.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr23:148798185 G>T did not map to a codon.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr23:148798035 T>A did not map to a codon.
Sequencing variant TCGA-KK-A8IA-01A-11D-A364-08 chr23:151093030 C>T did not map to a codon.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr23:151869831 C>T did not map to a codon.
Sequencing variant TCGA-HC-7232-01A-11D-2114-08 chr23:151869993 A>C did not map to a codon.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr23:151869831 C>T did not map to a codon.
Sequencing variant TCGA-XJ-A83G-01A-11D-A34U-08 chr23:151869897 G>T did not map to a codon.
Sequencing variant TCGA-YL-A8HJ-01A-11D-A364-08 chr23:151870215 A>T did not map to a codon.
Sequencing variant TCGA-YL-A9WI-01A-11D-A377-08 chr23:140996225 C>A did not map to a codon.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr23:140985096 C>A did not map to a codon.
Sequencing variant TCGA-EJ-7788-01A-11D-2114-08 chr23:140983189 C>A did not map to a codon.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr23:51639837 C>T did not map to a codon.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr23:149638073 G>T did not map to a codon.
Sequencing variant TCGA-VP-A87E-01A-31D-A34U-08 chr23:149639451 C>G did not map to a codon.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr1:117944806 G>T did not map to a codon.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr5:109106194 C>A maps to NM_002372.2 P383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr5:109159446 C>A maps to NM_002372.2 P825P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7233-01A-11D-2114-08 chr23:43571168 T>A did not map to a codon.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr15:43815431 A>G maps to ENST00000382031 E825E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr15:43814444 C>A maps to ENST00000382031 P496P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y6-A8TL-01A-21D-A377-08 chr5:71492634 G>A maps to NM_005909.3 E1151E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7075-01A-11D-1961-08 chr19:17831812 C>A maps to NM_018174.4 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NF-01A-11D-A33T-08 chr2:210588328 T>A maps to NM_001039538.1 L396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr17:67513025 C>T maps to NM_002758.3 C38C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8266-01A-11D-2260-08 chr11:65375264 G>A maps to NM_002419.3 H364H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6361-01A-21D-1961-08 chr12:53878998 C>G did not map to a codon.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr2:128066228 C>A maps to NM_006609.3 T522T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr2:128079649 G>T maps to NM_006609.3 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7783-01A-11D-2114-08 chr6:136990478 C>A maps to NM_005923.3 A436A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr2:102456433 C>A maps to NM_145686.2 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Z-01A-12D-A26M-08 chr23:20060692 A>G did not map to a codon.
Sequencing variant TCGA-G9-7519-01A-11D-2260-08 chr23:135314291 G>T did not map to a codon.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr23:135309467 T>A did not map to a codon.
Sequencing variant TCGA-YL-A8HO-01A-11D-A364-08 chr23:135314094 C>A did not map to a codon.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr1:206858780 C>G maps to NM_032960.2 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr20:31427558 C>G maps to NM_012325.2 S165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr20:31424468 A>G maps to NM_012325.2 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QY-01A-11D-A377-08 chr1:220791997 A>G maps to NM_018650.3 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr19:12978319 C>T maps to NM_014975.2 H724H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr1:46497979 C>T maps to NM_015112.2 I1106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr1:46493408 A>T maps to NM_015112.2 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr5:138643656 A>C maps to ENST00000394800 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QX-01A-11D-A377-08 chr18:47801394 G>A maps to ENST00000424334 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr18:51690930 G>T maps to NM_003927.3 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B3-01A-11D-A33T-08 chr23:131516261 C>A did not map to a codon.
Sequencing variant TCGA-VN-A88K-01A-11D-A34U-08 chr16:84124505 A>T maps to NM_003791.2 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6M7-01A-11D-A31L-08 chr20:54823919 G>T maps to ENST00000371389 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr18:13826432 C>A maps to NM_005913.2 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A9DI-01A-11D-A377-08 chr22:43529099 C>T maps to NM_173467.4 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr13:113732743 G>A maps to NM_001112732.1 R633R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr3:183059414 C>A maps to NM_015078.2 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IL-01A-11D-A364-08 chr10:13240782 A>G maps to NM_182751.2 S739S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr1:85510884 G>A maps to NM_018298.9 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr1:85498462 C>A maps to NM_018298.9 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6333-01A-12D-1961-08 chr15:95013612 G>A maps to NM_018349.3 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr15:94928744 C>A maps to NM_018349.3 P593P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr7:114655933 C>A maps to NM_199072.4 S338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr14:47504409 T>C maps to NM_001113498.2 K541K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87K-01A-11D-A34U-08 chr14:47600971 C>T maps to NM_001113498.2 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr6:90383965 G>T maps to NM_014611.1 P4368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6329-01A-13D-1961-08 chr6:90426385 G>A maps to NM_014611.1 D2242D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr23:153296741 G>T did not map to a codon.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr17:37566850 G>T maps to NM_004774.3 P541P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr23:70349257 C>T did not map to a codon.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr23:70349257 C>T did not map to a codon.
Sequencing variant TCGA-EJ-7792-01A-11D-2114-08 chr23:70348453 G>T did not map to a codon.
Sequencing variant TCGA-G9-7519-01A-11D-2260-08 chr23:70349254 G>C did not map to a codon.
Sequencing variant TCGA-KC-A7F3-01A-21D-A33T-08 chr23:70349257 C>T did not map to a codon.
Sequencing variant TCGA-VP-A87J-01A-11D-A34U-08 chr23:70349254 G>C did not map to a codon.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr3:150877857 C>A maps to NM_053002.4 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr17:60140572 G>A maps to NM_005121.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5763-01A-11D-1576-08 chr12:116446660 C>A maps to NM_015335.4 V519V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83M-01A-11D-A34U-08 chr22:20937035 T>A did not map to a codon.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr19:16688031 G>T maps to NM_004831.3 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr9:134889830 T>C maps to NM_004269.2 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr1:3519043 C>A maps to ENST00000452816 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr19:42840496 C>A maps to ENST00000251268 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr7:116339269 C>A maps to NM_001127500.1 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WW-A8ZI-01A-11D-A377-08 chr1:171761208 C>T maps to NM_015935.4 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr15:82336241 G>T maps to NM_032246.3 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr12:8804282 G>T maps to NM_003480.2 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr2:228197204 C>A maps to NM_020194.4 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr8:8749968 C>A maps to NM_004225.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr8:8748566 C>A maps to NM_004225.2 E668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83I-01A-11D-A364-08 chr3:196742334 C>T maps to NM_005929.5 K378K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr1:12058936 T>A did not map to a codon.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr3:158541296 G>T maps to NM_022736.2 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AP-01A-12D-A33T-08 chr15:41961929 G>T maps to ENST00000219905 E280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88I-01A-11D-A34U-08 chr15:42003249 C>G maps to ENST00000219905 Y929*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr7:141754595 C>T maps to ENST00000475668 L1068L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr2:135076249 C>A maps to NM_002410.3 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr5:43280300 T>C maps to NM_153361.2 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83N-01A-11D-A34U-08 chr10:131506293 C>A maps to NM_002412.3 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr16:4714729 G>T maps to NM_015246.2 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QW-01A-11D-A377-08 chr1:222838750 A>T maps to NM_198551.2 G1838G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8S8-01A-11D-A377-08 chr23:10417582 T>C did not map to a codon.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr23:107159357 A>G did not map to a codon.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr1:12082417 C>A maps to NM_021933.2 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr7:7645693 T>C maps to NM_019005.3 S841S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr10:129923868 G>T maps to NM_002417.4 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr10:129900971 G>C maps to NM_002417.4 P3044P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7213-01A-11D-2114-08 chr10:129899950 G>A maps to NM_002417.4 R3092R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr10:129905900 C>T maps to NM_002417.4 Q1401Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr20:10393193 G>T maps to NM_170784.1 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E0-01A-11D-A30X-08 chr22:40816927 G>C maps to NM_020831.3 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr22:50500056 G>A maps to NM_015166.3 D363D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr11:118343970 T>C maps to NM_001197104.1 A699A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr12:49415604 G>T maps to NM_003482.3 P5524P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr12:49443871 C>A maps to NM_003482.3 E1167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr12:49430958 G>A maps to NM_003482.3 Q3394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E5-01A-11D-A30X-08 chr12:49434306 G>A maps to NM_003482.3 Q2416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr7:151879330 G>A maps to ENST00000355193 Q1872*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NH-01A-12D-A33T-08 chr7:151873584 G>A maps to ENST00000355193 Q2985*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CL-01A-11D-A34U-08 chr7:151855998 C>T maps to ENST00000355193 E3873E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IF-01A-11D-A364-08 chr7:151878019 G>A maps to ENST00000355193 Q2309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8II-01A-11D-A364-08 chr7:151877200 A>C maps to ENST00000355193 L2387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QY-01A-11D-A377-08 chr7:151860194 T>C maps to ENST00000355193 Q3489Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr19:6216423 C>T maps to NM_005934.3 R433R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr6:168297652 G>T did not map to a codon.
Sequencing variant TCGA-KC-A7F3-01A-21D-A33T-08 chr6:168352504 C>T maps to ENST00000400822 Q1483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr17:36865472 G>T maps to NM_005937.3 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6333-01A-12D-1961-08 chr3:154861329 A>G maps to NM_007289.2 E429E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7793-01A-31D-2260-08 chr8:89128876 C>T maps to NM_005941.4 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-8200-01A-11D-A29Q-08 chr8:89128917 T>G maps to NM_005941.4 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6499-01A-12D-1961-08 chr12:132335620 G>T maps to NM_016155.4 A538A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr16:55532276 C>A maps to NM_004530.4 P562P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr11:102563707 C>A maps to NM_022122.2 G420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr11:102710882 A>G maps to NM_002422.3 D297D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr4:90816529 T>C maps to NM_007351.2 N136N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6DY-01A-12D-A30X-08 chr6:39877612 C>A maps to ENST00000425303 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr20:49576641 C>A maps to NM_014484.3 A421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr6:29627138 G>C maps to NM_002433.4 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A872-01A-11D-A34U-08 chr11:75438517 C>A maps to NM_025098.2 Y103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr2:74690102 G>T maps to NM_006302.2 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr12:62946845 G>A maps to ENST00000393630 V1035V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7750-01A-11D-2114-08 chr23:102931634 G>A did not map to a codon.
Sequencing variant TCGA-KK-A8IB-01A-11D-A364-08 chr12:122107368 T>C maps to NM_173855.4 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A720-01A-12D-A32B-08 chr10:99376043 C>T maps to NM_001098831.1 K139K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr23:14932666 G>T did not map to a codon.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr6:132645228 T>G maps to NM_015529.2 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IA-01A-11D-A364-08 chr2:71361866 T>C maps to NM_005791.2 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7750-01A-11D-2114-08 chr17:41957293 G>A maps to NM_005374.3 S403S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SP-01B-11D-A377-08 chr11:18955896 C>G maps to NM_147199.3 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr17:34964757 C>A maps to NM_024864.3 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr11:59573831 G>T maps to NM_017840.3 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr2:75879652 T>C maps to NM_014763.3 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7708-01A-11D-2114-08 chr6:43023653 G>A maps to NM_015950.3 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7742-01A-11D-2114-08 chr19:3762706 C>G maps to NM_172251.2 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr2:105706376 G>C did not map to a codon.
Sequencing variant TCGA-EJ-7314-01A-31D-2114-08 chr11:60164140 T>C maps to NM_032597.3 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr2:48027254 C>A maps to NM_000179.2 P711P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr12:120791156 G>T maps to NM_002442.2 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr3:135913889 G>T maps to NM_018133.3 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr16:812727 C>A maps to NM_013404.4 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7314-01A-31D-2114-08 chr23:64949441 A>C did not map to a codon.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr23:131207113 T>A did not map to a codon.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chr23:131188792 A>G did not map to a codon.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr8:98701312 G>T maps to NM_178812.3 G265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-8198-01A-11D-2260-08 chr8:98657099 G>A maps to NM_178812.3 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7519-01A-11D-2260-08 chr8:97269340 T>C maps to NM_015942.3 E112E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr2:242039185 C>A maps to NM_182501.3 G49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88L-01A-11D-A34U-08 chr8:66619383 C>A maps to NM_014637.3 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Y-01A-11D-A26M-08 chr15:31197978 T>C maps to NM_014967.4 G371G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I9-01A-11D-A364-08 chr11:95595462 A>G maps to NM_016156.5 Y110Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr22:30416461 C>A maps to NM_021090.3 A938A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8468-01A-21D-2395-08 chr22:30416350 G>A maps to NM_021090.3 R901R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr8:17169088 C>T maps to NM_004686.4 R344R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6G3-01A-11D-A30X-08 chr1:11169350 G>T maps to NM_004958.3 L2508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WW-01A-11D-A377-08 chr1:11189829 G>C maps to NM_004958.3 S1893S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8D0-01A-11D-A364-08 chr4:100543848 G>A maps to ENST00000511045 K870K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr8:17611560 G>A maps to NM_001001924.2 Q586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr13:29599665 C>T maps to NM_001033602.2 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67T-01A-11D-A30X-08 chr13:29599578 C>T maps to NM_001033602.2 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83M-01A-11D-A34U-08 chr11:26586955 A>G maps to NM_001135091.1 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr19:9075832 C>T maps to NM_024690.2 E3871E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7328-01A-31D-2114-08 chr19:9082694 T>A maps to NM_024690.2 T3040T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7789-01A-11D-2114-08 chr19:9057079 G>T maps to NM_024690.2 I10122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr19:9082880 G>T maps to NM_024690.2 P2978P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr19:9086743 T>A maps to NM_024690.2 R1691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7F6-01A-11D-A33T-08 chr19:9086804 A>G maps to NM_024690.2 S1670S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IC-01A-11D-A364-08 chr19:9045762 G>A maps to NM_024690.2 T11956T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VV-01A-11D-A377-08 chr7:100682352 C>A maps to NM_001040105.1 I2552I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr7:100675140 C>A maps to NM_001040105.1 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr7:100693834 T>C maps to NM_001040105.1 L4265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7785-01A-11D-2114-08 chr7:100681500 C>T maps to NM_001040105.1 S2268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr11:1081736 C>T maps to ENST00000441003 N555N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr11:1255480 G>A maps to ENST00000447027 A811A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7318-01B-11D-A32B-08 chr11:1271276 C>G maps to ENST00000447027 T4392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88Q-01A-11D-A34U-08 chr11:1248356 C>T maps to ENST00000447027 N186N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A6RA-01A-11D-A33T-08 chr6:49412359 A>C maps to NM_000255.3 S556S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr23:3242965 C>A did not map to a codon.
Sequencing variant TCGA-J4-A83I-01A-11D-A364-08 chr23:3235404 G>C did not map to a codon.
Sequencing variant TCGA-V1-A8X3-01A-11D-A377-08 chr23:3240658 T>C did not map to a codon.
Sequencing variant TCGA-YL-A8HO-01A-11D-A364-08 chr23:3240571 C>T did not map to a codon.
Sequencing variant TCGA-YL-A8SP-01B-11D-A377-08 chr23:3238697 C>T did not map to a codon.
Sequencing variant TCGA-YL-A9WH-01A-11D-A377-08 chr23:3227765 G>C did not map to a codon.
Sequencing variant TCGA-G9-6366-01A-11D-2114-08 chr12:102072012 T>A maps to NM_002465.2 P1081P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76X-01A-11D-A33T-08 chr13:77738586 A>G did not map to a codon.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr12:81110949 G>T maps to NM_005593.2 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr17:10404783 C>T maps to NM_005963.3 E1127E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr3:108112994 G>A maps to NM_014981.1 S1734S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr17:10448738 G>A maps to NM_017534.5 Y143Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr17:10446276 C>T maps to NM_017534.5 K273K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr17:10355524 G>A maps to NM_017533.2 A1157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A721-01A-12D-A32B-08 chr17:10355470 G>A maps to NM_017533.2 F1175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CN-01A-11D-A34U-08 chr14:23885341 G>T maps to NM_000257.2 R1608R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr17:10295963 C>A did not map to a codon.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr17:10296219 C>T maps to NM_002472.2 Q1797Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr22:36696286 C>T maps to NM_002473.4 E954E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr6:16146915 T>A maps to NM_013262.3 R424R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr6:16145413 C>A maps to NM_013262.3 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr3:123456318 G>T maps to NM_053025.3 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QZ-01A-11D-A377-08 chr6:2680488 G>A maps to NM_001012418.3 Q242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AP-01A-12D-A33T-08 chr17:18052095 C>T maps to ENST00000205890 R2262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr22:26422471 C>A maps to ENST00000407587 R2180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr17:30986137 G>A maps to NM_015194.1 F780F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr19:8595448 G>T maps to NM_012335.3 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8266-01A-11D-2260-08 chr10:26462762 A>G maps to NM_017433.4 K1190K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr2:171260842 C>A maps to NM_138995.3 P788P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr18:47516880 C>A maps to NM_001080467.2 E256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr11:76868350 G>A maps to NM_000260.3 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7078-01A-11D-2114-08 chr11:76893184 C>T maps to NM_000260.3 D1031D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CL-01A-11D-A34U-08 chr2:128335736 C>T maps to ENST00000389524 N293N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr18:3129368 G>T maps to NM_003803.3 P885P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr18:3135566 C>A maps to NM_003803.3 V729V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr1:24388586 C>A maps to ENST00000330966 L1264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7740-01A-11D-2114-08 chr1:24419566 C>T maps to ENST00000330966 K321K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WJ-01A-11D-A377-08 chr10:69881644 T>C maps to NM_032578.2 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7075-01A-11D-1961-08 chr3:40211571 C>A maps to NM_015460.2 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr1:59147848 A>T maps to NM_001085487.1 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr10:76788960 T>G maps to NM_012330.2 L1460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr20:62839623 C>A maps to NM_004535.2 R359R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr21:30255332 A>G maps to NM_013240.3 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr12:112516058 A>G maps to NM_024953.3 Y199Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr3:175041962 G>T did not map to a codon.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr12:57485186 C>A maps to NM_005967.3 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr17:42085836 C>T maps to NM_153006.2 G491G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76W-01A-11D-A33T-08 chr4:89618404 G>A maps to NM_153757.2 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7218-01B-11D-A32B-08 chr3:50334945 A>C maps to NM_012191.2 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr2:15378657 C>T maps to NM_015909.2 E1959E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr3:47036898 A>G maps to NM_015175.1 A558A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E1-01A-11D-A30X-08 chr3:47038460 C>A maps to NM_015175.1 I858I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SQ-01B-11D-A377-08 chr1:16893755 T>C maps to NM_017940.3 E919E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7314-01A-31D-2114-08 chr1:148004649 T>C maps to ENST00000310701 E893E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr19:19338462 T>C maps to NM_004386.2 Y678Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr12:6640147 C>A maps to NM_014865.3 P1342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr11:134054636 C>T maps to NM_015261.2 K782K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IG-01A-11D-A364-08 chr19:39691042 G>A maps to NM_001001414.1 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7785-01A-11D-2114-08 chr1:36028871 G>T maps to NM_001014839.1 G485G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AV-01A-11D-A32B-08 chr1:36026231 G>T maps to NM_001014839.1 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8261-01A-11D-2260-08 chr2:106497793 G>A maps to NM_001004720.2 K79K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5763-01A-11D-1576-08 chr2:183846058 A>G maps to NM_205842.1 H424H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7F3-01A-21D-A33T-08 chr2:183847592 A>G maps to NM_205842.1 H394H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IL-01A-11D-A364-08 chr2:133538753 A>G maps to NM_207363.2 A1640A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BL-01A-31D-A257-08 chr2:232320220 A>G maps to NM_005381.2 G649G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr2:24933957 C>A maps to NM_003743.4 A859A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr10:51584845 G>A maps to NM_001145260.1 R331R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8ML-01A-11D-A377-08 chr10:51584629 C>G maps to NM_001145260.1 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8ML-01A-11D-A377-08 chr10:51584700 C>G maps to NM_001145260.1 S283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr17:15976857 A>C maps to ENST00000395857 T1248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7212-01A-11D-2114-08 chr17:15971375 G>A maps to ENST00000395857 Q1541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:160314572 C>A maps to NM_015331.2 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr17:8350175 G>T maps to ENST00000402554 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QW-01A-11D-A377-08 chr3:179341803 T>A maps to NM_002492.2 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr9:32573052 C>A maps to NM_002493.3 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87E-01A-31D-A34U-08 chr2:152359339 C>T maps to NM_001164507.1 E7965E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7315-01A-31D-2114-08 chr12:8242591 A>G maps to NM_015509.3 K52K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8X3-01A-11D-A377-08 chr6:11213710 G>A maps to NM_006403.3 Q88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr1:198233328 A>G maps to NM_133494.2 E112E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8CY-01A-11D-A364-08 chr11:20869194 G>A maps to NM_006157.3 K134K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6G1-01A-11D-A30X-08 chr2:233899739 C>A maps to NM_005383.2 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr10:105350077 C>A maps to NM_004210.4 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr17:7224436 G>A maps to NM_032442.2 G1118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr17:7222512 G>A maps to NM_032442.2 F1180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88Q-01A-11D-A34U-08 chr17:37762552 C>A maps to NM_006160.3 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr7:31378576 G>A maps to NM_022728.2 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87J-01A-11D-A34U-08 chr17:29576013 A>G maps to NM_001042492.2 S1329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A721-01A-12D-A32B-08 chr1:204985657 T>C maps to ENST00000367172 S1345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr14:24838790 C>A maps to NM_001136022.1 R126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr9:94172249 G>C maps to NM_005384.2 S256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr23:17750101 A>G did not map to a codon.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr1:236180448 C>A maps to NM_002508.2 V751V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I8-01A-11D-A364-08 chr14:52508860 A>T maps to NM_007361.3 L596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr14:51288705 C>A maps to NM_020921.3 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83I-01A-11D-A364-08 chr12:772598 C>T maps to NM_016533.4 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr5:37020936 C>A maps to NM_133433.3 S1762S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr3:52526218 C>T maps to NM_007184.3 R1412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr1:161088965 C>A maps to NM_005600.2 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FS-01A-11D-A34U-08 chr23:119077406 A>G did not map to a codon.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr6:28227526 G>A maps to NM_001007531.1 E126E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr5:172659607 C>A maps to NM_004387.3 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SJ-01B-11D-A377-08 chr10:134598509 G>A maps to NM_177400.2 D248D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr17:33462275 C>T maps to NM_018096.3 R402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr23:5821236 G>C did not map to a codon.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr23:5811274 G>T did not map to a codon.
Sequencing variant TCGA-YL-A8S9-01A-11D-A377-08 chr17:26488194 C>T maps to NM_016231.4 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SC-01A-11D-A377-08 chr5:65077142 T>C maps to NM_020726.4 Y239Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr2:32474763 G>T maps to NM_021209.4 P723P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr16:57088674 G>A maps to NM_032206.3 T1173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IJ-01A-11D-A34U-08 chr19:56369967 T>A maps to NM_134444.4 A403A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QX-01A-11D-A377-08 chr19:56369988 C>T maps to NM_134444.4 D410D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr19:56539872 A>G maps to NM_153447.4 L758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7F3-01A-21D-A33T-08 chr19:56515210 G>C maps to NM_153447.4 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr19:56459477 C>A maps to NM_176811.2 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WL-01A-11D-A377-08 chr19:56223889 C>A maps to NM_176820.2 G856G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7736-01A-11D-2114-08 chr11:119043648 T>C maps to NM_024618.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr1:892348 G>T maps to NM_015658.3 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr7:30491718 G>T maps to NM_006092.2 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SR-01B-11D-A377-08 chr1:6592682 T>A maps to NM_024654.4 K459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6367-01A-11D-1786-08 chr2:203149109 G>T maps to NM_015934.3 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr12:117660555 C>T maps to ENST00000338101 L1347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TB-01A-11D-A364-08 chr12:117657906 G>A maps to ENST00000338101 D1415D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr1:162313728 A>G maps to NM_014697.2 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr1:120539833 A>T maps to NM_024408.2 C179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr6:32164198 C>A did not map to a codon.
Sequencing variant TCGA-G9-6385-01A-11D-1786-08 chr6:32163813 C>T maps to NM_004557.3 A1804A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83H-01A-11D-A34U-08 chr6:32180341 C>A maps to NM_004557.3 G863G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr14:26949215 G>T maps to ENST00000449198 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr14:26917260 T>C maps to ENST00000449198 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr11:66192367 C>T maps to NM_178864.3 D669D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr11:108032026 A>G maps to NM_002519.2 S1262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr11:108068118 A>G maps to NM_002519.2 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr20:62737950 C>T maps to NM_005286.2 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8D1-01A-11D-A364-08 chr7:44575522 C>A maps to NM_013389.2 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A71Y-01A-22D-A32B-08 chr7:44553093 A>C maps to NM_013389.2 G1344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr20:57290252 C>T maps to NM_024663.3 A481A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WJ-01A-11D-A377-08 chr2:110922635 T>A maps to NM_000272.3 K241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr1:5964827 C>T maps to NM_015102.2 K664K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-8200-01A-11D-A29Q-08 chr1:179526350 G>A maps to NM_014625.2 D183D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SJ-01B-11D-A377-08 chr7:98257787 C>T maps to NM_002523.2 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr7:25264784 G>A maps to NM_022150.3 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr4:164272283 A>C maps to NM_006174.2 R287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MU-01A-11D-A377-08 chr1:161203128 C>A did not map to a codon.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr15:96880727 C>A maps to NM_021005.3 S374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SJ-01B-11D-A377-08 chr10:115364398 C>T maps to ENST00000369358 W1407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr21:16338591 G>T maps to NM_003489.3 S641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr2:206562331 C>A maps to NM_201266.1 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7748-01A-11D-2114-08 chr2:206641225 G>A maps to NM_018534.3 E899E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7521-01A-11D-2260-08 chr5:176720971 T>A maps to NM_022455.4 S2201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr23:152037458 A>G did not map to a codon.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr20:1433674 C>T did not map to a codon.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr20:1433743 C>A maps to ENST00000476071 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr20:1435725 G>T maps to ENST00000476071 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr1:46818650 C>A maps to NM_199044.2 S235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6333-01A-12D-1961-08 chr10:104866419 A>C maps to NM_001134373.1 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr11:132081913 A>C did not map to a codon.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr1:107961229 G>A maps to NM_001113228.1 P372P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-HC-7230-01A-11D-2114-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HC-7230-01A-11D-2114-08 chr1:108023233 G>A maps to NM_001113226.1 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr9:135073942 G>T maps to NM_032536.2 R268R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6361-01A-21D-1961-08 chr8:110308623 C>A maps to NM_032869.3 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6353-01A-11D-1961-08 chr9:34343326 C>T maps to NM_147173.1 H111H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6G3-01A-11D-A30X-08 chr7:135279305 T>C maps to NM_015135.2 A614A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr3:13393390 C>T maps to NM_024923.2 R941R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr3:13370361 C>A maps to NM_024923.2 G1399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr1:153998192 C>A did not map to a codon.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr1:154067629 A>T maps to NM_207308.2 A656A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr1:153965385 G>T maps to NM_207308.2 P1864P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr9:134090729 G>T maps to ENST00000451030 G1909G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr12:102471268 C>A maps to NM_024057.2 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87D-01A-11D-A34U-08 chr16:28549402 G>A maps to NM_001042483.1 H80H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr6:118015305 C>A maps to NM_138459.3 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IP-01A-11D-A31L-08 chr23:102337985 G>A did not map to a codon.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr14:24880586 C>A maps to NM_025081.2 S858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr10:126091507 C>A maps to NM_000274.3 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr2:192549020 G>T maps to NM_001031716.2 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr1:228456387 C>T maps to NM_001098623.1 R1673R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr1:228462474 G>T maps to NM_001098623.1 L1962L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6333-01A-12D-1961-08 chr1:228433201 G>C maps to NM_001098623.1 V1190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr1:228482723 C>A maps to NM_001098623.1 S3880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7211-01A-11D-2114-08 chr1:228466408 G>A maps to NM_001098623.1 V2293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HO-01A-11D-A364-08 chr8:133053366 G>A maps to ENST00000262283 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr4:48851970 T>C maps to NM_001168254.1 C88C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HM-01A-11D-A364-08 chr23:128679012 A>C did not map to a codon.
Sequencing variant TCGA-ZG-A8QX-01A-11D-A377-08 chr9:131231506 C>T maps to NM_153435.1 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7314-01A-31D-2114-08 chr23:123839058 G>A did not map to a codon.
Sequencing variant TCGA-YL-A9WJ-01A-11D-A377-08 chr23:123514727 C>T did not map to a codon.
Sequencing variant TCGA-G9-7519-01A-11D-2260-08 chr5:167673769 C>A maps to NM_001122679.1 V1933V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr4:183522254 C>A maps to NM_001080477.1 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr4:183522161 C>A maps to NM_001080477.1 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr4:183714865 C>A maps to NM_001080477.1 T2347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7170-01A-11D-2114-08 chr4:183675932 C>T maps to NM_001080477.1 L1471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr11:78443390 T>C maps to NM_001098816.2 A1036A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr11:78381218 G>A maps to NM_001098816.2 Y2057Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr23:70767812 T>G did not map to a codon.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr1:114524120 C>A maps to NM_020190.2 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8S9-01A-11D-A377-08 chr15:53080998 G>A maps to NM_004498.1 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr3:193332787 C>T maps to NM_130837.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7F6-01A-11D-A33T-08 chr11:123886346 C>T maps to ENST00000375021 D22D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IP-01A-11D-A31L-08 chr11:123886914 C>T maps to NM_001004462.1 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr11:123909642 G>A maps to NM_001004463.1 D22D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr11:123893784 C>T maps to NM_001001953.1 D22D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I6-01A-11D-A364-08 chr19:15852462 C>T maps to NM_013938.1 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr1:158368836 C>T maps to NM_001004475.1 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IB-01A-11D-A364-08 chr1:158369195 G>A maps to NM_001004475.1 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr1:158576524 C>T maps to NM_001004478.1 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr1:158576872 C>T maps to NM_001004478.1 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr9:107361056 A>T maps to NM_001004482.1 L213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr23:130678845 C>A did not map to a codon.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr23:130678203 C>T did not map to a codon.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr17:3119034 G>T maps to NM_014565.2 G41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr9:125316128 C>A maps to NM_001004457.1 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6333-01A-12D-1961-08 chr7:143806791 G>T maps to NM_001005480.2 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr7:143771566 G>A maps to NM_001004488.1 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr7:99474213 G>T maps to NM_001005276.1 S148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7331-01A-11D-2114-08 chr11:6789257 G>A maps to NM_001004490.1 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr1:248128878 C>A maps to NM_001004491.1 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr1:247614411 G>T maps to NM_001004492.1 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr6:29142062 T>A maps to NM_030905.2 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7789-01A-11D-2114-08 chr1:248201937 G>T maps to NM_001004686.2 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:248343967 C>T maps to NM_001004688.1 H227H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr1:248616337 C>T maps to NM_001004136.1 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Z-01A-12D-A26M-08 chr1:248801911 C>G maps to NM_001001827.1 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr1:248525214 C>T maps to NM_001004696.1 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr5:180582178 G>A maps to NM_206880.1 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WH-01A-11D-A377-08 chr17:3195618 A>G maps to ENST00000397187 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr17:3181632 G>A maps to NM_002551.3 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IC-01A-11D-A364-08 chr11:55371195 G>A maps to NM_001004700.1 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VT-01A-11D-A377-08 chr11:49974309 A>C maps to NM_001001955.2 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7327-01A-11D-2114-08 chr17:56247417 C>A maps to NM_001004707.3 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr14:22133361 G>A maps to NM_001001912.1 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MF-01A-11D-A364-08 chr11:4928815 C>T maps to NM_001004749.1 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr11:4791051 A>T maps to ENST00000380383 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88O-01A-11D-A34U-08 chr11:5080815 G>A maps to NM_001005164.2 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr11:5905956 C>T maps to NM_001005165.1 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr11:6048226 T>C maps to NM_001001917.2 K236K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A720-01A-12D-A32B-08 chr14:21624013 C>G maps to NM_001004731.1 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Z-01A-12D-A26M-08 chr11:55541086 T>C maps to NM_001001967.1 H58H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VL-01A-21D-A377-08 chr11:55606970 T>A maps to NM_001005496.1 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QZ-01A-11D-A377-08 chr3:98109898 G>A maps to NM_001005516.1 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr11:56258762 C>T maps to NM_001005282.1 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr11:56043917 C>T maps to NM_001004745.1 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YJ-A8SW-01A-11D-A377-08 chr2:240969798 G>A maps to NM_001005853.1 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr12:55715237 C>A maps to NM_001005182.1 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr12:55945162 C>A maps to NM_001005494.1 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr12:55945168 C>G maps to NM_001005494.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chr12:55794776 T>C maps to NM_001005518.1 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr12:55820711 C>T maps to NM_001005183.1 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr1:158669836 G>T maps to NM_001005279.1 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr1:158687668 G>T maps to ENST00000368146 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A875-01A-31D-A34U-08 chr1:158735833 C>A maps to NM_001005185.1 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6499-01A-12D-1961-08 chr11:123813654 C>A maps to NM_001005187.1 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr19:14938094 C>A maps to NM_017506.1 *320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr19:14910837 G>C maps to NM_198944.1 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr19:9324895 C>A maps to NM_001005191.2 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr7:102087366 C>T maps to NM_032831.2 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr3:31710252 C>T maps to NM_017784.4 W659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr3:31703608 C>A did not map to a codon.
Sequencing variant TCGA-KK-A8IB-01A-11D-A364-08 chr8:90933336 C>T maps to NM_001126111.1 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr2:19553371 C>T maps to NM_145260.2 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7212-01A-11D-2114-08 chr17:72926527 T>C maps to NM_178160.2 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IG-01A-11D-A364-08 chr17:72926515 G>A maps to NM_178160.2 W262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7750-01A-11D-2114-08 chr11:63764356 G>T maps to ENST00000422031 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr4:146058590 C>T maps to ENST00000447906 Q1112Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7708-01A-11D-2114-08 chr4:146058890 A>C maps to ENST00000447906 V1012V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr2:63280184 C>A maps to NM_014562.3 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FS-01A-11D-A34U-08 chr2:63282952 G>A maps to NM_014562.3 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr17:1946352 C>A maps to NM_080822.2 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr3:25833003 T>C maps to NM_017897.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5763-01A-11D-1576-08 chr12:133197606 T>C maps to NM_170683.2 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7821-01A-12D-2114-08 chr23:78216115 A>T did not map to a codon.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr5:131531125 C>A maps to NM_001142599.1 G473G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr20:43545422 G>T maps to NM_001124756.1 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr13:25672096 A>G maps to NM_030979.2 E587E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr22:43267419 G>A maps to NM_001184970.1 R468R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7818-01A-11D-2114-08 chr1:17548934 C>A maps to NM_013358.2 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8261-01A-11D-2260-08 chr1:17690078 C>T maps to NM_012387.2 N607N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr11:77051798 C>A maps to NM_001128620.1 V336V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr20:9546932 T>C maps to NM_177990.2 K363K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HK-01A-11D-A364-08 chr11:35456158 C>G maps to NM_015430.2 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CP-01A-11D-A34U-08 chr12:56720444 T>C maps to NM_001127460.2 T406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr12:56722257 G>A maps to NM_001127460.2 Y150Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr13:28840862 G>T maps to NM_175854.7 E475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IF-01A-11D-A364-08 chr11:124489287 G>A maps to NM_052959.2 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IF-01A-11D-A364-08 chr11:124489569 G>A maps to NM_052959.2 E306E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IF-01A-11D-A364-08 chr11:124489635 G>C maps to NM_052959.2 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr16:50250027 C>A maps to NM_001040284.2 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83G-01A-11D-A34U-08 chr14:73719405 C>T maps to ENST00000427855 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-7775-01A-11D-2114-08 chr9:119065087 T>C maps to NM_002581.3 F1002F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88O-01A-11D-A34U-08 chr9:119106932 C>T maps to NM_002581.3 S1241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr16:3021852 C>T maps to NM_152341.3 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A5OB-01A-11D-A29Q-08 chr6:52268631 C>T maps to ENST00000361841 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chr16:67694961 T>C maps to NM_016948.2 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr1:226550821 G>T maps to NM_001618.3 P942P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr3:122340366 G>T maps to NM_001113523.1 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr3:122259685 G>C maps to NM_031458.2 T501T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7328-01A-31D-2114-08 chr23:150832694 C>G did not map to a codon.
Sequencing variant TCGA-HC-A8D1-01A-11D-A364-08 chr23:150840967 A>G did not map to a codon.
Sequencing variant TCGA-KK-A8IK-01A-11D-A364-08 chr23:150791529 C>T did not map to a codon.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr2:242066483 C>A maps to ENST00000358649 E616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr11:125648647 C>A maps to NM_212555.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76W-01A-11D-A33T-08 chr3:51992298 G>A maps to NM_033010.2 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr5:141242916 C>T maps to NM_032420.2 V993V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr23:91134000 G>T did not map to a codon.
Sequencing variant TCGA-HC-7744-01A-11D-2114-08 chr23:91132875 G>T did not map to a codon.
Sequencing variant TCGA-XJ-A83G-01A-11D-A34U-08 chr23:91090585 A>T did not map to a codon.
Sequencing variant TCGA-ZG-A8QX-01A-11D-A377-08 chr10:55955441 C>T did not map to a codon.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr4:138451633 C>A maps to NM_019035.3 E537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr4:138452261 T>C maps to NM_019035.3 Q327Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr23:99551704 T>C did not map to a codon.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr23:99662670 C>A did not map to a codon.
Sequencing variant TCGA-EJ-7318-01B-11D-A32B-08 chr23:99662942 C>T did not map to a codon.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr13:61986617 G>T maps to NM_022843.3 P538P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8W3-01A-11D-A377-08 chr5:140168037 G>T maps to NM_018900.2 L721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr5:140237081 G>A maps to NM_018901.2 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr5:140250898 G>A maps to NM_018902.3 T737T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr5:140256667 G>A maps to NM_018903.2 A537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr5:140183010 C>T maps to NM_018906.2 S743S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr5:140201749 C>A maps to NM_018908.2 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr5:140202763 G>A maps to NM_018908.2 P468P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I9-01A-11D-A364-08 chr5:140202970 C>T maps to NM_018908.2 R537R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NF-01A-11D-A33T-08 chr5:140209757 G>T maps to NM_018909.2 V694V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FS-01A-11D-A34U-08 chr5:140215503 G>T maps to NM_018910.2 A512A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MU-01A-11D-A377-08 chr5:140215500 C>T maps to NM_018910.2 H511H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MU-01A-11D-A377-08 chr5:140222413 C>A maps to NM_018911.2 S503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BV-01A-31D-A26M-08 chr5:140432440 A>C maps to NM_013340.2 R462R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AV-01A-11D-A32B-08 chr5:140432291 G>T maps to NM_013340.2 E413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr5:140572700 A>G maps to NM_018930.3 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr5:140595716 G>T maps to NM_018933.2 P674P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7230-01A-11D-2114-08 chr5:140595971 A>G maps to NM_018933.2 S759S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr5:140627359 C>T maps to NM_018935.2 D738D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7233-01A-11D-2114-08 chr5:140475282 G>T maps to NM_018936.2 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67T-01A-11D-A30X-08 chr5:140474538 G>T maps to NM_018936.2 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr5:140502608 C>A maps to NM_018938.2 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83I-01A-11D-A364-08 chr5:140531919 G>A maps to NM_018939.2 S694S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr5:140554609 C>T maps to NM_018940.2 R732*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr5:140558061 T>A maps to NM_019120.2 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr5:140794394 G>A maps to NM_018913.2 S551S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr5:140795087 G>A maps to NM_018913.2 T782T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr5:140812029 C>A maps to NM_003735.2 P568P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TK-A8OK-01A-22D-A364-08 chr5:140811042 A>G maps to NM_003735.2 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr5:140720421 G>A maps to NM_018915.2 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr5:140723734 G>T maps to NM_018916.3 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr5:140735372 C>T maps to NM_018917.2 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7737-01A-11D-2114-08 chr5:140735009 C>T maps to NM_018917.2 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr5:140745591 C>A maps to NM_018918.2 P565P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr5:140773099 G>A maps to NM_032088.1 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SH-01B-11D-A377-08 chr5:140772817 G>A maps to NM_032088.1 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IB-01A-11D-A364-08 chr5:140783253 G>T maps to NM_018921.2 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr5:140857426 C>A maps to NM_002588.2 R582R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr13:113849440 T>C did not map to a codon.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr7:82545721 G>T maps to NM_033026.5 P3860P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr7:82545751 C>T maps to NM_033026.5 Q3850Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A71Y-01A-22D-A32B-08 chr7:82430882 T>C maps to NM_033026.5 Q4986Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr14:71514562 G>A maps to NM_014982.2 L1400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QY-01A-11D-A377-08 chr1:233394211 G>A maps to NM_014801.3 Q466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr21:41301035 G>C maps to NM_006198.2 *63Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr15:101938638 A>C maps to NM_002570.3 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr1:55521762 C>T maps to NM_174936.3 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr5:148747556 G>A maps to NM_024028.3 E275E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr6:165832168 C>A maps to NM_001130690.1 E318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr11:14808095 G>T maps to NM_000922.3 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr1:145015937 C>T maps to NM_001198832.1 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7328-01A-31D-2114-08 chr1:144916718 G>A maps to NM_014644.4 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8W3-01A-11D-A377-08 chr10:95399904 T>C maps to NM_006204.3 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FS-01A-11D-A34U-08 chr21:44190854 G>T maps to NM_002606.2 E545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr8:17447025 G>A maps to NM_006207.2 E35E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr2:10929047 A>T maps to ENST00000381611 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr16:20370790 C>T maps to NM_174924.1 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr23:24516990 C>T did not map to a codon.
Sequencing variant TCGA-EJ-A8FS-01A-11D-A34U-08 chr5:32089031 T>C maps to NM_178140.2 P1826P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr5:32090292 C>A maps to NM_178140.2 R2247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A48F-01A-11D-A257-08 chr5:32089964 A>G maps to NM_178140.2 A2137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6M7-01A-11D-A31L-08 chr5:32089673 G>A maps to NM_178140.2 A2040A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr23:153073954 G>A did not map to a codon.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr3:73440204 C>A maps to NM_015009.1 T439T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr1:156877419 C>T maps to NM_001080471.1 S221S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-KK-A8IA-01A-11D-A364-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-XQ-A8TB-01A-11D-A364-08 chr19:57326530 G>A maps to NM_006210.2 D1093D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I6-01A-11D-A364-08 chr11:45937358 C>T maps to NM_057174.2 W85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52B-01A-11D-A26M-08 chr8:77895774 G>A maps to NM_001172087.1 Q214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46D-01A-21D-A257-08 chr6:143780271 G>T maps to NM_003630.2 E42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A875-01A-31D-A34U-08 chr3:179605497 C>T maps to NM_016559.1 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7736-01A-11D-2114-08 chr23:54989708 C>T did not map to a codon.
Sequencing variant TCGA-ZG-A8QY-01A-11D-A377-08 chr10:3177926 G>A did not map to a codon.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr23:77369511 G>T did not map to a codon.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr11:100962583 C>A maps to NM_000926.4 G605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83G-01A-11D-A34U-08 chr1:28764898 G>T maps to NM_023923.3 G2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr23:22132641 C>A did not map to a codon.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr5:133914475 G>A maps to ENST00000448712 G674G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr23:46887490 G>A did not map to a codon.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr4:129778548 C>A maps to NM_199320.2 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr20:34389528 T>G did not map to a codon.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr20:34458922 A>G maps to NM_016436.4 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr6:64404529 G>A maps to NM_015153.2 Q852Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr23:54029073 A>C did not map to a codon.
Sequencing variant TCGA-KK-A8IC-01A-11D-A364-08 chr6:79672823 C>T maps to NM_017934.5 L1175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7230-01A-11D-2114-08 chr23:71840633 A>T did not map to a codon.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr11:118501982 G>T maps to NM_015157.2 G629G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr11:118498441 C>A maps to NM_015157.2 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr11:118516356 C>T maps to NM_015157.2 D1135D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WV-01A-11D-A377-08 chr11:118514552 C>T maps to NM_015157.2 S971S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr7:77567151 C>T maps to ENST00000427986 N488N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7736-01A-11D-2114-08 chr10:60994190 T>C maps to NM_032439.3 D78D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr10:99426204 C>G maps to ENST00000416867 Y335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SL-01B-21D-A377-08 chr22:21097022 G>T maps to NM_058004.2 T1104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Z-01A-12D-A26M-08 chr13:73396006 A>G maps to NM_006346.2 K231K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr2:229890758 T>A maps to NM_017933.4 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr23:15342938 T>C did not map to a codon.
Sequencing variant TCGA-2A-A8VT-01A-11D-A377-08 chr10:98386516 G>A maps to NM_152309.2 T539T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr10:98412455 G>T maps to NM_152309.2 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr1:204433186 C>A maps to NM_002646.3 V421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr18:39607409 T>C maps to ENST00000398870 Y497Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr3:178952025 C>A maps to NM_006218.2 A1027A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr19:18273221 G>T maps to NM_005027.2 E339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6DY-01A-12D-A30X-08 chr1:46527680 C>T maps to NM_001114172.1 E228E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FD-01A-11D-A33T-08 chr3:130452641 T>C maps to NM_014602.2 E400E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr17:8792522 C>T maps to NM_001142633.1 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WI-01A-11D-A377-08 chr12:57994721 C>T maps to NM_024779.4 S314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr19:3643242 G>A maps to NM_012398.2 Y549Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FU-01A-11D-A364-08 chr9:130688197 G>A maps to NM_001135219.1 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr17:27380588 C>A maps to NM_016518.2 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7328-01A-31D-2114-08 chr10:103990273 T>C maps to NM_005029.3 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A879-01A-11D-A34U-08 chr22:25147434 A>G maps to NM_001008496.2 D336D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A878-01A-31D-A34U-08 chr16:2161024 G>A maps to NM_001009944.2 G1381G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr4:88957412 C>A maps to NM_000297.2 R251R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6329-01A-13D-1961-08 chr10:102048746 G>A maps to NM_016112.2 Q773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr22:46658214 G>T maps to NM_006071.1 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr6:51609252 C>A maps to NM_138694.3 L3362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr6:51524057 G>A maps to NM_138694.3 C3622C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8472-01A-11D-2395-08 chr8:110420308 T>A maps to ENST00000426474 V615V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr1:186915808 A>G maps to NM_024420.2 K358K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SL-01B-21D-A377-08 chr1:186925323 C>G maps to NM_024420.2 S476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I5-01A-11D-A364-08 chr15:42279574 T>G did not map to a codon.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr15:42446633 C>T maps to ENST00000397272 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr20:9416221 T>G maps to NM_001172646.1 L847*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr16:81942028 C>A maps to NM_002661.2 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr16:81944187 C>T maps to NM_002661.2 Y599Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr1:2419085 C>A maps to NM_014638.2 Y388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr17:4713046 C>A maps to NM_002663.3 R226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr19:40880401 C>A maps to NM_012268.2 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AP-01A-12D-A33T-08 chr8:144990641 C>G maps to NM_201380.2 A4586A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6DY-01A-12D-A30X-08 chr12:19436439 C>T maps to ENST00000429027 Q514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr7:30084732 G>T maps to ENST00000440706 G51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr6:151130590 C>A maps to NM_001029884.1 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr19:39907505 C>A maps to NM_022835.2 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr2:208866225 C>A maps to NM_001080475.2 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr1:150131387 C>A maps to ENST00000443480 P331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chr4:128818020 G>T maps to NM_014264.4 V923V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7213-01A-11D-2114-08 chr3:146246433 T>C maps to NM_021105.2 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7213-01A-11D-2114-08 chr3:146307580 C>T maps to NM_001085420.1 K212K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YJ-A8SW-01A-11D-A377-08 chr17:37243902 G>A maps to NM_020405.4 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CP-01A-11D-A34U-08 chr22:50720453 C>G maps to NM_012401.2 P1058P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr23:153039435 C>T did not map to a codon.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr12:94641722 C>A maps to NM_005761.1 P811P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HJ-01A-11D-A364-08 chr1:156203418 G>T maps to NM_007221.3 E90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr6:160237000 T>C maps to NM_173516.1 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr23:152158950 T>G did not map to a codon.
Sequencing variant TCGA-J4-A83K-01A-11D-A34U-08 chr19:46997771 C>T maps to NM_020709.1 Q317Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr6:36270247 T>C did not map to a codon.
Sequencing variant TCGA-J4-A6M7-01A-11D-A31L-08 chr23:7880087 A>G did not map to a codon.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr9:140379165 C>A maps to NM_001098537.1 T740T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr23:84561265 G>T did not map to a codon.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr23:24861701 A>G did not map to a codon.
Sequencing variant TCGA-J4-8198-01A-11D-2260-08 chr11:74303720 T>G maps to NM_006591.1 Y6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr17:26680001 G>A maps to NM_015584.3 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr17:62492846 A>G maps to NM_007215.3 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr17:62492984 C>A maps to NM_007215.3 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr17:62492935 C>A maps to NM_007215.3 E51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65G-01A-21D-A29Q-08 chr3:121208387 A>G maps to ENST00000393672 N1266N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr17:7399793 C>A maps to NM_000937.4 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr4:57876616 A>C maps to NM_000938.1 R499R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr1:145601556 G>T maps to NM_006468.6 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr8:22105703 A>G maps to NM_001722.2 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr7:53104000 C>A maps to NM_182595.3 R213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr9:134390830 C>A maps to NM_007171.3 P420P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr8:43147833 C>G maps to NM_001005365.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SH-01B-11D-A377-08 chr2:131976100 C>T maps to NM_001083538.1 N42N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr2:130832649 C>A maps to NM_001099771.2 E799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr8:128428779 A>C maps to NM_001159542.1 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr7:39500236 T>A maps to NM_007252.3 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52B-01A-11D-A26M-08 chr5:54771250 G>T maps to NM_003711.2 S29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr4:23815647 G>A maps to NM_013261.3 D486D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CL-01A-11D-A34U-08 chr5:149212574 C>G maps to NM_133263.3 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr23:18842130 A>G did not map to a codon.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr23:18775836 C>A did not map to a codon.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr4:76813114 G>A maps to NM_006239.2 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65E-01A-11D-A29Q-08 chr19:49653358 G>C maps to NM_003660.2 R1183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr19:49633699 C>T maps to NM_003660.2 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr2:170493831 C>A maps to NM_004792.2 P688P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7748-01A-11D-2114-08 chr2:170493057 A>G maps to NM_004792.2 K430K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr6:149826609 T>C maps to NM_139126.2 K486K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr15:43827081 G>A maps to NM_001130858.2 T1364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr14:60749575 C>A maps to NM_177952.2 S125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CP-01A-11D-A34U-08 chr1:161140215 G>A maps to NM_001122764.1 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FS-01A-11D-A34U-08 chr14:104212713 T>C maps to NM_015316.2 K382K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr14:104251153 G>A maps to NM_015316.2 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr8:145722825 C>T maps to NM_032902.5 D83D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HK-01A-11D-A364-08 chr8:145726590 C>T maps to NM_032902.5 Q373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr7:113518487 C>A maps to NM_002711.3 E887*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FS-01A-11D-A34U-08 chr7:113519778 G>C maps to NM_002711.3 P456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8D0-01A-11D-A364-08 chr7:113519010 T>C maps to NM_002711.3 E712E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IL-01A-11D-A364-08 chr7:113519340 A>G maps to NM_002711.3 H602H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr17:48216820 G>T maps to NM_032595.3 P662P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr5:145969653 C>A maps to ENST00000394414 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88P-01A-11D-A34U-08 chr5:146080618 G>A maps to ENST00000394414 R119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7318-01B-11D-A32B-08 chr3:135722331 C>T maps to NM_002718.4 I664I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr23:307978 G>T did not map to a codon.
Sequencing variant TCGA-HC-A76W-01A-11D-A33T-08 chr11:64694284 G>T maps to NM_006244.3 E101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr6:32122415 G>A maps to NM_138717.1 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr10:47087379 G>T maps to NM_005972.4 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FD-01A-11D-A33T-08 chr1:12854345 G>A maps to NM_023013.2 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7075-01A-11D-1961-08 chr1:12884844 G>A maps to NM_001146344.1 G422G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CK-01A-11D-A34U-08 chr1:12887307 C>T maps to NM_001146344.1 Q183Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IP-01A-11D-A31L-08 chr12:11461247 C>T maps to NM_002723.3 K223K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr15:91524743 T>C maps to NM_003981.2 Q219Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr11:129772216 G>T maps to NM_020228.2 T1158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr8:70978695 T>C maps to NM_024504.2 G319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr21:43281788 C>A maps to NM_022115.3 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr1:3328641 C>T maps to NM_022114.3 S627S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WH-01A-11D-A377-08 chr1:3328821 C>T maps to NM_022114.3 G687G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr4:81123290 C>A maps to NM_001099403.1 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NJ-01A-22D-A34U-08 chr5:23526963 T>C maps to NM_020227.2 F589F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr20:47317358 C>A maps to NM_020820.3 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr1:186275975 C>A maps to NM_005807.3 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IH-01A-11D-A364-08 chr12:120110137 G>A maps to NM_006253.4 Q64Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr19:14204547 C>A maps to NM_002730.3 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A4JI-01A-11D-A257-08 chr17:66519942 T>C maps to NM_212472.1 D142D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7783-01A-11D-2114-08 chr19:54395834 C>T maps to NM_002739.3 N253N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QW-01A-11D-A377-08 chr19:47219513 G>A maps to ENST00000449438 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WL-01A-11D-A377-08 chr8:48776072 C>A maps to NM_006904.6 V1878V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7818-01A-11D-2114-08 chr11:20409623 G>T maps to NM_005788.3 E30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WV-01A-11D-A377-08 chr11:20424496 C>T maps to NM_005788.3 F246F. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CH-5771-01A-21D-1576-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr14:23397823 C>A maps to NM_006109.3 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chr14:23395505 C>G did not map to a codon.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr1:107600026 C>T maps to NM_018137.2 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr2:68882251 G>T maps to NM_138964.2 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88O-01A-11D-A34U-08 chr20:5283270 G>T maps to NM_144773.2 Y190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A725-01A-12D-A32B-08 chr4:16019993 G>A maps to NM_006017.2 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WS-01A-11D-A377-08 chr5:177419967 G>A maps to NM_006261.4 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chr1:214171236 C>T maps to NM_002763.3 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr17:74308970 C>A maps to NM_002766.2 E327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SF-01A-11D-A377-08 chr19:50123645 G>A maps to NM_020719.1 A1845A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr5:120022391 T>C maps to NM_016644.1 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr19:5784047 T>C maps to NM_001134316.1 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr12:10999751 G>T maps to NM_007244.2 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr22:45128195 G>C maps to ENST00000352766 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr23:37285149 G>A did not map to a codon.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr16:2770146 C>T maps to NM_031948.3 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SL-01B-21D-A377-08 chr16:58314535 G>A maps to NM_001080492.1 Y260Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr10:25160953 G>A maps to NM_020200.5 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46D-01A-21D-A257-08 chr19:40901384 C>T maps to NM_181882.2 K958K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7750-01A-11D-2114-08 chr19:40903196 G>A maps to NM_181882.2 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SK-01B-21D-A377-08 chr9:80923473 T>C maps to ENST00000421149 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr5:139215339 G>T maps to NM_032289.2 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr8:18729461 C>A maps to ENST00000440756 V304V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TK-A8OK-01A-22D-A364-08 chr2:113958985 G>A maps to NM_012455.2 Q1055Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr19:43519266 C>A did not map to a codon.
Sequencing variant TCGA-ZG-A8QY-01A-11D-A377-08 chr19:43244509 G>A maps to NM_021016.3 C9C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr19:43680256 G>T maps to ENST00000270059 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A4JI-01A-11D-A257-08 chr19:43439763 G>A maps to NM_002783.2 D74D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr18:23759095 T>C did not map to a codon.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr14:24614266 C>A maps to ENST00000429021 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr13:20356678 C>A maps to NM_001042414.1 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8ID-01A-11D-A364-08 chr19:804111 G>T maps to NM_002819.4 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IJ-01A-11D-A34U-08 chr1:45295345 A>T maps to NM_003738.4 I341I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr10:27702747 C>T maps to NM_001034842.3 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr10:89690801 G>A did not map to a codon.
Sequencing variant TCGA-HC-7230-01A-11D-2114-08 chr10:89692848 G>A maps to NM_000314.4 W111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr2:209302259 A>T did not map to a codon.
Sequencing variant TCGA-EJ-5505-01A-01D-1576-08 chr2:209358095 G>T maps to NM_005048.2 V455V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr2:209292994 G>T maps to NM_005048.2 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67T-01A-11D-A30X-08 chr2:209307105 C>T maps to NM_005048.2 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr12:28116546 G>T maps to ENST00000354417 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SA-01A-21D-A377-08 chr7:136936040 G>A maps to NM_002825.5 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr9:96850148 C>A maps to ENST00000434261 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FA-01A-21D-A33T-08 chr9:96860385 C>G maps to ENST00000434261 S513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WI-01A-11D-A377-08 chr3:47437634 T>C maps to NM_015466.2 F29F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr9:112185101 C>T maps to NM_002829.3 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr12:7061280 C>T maps to ENST00000416215 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr15:75819590 C>T maps to NM_002833.2 Q25Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr1:198719700 C>T maps to ENST00000271610 F1051F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr1:198711450 T>C maps to ENST00000271610 Y884Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr9:8465564 C>A maps to NM_002839.3 L1205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A879-01A-11D-A34U-08 chr9:8636727 C>A maps to NM_002839.3 G61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr10:129867973 G>T maps to NM_006504.4 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IC-01A-11D-A364-08 chr10:129854463 C>T maps to NM_006504.4 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr11:48161137 G>A maps to NM_002843.3 E751E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr18:8113636 C>A maps to NM_001105244.1 L670L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr12:15710428 G>T maps to NM_030667.1 E867*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7794-01A-11D-2114-08 chr12:15742394 C>T maps to NM_030667.1 G1139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr7:121652282 G>A maps to NM_002851.2 E1061E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E0-01A-11D-A30X-08 chr2:20463105 A>C maps to ENST00000361078 P691P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr19:45389442 C>A maps to NM_001042724.1 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6336-01A-11D-1786-08 chr8:52320733 G>T maps to NM_144651.4 I1150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FA-01A-21D-A33T-08 chr14:51383368 G>C maps to NM_002863.4 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr11:64525942 C>A maps to NM_005609.2 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr10:100154986 C>A maps to NM_032709.2 G251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr12:9318702 C>A maps to NM_002864.2 E735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr17:29849384 C>A maps to NM_032932.3 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WW-A8ZI-01A-11D-A377-08 chr5:176728924 C>G did not map to a codon.
Sequencing variant TCGA-HC-A632-01A-11D-A29Q-08 chr4:140393994 T>C maps to NM_031296.1 H135H. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CH-5739-01A-11D-1576-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-J4-A6G3-01A-11D-A30X-08 chr17:72736965 C>T maps to NM_001006638.2 D51D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr19:18313412 C>T maps to NM_002866.4 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr23:102755041 G>T did not map to a codon.
Sequencing variant TCGA-KK-A8II-01A-11D-A364-08 chr1:229431651 C>T maps to NM_004578.2 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FA-01A-21D-A33T-08 chr2:130738002 A>G maps to NM_032144.2 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr23:13727113 C>T did not map to a codon.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr17:5264855 A>G maps to NM_004703.4 Q483Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83I-01A-11D-A364-08 chr17:5264970 G>C did not map to a codon.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr9:125760996 C>A maps to NM_012197.3 P442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr8:117878923 G>A maps to NM_006265.2 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SO-01B-31D-A377-08 chr8:117859876 T>G maps to NM_006265.2 R586R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7F3-01A-21D-A33T-08 chr7:4874798 G>A maps to NM_018059.4 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr6:150209735 C>A maps to NM_139165.1 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr6:150211084 C>A maps to NM_139165.1 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr5:34826504 C>G maps to NM_001145521.1 S907*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr14:36039875 T>G maps to NM_194301.2 T1975T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr20:37194024 G>T maps to NM_020336.2 G1241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr9:129930976 C>A maps to NM_014636.2 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr8:85441792 C>G maps to NM_001100391.1 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7523-01A-11D-2260-08 chr7:45222941 C>T maps to NM_005856.2 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr2:109365451 C>T maps to NM_006267.4 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WI-01A-11D-A377-08 chr9:6015580 C>A maps to NM_012416.2 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8W3-01A-11D-A377-08 chr6:13625975 T>C maps to NM_005493.2 A656A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr17:2908721 C>A maps to NM_015085.4 P420P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr9:134497350 C>T maps to NM_198679.1 S580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr17:38348922 C>A maps to ENST00000456989 P573P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6336-01A-11D-1786-08 chr13:114780694 C>T maps to ENST00000389544 K472K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr20:35668628 G>T maps to NM_002895.2 P610P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr20:35668589 C>T maps to NM_002895.2 K623K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7233-01A-11D-2114-08 chr16:53485705 T>C maps to NM_005611.3 C243C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87D-01A-11D-A34U-08 chr21:15592039 C>T maps to NM_144770.3 R85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SJ-01B-11D-A377-08 chr20:34240453 A>G maps to NM_001198838.1 L931L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr6:155131225 C>G maps to NM_014892.3 S435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr5:145641191 G>A maps to NM_018989.1 W671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr20:34312595 C>A maps to NM_184234.1 G195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr2:238738069 C>A maps to NM_001080504.2 S938S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SA-01A-21D-A377-08 chr2:238737874 T>C maps to NM_001080504.2 A873A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46D-01A-21D-A257-08 chr3:50005400 T>C maps to NM_005777.2 Y181Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr23:135961212 G>T did not map to a codon.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr10:48390796 C>A maps to NM_002900.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr15:65041349 C>A did not map to a codon.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr9:125622391 G>T maps to NM_001100588.1 P551P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr13:50123714 G>A maps to NM_018191.3 Y308Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HO-01A-11D-A364-08 chr14:24642194 C>T maps to NM_005132.2 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AU-01A-11D-A32B-08 chr12:21626536 T>C maps to NM_032941.2 V465V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr17:73658780 C>A maps to NM_004259.5 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr1:120342380 C>T maps to NM_032044.3 Q90Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr5:141017908 C>G maps to NM_173828.4 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65E-01A-11D-A29Q-08 chr7:103341382 C>T maps to ENST00000428762 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr7:103234872 G>T maps to ENST00000428762 P1202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr12:18237548 C>A maps to NM_024730.2 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr2:100055180 C>T maps to NM_016316.2 K365K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr17:33344574 G>A maps to NM_001017368.1 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QZ-01A-11D-A377-08 chr16:74670337 T>C maps to NM_018124.3 V444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IP-01A-11D-A31L-08 chr19:14083866 G>A maps to NM_002918.4 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FN-01A-11D-A34U-08 chr9:3293174 G>A maps to NM_134428.1 H211H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr12:107144483 C>A maps to ENST00000357881 P625P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6353-01A-11D-1961-08 chr6:117248235 C>A maps to NM_173560.3 P644P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QW-01A-11D-A377-08 chr13:37399673 T>C did not map to a codon.
Sequencing variant TCGA-HC-8261-01A-11D-2260-08 chr23:71351090 C>T did not map to a codon.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr1:183881371 C>A maps to NM_015149.3 P608P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr2:108487616 G>T maps to NM_182588.2 G1053*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr8:54791831 A>T maps to NM_170587.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr1:163122354 C>T maps to NM_003617.3 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MF-01A-11D-A364-08 chr5:63890652 C>T maps to NM_001029875.1 Q194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I5-01A-11D-A364-08 chr19:33167291 A>G maps to NM_207391.2 Q41Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr2:227729678 G>A maps to NM_001167608.1 W90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr17:74467834 G>A maps to NM_024599.5 A817A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr16:726865 C>A maps to NM_003961.1 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr5:95067625 G>T maps to NM_014899.3 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SK-01B-21D-A377-08 chr5:95067674 G>T maps to NM_014899.3 E39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr14:63671715 C>T maps to NM_020663.3 N43N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr19:33535270 C>A did not map to a codon.
Sequencing variant TCGA-HI-7170-01A-11D-2114-08 chr17:12847398 G>A maps to NM_014859.4 E249E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83H-01A-11D-A34U-08 chr12:123915095 C>T maps to NM_145058.1 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr14:24808679 C>A maps to NM_006871.3 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr14:21250157 C>T maps to NM_005615.4 N100N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr1:182550488 G>A maps to NM_021133.3 R592R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88K-01A-11D-A34U-08 chr23:119005302 C>T did not map to a codon.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr8:125498994 G>T maps to NM_007218.3 G369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr2:7160685 G>A maps to NM_014746.3 Q128Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr21:30318242 C>A maps to NM_015565.2 L1264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr13:25376710 T>A did not map to a codon.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr13:25376710 T>A did not map to a codon.
Sequencing variant TCGA-ZG-A8QX-01A-11D-A377-08 chr13:25348979 C>T maps to ENST00000381927 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83I-01A-11D-A364-08 chr9:104314096 A>G maps to NM_019592.5 Q468Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr22:30776080 C>T maps to NM_001017981.1 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6333-01A-12D-1961-08 chr22:30776080 C>A maps to NM_001017981.1 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-7775-01A-11D-2114-08 chr7:5780783 A>C maps to NM_207111.2 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SC-01A-11D-A377-08 chr1:44877960 C>T maps to ENST00000453887 N64N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr13:26788079 G>A maps to NM_005977.3 Q647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr6:117663707 C>A did not map to a codon.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr6:117645560 C>A maps to NM_002944.2 E1859*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr6:117662660 G>A maps to NM_002944.2 L1602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr8:55540710 T>A maps to NM_006269.1 C1423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A71Y-01A-22D-A32B-08 chr8:55533942 C>G maps to NM_006269.1 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88N-01A-11D-A364-08 chr8:55540776 T>A maps to NM_006269.1 S1445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IL-01A-11D-A364-08 chr8:10468856 C>T maps to NM_178857.5 A917A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr1:68906684 T>C did not map to a codon.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr14:21796692 C>A maps to NM_020366.3 Y1002*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7170-01A-11D-2114-08 chr14:21790126 G>T maps to NM_020366.3 E576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MJ-01A-11D-A364-08 chr12:113307698 C>A maps to NM_001143854.1 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B1-01A-11D-A32B-08 chr6:35437257 G>T maps to NM_007104.4 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7F3-01A-21D-A33T-08 chr3:23960790 C>T maps to NM_002948.2 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr2:101619171 C>A maps to NM_000993.4 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr8:146015221 C>A maps to NM_000973.3 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr10:15145357 G>A maps to NM_183005.3 K15K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr20:36686046 G>T did not map to a codon.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr23:20185707 C>A did not map to a codon.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr23:83411184 A>T did not map to a codon.
Sequencing variant TCGA-HC-7209-01A-11D-2114-08 chr3:39450136 T>G maps to ENST00000443003 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr17:78796033 C>A maps to NM_020761.2 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr20:17622554 T>A maps to ENST00000377813 K691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XA-A8JR-01A-11D-A364-08 chr6:7240689 T>A maps to NM_001003699.3 C1276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7820-01A-11D-2114-08 chr11:4130914 C>A maps to NM_001033.3 Y143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr10:99139074 G>T maps to NM_015179.3 P591P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr17:48557075 T>C maps to NM_018346.1 C74C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6329-01A-13D-1961-08 chr20:62320907 G>T maps to ENST00000482936 T644T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B1-01A-11D-A32B-08 chr15:41769658 C>T maps to NM_015138.4 Y562Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr3:46539656 C>A maps to NM_031440.1 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8S9-01A-11D-A377-08 chr10:70105525 C>A maps to NM_017987.4 *642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88L-01A-11D-A34U-08 chr7:87369181 T>C maps to NM_138290.2 N195N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr3:72428399 A>T did not map to a codon.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr19:39039026 C>A maps to NM_000540.2 P4083P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7740-01A-11D-2114-08 chr19:38934380 C>T maps to NM_000540.2 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr1:237754088 T>A maps to NM_001035.2 A1319A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6333-01A-12D-1961-08 chr1:237711847 G>A maps to NM_001035.2 A1008A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr1:237756846 T>C maps to NM_001035.2 D1449D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88L-01A-11D-A34U-08 chr1:237923149 T>C maps to NM_001035.2 C3800C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr15:33835895 C>T maps to NM_001036.3 D240D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46I-01A-12D-A26M-08 chr15:33941373 C>T maps to NM_001036.3 D1360D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6M7-01A-11D-A31L-08 chr15:33795932 C>T maps to NM_001036.3 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IP-01A-11D-A31L-08 chr15:34015066 C>T maps to NM_001036.3 D2257D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8X3-01A-11D-A377-08 chr15:34157423 A>C maps to NM_001036.3 G4870G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:153516336 G>A maps to NM_002961.2 N68N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr4:6695685 C>T maps to NM_005980.2 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr19:10335296 A>T maps to NM_004230.3 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr19:10625417 G>A maps to NM_001166215.1 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr3:45761022 A>G maps to NM_014016.3 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr2:234237187 C>T maps to NM_000541.4 R193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6366-01A-11D-2114-08 chr2:234237162 C>T maps to NM_000541.4 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr23:134990667 A>C did not map to a codon.
Sequencing variant TCGA-CH-5763-01A-11D-1576-08 chr17:48193047 C>T maps to NM_174920.2 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7523-01A-11D-2260-08 chr6:130467206 A>G maps to ENST00000457563 N405N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr19:39866396 C>A maps to NM_018028.2 R259R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6G3-01A-11D-A30X-08 chr7:92734006 T>C maps to NM_017654.3 V468V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I8-01A-11D-A364-08 chr7:92735119 T>C maps to NM_017654.3 K97K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7750-01A-11D-2114-08 chr22:50862021 C>T maps to ENST00000216061 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7218-01B-11D-A32B-08 chr23:128927060 C>A did not map to a codon.
Sequencing variant TCGA-M7-A725-01A-12D-A32B-08 chr2:200233397 A>T maps to NM_001172509.1 Y210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6333-01A-12D-1961-08 chr14:51132077 C>A maps to NM_021818.2 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr22:50905972 C>A maps to ENST00000337034 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8S8-01A-11D-A377-08 chr11:9838384 A>G did not map to a codon.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr12:123834910 A>G maps to NM_001167856.1 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr19:1113560 C>T maps to NM_014963.2 Q740Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87B-01A-11D-A34U-08 chr6:28554184 G>A maps to NM_052923.1 L104L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CH-5748-01A-11D-1576-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr17:1543258 G>T maps to NM_003693.2 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr10:102107909 C>A maps to NM_005063.4 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E1-01A-11D-A30X-08 chr15:51975310 A>G maps to NM_013243.3 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr11:62038407 G>C maps to NM_002411.2 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7331-01A-11D-2114-08 chr1:41494398 C>A did not map to a codon.
Sequencing variant TCGA-EJ-7785-01A-11D-2114-08 chr3:38802755 G>T maps to NM_006514.2 G270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7791-01A-11D-2114-08 chr3:38835294 C>T maps to NM_006514.2 E69E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7708-01A-11D-2114-08 chr3:38766806 T>C did not map to a codon.
Sequencing variant TCGA-KK-A8ID-01A-11D-A364-08 chr3:38924807 C>A maps to ENST00000302328 L1045L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr2:166852623 C>A maps to NM_001165963.1 G1494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr2:166848588 G>T maps to NM_001165963.1 P1732P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr2:166908357 G>A maps to NM_001165963.1 Q279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr11:118039352 G>A maps to NM_004588.4 Q62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7230-01A-11D-2114-08 chr11:123516293 C>T did not map to a codon.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr17:62022836 G>T maps to NM_000334.4 S1201S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-YL-A8HL-01A-11D-A364-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr2:167262809 A>T maps to NM_002976.2 I1443I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr16:23364120 G>T did not map to a codon.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr17:45915952 G>T maps to NM_138355.3 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SC-01A-11D-A377-08 chr11:65302784 G>T maps to NM_020680.3 E440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr1:161326631 T>C did not map to a codon.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr7:3681626 A>T maps to NM_152744.3 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88P-01A-11D-A34U-08 chr7:4119140 T>G maps to NM_152744.3 P1083P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr17:75205503 C>G maps to NM_001039573.2 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr16:5038193 G>A maps to NM_014692.1 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr9:139357509 G>T maps to NM_014866.1 P1574P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr14:39543646 C>A maps to NM_006364.2 E359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr9:91972383 C>A maps to NM_024077.3 P724P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr17:80282490 T>A maps to NM_003004.2 R124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr15:101816763 G>T maps to NM_018445.4 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr7:84694821 A>G maps to NM_152754.2 D212D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MG-01A-11D-A364-08 chr9:91994251 G>A maps to NM_006378.3 P652P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr10:102737390 G>A maps to NM_017893.2 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr15:48054505 A>G maps to NM_153618.1 K216K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr10:13361210 G>T maps to NM_012247.4 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IL-01A-11D-A364-08 chr2:242289492 C>T maps to ENST00000391972 R365R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr23:118767428 C>A did not map to a codon.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr16:1990837 G>T maps to ENST00000399753 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr14:94756666 T>C maps to NM_001100607.1 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr18:61223487 C>A maps to ENST00000382768 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr7:100775169 T>C maps to NM_000602.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr7:100775171 G>A maps to NM_000602.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr2:224849667 C>A did not map to a codon.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr17:1679917 C>T maps to NM_002615.4 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr11:57367488 C>A maps to ENST00000403558 S97S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-HC-A4ZV-01A-11D-A26M-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr3:9482198 G>A maps to ENST00000407969 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr3:9512273 C>A maps to ENST00000407969 P971P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr22:26688422 C>A maps to NM_021115.4 S49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr22:30736750 T>C maps to NM_005877.4 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr11:65820562 C>A maps to NM_006842.2 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr16:70589036 G>A maps to NM_012426.4 K546K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BL-01A-31D-A257-08 chr4:154709576 G>A maps to NM_003013.2 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A6RC-01A-11D-A32B-08 chr19:19120891 G>A maps to NM_001017392.3 L704L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IJ-01A-11D-A34U-08 chr19:19115403 C>T maps to NM_001017392.3 V834V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8D0-01A-11D-A364-08 chr23:1712836 T>A did not map to a codon.
Sequencing variant TCGA-VN-A88Q-01A-11D-A34U-08 chr11:94800908 C>A maps to NM_032102.2 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr6:166733744 C>A did not map to a codon.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr5:156184678 C>T maps to NM_000337.5 C221C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr7:94214813 G>T maps to NM_001099401.1 P462P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7230-01A-11D-2114-08 chr1:67147852 G>A maps to ENST00000237247 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr6:134493333 C>A maps to NM_001143676.1 P356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A5OB-01A-11D-A29Q-08 chr3:20215803 T>G maps to NM_001012410.3 R407R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr3:20219806 G>T maps to NM_001012410.3 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr3:20219788 G>T maps to NM_001012410.3 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr10:72629557 C>A maps to NM_003901.3 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88K-01A-11D-A34U-08 chr9:130507028 C>T maps to NM_170600.2 W538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr1:249118996 G>T maps to NM_030645.1 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr9:17791306 C>T maps to NM_003026.2 Q235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7783-01A-11D-2114-08 chr10:105361686 C>A maps to ENST00000369774 V1096V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr5:171821587 T>G maps to NM_001017995.2 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr4:8235131 G>A maps to NM_018986.3 G1058G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr4:8221137 C>A maps to NM_018986.3 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr15:49255146 G>T maps to NM_203349.3 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr16:46649931 G>T maps to NM_024745.4 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WH-01A-11D-A377-08 chr1:154459159 C>G did not map to a codon.
Sequencing variant TCGA-EJ-7318-01B-11D-A32B-08 chr13:26620947 C>T maps to NM_001007538.1 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WJ-01A-11D-A377-08 chr19:41096645 G>T maps to NM_138392.3 L593L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr17:18238891 G>T maps to NM_004169.3 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr23:601571 G>A did not map to a codon.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr23:591825 A>T did not map to a codon.
Sequencing variant TCGA-HC-A48F-01A-11D-A257-08 chr6:146264542 G>A maps to ENST00000367503 R658R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6G3-01A-11D-A30X-08 chr5:132158688 C>T maps to NM_001172700.1 L786L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr23:9912814 C>T did not map to a codon.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr4:77675724 C>A maps to NM_020859.3 P1363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8261-01A-11D-2260-08 chr4:77677869 C>T maps to NM_020859.3 Q1660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr3:113286503 C>A maps to ENST00000393830 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr11:117066582 C>T maps to NM_001040455.1 H796H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SK-01B-21D-A377-08 chr11:117052520 A>G did not map to a codon.
Sequencing variant TCGA-HC-A8D1-01A-11D-A364-08 chr20:3673296 G>A maps to NM_023068.3 L1301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HO-01A-11D-A364-08 chr19:51918363 T>G did not map to a codon.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr19:50461936 C>A maps to NM_052884.2 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr19:51628470 T>G maps to NM_014441.2 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr11:111594483 C>A maps to NM_015191.1 S804S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr6:100841441 G>T maps to ENST00000262901 P497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr6:100841375 G>T maps to ENST00000262901 V519V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr19:16952649 C>A maps to NM_015260.1 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr1:232579421 G>T maps to NM_020808.3 P1121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SO-01B-31D-A377-08 chr1:232649717 G>A maps to NM_020808.3 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SO-01B-31D-A377-08 chr19:38610374 G>A maps to NM_015073.1 V907V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr17:79873381 G>A maps to NM_016538.2 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr2:45233548 C>T maps to NM_016932.4 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr6:31927104 C>A maps to NM_006929.4 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr6:31930233 C>A maps to NM_006929.4 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr5:54635835 A>G did not map to a codon.
Sequencing variant TCGA-FC-A5OB-01A-11D-A29Q-08 chr13:103701636 A>G did not map to a codon.
Sequencing variant TCGA-HC-8266-01A-11D-2260-08 chr2:219249917 C>A maps to NM_000578.3 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr16:67980428 C>A maps to NM_005072.4 L783L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WS-01A-11D-A377-08 chr20:44670162 C>A maps to NM_001134771.1 A373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr15:34531250 C>A maps to NM_133647.1 G849G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87D-01A-11D-A34U-08 chr15:34528967 C>A maps to NM_133647.1 E995*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HM-01A-11D-A364-08 chr15:34527451 C>T maps to NM_133647.1 K1097K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr7:100463780 C>A maps to NM_020246.2 R767R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr18:43311097 C>A maps to NM_001146037.1 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr18:43248312 G>A did not map to a codon.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr6:111540219 C>A maps to NM_018593.4 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr17:66267451 T>C maps to NM_004694.4 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr12:60098740 T>C maps to NM_004731.3 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VV-01A-11D-A377-08 chr11:22382483 G>A maps to NM_020346.2 W205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QY-01A-11D-A377-08 chr12:100811861 G>T maps to NM_139319.2 G451G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr20:61594047 C>A maps to NM_022082.3 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr21:46951360 G>T maps to NM_194255.1 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr11:35333903 C>A maps to NM_004171.3 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr14:23821249 C>T maps to NM_020372.2 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A8O0-01A-41D-A377-08 chr11:63176238 C>T maps to NM_080866.2 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NM-01A-21D-A33T-08 chr5:138714918 G>T maps to NM_152685.3 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Z-01A-12D-A26M-08 chr15:48431346 C>A maps to NM_205850.2 I351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr17:79682750 C>A maps to ENST00000331531 P119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83H-01A-11D-A34U-08 chr2:172666118 G>A maps to NM_003705.3 G434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr7:95750980 A>G maps to NM_001160210.1 I610I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr14:37149904 C>A maps to NM_030631.3 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr6:46623670 C>A maps to NM_004277.3 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8470-01A-11D-2395-08 chr10:101373522 G>A maps to NM_031212.3 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr12:98989598 C>A maps to NM_213611.2 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr5:110097208 C>T maps to NM_138773.1 D328D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A875-01A-31D-A34U-08 chr5:110097083 C>T maps to NM_138773.1 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr12:58014047 G>T maps to NM_133489.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88P-01A-11D-A34U-08 chr17:78222019 C>T maps to NM_173626.3 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr5:149360520 T>A maps to NM_000112.3 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr6:35980013 G>T maps to NM_052961.3 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr1:205901875 G>T maps to NM_134325.2 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WW-01A-11D-A377-08 chr15:85461835 G>T did not map to a codon.
Sequencing variant TCGA-VP-A87B-01A-11D-A34U-08 chr15:45555256 A>T did not map to a codon.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr4:9828094 T>G maps to NM_020041.2 R517R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr2:32418957 G>T maps to NM_001193513.1 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MJ-01A-11D-A364-08 chr8:118169933 C>T maps to NM_173851.2 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8266-01A-11D-2260-08 chr4:42072552 G>A maps to NM_006345.3 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr4:25678364 C>T maps to NM_006424.2 A689A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr6:118475606 G>T did not map to a codon.
Sequencing variant TCGA-HC-7230-01A-11D-2114-08 chr21:43967226 A>C maps to NM_018964.3 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr2:165809220 A>G maps to ENST00000409662 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7510-01A-11D-2260-08 chr2:165765266 C>A maps to ENST00000409662 V270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr12:46757762 C>G maps to NM_018976.4 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7F3-01A-21D-A33T-08 chr14:61503801 C>T maps to NM_001172702.1 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88O-01A-11D-A34U-08 chr2:196545260 A>G maps to NM_001127257.1 K165K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8261-01A-11D-2260-08 chr12:56628744 T>A maps to NM_001135195.1 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr11:57182086 C>A did not map to a codon.
Sequencing variant TCGA-FC-A4JI-01A-11D-A257-08 chr1:75805313 A>G maps to NM_152697.4 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6499-01A-12D-1961-08 chr1:75708579 C>T maps to NM_152697.4 K154K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A6RC-01A-11D-A32B-08 chr1:8390956 C>T maps to ENST00000377479 P502P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr5:33947261 G>A maps to NM_001012509.2 C458C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8469-01A-11D-2395-08 chr17:42340028 G>A maps to NM_000342.3 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65E-01A-11D-A29Q-08 chr2:162804173 T>C maps to NM_001178015.1 F734F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IG-01A-11D-A364-08 chr2:27907926 A>G maps to NM_018158.2 E633E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr11:26743039 G>T maps to NM_178498.3 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E0-01A-11D-A30X-08 chr11:26725365 T>C maps to NM_178498.3 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr16:31499067 G>A maps to ENST00000431354 W291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr16:31498983 C>G maps to ENST00000431354 Y263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr3:10976881 C>A maps to NM_014229.1 P581P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr23:115572206 G>T did not map to a codon.
Sequencing variant TCGA-EJ-A65J-01A-11D-A30X-08 chr19:49797194 G>A maps to NM_014037.2 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr5:149581947 G>T maps to NM_014228.3 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr19:33706824 G>T maps to NM_019849.2 S69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr8:17400869 C>T maps to NM_001164771.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Z-01A-12D-A26M-08 chr8:17418004 G>A maps to NM_001164771.1 Q529Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr16:87874705 C>A maps to NM_003486.5 V240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87D-01A-11D-A34U-08 chr1:173495814 A>G maps to NM_178527.3 A784A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr2:103141514 C>A maps to NM_001011552.3 P617P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr16:67305046 C>T maps to NM_004594.2 T875T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr12:21392116 T>C maps to NM_006446.4 H690H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr11:74904263 C>A maps to NM_007256.4 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr5:101813485 G>A maps to NM_173488.3 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5515-01A-01D-1576-08 chr17:33690214 G>T maps to NM_152270.3 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr17:33749993 C>A maps to NM_018042.3 V18V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7818-01A-11D-2114-08 chr10:98806791 C>T maps to NM_003061.2 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr4:20255608 C>A maps to ENST00000273739 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr4:20255578 C>A maps to ENST00000273739 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr13:84454930 G>A maps to NM_052910.1 R238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8472-01A-11D-2395-08 chr23:144906345 C>T did not map to a codon.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr23:144906445 G>T did not map to a codon.
Sequencing variant TCGA-KK-A8IJ-01A-11D-A34U-08 chr3:164907133 G>A maps to NM_014926.2 I495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr23:142716668 G>A did not map to a codon.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr13:88327879 C>A maps to NM_015567.1 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr23:128599697 G>T did not map to a codon.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr1:152857071 C>T maps to NM_030663.2 C58C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83H-01A-11D-A34U-08 chr22:39908031 G>C did not map to a codon.
Sequencing variant TCGA-YL-A8SJ-01B-11D-A377-08 chr17:18219933 G>A maps to NM_144775.2 Q277Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr16:18866182 T>C maps to ENST00000389467 L1426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr16:18844356 G>T maps to ENST00000389467 P2899P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr17:2076131 C>T maps to NM_017575.4 S1059S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr1:183514074 C>A maps to ENST00000367537 P663P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FS-01A-11D-A34U-08 chr1:183514378 C>T maps to ENST00000367537 Q765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr14:70461180 C>A maps to NM_001034852.1 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr14:70480115 G>A maps to NM_001034852.1 G318G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6385-01A-11D-1786-08 chr9:33056917 C>T maps to NM_018225.2 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SC-01A-11D-A377-08 chr9:33057682 A>G maps to NM_018225.2 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A879-01A-11D-A34U-08 chr6:84290294 A>G maps to NM_014841.2 L725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr14:62233592 G>T did not map to a codon.
Sequencing variant TCGA-VN-A88O-01A-11D-A34U-08 chr20:1281298 G>T maps to ENST00000381876 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr2:70122251 C>A maps to NM_006857.1 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr2:70130360 C>T maps to NM_006857.1 Q133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr2:70515271 G>T maps to NM_003096.2 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr8:121554094 T>A maps to NM_021021.3 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A6RA-01A-11D-A33T-08 chr3:63638398 T>C maps to NM_001080537.1 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr15:75899624 C>A maps to ENST00000371091 E220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr17:46198731 C>A maps to NM_152244.1 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr23:70280883 C>A did not map to a codon.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr7:17885262 G>A maps to ENST00000417048 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr8:101589257 G>A maps to NM_152628.3 Q406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr8:101612610 A>T maps to NM_152628.3 L247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr15:75941790 C>T maps to NM_153271.1 D116D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HM-01A-11D-A364-08 chr3:125176112 A>G maps to NM_003794.2 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr8:22423993 C>A maps to NM_005775.4 R363R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8CY-01A-11D-A364-08 chr4:7741957 C>T maps to NM_020777.2 N1149N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I5-01A-11D-A364-08 chr13:112722310 G>A maps to NM_005986.2 K113K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr11:16071442 G>T maps to NM_001145819.1 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WH-01A-11D-A377-08 chr11:16117661 C>T maps to NM_001145819.1 K340K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I9-01A-11D-A364-08 chr12:53776770 C>A maps to NM_138473.2 S347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr2:231155226 A>G maps to NM_007237.4 P591P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SC-01A-11D-A377-08 chr17:46002396 G>A maps to NM_003110.5 Q495Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr2:174777795 A>G did not map to a codon.
Sequencing variant TCGA-V1-A8WL-01A-11D-A377-08 chr2:215274873 A>G maps to NM_024532.3 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr17:26910635 G>A maps to NM_006461.3 Q860*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YJ-A8SW-01A-11D-A377-08 chr10:22634709 G>A maps to ENST00000376603 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr9:35811259 G>T maps to NM_001039592.1 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr17:49054553 C>A maps to ENST00000376407 V1147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7078-01A-11D-2114-08 chr23:140785742 T>A did not map to a codon.
Sequencing variant TCGA-XA-A8JR-01A-11D-A364-08 chr23:140785701 C>T did not map to a codon.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr23:144337273 G>T did not map to a codon.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr23:144337211 G>T did not map to a codon.
Sequencing variant TCGA-J9-A8CK-01A-11D-A34U-08 chr23:144337276 T>C did not map to a codon.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr2:32368484 G>T did not map to a codon.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr3:57108292 T>A maps to NM_181727.1 *191K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8ID-01A-11D-A364-08 chr17:48626525 G>C maps to NM_022827.2 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BR-01A-32D-A257-08 chr1:16727314 C>A maps to NM_198546.1 R358R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr1:48865160 T>C maps to NM_019073.2 K214K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr5:95018261 G>T maps to NM_031952.3 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BL-01A-31D-A257-08 chr8:145094891 C>T maps to NM_198572.2 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr7:44040842 C>A maps to NM_175064.2 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr2:220331956 C>T maps to NM_005876.4 A981A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr2:220350131 A>G maps to NM_005876.4 L2558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr1:16257093 C>T maps to NM_015001.2 S1453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YJ-A8SW-01A-11D-A377-08 chr1:16260825 G>A maps to NM_015001.2 V2697V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr15:69238016 C>A maps to NM_145658.3 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr19:49131474 G>T maps to NM_020126.3 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7318-01B-11D-A32B-08 chr2:228883535 A>G maps to NM_001142644.1 H678H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr12:101876610 A>G maps to ENST00000299272 Q84Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr18:12463457 G>T maps to NM_001128626.1 P510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YJ-A8SW-01A-11D-A377-08 chr16:29675594 C>A maps to NM_003123.3 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr11:13984531 G>C maps to NM_006108.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr19:38881007 G>T maps to NM_001042522.1 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr19:38882638 C>A maps to NM_001042522.1 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7209-01A-11D-2114-08 chr1:152975780 G>A maps to NM_005416.2 E95E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr23:155003969 T>A did not map to a codon.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr5:141694232 C>T maps to NM_030964.3 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr1:158612200 C>T maps to NM_003126.2 K1579K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr1:158585064 G>A maps to NM_003126.2 D2243D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr1:158605701 C>A did not map to a codon.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr1:158639552 T>C maps to NM_003126.2 K541K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AP-01A-12D-A33T-08 chr1:158606499 C>A maps to NM_003126.2 G1747G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr14:65246523 C>T maps to ENST00000389723 L1468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr2:54753665 G>A maps to NM_003128.2 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr19:41062019 G>A maps to NM_020971.2 V1705V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7233-01A-11D-2114-08 chr19:41007897 C>T maps to NM_020971.2 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AV-01A-11D-A32B-08 chr19:41078059 T>C maps to NM_020971.2 A2485A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr15:42147469 C>T maps to ENST00000320955 A3125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr9:94797093 G>T maps to NM_006415.2 P442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr9:94877637 C>A maps to NM_006415.2 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6499-01A-12D-1961-08 chr11:18655744 C>A maps to NM_194285.2 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65J-01A-11D-A30X-08 chr15:45968453 A>G maps to NM_021199.2 K270K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8S9-01A-11D-A377-08 chr15:45968417 C>T maps to NM_021199.2 N258N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr2:45773896 A>G maps to NM_018079.4 Y616Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr12:64485103 C>A maps to NM_020762.2 P495P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8ID-01A-11D-A364-08 chr12:64502787 G>A maps to NM_020762.2 V630V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FA-01A-21D-A33T-08 chr1:206610381 C>G maps to ENST00000414359 A464A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chr23:153046770 G>T did not map to a codon.
Sequencing variant TCGA-EJ-7789-01A-11D-2114-08 chr23:38016272 A>T did not map to a codon.
Sequencing variant TCGA-HC-7233-01A-11D-2114-08 chr22:26884137 T>C maps to NM_001013694.2 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IA-01A-11D-A364-08 chr12:119583286 G>A maps to NM_194286.2 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr20:60737904 C>A maps to NM_198935.1 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8ID-01A-11D-A364-08 chr5:80809506 T>G maps to ENST00000380182 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr11:67074409 G>T maps to NM_017857.3 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7212-01A-11D-2114-08 chr14:38679034 T>A maps to NM_001049.2 C147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SK-01B-21D-A377-08 chr23:48207019 A>T did not map to a codon.
Sequencing variant TCGA-EJ-7785-01A-11D-2114-08 chr23:48054233 G>A did not map to a codon.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr23:48049695 G>T did not map to a codon.
Sequencing variant TCGA-KK-A7AV-01A-11D-A32B-08 chr23:48054446 G>A did not map to a codon.
Sequencing variant TCGA-YL-A8SO-01B-31D-A377-08 chr23:48053625 A>G did not map to a codon.
Sequencing variant TCGA-2A-A8W3-01A-11D-A377-08 chr8:134472108 C>T maps to NM_173344.2 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr8:134488180 G>C maps to NM_173344.2 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr1:44386557 C>A maps to NM_174963.2 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr1:77510217 C>A maps to NM_030965.1 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr15:92981723 C>A maps to NM_006011.3 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr18:44260211 C>A maps to NM_013305.4 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr3:52547909 C>A maps to NM_015136.2 P1120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr12:104107523 G>T maps to NM_017564.9 T1505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr12:104107520 C>T maps to NM_017564.9 Y1504Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr3:36524553 C>T maps to NM_003149.1 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr23:123200044 G>T did not map to a codon.
Sequencing variant TCGA-HC-7232-01A-11D-2114-08 chr23:123179181 C>G did not map to a codon.
Sequencing variant TCGA-VP-A87E-01A-31D-A34U-08 chr23:123179075 T>C did not map to a codon.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr2:74072295 A>G maps to NM_213622.1 K94K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr23:67937674 C>T did not map to a codon.
Sequencing variant TCGA-HC-A8CY-01A-11D-A364-08 chr2:191851585 C>T maps to NM_007315.3 R405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr17:40474447 A>G maps to NM_139276.2 A651A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6DY-01A-12D-A30X-08 chr1:47755172 A>T maps to NM_001048166.1 C319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr6:31940214 C>T maps to NM_032454.1 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6361-01A-21D-1961-08 chr2:242438193 G>T maps to NM_006374.3 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr7:23826530 T>A maps to NM_031414.3 P825P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7327-01A-11D-2114-08 chr12:27467470 C>A maps to NM_015000.3 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr9:35101708 G>T maps to NM_013442.1 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83G-01A-11D-A34U-08 chr15:74472522 G>A maps to ENST00000449139 R673R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr15:43896962 G>A maps to NM_153700.2 R1338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr23:7171275 G>T did not map to a codon.
Sequencing variant TCGA-M7-A71Y-01A-22D-A32B-08 chr20:57251291 T>A maps to NM_001001433.1 L308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr11:59559663 C>A maps to NM_004177.4 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr9:130438177 T>C maps to NM_003165.3 Y402Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr2:84670409 C>A maps to NM_003849.3 E106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr10:104264004 G>T maps to NM_016169.3 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr16:28631395 C>T maps to NM_177536.2 W42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr2:108998895 C>A maps to NM_006588.2 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr4:70721016 A>T did not map to a codon.
Sequencing variant TCGA-G9-7522-01A-11D-2260-08 chr22:39134910 C>T maps to ENST00000405018 W603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83G-01A-11D-A34U-08 chr22:39141778 G>A maps to ENST00000405018 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr19:39964092 G>A maps to NM_003169.3 L808L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HJ-01A-11D-A364-08 chr17:27011734 C>A maps to NM_003170.3 S787S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr10:70940277 C>T maps to NM_003171.3 D77D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CP-01A-11D-A34U-08 chr10:70940178 C>T maps to NM_003171.3 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7232-01A-11D-2114-08 chr22:24581634 G>A maps to NM_019601.3 R359R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr1:149885320 C>T maps to NM_014849.3 K24K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8469-01A-11D-2395-08 chr5:75490816 A>G maps to NM_014979.1 K218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52B-01A-11D-A26M-08 chr9:113312164 C>A maps to ENST00000374463 E251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7789-01A-11D-2114-08 chr6:10928670 C>T maps to NM_001040274.2 F492F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7794-01A-11D-2114-08 chr19:46334799 C>T maps to NM_004819.2 K480K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr22:33260925 T>C maps to NM_003490.3 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A71Y-01A-22D-A32B-08 chr6:86333755 C>A maps to NM_006372.4 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr6:152708416 G>T maps to NM_182961.2 P2759P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr6:152832184 T>A maps to NM_182961.2 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65E-01A-11D-A29Q-08 chr6:152647579 G>A maps to NM_182961.2 N5048N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr14:64518895 C>A maps to NM_182914.2 P2755P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr14:64580249 C>T maps to NM_182914.2 D4267D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr23:49050743 G>T did not map to a codon.
Sequencing variant TCGA-G9-6361-01A-21D-1961-08 chr11:66812167 C>T maps to NM_001177880.1 N314N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr18:40853619 T>A maps to NM_020783.3 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr11:85459456 A>T maps to NM_001162953.1 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr23:99956497 C>A did not map to a codon.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr6:166580169 G>T maps to NM_003181.2 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr6:132874238 C>A maps to NM_053278.1 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6M7-01A-11D-A31L-08 chr6:149700268 A>G maps to NM_015093.4 T406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7331-01A-11D-2114-08 chr10:123843718 A>T maps to NM_206862.2 G568G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr4:104577478 G>A maps to NM_001059.2 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr4:7056216 G>T maps to NM_152293.2 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr23:70613198 T>C did not map to a codon.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr17:34147367 C>T maps to NM_139215.1 Q73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr9:32633777 C>A maps to NM_153809.2 R600R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr8:120759088 G>T maps to NM_003184.3 P988P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65J-01A-11D-A30X-08 chr11:62554329 A>T maps to NM_006473.2 A477A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76W-01A-11D-A33T-08 chr9:108425067 G>A maps to NM_005421.2 Q97Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8264-01B-11D-2395-08 chr2:160035656 C>G maps to NM_033394.2 A831A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8468-01A-21D-2395-08 chr17:61432334 C>A maps to ENST00000389520 T648T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr1:234556447 C>T maps to NM_005646.3 Q1185Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr7:38305253 G>A maps to ENST00000443402 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7821-01A-12D-2114-08 chr1:150471025 A>G maps to NM_025150.3 R429R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:6634740 C>A maps to NM_138697.3 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr5:9629678 G>A maps to NM_019599.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr12:11214314 T>A maps to ENST00000422992 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7736-01A-11D-2114-08 chr3:10320071 C>A maps to NM_014760.3 R691R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr4:38016161 G>T maps to NM_015173.2 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88O-01A-11D-A34U-08 chr4:38097622 A>G maps to NM_015173.2 V770V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr4:26622237 T>C maps to NM_018317.2 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7510-01A-11D-2260-08 chr6:37280703 G>C maps to NM_017772.2 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr6:13316808 G>T maps to NM_016495.4 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr23:106064138 G>T did not map to a codon.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr6:42713802 G>A maps to NM_003192.2 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr17:80726351 T>C maps to NM_005993.4 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr3:176755960 C>G did not map to a codon.
Sequencing variant TCGA-EJ-A7NH-01A-12D-A33T-08 chr6:85446894 C>T maps to NM_001080508.1 Q444Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B3-01A-11D-A33T-08 chr23:101396001 G>A did not map to a codon.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr16:2827128 C>T did not map to a codon.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr1:24083515 G>T maps to NM_003198.2 E746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr5:145843327 C>A maps to NM_006706.3 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SH-01B-11D-A377-08 chr15:57484402 A>G maps to NM_207036.1 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr22:42610894 A>G maps to NM_005650.1 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr19:1615476 C>T maps to NM_003200.2 K543K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr10:114711013 C>A maps to NM_030756.4 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IB-01A-11D-A364-08 chr10:114925328 C>T maps to NM_030756.4 C463C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr1:152057904 G>T maps to NM_001008536.1 P751P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WV-01A-11D-A377-08 chr11:67817999 C>T maps to NM_006019.3 G761G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr5:149755318 C>T maps to ENST00000451292 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IK-01A-11D-A364-08 chr12:124163787 T>G maps to NM_024809.3 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr1:179638342 T>C maps to ENST00000444136 N888N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr1:151752576 C>A maps to NM_001083965.1 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr14:102904420 C>A maps to NM_014844.3 S819S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr19:14674847 C>A maps to ENST00000436007 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr16:1556316 C>T maps to NM_016111.3 Q705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr23:69844761 T>C did not map to a codon.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr23:107225169 A>G did not map to a codon.
Sequencing variant TCGA-YL-A9WI-01A-11D-A377-08 chr8:30699597 T>C maps to NM_031271.3 R2312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B4-01A-11D-A32B-08 chr1:36055548 G>A maps to NM_178548.3 G268G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr23:132351871 G>A did not map to a codon.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr8:133925307 C>T maps to NM_003235.4 G1392G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A876-01A-11D-A34U-08 chr16:31485242 C>T maps to NM_001042454.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr1:92262993 A>T maps to NM_003243.4 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr1:92185485 C>T maps to NM_003243.4 E459E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A720-01A-12D-A32B-08 chr2:105924086 C>A maps to NM_004257.4 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr19:375679 C>T maps to NM_016585.3 E97E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr2:88478452 G>A maps to NM_018271.3 Q241Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr17:79848573 G>T maps to NM_005782.3 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CP-01A-11D-A34U-08 chr22:29924167 T>C did not map to a codon.
Sequencing variant TCGA-HC-7079-01A-11D-1961-08 chr1:36755263 G>T maps to NM_005119.3 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr2:137814398 T>G maps to ENST00000272643 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6329-01A-13D-1961-08 chr2:137814554 G>T maps to ENST00000272643 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr2:39982550 T>A did not map to a codon.
Sequencing variant TCGA-KK-A8IG-01A-11D-A364-08 chr11:119291594 G>A maps to NM_006288.3 I7I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr6:155451341 C>T maps to ENST00000456144 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87D-01A-11D-A34U-08 chr6:155500567 G>A maps to ENST00000456144 K895K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr19:4816547 G>T maps to NM_182919.2 P614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VO-01A-11D-A377-08 chr1:43779587 C>T maps to NM_005424.2 I786I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr1:43779602 G>T maps to NM_005424.2 L791L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7210-01A-11D-2114-08 chr4:90034421 A>G maps to NM_145715.2 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr11:65123662 A>G maps to NM_145719.2 K128K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I8-01A-11D-A364-08 chr11:65123572 G>A maps to NM_145719.2 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FA-01A-21D-A33T-08 chr5:156381615 G>A maps to NM_138379.2 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7318-01B-11D-A32B-08 chr19:2427322 C>A did not map to a codon.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr17:900588 C>A maps to NM_013337.2 C69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr17:904322 C>A maps to NM_013337.2 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65J-01A-11D-A30X-08 chr6:54216176 C>T maps to NM_014464.3 Q370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76W-01A-11D-A33T-08 chr19:3731955 C>T maps to NM_014428.1 Q232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr2:171862700 A>G maps to ENST00000360843 G641G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr17:60654068 G>A did not map to a codon.
Sequencing variant TCGA-VP-A879-01A-11D-A34U-08 chr17:60685505 A>G maps to ENST00000326270 A714A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr15:62978868 G>T maps to NM_015059.2 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7209-01A-11D-2114-08 chr4:38798748 C>T maps to NM_003263.3 K568K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IK-01A-11D-A364-08 chr23:12939903 T>G did not map to a codon.
Sequencing variant TCGA-M7-A721-01A-12D-A32B-08 chr23:12938244 C>T did not map to a codon.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr10:102849596 G>A maps to NM_001085398.1 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr3:149040065 C>A maps to NM_138786.3 G190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88I-01A-11D-A34U-08 chr3:149192702 C>G maps to NM_004617.2 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr15:83781632 C>A maps to NM_023003.3 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IB-01A-11D-A364-08 chr12:27152540 C>T maps to NM_016551.2 Q105Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr8:105367307 C>T maps to NM_030788.2 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7791-01A-11D-2114-08 chr14:24661452 C>T maps to NM_006405.5 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr9:75445551 T>G maps to NM_138691.2 A738A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr15:81625416 G>T maps to ENST00000454937 P885P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr19:54676749 G>T maps to NM_001145303.1 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr16:19041571 T>C maps to NM_024847.3 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IF-01A-11D-A364-08 chr16:19020720 G>T maps to NM_024847.3 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VL-01A-21D-A377-08 chr14:75602589 C>G did not map to a codon.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr2:193056698 T>C maps to NM_016192.2 E63E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr11:60688428 C>A maps to NM_024092.2 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr4:4239661 G>A maps to ENST00000382753 C133C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr2:98451388 C>A did not map to a codon.
Sequencing variant TCGA-KK-A8I6-01A-11D-A364-08 chr11:120198156 T>C maps to NM_001198670.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr19:48836661 C>A maps to NM_018273.2 V398V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr19:42819343 C>A maps to ENST00000406159 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SO-01B-31D-A377-08 chr19:5751815 C>G maps to NM_152784.3 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr7:150500856 C>A maps to NM_018487.2 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr2:120438840 C>A maps to NM_030577.2 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A876-01A-11D-A34U-08 chr10:104232672 C>T maps to NM_024789.3 D297D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83N-01A-11D-A34U-08 chr6:159046200 G>A maps to NM_020823.1 V477V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr1:9662325 C>A maps to NM_001130924.2 R386R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr22:25331313 C>A maps to ENST00000423535 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr2:27258871 G>A maps to NM_017727.4 Q224Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I5-01A-11D-A364-08 chr23:102968707 T>A did not map to a codon.
Sequencing variant TCGA-V1-A8X3-01A-11D-A377-08 chr3:12785417 G>A maps to ENST00000431022 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65E-01A-11D-A29Q-08 chr3:100287664 G>C did not map to a codon.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chr1:54284689 T>C maps to NM_018087.4 E219E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr12:64173823 C>T maps to NM_014254.1 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6499-01A-12D-1961-08 chr1:226059716 G>A maps to NM_014698.2 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88P-01A-11D-A34U-08 chr3:69087801 A>C maps to NM_007114.2 R688R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr21:42839792 C>T maps to NM_001135099.1 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8D0-01A-11D-A364-08 chr21:42866284 G>C maps to NM_001135099.1 S116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IJ-01A-11D-A34U-08 chr22:37485724 G>A maps to ENST00000381792 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8ID-01A-11D-A364-08 chr19:2410385 C>A maps to NM_182973.1 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8ID-01A-11D-A364-08 chr12:83424605 C>T maps to NM_152588.1 F700F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr12:88568464 T>C maps to NM_181783.3 D427D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WV-01A-11D-A377-08 chr12:88560142 A>G maps to NM_181783.3 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr7:150779389 C>A maps to NM_031434.3 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7079-01A-11D-1961-08 chr18:66344376 C>A maps to NM_019022.3 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7794-01A-11D-2114-08 chr8:22880192 G>T maps to NM_003842.4 A438A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr6:47200571 C>A maps to NM_014452.3 G633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5763-01A-11D-1576-08 chr4:122075726 A>G maps to ENST00000509841 C234C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr4:122063931 C>A did not map to a codon.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr3:195594756 C>A maps to NM_001010938.1 S867S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr11:57077241 G>T maps to NM_033396.2 P981P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr10:93600427 A>G maps to NM_025235.3 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7075-01A-11D-1961-08 chr1:175054614 C>T maps to NM_022093.1 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XA-A8JR-01A-11D-A364-08 chr11:1860931 A>G maps to ENST00000381906 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7230-01A-11D-2114-08 chr5:72195833 A>G maps to NM_002270.3 A780A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A9DI-01A-11D-A377-08 chr7:47408547 G>A maps to NM_022748.11 P565P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6499-01A-12D-1961-08 chr17:38638447 A>T maps to NM_032865.5 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr6:32023934 G>T maps to ENST00000375244 T2720T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr6:32021195 G>A maps to ENST00000375244 R2920R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7797-01A-11D-2260-08 chr6:32010243 C>G maps to ENST00000375244 G4066G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr6:32036413 C>T maps to ENST00000375244 G1991G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QZ-01A-11D-A377-08 chr6:32013020 G>A maps to ENST00000375244 T3563T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IG-01A-11D-A364-08 chr20:39725935 T>C maps to NM_003286.2 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr3:133342925 T>C maps to NM_007027.3 V966V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr9:32543931 A>C maps to NM_005802.4 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr8:59720735 C>A maps to NM_014729.2 S495S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5515-01A-01D-1576-08 chr16:52484401 C>T maps to ENST00000407228 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VT-01A-11D-A377-08 chr17:7579591 T>C did not map to a codon.
Sequencing variant TCGA-HC-7213-01A-11D-2114-08 chr17:7578554 C>T did not map to a codon.
Sequencing variant TCGA-KC-A7FA-01A-21D-A33T-08 chr17:7576850 A>C did not map to a codon.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr8:95942871 G>T maps to NM_033285.3 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr12:113733847 A>T maps to NM_001143819.1 P878P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I9-01A-11D-A364-08 chr12:72372849 C>T maps to ENST00000389376 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr16:67424506 C>A maps to NM_016140.2 E73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SO-01B-31D-A377-08 chr1:186326599 T>C maps to NM_003292.2 Q551Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr19:48305094 G>T maps to NM_198479.2 P391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr20:30363691 G>T maps to ENST00000340513 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr12:112572541 C>A maps to NM_006700.2 C16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr3:42251445 C>A maps to NM_001042646.1 T644T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr21:45503101 T>C maps to NM_003274.4 A719A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7232-01A-11D-2114-08 chr6:30121515 G>A maps to NM_052828.2 C379C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8ID-01A-11D-A364-08 chr6:30124742 G>A maps to NM_006778.3 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr17:54969321 G>A maps to NM_005082.4 R544R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr19:59059686 C>G maps to NM_005762.2 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HO-01A-11D-A364-08 chr19:59060744 G>A maps to NM_005762.2 E570E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr11:120008333 G>T maps to NM_012101.3 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr1:115005787 G>A maps to NM_015906.3 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WH-01A-11D-A377-08 chr1:114968070 C>T maps to NM_015906.3 Q565Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B4-01A-11D-A32B-08 chr8:27151800 C>A maps to NM_171982.3 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr11:89531567 T>C maps to NM_020358.2 K363K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr11:5686408 C>T maps to NM_033034.2 W371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr5:180687286 G>T maps to NM_032765.2 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CL-01A-11D-A34U-08 chr4:165962534 C>G maps to NM_152620.2 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr1:33612957 C>A maps to NM_018207.2 V416V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SU-A7E7-01A-22D-A33T-08 chr10:104414838 G>A maps to NM_030912.2 E223E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SA-01A-21D-A377-08 chr14:51560841 T>A maps to ENST00000338969 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8469-01A-11D-2395-08 chr22:38121844 C>T maps to NM_001039141.2 A1094A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SP-01B-11D-A377-08 chr22:38121967 A>G maps to NM_001039141.2 L1135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7331-01A-11D-2114-08 chr19:6750304 G>A maps to ENST00000313244 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7792-01A-11D-2114-08 chr19:6743804 C>T maps to ENST00000313244 D200D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NM-01A-21D-A33T-08 chr22:20104420 C>T maps to ENST00000439169 E3E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SO-01B-31D-A377-08 chr14:104000980 G>A maps to ENST00000299201 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr22:46733730 G>T maps to NM_018006.4 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr8:72963063 G>A maps to NM_007332.2 G618G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NH-01A-12D-A33T-08 chr8:72936046 A>G did not map to a codon.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr13:38213400 T>C maps to NM_003306.1 Q710Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr23:111025268 G>T did not map to a codon.
Sequencing variant TCGA-YL-A8HM-01A-11D-A364-08 chr23:111095550 G>A did not map to a codon.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr15:31294405 G>A maps to NM_002420.4 I1477I. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CH-5739-01A-11D-1576-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr9:77448964 T>C maps to NM_017662.4 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr9:77390916 G>T maps to NM_017662.4 Y1095*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A8O0-01A-41D-A377-08 chr8:116632179 C>A maps to NM_014112.2 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr7:98508783 G>T maps to ENST00000359863 E633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr7:98569471 C>A maps to ENST00000359863 P2574P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr7:98565106 G>T did not map to a codon.
Sequencing variant TCGA-YJ-A8SW-01A-11D-A377-08 chr7:98522823 G>T maps to ENST00000359863 L971L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A5OB-01A-11D-A29Q-08 chr7:130357703 G>A maps to NM_052933.2 Q134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WJ-01A-11D-A377-08 chr18:73000202 G>A maps to NM_005786.4 V902V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr19:50248601 C>T maps to NM_021733.1 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr16:67859050 G>T maps to ENST00000339830 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr23:38540489 G>C did not map to a codon.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr12:3390976 C>T maps to ENST00000407263 I214I. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-G9-6366-01A-11D-2114-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr11:43513625 C>T maps to NM_018259.5 D1069D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr10:75104885 G>T maps to NM_145170.3 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr10:75029380 G>A maps to NM_145170.3 V1076V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IA-01A-11D-A364-08 chr3:39174616 A>G maps to ENST00000301819 Q887Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QZ-01A-11D-A377-08 chr1:55266617 G>A maps to NM_001114108.1 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A878-01A-31D-A34U-08 chr4:147628686 G>A maps to ENST00000513335 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87D-01A-11D-A34U-08 chr2:178481830 A>G maps to NM_152275.3 Y533Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr2:74719547 G>T maps to NM_022492.4 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7510-01A-11D-2260-08 chr22:46685403 G>A maps to NM_017931.2 E396E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr2:47256511 T>A maps to ENST00000394850 P597P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I4-01A-11D-A364-08 chr2:113260503 G>A maps to NM_153712.4 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FN-01A-11D-A34U-08 chr22:43576900 C>T maps to NM_015140.3 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr3:9855029 G>A did not map to a codon.
Sequencing variant TCGA-FC-A8O0-01A-41D-A377-08 chr17:46862422 C>T maps to NM_001130918.1 T634T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr2:179395543 G>T maps to NM_133378.4 P32698P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7218-01B-11D-A32B-08 chr2:179615124 A>C maps to ENST00000375038 L4003*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr2:179440958 C>T maps to NM_133378.4 Q20732Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr2:179399092 T>C maps to NM_133378.4 K31515K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr2:179537131 A>G did not map to a codon.
Sequencing variant TCGA-G9-7510-01A-11D-2260-08 chr2:179456527 A>G maps to NM_133378.4 G17438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr2:179397721 A>T maps to NM_133378.4 Y31972*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IA-01A-11D-A364-08 chr2:179432009 T>G maps to NM_133378.4 V23715V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MJ-01A-11D-A364-08 chr2:179403721 C>T maps to NM_133378.4 L30412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A878-01A-31D-A34U-08 chr2:179629395 G>A maps to NM_133378.4 G3282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr2:132237010 G>C maps to NM_080386.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr17:40764503 C>A maps to NM_001070.4 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr17:40811927 C>T maps to NM_016437.2 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr6:35477697 C>A maps to NM_003322.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr6:158873274 C>A maps to NM_020245.3 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr17:1198823 C>A maps to NM_172367.2 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr18:9888098 T>G maps to NM_001098529.1 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65E-01A-11D-A29Q-08 chr1:145441199 C>T maps to NM_006472.3 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6366-01A-11D-2114-08 chr19:10468471 C>A maps to NM_003331.4 E812*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6499-01A-12D-1961-08 chr7:66489942 G>A maps to NM_018264.2 Q306Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YJ-A8SW-01A-11D-A377-08 chr21:44514889 A>G maps to NM_001025203.1 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8X3-01A-11D-A377-08 chr9:139975260 G>A maps to NM_207309.2 R433R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr9:33986766 G>T maps to NM_018449.2 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87J-01A-11D-A34U-08 chr9:33943521 C>A maps to NM_018449.2 G537G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76W-01A-11D-A33T-08 chr11:122659911 C>T maps to NM_032873.4 S292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr12:125398089 C>T maps to NM_021009.5 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr4:103720583 G>T maps to NM_181890.1 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8ID-01A-11D-A364-08 chr15:25605554 C>T maps to NM_000462.2 V579V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5763-01A-11D-1576-08 chr11:5529390 T>C maps to NM_017481.2 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6353-01A-11D-1961-08 chr11:5536504 G>T maps to NM_145053.4 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I6-01A-11D-A364-08 chr11:5537356 G>A maps to NM_145053.4 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr15:43328435 C>A maps to NM_174916.2 L710L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr2:170938347 C>T maps to ENST00000442603 L1917L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr1:19477099 G>T maps to ENST00000375267 P2467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83M-01A-11D-A34U-08 chr1:19480293 G>A maps to ENST00000375267 Q2200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7791-01A-11D-2114-08 chr8:103298846 T>C did not map to a codon.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr17:42293126 G>A maps to NM_014233.2 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr11:62444224 C>A maps to NM_015853.3 G302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IB-01A-11D-A364-08 chr8:59343159 G>T maps to NM_001077619.1 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I5-01A-11D-A364-08 chr2:136527362 G>A maps to NM_014607.3 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FD-01A-11D-A33T-08 chr3:196089431 C>A maps to NM_015562.1 E321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr11:18579844 G>C maps to NM_001040697.1 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr2:234628278 C>A maps to NM_007120.2 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46D-01A-21D-A257-08 chr2:234527190 G>T maps to NM_019076.4 G280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83G-01A-11D-A34U-08 chr4:70361504 C>T maps to NM_021139.2 K25K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6366-01A-11D-2114-08 chr12:100452767 A>G maps to NM_015054.1 L763L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8472-01A-11D-2395-08 chr15:54306248 C>G maps to ENST00000260323 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr15:54792333 A>G maps to ENST00000260323 E1706E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88P-01A-11D-A34U-08 chr15:54847664 G>A maps to ENST00000260323 T1971T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr10:73050840 C>A maps to NM_170744.3 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8X3-01A-11D-A377-08 chr8:35406945 C>T maps to ENST00000416672 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr17:73811287 G>T maps to NM_001080419.1 S381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7327-01A-11D-2114-08 chr22:30163413 A>G maps to ENST00000406782 K9K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IJ-01A-11D-A34U-08 chr1:229773317 T>A maps to NM_014777.2 L986L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr1:216256914 A>T maps to ENST00000366943 L1727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8S8-01A-11D-A377-08 chr19:17374838 C>A maps to NM_031941.3 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr13:27649443 T>A maps to NM_182488.3 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A632-01A-11D-A29Q-08 chr12:62777655 A>G maps to ENST00000280377 G375G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr17:20910261 G>A maps to ENST00000455117 T491T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76X-01A-11D-A33T-08 chr17:20922441 T>A maps to ENST00000455117 K227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr11:113704217 G>C maps to NM_020886.2 S228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65E-01A-11D-A29Q-08 chr12:109523651 G>T maps to NM_032663.3 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chr1:78194271 G>A maps to NM_015017.3 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr2:61415487 C>A maps to NM_014709.3 E3464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8W3-01A-11D-A377-08 chr11:77917054 C>T maps to NM_020798.2 I455I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr11:77911273 C>T maps to NM_020798.2 F344F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6333-01A-12D-1961-08 chr17:76803038 A>C did not map to a codon.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr2:219353101 G>T maps to NM_020935.2 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I5-01A-11D-A364-08 chr7:6187372 C>T maps to ENST00000404835 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr12:6961391 C>A maps to NM_001098536.1 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7793-01A-31D-2260-08 chr15:50833425 T>C maps to ENST00000456636 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr10:11505705 C>T maps to NM_001080491.2 A424A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8261-01A-11D-2260-08 chr15:50790906 T>C maps to NM_005154.3 Y1051Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr23:40999969 A>G did not map to a codon.
Sequencing variant TCGA-YL-A8SL-01B-21D-A377-08 chr23:41082489 C>T did not map to a codon.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr12:101764853 C>T maps to NM_014503.2 L2236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8470-01A-11D-2395-08 chr8:117783945 T>A maps to NM_032334.2 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr6:145093096 A>G maps to NM_007124.2 Q2850Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59X-01A-11D-A29Q-08 chr6:144837471 T>C maps to NM_007124.2 N1784N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr1:116202354 C>A maps to NM_001172412.1 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr1:160394000 G>A maps to NM_020335.2 Q411Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr6:30884892 G>T maps to NM_001167734.1 V285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AP-01A-12D-A33T-08 chr19:6850725 A>C maps to NM_005428.2 G725G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HM-01A-11D-A364-08 chr19:6854099 C>A maps to NM_005428.2 I825I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr1:108185309 G>T maps to NM_006113.4 P615P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr1:108247661 A>G maps to NM_006113.4 Y508Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CL-01A-11D-A34U-08 chr1:108231001 C>T did not map to a codon.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr5:82815918 G>A maps to NM_004385.4 E598E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FN-01A-11D-A34U-08 chr23:7811725 A>G did not map to a codon.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr7:100807836 G>A maps to NM_003378.3 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SO-01B-31D-A377-08 chr6:117589487 A>C maps to NM_182645.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr3:87018022 G>A maps to NM_016206.2 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr3:38038578 C>A maps to NM_015873.3 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr7:158851251 C>A maps to ENST00000402066 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr9:79834913 C>A maps to ENST00000376646 R267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7314-01A-31D-2114-08 chr8:100866332 C>T maps to NM_017890.3 V3597V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7331-01A-11D-2114-08 chr15:62212806 C>A maps to NM_020821.2 G2368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7209-01A-11D-2114-08 chr20:2842495 G>A maps to NM_022575.2 G315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83G-01A-11D-A34U-08 chr2:86790450 G>C maps to NM_016079.3 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7F3-01A-21D-A33T-08 chr8:145649502 G>A maps to NM_183057.1 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr15:91549290 T>A did not map to a codon.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr13:53008974 C>A maps to NM_016075.2 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr12:123355527 G>T maps to NM_024667.2 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr23:65252420 T>C did not map to a codon.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr11:61034969 C>T maps to NM_152718.2 P643P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr12:6153555 C>A maps to NM_000552.3 L781L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr12:6172164 C>T maps to NM_000552.3 E496E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr10:28822944 G>A maps to NM_016628.3 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YJ-A8SW-01A-11D-A377-08 chr23:48547129 G>A did not map to a codon.
Sequencing variant TCGA-VP-A87B-01A-11D-A34U-08 chr12:14940328 C>A maps to NM_016312.2 G532G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr22:42423016 C>A maps to NM_152613.2 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7521-01A-11D-2260-08 chr7:73112191 C>G maps to ENST00000423497 G291G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WH-01A-11D-A377-08 chr23:48458009 A>T did not map to a codon.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr4:177052765 C>A maps to NM_170710.4 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr9:116079079 G>C maps to NM_001012361.2 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr2:29148006 T>G maps to NM_015131.1 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr1:109538406 C>A maps to NM_001142550.1 E504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr3:113152409 A>T did not map to a codon.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr1:241958522 C>A maps to NM_144625.4 P994P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr8:124096567 G>T maps to NM_145647.3 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr18:54591237 G>A maps to NM_015285.2 L1204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88Q-01A-11D-A34U-08 chr18:54547217 T>C maps to NM_015285.2 S1116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IG-01A-11D-A364-08 chr15:85189498 A>G maps to NM_032856.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7783-01A-11D-2114-08 chr16:703784 G>A maps to NM_145294.4 K473K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7233-01A-11D-2114-08 chr4:6302430 G>A maps to NM_006005.3 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SK-01B-21D-A377-08 chr4:6302391 G>A maps to NM_006005.3 K290K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8CY-01A-11D-A364-08 chr12:65461529 A>G maps to NM_007191.4 N193N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7F3-01A-21D-A33T-08 chr17:66440640 G>A maps to NM_017983.5 N141N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr20:43355878 G>A maps to NM_003881.2 Q228Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr23:54359993 C>T did not map to a codon.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr12:49374246 C>T maps to NM_005430.3 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7327-01A-11D-2114-08 chr23:10058809 G>A did not map to a codon.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr19:7691146 C>A maps to NM_020196.2 E178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr17:6673969 T>C maps to NM_017523.2 C172C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TK-A8OK-01A-22D-A364-08 chr22:29195089 A>C maps to ENST00000403532 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83N-01A-11D-A34U-08 chr2:31604514 C>T maps to NM_000379.3 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A632-01A-11D-A29Q-08 chr23:2726250 C>T did not map to a codon.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr2:168099281 T>G maps to NM_152381.5 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87K-01A-11D-A34U-08 chr2:168067308 T>A maps to NM_152381.5 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chr23:37553557 A>G did not map to a codon.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr9:100447234 T>A maps to NM_000380.3 K215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr10:111633185 C>A did not map to a codon.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr23:128894499 C>T did not map to a codon.
Sequencing variant TCGA-EJ-A7NM-01A-21D-A33T-08 chr13:21401282 G>A maps to NM_022459.4 Q255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FD-01A-11D-A33T-08 chr8:21833902 C>T maps to ENST00000434536 Q221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FD-01A-11D-A33T-08 chr8:21842351 T>A did not map to a codon.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr1:180772719 C>A maps to NM_004736.3 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr1:180793907 A>T maps to NM_004736.3 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr5:82499424 G>T maps to NM_022406.2 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr22:42052955 C>A maps to NM_001469.3 P447P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr23:67731783 A>T did not map to a codon.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr14:75264384 C>T maps to NM_019589.2 P795P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7820-01A-11D-2114-08 chr4:69198539 T>C maps to NM_001031732.2 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59X-01A-11D-A29Q-08 chr5:112889506 C>T maps to NM_022828.3 Q670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A725-01A-12D-A32B-08 chr23:21875523 G>A did not map to a codon.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr7:100348485 C>A maps to ENST00000349350 V496V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I5-01A-11D-A364-08 chr7:100371058 C>A maps to ENST00000349350 T1859T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7708-01A-11D-2114-08 chr2:98351130 C>T maps to NM_001079.3 C346C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7820-01A-11D-2114-08 chr3:167000275 T>C maps to ENST00000307529 K668K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8CY-01A-11D-A364-08 chr3:167045901 T>C maps to ENST00000307529 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6329-01A-13D-1961-08 chr3:101384240 G>C maps to NM_014415.3 S397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NH-01A-12D-A33T-08 chr6:31868518 T>C maps to NM_181842.2 E188E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr19:36207473 C>A maps to NM_014383.1 Y428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr9:129642272 C>T maps to ENST00000319119 Q199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7218-01B-11D-A32B-08 chr1:197169425 G>A maps to NM_194314.2 Q60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IL-01A-11D-A364-08 chr11:130109741 C>T maps to ENST00000397753 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr20:62384050 C>T maps to NM_025224.2 K462K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr1:154988947 C>A maps to ENST00000417934 P503P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr1:37948983 C>A maps to NM_025079.2 P524P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr13:46544600 C>A did not map to a codon.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr23:117959281 G>A did not map to a codon.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr16:87451233 C>A maps to NM_015144.2 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr23:77913570 G>A did not map to a codon.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr23:74637001 G>T did not map to a codon.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr12:77222205 C>A maps to NM_015336.2 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87B-01A-11D-A34U-08 chr23:128944943 C>T did not map to a codon.
Sequencing variant TCGA-FC-A4JI-01A-11D-A257-08 chr2:145156430 A>G maps to NM_014795.3 L775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7F3-01A-21D-A33T-08 chr2:145157535 T>C maps to NM_014795.3 T406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr12:72036213 A>C did not map to a codon.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr12:72056880 C>A maps to NM_144982.4 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr16:72821571 C>A maps to NM_006885.3 E3535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FD-01A-11D-A33T-08 chr16:72845537 G>A maps to NM_006885.3 Q1268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WH-01A-11D-A377-08 chr16:72828629 C>A maps to NM_006885.3 E2651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr8:77617576 C>A maps to NM_024721.4 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YJ-A8SW-01A-11D-A377-08 chr8:77767001 A>G maps to NM_024721.4 E2615E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7079-01A-11D-1961-08 chr15:42740782 G>T maps to NM_022473.1 S851S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CP-01A-11D-A34U-08 chr15:42720230 G>T maps to NM_022473.1 V1638V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr19:57065053 C>G maps to NM_020828.1 G300G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6333-01A-12D-1961-08 chr19:57065371 G>T maps to NM_020828.1 V406V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr19:57065051 G>C did not map to a codon.
Sequencing variant TCGA-KK-A8I9-01A-11D-A364-08 chr20:50769704 A>T maps to NM_018197.2 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr8:106815537 C>A maps to NM_012082.3 P1076P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr23:24229056 C>A did not map to a codon.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr14:68220895 C>A maps to NM_015346.3 V2340V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7818-01A-11D-2114-08 chr8:124267244 A>G maps to NM_007222.3 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr20:39830760 G>T maps to NM_015035.3 P932P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7740-01A-11D-2114-08 chr20:39832182 G>A maps to NM_015035.3 P458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IA-01A-11D-A364-08 chr3:147128234 G>A maps to NM_003412.3 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr23:136652079 C>A did not map to a codon.
Sequencing variant TCGA-HC-7232-01A-11D-2114-08 chr13:100622585 C>T maps to NM_033132.3 E448E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr19:58101496 C>T maps to NM_001010879.2 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7750-01A-11D-2114-08 chr19:57301239 C>T maps to NM_001146326.1 Q159Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr7:99117480 C>A maps to NM_014569.3 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr10:81051938 C>A maps to NM_020338.3 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr10:81050861 C>A maps to NM_020338.3 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr23:70472906 C>A did not map to a codon.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr23:70471026 C>A did not map to a codon.
Sequencing variant TCGA-HC-A76W-01A-11D-A33T-08 chr23:70462904 G>C did not map to a codon.
Sequencing variant TCGA-KC-A4BV-01A-31D-A26M-08 chr23:70462163 A>C did not map to a codon.
Sequencing variant TCGA-VN-A88K-01A-11D-A34U-08 chr5:43175081 C>T maps to ENST00000509156 N573N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7708-01A-11D-2114-08 chr19:36728179 A>T maps to NM_007145.2 K280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr19:58213659 A>G maps to NM_001085384.1 C219C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr19:35232874 C>G maps to ENST00000392232 S574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VO-01A-11D-A377-08 chr23:47836947 C>T did not map to a codon.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr23:47837102 G>T did not map to a codon.
Sequencing variant TCGA-VP-A876-01A-11D-A34U-08 chr23:47835729 T>C did not map to a codon.
Sequencing variant TCGA-EJ-7792-01A-11D-2114-08 chr3:44684196 C>T maps to NM_006991.3 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83H-01A-11D-A34U-08 chr11:123597403 C>A maps to NM_003455.2 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr20:52198351 C>T maps to NM_006526.2 K338K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr19:44564708 G>A maps to NM_013361.4 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7F6-01A-11D-A33T-08 chr19:44933128 G>A maps to NM_014518.2 F609F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr19:44515530 C>A maps to NM_006300.3 S447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr17:5009562 G>T maps to NM_014519.2 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A4JI-01A-11D-A257-08 chr18:74620422 A>G maps to NM_007345.3 A813A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6499-01A-12D-1961-08 chr18:74587565 C>A maps to NM_007345.3 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr18:74592172 C>A maps to NM_007345.3 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr16:89789104 T>A maps to NM_001113525.1 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VO-01A-11D-A377-08 chr19:44891644 G>A maps to NM_152354.3 H254H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr6:87969898 A>G maps to NM_015021.1 Q2184Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B4-01A-11D-A32B-08 chr20:25657356 G>A maps to NM_015655.2 F189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr10:38343825 T>C maps to NM_006954.1 D258D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr20:32379197 G>T maps to ENST00000375200 E814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88Q-01A-11D-A34U-08 chr10:64136572 A>G maps to NM_199451.2 K207K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8266-01A-11D-2260-08 chr8:28206325 C>T maps to NM_018660.2 K484K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr14:74364846 C>A maps to NM_021188.1 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr19:22001954 T>G maps to NM_003423.2 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr16:3440103 T>A maps to ENST00000396852 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr23:134494803 C>A did not map to a codon.
Sequencing variant TCGA-G9-6499-01A-12D-1961-08 chr23:134494269 C>A did not map to a codon.
Sequencing variant TCGA-EJ-A7NM-01A-21D-A33T-08 chr9:109701287 C>G maps to NM_021224.4 A2109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7075-01A-11D-1961-08 chr9:109736550 C>A maps to NM_021224.4 R2277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr9:109688259 C>A maps to NM_021224.4 P689P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QX-01A-11D-A377-08 chr19:53344799 G>A maps to NM_001008801.1 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7210-01A-11D-2114-08 chr2:27822523 C>T maps to NM_032434.2 Q118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HO-01A-11D-A364-08 chr18:74091975 T>A maps to ENST00000443185 G698G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr4:10447769 T>A maps to NM_053042.2 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88P-01A-11D-A34U-08 chr4:10447286 G>C maps to NM_053042.2 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QW-01A-11D-A377-08 chr18:22807245 C>T maps to NM_015461.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr19:52937266 G>A maps to NM_001143939.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr19:31039789 G>T maps to NM_014717.1 L1088L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8CY-01A-11D-A364-08 chr19:30935473 C>T maps to NM_014717.1 N335N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr19:58049136 C>A maps to ENST00000376233 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WJ-01A-11D-A377-08 chr19:2833763 A>T maps to NM_001102651.1 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr19:2877441 G>A maps to NM_024967.1 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr19:7075114 C>T maps to NM_024341.2 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8468-01A-21D-2395-08 chr19:9453236 A>G maps to NM_032497.1 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr19:53008032 G>T maps to NM_001099694.1 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr19:56090150 C>T maps to NM_152600.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr19:58370391 C>A maps to NM_032828.2 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr15:85326136 G>A maps to NM_014630.2 E77E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr1:26496948 C>A maps to NM_015871.4 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr16:3487539 T>G did not map to a codon.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr19:53270591 A>C maps to NM_198457.2 Y139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I9-01A-11D-A364-08 chr19:58499975 G>A maps to NM_025027.3 H97H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr19:38190149 G>T maps to NM_032689.4 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8472-01A-11D-2395-08 chr5:123984771 C>A maps to NM_020747.2 G435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr5:124036818 C>A maps to NM_020747.2 V350V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr19:52620074 G>T maps to NM_178523.3 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr16:30793263 G>T maps to NM_001080417.1 P795P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr16:30794664 G>T maps to NM_001080417.1 I328I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7075-01A-11D-1961-08 chr23:47919355 C>A did not map to a codon.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr12:48737262 C>A maps to NM_152320.2 G270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr1:40928285 C>A maps to NM_023070.2 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HM-01A-11D-A364-08 chr16:31090752 C>T maps to NM_014699.3 L1036L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AU-01A-11D-A32B-08 chr1:182025560 C>A maps to NM_001009992.1 E529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YJ-A8SW-01A-11D-A377-08 chr19:53668834 G>C maps to NM_024733.3 S303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr16:31072439 G>T maps to NM_001172669.1 P626P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr1:227842074 C>T maps to NM_178549.3 Q97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr1:26691328 C>A maps to ENST00000436292 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr1:151262650 C>A maps to NM_020832.1 P1006P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr16:30581353 C>A maps to NM_145271.3 G238G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr16:30620888 A>C maps to NM_138447.1 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8W3-01A-11D-A377-08 chr17:80790120 T>G maps to NM_024702.2 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr17:80788497 C>T maps to NM_024702.2 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6385-01A-11D-1786-08 chr19:52793388 G>A maps to NM_001010851.2 Q115Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr7:149133689 G>A maps to ENST00000440594 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr9:99581088 T>A maps to NM_001001662.1 K406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr19:12501648 T>A maps to NM_001080821.2 V521V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CL-01A-11D-A34U-08 chr2:185802144 T>A maps to NM_194250.1 C674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr19:53456130 C>A did not map to a codon.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:146824229 G>A maps to ENST00000508784 Q61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr13:115090480 G>A maps to NM_032436.2 E388E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr13:115089997 C>A maps to NM_032436.2 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QW-01A-11D-A377-08 chr19:53117663 A>G maps to NM_018300.3 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88O-01A-11D-A34U-08 chr17:33289178 G>T maps to NM_052857.3 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SO-01B-31D-A377-08 chr19:52658799 A>G maps to NM_001102657.1 Y712Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CN-01A-11D-A34U-08 chr19:23544859 T>A maps to NM_003430.2 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr19:22574556 C>A maps to NM_001098626.1 E494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WH-01A-11D-A377-08 chr22:29438480 A>G did not map to a codon.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr19:5456786 C>T maps to NM_181710.3 Q429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr11:60640727 C>T maps to NM_207341.2 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IB-01A-11D-A364-08 chr10:126672052 A>G maps to NM_017580.2 E568E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8S9-01A-11D-A377-08 chr10:126662250 A>G maps to NM_017580.2 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7170-01A-11D-2114-08 chr23:15809136 G>T did not map to a codon.
Sequencing variant TCGA-J4-A83K-01A-11D-A34U-08 chr6:28097611 C>T maps to NM_025231.1 Q311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr1:45484151 G>A maps to NM_020883.1 L1178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr1:45501858 C>A maps to NM_020883.1 L669L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr15:66821853 G>A maps to NM_017975.3 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr17:3979977 C>A maps to NM_015113.3 E1063*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59X-01A-11D-A29Q-08 chr17:3959635 T>C maps to NM_015113.3 Q1723Q. Only missense variants will be evaluated by CHASM.
