5843 NP_001070868 G627C not found in SNVbox database
126 NP_001070868 W63S not found in SNVbox database
799 NP_705833 V669F not found in SNVbox database
1242 NP_705833 W972C not found in SNVbox database
1261 NP_001070868 R268W not found in SNVbox database
1590 NP_001070868 P766A not found in SNVbox database
1699 NP_001070868 E503G not found in SNVbox database
2263 NP_705833 A452T not found in SNVbox database
2998 NP_001070868 R592G not found in SNVbox database
3148 NP_705833 G243A not found in SNVbox database
3721 NP_001070868 K157N not found in SNVbox database
3860 NP_001070868 V60I not found in SNVbox database
4048 NP_001070868 E15D not found in SNVbox database
4109 NP_001070868 L468M not found in SNVbox database
4261 NP_705833 R185C not found in SNVbox database
4576 NP_705833 E203D not found in SNVbox database
Sequencing variant TCGA-4K-AA1I-01A-11D-A435-10 chr6:44268394 G>A maps to NM_020745.2 H949H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALR-01A-21D-A42Y-10 chr2:215910733 G>T maps to NM_173076.2 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG8-01A-31D-A42Y-10 chr9:139906168 G>A maps to ENST00000355090 V1886V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF1-01A-11D-A42Y-10 chr16:2339581 G>T maps to NM_001089.2 A851A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOD-01A-11D-A435-10 chr16:2358478 G>A maps to NM_001089.2 A419A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A912-01A-11D-A435-10 chr17:67124786 A>G maps to NM_080284.2 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAL7-01A-11D-A42Y-10 chr19:1047262 C>A maps to NM_019112.3 S651S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V5-01A-11D-A435-10 chr19:1047522 C>T maps to NM_019112.3 G713G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANJ-01A-11D-A435-10 chr17:66992071 G>T maps to NM_080283.3 P1173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A912-01A-11D-A435-10 chr7:150725640 C>T maps to ENST00000297504 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr16:48244963 C>T maps to NM_032583.3 G501G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0B-01A-11D-A435-10 chr16:48180306 G>T maps to NM_033226.2 S10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFG-01A-11D-A42Y-10 chr23:152991227 C>A did not map to a codon.
Sequencing variant TCGA-2G-AAHT-01A-11D-A42Y-10 chr23:153008730 G>T did not map to a codon.
Sequencing variant TCGA-2G-AALR-01A-21D-A42Y-10 chr23:153001576 G>C did not map to a codon.
Sequencing variant TCGA-ZM-AA0H-01A-11D-A435-10 chr23:153008787 G>A did not map to a codon.
Sequencing variant TCGA-ZM-AA06-01A-12D-A435-10 chr1:94964162 A>T maps to ENST00000454898 R488R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V3-01A-11D-A435-10 chr7:150913106 G>T maps to NM_005692.3 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOD-01A-11D-A435-10 chr14:23067199 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAGN-01A-11D-A42Y-10 chr19:17405201 G>T maps to NM_024527.4 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKL-01A-11D-A42Y-10 chr9:133759941 C>T maps to NM_007313.2 H774H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AAAL-01A-11D-A435-10 chr9:136131247 G>T maps to NM_020469.2 V289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKG-01A-11D-A42Y-10 chr6:26598338 G>T did not map to a codon.
Sequencing variant TCGA-SO-A8JP-01A-11D-A435-10 chr3:127396683 G>T maps to NM_172027.2 E343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAEW-01A-11D-A42Y-10 chr11:34184246 G>A maps to NM_145804.2 S698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JY-01A-11D-A435-10 chr11:34186250 G>T maps to NM_145804.2 S657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH2-01A-11D-A42Y-10 chr1:1229471 G>T maps to NM_030649.2 T749T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGE-01A-21D-A42Y-10 chr11:108018053 C>T maps to NM_000019.3 Y407Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V5-01A-11D-A435-10 chr17:61574510 G>T maps to NM_000789.3 G1235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA05-01A-12D-A435-10 chr14:23530744 T>G maps to NM_014977.3 P1120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGJ-01A-11D-A42Y-10 chr2:135630211 G>T did not map to a codon.
Sequencing variant TCGA-XE-AAO4-01A-11D-A435-10 chr14:74059004 C>G maps to NM_152331.3 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0B-01A-11D-A435-10 chr23:23740076 G>A did not map to a codon.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr12:6749615 G>A maps to NM_032489.2 Q384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGC-01A-21D-A42Y-10 chr4:185701509 G>T maps to NM_001995.2 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr16:20477038 C>T maps to NM_001010845.2 C126C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALZ-01A-11D-A42Y-10 chr2:98274701 G>A maps to NM_005735.3 D245D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84Y-01A-11D-A435-10 chr3:53905292 C>G maps to NM_022899.4 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94I-01A-11D-A435-10 chr2:148657361 C>G maps to NM_001616.3 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X3-A8G4-01A-11D-A435-10 chr10:127789651 C>T maps to NM_003474.4 A303A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH3-01A-11D-A42Y-10 chr5:156936421 G>T maps to ENST00000430702 T266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF8-01A-11D-A42Y-10 chr8:39695677 G>A maps to NM_001464.3 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGG-01A-11D-A42Y-10 chr8:24151703 T>G maps to NM_014265.4 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGC-01A-21D-A42Y-10 chr8:39079163 T>G maps to NM_145004.5 T423T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH4-01A-12D-A42Y-10 chr20:3653451 C>T maps to NM_025220.2 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKL-01A-11D-A42Y-10 chr19:8665877 G>A maps to NM_030957.2 D248D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALR-01A-21D-A42Y-10 chr19:8649875 G>T maps to NM_030957.2 G1035G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr5:33614433 G>T maps to NM_030955.2 I812I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84W-01A-11D-A435-10 chr15:100821451 G>T maps to NM_139057.2 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94D-01A-11D-A435-10 chr15:100636612 G>A maps to NM_139057.2 D695D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AAAL-01A-11D-A435-10 chr5:128984529 A>G maps to NM_133638.3 K675K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0B-01A-11D-A435-10 chr21:28296506 G>T maps to NM_007038.3 A886A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SB-A76C-01A-11D-A435-10 chr3:64633627 G>A maps to NM_182920.1 C566C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGI-01A-11D-A42Y-10 chr9:136404995 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAG5-01A-11D-A42Y-10 chr1:150526210 C>A maps to ENST00000369039 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGF-01A-31D-A42Y-10 chr8:145617337 G>T maps to NM_174922.3 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1I-01A-11D-A435-10 chr7:45614333 G>A maps to NM_021116.2 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGY-01A-11D-A42Y-10 chr5:7743790 C>T maps to NM_020546.2 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A89B-01A-11D-A435-10 chr5:7396570 C>A maps to NM_020546.2 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr14:24795331 G>A maps to NM_139247.3 T536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94D-01A-11D-A435-10 chr3:123049764 C>T maps to NM_183357.2 E539E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF8-01A-11D-A42Y-10 chr16:50338323 G>T maps to NM_001114.3 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGJ-01A-11D-A42Y-10 chr4:2895780 T>C maps to NM_014189.2 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALR-01A-21D-A42Y-10 chr4:100235055 G>A maps to NM_000668.4 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFI-01A-21D-A42Y-10 chr20:49509507 G>T maps to NM_181442.1 Y581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKL-01A-11D-A42Y-10 chr20:49508787 G>A maps to NM_181442.1 G821G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFV-01A-11D-A42Y-10 chr1:203098166 C>T maps to NM_001048230.1 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1I-01A-11D-A435-10 chr15:73044819 T>C maps to NM_031284.4 V451V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG3-01A-11D-A42Y-10 chr13:114088090 C>A maps to NM_138430.3 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr8:26721625 A>G maps to ENST00000356368 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V3-01A-11D-A435-10 chr20:4202382 C>T maps to NM_000678.3 P502P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AAAL-01A-11D-A435-10 chr2:96781576 G>A maps to NM_000682.5 C104C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOC-01A-11D-A435-10 chr12:19593199 C>T maps to NM_001114176.1 Y189Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90P-01A-11D-A435-10 chr23:147891441 C>T did not map to a codon.
Sequencing variant TCGA-2G-AAF4-01A-11D-A42Y-10 chr17:76198676 G>T maps to NM_001145526.1 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84W-01A-11D-A435-10 chr2:27276345 C>T maps to NM_021831.5 Q98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGA-01A-11D-A42Y-10 chr8:41478444 C>T maps to NM_178819.3 D432D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG5-01A-11D-A42Y-10 chr7:16918208 A>G maps to NM_176813.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFO-01A-31D-A42Y-10 chr20:32868922 A>G maps to NM_000687.2 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG9-01A-11D-A42Y-10 chr1:27875917 G>A maps to NM_001029882.2 S903S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGT-01A-11D-A42Y-10 chr1:27878461 G>A maps to NM_001029882.2 H55H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANI-01A-11D-A435-10 chr11:62294253 C>T maps to NM_001620.1 K2545K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A8S2-01A-11D-A435-10 chr14:105415679 G>T maps to NM_138420.2 L2036L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGM-01A-11D-A42Y-10 chr23:129264041 T>C did not map to a codon.
Sequencing variant TCGA-VF-A8AB-01A-31D-A435-10 chr22:21334369 G>T maps to NM_144704.2 E572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2X-A9D5-01A-11D-A435-10 chr9:130635028 T>C maps to ENST00000223836 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0H-01A-11D-A435-10 chr1:33476434 C>A did not map to a codon.
Sequencing variant TCGA-2G-AAHT-01A-11D-A42Y-10 chr9:4741003 A>G maps to NM_016282.3 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94I-01A-11D-A435-10 chr14:96858505 G>A maps to NM_152327.2 E5E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGY-01A-11D-A42Y-10 chr15:86118560 G>T did not map to a codon.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr15:86266550 G>T maps to NM_006738.4 E2253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A8S3-01B-11D-A435-10 chr19:15510123 G>T maps to NM_014371.2 R382R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGC-01A-21D-A42Y-10 chr6:109867321 T>G maps to NM_001145128.2 P991P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr1:109377672 G>T maps to NM_152763.3 P514P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHC-01A-11D-A42Y-10 chr4:74272366 G>A maps to NM_000477.5 Q53Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr4:74283803 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAG0-01A-11D-A42Y-10 chr19:49971738 G>T maps to NM_153329.3 L680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHT-01A-11D-A42Y-10 chr10:97370020 G>A maps to NM_002860.3 H713H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1G-01A-11D-A435-10 chr10:97397133 G>T maps to NM_002860.3 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFJ-01A-11D-A42Y-10 chr1:19216598 G>T maps to NM_003748.3 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALG-01A-11D-A42Y-10 chr1:19216532 G>T maps to NM_003748.3 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALN-01A-11D-A42Y-10 chr16:30080965 G>A maps to ENST00000395248 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0B-01A-11D-A435-10 chr11:111706993 G>T maps to ENST00000428306 S724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H5-01A-11D-A435-10 chr2:29462643 G>T maps to NM_004304.3 R753R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0D-01A-11D-A435-10 chr2:30143261 G>T maps to NM_004304.3 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO3-01A-11D-A435-10 chr17:18087631 G>A maps to ENST00000261650 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAEX-01A-11D-A42Y-10 chr19:36501929 G>T maps to ENST00000455847 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGJ-01A-11D-A42Y-10 chr2:233321405 G>A did not map to a codon.
Sequencing variant TCGA-2G-AAFL-01A-21D-A42Y-10 chr15:85401529 G>A maps to NM_020778.4 E1389E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALO-01A-12D-A42Y-10 chr15:85400647 C>T maps to NM_020778.4 S1095S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGJ-01A-11D-A42Y-10 chr2:233246465 C>A maps to NM_001632.3 A523A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALX-01A-11D-A42Y-10 chr2:233271627 C>G maps to NM_031313.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM4-01A-11D-A435-10 chr3:46728532 G>T maps to NM_147129.3 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A8D5-01A-11D-A435-10 chr2:202195504 G>T maps to NM_139163.2 Y192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGT-01A-11D-A42Y-10 chr5:34004801 C>A maps to NM_001167595.1 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM4-01A-11D-A435-10 chr5:34007932 G>T maps to NM_001167595.1 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGP-01A-11D-A42Y-10 chr11:46439569 G>A maps to ENST00000458649 A1003A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84X-01A-11D-A435-10 chr11:46563784 G>T maps to ENST00000458649 G594G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A89B-01A-11D-A435-10 chr11:46419164 G>T maps to ENST00000458649 T1244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAL7-01A-11D-A42Y-10 chr23:109561070 C>A did not map to a codon.
Sequencing variant TCGA-WZ-A8D5-01A-11D-A435-10 chr23:109561070 C>A did not map to a codon.
Sequencing variant TCGA-2G-AALT-01A-11D-A42Y-10 chr2:128628895 G>T maps to NM_031445.2 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0H-01A-11D-A435-10 chr1:104160106 T>C maps to NM_000699.2 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALG-01A-11D-A42Y-10 chr9:140069898 G>A maps to NM_013366.3 S682S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM2-01A-11D-A435-10 chr12:121775138 C>T maps to NM_016237.4 K238K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFM-01A-11D-A42Y-10 chr14:21162163 G>A maps to NM_001097577.2 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKM-01A-11D-A42Y-10 chr14:21162160 T>G maps to NM_001097577.2 R146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOD-01A-11D-A435-10 chr11:101775578 C>T maps to NM_178127.4 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGN-01A-11D-A42Y-10 chr8:41575644 G>A maps to ENST00000415018 A395A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-XY-A8S3-01B-11D-A435-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-2G-AALO-01A-12D-A42Y-10 chr17:54558037 G>A maps to NM_153228.2 W653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOB-01A-11D-A435-10 chr5:139819757 G>A maps to ENST00000253810 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGN-01A-11D-A42Y-10 chr2:241492363 G>A maps to ENST00000401804 Y149Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH4-01A-12D-A42Y-10 chr16:89347465 C>T maps to NM_013275.4 S1828S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JY-01A-11D-A435-10 chr16:89341535 G>T maps to NM_013275.4 R2512R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOD-01A-11D-A435-10 chr16:89346814 G>T maps to NM_013275.4 P2045P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90Y-01A-11D-A435-10 chr11:67066579 C>T maps to NM_207354.2 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAL7-01A-11D-A42Y-10 chr10:99337613 G>T maps to NM_020349.2 E76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALR-01A-21D-A42Y-10 chr9:67968312 G>A maps to NM_001012419.1 V624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFM-01A-11D-A42Y-10 chr19:4216045 A>G maps to ENST00000262970 P513P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H4-01A-31D-A435-10 chr12:52282493 G>T maps to NM_182608.3 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84X-01A-11D-A435-10 chr5:79855371 A>T maps to NM_001004441.2 L156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGA-01A-11D-A42Y-10 chr1:145560170 G>T maps to NM_144698.3 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGC-01A-21D-A42Y-10 chr4:125599936 C>T maps to NM_020337.2 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr6:90276739 C>G maps to ENST00000339746 L15L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-2G-AAGX-01A-11D-A42Y-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-2G-AALY-01A-11D-A42Y-10 chr11:69972214 G>T maps to NM_018043.5 V337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGP-01A-11D-A42Y-10 chr11:26547226 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAH4-01A-12D-A42Y-10 chr17:40997659 C>T maps to NM_009590.2 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0E-01A-12D-A435-10 chr2:201467016 C>T maps to NM_001159.3 C149C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V3-01A-11D-A435-10 chr19:16337285 C>T maps to NM_001130524.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH3-01A-11D-A42Y-10 chr11:993798 C>T maps to ENST00000332231 C533C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X3-A8G4-01A-11D-A435-10 chr7:99699563 G>A maps to ENST00000429084 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALP-01A-12D-A42Y-10 chr12:99052953 A>G maps to NM_181861.1 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AAAL-01A-11D-A435-10 chr12:99052953 A>G maps to NM_181861.1 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H4-01A-31D-A435-10 chr12:99056498 A>G maps to NM_181861.1 K290K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALQ-01A-12D-A42Y-10 chr19:1467049 C>T maps to NM_005883.2 C1250C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOD-01A-11D-A435-10 chr11:57004400 G>T maps to NM_005161.4 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr11:116708058 A>C did not map to a codon.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr1:161192312 C>T did not map to a codon.
Sequencing variant TCGA-2G-AAEX-01A-11D-A42Y-10 chr2:21255320 G>T maps to NM_000384.2 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGF-01A-31D-A42Y-10 chr2:21256355 G>T maps to NM_000384.2 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84W-01A-11D-A435-10 chr2:21224910 T>C maps to NM_000384.2 K4461K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr2:21232320 G>T maps to NM_000384.2 T2473T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V5-01A-11D-A435-10 chr6:41029396 C>G maps to NM_006789.3 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKG-01A-11D-A42Y-10 chr22:39357585 T>C maps to NM_001193289.1 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90W-01A-11D-A435-10 chr22:39357585 T>C maps to NM_001193289.1 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A89B-01A-11D-A435-10 chr22:39382073 C>T maps to ENST00000402182 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SB-A76C-01A-11D-A435-10 chr7:30963099 G>T maps to ENST00000509504 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGC-01A-21D-A42Y-10 chr2:241621834 C>A maps to NM_001102467.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAEX-01A-11D-A42Y-10 chr23:66766275 G>T did not map to a codon.
Sequencing variant TCGA-2G-AALS-01A-12D-A42Y-10 chr23:66766584 G>T did not map to a codon.
Sequencing variant TCGA-4K-AAAL-01A-11D-A435-10 chr23:66766355 T>C did not map to a codon.
Sequencing variant TCGA-WZ-A8D5-01A-11D-A435-10 chr11:72404839 C>T maps to NM_001040118.2 L1235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALP-01A-12D-A42Y-10 chr5:141059696 G>A maps to NM_022481.5 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGJ-01A-11D-A42Y-10 chr8:143694936 G>A maps to NM_015193.3 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A89B-01A-11D-A435-10 chr8:68128854 T>A maps to NM_006421.3 P1552P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHG-01A-11D-A42Y-10 chr16:24965935 G>A maps to NM_001006634.1 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84X-01A-11D-A435-10 chr16:24965935 G>A maps to NM_001006634.1 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A8S2-01A-11D-A435-10 chr16:24942405 G>T maps to NM_001006634.1 P738P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO3-01A-11D-A435-10 chr11:110561319 G>A maps to NM_020809.2 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOF-01A-11D-A435-10 chr11:110451482 G>T maps to NM_020809.2 S729S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG7-01A-11D-A42Y-10 chr1:161026273 G>T maps to NM_001025598.1 Y83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGZ-01A-11D-A42Y-10 chr3:119120672 A>G maps to NM_020754.2 K358K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X3-A8G4-01A-11D-A435-10 chr11:128839437 C>T maps to NM_001142685.1 E1876E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM4-01A-11D-A435-10 chr23:130215790 C>G did not map to a codon.
Sequencing variant TCGA-YU-A90W-01A-11D-A435-10 chr23:130219012 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAFI-01A-21D-A42Y-10 chr23:153174573 G>T did not map to a codon.
Sequencing variant TCGA-S6-A8JW-01A-11D-A435-10 chr23:153173196 G>T did not map to a codon.
Sequencing variant TCGA-SN-A84W-01A-11D-A435-10 chr23:153174595 G>T did not map to a codon.
Sequencing variant TCGA-ZM-AA05-01A-12D-A435-10 chr23:153187250 G>T did not map to a codon.
Sequencing variant TCGA-ZM-AA0D-01A-11D-A435-10 chr23:11197552 C>A did not map to a codon.
Sequencing variant TCGA-2G-AAH3-01A-11D-A42Y-10 chr19:42410874 C>T maps to NM_199002.1 C907C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84Y-01A-11D-A435-10 chr19:42399473 G>T maps to NM_199002.1 R325R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFL-01A-21D-A42Y-10 chr1:3396389 G>T maps to NM_014448.3 E635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A6IS-01A-11D-A435-10 chr2:131803740 G>T maps to NM_015320.2 R684R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALR-01A-21D-A42Y-10 chr23:135763030 G>C did not map to a codon.
Sequencing variant TCGA-YU-A94I-01A-11D-A435-10 chr1:27057900 C>T maps to NM_006015.4 Q537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGJ-01A-11D-A42Y-10 chr6:157100004 C>A maps to ENST00000367148 G314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAL7-01A-11D-A42Y-10 chr6:157100004 C>A maps to ENST00000367148 G314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1H-01A-11D-A435-10 chr6:157100004 C>A maps to ENST00000367148 G314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM4-01A-11D-A435-10 chr1:235345257 G>A maps to NM_016374.5 V992V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGW-01A-11D-A42Y-10 chr2:97217881 G>T maps to NM_212481.1 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHT-01A-11D-A42Y-10 chr15:72767234 C>T maps to NM_005744.3 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKM-01A-11D-A42Y-10 chr15:72767234 C>T maps to NM_005744.3 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H1-01A-11D-A435-10 chr15:72767234 C>T maps to NM_005744.3 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0N-01A-21D-A435-10 chr11:64786159 C>T maps to NM_001667.3 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0B-01A-11D-A435-10 chr16:57283711 C>T maps to NM_012106.3 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84Y-01A-11D-A435-10 chr10:18948571 G>T maps to NM_178815.3 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM2-01A-11D-A435-10 chr6:109274549 G>A maps to NM_032131.4 T637T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH2-01A-11D-A42Y-10 chr10:23297851 A>G maps to NM_173081.3 K679K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOB-01A-11D-A435-10 chr16:31476520 G>C maps to NM_024742.2 *726S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFV-01A-11D-A42Y-10 chr3:137942566 C>T maps to ENST00000469044 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG3-01A-11D-A42Y-10 chr23:101857553 C>A did not map to a codon.
Sequencing variant TCGA-XE-AAO4-01A-11D-A435-10 chr23:101858296 C>T did not map to a codon.
Sequencing variant TCGA-XE-AANV-01A-11D-A435-10 chr15:80883969 G>A maps to NM_014862.3 W660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JX-01A-11D-A435-10 chr3:35724363 G>T maps to ENST00000458225 E52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALY-01A-11D-A42Y-10 chr23:69501570 G>T did not map to a codon.
Sequencing variant TCGA-XE-AAO4-01A-11D-A435-10 chr5:90667228 G>T maps to NM_020801.2 C411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGP-01A-11D-A42Y-10 chr23:3030574 G>A did not map to a codon.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr23:3019219 C>T did not map to a codon.
Sequencing variant TCGA-2G-AAFO-01A-31D-A42Y-10 chr17:66339909 G>A maps to NM_014960.3 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF8-01A-11D-A42Y-10 chr22:19965525 C>T maps to NM_001670.2 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGE-01A-21D-A42Y-10 chr23:25025373 G>A did not map to a codon.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr23:25033724 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAGE-01A-21D-A42Y-10 chr1:23763529 C>A maps to NM_017707.3 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1I-01A-11D-A435-10 chr1:76388025 G>T maps to NM_080868.2 Y140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGI-01A-11D-A42Y-10 chr10:73970548 C>T maps to NM_001198800.1 E51E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHC-01A-11D-A42Y-10 chr12:103352217 C>T maps to NM_004316.3 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGE-01A-21D-A42Y-10 chr7:65552332 A>G maps to NM_000048.3 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANJ-01A-11D-A435-10 chr2:70187845 C>T maps to NM_152792.2 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAL5-01A-11D-A42Y-10 chr1:176853486 T>A maps to ENST00000281881 K1080*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr1:176852035 G>T maps to ENST00000281881 I1115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFO-01A-31D-A42Y-10 chr10:89530768 A>G maps to NM_032810.2 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG9-01A-11D-A42Y-10 chr8:124382187 A>G maps to NM_014109.3 D268D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG9-01A-11D-A42Y-10 chr2:175979434 G>C maps to NM_001880.2 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG3-01A-11D-A42Y-10 chr11:64677637 A>G maps to ENST00000421419 H579H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAL5-01A-11D-A42Y-10 chr11:64662854 C>A maps to ENST00000421419 L1831L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V3-01A-11D-A435-10 chr11:64668088 G>T maps to ENST00000421419 G1449G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90Q-01A-11D-A435-10 chr11:64678132 G>T maps to ENST00000421419 P554P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHP-01A-12D-A42Y-10 chr14:96781834 G>T maps to NM_018036.5 S1149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG8-01A-31D-A42Y-10 chr2:242610197 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAG3-01A-11D-A42Y-10 chr2:38527451 G>A maps to NM_001135673.1 Q364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JW-01A-11D-A435-10 chr11:108121538 G>T maps to NM_000051.3 G449G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALG-01A-11D-A42Y-10 chr12:7045068 T>C maps to NM_001940.3 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM3-01A-11D-A435-10 chr12:7045914 G>A maps to NM_001940.3 Q495Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO4-01A-11D-A435-10 chr5:160114832 G>T maps to NM_025153.2 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAEX-01A-11D-A42Y-10 chr13:113530167 G>T maps to NM_032189.3 V1080V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGX-01A-11D-A42Y-10 chr13:113508739 G>T maps to NM_032189.3 L713L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANJ-01A-11D-A435-10 chr13:25265282 C>T maps to NM_001185085.1 F327F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AB-01A-31D-A435-10 chr19:19770790 G>A maps to NM_020410.2 Y134Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAL7-01A-11D-A42Y-10 chr1:160109763 G>T maps to NM_000702.3 R1008R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAL7-01A-11D-A42Y-10 chr19:42482470 G>T maps to ENST00000441343 C546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM3-01A-11D-A435-10 chr19:42474677 G>A maps to ENST00000441343 D760D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGM-01A-11D-A42Y-10 chr1:160151731 A>G maps to NM_144699.3 L960L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90W-01A-11D-A435-10 chr16:28914469 T>A did not map to a codon.
Sequencing variant TCGA-2G-AAGJ-01A-11D-A42Y-10 chr12:90018055 A>G maps to ENST00000428670 F416F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2X-A9D5-01A-11D-A435-10 chr1:203669389 G>T maps to NM_001001396.1 E236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2X-A9D6-01A-11D-A435-10 chr16:84456000 G>A maps to ENST00000416219 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF8-01A-11D-A42Y-10 chr19:36041522 G>T maps to NM_000704.2 Y1034*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALY-01A-11D-A42Y-10 chr21:27102057 G>A maps to NM_001003701.1 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V5-01A-11D-A435-10 chr21:35288043 C>T maps to NM_001697.2 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHN-01A-11D-A42Y-10 chr23:153661315 C>T did not map to a codon.
Sequencing variant TCGA-YU-A90Q-01A-11D-A435-10 chr17:40653234 G>T maps to NM_001130020.1 L646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALR-01A-21D-A42Y-10 chr16:2569647 C>T maps to NM_001694.3 Q124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2X-A9D5-01A-11D-A435-10 chr8:54742087 A>G maps to NM_015941.2 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALF-01A-11D-A42Y-10 chr4:42524316 C>A did not map to a codon.
Sequencing variant TCGA-2G-AAH3-01A-11D-A42Y-10 chr13:26436475 G>A maps to NM_016529.4 W1038*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGO-01A-11D-A42Y-10 chr23:76855028 T>C did not map to a codon.
Sequencing variant TCGA-2G-AAGP-01A-11D-A42Y-10 chr23:76938654 T>C did not map to a codon.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr23:76855028 T>C did not map to a codon.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr7:70249952 T>C maps to NM_015570.2 P724P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA06-01A-12D-A435-10 chr23:69458084 G>T did not map to a codon.
Sequencing variant TCGA-XE-A8H5-01A-11D-A435-10 chr23:69263369 A>G did not map to a codon.
Sequencing variant TCGA-XE-A9SE-01A-21D-A435-10 chr17:63554671 G>T maps to NM_004655.3 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SO-A8JP-01A-11D-A435-10 chr17:79174196 G>T maps to ENST00000269392 R280R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOD-01A-11D-A435-10 chr8:103841636 T>C maps to NM_148174.2 E366E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X3-A8G4-01A-11D-A435-10 chr1:193150314 T>C maps to NM_003783.3 K126K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFG-01A-11D-A42Y-10 chr6:33245603 G>T maps to NM_003782.3 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFZ-01A-11D-A42Y-10 chr21:41032932 G>A maps to NM_033172.1 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V3-01A-11D-A435-10 chr17:81006577 G>T maps to NM_001009905.1 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOC-01A-11D-A435-10 chr11:375477 C>T maps to NM_178537.4 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFO-01A-31D-A42Y-10 chr21:11058339 A>C did not map to a codon.
Sequencing variant TCGA-2G-AAFO-01A-31D-A42Y-10 chr21:11058347 C>A did not map to a codon.
Sequencing variant TCGA-2G-AALX-01A-11D-A42Y-10 chr8:143614694 G>T maps to NM_001702.2 L1146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AD-01A-11D-A435-10 chr8:143566120 C>T maps to NM_001702.2 N768N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALW-01A-11D-A42Y-10 chr22:38503887 G>T maps to NM_025045.4 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKO-01A-11D-A42Y-10 chr6:33543580 C>T maps to ENST00000360661 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AC-01A-11D-A435-10 chr5:17275705 G>T maps to NM_006317.3 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOC-01A-11D-A435-10 chr7:72861684 A>G maps to NM_032408.3 S1251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA06-01A-12D-A435-10 chr12:56995803 T>C maps to NM_013449.3 Q1201Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGE-01A-21D-A42Y-10 chr7:33388729 C>T maps to NM_198428.2 Y460Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr7:33313524 C>T maps to NM_198428.2 Q325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JW-01A-11D-A435-10 chr1:156617453 G>A maps to NM_021948.3 W207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0N-01A-21D-A435-10 chr23:152981135 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAGA-01A-11D-A42Y-10 chr12:24995151 G>A maps to NM_001178093.1 Y239Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHA-01A-11D-A42Y-10 chr12:12232367 C>T maps to NM_138722.1 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALO-01A-12D-A42Y-10 chr1:114429212 G>A maps to NM_001010922.2 N65N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X3-A8G4-01A-11D-A435-10 chr19:45261636 C>T maps to NM_005178.4 N342N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG0-01A-11D-A42Y-10 chr1:147092150 T>C maps to NM_004326.2 S730S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0E-01A-12D-A435-10 chr1:147084714 T>C maps to NM_004326.2 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA05-01A-12D-A435-10 chr11:118769750 G>A maps to NM_182557.2 D1291D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALO-01A-12D-A42Y-10 chr23:39916462 G>A did not map to a codon.
Sequencing variant TCGA-2G-AAF1-01A-11D-A42Y-10 chr23:129148077 A>C did not map to a codon.
Sequencing variant TCGA-2X-A9D6-01A-11D-A435-10 chr11:27681194 T>C did not map to a codon.
Sequencing variant TCGA-XY-A8S2-01A-11D-A435-10 chr11:27681194 T>C did not map to a codon.
Sequencing variant TCGA-VF-A8AE-01A-11D-A435-10 chr6:107390549 G>T maps to NM_001080450.2 R615R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOJ-01A-12D-A435-10 chr4:42145559 C>T maps to NM_207406.3 E313E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0H-01A-11D-A435-10 chr4:42145559 C>T maps to NM_207406.3 E313E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHC-01A-11D-A42Y-10 chr8:65494285 C>T maps to NM_152414.3 G313G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H4-01A-31D-A435-10 chr8:65494204 G>T maps to NM_152414.3 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84Y-01A-11D-A435-10 chr20:61637700 G>T maps to NM_080606.3 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGE-01A-21D-A42Y-10 chr10:60560686 A>G maps to NM_001080512.1 R632R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANV-01A-11D-A435-10 chr9:95481137 G>T maps to NM_001003800.1 R597R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94D-01A-11D-A435-10 chr22:18220953 C>T maps to NM_197966.1 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALW-01A-11D-A42Y-10 chr2:127825792 G>T maps to NM_139343.1 C186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHN-01A-11D-A42Y-10 chr12:51685421 G>A maps to NM_016293.2 Q490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr11:102221244 C>T maps to NM_001166.3 C220C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SB-A6J6-01A-11D-A435-10 chr2:32718724 C>G maps to NM_016252.3 S2820*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF1-01A-11D-A42Y-10 chr4:79792129 A>G maps to NM_198892.1 Q475Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG0-01A-11D-A42Y-10 chr4:79793946 C>T maps to NM_198892.1 A596A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGC-01A-21D-A42Y-10 chr14:54417211 G>A maps to NM_130850.2 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHA-01A-11D-A42Y-10 chr10:133784437 C>A maps to NM_004052.2 E107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr6:3119018 G>T maps to NM_004332.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG7-01A-11D-A42Y-10 chr17:65890192 G>T maps to ENST00000321892 E945*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFM-01A-11D-A42Y-10 chr23:154348400 G>T did not map to a codon.
Sequencing variant TCGA-2G-AALX-01A-11D-A42Y-10 chr23:154305543 G>A did not map to a codon.
Sequencing variant TCGA-2G-AAHP-01A-12D-A42Y-10 chr22:50217263 G>A maps to ENST00000342989 C234C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X3-A8G4-01A-11D-A435-10 chr9:136915675 G>T maps to NM_007371.3 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFY-01A-11D-A42Y-10 chr19:15350232 C>T maps to NM_058243.2 Q1182Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF8-01A-11D-A42Y-10 chr5:137502366 G>T maps to NM_139199.1 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V5-01A-11D-A435-10 chr17:59934455 T>C maps to NM_032043.2 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGC-01A-21D-A42Y-10 chr11:66109597 G>T maps to NM_001024957.1 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H4-01A-31D-A435-10 chr11:66108710 C>T maps to NM_001024957.1 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH8-01A-11D-A42Y-10 chr3:9783074 G>T maps to NM_001003694.1 R602R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JY-01A-11D-A435-10 chr23:135572572 T>G did not map to a codon.
Sequencing variant TCGA-YU-AA61-01A-11D-A435-10 chr11:1467101 G>T maps to NM_003957.2 A397A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGJ-01A-11D-A42Y-10 chr23:79959061 G>T did not map to a codon.
Sequencing variant TCGA-2G-AALO-01A-12D-A42Y-10 chr23:79932397 T>C did not map to a codon.
Sequencing variant TCGA-2G-AAH3-01A-11D-A42Y-10 chr11:62458259 T>C maps to NM_001130702.1 T384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A89B-01A-11D-A435-10 chr19:577975 C>A maps to NM_001728.2 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr9:116116548 G>T maps to NM_017688.2 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG0-01A-11D-A42Y-10 chr11:122848422 G>C maps to NM_001098169.1 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAEW-01A-11D-A42Y-10 chr12:108010913 G>T maps to NM_001018072.1 E684*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-2G-AAFJ-01A-11D-A42Y-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-VF-A8AA-01A-11D-A435-10 chr1:45275920 G>A maps to NM_001136537.1 E41E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A89B-01A-11D-A435-10 chr4:75719475 G>T maps to NM_001729.2 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1G-01A-11D-A435-10 chr23:100625018 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAG5-01A-11D-A42Y-10 chr6:26411340 A>G maps to NM_007048.5 G323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SB-A76C-01A-11D-A435-10 chr10:103221769 C>T maps to NM_033637.2 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFH-01A-12D-A42Y-10 chr11:116633789 G>T maps to NM_032725.3 S172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG8-01A-31D-A42Y-10 chr17:56387454 G>T maps to NM_004758.2 S1255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALG-01A-11D-A42Y-10 chr17:56386621 T>C maps to NM_004758.2 E1337E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG8-01A-31D-A42Y-10 chr10:21784696 G>T maps to NM_001010911.2 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2X-A9D5-01A-11D-A435-10 chr10:124459131 G>T maps to NM_001010912.1 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGY-01A-11D-A42Y-10 chr10:73511466 G>A maps to NM_022153.1 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGY-01A-11D-A42Y-10 chr10:124713658 G>T maps to NM_024942.3 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALS-01A-12D-A42Y-10 chr11:16760381 C>T maps to NM_014267.5 D19D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKO-01A-11D-A42Y-10 chr11:111168757 C>T did not map to a codon.
Sequencing variant TCGA-2G-AALN-01A-11D-A42Y-10 chr11:111167556 A>T did not map to a codon.
Sequencing variant TCGA-2G-AAFJ-01A-11D-A42Y-10 chr12:13526326 C>G maps to ENST00000318426 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGN-01A-11D-A42Y-10 chr12:103696284 C>T maps to NM_001099336.1 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAL5-01A-11D-A42Y-10 chr12:113629501 G>A maps to NM_032848.1 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGN-01A-11D-A42Y-10 chr14:105964250 G>A maps to ENST00000392523 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W4-A7U2-01A-11D-A435-10 chr15:34640734 T>C maps to ENST00000438749 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF1-01A-11D-A42Y-10 chr15:40544584 A>G maps to NM_001039905.1 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84Y-01A-11D-A435-10 chr16:2514566 G>A maps to NM_025108.2 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANI-01A-11D-A435-10 chr16:19718522 C>T maps to NM_001012991.2 W362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1I-01A-11D-A435-10 chr16:5112522 C>T maps to ENST00000350219 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JX-01A-11D-A435-10 chr17:58503677 G>T maps to NM_181707.2 E104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKM-01A-11D-A42Y-10 chr17:79507957 G>A maps to NM_025161.5 Q845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84W-01A-11D-A435-10 chr17:79517781 A>G maps to NM_025161.5 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOD-01A-11D-A435-10 chr17:71232214 A>G maps to NM_017941.4 Q198Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGV-01A-11D-A42Y-10 chr19:1236072 T>C maps to ENST00000382477 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM4-01A-11D-A435-10 chr19:1236042 G>T maps to ENST00000382477 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94D-01A-11D-A435-10 chr19:2275720 G>T maps to NM_198532.2 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAL7-01A-11D-A42Y-10 chr19:13996847 C>T maps to ENST00000454313 K563K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A9T9-01A-11D-A435-10 chr11:47612008 G>T maps to NM_031909.2 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFY-01A-11D-A42Y-10 chr16:1143812 G>A maps to NM_207419.3 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFN-01A-31D-A42Y-10 chr1:169390744 T>C maps to ENST00000367806 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr1:75086439 G>T maps to NM_001002912.4 Y326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X3-A8G4-01A-11D-A435-10 chr1:55271836 C>T maps to NM_001110533.1 V16V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM3-01A-11D-A435-10 chr1:109650647 A>T maps to NM_001122961.1 Y19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr1:228288912 G>T maps to NM_024319.2 C237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHT-01A-11D-A42Y-10 chr1:34643422 G>A maps to NM_001134734.1 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGG-01A-11D-A42Y-10 chr2:241835039 G>A maps to NM_001085437.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2X-A9D5-01A-11D-A435-10 chr5:41917161 G>T maps to NM_175921.4 E216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHG-01A-11D-A42Y-10 chr5:131811503 C>T maps to ENST00000378953 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH8-01A-11D-A42Y-10 chr6:121526288 T>G maps to ENST00000275159 I834I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84X-01A-11D-A435-10 chr6:127898392 G>T maps to NM_001010905.1 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKO-01A-11D-A42Y-10 chr6:170175416 G>T maps to NM_018341.1 E457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF6-01A-11D-A42Y-10 chr7:6634133 G>T maps to NM_024067.2 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr7:134851457 T>G maps to NM_024033.2 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANR-01A-11D-A435-10 chr7:112462250 G>T maps to NM_152556.2 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM3-01A-11D-A435-10 chr9:139741763 G>A maps to NM_001080482.2 V966V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAL5-01A-11D-A42Y-10 chr9:91606482 C>T maps to NM_001001938.3 D115D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH3-01A-11D-A42Y-10 chr9:136270538 G>T maps to NM_153710.3 L679L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SO-A8JP-01A-11D-A435-10 chr8:61144875 C>T maps to NM_004056.4 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG6-01A-11D-A42Y-10 chr19:13423557 G>T maps to NM_023035.2 S532S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SO-A8JP-01A-11D-A435-10 chr19:13443725 G>T maps to NM_023035.2 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAEX-01A-11D-A42Y-10 chr12:2743460 A>C did not map to a codon.
Sequencing variant TCGA-WZ-A7V3-01A-11D-A435-10 chr16:1245463 G>T maps to NM_021098.2 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALF-01A-11D-A42Y-10 chr22:40055122 T>G did not map to a codon.
Sequencing variant TCGA-ZM-AA0E-01A-12D-A435-10 chr22:40061520 G>T maps to NM_021096.3 P1290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGZ-01A-11D-A42Y-10 chr7:81693630 A>T maps to NM_000722.2 I256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKD-01A-31D-A42Y-10 chr8:91078130 G>A maps to NM_004929.2 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALP-01A-12D-A42Y-10 chr12:54108459 A>G maps to NM_020898.2 S468S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGJ-01A-11D-A42Y-10 chr7:134620436 A>G did not map to a codon.
Sequencing variant TCGA-2G-AALN-01A-11D-A42Y-10 chr10:5567449 C>T maps to NM_005185.2 D134D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFV-01A-11D-A42Y-10 chr10:12595238 A>G maps to NM_153498.2 E36E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF4-01A-11D-A42Y-10 chr5:149607839 G>T maps to NM_015981.3 C384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V5-01A-11D-A435-10 chr4:114378549 C>A maps to ENST00000515496 R469R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0E-01A-12D-A435-10 chr10:75585051 G>T maps to ENST00000423381 P380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG7-01A-11D-A42Y-10 chr1:20811815 G>A maps to NM_018584.5 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALT-01A-11D-A42Y-10 chr5:110819953 A>G maps to NM_001744.4 K404K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANI-01A-11D-A435-10 chr3:12851758 G>T maps to NM_001162499.1 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKM-01A-11D-A42Y-10 chr15:42684847 G>T maps to NM_000070.2 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFJ-01A-11D-A42Y-10 chr19:36632053 C>T maps to NM_001749.2 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFM-01A-11D-A42Y-10 chr19:36632053 C>T maps to NM_001749.2 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGO-01A-11D-A42Y-10 chr19:36632053 C>T maps to NM_001749.2 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGT-01A-11D-A42Y-10 chr19:36632053 C>T maps to NM_001749.2 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr19:36632053 C>T maps to NM_001749.2 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALX-01A-11D-A42Y-10 chr19:36631957 C>G maps to NM_001749.2 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALY-01A-11D-A42Y-10 chr19:36632053 C>T maps to NM_001749.2 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANR-01A-11D-A435-10 chr19:36632053 C>T maps to NM_001749.2 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOF-01A-11D-A435-10 chr19:36631957 C>G maps to NM_001749.2 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOL-01A-11D-A435-10 chr19:36632053 C>T maps to NM_001749.2 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A8S3-01B-11D-A435-10 chr19:36632053 C>T maps to NM_001749.2 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG3-01A-11D-A42Y-10 chr22:37912201 G>T maps to NM_014550.3 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG9-01A-11D-A42Y-10 chr22:37891565 C>T maps to NM_014550.3 E777E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SB-A76C-01A-11D-A435-10 chr9:139262097 C>T maps to NM_052813.4 T420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFJ-01A-11D-A42Y-10 chr13:111299557 G>T maps to NM_024537.2 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG8-01A-31D-A42Y-10 chr15:40933156 A>G maps to NM_170589.3 Q1936Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF6-01A-11D-A42Y-10 chr7:94167042 T>G maps to NM_022900.4 L368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHP-01A-12D-A42Y-10 chr7:94147625 A>G maps to NM_022900.4 E114E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHC-01A-11D-A42Y-10 chr23:41390359 T>C did not map to a codon.
Sequencing variant TCGA-2G-AAF1-01A-11D-A42Y-10 chr16:2229741 G>T maps to NM_020764.3 P1209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG6-01A-11D-A42Y-10 chr16:2230284 G>T maps to NM_020764.3 P1028P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JY-01A-11D-A435-10 chr16:2231334 G>T maps to NM_020764.3 P678P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFJ-01A-11D-A42Y-10 chr17:73498805 C>G maps to NM_020753.3 G783G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90P-01A-11D-A435-10 chr17:73498037 G>T maps to NM_020753.3 P1039P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF8-01A-11D-A42Y-10 chr2:202137404 G>A maps to NM_001080125.1 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGZ-01A-11D-A42Y-10 chr3:121981252 G>T maps to NM_001178065.1 A457A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKG-01A-11D-A42Y-10 chr3:122002840 C>T maps to NM_001178065.1 R690R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr3:121980485 G>T maps to NM_001178065.1 E202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA06-01A-12D-A435-10 chr11:119149217 A>G did not map to a codon.
Sequencing variant TCGA-2G-AALG-01A-11D-A42Y-10 chr17:46154241 C>T maps to ENST00000442683 W42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOB-01A-11D-A435-10 chr22:39262864 C>T maps to NM_014292.3 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGN-01A-11D-A42Y-10 chr9:131598072 G>A maps to NM_004059.4 C280C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM2-01A-11D-A435-10 chr16:57552623 G>A maps to NM_033212.3 D317D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AA-01A-11D-A435-10 chr16:57550225 C>T maps to NM_033212.3 E466E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90Y-01A-11D-A435-10 chr19:15132448 G>T maps to NM_173482.2 G355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALZ-01A-11D-A42Y-10 chr23:48922189 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAG8-01A-31D-A42Y-10 chr7:128441310 G>T maps to NM_022742.3 E140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG9-01A-11D-A42Y-10 chr17:18446964 T>A did not map to a codon.
Sequencing variant TCGA-2G-AAGE-01A-21D-A42Y-10 chr17:18528522 C>T did not map to a codon.
Sequencing variant TCGA-WZ-A7V5-01A-11D-A435-10 chr17:18513399 G>A did not map to a codon.
Sequencing variant TCGA-VF-A8AD-01A-11D-A435-10 chr7:76889505 G>A maps to NM_020879.2 K313K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0H-01A-11D-A435-10 chr19:11534698 C>G did not map to a codon.
Sequencing variant TCGA-2G-AAG5-01A-11D-A42Y-10 chr19:49912497 G>T maps to NM_144688.4 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SB-A6J6-01A-11D-A435-10 chr19:49920742 C>T maps to NM_144688.4 C555C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90Q-01A-11D-A435-10 chr4:77290776 C>T did not map to a codon.
Sequencing variant TCGA-2G-AAFJ-01A-11D-A42Y-10 chr17:78023946 C>T maps to NM_017950.2 Q342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKO-01A-11D-A42Y-10 chr12:119866559 C>T maps to NM_178499.3 R55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO3-01A-11D-A435-10 chr12:119954483 G>T maps to NM_178499.3 E314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0B-01A-11D-A435-10 chr12:120527872 C>T maps to NM_207311.2 Q520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2X-A9D5-01A-11D-A435-10 chr16:3080717 C>T maps to NM_001103175.1 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFY-01A-11D-A42Y-10 chr11:66360039 G>T maps to NM_018219.2 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG9-01A-11D-A42Y-10 chr14:91804417 C>T maps to NM_001080414.2 R327R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0D-01A-11D-A435-10 chr4:7044590 C>T maps to NM_153376.2 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A912-01A-11D-A435-10 chr19:41825731 A>G maps to NM_052848.1 E252E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH4-01A-12D-A42Y-10 chr23:50053934 T>C did not map to a codon.
Sequencing variant TCGA-XE-AANI-01A-11D-A435-10 chr5:159707574 G>T maps to NM_024565.5 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84X-01A-11D-A435-10 chr3:45942702 C>T maps to NM_031200.2 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH3-01A-11D-A42Y-10 chr3:132321046 C>A did not map to a codon.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr1:117564465 G>A maps to NM_004258.3 L763L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHN-01A-11D-A42Y-10 chr5:140011944 G>A maps to NM_001174105.1 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALQ-01A-12D-A42Y-10 chr1:158325336 G>T maps to NM_030893.3 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM4-01A-11D-A435-10 chr15:74000798 G>T maps to NM_001024736.1 E497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A6IS-01A-11D-A435-10 chr15:73995179 C>T maps to NM_001024736.1 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGG-01A-11D-A42Y-10 chr17:72469723 A>G maps to NM_007261.2 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1G-01A-11D-A435-10 chr1:207941163 C>T maps to NM_172359.2 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH0-01A-11D-A42Y-10 chr1:111440511 G>T maps to NM_000560.3 E196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALP-01A-12D-A42Y-10 chr20:23066499 C>A maps to NM_012072.3 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0H-01A-11D-A435-10 chr20:3785521 G>T maps to NM_021873.2 E553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAEX-01A-11D-A42Y-10 chr17:45234324 G>A maps to NM_001114091.1 R266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFH-01A-12D-A42Y-10 chr17:45234324 G>A maps to NM_001114091.1 R266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHP-01A-12D-A42Y-10 chr17:45219802 C>A did not map to a codon.
Sequencing variant TCGA-2G-AAHT-01A-11D-A42Y-10 chr17:45234322 T>C maps to NM_001114091.1 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1I-01A-11D-A435-10 chr17:45234324 G>A maps to NM_001114091.1 R266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOC-01A-11D-A435-10 chr1:227335122 G>A maps to ENST00000366766 Y277Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0D-01A-11D-A435-10 chr22:37964166 G>A maps to NM_152243.2 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH0-01A-11D-A42Y-10 chr22:19484955 G>T maps to NM_001178010.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A8S2-01A-11D-A435-10 chr8:25344850 G>A did not map to a codon.
Sequencing variant TCGA-2G-AAHG-01A-11D-A42Y-10 chr18:64172300 G>A maps to NM_021153.2 G689G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANV-01A-11D-A435-10 chr18:64211261 G>T maps to NM_021153.2 S387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JY-01A-11D-A435-10 chr20:44815230 G>T maps to NM_021248.1 I553I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHT-01A-11D-A42Y-10 chr20:58560109 C>T maps to NM_177980.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr5:26881346 G>T maps to NM_016279.3 L756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A912-01A-11D-A435-10 chr5:26890657 C>T maps to NM_016279.3 R423R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr5:176002408 G>T maps to NM_001171976.1 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALF-01A-11D-A42Y-10 chr7:105641931 G>T maps to NM_152750.4 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGP-01A-11D-A42Y-10 chr16:89761463 C>T maps to NM_052988.4 Y306Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A6IS-01A-11D-A435-10 chr7:39991319 C>T maps to NM_003718.4 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGF-01A-31D-A42Y-10 chr7:90741977 C>T maps to NM_012395.2 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V3-01A-11D-A435-10 chr17:46052881 C>A maps to NM_176096.1 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALZ-01A-11D-A42Y-10 chr14:50798951 C>T maps to ENST00000358473 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SO-A8JP-01A-11D-A435-10 chr23:18622107 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAM4-01A-11D-A435-10 chr9:21994302 G>T maps to ENST00000361570 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGJ-01A-11D-A42Y-10 chr9:22006137 G>T maps to NM_004936.3 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGM-01A-11D-A42Y-10 chr23:139866051 G>A did not map to a codon.
Sequencing variant TCGA-2G-AALT-01A-11D-A42Y-10 chr23:139866494 C>T did not map to a codon.
Sequencing variant TCGA-2G-AAH4-01A-12D-A42Y-10 chr16:22359013 G>T maps to NM_001802.1 R213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGX-01A-11D-A42Y-10 chr17:14139303 T>G maps to NM_001007530.1 R146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGZ-01A-11D-A42Y-10 chr4:85560084 T>C maps to NM_001263.3 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFH-01A-12D-A42Y-10 chr6:31084506 G>T maps to NM_001264.4 G295G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALP-01A-12D-A42Y-10 chr5:149546519 G>A maps to NM_001804.2 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90S-01A-11D-A435-10 chr23:72667530 T>C did not map to a codon.
Sequencing variant TCGA-2G-AAM2-01A-11D-A435-10 chr19:51983737 C>T maps to NM_001080405.1 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG7-01A-11D-A42Y-10 chr19:33792543 C>A maps to NM_004364.3 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A8D5-01A-11D-A435-10 chr20:48808331 G>T maps to NM_005194.2 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGJ-01A-11D-A42Y-10 chr22:17978522 C>T maps to ENST00000400579 R122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGY-01A-11D-A42Y-10 chr1:22307357 C>T maps to NM_007352.2 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG6-01A-11D-A42Y-10 chr1:151678721 T>C maps to NM_007185.4 Q368Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH8-01A-11D-A42Y-10 chr1:151678745 C>T maps to NM_007185.4 Q360Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHN-01A-11D-A42Y-10 chr1:151679177 G>A maps to NM_007185.4 Q319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKD-01A-31D-A42Y-10 chr1:151678745 C>T maps to NM_007185.4 Q360Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X3-A8G4-01A-11D-A435-10 chr1:151678745 C>T maps to NM_007185.4 Q360Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84Y-01A-11D-A435-10 chr18:34844655 G>T maps to NM_020180.3 I410I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H5-01A-11D-A435-10 chr15:72608194 G>A maps to NM_052840.4 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFH-01A-12D-A42Y-10 chr22:46765083 T>C maps to NM_014246.1 K2648K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG9-01A-11D-A42Y-10 chr22:46804954 G>T maps to NM_014246.1 R1722R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90Y-01A-11D-A435-10 chr22:46931225 G>A maps to NM_014246.1 G614G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOJ-01A-12D-A435-10 chr16:90038252 G>T maps to NM_145039.3 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF8-01A-11D-A42Y-10 chr23:100383721 C>A did not map to a codon.
Sequencing variant TCGA-2G-AAGJ-01A-11D-A42Y-10 chr16:81053826 G>A maps to NM_001100624.1 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANV-01A-11D-A435-10 chr16:67864335 G>A maps to NM_025082.3 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG8-01A-31D-A42Y-10 chr11:117267809 G>T maps to NM_014956.4 L1094L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALS-01A-12D-A42Y-10 chr16:55853458 C>T maps to NM_001025195.1 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AB-01A-31D-A435-10 chr19:4409386 C>T maps to NM_005483.2 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA06-01A-12D-A435-10 chr3:126571533 C>T maps to ENST00000508789 D153D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO6-01A-31D-A435-10 chr5:98239546 C>T maps to NM_001270.2 Q107Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H4-01A-31D-A435-10 chr19:16641680 G>A maps to NM_006387.5 Q229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90Q-01A-11D-A435-10 chr12:133424712 G>A maps to NM_001161344.1 D547D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A9T9-01A-11D-A435-10 chr14:93397925 G>A maps to NM_001275.3 E229E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr1:203198778 G>A did not map to a codon.
Sequencing variant TCGA-2G-AAFL-01A-21D-A42Y-10 chr23:85218960 G>A did not map to a codon.
Sequencing variant TCGA-ZM-AA0D-01A-11D-A435-10 chr7:29438102 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAG8-01A-31D-A42Y-10 chr7:150935130 G>T maps to NM_019015.1 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90W-01A-11D-A435-10 chr23:109924729 T>C did not map to a codon.
Sequencing variant TCGA-YU-A94D-01A-11D-A435-10 chr23:109963071 C>T did not map to a codon.
Sequencing variant TCGA-ZM-AA0N-01A-21D-A435-10 chr11:74424503 G>T maps to NM_015424.3 Y72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALN-01A-11D-A42Y-10 chr2:175614727 G>A maps to NM_001039523.2 I341I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKO-01A-11D-A42Y-10 chr8:27327403 G>T maps to NM_000742.3 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKL-01A-11D-A42Y-10 chr15:78922240 G>T maps to NM_000750.3 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALS-01A-12D-A42Y-10 chr3:142840932 C>G maps to NM_004267.3 Y425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANJ-01A-11D-A435-10 chr3:142840362 C>T maps to NM_004267.3 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84W-01A-11D-A435-10 chr10:73768165 C>T maps to NM_004273.4 A459A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALN-01A-11D-A42Y-10 chr16:75563574 C>T maps to NM_024533.3 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr16:75563910 G>T maps to NM_024533.3 C124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM4-01A-11D-A435-10 chr16:75513050 G>A maps to NM_021615.4 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H1-01A-11D-A435-10 chr19:19655438 C>T maps to NM_153221.2 S695S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFZ-01A-11D-A42Y-10 chr12:120128069 G>C maps to ENST00000392521 P2024P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A9T9-01A-11D-A435-10 chr9:130941501 C>T maps to NM_012127.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0N-01A-21D-A435-10 chr3:33543149 G>T maps to ENST00000359576 G1485G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGF-01A-31D-A42Y-10 chr16:1505138 G>T maps to ENST00000382745 S365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84Y-01A-11D-A435-10 chr16:1510493 G>T maps to ENST00000382745 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFM-01A-11D-A42Y-10 chr1:16383401 C>T maps to NM_000085.3 A685A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHN-01A-11D-A42Y-10 chr1:16383401 C>T maps to NM_000085.3 A685A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFZ-01A-11D-A42Y-10 chr13:96085989 G>A did not map to a codon.
Sequencing variant TCGA-S6-A8JW-01A-11D-A435-10 chr21:37833708 G>A maps to NM_001146077.1 C95C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2X-A9D6-01A-11D-A435-10 chr23:106172011 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAGY-01A-11D-A42Y-10 chr4:141311835 G>T maps to NM_004362.2 I566I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JW-01A-11D-A435-10 chr16:28495342 G>T maps to NM_000086.2 A258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOJ-01A-12D-A435-10 chr11:57427263 C>T maps to NM_006831.2 Q106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAL5-01A-11D-A42Y-10 chr11:72145170 G>A maps to NM_030813.3 C116C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84X-01A-11D-A435-10 chr5:1331992 G>T maps to NM_030782.3 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGP-01A-11D-A42Y-10 chr3:140281040 G>T maps to NM_022131.2 V701V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGI-01A-11D-A42Y-10 chr12:7302200 C>A maps to NM_014718.3 P719P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALR-01A-21D-A42Y-10 chr5:175823487 G>T maps to NM_007097.2 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AB-01A-31D-A435-10 chr17:57746270 C>T maps to NM_004859.3 Y754Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr22:19263275 G>T maps to NM_007098.3 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A89B-01A-11D-A435-10 chr14:23847655 C>T maps to ENST00000339180 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANI-01A-11D-A435-10 chr8:88363931 T>C maps to NM_173538.2 N354N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr23:150908186 C>T did not map to a codon.
Sequencing variant TCGA-2G-AAGX-01A-11D-A42Y-10 chr16:57993940 C>T maps to NM_001297.4 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGI-01A-11D-A42Y-10 chr23:21450745 C>A did not map to a codon.
Sequencing variant TCGA-2G-AAHP-01A-12D-A42Y-10 chr23:21519641 C>T did not map to a codon.
Sequencing variant TCGA-2G-AAGZ-01A-11D-A42Y-10 chr10:101089339 G>T maps to NM_020348.2 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFH-01A-12D-A42Y-10 chr2:97482997 C>T maps to NM_017623.4 D328D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0B-01A-11D-A435-10 chr17:40125921 C>T maps to NM_033133.4 Q416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0E-01A-12D-A435-10 chr9:17135089 G>A maps to NM_017738.2 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALX-01A-11D-A42Y-10 chr3:74548916 G>T maps to NM_020872.1 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFN-01A-31D-A42Y-10 chr3:3067876 G>T maps to NM_175607.1 S526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1G-01A-11D-A435-10 chr16:76496002 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAGZ-01A-11D-A42Y-10 chr7:51095411 G>C maps to ENST00000395542 R1209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFV-01A-11D-A42Y-10 chr16:70515314 G>T maps to NM_015386.2 R728R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90Q-01A-11D-A435-10 chr16:23415149 T>C maps to NM_153603.3 K556K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84X-01A-11D-A435-10 chr16:69369197 G>T maps to NM_032382.4 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0H-01A-11D-A435-10 chr6:33139320 G>T maps to NM_080680.2 R1061R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84W-01A-11D-A435-10 chr6:75798828 G>T maps to ENST00000322507 G3001G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGS-01A-11D-A42Y-10 chr8:121220568 T>C maps to NM_021110.1 A430A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALP-01A-12D-A42Y-10 chr8:121215960 G>T maps to NM_021110.1 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1I-01A-11D-A435-10 chr8:121344414 A>G maps to NM_021110.1 P1565P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SB-A76C-01A-11D-A435-10 chr8:121219206 G>T maps to NM_021110.1 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFV-01A-11D-A42Y-10 chr1:32137260 C>A did not map to a codon.
Sequencing variant TCGA-2G-AAG8-01A-31D-A42Y-10 chr1:32156171 G>A maps to NM_001856.3 G480G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHL-01A-11D-A42Y-10 chr7:94042435 T>C maps to NM_000089.3 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOJ-01A-12D-A435-10 chr9:117002728 C>A maps to NM_032888.2 R933R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94D-01A-11D-A435-10 chr23:107683386 G>T did not map to a codon.
Sequencing variant TCGA-YU-A94D-01A-11D-A435-10 chr23:107929305 G>A did not map to a codon.
Sequencing variant TCGA-XE-AAO6-01A-31D-A435-10 chr23:107457452 G>T did not map to a codon.
Sequencing variant TCGA-XE-AAOF-01A-11D-A435-10 chr23:107430449 T>C did not map to a codon.
Sequencing variant TCGA-XY-A8S3-01B-11D-A435-10 chr21:47421227 G>T maps to NM_001848.2 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHP-01A-12D-A42Y-10 chr3:130134523 A>G maps to ENST00000312481 K1599K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGK-01A-11D-A42Y-10 chr19:18896611 C>A maps to NM_000095.2 V513V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALF-01A-11D-A42Y-10 chr15:69011559 A>G maps to NM_006091.3 G386G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr16:4414862 C>T maps to NM_024535.3 A319A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H5-01A-11D-A435-10 chr4:73935348 G>A maps to NM_173827.2 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHL-01A-11D-A42Y-10 chr16:85838604 T>C maps to NM_001861.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84W-01A-11D-A435-10 chr2:98264519 C>T maps to NM_001862.2 C113C. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-YU-A94D-01A-11D-A435-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-2G-AAG5-01A-11D-A42Y-10 chr19:17004137 C>T maps to ENST00000443236 G1870G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALQ-01A-12D-A42Y-10 chr19:17038839 G>T maps to ENST00000443236 R1174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-AA4L-01A-11D-A435-10 chr19:17039936 A>G maps to ENST00000443236 L1044L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALG-01A-11D-A42Y-10 chr17:28758788 G>T did not map to a codon.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr17:28754502 G>T maps to NM_001304.4 T648T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALT-01A-11D-A42Y-10 chr12:69264139 G>T maps to NM_001874.4 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SO-A8JP-01A-11D-A435-10 chr16:89655120 G>T maps to NM_014427.4 R397R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1H-01A-11D-A435-10 chr8:145622454 C>T maps to NM_013291.2 A853A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1I-01A-11D-A435-10 chr8:145623294 G>A maps to NM_013291.2 C649C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JY-01A-11D-A435-10 chr8:145622523 G>T maps to NM_013291.2 G830G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOD-01A-11D-A435-10 chr2:9568892 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAM4-01A-11D-A435-10 chr11:68530186 G>T maps to NM_001876.3 R595R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALX-01A-11D-A42Y-10 chr22:51016323 G>T maps to NM_152245.2 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0E-01A-12D-A435-10 chr19:50215118 G>A maps to NM_152359.2 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKO-01A-11D-A42Y-10 chr1:207749011 G>A maps to NM_000651.4 P1508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO4-01A-11D-A435-10 chr1:207751171 A>C maps to NM_000651.4 P1520P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1H-01A-11D-A435-10 chr22:50319191 G>T maps to NM_001135101.1 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AE-01A-11D-A435-10 chr8:67089598 C>T maps to NM_000756.2 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A8D5-01A-11D-A435-10 chr3:97662071 G>T maps to ENST00000182096 G995*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHT-01A-11D-A42Y-10 chr16:21289539 G>T maps to NM_001888.3 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG5-01A-11D-A42Y-10 chr23:1422910 A>G did not map to a codon.
Sequencing variant TCGA-SB-A76C-01A-11D-A435-10 chr22:37326717 G>A maps to ENST00000262825 E292E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALQ-01A-12D-A42Y-10 chr1:36937223 G>A maps to NM_156039.3 S365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKG-01A-11D-A42Y-10 chr10:43659371 C>T maps to NM_018590.3 R347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALO-01A-12D-A42Y-10 chr10:43659371 C>T maps to NM_018590.3 R347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALT-01A-11D-A42Y-10 chr10:43659371 C>T maps to NM_018590.3 R347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGF-01A-31D-A42Y-10 chr8:3226878 G>T maps to NM_033225.5 G932G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGV-01A-11D-A42Y-10 chr8:3216722 G>A maps to NM_033225.5 C1085C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGW-01A-11D-A42Y-10 chr8:3855558 G>C maps to NM_033225.5 Y228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOB-01A-11D-A435-10 chr8:2944634 G>A maps to NM_033225.5 L2486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2X-A9D6-01A-11D-A435-10 chr1:34554768 G>A maps to ENST00000373381 H31H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANI-01A-11D-A435-10 chr1:33998695 G>T maps to ENST00000373381 T3335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKL-01A-11D-A42Y-10 chr15:75968619 C>T maps to NM_001897.4 V2080V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFV-01A-11D-A42Y-10 chr23:153881675 A>C did not map to a codon.
Sequencing variant TCGA-2G-AAGO-01A-11D-A42Y-10 chr23:153881675 A>C did not map to a codon.
Sequencing variant TCGA-2G-AAG3-01A-11D-A42Y-10 chr10:126678128 G>T maps to NM_022802.2 P972P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGS-01A-11D-A42Y-10 chr20:56094263 T>C maps to ENST00000423479 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H1-01A-11D-A435-10 chr1:70877109 A>G maps to NM_001902.5 K4K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGO-01A-11D-A42Y-10 chr5:11397160 C>T maps to NM_001332.2 T198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H5-01A-11D-A435-10 chr5:11098815 T>C maps to NM_001332.2 K836K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH0-01A-11D-A42Y-10 chr23:16685815 T>C did not map to a codon.
Sequencing variant TCGA-2G-AAH4-01A-12D-A42Y-10 chr23:16711310 G>T did not map to a codon.
Sequencing variant TCGA-XE-AAOC-01A-11D-A435-10 chr14:25043630 G>T maps to NM_001911.2 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALZ-01A-11D-A42Y-10 chr9:99797976 T>C did not map to a codon.
Sequencing variant TCGA-2G-AAGS-01A-11D-A42Y-10 chr7:117407170 G>A maps to NM_033427.2 C946C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH0-01A-11D-A42Y-10 chr17:55962850 T>C maps to NM_017949.1 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOF-01A-11D-A435-10 chr17:55962727 G>T maps to NM_017949.1 I66I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF4-01A-11D-A42Y-10 chr6:43156417 G>T maps to ENST00000354495 R715R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFH-01A-12D-A42Y-10 chr6:43153341 G>T maps to ENST00000354495 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHP-01A-12D-A42Y-10 chr6:43183046 C>T maps to ENST00000354495 S1973S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A6IS-01A-11D-A435-10 chr6:43166533 G>T maps to ENST00000354495 L997L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF4-01A-11D-A42Y-10 chr7:101877520 G>T did not map to a codon.
Sequencing variant TCGA-VF-A8AC-01A-11D-A435-10 chr7:101882799 G>T maps to ENST00000360264 E1286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A6IS-01A-11D-A435-10 chr12:111776096 G>T maps to NM_015267.3 R1068R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFJ-01A-11D-A42Y-10 chr10:101997852 G>T maps to NM_018294.4 R394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90W-01A-11D-A435-10 chr11:107309826 G>T maps to NM_152434.2 S218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG6-01A-11D-A42Y-10 chr18:47810854 G>T maps to NM_001101654.1 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHP-01A-12D-A42Y-10 chr18:47810350 A>T maps to NM_001101654.1 T446T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF1-01A-11D-A42Y-10 chr23:45017125 G>T did not map to a codon.
Sequencing variant TCGA-XE-AAOD-01A-11D-A435-10 chr23:40489932 G>T did not map to a codon.
Sequencing variant TCGA-VF-A8AA-01A-11D-A435-10 chr23:134294392 C>T did not map to a codon.
Sequencing variant TCGA-XY-A89B-01A-11D-A435-10 chr23:37665736 C>T did not map to a codon.
Sequencing variant TCGA-2G-AAH4-01A-12D-A42Y-10 chr23:83129488 A>G did not map to a codon.
Sequencing variant TCGA-2G-AAHA-01A-11D-A42Y-10 chr23:83129488 A>G did not map to a codon.
Sequencing variant TCGA-2G-AALW-01A-11D-A42Y-10 chr23:83128816 A>G did not map to a codon.
Sequencing variant TCGA-2G-AAGJ-01A-11D-A42Y-10 chr10:104593812 T>A maps to NM_000102.3 K245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALZ-01A-11D-A42Y-10 chr10:104591289 C>T maps to NM_000102.3 W406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFN-01A-31D-A42Y-10 chr15:75015056 C>A maps to NM_000499.3 G128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG5-01A-11D-A42Y-10 chr6:32008456 C>T maps to NM_000500.5 Y377Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG0-01A-11D-A42Y-10 chr4:108853023 G>T maps to NM_183075.2 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOC-01A-11D-A435-10 chr19:15733938 G>T maps to NM_007253.3 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AD-01A-11D-A435-10 chr1:47533215 C>A maps to NM_178134.2 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90Y-01A-11D-A435-10 chr1:57480874 C>T maps to ENST00000371231 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGW-01A-11D-A42Y-10 chr5:39377193 A>G maps to NM_001343.2 T565T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGG-01A-11D-A42Y-10 chr9:124528808 G>T maps to ENST00000408936 S499S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2X-A9D6-01A-11D-A435-10 chr13:72440445 G>A maps to ENST00000359684 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO3-01A-11D-A435-10 chr13:72440445 G>A maps to ENST00000359684 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A9T9-01A-11D-A435-10 chr13:72440445 G>A maps to ENST00000359684 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H1-01A-11D-A435-10 chr19:47151864 A>C maps to NM_145056.2 G588G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALF-01A-11D-A42Y-10 chr16:90075812 C>T maps to ENST00000392973 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH4-01A-12D-A42Y-10 chr19:49136910 G>T maps to NM_001352.3 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr23:125686304 G>A did not map to a codon.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr8:104438340 G>T maps to NM_015420.6 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGV-01A-11D-A42Y-10 chr14:69521080 A>G maps to NM_003861.2 P774P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94D-01A-11D-A435-10 chr23:27998406 G>T did not map to a codon.
Sequencing variant TCGA-2G-AALY-01A-11D-A42Y-10 chr18:51053065 G>T maps to NM_005215.3 V1397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOC-01A-11D-A435-10 chr18:50278478 C>T maps to NM_005215.3 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAEW-01A-11D-A42Y-10 chr6:24301980 G>T maps to NM_016356.3 V173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANV-01A-11D-A435-10 chr11:6643166 G>T maps to NM_003737.2 S3247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF8-01A-11D-A42Y-10 chr13:95121165 G>T maps to NM_001129889.1 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALF-01A-11D-A42Y-10 chr13:95131233 G>A maps to NM_001129889.1 H92H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AB-01A-31D-A435-10 chr11:61071378 C>A maps to NM_001923.3 V930V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AC-01A-11D-A435-10 chr14:53522375 A>G did not map to a codon.
Sequencing variant TCGA-2G-AAHC-01A-11D-A42Y-10 chr10:74034543 G>T maps to NM_019058.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1I-01A-11D-A435-10 chr10:74034750 C>T maps to NM_019058.2 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGF-01A-31D-A42Y-10 chr11:108594023 A>G maps to NM_004398.2 K600K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGZ-01A-11D-A42Y-10 chr12:31237979 G>A maps to NM_030653.3 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALS-01A-12D-A42Y-10 chr22:38881966 A>G maps to NM_001098504.1 P723P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGW-01A-11D-A42Y-10 chr12:49231065 G>A maps to NM_004818.2 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH3-01A-11D-A42Y-10 chr23:41205589 G>C did not map to a codon.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr24:15026885 G>T did not map to a codon.
Sequencing variant TCGA-XE-A8H5-01A-11D-A435-10 chr5:176938911 G>T maps to NM_016222.2 A583A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr6:74124406 A>G maps to NM_018665.2 A581A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-SN-A84W-01A-11D-A435-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-2G-AAG9-01A-11D-A42Y-10 chr11:118627001 G>T maps to NM_004397.4 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr19:6476885 G>T maps to NM_024898.2 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHC-01A-11D-A42Y-10 chr1:115130379 T>C maps to ENST00000393274 A875A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHP-01A-12D-A42Y-10 chr1:111739830 G>T maps to NM_024901.3 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGG-01A-11D-A42Y-10 chr15:65962391 G>T maps to ENST00000443035 P1533P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALG-01A-11D-A42Y-10 chr1:153914770 G>T maps to NM_014856.2 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1I-01A-11D-A435-10 chr1:153914439 C>T maps to NM_014856.2 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JY-01A-11D-A435-10 chr22:32193621 T>C maps to NM_001136029.1 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGF-01A-31D-A42Y-10 chr17:5383845 G>T maps to NM_016041.3 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGE-01A-21D-A42Y-10 chr15:89056262 A>G maps to NM_017996.3 P535P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO3-01A-11D-A435-10 chr15:89056262 A>G maps to NM_017996.3 P535P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGY-01A-11D-A42Y-10 chr9:117185776 G>T maps to NM_015404.3 G481G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94D-01A-11D-A435-10 chr9:117266553 T>C maps to NM_015404.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG6-01A-11D-A42Y-10 chr2:234368883 C>A maps to NM_152879.2 C958*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFO-01A-31D-A42Y-10 chr11:46394019 C>A maps to NM_001105540.1 R512R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JX-01A-11D-A435-10 chr3:47891549 G>T maps to NM_138615.2 L1175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SO-A8JP-01A-11D-A435-10 chr10:127526836 G>A maps to NM_018180.2 F667F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANR-01A-11D-A435-10 chr19:47876119 G>A maps to NM_014681.5 P634P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0E-01A-12D-A435-10 chr14:80669619 A>C maps to NM_001007023.2 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1H-01A-11D-A435-10 chr21:47969713 C>T maps to ENST00000318711 H852H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H1-01A-11D-A435-10 chr21:47965816 A>G maps to ENST00000318711 G780G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFM-01A-11D-A42Y-10 chr1:68512244 T>G did not map to a codon.
Sequencing variant TCGA-2G-AAKG-01A-11D-A42Y-10 chr15:40656717 G>A maps to NM_033510.1 R192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO3-01A-11D-A435-10 chr15:40660379 G>A maps to NM_033510.1 L689L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOJ-01A-12D-A435-10 chr15:40660082 C>T maps to NM_033510.1 G590G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF8-01A-11D-A42Y-10 chr23:69665374 G>T did not map to a codon.
Sequencing variant TCGA-XE-AANR-01A-11D-A435-10 chr23:69713236 G>T did not map to a codon.
Sequencing variant TCGA-SB-A6J6-01A-11D-A435-10 chr17:7100102 C>T maps to NM_001365.3 E395E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGY-01A-11D-A42Y-10 chr10:79581551 G>T maps to NM_004747.3 S897*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGT-01A-11D-A42Y-10 chr8:1626713 C>T maps to ENST00000357934 L817L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALX-01A-11D-A42Y-10 chr15:41228736 G>T maps to NM_019074.3 E518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKL-01A-11D-A42Y-10 chr2:172967029 G>C maps to NM_004405.3 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-AA4L-01A-11D-A435-10 chr2:172967029 G>C maps to NM_004405.3 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGM-01A-11D-A42Y-10 chr23:32456428 C>T did not map to a codon.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr23:31196890 G>T did not map to a codon.
Sequencing variant TCGA-XY-A8S2-01A-11D-A435-10 chr23:31950248 G>C did not map to a codon.
Sequencing variant TCGA-ZM-AA06-01A-12D-A435-10 chr23:31462742 G>T did not map to a codon.
Sequencing variant TCGA-ZM-AA06-01A-12D-A435-10 chr23:32663130 C>A did not map to a codon.
Sequencing variant TCGA-YU-A90Q-01A-11D-A435-10 chr5:78328618 G>T maps to NM_013391.2 R470R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA06-01A-12D-A435-10 chr5:78347181 T>G maps to NM_013391.2 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG9-01A-11D-A42Y-10 chr19:46274630 G>T maps to NM_004409.3 R542R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANR-01A-11D-A435-10 chr19:42352957 G>A maps to ENST00000427618 W181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H4-01A-31D-A435-10 chr19:46287527 G>A maps to NM_004943.1 G666G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOD-01A-11D-A435-10 chr12:124256227 G>T maps to NM_207437.3 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AD-01A-11D-A435-10 chr17:76556824 T>C maps to ENST00000389840 K676K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGA-01A-11D-A42Y-10 chr17:7702428 G>A maps to NM_020877.2 S2856S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V5-01A-11D-A435-10 chr17:7637851 A>T maps to NM_020877.2 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V5-01A-11D-A435-10 chr17:7726882 C>T maps to NM_020877.2 Q3756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF1-01A-11D-A42Y-10 chr16:21073931 C>T maps to NM_017539.1 P1197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH0-01A-11D-A42Y-10 chr16:21132079 C>T maps to NM_017539.1 A560A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AC-01A-11D-A435-10 chr5:13830170 C>G maps to NM_001369.2 V2071V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V5-01A-11D-A435-10 chr5:13839637 C>A did not map to a codon.
Sequencing variant TCGA-2G-AAH0-01A-11D-A42Y-10 chr6:38899769 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAFL-01A-21D-A42Y-10 chr17:11502132 C>T maps to NM_001372.3 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG3-01A-11D-A42Y-10 chr17:11833286 A>T maps to NM_001372.3 P3994P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AE-01A-11D-A435-10 chr17:11502150 G>T maps to NM_001372.3 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V5-01A-11D-A435-10 chr17:11583112 C>T maps to NM_001372.3 S1131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHC-01A-11D-A42Y-10 chr3:132199259 G>T maps to NM_015268.3 V940V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM3-01A-11D-A435-10 chr2:25174378 T>C maps to NM_016544.2 K191K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFN-01A-31D-A42Y-10 chr1:84880406 C>T maps to NM_021233.2 G314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V3-01A-11D-A435-10 chr9:139256496 A>G maps to NM_001080849.1 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO4-01A-11D-A435-10 chr9:130965793 G>T maps to ENST00000372923 R15R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr12:32861094 G>T maps to ENST00000381000 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A912-01A-11D-A435-10 chr1:171810828 G>T maps to ENST00000359070 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84Y-01A-11D-A435-10 chr19:10260599 C>A maps to NM_001130823.1 A770A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0E-01A-12D-A435-10 chr19:10291230 A>G maps to NM_001130823.1 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM4-01A-11D-A435-10 chr2:25523019 G>T maps to NM_175629.1 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANI-01A-11D-A435-10 chr2:25505571 G>A maps to NM_175629.1 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr21:45679567 G>A maps to NM_013369.2 Q60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHP-01A-12D-A42Y-10 chr23:117680025 C>G did not map to a codon.
Sequencing variant TCGA-XY-A9T9-01A-11D-A435-10 chr23:117742319 G>T did not map to a codon.
Sequencing variant TCGA-XE-AANI-01A-11D-A435-10 chr3:51251593 C>T maps to NM_004947.4 Q390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG5-01A-11D-A42Y-10 chr7:111400314 G>A maps to ENST00000428084 L1362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOJ-01A-12D-A435-10 chr1:62979204 C>A maps to ENST00000371140 E1398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGT-01A-11D-A42Y-10 chr19:3491804 C>T maps to NM_001145165.1 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGW-01A-11D-A42Y-10 chr4:3494688 C>T maps to ENST00000389653 Q326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGW-01A-11D-A42Y-10 chr9:131851280 C>T maps to NM_020438.4 Q238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A8D5-01A-11D-A435-10 chr19:2226653 G>T maps to ENST00000221482 G1378G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAEX-01A-11D-A42Y-10 chr6:30919138 A>G maps to NM_080870.3 E966E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SO-A8JP-01A-11D-A435-10 chr6:30917806 C>T maps to NM_080870.3 H522H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHN-01A-11D-A42Y-10 chr19:38709683 G>A maps to NM_001135155.1 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2X-A9D6-01A-11D-A435-10 chr1:44437572 G>T maps to NM_001384.4 V333V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM4-01A-11D-A435-10 chr11:66276583 A>T maps to NM_005700.3 S692S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JX-01A-11D-A435-10 chr11:66272123 G>T maps to NM_005700.3 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94I-01A-11D-A435-10 chr11:66260274 G>A maps to NM_005700.3 W359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JX-01A-11D-A435-10 chr9:140005138 C>T maps to NM_013379.2 Q480Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A6IS-01A-11D-A435-10 chr9:140006325 A>C maps to NM_013379.2 G402G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANV-01A-11D-A435-10 chr1:97839131 G>T maps to NM_000110.3 G681G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH4-01A-12D-A42Y-10 chr18:28671011 A>G maps to ENST00000438199 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGT-01A-11D-A42Y-10 chr11:117376427 G>T maps to NM_020693.2 P661P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGI-01A-11D-A42Y-10 chr18:29122742 C>T maps to NM_001943.3 S754S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-2G-AAF1-01A-11D-A42Y-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-2G-AAF4-01A-11D-A42Y-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-2G-AAFG-01A-11D-A42Y-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-2G-AAFL-01A-21D-A42Y-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-2G-AAGV-01A-11D-A42Y-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-2G-AAHC-01A-11D-A42Y-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-2G-AAHT-01A-11D-A42Y-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-2G-AAKM-01A-11D-A42Y-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-2G-AAKO-01A-11D-A42Y-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-2G-AAM4-01A-11D-A435-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-YU-AA61-01A-11D-A435-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-ZM-AA05-01A-12D-A435-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-ZM-AA0F-01A-21D-A435-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-S6-A8JW-01A-11D-A435-10 chr20:18724892 G>A maps to NM_080820.4 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOB-01A-11D-A435-10 chr7:76112032 C>T maps to NM_020892.2 H159H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr7:107207562 A>G maps to NM_181581.1 K16K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFV-01A-11D-A42Y-10 chr1:221879722 G>A maps to NM_007207.3 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AAAL-01A-11D-A435-10 chr20:30454892 G>T maps to NM_080611.3 S40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGF-01A-31D-A42Y-10 chr11:1579109 G>A maps to NM_004420.2 H245H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr23:152914703 C>A did not map to a codon.
Sequencing variant TCGA-2G-AAGJ-01A-11D-A42Y-10 chr1:1273784 G>A maps to ENST00000378888 H457H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM2-01A-11D-A435-10 chr14:102496590 G>T maps to NM_001376.4 V3285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALG-01A-11D-A42Y-10 chr3:32582555 G>T maps to NM_016141.3 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1G-01A-11D-A435-10 chr3:32578557 G>C maps to NM_016141.3 Y259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALY-01A-11D-A42Y-10 chr11:103093788 G>A maps to NM_001080463.1 L3109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JX-01A-11D-A435-10 chr2:44021860 A>C maps to NM_015522.3 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0B-01A-11D-A435-10 chr2:44028792 G>T maps to NM_001193464.1 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOL-01A-11D-A435-10 chr21:38884386 T>C maps to NM_001396.3 H615H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGK-01A-11D-A42Y-10 chr2:71795193 G>T maps to NM_001130987.1 L893L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGE-01A-21D-A42Y-10 chr6:20402609 C>T maps to NM_001949.3 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALW-01A-11D-A42Y-10 chr16:2284681 G>A maps to NM_004424.3 R564R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH3-01A-11D-A42Y-10 chr16:23540941 G>A maps to NM_001083614.1 C411C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG3-01A-11D-A42Y-10 chr8:110569201 C>A maps to ENST00000276658 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALP-01A-12D-A42Y-10 chr5:158524092 G>T maps to NM_024007.3 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOD-01A-11D-A435-10 chr5:158135161 G>T maps to NM_024007.3 T523T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGJ-01A-11D-A42Y-10 chr23:48385672 G>T did not map to a codon.
Sequencing variant TCGA-2G-AALW-01A-11D-A42Y-10 chr10:74899093 G>T maps to NM_001135752.1 S498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF1-01A-11D-A42Y-10 chr10:135180454 G>T maps to NM_004092.3 S186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AD-01A-11D-A435-10 chr23:69176946 G>A did not map to a codon.
Sequencing variant TCGA-VF-A8AD-01A-11D-A435-10 chr23:65819572 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAGA-01A-11D-A42Y-10 chr2:109527397 G>A maps to ENST00000376651 D220D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA06-01A-12D-A435-10 chr13:78492306 G>A maps to ENST00000377211 N224N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2X-A9D5-01A-11D-A435-10 chr20:62119704 G>T maps to NM_001958.2 G446G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH3-01A-11D-A42Y-10 chr16:22291563 G>T maps to NM_013302.3 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X3-A8G4-01A-11D-A435-10 chr16:22274453 C>T maps to NM_013302.3 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A8S2-01A-11D-A435-10 chr16:22268121 C>T maps to NM_013302.3 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANV-01A-11D-A435-10 chr1:245245456 G>T maps to ENST00000421886 E222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFZ-01A-11D-A42Y-10 chr3:19975291 T>A maps to NM_144715.3 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALX-01A-11D-A42Y-10 chr1:15736568 G>A maps to NM_024329.5 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHP-01A-12D-A42Y-10 chr13:107145462 G>T maps to NM_004093.2 G309G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A89B-01A-11D-A435-10 chr17:7612494 C>T maps to NM_001406.3 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALS-01A-12D-A42Y-10 chr14:23828819 T>G maps to NM_005864.2 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGG-01A-11D-A42Y-10 chr5:38448403 G>T maps to ENST00000354891 T830T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr7:55223544 C>T maps to NM_005228.3 H304H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG7-01A-11D-A42Y-10 chr19:41306599 C>A maps to NM_053046.2 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90S-01A-11D-A435-10 chr9:140707982 G>T did not map to a codon.
Sequencing variant TCGA-YU-A912-01A-11D-A435-10 chr9:140729281 C>T maps to NM_024757.4 C1258C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGA-01A-11D-A42Y-10 chr23:20148689 C>A did not map to a codon.
Sequencing variant TCGA-ZM-AA0N-01A-21D-A435-10 chr23:24078273 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAGZ-01A-11D-A42Y-10 chr7:2404051 C>T maps to ENST00000314800 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGP-01A-11D-A42Y-10 chr15:44829570 C>T maps to NM_003758.2 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94I-01A-11D-A435-10 chr12:53410338 C>G maps to ENST00000438209 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANV-01A-11D-A435-10 chr4:99812428 C>T maps to NM_001130679.1 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JX-01A-11D-A435-10 chr1:21205926 A>G maps to NM_001198801.1 T817T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALR-01A-21D-A42Y-10 chr10:81272626 G>A maps to NM_001099692.1 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A8S2-01A-11D-A435-10 chr17:12921084 C>T maps to NM_018127.6 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFO-01A-31D-A42Y-10 chr23:129215227 A>G did not map to a codon.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr11:34527230 C>T maps to NM_198381.1 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKD-01A-31D-A42Y-10 chr20:45014803 G>A maps to ENST00000439931 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALQ-01A-12D-A42Y-10 chr20:45000325 G>A maps to ENST00000439931 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AD-01A-11D-A435-10 chr20:45014803 G>A maps to ENST00000439931 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W4-A7U4-01A-12D-A435-10 chr20:45017781 C>T maps to ENST00000439931 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1G-01A-11D-A435-10 chr16:67235502 G>A maps to NM_024712.3 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFH-01A-12D-A42Y-10 chr18:33726313 G>A maps to ENST00000442325 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANV-01A-11D-A435-10 chr16:1825968 C>A maps to NM_001010865.1 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANI-01A-11D-A435-10 chr2:27305626 C>T maps to NM_007046.3 H396H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALQ-01A-12D-A42Y-10 chr10:119307661 A>G maps to NM_004098.3 K226K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALR-01A-21D-A42Y-10 chr9:130578303 G>A maps to NM_001114753.1 P590P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALS-01A-12D-A42Y-10 chr9:139943413 G>T maps to NM_203468.1 G421G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SB-A76C-01A-11D-A435-10 chr22:41531830 G>T maps to NM_001429.3 G515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AB-01A-31D-A435-10 chr12:132547104 G>A maps to ENST00000333577 Q2767Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X3-A8G4-01A-11D-A435-10 chr12:132446459 G>A maps to ENST00000333577 E432E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOD-01A-11D-A435-10 chr12:132547146 G>A maps to ENST00000333577 Q2781Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84W-01A-11D-A435-10 chr1:29359660 C>T maps to NM_001166005.1 Y423Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90W-01A-11D-A435-10 chr1:29314194 A>G maps to NM_001166005.1 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGF-01A-31D-A42Y-10 chr15:43500506 G>A maps to NM_000119.2 C362C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AC-01A-11D-A435-10 chr10:32575640 G>T maps to NM_025209.2 R458R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr7:143094682 C>T maps to NM_005232.4 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH4-01A-12D-A42Y-10 chr1:38227155 G>T maps to NM_001099439.1 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94I-01A-11D-A435-10 chr1:38227302 G>T maps to NM_001099439.1 Y208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHP-01A-12D-A42Y-10 chr4:66270180 G>A maps to NM_004439.5 S567S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr4:66217147 G>T maps to NM_004439.5 R823R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SB-A76C-01A-11D-A435-10 chr1:23111036 G>T maps to ENST00000400191 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A89B-01A-11D-A435-10 chr1:23111393 G>T maps to ENST00000400191 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGI-01A-11D-A42Y-10 chr7:142562073 C>T maps to NM_004445.3 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALW-01A-11D-A42Y-10 chr7:142562073 C>T maps to NM_004445.3 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr7:142565384 G>T maps to NM_004445.3 P590P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANI-01A-11D-A435-10 chr7:142566830 G>T maps to NM_004445.3 L796L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA06-01A-12D-A435-10 chr7:142562073 C>T maps to NM_004445.3 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AAAL-01A-11D-A435-10 chr7:100320333 G>A maps to NM_000799.2 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H1-01A-11D-A435-10 chr19:11492418 G>T maps to NM_000121.3 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH8-01A-11D-A42Y-10 chr8:144946191 C>T maps to NM_031308.1 R410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SB-A6J6-01A-11D-A435-10 chr8:144940689 G>A maps to NM_031308.1 S2244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V5-01A-11D-A435-10 chr8:144940449 G>C maps to NM_031308.1 A2324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA05-01A-12D-A435-10 chr8:144940500 G>A maps to NM_031308.1 V2307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0F-01A-21D-A435-10 chr8:144940632 C>T maps to NM_031308.1 L2263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALT-01A-11D-A42Y-10 chr1:220195788 G>A maps to NM_004446.2 R339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFO-01A-31D-A42Y-10 chr12:15803896 G>A maps to NM_004447.5 R432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKO-01A-11D-A42Y-10 chr17:27182147 T>C maps to NM_005702.2 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGA-01A-11D-A42Y-10 chr17:37879598 G>T maps to NM_004448.2 V658V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGY-01A-11D-A42Y-10 chr17:37868701 G>T did not map to a codon.
Sequencing variant TCGA-XE-A8H1-01A-11D-A435-10 chr10:50708742 C>A did not map to a codon.
Sequencing variant TCGA-2G-AAFV-01A-11D-A42Y-10 chr23:71425588 G>T did not map to a codon.
Sequencing variant TCGA-2G-AALN-01A-11D-A42Y-10 chr21:39947609 G>T maps to NM_001136154.1 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM4-01A-11D-A435-10 chr20:34136277 G>T maps to ENST00000447986 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90W-01A-11D-A435-10 chr8:642585 G>A maps to NM_207332.1 R66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90W-01A-11D-A435-10 chr17:62144206 G>T maps to NM_001433.3 Y222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr12:53685532 G>T maps to NM_012291.4 G1860G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGK-01A-11D-A42Y-10 chr2:239040288 C>T maps to NM_194312.2 N978N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90S-01A-11D-A435-10 chr11:64082665 A>G maps to NM_004451.3 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGI-01A-11D-A42Y-10 chr12:56532267 G>A maps to NM_001184796.1 R816R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOC-01A-11D-A435-10 chr7:158552221 G>T maps to NM_020728.2 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGV-01A-11D-A42Y-10 chr1:157095427 A>G maps to NM_001145312.1 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFN-01A-31D-A42Y-10 chr1:157062557 G>T maps to NM_001004341.2 G323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AE-01A-11D-A435-10 chr12:11905469 G>T maps to NM_001987.4 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AE-01A-11D-A435-10 chr19:7927944 G>T maps to NM_001159944.1 E679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H1-01A-11D-A435-10 chr10:94773972 G>T maps to NM_019053.4 V706V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHP-01A-12D-A42Y-10 chr10:99196204 G>T maps to NM_016046.3 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-AA61-01A-11D-A435-10 chr10:99205530 C>T maps to NM_016046.3 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A8S2-01A-11D-A435-10 chr11:108384983 G>T maps to NM_015065.2 S417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V3-01A-11D-A435-10 chr6:65016864 G>T maps to ENST00000370616 C2063*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0H-01A-11D-A435-10 chr6:159188481 T>G maps to NM_001111077.1 A469A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALZ-01A-11D-A42Y-10 chr5:176831070 G>A maps to NM_000505.3 Q347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A8D5-01A-11D-A435-10 chr13:113770082 G>T maps to NM_000131.3 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-AA4L-01A-11D-A435-10 chr13:113772844 G>T maps to NM_000131.3 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH3-01A-11D-A42Y-10 chr23:154157223 T>C did not map to a codon.
Sequencing variant TCGA-SO-A8JP-01A-11D-A435-10 chr23:154133088 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAGS-01A-11D-A42Y-10 chr11:61584182 G>T maps to NM_013402.4 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHA-01A-11D-A42Y-10 chr1:50907169 G>T maps to NM_007051.2 S632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AC-01A-11D-A435-10 chr5:175875461 G>A maps to NM_014613.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr2:96078219 G>T maps to NM_016044.2 E242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOL-01A-11D-A435-10 chr17:293281 G>T maps to NM_182705.2 Y36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKL-01A-11D-A42Y-10 chr23:55172629 G>A did not map to a codon.
Sequencing variant TCGA-2G-AAKL-01A-11D-A42Y-10 chr23:55172644 C>G did not map to a codon.
Sequencing variant TCGA-2G-AALS-01A-12D-A42Y-10 chr23:55172629 G>A did not map to a codon.
Sequencing variant TCGA-2X-A9D5-01A-11D-A435-10 chr23:55172629 G>A did not map to a codon.
Sequencing variant TCGA-2X-A9D5-01A-11D-A435-10 chr23:55172644 C>G did not map to a codon.
Sequencing variant TCGA-SB-A76C-01A-11D-A435-10 chr23:55172717 G>T did not map to a codon.
Sequencing variant TCGA-WZ-A7V4-01A-11D-A435-10 chr23:55172629 G>A did not map to a codon.
Sequencing variant TCGA-WZ-A7V4-01A-11D-A435-10 chr23:55172644 C>G did not map to a codon.
Sequencing variant TCGA-XE-AAO4-01A-11D-A435-10 chr23:55172644 C>G did not map to a codon.
Sequencing variant TCGA-YU-A90Q-01A-11D-A435-10 chr23:55172629 G>A did not map to a codon.
Sequencing variant TCGA-YU-A90Q-01A-11D-A435-10 chr23:55172644 C>G did not map to a codon.
Sequencing variant TCGA-2G-AAEW-01A-11D-A42Y-10 chr19:1881262 G>A maps to NM_031213.3 C101C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAEW-01A-11D-A42Y-10 chr19:1881346 A>G maps to NM_031213.3 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGN-01A-11D-A42Y-10 chr19:1881394 T>C maps to NM_031213.3 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH2-01A-11D-A42Y-10 chr19:1877408 G>T maps to NM_031213.3 S292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A912-01A-11D-A435-10 chr19:1881262 G>A maps to NM_031213.3 C101C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHN-01A-11D-A42Y-10 chr2:45629 G>A maps to NM_001077710.2 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG6-01A-11D-A42Y-10 chr23:54209317 A>G did not map to a codon.
Sequencing variant TCGA-WZ-A7V5-01A-11D-A435-10 chr4:187077205 A>T maps to ENST00000356371 K437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFL-01A-21D-A42Y-10 chr5:118965472 C>T maps to ENST00000420106 R4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2X-A9D5-01A-11D-A435-10 chr2:187559028 A>G maps to NM_177454.3 Q43Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHG-01A-11D-A42Y-10 chr14:94395419 G>T maps to NM_138344.3 G325G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFJ-01A-11D-A42Y-10 chr19:35716024 G>T maps to NM_152481.1 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOC-01A-11D-A435-10 chr22:49042515 C>T maps to ENST00000336769 Q74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALW-01A-11D-A42Y-10 chr9:99699463 A>G maps to NM_001170741.1 A367A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0B-01A-11D-A435-10 chr23:153736635 G>T did not map to a codon.
Sequencing variant TCGA-YU-A90W-01A-11D-A435-10 chr3:194407932 C>A maps to NM_153690.4 R126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM4-01A-11D-A435-10 chr6:82461789 T>G maps to ENST00000369756 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr1:27332835 G>T maps to NM_052943.3 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHC-01A-11D-A42Y-10 chr23:37028093 A>G did not map to a codon.
Sequencing variant TCGA-2G-AAM3-01A-11D-A435-10 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr23:37028068 T>C did not map to a codon.
Sequencing variant TCGA-ZM-AA05-01A-12D-A435-10 chr5:137681244 G>T maps to NM_001135647.1 E290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKG-01A-11D-A42Y-10 chr1:177249620 C>T maps to NM_021165.2 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA06-01A-12D-A435-10 chr11:95521720 G>T maps to NM_144664.4 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGP-01A-11D-A42Y-10 chr8:124219615 C>G maps to NM_032899.4 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH3-01A-11D-A42Y-10 chr8:144810754 G>T maps to NM_198488.3 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGW-01A-11D-A42Y-10 chr16:5141851 C>T maps to NM_201400.2 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84X-01A-11D-A435-10 chr8:12042850 C>G did not map to a codon.
Sequencing variant TCGA-2G-AAHA-01A-11D-A42Y-10 chr6:17602825 G>T maps to NM_016255.2 E240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AAAL-01A-11D-A435-10 chr6:17602825 G>T maps to NM_016255.2 E240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H4-01A-31D-A435-10 chr6:17602825 G>T maps to NM_016255.2 E240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr16:85139013 G>T maps to ENST00000393246 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAEW-01A-11D-A42Y-10 chr15:38776808 T>A maps to NM_173611.2 G417G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHT-01A-11D-A42Y-10 chr15:38776832 T>A maps to NM_173611.2 G425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOJ-01A-12D-A435-10 chr15:38776832 T>A maps to NM_173611.2 G425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A8S2-01A-11D-A435-10 chr15:38776808 T>A maps to NM_173611.2 G417G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0H-01A-11D-A435-10 chr15:38762578 G>A maps to NM_173611.2 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84W-01A-11D-A435-10 chr23:8763194 C>T did not map to a codon.
Sequencing variant TCGA-2G-AAGJ-01A-11D-A42Y-10 chr16:89851353 G>A maps to NM_000135.2 R460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALP-01A-12D-A42Y-10 chr23:14868778 A>G did not map to a codon.
Sequencing variant TCGA-2G-AAGK-01A-11D-A42Y-10 chr3:10089632 G>T maps to NM_033084.3 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALZ-01A-11D-A42Y-10 chr3:10091152 C>T maps to NM_033084.3 N503N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOJ-01A-12D-A435-10 chr3:10091152 C>T maps to NM_033084.3 N503N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94I-01A-11D-A435-10 chr3:10132047 C>T maps to NM_033084.3 G1252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2X-A9D5-01A-11D-A435-10 chr14:45606272 G>T maps to NM_020937.2 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFN-01A-31D-A42Y-10 chr10:127585220 C>T maps to NM_145235.3 Q4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKL-01A-11D-A42Y-10 chr10:127585220 C>T maps to NM_145235.3 Q4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A8D5-01A-11D-A435-10 chr10:127585220 C>T maps to NM_145235.3 Q4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H5-01A-11D-A435-10 chr10:127585220 C>T maps to NM_145235.3 Q4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH2-01A-11D-A42Y-10 chr6:5404836 G>T maps to NM_006567.3 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAL5-01A-11D-A42Y-10 chr7:150774451 C>A maps to NM_006712.3 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SB-A6J6-01A-11D-A435-10 chr2:170403078 G>A maps to NM_024622.3 N450N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGM-01A-11D-A42Y-10 chr5:150917381 C>T maps to NM_001447.2 A3055A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH4-01A-12D-A42Y-10 chr11:92535074 G>T maps to ENST00000298047 G2966*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90W-01A-11D-A435-10 chr11:92257929 G>T maps to ENST00000298047 V1141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKG-01A-11D-A42Y-10 chr4:126237898 T>C maps to NM_024582.4 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AD-01A-11D-A435-10 chr4:126240962 G>T maps to NM_024582.4 G1133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALP-01A-12D-A42Y-10 chr23:150891212 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAM3-01A-11D-A435-10 chr22:45927185 C>T maps to ENST00000348697 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SO-A8JP-01A-11D-A435-10 chr22:45928976 G>T maps to ENST00000348697 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG6-01A-11D-A42Y-10 chr3:13612700 G>A maps to NM_001165035.1 E282E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH0-01A-11D-A42Y-10 chr3:13612700 G>A maps to NM_001165035.1 E282E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0N-01A-21D-A435-10 chr15:48703417 G>T maps to NM_000138.4 I2795I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFG-01A-11D-A42Y-10 chr5:127623057 G>T maps to NM_001999.3 S2274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHA-01A-11D-A42Y-10 chr5:127800525 G>A maps to NM_001999.3 C239C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SO-A8JP-01A-11D-A435-10 chr5:127648440 A>G maps to NM_001999.3 D1588D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGJ-01A-11D-A42Y-10 chr19:8212312 G>A maps to NM_032447.3 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGX-01A-11D-A42Y-10 chr19:8183823 A>G maps to NM_032447.3 C1098C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALO-01A-12D-A42Y-10 chr10:104181701 C>T maps to NM_024326.3 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1G-01A-11D-A435-10 chr8:28304722 G>A maps to NM_172366.2 Q270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG7-01A-11D-A42Y-10 chr10:5951127 A>G maps to NM_032807.3 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H5-01A-11D-A435-10 chr1:11710790 C>G maps to NM_012168.4 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF8-01A-11D-A42Y-10 chr3:121340830 G>T maps to NM_016298.3 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGX-01A-11D-A42Y-10 chr2:73496314 G>T maps to ENST00000295133 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH4-01A-12D-A42Y-10 chr17:18673362 T>C maps to ENST00000395665 G657G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr17:18681823 T>A maps to ENST00000395665 L791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V3-01A-11D-A435-10 chr5:171303294 G>T maps to NM_012300.2 T384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH4-01A-12D-A42Y-10 chr10:103371158 C>T maps to ENST00000331272 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0D-01A-11D-A435-10 chr9:139835403 G>T maps to NM_018998.2 S559S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM4-01A-11D-A435-10 chr19:40421235 G>A maps to NM_003890.2 G895G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALR-01A-21D-A42Y-10 chr19:17888999 G>A maps to NM_015122.2 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHP-01A-12D-A42Y-10 chr11:61563051 C>T maps to NM_004111.4 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF6-01A-11D-A42Y-10 chr2:97361796 G>T maps to NM_001113382.1 E1383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOL-01A-11D-A435-10 chr15:91435301 G>T maps to NM_002005.3 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H4-01A-31D-A435-10 chr3:62355877 G>A maps to NM_018008.3 A420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AD-01A-11D-A435-10 chr19:35842504 G>T maps to NM_005303.2 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALZ-01A-11D-A42Y-10 chr19:35940861 C>T maps to NM_005306.2 C82C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF4-01A-11D-A42Y-10 chr23:54496514 C>G did not map to a codon.
Sequencing variant TCGA-2G-AAGM-01A-11D-A42Y-10 chr23:54497048 G>A did not map to a codon.
Sequencing variant TCGA-ZM-AA06-01A-12D-A435-10 chr23:54476098 T>A did not map to a codon.
Sequencing variant TCGA-2G-AALT-01A-11D-A42Y-10 chr9:95797715 C>T maps to NM_033086.2 Q675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGF-01A-31D-A42Y-10 chr12:32734924 G>T maps to NM_139241.2 E42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0F-01A-21D-A435-10 chr3:14940333 G>T did not map to a codon.
Sequencing variant TCGA-WZ-A7V5-01A-11D-A435-10 chr5:44305288 T>C maps to NM_004465.1 E145E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JX-01A-11D-A435-10 chr17:7343089 C>T maps to NM_004112.2 R51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFI-01A-21D-A42Y-10 chr3:192125817 T>C maps to NM_021032.4 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AAAL-01A-11D-A435-10 chr12:4554547 G>T maps to NM_020996.1 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0E-01A-12D-A435-10 chr10:123256222 G>T maps to ENST00000351936 V582V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOD-01A-11D-A435-10 chr4:1016153 G>A maps to NM_021923.3 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA06-01A-12D-A435-10 chr9:133805021 G>T maps to NM_001145106.1 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JY-01A-11D-A435-10 chr4:54257227 A>G maps to NM_030917.3 K186K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALQ-01A-12D-A42Y-10 chr19:56109216 G>T maps to NM_032836.2 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90W-01A-11D-A435-10 chr12:2908332 G>C maps to NM_002014.3 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V4-01A-11D-A435-10 chr19:18650504 C>A maps to NM_012181.3 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84X-01A-11D-A435-10 chr1:152276831 G>C maps to NM_002016.1 S3510S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHT-01A-11D-A42Y-10 chr1:152327657 T>A maps to NM_001014342.2 T868T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO6-01A-31D-A435-10 chr1:152328050 T>C maps to NM_001014342.2 S737S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALY-01A-11D-A42Y-10 chr17:18154277 G>A maps to NM_002018.2 G550G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X3-A8G4-01A-11D-A435-10 chr17:18150240 G>A maps to NM_002018.2 Y934Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFL-01A-21D-A42Y-10 chr23:153595837 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAGW-01A-11D-A42Y-10 chr23:153589788 G>A did not map to a codon.
Sequencing variant TCGA-2G-AAL5-01A-11D-A42Y-10 chr23:153583389 C>G did not map to a codon.
Sequencing variant TCGA-2G-AAFG-01A-11D-A42Y-10 chr7:128490067 A>G maps to NM_001458.4 E1746E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKD-01A-31D-A42Y-10 chr7:128478445 G>T maps to NM_001458.4 V391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG6-01A-11D-A42Y-10 chr11:63884329 G>A maps to NM_013280.4 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr11:63884329 G>T maps to NM_013280.4 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG9-01A-11D-A42Y-10 chr13:28644723 C>A maps to NM_004119.2 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr13:28578253 G>A maps to NM_004119.2 R973*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM2-01A-11D-A435-10 chr5:180052903 G>T maps to NM_182925.4 P462P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM3-01A-11D-A435-10 chr5:180038335 G>T maps to NM_182925.4 A1227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W4-A7U2-01A-11D-A435-10 chr5:180048755 G>A maps to NM_182925.4 H602H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANJ-01A-11D-A435-10 chr14:76045332 C>A maps to NM_017791.2 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAEX-01A-11D-A42Y-10 chr1:240371510 C>G maps to ENST00000406993 P1276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGX-01A-11D-A42Y-10 chr1:240371516 T>A maps to ENST00000406993 L1278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALW-01A-11D-A42Y-10 chr1:240371579 A>T maps to ENST00000406993 P1299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1H-01A-11D-A435-10 chr1:240371501 C>T maps to ENST00000406993 P1273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO6-01A-31D-A435-10 chr1:240371516 T>A maps to ENST00000406993 L1278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A8S3-01B-11D-A435-10 chr1:240371138 C>T maps to ENST00000406993 P1152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A912-01A-11D-A435-10 chr1:240371243 G>A maps to ENST00000406993 P1187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X3-A8G4-01A-11D-A435-10 chr17:43323270 G>A maps to NM_005892.3 W1007*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AD-01A-11D-A435-10 chr17:80680734 G>T maps to NM_024619.3 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V3-01A-11D-A435-10 chr9:132678244 C>T maps to NM_015033.2 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr11:47744590 A>T maps to NM_015308.2 P914P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH2-01A-11D-A42Y-10 chr3:172065070 G>T maps to NM_022763.3 E812*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGA-01A-11D-A42Y-10 chr8:42940419 C>T maps to NM_002027.2 Q379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG3-01A-11D-A42Y-10 chr11:49204789 A>G maps to NM_004476.1 Y277Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHP-01A-12D-A42Y-10 chr11:49204789 A>G maps to NM_004476.1 Y277Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKO-01A-11D-A42Y-10 chr11:49204789 A>G maps to NM_004476.1 Y277Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALF-01A-11D-A42Y-10 chr11:49204789 A>G maps to NM_004476.1 Y277Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALS-01A-12D-A42Y-10 chr11:49204789 A>G maps to NM_004476.1 Y277Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AB-01A-31D-A435-10 chr11:49204789 A>G maps to NM_004476.1 Y277Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO6-01A-31D-A435-10 chr11:49204789 A>G maps to NM_004476.1 Y277Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0E-01A-12D-A435-10 chr11:49204789 A>G maps to NM_004476.1 Y277Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANI-01A-11D-A435-10 chr14:75747997 G>T maps to NM_005252.3 T338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG9-01A-11D-A42Y-10 chr19:45971879 C>A maps to NM_006732.2 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A8S3-01B-11D-A435-10 chr19:46375769 G>T maps to NM_004497.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGK-01A-11D-A42Y-10 chr9:117486 C>T maps to NM_207305.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGJ-01A-11D-A42Y-10 chr1:47882403 G>T maps to NM_012186.2 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANV-01A-11D-A435-10 chr7:4799056 G>T maps to ENST00000450194 A487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALN-01A-11D-A42Y-10 chr12:2968304 A>G maps to NM_202002.1 P635P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM4-01A-11D-A435-10 chr12:2973634 G>T maps to NM_202002.1 R373R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOL-01A-11D-A435-10 chr7:114304485 G>T maps to NM_148898.3 P691P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA05-01A-12D-A435-10 chr23:49113924 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr6:41555160 G>C maps to NM_001012426.1 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAEX-01A-11D-A42Y-10 chr6:1313400 C>G maps to NM_033260.3 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGS-01A-11D-A42Y-10 chr9:130572099 G>T maps to NM_004957.4 E400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFY-01A-11D-A42Y-10 chr4:79460491 G>T maps to NM_025074.6 V3781V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84Y-01A-11D-A435-10 chr4:79284685 G>A maps to NM_025074.6 Q814Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2X-A9D5-01A-11D-A435-10 chr10:13838518 G>T maps to NM_018027.3 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFH-01A-12D-A42Y-10 chr23:12734430 G>T did not map to a codon.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr23:12736056 G>A did not map to a codon.
Sequencing variant TCGA-X3-A8G4-01A-11D-A435-10 chr13:32735279 G>T did not map to a codon.
Sequencing variant TCGA-YU-A94I-01A-11D-A435-10 chr13:32776177 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAGM-01A-11D-A42Y-10 chr4:48537739 G>T maps to NM_015030.1 V2166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALP-01A-12D-A42Y-10 chr19:4307980 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAL5-01A-11D-A42Y-10 chr5:121187744 G>T maps to NM_177478.1 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGP-01A-11D-A42Y-10 chr16:71317852 A>C maps to NM_018348.5 G657G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALS-01A-12D-A42Y-10 chr1:78430878 T>C maps to ENST00000436586 K191K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H5-01A-11D-A435-10 chr9:133510063 C>T maps to NM_003934.1 S507S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG5-01A-11D-A42Y-10 chr1:24194761 C>G maps to NM_000147.4 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr6:143825111 G>A maps to NM_032020.4 D230D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0B-01A-11D-A435-10 chr14:66028472 C>T maps to NM_178155.1 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOF-01A-11D-A435-10 chr2:208632212 G>T maps to NM_003468.3 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG9-01A-11D-A42Y-10 chr7:72849812 A>G maps to NM_003508.2 G492G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG5-01A-11D-A42Y-10 chr23:153764199 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAGS-01A-11D-A42Y-10 chr23:153762707 G>T did not map to a codon.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr23:153760881 G>T did not map to a codon.
Sequencing variant TCGA-SN-A84Y-01A-11D-A435-10 chr4:144378922 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAGN-01A-11D-A42Y-10 chr11:77938072 G>T maps to NM_080491.2 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALZ-01A-11D-A42Y-10 chr23:153928304 G>A did not map to a codon.
Sequencing variant TCGA-2G-AAGY-01A-11D-A42Y-10 chr22:17488890 G>T maps to NM_001037814.1 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH2-01A-11D-A42Y-10 chr4:47163289 C>T maps to NM_000812.3 Q89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGM-01A-11D-A42Y-10 chr23:151138733 C>T did not map to a codon.
Sequencing variant TCGA-2G-AAHT-01A-11D-A42Y-10 chr23:151123180 T>A did not map to a codon.
Sequencing variant TCGA-S6-A8JY-01A-11D-A435-10 chr23:151123959 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAFI-01A-21D-A42Y-10 chr4:877843 G>T maps to NM_005255.2 Y412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGK-01A-11D-A42Y-10 chr11:68455485 C>T maps to NM_015973.3 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKD-01A-31D-A42Y-10 chr2:242742845 C>G maps to NM_022134.2 Y154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGC-01A-21D-A42Y-10 chr9:101589070 A>G maps to NM_024642.3 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84Y-01A-11D-A435-10 chr4:174169130 G>T maps to NM_017423.2 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AB-01A-31D-A435-10 chr18:74962794 G>T maps to NM_001480.3 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGE-01A-21D-A42Y-10 chr9:34649410 T>C maps to NM_000155.2 A303A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1G-01A-11D-A435-10 chr19:36033898 G>T maps to NM_014364.4 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0H-01A-11D-A435-10 chr21:34889724 C>T maps to NM_001136006.1 V631V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SB-A6J6-01A-11D-A435-10 chr9:89560989 G>T maps to NM_002048.2 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84X-01A-11D-A435-10 chr9:89561082 G>T maps to NM_002048.2 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA05-01A-12D-A435-10 chr16:90097757 G>T maps to NM_001481.2 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGG-01A-11D-A42Y-10 chr23:48652264 A>G did not map to a codon.
Sequencing variant TCGA-YU-A90S-01A-11D-A435-10 chr23:48651621 C>T did not map to a codon.
Sequencing variant TCGA-2G-AAHP-01A-12D-A42Y-10 chr19:19606950 G>T maps to ENST00000404158 G302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94I-01A-11D-A435-10 chr1:153784506 C>T maps to NM_020699.2 T507T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SO-A8JP-01A-11D-A435-10 chr22:30685381 G>T maps to NM_001037666.2 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr6:10586755 C>G maps to NM_145655.3 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGV-01A-11D-A42Y-10 chr5:74324716 A>G maps to NM_016591.2 C382C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKO-01A-11D-A42Y-10 chr8:75262791 G>T maps to NM_018972.2 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHN-01A-11D-A42Y-10 chr2:20870839 C>G maps to NM_182828.2 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr2:20870821 G>T maps to NM_182828.2 A330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOF-01A-11D-A435-10 chr23:69647058 G>T did not map to a codon.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr23:14027164 G>T did not map to a codon.
Sequencing variant TCGA-SB-A6J6-01A-11D-A435-10 chr17:42989135 G>T maps to NM_002055.3 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGG-01A-11D-A42Y-10 chr1:92948550 G>T maps to NM_005263.3 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84W-01A-11D-A435-10 chr1:92946382 T>C maps to NM_005263.3 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SB-A6J6-01A-11D-A435-10 chr16:67709570 C>T maps to NM_030819.3 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-AA4L-01A-11D-A435-10 chr16:67709828 G>T maps to NM_030819.3 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANJ-01A-11D-A435-10 chr22:38027038 G>T maps to ENST00000381756 P504P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG9-01A-11D-A42Y-10 chr16:23481478 C>T maps to NM_015044.4 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFG-01A-11D-A42Y-10 chr17:73236093 G>T maps to NM_138619.2 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr17:40342274 G>T maps to NM_032484.4 G434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AE-01A-11D-A435-10 chr7:100279559 G>T maps to NM_022574.4 T994T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JY-01A-11D-A435-10 chr23:100653455 G>C did not map to a codon.
Sequencing variant TCGA-XE-AAOD-01A-11D-A435-10 chr11:134226236 G>T maps to NM_138342.3 E201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF8-01A-11D-A42Y-10 chr16:74516991 G>T maps to NM_012201.5 Y534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF8-01A-11D-A42Y-10 chr7:42063135 G>T maps to NM_000168.5 V476V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90P-01A-11D-A435-10 chr8:144351631 A>T maps to NM_138465.3 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHL-01A-11D-A42Y-10 chr9:3829448 G>T maps to NM_001042413.1 P839P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1G-01A-11D-A435-10 chr2:191746157 C>T maps to NM_014905.3 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANI-01A-11D-A435-10 chr1:1262374 C>T maps to NM_001029885.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H1-01A-11D-A435-10 chr19:48204804 C>T maps to NM_015711.3 S1272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOD-01A-11D-A435-10 chr23:120182070 C>A did not map to a codon.
Sequencing variant TCGA-2G-AAGV-01A-11D-A42Y-10 chr20:62221507 G>C maps to NM_012384.3 P509P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A6IS-01A-11D-A435-10 chr20:62221816 C>T maps to NM_012384.3 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0H-01A-11D-A435-10 chr19:39819173 G>T maps to NM_004877.2 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGK-01A-11D-A42Y-10 chr6:16290844 G>T maps to NM_006877.3 E284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM3-01A-11D-A435-10 chr17:63052636 G>T maps to NM_006572.4 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGW-01A-11D-A42Y-10 chr18:11824996 G>T maps to NM_182978.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAL5-01A-11D-A42Y-10 chr9:80430536 G>T maps to NM_002072.3 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOF-01A-11D-A435-10 chr9:80646046 G>A maps to NM_002072.3 D35D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGP-01A-11D-A42Y-10 chr5:180668626 C>A maps to NM_006098.4 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF8-01A-11D-A42Y-10 chr23:54578730 G>T did not map to a codon.
Sequencing variant TCGA-S6-A8JY-01A-11D-A435-10 chr23:54584945 C>T did not map to a codon.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr23:54584982 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAFJ-01A-11D-A42Y-10 chr1:231403536 A>T maps to NM_014236.3 I389I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A8S2-01A-11D-A435-10 chr1:231401775 G>T maps to NM_014236.3 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AB-01A-31D-A435-10 chr1:155726781 C>T maps to ENST00000368331 R1828R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG7-01A-11D-A42Y-10 chr10:113924338 C>T maps to NM_020918.4 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SB-A6J6-01A-11D-A435-10 chr1:156568271 G>T maps to NM_015590.3 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKG-01A-11D-A42Y-10 chr17:42513866 G>T maps to NM_001002909.2 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG9-01A-11D-A42Y-10 chr23:133119395 C>G did not map to a codon.
Sequencing variant TCGA-2G-AALQ-01A-12D-A42Y-10 chr23:133119395 C>G did not map to a codon.
Sequencing variant TCGA-2G-AALW-01A-11D-A42Y-10 chr23:133119395 C>G did not map to a codon.
Sequencing variant TCGA-XY-A8S2-01A-11D-A435-10 chr23:133119395 C>G did not map to a codon.
Sequencing variant TCGA-2G-AAF6-01A-11D-A42Y-10 chr13:92345960 G>A maps to NM_004466.4 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGJ-01A-11D-A42Y-10 chr12:50501423 G>A maps to NM_005276.2 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALR-01A-21D-A42Y-10 chr2:157435486 T>C maps to NM_000408.4 I618I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AD-01A-11D-A435-10 chr7:1132182 G>T maps to NM_001505.2 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A8D5-01A-11D-A435-10 chr14:63779820 G>A maps to ENST00000314140 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94I-01A-11D-A435-10 chr4:176923707 C>T did not map to a codon.
Sequencing variant TCGA-XE-AANR-01A-11D-A435-10 chr23:13825788 G>T did not map to a codon.
Sequencing variant TCGA-WZ-A8D5-01A-11D-A435-10 chr1:27216506 C>T maps to NM_018066.3 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr23:135405333 G>T did not map to a codon.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr6:47678469 G>T did not map to a codon.
Sequencing variant TCGA-SN-A84W-01A-11D-A435-10 chr10:134912176 G>T maps to ENST00000368577 T596T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94I-01A-11D-A435-10 chr8:37687461 G>T maps to NM_032777.9 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANR-01A-11D-A435-10 chr14:59930939 G>T maps to NM_022571.5 I335I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFY-01A-11D-A42Y-10 chr7:37780114 C>T maps to NM_181791.1 F40F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH4-01A-12D-A42Y-10 chr12:6933729 T>G maps to NM_019858.1 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94I-01A-11D-A435-10 chr12:6933729 T>G maps to NM_019858.1 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA06-01A-12D-A435-10 chr12:6933750 G>T maps to NM_019858.1 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANR-01A-11D-A435-10 chr7:107115389 G>A maps to NM_005295.2 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SO-A8JP-01A-11D-A435-10 chr10:125426013 C>T maps to NM_153442.3 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90W-01A-11D-A435-10 chr2:133174782 G>A maps to NM_001508.2 Q56Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr2:105858881 C>T maps to NM_007227.3 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr6:110301310 C>T maps to ENST00000414000 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90Q-01A-11D-A435-10 chr6:110300884 C>A maps to ENST00000414000 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA06-01A-12D-A435-10 chr6:110300641 G>T maps to ENST00000414000 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGA-01A-11D-A42Y-10 chr23:19026143 G>T did not map to a codon.
Sequencing variant TCGA-XE-A8H5-01A-11D-A435-10 chr23:101909825 A>T did not map to a codon.
Sequencing variant TCGA-XE-A8H5-01A-11D-A435-10 chr23:101909833 C>A did not map to a codon.
Sequencing variant TCGA-XE-AAOD-01A-11D-A435-10 chr23:101971348 G>T did not map to a codon.
Sequencing variant TCGA-YU-A90W-01A-11D-A435-10 chr17:7217004 T>A maps to NM_004489.4 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH3-01A-11D-A42Y-10 chr1:109461326 G>A maps to NM_013296.4 G452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF1-01A-11D-A42Y-10 chr19:35504212 G>A maps to NM_020895.3 E220E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90Y-01A-11D-A435-10 chr22:47022779 G>T maps to NM_015124.2 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGG-01A-11D-A42Y-10 chr17:37901195 C>T maps to ENST00000445327 Q347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AC-01A-11D-A435-10 chr17:37903137 G>T maps to ENST00000445327 R552R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFN-01A-31D-A42Y-10 chr9:37428555 G>T maps to ENST00000377824 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHC-01A-11D-A42Y-10 chr23:122599614 C>T did not map to a codon.
Sequencing variant TCGA-VF-A8AD-01A-11D-A435-10 chr16:9862935 C>T maps to NM_000833.3 E789E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGS-01A-11D-A42Y-10 chr12:13717471 G>T maps to NM_000834.3 R900R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALO-01A-12D-A42Y-10 chr12:13761689 A>G maps to NM_000834.3 P619P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF1-01A-11D-A42Y-10 chr23:48839805 G>T did not map to a codon.
Sequencing variant TCGA-2X-A9D5-01A-11D-A435-10 chr10:121086094 C>T maps to NM_005308.2 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0N-01A-21D-A435-10 chr11:88338025 G>A maps to NM_001143831.2 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFO-01A-31D-A42Y-10 chr19:48956275 C>T maps to NM_031485.3 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM3-01A-11D-A435-10 chr8:144644685 G>T maps to NM_024736.6 E403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOC-01A-11D-A435-10 chr8:144644276 G>T maps to NM_024736.6 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V3-01A-11D-A435-10 chr17:3627690 C>T maps to NM_031965.2 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X3-A8G4-01A-11D-A435-10 chr9:124094757 G>C maps to NM_000177.4 T742T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO3-01A-11D-A435-10 chr9:124088833 G>T maps to NM_000177.4 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALQ-01A-12D-A42Y-10 chr16:11990538 C>A maps to NM_002094.3 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFN-01A-31D-A42Y-10 chr14:81670289 A>T maps to NM_015859.2 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKM-01A-11D-A42Y-10 chr11:18387385 G>A maps to NM_005316.3 W539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO4-01A-11D-A435-10 chr7:74105441 T>C maps to NM_032999.2 Y79Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JY-01A-11D-A435-10 chr6:43592664 G>T maps to NM_019096.3 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGK-01A-11D-A42Y-10 chr19:17449510 G>T maps to NM_133644.3 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A89B-01A-11D-A435-10 chr1:42619174 G>C maps to NM_007102.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHG-01A-11D-A42Y-10 chr17:7909964 G>T maps to NM_000180.3 P437P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOL-01A-11D-A435-10 chr1:228335313 A>G did not map to a codon.
Sequencing variant TCGA-W4-A7U4-01A-12D-A435-10 chr2:127413733 C>G did not map to a codon.
Sequencing variant TCGA-2G-AAG8-01A-31D-A42Y-10 chr19:49472836 G>T maps to NM_002103.4 S641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1G-01A-11D-A435-10 chr19:49473876 G>T maps to NM_002103.4 R579R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-XE-AAO4-01A-11D-A435-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-XE-AAO4-01A-11D-A435-10 chr5:134678954 G>A maps to ENST00000432382 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGI-01A-11D-A42Y-10 chr2:43015710 G>T maps to NM_012205.2 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOJ-01A-12D-A435-10 chr1:156595121 C>T maps to NM_021817.2 G323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGN-01A-11D-A42Y-10 chr19:52216944 G>T maps to NM_001523.2 S491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO3-01A-11D-A435-10 chr19:36104634 G>T maps to NM_015302.1 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V5-01A-11D-A435-10 chr9:19070215 C>A did not map to a codon.
Sequencing variant TCGA-4K-AA1I-01A-11D-A435-10 chr23:152722098 G>T did not map to a codon.
Sequencing variant TCGA-VF-A8AB-01A-31D-A435-10 chr23:152734604 G>T did not map to a codon.
Sequencing variant TCGA-XE-AAO6-01A-31D-A435-10 chr23:152721205 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAF8-01A-11D-A42Y-10 chr5:156535961 C>G maps to NM_032782.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKO-01A-11D-A42Y-10 chr23:153223523 G>T did not map to a codon.
Sequencing variant TCGA-2G-AALN-01A-11D-A42Y-10 chr23:153217301 C>T did not map to a codon.
Sequencing variant TCGA-2G-AALY-01A-11D-A42Y-10 chr23:153215723 C>T did not map to a codon.
Sequencing variant TCGA-SN-A84X-01A-11D-A435-10 chr23:153217372 C>T did not map to a codon.
Sequencing variant TCGA-2G-AAF8-01A-11D-A42Y-10 chr5:45353276 G>T maps to NM_021072.2 Y434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H4-01A-31D-A435-10 chr19:590562 G>A maps to NM_001194.3 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGZ-01A-11D-A42Y-10 chr1:155258013 T>C maps to NM_020897.1 G695G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFG-01A-11D-A42Y-10 chr15:73660062 C>A maps to NM_005477.2 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr15:73617653 G>A maps to NM_005477.2 S574S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X3-A8G4-01A-11D-A435-10 chr3:13545732 C>T maps to NM_024827.3 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGK-01A-11D-A42Y-10 chr17:42160954 G>A maps to NM_001015053.1 C808C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHC-01A-11D-A42Y-10 chr23:71571680 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAGV-01A-11D-A42Y-10 chr2:37234396 G>T maps to NM_019024.1 R1525R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0H-01A-11D-A435-10 chr2:37235844 T>C maps to NM_019024.1 L1477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A6IS-01A-11D-A435-10 chr2:197092903 A>C maps to NM_020760.1 L1280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84X-01A-11D-A435-10 chr3:124716649 G>T maps to NM_020733.1 R1179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AAAL-01A-11D-A435-10 chr11:124805884 T>C maps to NM_152722.4 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG9-01A-11D-A42Y-10 chr23:65428067 G>T did not map to a codon.
Sequencing variant TCGA-YU-A94D-01A-11D-A435-10 chr23:65479953 T>A did not map to a codon.
Sequencing variant TCGA-XE-A8H5-01A-11D-A435-10 chr15:64039939 G>T maps to ENST00000261887 L779L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGN-01A-11D-A42Y-10 chr4:89338643 C>T maps to NM_017912.3 I542I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JW-01A-11D-A435-10 chr4:89304512 G>T maps to NM_017912.3 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF8-01A-11D-A42Y-10 chr3:193854207 G>A maps to NM_005524.2 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr17:43227330 C>T maps to NM_006460.2 D258D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFY-01A-11D-A42Y-10 chr22:21799537 C>A maps to NM_015094.2 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFM-01A-11D-A42Y-10 chr19:40886727 G>T maps to NM_144685.3 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHP-01A-12D-A42Y-10 chr16:30005337 T>C maps to NM_003609.3 G376G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFH-01A-12D-A42Y-10 chr6:26045697 G>A maps to NM_003531.2 Q20Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H5-01A-11D-A435-10 chr6:26045833 C>T maps to NM_003531.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOC-01A-11D-A435-10 chr6:26271525 G>A maps to NM_003534.2 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOB-01A-11D-A435-10 chr6:143092506 C>T maps to NM_006734.3 P1123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAEX-01A-11D-A42Y-10 chr1:42048122 G>T maps to NM_024503.3 S782S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHP-01A-12D-A42Y-10 chr1:42046700 G>A maps to NM_024503.3 S1256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr2:234750713 C>A maps to NM_018410.3 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALZ-01A-11D-A42Y-10 chr6:32917165 G>A maps to NM_006120.3 N221N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGV-01A-11D-A42Y-10 chr6:29797393 G>A maps to ENST00000376828 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAL7-01A-11D-A42Y-10 chr11:118958996 C>T maps to NM_000190.3 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFY-01A-11D-A42Y-10 chr19:3573770 G>T maps to NM_006339.2 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGA-01A-11D-A42Y-10 chr23:150156377 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAH8-01A-11D-A42Y-10 chr23:150156377 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAL5-01A-11D-A42Y-10 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-4K-AAAL-01A-11D-A435-10 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-XY-A8S2-01A-11D-A435-10 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-2G-AALG-01A-11D-A42Y-10 chr1:24151934 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAFO-01A-31D-A42Y-10 chr23:80370323 C>A did not map to a codon.
Sequencing variant TCGA-WZ-A8D5-01A-11D-A435-10 chr22:35661553 G>A maps to NM_001003681.2 K391K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH3-01A-11D-A42Y-10 chr16:4559435 C>T maps to NM_001127205.1 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKO-01A-11D-A42Y-10 chr17:36104626 G>T maps to NM_000458.2 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGY-01A-11D-A42Y-10 chr12:54677641 C>T maps to NM_031157.2 Y318Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90P-01A-11D-A435-10 chr19:8539105 G>C maps to NM_005968.3 G366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGZ-01A-11D-A42Y-10 chr11:62490078 G>A maps to NM_001079559.1 C363C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGT-01A-11D-A42Y-10 chr1:150680867 G>A maps to NM_032132.4 N137N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGC-01A-21D-A42Y-10 chr7:27238793 G>T maps to NM_000522.4 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH8-01A-11D-A42Y-10 chr7:27170153 G>T maps to NM_002141.4 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFL-01A-21D-A42Y-10 chr17:46655234 G>A maps to NM_024015.4 H149H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JX-01A-11D-A435-10 chr12:54367504 C>T maps to NM_014212.3 C160C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A89B-01A-11D-A435-10 chr12:54333052 C>T maps to NM_017410.2 Y121Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A8S2-01A-11D-A435-10 chr12:54448768 C>A maps to NM_153633.2 S192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOC-01A-11D-A435-10 chr2:176982178 C>T maps to NM_002148.3 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0E-01A-12D-A435-10 chr10:100184074 G>T maps to NM_000195.2 S464S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGZ-01A-11D-A42Y-10 chr10:103826172 T>C maps to NM_024747.4 S314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H1-01A-11D-A435-10 chr10:103825726 C>A maps to NM_024747.4 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGV-01A-11D-A42Y-10 chr4:84234378 G>T maps to NM_006665.5 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH2-01A-11D-A42Y-10 chr19:49657885 C>T maps to NM_002152.2 E203E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH2-01A-11D-A42Y-10 chr19:49657915 T>C maps to NM_002152.2 E193E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALX-01A-11D-A42Y-10 chr19:49657879 G>A maps to NM_002152.2 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V5-01A-11D-A435-10 chr19:49658347 G>T maps to NM_002152.2 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHG-01A-11D-A42Y-10 chr23:132092424 T>C did not map to a codon.
Sequencing variant TCGA-SN-A6IS-01A-11D-A435-10 chr23:53459353 G>T did not map to a codon.
Sequencing variant TCGA-YU-A94I-01A-11D-A435-10 chr5:118809606 T>C maps to NM_000414.3 N39N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANJ-01A-11D-A435-10 chr12:57178676 G>T maps to NM_003725.2 E205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2X-A9D5-01A-11D-A435-10 chr6:122744743 T>C maps to NM_004506.3 Y363Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKL-01A-11D-A42Y-10 chr19:16268132 T>G maps to NM_032855.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94I-01A-11D-A435-10 chr1:22200900 G>T maps to NM_005529.5 G1218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA05-01A-12D-A435-10 chr1:22213940 G>T maps to NM_005529.5 C310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0H-01A-11D-A435-10 chr13:31727057 G>T maps to NM_006644.2 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFJ-01A-11D-A42Y-10 chr6:87725555 T>C maps to NM_000865.2 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGN-01A-11D-A42Y-10 chr6:87725675 G>T maps to NM_000865.2 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFZ-01A-11D-A42Y-10 chr11:113775693 C>A maps to NM_006028.3 I13I. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-YU-A94D-01A-11D-A435-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-2G-AALR-01A-21D-A42Y-10 chr1:20005665 G>T maps to NM_000871.1 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94I-01A-11D-A435-10 chr2:74757159 T>G maps to NM_013247.4 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFL-01A-21D-A42Y-10 chr23:53622245 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAG8-01A-31D-A42Y-10 chr23:53672396 C>T did not map to a codon.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr23:53572038 G>T did not map to a codon.
Sequencing variant TCGA-XE-AANI-01A-11D-A435-10 chr23:53579360 G>T did not map to a codon.
Sequencing variant TCGA-ZM-AA06-01A-12D-A435-10 chr23:53585983 C>T did not map to a codon.
Sequencing variant TCGA-2G-AAEX-01A-11D-A42Y-10 chr16:70954859 G>T maps to NM_032821.2 Y2472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGY-01A-11D-A42Y-10 chr16:70913325 C>G maps to NM_032821.2 V3476V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGJ-01A-11D-A42Y-10 chr6:82924302 G>T maps to NM_015525.2 C615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGO-01A-11D-A42Y-10 chr19:10444834 C>A did not map to a codon.
Sequencing variant TCGA-2G-AALF-01A-11D-A42Y-10 chr19:10450224 C>T maps to NM_002162.3 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGK-01A-11D-A42Y-10 chr19:10402485 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAGY-01A-11D-A42Y-10 chr10:94214293 A>G maps to NM_004969.3 P989P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFH-01A-12D-A42Y-10 chr9:131939452 G>T maps to NM_203434.2 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHA-01A-11D-A42Y-10 chr12:6650730 G>T maps to NM_001193457.1 G519G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr12:6649684 G>T maps to NM_001193457.1 S560S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG8-01A-31D-A42Y-10 chr2:163174667 G>T maps to NM_022168.2 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKM-01A-11D-A42Y-10 chr3:129239030 G>T maps to NM_052985.2 E1268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH8-01A-11D-A42Y-10 chr16:1561123 G>T maps to NM_014714.3 R1404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AE-01A-11D-A435-10 chr16:1574555 G>T maps to NM_014714.3 C1046*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG9-01A-11D-A42Y-10 chr2:27677282 A>G maps to NM_015662.1 G1156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr2:27688722 G>T maps to NM_015662.1 G573G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF1-01A-11D-A42Y-10 chr11:118416168 G>A maps to NM_020153.3 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFZ-01A-11D-A42Y-10 chr16:1841104 C>T maps to NM_001146006.1 E476E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH2-01A-11D-A42Y-10 chr16:1840813 A>C maps to NM_001146006.1 G573G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALQ-01A-12D-A42Y-10 chr16:1840924 G>T maps to NM_001146006.1 P536P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGW-01A-11D-A42Y-10 chr11:68704479 G>T maps to NM_002180.2 A844A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFI-01A-21D-A42Y-10 chr23:130412688 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAH3-01A-11D-A42Y-10 chr11:133805638 C>G maps to NM_014987.1 V280V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALP-01A-12D-A42Y-10 chr11:133807351 G>T maps to NM_014987.1 R200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X3-A8G4-01A-11D-A435-10 chr11:133789874 G>A maps to NM_014987.1 R1249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKL-01A-11D-A42Y-10 chr2:219925069 C>T maps to NM_002181.3 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SB-A6J6-01A-11D-A435-10 chr5:140032729 G>A did not map to a codon.
Sequencing variant TCGA-2G-AAM3-01A-11D-A435-10 chr1:206650043 G>A maps to NM_014002.3 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANJ-01A-11D-A435-10 chr22:17589770 G>A maps to NM_014339.5 S554S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOJ-01A-12D-A435-10 chr22:17584445 G>T maps to NM_014339.5 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr3:53889324 C>T maps to NM_018725.3 C162C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H4-01A-31D-A435-10 chr3:9974649 C>T maps to NM_153461.2 G583G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFL-01A-21D-A42Y-10 chr22:50439248 G>T maps to NM_001001694.2 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H5-01A-11D-A435-10 chr11:71711469 G>A maps to NM_001145057.1 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM4-01A-11D-A435-10 chr16:27456039 G>T maps to NM_181079.4 E251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHC-01A-11D-A42Y-10 chr16:28511193 C>T maps to NM_145659.3 E170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHC-01A-11D-A42Y-10 chr16:28511196 T>C maps to NM_145659.3 E169E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKO-01A-11D-A42Y-10 chr16:28511196 T>C maps to NM_145659.3 E169E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A89B-01A-11D-A435-10 chr16:28511196 T>C maps to NM_145659.3 E169E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1H-01A-11D-A435-10 chr16:70690988 G>T maps to NM_152456.2 E123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAEW-01A-11D-A42Y-10 chr23:1501337 C>G did not map to a codon.
Sequencing variant TCGA-2G-AAGJ-01A-11D-A42Y-10 chr19:50399125 G>A maps to NM_172374.1 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO3-01A-11D-A435-10 chr19:50397674 G>T maps to NM_172374.1 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOC-01A-11D-A435-10 chr16:27353569 C>T maps to NM_000418.2 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH3-01A-11D-A42Y-10 chr23:155234956 G>T did not map to a codon.
Sequencing variant TCGA-2G-AALP-01A-12D-A42Y-10 chr23:155239820 G>A did not map to a codon.
Sequencing variant TCGA-X3-A8G4-01A-11D-A435-10 chr23:155239803 C>G did not map to a codon.
Sequencing variant TCGA-XE-A8H1-01A-11D-A435-10 chr1:166890442 G>T maps to NM_199351.2 S462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG3-01A-11D-A42Y-10 chr19:10798136 G>A maps to NM_017620.2 P729P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA05-01A-12D-A435-10 chr19:10798067 T>G maps to NM_017620.2 G706G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AD-01A-11D-A435-10 chr11:61897742 C>T maps to NM_001040694.1 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHA-01A-11D-A42Y-10 chr2:74684837 G>A maps to ENST00000452361 P306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF8-01A-11D-A42Y-10 chr4:143129611 C>T maps to NM_003866.2 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF6-01A-11D-A42Y-10 chr10:134523942 G>T maps to NM_005539.3 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGC-01A-21D-A42Y-10 chr9:139327037 G>T maps to NM_019892.3 S427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALR-01A-21D-A42Y-10 chr22:31522466 C>T maps to ENST00000331075 I459I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SO-A8JP-01A-11D-A435-10 chr11:71942579 G>T maps to NM_001567.3 V512V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF6-01A-11D-A42Y-10 chr19:7143085 G>T maps to NM_000208.2 R761R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKM-01A-11D-A42Y-10 chr13:51961632 C>T maps to NM_012141.2 W261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGV-01A-11D-A42Y-10 chr13:98634776 A>G maps to NM_002271.4 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALY-01A-11D-A42Y-10 chr13:98667827 T>C maps to NM_002271.4 F808F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH3-01A-11D-A42Y-10 chr3:158983107 T>C maps to NM_001042705.2 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF1-01A-11D-A42Y-10 chr5:75969833 C>A maps to NM_006633.2 P1089P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr3:12977108 G>T maps to ENST00000429247 I469I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALS-01A-12D-A42Y-10 chr23:53279933 G>T did not map to a codon.
Sequencing variant TCGA-XE-A8H5-01A-11D-A435-10 chr23:53263991 T>G did not map to a codon.
Sequencing variant TCGA-2G-AAGF-01A-31D-A42Y-10 chr23:153278097 C>G did not map to a codon.
Sequencing variant TCGA-2G-AAHT-01A-11D-A42Y-10 chr19:46388366 C>T maps to NM_015649.1 W222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGE-01A-21D-A42Y-10 chr1:234745192 G>T maps to NM_182972.2 C16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2X-A9D6-01A-11D-A435-10 chr1:234745105 G>T maps to NM_182972.2 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AD-01A-11D-A435-10 chr1:209968741 C>T maps to NM_006147.2 W134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFY-01A-11D-A42Y-10 chr11:615252 G>T maps to NM_004031.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALW-01A-11D-A42Y-10 chr14:24634054 C>T maps to NM_006084.4 C294C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH4-01A-12D-A42Y-10 chr19:44097050 G>T maps to NM_001007561.2 G333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGA-01A-11D-A42Y-10 chr13:110434902 G>A maps to NM_003749.2 A1166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM2-01A-11D-A435-10 chr13:110435931 G>T maps to NM_003749.2 Y823*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2X-A9D6-01A-11D-A435-10 chr13:110436411 C>A maps to NM_003749.2 A663A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A9SE-01A-21D-A435-10 chr13:110435298 C>T maps to NM_003749.2 P1034P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANJ-01A-11D-A435-10 chr13:110436261 G>T maps to NM_003749.2 T713T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr5:3600084 C>T maps to NM_024337.3 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALQ-01A-12D-A42Y-10 chr5:2751509 G>T maps to NM_033267.4 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1H-01A-11D-A435-10 chr5:2749898 G>T maps to NM_033267.4 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA06-01A-12D-A435-10 chr5:2749802 C>T maps to NM_033267.4 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr5:1879732 C>T maps to NM_016358.2 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM3-01A-11D-A435-10 chr16:55363164 G>T maps to NM_024335.2 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGV-01A-11D-A42Y-10 chr19:18548462 G>T maps to NM_016368.4 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V3-01A-11D-A435-10 chr2:182358130 G>A maps to NM_000885.4 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A89B-01A-11D-A435-10 chr2:182400166 C>T maps to NM_000885.4 F1004F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFY-01A-11D-A42Y-10 chr12:54791247 G>T maps to NM_002205.2 T989T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF4-01A-11D-A42Y-10 chr2:173349558 A>G maps to ENST00000264106 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X3-A8G4-01A-11D-A435-10 chr12:56088586 G>T maps to ENST00000347027 S768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF6-01A-11D-A42Y-10 chr16:30532937 G>T maps to NM_002209.2 L1155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AAAL-01A-11D-A435-10 chr16:30531260 G>T maps to NM_002209.2 L1104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANJ-01A-11D-A435-10 chr21:46308740 G>T maps to NM_000211.3 G649G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A8S2-01A-11D-A435-10 chr21:46311734 G>T maps to NM_000211.3 C467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr3:124592307 G>T maps to NM_002213.3 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALF-01A-11D-A42Y-10 chr7:20406738 T>G maps to NM_002214.2 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W4-A7U2-01A-11D-A435-10 chr3:52852481 G>T maps to ENST00000485816 I721I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALY-01A-11D-A42Y-10 chr10:7618458 G>T maps to ENST00000256861 P645P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFJ-01A-11D-A42Y-10 chr3:4774831 C>A maps to ENST00000356617 R1757R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGG-01A-11D-A42Y-10 chr3:4687294 G>A maps to ENST00000356617 E242E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGJ-01A-11D-A42Y-10 chr3:4718332 G>T maps to ENST00000356617 E935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H5-01A-11D-A435-10 chr3:4730229 C>T maps to ENST00000356617 Q1248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A89B-01A-11D-A435-10 chr12:26636702 C>T maps to NM_002223.2 K1980K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JX-01A-11D-A435-10 chr6:33639003 G>A maps to ENST00000374316 R883R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W4-A7U2-01A-11D-A435-10 chr16:19126253 C>T maps to NM_001034841.3 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFL-01A-21D-A42Y-10 chr21:35144497 G>A maps to NM_003024.2 E392E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SB-A6J6-01A-11D-A435-10 chr1:152883010 T>A maps to NM_005547.2 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALT-01A-11D-A42Y-10 chr14:105615088 G>T maps to NM_002226.3 C671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SO-A8JP-01A-11D-A435-10 chr14:105609507 C>T did not map to a codon.
Sequencing variant TCGA-VF-A8AD-01A-11D-A435-10 chr19:17945937 G>A maps to NM_000215.3 I667I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGK-01A-11D-A42Y-10 chr5:147051342 G>T maps to NM_014790.3 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A8D5-01A-11D-A435-10 chr10:133976880 C>A maps to NM_001105521.2 R795R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A8S3-01B-11D-A435-10 chr10:133955459 C>T maps to NM_001105521.2 Q504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGT-01A-11D-A42Y-10 chr10:64928258 G>T maps to NM_032776.1 S2490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V3-01A-11D-A435-10 chr20:42788658 G>T maps to NM_020433.4 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALP-01A-12D-A42Y-10 chr17:39912436 G>A maps to NM_021991.2 P692P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALT-01A-11D-A42Y-10 chr17:39921059 G>A maps to NM_021991.2 Q355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V5-01A-11D-A435-10 chr17:39925794 G>T maps to NM_021991.2 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFY-01A-11D-A42Y-10 chr3:124114182 G>T maps to NM_001024660.3 E720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAL5-01A-11D-A42Y-10 chr9:745198 G>A maps to NM_015158.2 T1341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGN-01A-11D-A42Y-10 chr19:11303935 G>T maps to NM_015493.6 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94D-01A-11D-A435-10 chr11:30033832 C>T maps to NM_002233.2 E131E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOF-01A-11D-A435-10 chr3:156232195 G>A maps to NM_172159.3 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANJ-01A-11D-A435-10 chr1:6142260 G>T maps to NM_003636.3 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90P-01A-11D-A435-10 chr19:50831871 C>T maps to NM_004977.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A9SE-01A-21D-A435-10 chr1:112524652 C>T maps to ENST00000315987 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKL-01A-11D-A42Y-10 chr20:49621193 G>T maps to NM_002237.3 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGW-01A-11D-A42Y-10 chr17:40323896 G>A maps to NM_012285.2 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0B-01A-11D-A435-10 chr14:63447862 A>G maps to NM_139318.3 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG8-01A-31D-A42Y-10 chr2:163253437 C>A maps to NM_033272.2 G809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALW-01A-11D-A42Y-10 chr2:163374507 G>A maps to NM_033272.2 C208C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A9T9-01A-11D-A435-10 chr11:17409230 G>T maps to NM_000525.3 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AD-01A-11D-A435-10 chr2:26950832 C>T maps to NM_002246.2 F194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFN-01A-31D-A42Y-10 chr11:65363218 G>A maps to NM_033347.1 R9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H1-01A-11D-A435-10 chr1:154698448 G>T maps to NM_002249.4 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG8-01A-31D-A42Y-10 chr11:2591883 G>T maps to NM_000218.2 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHN-01A-11D-A42Y-10 chr20:62038605 G>T maps to NM_172107.2 Y670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFH-01A-12D-A42Y-10 chr20:43726454 G>A maps to NM_002251.3 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALZ-01A-11D-A42Y-10 chr2:18113147 C>T maps to NM_002252.3 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAEX-01A-11D-A42Y-10 chr9:138662152 G>A maps to ENST00000298480 Q543Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAEX-01A-11D-A42Y-10 chr9:2717879 A>T maps to NM_133497.2 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALO-01A-12D-A42Y-10 chr18:24127402 G>T maps to NM_001142730.1 R366R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGO-01A-11D-A42Y-10 chr17:7256674 G>T maps to NM_001002914.2 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF8-01A-11D-A42Y-10 chr16:67333330 G>T maps to NM_001100915.1 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X3-A8G4-01A-11D-A435-10 chr7:66094065 G>T maps to ENST00000451741 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALR-01A-21D-A42Y-10 chr11:67018077 A>G maps to NM_012308.2 E859E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO4-01A-11D-A435-10 chr11:66948810 C>T maps to NM_012308.2 Q68*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-2G-AAGV-01A-11D-A42Y-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-2G-AAFV-01A-11D-A42Y-10 chr2:86707432 T>C maps to NM_001146688.1 P820P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOF-01A-11D-A435-10 chr5:137729062 T>C did not map to a codon.
Sequencing variant TCGA-XE-AAOC-01A-11D-A435-10 chr1:202710493 C>A did not map to a codon.
Sequencing variant TCGA-2G-AAH8-01A-11D-A42Y-10 chr23:53222377 G>T did not map to a codon.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr23:53227712 G>A did not map to a codon.
Sequencing variant TCGA-2G-AAF8-01A-11D-A42Y-10 chr24:21878488 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAGT-01A-11D-A42Y-10 chr17:7751801 G>T maps to NM_001080424.1 L732L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94D-01A-11D-A435-10 chr19:10597468 C>A maps to NM_203500.1 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A89B-01A-11D-A435-10 chr9:114132780 G>A maps to NM_001080398.1 I1814I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKO-01A-11D-A42Y-10 chr14:35593059 C>G maps to NM_014672.2 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2X-A9D5-01A-11D-A435-10 chr16:15719656 G>A maps to NM_014647.3 Q509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H4-01A-31D-A435-10 chr16:15692879 C>T maps to NM_014647.3 G1605G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALT-01A-11D-A42Y-10 chr5:5462345 C>T maps to NM_015325.1 Q967*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM4-01A-11D-A435-10 chr5:5464351 G>T maps to NM_015325.1 L1635L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr4:123249483 G>T maps to NM_015312.3 E3741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA05-01A-12D-A435-10 chr5:175777717 C>T maps to NM_020444.3 Q119Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOL-01A-11D-A435-10 chr10:24669919 T>C maps to NM_019590.3 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-AA61-01A-11D-A435-10 chr10:70760226 A>C maps to NM_015634.3 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOB-01A-11D-A435-10 chr7:138593754 C>T maps to NM_001164665.1 T1086T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH3-01A-11D-A42Y-10 chr1:1920329 G>A maps to ENST00000434971 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V4-01A-11D-A435-10 chr3:113376106 C>T maps to NM_001009899.2 Q1474Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A9T9-01A-11D-A435-10 chr3:113376115 C>T maps to NM_001009899.2 Q1471Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKL-01A-11D-A42Y-10 chr9:6007724 C>T maps to NM_001017969.2 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAEX-01A-11D-A42Y-10 chr8:28929815 G>T maps to NM_015254.3 G1513G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94D-01A-11D-A435-10 chr1:200529864 T>C maps to NM_014875.2 K1405K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr3:44828006 G>T maps to NM_020242.2 G194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOC-01A-11D-A435-10 chr20:16385485 G>A maps to NM_024704.4 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGY-01A-11D-A42Y-10 chr1:21044034 G>A maps to NM_020816.2 D55D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AB-01A-31D-A435-10 chr1:21031249 G>T maps to NM_020816.2 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGW-01A-11D-A42Y-10 chr12:39735382 C>T maps to ENST00000395670 E615E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALN-01A-11D-A42Y-10 chr12:39735382 C>T maps to ENST00000395670 E615E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SO-A8JP-01A-11D-A435-10 chr12:39735382 C>T maps to ENST00000395670 E615E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A912-01A-11D-A435-10 chr12:39735382 C>T maps to ENST00000395670 E615E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFJ-01A-11D-A42Y-10 chr1:200974465 G>T maps to NM_017596.2 C234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84W-01A-11D-A435-10 chr1:200974450 G>T maps to NM_017596.2 C239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr1:200948727 G>T maps to NM_017596.2 S1352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V3-01A-11D-A435-10 chr14:104643747 G>T maps to NM_015656.1 G1541G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFV-01A-11D-A42Y-10 chr1:245851504 G>T maps to NM_018012.3 L1740L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AAAL-01A-11D-A435-10 chr1:245861583 C>T maps to NM_018012.3 Q2001*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO6-01A-31D-A435-10 chr2:26203244 G>C maps to NM_002254.6 Y514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0H-01A-11D-A435-10 chr12:57965875 G>A maps to NM_004984.2 K465K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AC-01A-11D-A435-10 chr15:90174727 C>A maps to NM_198525.2 E1037*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOC-01A-11D-A435-10 chr8:145692489 C>T maps to NM_145754.2 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H1-01A-11D-A435-10 chr16:57803626 G>T maps to NM_005550.3 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr19:55285079 C>A maps to ENST00000291633 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84W-01A-11D-A435-10 chr1:204159650 C>T maps to ENST00000306118 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG0-01A-11D-A42Y-10 chr4:39448346 C>A maps to NM_175737.3 A667A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALS-01A-12D-A42Y-10 chr11:66033607 C>A maps to NM_022822.2 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALF-01A-11D-A42Y-10 chr15:31619960 G>C maps to NM_015995.2 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGJ-01A-11D-A42Y-10 chr23:56295890 G>C did not map to a codon.
Sequencing variant TCGA-XE-AANI-01A-11D-A435-10 chr6:42985043 T>G maps to NM_057161.2 Y38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V5-01A-11D-A435-10 chr3:49213206 G>A maps to NM_173546.2 E346E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAL7-01A-11D-A42Y-10 chr23:117043474 G>A did not map to a codon.
Sequencing variant TCGA-2G-AAFI-01A-21D-A42Y-10 chr18:30350530 G>T maps to NM_020805.1 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr23:24024351 C>A did not map to a codon.
Sequencing variant TCGA-2G-AAGS-01A-11D-A42Y-10 chr4:166220780 G>T maps to NM_001161521.1 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALQ-01A-12D-A42Y-10 chr15:86311958 G>A maps to NM_022480.3 Y361Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGC-01A-21D-A42Y-10 chr19:18779074 C>T maps to NM_018316.1 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AC-01A-11D-A435-10 chr23:21675218 C>T did not map to a codon.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr7:23213658 C>T maps to NM_001031710.2 Y501Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A8D5-01A-11D-A435-10 chr19:51528036 T>C maps to NM_144947.1 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA05-01A-12D-A435-10 chr19:51534067 G>A maps to NM_019598.2 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALW-01A-11D-A42Y-10 chr19:51453208 C>A maps to NM_012427.4 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKL-01A-11D-A42Y-10 chr12:123057482 G>A did not map to a codon.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr12:123087234 G>T maps to NM_014708.4 L1591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF6-01A-11D-A42Y-10 chr16:3017028 C>T maps to NM_172229.1 G253G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALT-01A-11D-A42Y-10 chr17:39743002 G>A maps to NM_000526.4 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALN-01A-11D-A42Y-10 chr12:53045776 G>C maps to NM_000423.2 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr17:38854820 T>C maps to NM_019016.2 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANJ-01A-11D-A435-10 chr17:39507010 G>T maps to NM_004138.2 Y3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO6-01A-31D-A435-10 chr17:39644940 G>T maps to NM_003771.4 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGZ-01A-11D-A42Y-10 chr17:39578410 G>A maps to NM_003770.4 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOL-01A-11D-A435-10 chr12:52841623 G>A maps to NM_005555.3 V454V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM2-01A-11D-A435-10 chr12:52985289 G>T maps to NM_080747.2 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF1-01A-11D-A42Y-10 chr12:53002213 G>T maps to NM_175068.2 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH8-01A-11D-A42Y-10 chr12:52827740 A>G maps to ENST00000252245 C170C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGG-01A-11D-A42Y-10 chr12:52681794 G>T maps to NM_002281.3 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALP-01A-12D-A42Y-10 chr17:39723689 C>T maps to NM_000226.3 G569G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90W-01A-11D-A435-10 chr17:39728193 A>C maps to NM_000226.3 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94I-01A-11D-A435-10 chr17:39728193 A>C maps to NM_000226.3 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHT-01A-11D-A42Y-10 chr21:46057777 G>T maps to NM_181688.1 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90Q-01A-11D-A435-10 chr21:46057831 T>A maps to NM_181688.1 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFM-01A-11D-A42Y-10 chr21:45970729 C>A maps to NM_198693.2 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHL-01A-11D-A42Y-10 chr21:45971146 G>A maps to NM_198693.2 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHA-01A-11D-A42Y-10 chr21:45994675 A>G maps to NM_198687.1 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SB-A6J6-01A-11D-A435-10 chr21:45993850 C>T maps to NM_198687.1 C72C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84X-01A-11D-A435-10 chr21:45993850 C>T maps to NM_198687.1 C72C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AD-01A-11D-A435-10 chr21:31768920 T>C maps to NM_181599.2 *173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AB-01A-31D-A435-10 chr17:39280272 G>T maps to NM_031854.2 T34T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-WZ-A8D5-01A-11D-A435-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-4K-AA1G-01A-11D-A435-10 chr11:1629384 A>G maps to ENST00000359229 C161C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKO-01A-11D-A42Y-10 chr11:1651441 G>C maps to NM_001001480.2 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALN-01A-11D-A42Y-10 chr11:1651441 G>C maps to NM_001001480.2 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALQ-01A-12D-A42Y-10 chr11:1651441 G>C maps to NM_001001480.2 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A6IS-01A-11D-A435-10 chr11:1651126 C>T maps to NM_001001480.2 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JY-01A-11D-A435-10 chr11:71238417 T>C maps to ENST00000422553 C24C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGY-01A-11D-A42Y-10 chr11:71249544 C>T maps to NM_021046.2 C148C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO3-01A-11D-A435-10 chr2:143685254 G>A maps to NM_003937.2 K106K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGO-01A-11D-A42Y-10 chr1:201356275 G>T maps to NM_005558.3 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGP-01A-11D-A42Y-10 chr18:7023226 G>T maps to NM_005559.2 G879G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr6:129204395 G>A maps to NM_000426.3 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALR-01A-21D-A42Y-10 chr6:129637313 C>T maps to NM_000426.3 S1352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A9T9-01A-11D-A435-10 chr18:21427620 C>T maps to ENST00000416669 S1377S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHP-01A-12D-A42Y-10 chr20:60886011 C>A maps to NM_005560.3 G3409G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAL5-01A-11D-A42Y-10 chr20:60887506 G>A maps to NM_005560.3 L3103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG9-01A-11D-A42Y-10 chr23:37431144 G>A did not map to a codon.
Sequencing variant TCGA-2G-AAG0-01A-11D-A42Y-10 chr8:98817594 G>T maps to ENST00000378722 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALX-01A-11D-A42Y-10 chr8:98788290 C>A maps to ENST00000378722 C155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH2-01A-11D-A42Y-10 chr12:50869340 C>T maps to ENST00000429001 C629C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH0-01A-11D-A42Y-10 chr10:861004 G>T maps to NM_015155.1 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0B-01A-11D-A435-10 chr10:860953 G>T maps to NM_015155.1 P584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANR-01A-11D-A435-10 chr13:21562307 G>T maps to NM_014572.2 C537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGJ-01A-11D-A42Y-10 chr4:18023326 G>A maps to NM_001166139.1 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFJ-01A-11D-A42Y-10 chr1:22141107 G>C maps to NM_001013693.2 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H5-01A-11D-A435-10 chr22:44893009 G>A maps to NM_032287.2 R143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JY-01A-11D-A435-10 chr5:135287020 G>T maps to NM_002302.2 C60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHA-01A-11D-A42Y-10 chr1:43213950 G>T maps to NM_022356.3 V586V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM4-01A-11D-A435-10 chr1:236706864 G>A maps to NM_201545.1 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAL7-01A-11D-A42Y-10 chr19:49519471 C>A maps to NM_000894.2 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH4-01A-12D-A42Y-10 chr7:103969250 C>T maps to NM_199000.2 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2X-A9D5-01A-11D-A435-10 chr7:103969250 C>T maps to NM_199000.2 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALX-01A-11D-A42Y-10 chr12:113907119 C>A maps to NM_022363.2 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALY-01A-11D-A42Y-10 chr12:113906209 C>T did not map to a codon.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr1:75602876 C>A maps to NM_001001933.1 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHA-01A-11D-A42Y-10 chr22:30642575 T>G did not map to a codon.
Sequencing variant TCGA-XE-AANI-01A-11D-A435-10 chr19:48636322 G>T maps to NM_000234.1 P547P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SO-A8JP-01A-11D-A435-10 chr19:54724043 T>A maps to NM_001081450.1 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W4-A7U4-01A-12D-A435-10 chr20:62369749 C>T maps to NM_017806.2 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFV-01A-11D-A42Y-10 chr19:2291165 G>T maps to NM_001101391.1 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGK-01A-11D-A42Y-10 chr19:42914476 G>T maps to NM_005357.2 G467G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG6-01A-11D-A42Y-10 chr15:75111136 C>T maps to NM_021819.2 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFL-01A-21D-A42Y-10 chr3:8543417 G>T did not map to a codon.
Sequencing variant TCGA-ZM-AA0H-01A-11D-A435-10 chr22:50944794 G>T maps to NM_033200.2 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1G-01A-11D-A435-10 chr1:87797775 C>T maps to NM_006769.3 C26C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALY-01A-11D-A42Y-10 chr13:76427263 C>T maps to ENST00000357063 S1397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-AA61-01A-11D-A435-10 chr13:76391408 C>T maps to ENST00000357063 Q617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM4-01A-11D-A435-10 chr7:123302962 T>A maps to NM_207163.1 P441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AAAL-01A-11D-A435-10 chr19:49001925 A>G maps to NM_001080434.1 P829P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W4-A7U2-01A-11D-A435-10 chr11:194440 C>T maps to NM_145651.2 D93D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84Y-01A-11D-A435-10 chr19:5720013 G>T maps to NM_004793.2 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHC-01A-11D-A42Y-10 chr2:100916314 A>T maps to NM_198461.3 G377G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH3-01A-11D-A42Y-10 chr1:153233514 C>T maps to NM_000427.2 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM2-01A-11D-A435-10 chr1:153233514 C>T maps to NM_000427.2 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr1:153233475 G>T maps to NM_000427.2 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO6-01A-31D-A435-10 chr1:153233514 C>T maps to NM_000427.2 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94D-01A-11D-A435-10 chr1:153233505 C>T maps to NM_000427.2 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALW-01A-11D-A42Y-10 chr10:100017442 G>T maps to NM_032211.6 V408V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1I-01A-11D-A435-10 chr6:160958955 G>A maps to NM_005577.2 L1925L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84X-01A-11D-A435-10 chr6:160978592 C>A maps to NM_005577.2 E1548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGS-01A-11D-A42Y-10 chr19:14262419 G>T maps to NM_001008701.2 P1230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANI-01A-11D-A435-10 chr4:62679543 C>T maps to ENST00000506720 Q473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JW-01A-11D-A435-10 chr2:11935589 G>T maps to ENST00000396099 P627P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALX-01A-11D-A42Y-10 chr18:2951053 G>A maps to NM_014646.2 R197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A6IS-01A-11D-A435-10 chr18:2931428 G>T maps to NM_014646.2 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAEW-01A-11D-A42Y-10 chr7:100173406 T>C did not map to a codon.
Sequencing variant TCGA-XE-AANV-01A-11D-A435-10 chr7:100183684 A>C maps to NM_002319.3 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGN-01A-11D-A42Y-10 chr19:39804794 T>G maps to NM_020862.1 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94I-01A-11D-A435-10 chr19:36435791 C>T maps to NM_024509.1 T586T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALP-01A-12D-A42Y-10 chr7:133812183 A>T maps to NM_144648.1 R22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALF-01A-11D-A42Y-10 chr12:57600262 G>A maps to NM_002332.2 E3866E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANR-01A-11D-A435-10 chr12:57588469 G>T maps to NM_002332.2 E2727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X3-A8G4-01A-11D-A435-10 chr2:170115532 A>C did not map to a codon.
Sequencing variant TCGA-2G-AAGI-01A-11D-A42Y-10 chr19:33697229 C>T maps to NM_002333.3 C518C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGZ-01A-11D-A42Y-10 chr19:33696437 C>T maps to NM_002333.3 C254C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG8-01A-31D-A42Y-10 chr11:46898069 C>T maps to ENST00000256991 L1206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFL-01A-21D-A42Y-10 chr11:68216456 C>T maps to NM_002335.2 S1589S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84X-01A-11D-A435-10 chr11:68115708 C>T maps to NM_002335.2 H162H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AE-01A-11D-A435-10 chr11:68115597 G>A maps to NM_002335.2 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGI-01A-11D-A42Y-10 chr22:25755834 G>A maps to NM_001135772.1 D75D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF6-01A-11D-A42Y-10 chr12:12303883 G>T maps to NM_002336.2 P960P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF8-01A-11D-A42Y-10 chr9:26996465 G>T maps to NM_022901.2 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALO-01A-12D-A42Y-10 chr11:76370932 C>T maps to NM_001128922.1 L568L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALQ-01A-12D-A42Y-10 chr11:76370908 G>A maps to NM_001128922.1 C576C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGN-01A-11D-A42Y-10 chr17:62892946 G>A maps to NM_199340.2 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALS-01A-12D-A42Y-10 chr17:30374804 A>G maps to ENST00000327564 P783P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr1:70650539 G>T maps to NM_017768.4 C155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGA-01A-11D-A42Y-10 chr17:79988251 C>T maps to NM_144999.2 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALF-01A-11D-A42Y-10 chr17:45914164 G>A maps to NM_033413.3 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84W-01A-11D-A435-10 chr1:3712536 A>G maps to NM_020710.2 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKM-01A-11D-A42Y-10 chr17:48460489 T>C maps to NM_018509.3 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGN-01A-11D-A42Y-10 chr4:52861267 C>T maps to NM_001024611.1 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGZ-01A-11D-A42Y-10 chr4:52861138 G>A maps to NM_001024611.1 N683N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHN-01A-11D-A42Y-10 chr4:52883328 T>A maps to NM_001024611.1 K151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO3-01A-11D-A435-10 chr1:70504281 T>C maps to NM_020794.2 P887P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGG-01A-11D-A42Y-10 chr1:90048811 C>T maps to NM_015350.2 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JX-01A-11D-A435-10 chr3:37100308 G>T maps to NM_006309.2 G614G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGP-01A-11D-A42Y-10 chr15:101555581 T>A maps to NM_024652.3 G528G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90Q-01A-11D-A435-10 chr15:101593437 G>A maps to NM_024652.3 L1289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X3-A8G4-01A-11D-A435-10 chr12:40713815 T>A maps to NM_198578.3 C1618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGE-01A-21D-A42Y-10 chr9:130216850 G>T maps to NM_001005374.2 R15R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AC-01A-11D-A435-10 chr21:47642608 G>T maps to NM_002340.5 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOL-01A-11D-A435-10 chr21:47642635 G>T maps to NM_002340.5 C112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG0-01A-11D-A42Y-10 chr14:24780817 G>T maps to ENST00000336557 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr11:65310633 G>A maps to NM_001130144.2 G846G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A9T9-01A-11D-A435-10 chr15:41804957 G>A maps to NM_002344.5 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AA-01A-11D-A435-10 chr16:239208 G>A maps to NM_201412.1 A368A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFM-01A-11D-A42Y-10 chr4:4285379 G>T maps to NM_017816.2 C30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFY-01A-11D-A42Y-10 chr19:43967281 C>T maps to NM_014400.2 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHP-01A-12D-A42Y-10 chr19:43967293 G>A maps to NM_014400.2 N176N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOC-01A-11D-A435-10 chr8:54965241 C>T maps to ENST00000419058 W155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAL7-01A-11D-A42Y-10 chr1:24120781 C>T maps to NM_007260.2 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr1:235922555 C>T maps to NM_000081.2 V2199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A9SE-01A-21D-A435-10 chr22:21348865 G>T maps to NM_006767.3 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHP-01A-12D-A42Y-10 chr10:102766681 T>G maps to NM_032429.2 G589G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGK-01A-11D-A42Y-10 chr13:36050492 T>G did not map to a codon.
Sequencing variant TCGA-2G-AAGY-01A-11D-A42Y-10 chr13:36049615 G>T maps to NM_005584.4 G220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALG-01A-11D-A42Y-10 chr1:39783025 A>G maps to ENST00000361689 K1248K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr1:39852902 C>T maps to ENST00000361689 Q2735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANR-01A-11D-A435-10 chr1:39801334 A>G maps to ENST00000289893 K1465K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGY-01A-11D-A42Y-10 chr11:63918711 G>A maps to NM_014067.3 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAL7-01A-11D-A42Y-10 chr1:166961962 C>T maps to NM_032858.1 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHN-01A-11D-A42Y-10 chr19:35786621 G>T maps to NM_002361.3 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AAAL-01A-11D-A435-10 chr19:35790580 G>T maps to NM_002361.3 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANJ-01A-11D-A435-10 chr19:35790584 G>T maps to NM_002361.3 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGE-01A-21D-A42Y-10 chr23:151303918 G>A did not map to a codon.
Sequencing variant TCGA-4K-AAAL-01A-11D-A435-10 chr23:148794833 C>A did not map to a codon.
Sequencing variant TCGA-YU-AA4L-01A-11D-A435-10 chr23:151899527 C>T did not map to a codon.
Sequencing variant TCGA-2G-AAL7-01A-11D-A42Y-10 chr23:30269095 C>T did not map to a codon.
Sequencing variant TCGA-2G-AAGO-01A-11D-A42Y-10 chr23:27840131 G>T did not map to a codon.
Sequencing variant TCGA-YU-A94D-01A-11D-A435-10 chr23:27839492 G>A did not map to a codon.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr23:30254693 C>T did not map to a codon.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr23:30261214 T>C did not map to a codon.
Sequencing variant TCGA-2G-AAGE-01A-21D-A42Y-10 chr23:140995246 A>G did not map to a codon.
Sequencing variant TCGA-4K-AAAL-01A-11D-A435-10 chr23:140994162 A>T did not map to a codon.
Sequencing variant TCGA-4K-AAAL-01A-11D-A435-10 chr23:140994164 A>T did not map to a codon.
Sequencing variant TCGA-XE-AAO4-01A-11D-A435-10 chr23:140994526 C>T did not map to a codon.
Sequencing variant TCGA-2G-AAGJ-01A-11D-A42Y-10 chr23:51637752 C>A did not map to a codon.
Sequencing variant TCGA-ZM-AA0E-01A-12D-A435-10 chr23:75004548 T>C did not map to a codon.
Sequencing variant TCGA-2G-AAKD-01A-31D-A42Y-10 chr15:23889163 G>T maps to NM_019066.4 P1242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFG-01A-11D-A42Y-10 chr3:65425593 C>T maps to NM_001033057.1 Q410Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JX-01A-11D-A435-10 chr3:65425584 C>T maps to NM_001033057.1 Q413Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOL-01A-11D-A435-10 chr1:114215975 A>G maps to NM_001142782.1 R1026R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V3-01A-11D-A435-10 chr12:10762453 A>G maps to NM_018048.3 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGT-01A-11D-A42Y-10 chr11:95825253 C>T maps to NM_032427.1 Q647Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0F-01A-21D-A435-10 chr11:95825253 C>T maps to NM_032427.1 Q647Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0N-01A-21D-A435-10 chr11:95825262 C>T maps to NM_032427.1 Q644Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGY-01A-11D-A42Y-10 chr4:140640914 C>T maps to ENST00000509479 G993G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGM-01A-11D-A42Y-10 chr23:149639634 A>T did not map to a codon.
Sequencing variant TCGA-ZM-AA0F-01A-21D-A435-10 chr23:149639634 A>T did not map to a codon.
Sequencing variant TCGA-2G-AAHT-01A-11D-A42Y-10 chr5:109103371 G>A maps to NM_002372.2 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH2-01A-11D-A42Y-10 chr19:12774208 C>T maps to NM_000528.3 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALY-01A-11D-A42Y-10 chr4:6599003 C>T maps to NM_015274.1 Q408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHL-01A-11D-A42Y-10 chr15:75654242 G>A maps to NM_006715.2 Q352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SO-A8JP-01A-11D-A435-10 chr15:75650585 G>T maps to NM_006715.2 R835R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AE-01A-11D-A435-10 chr1:38260363 G>T maps to NM_001113482.1 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SB-A76C-01A-11D-A435-10 chr23:43603152 G>T did not map to a codon.
Sequencing variant TCGA-YU-AA4L-01A-11D-A435-10 chr23:43590941 G>T did not map to a codon.
Sequencing variant TCGA-SN-A84X-01A-11D-A435-10 chr5:71495133 G>T maps to NM_005909.3 L1984L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFL-01A-21D-A42Y-10 chr19:17837104 G>A maps to NM_018174.4 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG0-01A-11D-A42Y-10 chr19:17838361 C>A maps to NM_018174.4 G723G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH4-01A-12D-A42Y-10 chr19:17837038 G>T maps to NM_018174.4 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANJ-01A-11D-A435-10 chr19:4110626 G>T maps to NM_030662.3 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84W-01A-11D-A435-10 chr15:67835783 G>T maps to NM_145160.1 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM3-01A-11D-A435-10 chr11:65380519 G>A maps to NM_002419.3 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JY-01A-11D-A435-10 chr11:65380777 G>T maps to NM_002419.3 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFL-01A-21D-A42Y-10 chr6:161533754 G>A maps to NM_005922.2 A1525A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGF-01A-31D-A42Y-10 chr1:27684930 G>T maps to NM_004672.3 R919R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH4-01A-12D-A42Y-10 chr6:91254349 G>T maps to NM_145331.1 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM2-01A-11D-A435-10 chr14:55529373 C>T maps to NM_144578.3 T19T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGN-01A-11D-A42Y-10 chr22:51044139 C>T maps to ENST00000329492 P663P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO4-01A-11D-A435-10 chr22:51039297 G>T maps to ENST00000329492 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALP-01A-12D-A42Y-10 chr16:1818242 G>A maps to NM_015133.3 G1201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84X-01A-11D-A435-10 chr5:179663446 C>T maps to NM_002752.4 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H5-01A-11D-A435-10 chr17:44060769 G>A maps to NM_001123066.3 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGK-01A-11D-A42Y-10 chr12:58152466 A>G maps to NM_138396.4 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGE-01A-21D-A42Y-10 chr11:63667567 G>T maps to NM_001039469.2 G252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X3-A8G4-01A-11D-A435-10 chr14:103946750 C>T maps to ENST00000335102 R527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKL-01A-11D-A42Y-10 chr19:45801077 T>G maps to NM_031417.3 G581G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFN-01A-31D-A42Y-10 chr12:57883072 G>A maps to NM_004990.2 W75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALN-01A-11D-A42Y-10 chr12:57883692 A>G maps to NM_004990.2 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84Y-01A-11D-A435-10 chr12:57898051 G>C maps to NM_004990.2 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG0-01A-11D-A42Y-10 chr1:31196428 G>A did not map to a codon.
Sequencing variant TCGA-2G-AAG5-01A-11D-A42Y-10 chr5:138651821 T>C maps to ENST00000394800 P358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHC-01A-11D-A42Y-10 chr18:58039042 T>C maps to NM_005912.2 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-AA4L-01A-11D-A435-10 chr5:112418570 T>G maps to NM_001085377.1 T590T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF1-01A-11D-A42Y-10 chr10:13230970 G>T maps to NM_182751.2 G437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFV-01A-11D-A42Y-10 chr6:52141939 G>T maps to ENST00000419835 R409R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGO-01A-11D-A42Y-10 chr21:47664964 G>A maps to NM_003906.3 G1598G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALO-01A-12D-A42Y-10 chr19:7595281 G>T maps to NM_020533.2 V490V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFL-01A-21D-A42Y-10 chr8:6302343 G>A maps to NM_024596.3 P367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGI-01A-11D-A42Y-10 chr15:94841502 G>T maps to NM_018349.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFV-01A-11D-A42Y-10 chr6:30673314 G>T maps to NM_014641.2 T1215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90S-01A-11D-A435-10 chr6:30681593 G>T maps to NM_014641.2 S168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGI-01A-11D-A42Y-10 chr6:37615065 G>T maps to ENST00000297153 T646T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF8-01A-11D-A42Y-10 chr6:90385225 G>T maps to NM_014611.1 R4240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFL-01A-21D-A42Y-10 chr11:86382932 G>T maps to NM_001014811.1 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH2-01A-11D-A42Y-10 chr17:37571337 G>A maps to NM_004774.3 Y480Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFI-01A-21D-A42Y-10 chr3:150881772 C>T maps to NM_053002.4 Q401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94D-01A-11D-A435-10 chr23:40569338 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAHA-01A-11D-A42Y-10 chr19:886141 C>T maps to NM_005481.2 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A912-01A-11D-A435-10 chr19:16687977 G>T maps to NM_004831.3 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKO-01A-11D-A42Y-10 chr17:17380477 T>C maps to NM_018019.2 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A9SE-01A-21D-A435-10 chr15:100214644 G>T maps to ENST00000338042 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF6-01A-11D-A42Y-10 chr16:3304632 G>A maps to NM_000243.2 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA05-01A-12D-A435-10 chr16:3304500 G>T maps to NM_000243.2 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH8-01A-11D-A42Y-10 chr5:126755896 C>T maps to NM_032446.2 Q530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAL7-01A-11D-A42Y-10 chr15:66262976 G>T maps to NM_032445.2 C271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALF-01A-11D-A42Y-10 chr1:3440790 G>T maps to ENST00000452816 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X3-A8G4-01A-11D-A435-10 chr1:3411237 G>A maps to ENST00000452816 C1388C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84X-01A-11D-A435-10 chr19:42872800 C>T maps to ENST00000251268 S2156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOB-01A-11D-A435-10 chr19:42873739 G>T maps to ENST00000251268 V2233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A89B-01A-11D-A435-10 chr19:42880075 G>T maps to ENST00000251268 E2563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A8S2-01A-11D-A435-10 chr9:36657332 A>C maps to NM_014791.2 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALY-01A-11D-A42Y-10 chr2:32168447 C>T maps to NM_015955.2 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG0-01A-11D-A42Y-10 chr7:15725826 C>A maps to NM_005924.4 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H4-01A-31D-A435-10 chr6:46766383 G>T did not map to a codon.
Sequencing variant TCGA-SN-A84W-01A-11D-A435-10 chr7:100028000 C>G maps to NM_019606.5 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAL5-01A-11D-A42Y-10 chr2:112760765 T>C did not map to a codon.
Sequencing variant TCGA-SO-A8JP-01A-11D-A435-10 chr15:81295325 G>T maps to NM_022566.2 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHG-01A-11D-A42Y-10 chr15:90320172 A>G maps to NM_001039958.1 G195G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A912-01A-11D-A435-10 chr15:90320172 A>G maps to NM_001039958.1 G195G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF6-01A-11D-A42Y-10 chr12:95867963 T>G maps to NM_006838.3 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGA-01A-11D-A42Y-10 chr16:767134 G>T maps to NM_024042.2 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AC-01A-11D-A435-10 chr14:21971824 G>T maps to NM_019852.3 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFM-01A-11D-A42Y-10 chr16:21611167 C>T maps to NM_016025.3 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALQ-01A-12D-A42Y-10 chr19:1556638 G>T maps to NM_001174118.1 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH4-01A-12D-A42Y-10 chr2:228211977 T>C maps to NM_020194.4 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W4-A7U2-01A-11D-A435-10 chr2:228194320 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAFH-01A-12D-A42Y-10 chr8:8749215 A>G maps to NM_004225.2 P451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGG-01A-11D-A42Y-10 chr8:8748681 G>T maps to NM_004225.2 C629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H1-01A-11D-A435-10 chr8:8748486 A>C maps to NM_004225.2 G694G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANI-01A-11D-A435-10 chr8:8749746 C>T maps to NM_004225.2 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH3-01A-11D-A42Y-10 chr1:12069690 C>T maps to NM_014874.3 D704D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALW-01A-11D-A42Y-10 chr3:158538115 G>T did not map to a codon.
Sequencing variant TCGA-XY-A89B-01A-11D-A435-10 chr4:2932978 G>T maps to NM_001146069.1 C379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFZ-01A-11D-A42Y-10 chr2:24246461 G>A maps to ENST00000338315 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFH-01A-12D-A42Y-10 chr1:205538280 C>T maps to NM_181644.4 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X3-A8G4-01A-11D-A435-10 chr3:127440000 G>A maps to NM_007283.5 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG7-01A-11D-A42Y-10 chr11:12244986 G>T maps to NM_014632.2 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr11:12263796 G>T maps to NM_014632.2 E792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A912-01A-11D-A435-10 chr22:18358227 G>T maps to NM_001136004.1 S830S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHT-01A-11D-A42Y-10 chr23:107084385 G>A did not map to a codon.
Sequencing variant TCGA-XE-AAOF-01A-11D-A435-10 chr22:24237062 G>T maps to NM_002415.1 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFG-01A-11D-A42Y-10 chr10:129905195 G>T maps to NM_002417.4 S1636S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH0-01A-11D-A42Y-10 chr10:129914215 T>C maps to NM_002417.4 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGY-01A-11D-A42Y-10 chr19:2043518 G>T maps to NM_199054.2 Y134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0N-01A-21D-A435-10 chr19:2039710 G>T maps to NM_199054.2 C433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A8S2-01A-11D-A435-10 chr17:56293604 C>G did not map to a codon.
Sequencing variant TCGA-2G-AALQ-01A-12D-A42Y-10 chr12:6858044 T>C maps to NM_005439.2 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFJ-01A-11D-A42Y-10 chr14:75508401 A>G maps to NM_001040108.1 D1127D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGO-01A-11D-A42Y-10 chr12:49444813 A>G maps to NM_003482.3 P884P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALZ-01A-11D-A42Y-10 chr12:49420274 C>T maps to NM_003482.3 E5158E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGG-01A-11D-A42Y-10 chr7:151845607 C>T maps to ENST00000355193 T4525T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH4-01A-12D-A42Y-10 chr7:152012229 G>A maps to ENST00000355193 Q195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHG-01A-11D-A42Y-10 chr7:151945312 A>G maps to ENST00000355193 L736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALF-01A-11D-A42Y-10 chr7:151921173 G>A maps to ENST00000355193 S1083S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANV-01A-11D-A435-10 chr7:151945088 G>A maps to ENST00000355193 N810N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOJ-01A-12D-A435-10 chr7:151962268 C>T maps to ENST00000355193 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGN-01A-11D-A42Y-10 chr19:36219738 C>T maps to NM_014727.1 Q1546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO3-01A-11D-A435-10 chr19:36212613 G>T maps to NM_014727.1 E789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH8-01A-11D-A42Y-10 chr7:104747053 G>A maps to NM_182931.2 P894P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84X-01A-11D-A435-10 chr7:104746450 G>T did not map to a codon.
Sequencing variant TCGA-2G-AALG-01A-11D-A42Y-10 chr9:20414369 G>A maps to NM_004529.2 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFM-01A-11D-A42Y-10 chr23:135055905 T>G did not map to a codon.
Sequencing variant TCGA-YU-AA61-01A-11D-A435-10 chr12:132326265 G>A maps to NM_016155.4 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1I-01A-11D-A435-10 chr1:1569980 C>T maps to ENST00000412415 R425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALF-01A-11D-A42Y-10 chr10:88702581 G>T maps to NM_024756.2 L653L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM4-01A-11D-A435-10 chr22:28195493 T>G maps to NM_002430.2 P346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A8S2-01A-11D-A435-10 chr22:28196363 G>T maps to NM_002430.2 G56G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A8S3-01B-11D-A435-10 chr22:28194893 C>T maps to NM_002430.2 Q546Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V3-01A-11D-A435-10 chr7:156802390 G>A maps to NM_005515.3 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H1-01A-11D-A435-10 chr20:49576173 G>T maps to NM_014484.3 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALW-01A-11D-A42Y-10 chr22:31337529 G>T maps to ENST00000397641 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH3-01A-11D-A42Y-10 chr23:106184799 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAH3-01A-11D-A42Y-10 chr9:13217200 G>T maps to ENST00000319217 G393G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALR-01A-21D-A42Y-10 chr13:20208028 C>A maps to ENST00000414242 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A9SE-01A-21D-A435-10 chr17:56355260 C>T maps to ENST00000340482 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SB-A76C-01A-11D-A435-10 chr23:154020463 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAH8-01A-11D-A42Y-10 chr10:18138581 G>T maps to NM_002438.2 E380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF8-01A-11D-A42Y-10 chr17:60758221 G>T maps to NM_006039.3 T845T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFO-01A-31D-A42Y-10 chr19:13879175 T>C maps to NM_032285.2 R125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A89B-01A-11D-A435-10 chr19:13879551 G>A did not map to a codon.
Sequencing variant TCGA-2G-AAEW-01A-11D-A42Y-10 chr12:93881368 G>T maps to NM_172177.2 G106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO4-01A-11D-A435-10 chr1:151735987 A>C did not map to a codon.
Sequencing variant TCGA-VF-A8AD-01A-11D-A435-10 chr15:89010688 C>T did not map to a codon.
Sequencing variant TCGA-XE-A8H1-01A-11D-A435-10 chr12:27863859 G>T maps to NM_021821.3 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKG-01A-11D-A42Y-10 chr2:95753179 T>C maps to NM_031902.3 K405K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90P-01A-11D-A435-10 chr6:31725946 G>C maps to ENST00000375742 V357V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A9SE-01A-21D-A435-10 chr16:815589 C>T maps to NM_013404.4 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOB-01A-11D-A435-10 chr16:815168 C>T maps to NM_013404.4 C190C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JY-01A-11D-A435-10 chr3:49725037 G>C maps to NM_020998.3 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JY-01A-11D-A435-10 chr3:49725085 G>A maps to NM_020998.3 N86N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG8-01A-31D-A42Y-10 chr3:49940448 G>T maps to NM_002447.2 Y198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKG-01A-11D-A42Y-10 chr11:62365526 G>A maps to NM_004739.2 Y153Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANI-01A-11D-A435-10 chr2:42836613 A>G maps to ENST00000405094 E69E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALP-01A-12D-A42Y-10 chr1:93580261 G>T maps to NM_007358.3 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKO-01A-11D-A42Y-10 chr10:135207792 C>T maps to NM_138384.2 C23C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHA-01A-11D-A42Y-10 chr14:64914954 A>G maps to NM_005956.3 K733K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V3-01A-11D-A435-10 chr1:11854011 G>T maps to ENST00000376585 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AD-01A-11D-A435-10 chr22:30416629 G>A maps to NM_021090.3 L994L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALW-01A-11D-A42Y-10 chr6:153323667 C>T maps to NM_019041.5 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALN-01A-11D-A42Y-10 chr1:155161883 G>T maps to ENST00000425082 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1G-01A-11D-A435-10 chr3:124646754 G>T maps to NM_033049.3 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF4-01A-11D-A42Y-10 chr19:9025603 A>G maps to NM_024690.2 L12284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALZ-01A-11D-A42Y-10 chr19:9033259 G>T maps to NM_024690.2 L12122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFJ-01A-11D-A42Y-10 chr7:100678917 G>A maps to NM_001040105.1 P1407P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFV-01A-11D-A42Y-10 chr7:100680099 G>A maps to NM_001040105.1 S1801S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKO-01A-11D-A42Y-10 chr7:100678917 G>A maps to NM_001040105.1 P1407P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALO-01A-12D-A42Y-10 chr7:100685847 T>A maps to NM_001040105.1 P3717P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA06-01A-12D-A435-10 chr7:100679220 G>T maps to NM_001040105.1 T1508T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFI-01A-21D-A42Y-10 chr11:1092959 C>A maps to ENST00000441003 T1593T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFJ-01A-11D-A42Y-10 chr11:1093292 C>G maps to ENST00000441003 T1704T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG3-01A-11D-A42Y-10 chr11:1092965 C>A maps to ENST00000441003 T1595T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGC-01A-21D-A42Y-10 chr11:1093436 G>C maps to ENST00000441003 T1752T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHT-01A-11D-A42Y-10 chr11:1092968 A>T maps to ENST00000441003 P1596P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALF-01A-11D-A42Y-10 chr11:1093433 C>T maps to ENST00000441003 T1751T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALX-01A-11D-A42Y-10 chr11:1093184 C>T maps to ENST00000441003 T1668T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALY-01A-11D-A42Y-10 chr11:1093433 C>T maps to ENST00000441003 T1751T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALZ-01A-11D-A42Y-10 chr11:1092899 A>T maps to ENST00000441003 P1573P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFI-01A-21D-A42Y-10 chr6:30954812 T>C maps to NM_001010909.2 N287N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr6:30955232 A>G maps to NM_001010909.2 T427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALN-01A-11D-A42Y-10 chr6:30954392 T>C maps to NM_001010909.2 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALR-01A-21D-A42Y-10 chr6:30954869 T>C maps to NM_001010909.2 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALN-01A-11D-A42Y-10 chr3:195510665 G>A maps to NM_018406.5 V2595V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALQ-01A-12D-A42Y-10 chr3:195512456 G>A maps to NM_018406.5 A1998A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr3:195508958 A>T maps to NM_018406.5 G3164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANJ-01A-11D-A435-10 chr3:195506558 A>G maps to NM_018406.5 G3964G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90Q-01A-11D-A435-10 chr3:195510779 G>A maps to NM_018406.5 H2557H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFL-01A-21D-A42Y-10 chr11:1271588 C>T maps to ENST00000447027 S4496S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALP-01A-12D-A42Y-10 chr11:1268036 G>A maps to ENST00000447027 P3312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFJ-01A-11D-A42Y-10 chr11:1017823 G>C maps to NM_005961.2 L1659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFM-01A-11D-A42Y-10 chr11:1017555 G>A maps to NM_005961.2 L1749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOD-01A-11D-A435-10 chr11:1016821 A>C maps to NM_005961.2 T1993T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHL-01A-11D-A42Y-10 chr1:20834436 G>T maps to NM_024544.2 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90W-01A-11D-A435-10 chr19:1360217 G>T maps to NM_032853.3 E101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr9:103340814 C>T maps to NM_001018116.1 F130F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr1:45796994 G>T maps to NM_001128425.1 T445T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAL5-01A-11D-A42Y-10 chr21:42767523 C>A maps to NM_002463.1 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG5-01A-11D-A42Y-10 chr23:3229353 C>T did not map to a codon.
Sequencing variant TCGA-2G-AAG3-01A-11D-A42Y-10 chr17:4445102 G>T maps to NM_001105538.1 G1057G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGX-01A-11D-A42Y-10 chr11:47365119 C>T maps to ENST00000399249 R382R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKM-01A-11D-A42Y-10 chr11:47355258 G>T maps to ENST00000399249 P1013P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAL5-01A-11D-A42Y-10 chr13:77672102 G>T maps to NM_015057.4 S3062S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94D-01A-11D-A435-10 chr13:77742670 G>T maps to NM_015057.4 T2002T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALW-01A-11D-A42Y-10 chr17:48585968 T>G maps to NM_032133.4 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA06-01A-12D-A435-10 chr17:48585968 T>G maps to NM_032133.4 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X3-A8G4-01A-11D-A435-10 chr17:10236458 G>T maps to NM_003802.2 V702V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM2-01A-11D-A435-10 chr19:50764814 G>T maps to NM_001145809.1 L836L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JY-01A-11D-A435-10 chr19:50760598 C>T maps to NM_001145809.1 D696D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JW-01A-11D-A435-10 chr17:10428648 G>T maps to NM_017534.5 L1518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA06-01A-12D-A435-10 chr17:10533024 G>T maps to NM_002470.2 T1895T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANI-01A-11D-A435-10 chr14:23874337 T>C did not map to a codon.
Sequencing variant TCGA-2G-AAFL-01A-21D-A42Y-10 chr17:18023050 G>T maps to ENST00000205890 E313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA06-01A-12D-A435-10 chr17:27437603 G>T maps to NM_078471.3 G979G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr19:8609309 G>A maps to NM_012335.3 C465C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1I-01A-11D-A435-10 chr15:52671829 G>A maps to ENST00000358212 L734L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH8-01A-11D-A42Y-10 chr11:76919802 G>T maps to NM_000260.3 V2002V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90P-01A-11D-A435-10 chr11:76913416 G>T maps to NM_000260.3 E1706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JY-01A-11D-A435-10 chr19:17316914 G>T maps to NM_004145.3 S1737S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGP-01A-11D-A42Y-10 chr11:17741613 G>T maps to NM_002478.4 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF8-01A-11D-A42Y-10 chr18:3173969 G>T maps to NM_003803.3 R380R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG8-01A-31D-A42Y-10 chr8:2000360 G>T maps to NM_003970.2 G65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H5-01A-11D-A435-10 chr1:24406586 G>A maps to ENST00000330966 G836G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFI-01A-21D-A42Y-10 chr10:69881407 A>G maps to NM_032578.2 E71E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFO-01A-31D-A42Y-10 chr4:40154442 G>T maps to NM_018177.3 T1729T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHP-01A-12D-A42Y-10 chr13:41894923 G>T maps to NM_024561.4 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOL-01A-11D-A435-10 chr11:89924797 C>A maps to NM_005467.3 I702I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A8S3-01B-11D-A435-10 chr11:89891356 C>T maps to NM_005467.3 R281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH2-01A-11D-A42Y-10 chr12:57112385 A>G maps to NM_001113203.1 G976G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHL-01A-11D-A42Y-10 chr12:57111377 A>G maps to NM_001113203.1 P1312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALT-01A-11D-A42Y-10 chr9:130829050 G>T maps to NM_197956.3 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90Q-01A-11D-A435-10 chr19:13988166 G>A maps to NM_001098622.1 E35E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFG-01A-11D-A42Y-10 chr23:92927245 G>C did not map to a codon.
Sequencing variant TCGA-XE-AANV-01A-11D-A435-10 chr23:92927834 G>T did not map to a codon.
Sequencing variant TCGA-XY-A8S2-01A-11D-A435-10 chr18:10526104 G>T maps to NM_003826.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr11:19914120 G>T maps to ENST00000396087 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANR-01A-11D-A435-10 chr2:15557680 G>A maps to NM_015909.2 D911D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V3-01A-11D-A435-10 chr3:47039153 G>T maps to NM_015175.1 G976G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHA-01A-11D-A42Y-10 chr1:19981663 C>T maps to NM_182744.2 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGG-01A-11D-A42Y-10 chr1:148009434 A>T maps to ENST00000310701 G629G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A8S3-01B-11D-A435-10 chr1:148579687 C>G maps to NM_001170755.1 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM4-01A-11D-A435-10 chr17:41345206 C>T maps to NM_005899.3 T390T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-2G-AAFM-01A-11D-A42Y-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-XE-AAOJ-01A-12D-A435-10 chr12:6637350 C>T maps to NM_014865.3 C1052C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AAAL-01A-11D-A435-10 chr11:134027844 G>A maps to NM_015261.2 S1384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFV-01A-11D-A42Y-10 chr2:97033083 G>T maps to NM_015341.3 A657A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGV-01A-11D-A42Y-10 chr1:36026279 C>T maps to NM_001014839.1 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGS-01A-11D-A42Y-10 chr7:74202920 G>A maps to NM_000265.4 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALR-01A-21D-A42Y-10 chr22:37261053 G>T maps to NM_013416.3 E71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr3:48717113 G>T maps to NM_016453.2 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr2:24952605 G>A maps to NM_003743.4 R1041R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAEW-01A-11D-A42Y-10 chr20:46264897 A>C maps to NM_181659.2 R590R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1H-01A-11D-A435-10 chr20:46279844 G>A maps to NM_181659.2 Q1257Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SB-A76C-01A-11D-A435-10 chr20:44690956 A>G maps to NM_020967.2 S574S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AE-01A-11D-A435-10 chr20:33345722 C>T maps to NM_014071.2 Q276Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A8D5-01A-11D-A435-10 chr6:126249821 G>T maps to NM_181782.4 G912*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGF-01A-31D-A42Y-10 chr12:124887101 C>T maps to NM_006312.4 Q496Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAL7-01A-11D-A42Y-10 chr12:124887101 C>T maps to NM_006312.4 Q496Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90W-01A-11D-A435-10 chr12:124887101 C>T maps to NM_006312.4 Q496Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X3-A8G4-01A-11D-A435-10 chr16:15790696 C>T maps to NM_001143979.1 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A8S3-01B-11D-A435-10 chr13:80055400 C>T maps to NM_019080.2 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGA-01A-11D-A42Y-10 chr9:140109563 G>A maps to NM_001144026.1 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGJ-01A-11D-A42Y-10 chr23:43817790 G>C did not map to a codon.
Sequencing variant TCGA-2G-AAGP-01A-11D-A42Y-10 chr20:35284910 G>A maps to ENST00000373803 Q295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr5:149932836 T>G maps to NM_001543.4 Y864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH8-01A-11D-A42Y-10 chr4:115751038 G>T maps to NM_022569.1 P802P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAL7-01A-11D-A42Y-10 chr19:19638551 C>A maps to ENST00000436926 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AC-01A-11D-A435-10 chr12:57629359 G>T maps to NM_020142.3 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W4-A7U4-01A-12D-A435-10 chr20:32247748 G>T maps to NM_031232.3 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A8S2-01A-11D-A435-10 chr18:56057875 A>G did not map to a codon.
Sequencing variant TCGA-2G-AAF4-01A-11D-A42Y-10 chr8:24814107 A>G did not map to a codon.
Sequencing variant TCGA-SN-A84W-01A-11D-A435-10 chr15:75646086 A>G maps to NM_024608.2 K242K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGZ-01A-11D-A42Y-10 chr3:27350471 G>T maps to ENST00000396636 R221R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFO-01A-31D-A42Y-10 chr10:5454762 C>A maps to NM_001047160.1 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHA-01A-11D-A42Y-10 chr16:47163243 A>G maps to NM_018092.3 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGC-01A-21D-A42Y-10 chr11:74716882 A>G maps to NM_006656.5 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94I-01A-11D-A435-10 chr17:7224485 G>T maps to NM_032442.2 S1102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG9-01A-11D-A42Y-10 chr17:37761787 C>T maps to NM_006160.3 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFH-01A-12D-A42Y-10 chr17:29496938 C>T maps to NM_001042492.2 D170D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFZ-01A-11D-A42Y-10 chr16:68119616 G>A maps to NM_173165.2 E11E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGW-01A-11D-A42Y-10 chr14:24841658 A>C maps to NM_001136022.1 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALO-01A-12D-A42Y-10 chr9:14116324 T>A maps to ENST00000397581 V422V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0H-01A-11D-A435-10 chr19:13192669 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAGK-01A-11D-A42Y-10 chr19:39390768 G>T maps to NM_002503.3 G33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOC-01A-11D-A435-10 chr3:101572305 T>C maps to NM_031419.3 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90Y-01A-11D-A435-10 chr1:116383280 C>A did not map to a codon.
Sequencing variant TCGA-2G-AAG9-01A-11D-A42Y-10 chr5:177576722 T>G maps to NM_017838.3 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG9-01A-11D-A42Y-10 chr23:17745673 G>T did not map to a codon.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr23:17750308 G>A did not map to a codon.
Sequencing variant TCGA-VF-A8AA-01A-11D-A435-10 chr23:17750308 G>A did not map to a codon.
Sequencing variant TCGA-2G-AAF8-01A-11D-A42Y-10 chr9:95888706 G>A maps to NM_004148.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFY-01A-11D-A42Y-10 chr20:25439018 C>T maps to NM_025176.4 R1281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGP-01A-11D-A42Y-10 chr6:28228081 T>C maps to NM_001007531.1 Y311Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2X-A9D6-01A-11D-A435-10 chr19:45656857 G>T maps to NM_198478.3 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SO-A8JP-01A-11D-A435-10 chr19:45661942 G>T maps to NM_198478.3 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH4-01A-12D-A42Y-10 chr23:118724146 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAFH-01A-12D-A42Y-10 chr14:36988466 G>T maps to NM_001079668.2 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG0-01A-11D-A42Y-10 chr14:36988451 C>T maps to NM_001079668.2 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALT-01A-11D-A42Y-10 chr14:37050567 G>T maps to NM_014360.2 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V5-01A-11D-A435-10 chr17:7311729 C>T maps to NM_020795.2 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH3-01A-11D-A42Y-10 chr23:70387351 A>C did not map to a codon.
Sequencing variant TCGA-XE-AAOD-01A-11D-A435-10 chr24:16953086 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAGI-01A-11D-A42Y-10 chr5:65108214 A>T maps to NM_020726.4 P659P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOJ-01A-12D-A435-10 chr2:32476308 G>T maps to NM_021209.4 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AAAL-01A-11D-A435-10 chr17:5440171 G>T maps to NM_033004.3 R987R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JY-01A-11D-A435-10 chr17:5436696 C>A maps to NM_033004.3 A1020A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr17:5461936 C>T maps to NM_033004.3 R693R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFN-01A-31D-A42Y-10 chr11:7081205 G>T maps to NM_176822.3 L905L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1I-01A-11D-A435-10 chr19:56515189 G>A maps to NM_153447.4 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF1-01A-11D-A42Y-10 chr11:281437 A>G maps to NM_138329.1 S568S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALF-01A-11D-A42Y-10 chr11:281494 C>T maps to NM_138329.1 P587P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKG-01A-11D-A42Y-10 chr16:4519317 G>A maps to NM_020677.3 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A8S2-01A-11D-A435-10 chr17:43173563 A>T maps to NM_021079.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANI-01A-11D-A435-10 chr10:15174828 G>T maps to ENST00000378143 R267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90W-01A-11D-A435-10 chr10:15210587 C>T maps to ENST00000378143 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALY-01A-11D-A42Y-10 chr7:30491537 G>T maps to NM_006092.2 R499R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOL-01A-11D-A435-10 chr9:95077300 G>A maps to NM_017948.5 R536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H1-01A-11D-A435-10 chr4:2949326 G>T maps to NM_003703.1 G475G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALP-01A-12D-A42Y-10 chr12:117657987 A>G maps to ENST00000338101 C1388C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr17:26125769 T>C maps to NM_000625.4 K22K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG5-01A-11D-A42Y-10 chr7:150706578 G>T maps to NM_000603.4 R806R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84W-01A-11D-A435-10 chr19:50060500 G>T maps to NM_015953.3 Y88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALS-01A-12D-A42Y-10 chr9:139405667 G>A maps to NM_017617.3 G841G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr9:139399282 G>T maps to NM_017617.3 Y1620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AE-01A-11D-A435-10 chr9:139412616 G>T maps to NM_017617.3 C409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOD-01A-11D-A435-10 chr9:139407985 G>T maps to NM_017617.3 Y737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHG-01A-11D-A42Y-10 chr1:120458444 G>T maps to NM_024408.2 P2300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO4-01A-11D-A435-10 chr1:120468322 C>T maps to NM_024408.2 R1372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOD-01A-11D-A435-10 chr19:15296449 G>A maps to NM_000435.2 S664S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALY-01A-11D-A42Y-10 chr23:100105255 A>G did not map to a codon.
Sequencing variant TCGA-XE-AANI-01A-11D-A435-10 chr8:53852979 G>T maps to NM_005285.3 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A6IS-01A-11D-A435-10 chr20:62738007 C>T maps to NM_005286.2 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AA-01A-11D-A435-10 chr18:21134852 C>T maps to NM_000271.4 P474P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF6-01A-11D-A42Y-10 chr10:72014844 C>T maps to ENST00000277942 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AE-01A-11D-A435-10 chr10:72015063 C>T maps to ENST00000277942 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr1:179533848 A>G maps to NM_014625.2 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0E-01A-12D-A435-10 chr8:21891642 G>T maps to NM_182795.1 E130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AB-01A-31D-A435-10 chr5:32712262 G>A maps to ENST00000265074 K127K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr23:30326686 G>C did not map to a codon.
Sequencing variant TCGA-4K-AA1I-01A-11D-A435-10 chr19:50881646 C>T maps to NM_007121.4 C141C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H1-01A-11D-A435-10 chr19:50885774 G>T maps to NM_007121.4 V433V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr1:161202703 G>T maps to NM_001077482.1 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94D-01A-11D-A435-10 chr1:161200618 G>T maps to NM_001077482.1 R310R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1G-01A-11D-A435-10 chr15:72106455 G>T maps to NM_014249.2 V366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO6-01A-31D-A435-10 chr4:149356893 A>G maps to ENST00000511528 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGI-01A-11D-A42Y-10 chr10:115383356 T>C maps to ENST00000369358 K804K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKL-01A-11D-A42Y-10 chr10:115423605 C>A maps to ENST00000369358 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALS-01A-12D-A42Y-10 chr7:107815785 A>G maps to ENST00000379032 P1056P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANR-01A-11D-A435-10 chr1:52255290 G>T maps to NM_002525.2 V1137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr2:50724691 G>A maps to ENST00000404971 G926G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A8S3-01B-11D-A435-10 chr11:64375420 C>T maps to NM_015080.3 T1462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHL-01A-11D-A42Y-10 chr5:176638276 A>T maps to NM_022455.4 G959G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A6IS-01A-11D-A435-10 chr20:1447418 G>T maps to ENST00000476071 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA06-01A-12D-A435-10 chr20:1424504 G>T maps to ENST00000476071 A336A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84X-01A-11D-A435-10 chr8:59571854 G>T maps to NM_001144772.1 I17I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGF-01A-31D-A42Y-10 chr2:18765887 G>C maps to ENST00000455492 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHC-01A-11D-A42Y-10 chr12:104190746 G>T maps to NM_001031701.2 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFM-01A-11D-A42Y-10 chr16:2097799 G>A maps to NM_002528.5 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0H-01A-11D-A435-10 chr1:107866929 G>A maps to NM_001113226.1 E91E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr1:156846299 G>T maps to NM_002529.3 E581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90P-01A-11D-A435-10 chr16:1838171 G>T maps to NM_012225.2 E212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFO-01A-31D-A42Y-10 chr23:51075766 T>A did not map to a codon.
Sequencing variant TCGA-2G-AAHG-01A-11D-A42Y-10 chr23:51076023 G>A did not map to a codon.
Sequencing variant TCGA-2G-AAL5-01A-11D-A42Y-10 chr23:51076023 G>A did not map to a codon.
Sequencing variant TCGA-2G-AALR-01A-21D-A42Y-10 chr23:51075900 G>A did not map to a codon.
Sequencing variant TCGA-S6-A8JX-01A-11D-A435-10 chr23:51076023 G>A did not map to a codon.
Sequencing variant TCGA-VF-A8AE-01A-11D-A435-10 chr23:51076094 C>A did not map to a codon.
Sequencing variant TCGA-ZM-AA0D-01A-11D-A435-10 chr23:51075900 G>A did not map to a codon.
Sequencing variant TCGA-SN-A84Y-01A-11D-A435-10 chr14:105639423 G>T maps to NM_177533.3 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A8S3-01B-11D-A435-10 chr16:4743825 C>T maps to NM_032349.3 Y33Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALP-01A-12D-A42Y-10 chr1:145586678 C>A maps to NM_001012758.2 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAEW-01A-11D-A42Y-10 chr19:41173906 C>T maps to NM_004756.3 Q432Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHL-01A-11D-A42Y-10 chr12:69135739 G>T maps to NM_020401.2 E884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA05-01A-12D-A435-10 chr7:135291661 A>G maps to NM_015135.2 P1023P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGY-01A-11D-A42Y-10 chr3:13373824 C>T maps to NM_024923.2 S1301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOC-01A-11D-A435-10 chr17:73208157 G>T did not map to a codon.
Sequencing variant TCGA-2G-AALP-01A-12D-A42Y-10 chr16:56855495 C>T maps to NM_014669.3 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO4-01A-11D-A435-10 chr1:224514121 G>T maps to NM_002533.2 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO4-01A-11D-A435-10 chr19:16860653 T>C maps to ENST00000438489 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr23:108784833 G>A did not map to a codon.
Sequencing variant TCGA-SB-A6J6-01A-11D-A435-10 chr14:24878058 G>A maps to NM_025081.2 G353G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALW-01A-11D-A42Y-10 chr12:113376379 G>T maps to NM_006187.2 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF8-01A-11D-A42Y-10 chr1:228468318 C>T maps to NM_001098623.1 P2673P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG3-01A-11D-A42Y-10 chr1:228465294 G>T did not map to a codon.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr1:228529820 G>T maps to NM_001098623.1 R6012R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V4-01A-11D-A435-10 chr1:228480320 G>T maps to NM_001098623.1 V3567V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A8S2-01A-11D-A435-10 chr1:228553856 C>T maps to NM_001098623.1 G6382G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AC-01A-11D-A435-10 chr2:220430189 G>T maps to NM_015311.2 T727T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALQ-01A-12D-A42Y-10 chr23:128691867 A>G did not map to a codon.
Sequencing variant TCGA-2G-AAFH-01A-12D-A42Y-10 chr9:131262419 C>T maps to NM_153435.1 S856S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFI-01A-21D-A42Y-10 chr22:50969175 G>T maps to NM_001014440.3 R216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGJ-01A-11D-A42Y-10 chr20:61436315 C>T maps to NM_007346.2 D35D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOB-01A-11D-A435-10 chr20:61443977 T>G maps to NM_007346.2 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF8-01A-11D-A42Y-10 chr3:9792838 G>T maps to NM_016821.2 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOD-01A-11D-A435-10 chr23:70793561 A>G did not map to a codon.
Sequencing variant TCGA-WZ-A8D5-01A-11D-A435-10 chr19:10024250 T>C did not map to a codon.
Sequencing variant TCGA-XE-AANI-01A-11D-A435-10 chr19:9965326 C>T maps to NM_058164.2 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFL-01A-21D-A42Y-10 chr1:114524090 C>T maps to NM_020190.2 D307D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOD-01A-11D-A435-10 chr21:34399700 C>T maps to NM_005806.2 Y177Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOB-01A-11D-A435-10 chr18:55103649 C>T maps to NM_004852.2 N234N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGT-01A-11D-A42Y-10 chr23:67333028 C>T did not map to a codon.
Sequencing variant TCGA-2G-AAFZ-01A-11D-A42Y-10 chr8:145113440 G>T maps to ENST00000360660 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHL-01A-11D-A42Y-10 chr8:145111361 G>T maps to ENST00000360660 R637R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGO-01A-11D-A42Y-10 chr6:154428664 G>A maps to NM_001145286.1 G410G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFZ-01A-11D-A42Y-10 chr11:123894600 G>T maps to NM_001001953.1 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AE-01A-11D-A435-10 chr1:158435623 C>A maps to NM_001004473.1 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG0-01A-11D-A42Y-10 chr11:123847414 G>A maps to NM_001004474.1 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V3-01A-11D-A435-10 chr1:247835617 G>T maps to NM_001005487.1 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOL-01A-11D-A435-10 chr17:3030494 G>T maps to ENST00000381953 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGP-01A-11D-A42Y-10 chr1:247614867 G>T maps to NM_001004492.1 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHC-01A-11D-A42Y-10 chr16:3406281 G>T maps to NM_012368.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALS-01A-12D-A42Y-10 chr16:3406386 C>T maps to NM_012368.2 C149C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAEW-01A-11D-A42Y-10 chr11:55110714 G>A maps to NM_001005274.1 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAEW-01A-11D-A42Y-10 chr11:55110738 G>A maps to NM_001005274.1 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALX-01A-11D-A42Y-10 chr11:55110714 G>A maps to NM_001005274.1 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1H-01A-11D-A435-10 chr11:5322648 G>A maps to NM_033179.2 C176C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AD-01A-11D-A435-10 chr11:5776662 C>T maps to NM_001005175.2 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84Y-01A-11D-A435-10 chr11:56409843 G>A maps to NM_001002925.1 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH8-01A-11D-A42Y-10 chr11:58126035 G>T maps to NM_001005489.1 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AB-01A-31D-A435-10 chr11:55761333 G>T maps to NM_003697.1 I256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1H-01A-11D-A435-10 chr11:56237577 A>G maps to NM_001004742.1 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGT-01A-11D-A42Y-10 chr11:6816324 G>A maps to NM_003696.2 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X3-A8G4-01A-11D-A435-10 chr11:6816714 G>T maps to NM_003696.2 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SO-A8JP-01A-11D-A435-10 chr1:247875952 G>T maps to NM_001005286.1 Y35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A6IS-01A-11D-A435-10 chr11:123624887 G>T maps to NM_001005188.1 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AC-01A-11D-A435-10 chr19:9226016 C>T maps to ENST00000293614 W141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF8-01A-11D-A42Y-10 chr11:124179873 A>G maps to NM_001002917.1 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGA-01A-11D-A42Y-10 chr7:102087324 C>T maps to NM_032831.2 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGC-01A-21D-A42Y-10 chr22:31266594 G>T maps to NM_030758.3 E345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0B-01A-11D-A435-10 chr22:31091148 G>T maps to NM_030758.3 E85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG9-01A-11D-A42Y-10 chr3:32022632 A>C maps to NM_017784.4 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SB-A76C-01A-11D-A435-10 chr2:26689999 G>T maps to NM_194248.2 S1443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALZ-01A-11D-A42Y-10 chr4:4204287 G>T maps to NM_177998.1 S206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHN-01A-11D-A42Y-10 chr23:48781268 C>T did not map to a codon.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr14:57268935 G>T maps to NM_021728.2 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG6-01A-11D-A42Y-10 chr1:111957532 C>T maps to ENST00000369728 Q594Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGW-01A-11D-A42Y-10 chr1:111957532 C>T maps to ENST00000369728 Q594Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALG-01A-11D-A42Y-10 chr1:111957532 C>T maps to ENST00000369728 Q594Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2X-A9D5-01A-11D-A435-10 chr1:111957532 C>T maps to ENST00000369728 Q594Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr1:111957532 C>T maps to ENST00000369728 Q594Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94D-01A-11D-A435-10 chr1:111957532 C>T maps to ENST00000369728 Q594Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2X-A9D6-01A-11D-A435-10 chr20:18037393 G>T maps to NM_021220.2 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0N-01A-21D-A435-10 chr14:23239417 G>A maps to NM_005015.3 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr1:40235514 G>T maps to NM_022120.1 A471A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANR-01A-11D-A435-10 chr12:121605292 C>T maps to NM_002562.5 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr23:69478691 G>T did not map to a codon.
Sequencing variant TCGA-YU-A94D-01A-11D-A435-10 chr23:1584417 T>C did not map to a codon.
Sequencing variant TCGA-XE-AAO3-01A-11D-A435-10 chr10:74768045 G>T maps to NM_000917.3 S513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF4-01A-11D-A42Y-10 chr12:56500420 G>T maps to NM_006191.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94I-01A-11D-A435-10 chr12:56505267 C>T maps to NM_006191.2 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKD-01A-31D-A42Y-10 chr13:25671121 C>T maps to NM_030979.2 Y262Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG9-01A-11D-A42Y-10 chr14:105834424 G>T maps to ENST00000458164 E201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AB-01A-31D-A435-10 chr1:17431435 G>T maps to NM_007365.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AB-01A-31D-A435-10 chr1:17431514 G>T maps to NM_007365.2 S45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr1:17718620 G>A maps to NM_207421.3 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG5-01A-11D-A42Y-10 chr19:39880018 G>A maps to NM_019088.2 Q122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr4:57316792 G>T maps to NM_001079525.1 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKD-01A-31D-A42Y-10 chr5:43539097 T>C maps to NM_006451.4 K258K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A8D5-01A-11D-A435-10 chr5:138700432 G>A did not map to a codon.
Sequencing variant TCGA-XE-A8H4-01A-31D-A435-10 chr23:110385386 T>G did not map to a codon.
Sequencing variant TCGA-2G-AAGJ-01A-11D-A42Y-10 chr16:23614908 G>A maps to NM_024675.3 L1144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHL-01A-11D-A42Y-10 chr4:169632801 T>C maps to NM_001166108.1 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF1-01A-11D-A42Y-10 chr9:112899360 A>T maps to NM_007203.4 K513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH0-01A-11D-A42Y-10 chr20:3888897 G>A maps to NM_153638.2 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANR-01A-11D-A435-10 chr5:167995710 C>T maps to NM_024594.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X3-A8G4-01A-11D-A435-10 chr14:73727425 C>T maps to ENST00000427855 C665C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGZ-01A-11D-A42Y-10 chr1:176671867 C>G maps to NM_020318.2 S1121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AA-01A-11D-A435-10 chr10:89473068 T>A did not map to a codon.
Sequencing variant TCGA-2G-AALF-01A-11D-A42Y-10 chr16:3021897 C>T maps to NM_152341.3 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG0-01A-11D-A42Y-10 chr7:139756946 G>A maps to NM_022750.2 Q157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGP-01A-11D-A42Y-10 chr3:122255024 C>G maps to NM_031458.2 S725S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGG-01A-11D-A42Y-10 chr11:59425074 G>A maps to NM_152716.2 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH0-01A-11D-A42Y-10 chr20:21687361 C>A maps to NM_006192.3 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALP-01A-12D-A42Y-10 chr20:21689975 G>T maps to NM_006192.3 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOD-01A-11D-A435-10 chr11:31816307 T>C maps to NM_001604.4 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHC-01A-11D-A42Y-10 chr2:113992972 G>T maps to NM_003466.3 S362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH2-01A-11D-A42Y-10 chr7:154738433 G>A maps to NM_007349.3 S1004S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFH-01A-12D-A42Y-10 chr3:52677349 G>T maps to ENST00000296302 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGJ-01A-11D-A42Y-10 chr6:32156159 T>A maps to NM_002586.4 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84X-01A-11D-A435-10 chr6:32157665 G>A maps to NM_002586.4 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGE-01A-21D-A42Y-10 chr11:66639223 G>T maps to NM_022172.2 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOD-01A-11D-A435-10 chr12:53865576 T>G maps to NM_005016.5 Y350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH2-01A-11D-A42Y-10 chr13:100959514 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAGF-01A-31D-A42Y-10 chr4:134072953 G>T maps to NM_032961.1 A553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGC-01A-21D-A42Y-10 chr5:141335640 G>T maps to NM_016580.2 I592I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr10:55568541 G>T maps to NM_001142769.1 G1761G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFN-01A-31D-A42Y-10 chr4:138450830 A>G maps to NM_019035.3 S804S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0H-01A-11D-A435-10 chr4:138452612 T>G maps to NM_019035.3 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGE-01A-21D-A42Y-10 chr5:140167608 T>C maps to NM_018900.2 S578S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AC-01A-11D-A435-10 chr5:140263826 G>T maps to NM_018904.2 A658A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGW-01A-11D-A42Y-10 chr5:140182665 G>T maps to NM_018906.2 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANJ-01A-11D-A435-10 chr5:140209499 G>T maps to NM_018909.2 S608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOL-01A-11D-A435-10 chr5:140209478 A>G maps to NM_018909.2 S601S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAEW-01A-11D-A42Y-10 chr5:140573921 C>T maps to NM_018930.3 N599N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALX-01A-11D-A42Y-10 chr5:140573921 C>T maps to NM_018930.3 N599N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H1-01A-11D-A435-10 chr5:140573921 C>T maps to NM_018930.3 N599N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H4-01A-31D-A435-10 chr5:140573921 C>T maps to NM_018930.3 N599N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF8-01A-11D-A42Y-10 chr5:140595251 G>T maps to NM_018933.2 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOB-01A-11D-A435-10 chr5:140594282 G>A maps to NM_018933.2 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOF-01A-11D-A435-10 chr5:140605293 G>A maps to NM_018934.2 V739V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-AA61-01A-11D-A435-10 chr5:140503154 G>T maps to NM_018938.2 A525A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG9-01A-11D-A42Y-10 chr5:140553993 G>T maps to NM_018940.2 A526A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGM-01A-11D-A42Y-10 chr5:140553993 G>T maps to NM_018940.2 A526A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH4-01A-12D-A42Y-10 chr5:140559195 G>T maps to NM_019120.2 A527A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG9-01A-11D-A42Y-10 chr5:140811891 C>A maps to NM_003735.2 Y522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGT-01A-11D-A42Y-10 chr5:140812464 G>A maps to NM_003735.2 A713A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGY-01A-11D-A42Y-10 chr5:140773213 A>T maps to NM_032088.1 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOD-01A-11D-A435-10 chr4:727492 G>T maps to NM_006315.4 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALP-01A-12D-A42Y-10 chr10:105110538 C>T maps to NM_001011663.1 E95E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOC-01A-11D-A435-10 chr20:56137902 T>C maps to NM_002591.3 D186D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH2-01A-11D-A42Y-10 chr14:24566125 T>C maps to NM_004563.2 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H1-01A-11D-A435-10 chr14:24567816 G>T maps to NM_004563.2 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOC-01A-11D-A435-10 chr7:82583011 T>G maps to NM_033026.5 P2419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALY-01A-11D-A42Y-10 chr21:47810694 G>A maps to NM_006031.5 K1317K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFM-01A-11D-A42Y-10 chr15:101922322 A>T maps to NM_002570.3 C501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGE-01A-21D-A42Y-10 chr23:24665185 C>T did not map to a codon.
Sequencing variant TCGA-VF-A8AC-01A-11D-A435-10 chr23:24605359 G>T did not map to a codon.
Sequencing variant TCGA-VF-A8AE-01A-11D-A435-10 chr10:105174893 G>T maps to NM_014976.1 E502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA06-01A-12D-A435-10 chr11:775092 G>T maps to NM_182612.2 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84Y-01A-11D-A435-10 chr11:72299853 G>A maps to NM_002599.3 C348C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr12:20769228 C>G maps to NM_000921.3 T445T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHG-01A-11D-A42Y-10 chr11:14666436 G>T maps to NM_000922.3 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGV-01A-11D-A42Y-10 chr19:10563984 C>T maps to NM_006202.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A9SE-01A-21D-A435-10 chr17:79620320 C>T maps to ENST00000331056 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A9T9-01A-11D-A435-10 chr11:103814198 G>T maps to NM_025208.4 Y251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGW-01A-11D-A42Y-10 chr5:149502624 G>T maps to NM_002609.3 P721P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALO-01A-12D-A42Y-10 chr5:149512313 G>T maps to NM_002609.3 R376R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SB-A6J6-01A-11D-A435-10 chr23:19369426 G>A did not map to a codon.
Sequencing variant TCGA-X3-A8G4-01A-11D-A435-10 chr7:95225506 G>A maps to NM_002612.3 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH4-01A-12D-A42Y-10 chr10:97006972 T>C maps to NM_020992.2 K228K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0D-01A-11D-A435-10 chr10:97006972 T>C maps to NM_020992.2 K228K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2X-A9D5-01A-11D-A435-10 chr16:66918753 G>A maps to NM_020786.2 W189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOC-01A-11D-A435-10 chr13:33222914 T>C maps to ENST00000400481 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALT-01A-11D-A42Y-10 chr13:28494403 G>C maps to NM_000209.3 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr5:32098546 C>T maps to NM_178140.2 N2675N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALF-01A-11D-A42Y-10 chr23:153071021 C>T did not map to a codon.
Sequencing variant TCGA-WZ-A8D5-01A-11D-A435-10 chr23:153069640 G>A did not map to a codon.
Sequencing variant TCGA-2G-AAHT-01A-11D-A42Y-10 chr11:66241454 T>C did not map to a codon.
Sequencing variant TCGA-2G-AAGA-01A-11D-A42Y-10 chr17:4575678 T>C maps to ENST00000301396 G1013G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALF-01A-11D-A42Y-10 chr17:17480329 G>A maps to NM_148172.1 C36C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGP-01A-11D-A42Y-10 chr1:7902772 G>A maps to ENST00000377532 A1197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JY-01A-11D-A435-10 chr1:160254905 G>T maps to NM_002857.3 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGO-01A-11D-A42Y-10 chr22:18568022 A>G maps to NM_017929.5 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W4-A7U2-01A-11D-A435-10 chr12:7354886 C>T maps to NM_001131023.1 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOD-01A-11D-A435-10 chr10:3161040 C>T maps to NM_002627.3 L504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V4-01A-11D-A435-10 chr12:133291444 C>T maps to NM_001170543.1 R65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALG-01A-11D-A42Y-10 chr10:50724863 A>G maps to ENST00000515869 P567P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANJ-01A-11D-A435-10 chr1:230503882 G>A maps to ENST00000321327 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGV-01A-11D-A42Y-10 chr1:10459761 G>T did not map to a codon.
Sequencing variant TCGA-XE-AANJ-01A-11D-A435-10 chr1:10464288 G>T maps to NM_002631.2 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AAAL-01A-11D-A435-10 chr17:76396832 C>A maps to NM_024419.3 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A8S2-01A-11D-A435-10 chr1:28793238 T>C maps to NM_023923.3 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM4-01A-11D-A435-10 chr1:33832792 C>T maps to ENST00000419414 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SB-A76C-01A-11D-A435-10 chr1:33796983 A>G maps to ENST00000419414 R657R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGG-01A-11D-A42Y-10 chr23:22208574 C>T did not map to a codon.
Sequencing variant TCGA-2G-AAHN-01A-11D-A42Y-10 chr5:133914248 C>T maps to ENST00000448712 Q599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH0-01A-11D-A42Y-10 chr23:46857585 G>T did not map to a codon.
Sequencing variant TCGA-2X-A9D6-01A-11D-A435-10 chr9:123631479 G>A maps to NM_015651.1 C198C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SO-A8JP-01A-11D-A435-10 chr9:96408039 G>T maps to NM_005392.3 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JY-01A-11D-A435-10 chr11:45955620 C>T maps to ENST00000257821 P648P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AE-01A-11D-A435-10 chr11:46001325 G>A maps to ENST00000257821 N115N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFO-01A-31D-A42Y-10 chr22:45279174 C>A maps to NM_138415.3 E463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHA-01A-11D-A42Y-10 chr17:7140046 G>T maps to NM_024297.2 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JW-01A-11D-A435-10 chr6:64423073 C>T maps to NM_015153.2 Q1864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr23:71829495 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAGN-01A-11D-A42Y-10 chr7:56148878 G>T maps to NM_006213.3 R344R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALR-01A-21D-A42Y-10 chr7:56155459 G>A maps to NM_006213.3 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A89B-01A-11D-A435-10 chr7:56148890 G>T maps to NM_006213.3 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAEX-01A-11D-A42Y-10 chr11:2950231 T>G maps to NM_003311.3 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALG-01A-11D-A42Y-10 chr17:47301802 G>A maps to NM_001143804.1 D228D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGX-01A-11D-A42Y-10 chr8:22079279 G>T maps to NM_014759.3 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH3-01A-11D-A42Y-10 chr8:22079279 G>T maps to NM_014759.3 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF6-01A-11D-A42Y-10 chr11:85685759 T>C maps to ENST00000393343 S653S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JW-01A-11D-A435-10 chr14:68066815 C>T maps to NM_004569.3 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF1-01A-11D-A42Y-10 chr9:35090664 A>G maps to NM_032634.2 P884P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H4-01A-31D-A435-10 chr16:626175 G>T maps to NM_148920.1 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V5-01A-11D-A435-10 chr17:26897966 C>A maps to NM_033198.3 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAEW-01A-11D-A42Y-10 chr20:44053177 C>A maps to NM_015937.4 A481A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AA-01A-11D-A435-10 chr11:17170257 G>A maps to NM_002645.2 G468G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGM-01A-11D-A42Y-10 chr1:204403712 G>A maps to NM_002646.3 S1180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGO-01A-11D-A42Y-10 chr17:8808103 G>T maps to NM_001142633.1 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO6-01A-31D-A435-10 chr17:8812423 G>T maps to NM_001142633.1 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG9-01A-11D-A42Y-10 chr23:48772440 T>G did not map to a codon.
Sequencing variant TCGA-2G-AAGM-01A-11D-A42Y-10 chr22:50356645 G>T maps to NM_001001852.3 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHN-01A-11D-A42Y-10 chr9:130689595 G>T maps to NM_001135219.1 R192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGI-01A-11D-A42Y-10 chr17:27380006 G>T maps to NM_016518.2 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H4-01A-31D-A435-10 chr17:65574358 G>T maps to NM_012417.2 G118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGC-01A-21D-A42Y-10 chr11:67259713 G>A maps to NM_004910.2 H1175H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A6IS-01A-11D-A435-10 chr12:123475098 G>A maps to NM_020845.2 I854I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGE-01A-21D-A42Y-10 chr17:6381974 G>T maps to NM_031220.3 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKO-01A-11D-A42Y-10 chr17:6358777 G>T maps to NM_031220.3 P935P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90W-01A-11D-A435-10 chr5:134364534 C>G maps to NM_002653.4 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFO-01A-31D-A42Y-10 chr16:2152492 C>T maps to NM_001009944.2 L3030L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SB-A6J6-01A-11D-A435-10 chr16:2160442 G>T maps to NM_001009944.2 G1575G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84W-01A-11D-A435-10 chr16:2165408 G>T maps to NM_001009944.2 S689S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO3-01A-11D-A435-10 chr16:2162856 C>T maps to NM_001009944.2 L1031L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHT-01A-11D-A42Y-10 chr16:81253924 G>T maps to NM_052892.3 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H4-01A-31D-A435-10 chr4:88964594 G>T maps to NM_000297.2 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFJ-01A-11D-A42Y-10 chr10:102052769 C>T maps to NM_016112.2 V605V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALZ-01A-11D-A42Y-10 chr22:46658493 G>A maps to NM_006071.1 N242N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF4-01A-11D-A42Y-10 chr8:110374853 G>A maps to ENST00000426474 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84Y-01A-11D-A435-10 chr8:110422125 T>C maps to ENST00000426474 T668T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90S-01A-11D-A435-10 chr9:131467790 C>A maps to NM_013355.3 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr2:159499038 G>T maps to NM_003628.3 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr19:48607858 G>T maps to NM_003706.2 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A8S2-01A-11D-A435-10 chr15:42446573 G>A maps to ENST00000397272 C89C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGZ-01A-11D-A42Y-10 chr22:38565262 G>A maps to NM_003560.2 C57C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84Y-01A-11D-A435-10 chr12:113826310 C>T maps to NM_173542.3 S550S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANJ-01A-11D-A435-10 chr15:40580987 G>T maps to NM_004573.2 C1162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF8-01A-11D-A42Y-10 chr17:43194019 G>T maps to NM_133373.3 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGF-01A-31D-A42Y-10 chr17:43195378 C>A maps to NM_133373.3 V414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-AA4L-01A-11D-A435-10 chr1:2418771 C>T maps to NM_014638.2 D357D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFY-01A-11D-A42Y-10 chr17:17109306 C>A maps to NM_178836.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1H-01A-11D-A435-10 chr8:144992666 G>T maps to NM_201380.2 P3911P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO6-01A-31D-A435-10 chr8:144992765 C>T maps to NM_201380.2 R3878R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-AA4L-01A-11D-A435-10 chr8:144996005 G>T maps to NM_201380.2 A2798A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SO-A8JP-01A-11D-A435-10 chr7:30129788 T>G maps to NM_032639.3 *441G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGT-01A-11D-A42Y-10 chr14:68024066 G>T maps to NM_020715.2 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALF-01A-11D-A42Y-10 chr1:909349 A>G maps to ENST00000379409 G576G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H5-01A-11D-A435-10 chr15:65153710 G>T maps to NM_025201.4 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFH-01A-12D-A42Y-10 chr19:4531720 G>T maps to NM_001013706.2 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1G-01A-11D-A435-10 chr1:45266603 G>A maps to NM_004073.2 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr3:145788626 G>T maps to NM_182943.2 C718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG0-01A-11D-A42Y-10 chr3:126734046 G>T maps to NM_032242.3 V966V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V3-01A-11D-A435-10 chr7:131817900 G>T maps to NM_020911.1 Y1832*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGJ-01A-11D-A42Y-10 chr3:48461312 C>T maps to NM_001130082.1 P794P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALX-01A-11D-A42Y-10 chr3:48454324 G>T maps to NM_001130082.1 G1560G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AAAL-01A-11D-A435-10 chr22:50727514 G>A maps to NM_012401.2 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGI-01A-11D-A42Y-10 chr23:153039473 A>C did not map to a codon.
Sequencing variant TCGA-2G-AAGW-01A-11D-A42Y-10 chr3:129325110 G>T maps to NM_015103.2 Y124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V3-01A-11D-A435-10 chr1:205814016 C>T maps to NM_152491.4 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H1-01A-11D-A435-10 chr15:74327859 G>A maps to NM_033239.2 W686*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGM-01A-11D-A42Y-10 chr7:6017230 G>T maps to NM_000535.5 A811A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr7:6026589 G>T maps to NM_000535.5 A602A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFG-01A-11D-A42Y-10 chr23:152939603 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAG5-01A-11D-A42Y-10 chr10:118386475 G>T maps to NM_005396.4 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGE-01A-21D-A42Y-10 chr23:152226010 A>G did not map to a codon.
Sequencing variant TCGA-ZM-AA06-01A-12D-A435-10 chr23:152226010 A>G did not map to a codon.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr23:152159583 G>T did not map to a codon.
Sequencing variant TCGA-X3-A8G4-01A-11D-A435-10 chr19:46998784 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAGV-01A-11D-A42Y-10 chr14:39644507 C>T maps to NM_002687.3 Q9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFY-01A-11D-A42Y-10 chr23:7868820 A>G did not map to a codon.
Sequencing variant TCGA-2G-AAGK-01A-11D-A42Y-10 chr23:7868820 A>G did not map to a codon.
Sequencing variant TCGA-2G-AAHA-01A-11D-A42Y-10 chr23:7868820 A>G did not map to a codon.
Sequencing variant TCGA-XE-AAO4-01A-11D-A435-10 chr23:7868820 A>G did not map to a codon.
Sequencing variant TCGA-YU-A90Q-01A-11D-A435-10 chr23:7868820 A>G did not map to a codon.
Sequencing variant TCGA-2G-AAFH-01A-12D-A42Y-10 chr19:7615463 C>T maps to NM_001166111.1 Q679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAEX-01A-11D-A42Y-10 chr9:140379045 G>A maps to NM_001098537.1 S780S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOB-01A-11D-A435-10 chr23:84634405 C>T did not map to a codon.
Sequencing variant TCGA-2G-AAGC-01A-21D-A42Y-10 chr1:151378738 C>T maps to NM_015100.3 P924P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGI-01A-11D-A42Y-10 chr23:24759593 G>T did not map to a codon.
Sequencing variant TCGA-XE-AAO4-01A-11D-A435-10 chr23:24833114 C>T did not map to a codon.
Sequencing variant TCGA-YU-A94I-01A-11D-A435-10 chr23:24751913 A>G did not map to a codon.
Sequencing variant TCGA-4K-AAAL-01A-11D-A435-10 chr19:50918214 C>T maps to ENST00000391817 V870V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHA-01A-11D-A42Y-10 chr11:74351711 A>G maps to NM_006591.1 K434K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKD-01A-31D-A42Y-10 chr2:113333029 G>T maps to NM_019014.4 A1044A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHG-01A-11D-A42Y-10 chr17:7407046 G>T maps to NM_000937.4 R1059R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0B-01A-11D-A435-10 chr17:7415173 G>T maps to NM_000937.4 L1382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOF-01A-11D-A435-10 chr11:62529310 C>T maps to NM_002696.2 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A8S2-01A-11D-A435-10 chr19:619020 G>T maps to NM_005035.3 P1081P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90Q-01A-11D-A435-10 chr7:72418900 G>A maps to ENST00000446813 P964P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGG-01A-11D-A42Y-10 chr7:53103897 G>T maps to NM_182595.3 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH8-01A-11D-A42Y-10 chr14:77769281 C>A maps to NM_013382.5 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFI-01A-21D-A42Y-10 chr7:94944671 G>T maps to NM_000446.5 S111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALP-01A-12D-A42Y-10 chr23:48372917 T>G did not map to a codon.
Sequencing variant TCGA-XE-AAOB-01A-11D-A435-10 chr23:48374125 G>T did not map to a codon.
Sequencing variant TCGA-XY-A89B-01A-11D-A435-10 chr23:48370300 C>T did not map to a codon.
Sequencing variant TCGA-ZM-AA0H-01A-11D-A435-10 chr2:132021541 C>T maps to NM_001083538.1 A838A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W4-A7U2-01A-11D-A435-10 chr14:19566035 C>T maps to NM_001005356.2 Y360Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0H-01A-11D-A435-10 chr19:42599533 G>A maps to ENST00000342301 F340F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGI-01A-11D-A42Y-10 chr11:120176444 G>A maps to NM_014352.2 K240K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM2-01A-11D-A435-10 chr10:71969412 A>G maps to NM_021129.3 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0B-01A-11D-A435-10 chr4:106367653 G>T maps to ENST00000357415 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM3-01A-11D-A435-10 chr4:23830065 G>T maps to NM_013261.3 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH3-01A-11D-A42Y-10 chr23:18845541 G>T did not map to a codon.
Sequencing variant TCGA-YU-A94D-01A-11D-A435-10 chr23:18845517 C>A did not map to a codon.
Sequencing variant TCGA-2G-AAGV-01A-11D-A42Y-10 chr12:42729725 G>T maps to NM_016488.6 E8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0B-01A-11D-A435-10 chr16:4934416 G>T maps to NM_002705.4 R1413R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94I-01A-11D-A435-10 chr17:58740736 A>T maps to NM_003620.3 K548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr17:56833453 G>A maps to NM_014906.3 E32E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHC-01A-11D-A42Y-10 chr19:38746834 G>T maps to NM_033256.1 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGT-01A-11D-A42Y-10 chr15:41108370 C>T maps to NM_001130143.1 W151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALG-01A-11D-A42Y-10 chr23:49142703 G>T did not map to a codon.
Sequencing variant TCGA-2G-AALP-01A-12D-A42Y-10 chr7:94539754 T>C maps to NM_001166160.1 D110D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOB-01A-11D-A435-10 chr19:52716239 C>A maps to NM_014225.5 C228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFV-01A-11D-A42Y-10 chr8:26217713 G>T maps to NM_001177591.1 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHA-01A-11D-A42Y-10 chr8:26217683 G>T did not map to a codon.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr8:26221300 G>T maps to NM_001177591.1 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG9-01A-11D-A42Y-10 chr23:306964 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAGZ-01A-11D-A42Y-10 chr10:103892851 C>T maps to NM_015062.3 D9D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H1-01A-11D-A435-10 chr10:103892978 G>T did not map to a codon.
Sequencing variant TCGA-WZ-A7V5-01A-11D-A435-10 chr6:32122904 G>T maps to NM_138717.1 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AA-01A-11D-A435-10 chr1:13474973 G>A maps to NM_001099850.1 H385H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALQ-01A-12D-A42Y-10 chr1:12921135 C>T maps to NM_023014.1 D309D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1I-01A-11D-A435-10 chr1:12921135 C>T maps to NM_023014.1 D309D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM4-01A-11D-A435-10 chr12:11506145 A>G maps to NM_005039.3 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG3-01A-11D-A42Y-10 chr12:11546213 T>G maps to NM_006248.3 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr12:11546003 A>T maps to NM_006248.3 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGZ-01A-11D-A42Y-10 chr12:11420651 C>T maps to NM_006249.4 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A89B-01A-11D-A435-10 chr12:11420720 A>G maps to NM_006249.4 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1G-01A-11D-A435-10 chr11:129772249 G>T maps to NM_020228.2 T1147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHT-01A-11D-A42Y-10 chr1:14105105 G>A maps to NM_012231.4 E272E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFY-01A-11D-A42Y-10 chr1:203453088 C>T maps to NM_201348.1 N259N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHP-01A-12D-A42Y-10 chr1:186276584 A>C maps to NM_005807.3 P578P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM4-01A-11D-A435-10 chr12:11035034 A>G maps to NM_006250.2 H100H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH2-01A-11D-A42Y-10 chr12:11083459 T>C maps to NM_001110213.1 H100H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKG-01A-11D-A42Y-10 chr3:64142836 C>A did not map to a codon.
Sequencing variant TCGA-2G-AALP-01A-12D-A42Y-10 chr23:49033371 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAFM-01A-11D-A42Y-10 chr7:624154 G>T maps to NM_002735.2 V253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO4-01A-11D-A435-10 chr11:6340566 G>T maps to NM_145040.2 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGT-01A-11D-A42Y-10 chr14:62016447 G>T maps to NM_006255.3 E651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHT-01A-11D-A42Y-10 chr10:6470240 G>T maps to NM_006257.2 I683I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH2-01A-11D-A42Y-10 chr19:11558369 G>A maps to ENST00000436195 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANI-01A-11D-A435-10 chr19:11546955 G>T maps to ENST00000436195 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A89B-01A-11D-A435-10 chr19:11558369 G>A maps to ENST00000436195 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90Y-01A-11D-A435-10 chr19:11558390 G>A maps to ENST00000436195 E329E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94I-01A-11D-A435-10 chr19:11558369 G>A maps to ENST00000436195 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0F-01A-21D-A435-10 chr19:11558369 G>A maps to ENST00000436195 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X3-A8G4-01A-11D-A435-10 chr19:47214194 G>A maps to ENST00000449438 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr8:48839865 G>T maps to NM_006904.6 G769G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A9T9-01A-11D-A435-10 chr8:48746931 C>G maps to NM_006904.6 L2658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90P-01A-11D-A435-10 chr1:214170541 C>T maps to NM_002763.3 Q222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JX-01A-11D-A435-10 chr13:113826049 C>A maps to ENST00000342783 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90S-01A-11D-A435-10 chr1:52876859 G>T maps to NM_032864.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr1:109238795 G>T maps to NM_018061.2 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGI-01A-11D-A42Y-10 chr17:74349754 C>T maps to NM_002766.2 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90S-01A-11D-A435-10 chr17:74349676 G>T maps to NM_002766.2 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF8-01A-11D-A42Y-10 chr19:42814215 C>G maps to NM_199285.2 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90Y-01A-11D-A435-10 chr19:5783885 G>T maps to NM_001134316.1 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO3-01A-11D-A435-10 chr16:855796 G>T maps to NM_001013638.1 G119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHC-01A-11D-A42Y-10 chr23:37312623 A>G did not map to a codon.
Sequencing variant TCGA-2G-AAGP-01A-11D-A42Y-10 chr4:119252935 T>G maps to NM_003619.3 G302G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84W-01A-11D-A435-10 chr9:33798036 T>C maps to NM_007343.3 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr16:31097417 G>T maps to NM_001039503.2 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHA-01A-11D-A42Y-10 chr19:40901936 C>A maps to NM_181882.2 V774V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALP-01A-12D-A42Y-10 chr2:113956424 G>T maps to NM_012455.2 R911R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr2:113953722 G>T did not map to a codon.
Sequencing variant TCGA-YU-A90S-01A-11D-A435-10 chr19:43699191 G>T maps to NM_002780.3 R315R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AE-01A-11D-A435-10 chr19:43411799 C>A maps to NM_002782.3 G305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AE-01A-11D-A435-10 chr16:67942634 G>T did not map to a codon.
Sequencing variant TCGA-ZM-AA06-01A-12D-A435-10 chr16:67969560 G>T maps to NM_002801.2 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-AA4L-01A-11D-A435-10 chr14:23504075 G>A maps to NM_002797.3 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA06-01A-12D-A435-10 chr14:90735758 T>G maps to NM_002802.2 G300G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALQ-01A-12D-A42Y-10 chr11:47445697 G>A maps to NM_002804.4 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AA-01A-11D-A435-10 chr19:6375400 C>A maps to NM_004158.2 R125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr1:45294671 C>A maps to NM_003738.4 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGY-01A-11D-A42Y-10 chr23:23398202 G>T did not map to a codon.
Sequencing variant TCGA-VF-A8AA-01A-11D-A435-10 chr23:23411680 C>G did not map to a codon.
Sequencing variant TCGA-2G-AAKG-01A-11D-A42Y-10 chr1:11580780 C>T maps to NM_020780.1 F746F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH4-01A-12D-A42Y-10 chr10:27702321 G>T maps to NM_001034842.3 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF8-01A-11D-A42Y-10 chr11:490431 G>A maps to NM_030783.1 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGS-01A-11D-A42Y-10 chr20:48166686 G>T maps to NM_000961.3 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOB-01A-11D-A435-10 chr1:186645691 G>T maps to NM_000963.2 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANJ-01A-11D-A435-10 chr6:43100168 C>T maps to NM_002821.3 D324D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr8:142437897 C>T maps to NM_032611.1 Y126Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM4-01A-11D-A435-10 chr11:47587434 G>T maps to NM_001143984.1 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH8-01A-11D-A42Y-10 chr18:12830953 C>T maps to NM_002828.2 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGY-01A-11D-A42Y-10 chr14:88945533 A>G maps to NM_007039.3 P747P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG9-01A-11D-A42Y-10 chr3:47447255 C>T maps to NM_015466.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGV-01A-11D-A42Y-10 chr9:8376060 T>C maps to NM_002839.3 R1512R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAEW-01A-11D-A42Y-10 chr1:44057117 G>T maps to NM_002840.3 V475V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFV-01A-11D-A42Y-10 chr1:44085235 G>T maps to NM_002840.3 E1642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO6-01A-31D-A435-10 chr1:44057099 G>A maps to NM_002840.3 A469A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr18:7774225 G>T maps to NM_001105244.1 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALN-01A-11D-A42Y-10 chr7:121682712 G>A maps to NM_002851.2 Q1951Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84W-01A-11D-A435-10 chr17:40556821 G>T maps to NM_012232.5 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAL7-01A-11D-A42Y-10 chr16:1537644 G>T maps to NM_001013658.1 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A6IS-01A-11D-A435-10 chr8:144899806 G>T maps to NM_078480.1 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO4-01A-11D-A435-10 chr1:31441218 G>A maps to ENST00000373741 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SO-A8JP-01A-11D-A435-10 chr5:139494332 G>A maps to NM_005859.4 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKO-01A-11D-A42Y-10 chr8:30889695 G>T maps to NM_013357.2 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1I-01A-11D-A435-10 chr2:61238920 T>G maps to NM_144709.2 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANV-01A-11D-A435-10 chr5:159546148 C>A maps to NM_001130864.1 E83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAL7-01A-11D-A42Y-10 chr2:1677520 G>T maps to NM_012293.1 I304I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0B-01A-11D-A435-10 chr2:1653130 G>T maps to NM_012293.1 T807T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH3-01A-11D-A42Y-10 chr12:133277882 G>A maps to NM_018663.1 W149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H1-01A-11D-A435-10 chr20:32307917 G>T maps to NM_007238.4 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGF-01A-31D-A42Y-10 chr8:144687881 G>T maps to NM_023078.3 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr11:64521404 C>T maps to NM_005609.2 T395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGP-01A-11D-A42Y-10 chr17:42030830 C>T maps to NM_004160.4 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOD-01A-11D-A435-10 chr3:49139868 G>A maps to NM_005051.1 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SO-A8JP-01A-11D-A435-10 chr4:122261655 A>G maps to NM_198179.2 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALT-01A-11D-A42Y-10 chr3:113798887 G>T maps to ENST00000485050 P306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGS-01A-11D-A42Y-10 chr17:29761076 G>T maps to NM_032932.3 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGX-01A-11D-A42Y-10 chr12:72148935 C>G maps to NM_014999.2 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHN-01A-11D-A42Y-10 chr22:23503702 G>T maps to NM_004914.2 P318P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-VF-A8AB-01A-31D-A435-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-XE-AAO6-01A-31D-A435-10 chr1:220340991 C>T maps to ENST00000358951 K944K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH3-01A-11D-A42Y-10 chr11:61669972 G>T maps to NM_013401.2 R314R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90Y-01A-11D-A435-10 chr11:61675531 C>T maps to NM_013401.2 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90W-01A-11D-A435-10 chr17:5212058 T>C maps to NM_004703.4 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGO-01A-11D-A42Y-10 chr16:28925901 A>C maps to NM_024816.2 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALR-01A-21D-A42Y-10 chr16:28925601 G>T maps to NM_024816.2 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A9SE-01A-21D-A435-10 chr9:127996189 T>C maps to NM_005833.3 C350C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA05-01A-12D-A435-10 chr17:79991662 G>T maps to NM_005052.2 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr12:1025812 G>A maps to NM_134424.2 C239C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHN-01A-11D-A42Y-10 chr7:4845283 G>A maps to NM_018059.4 L735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AD-01A-11D-A435-10 chr7:4874813 G>T maps to NM_018059.4 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKL-01A-11D-A42Y-10 chr17:17697104 G>A maps to ENST00000395776 Q281Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V5-01A-11D-A435-10 chr17:17697104 G>A maps to ENST00000395776 Q281Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGP-01A-11D-A42Y-10 chr23:17819966 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAG0-01A-11D-A42Y-10 chr9:135984156 G>T maps to NM_006266.2 Y227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG9-01A-11D-A42Y-10 chr20:32664876 C>T maps to NM_016732.1 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHA-01A-11D-A42Y-10 chr20:32664876 C>T maps to NM_016732.1 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2X-A9D6-01A-11D-A435-10 chr20:32664876 C>T maps to NM_016732.1 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1I-01A-11D-A435-10 chr20:32664876 C>T maps to NM_016732.1 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG9-01A-11D-A42Y-10 chr9:6014326 G>T maps to NM_012416.2 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG8-01A-31D-A42Y-10 chr22:41660688 G>T maps to NM_002883.2 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOJ-01A-12D-A435-10 chr17:2901630 G>A maps to NM_015085.4 V387V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGZ-01A-11D-A42Y-10 chr9:134497190 G>T maps to NM_198679.1 R634R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKD-01A-31D-A42Y-10 chr7:22348121 G>A maps to ENST00000344041 D19D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALY-01A-11D-A42Y-10 chr7:22176600 T>A maps to ENST00000344041 K609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFZ-01A-11D-A42Y-10 chr2:204312707 G>T maps to ENST00000374493 S588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SB-A6J6-01A-11D-A435-10 chr11:47469558 C>T maps to NM_005055.3 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOD-01A-11D-A435-10 chr17:38512393 T>G maps to NM_001145301.2 G435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG8-01A-31D-A42Y-10 chr3:141205996 C>T maps to ENST00000452898 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr3:141235272 G>T maps to ENST00000452898 G119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFN-01A-31D-A42Y-10 chr13:114778650 G>T maps to ENST00000389544 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALP-01A-12D-A42Y-10 chr1:178063807 C>T maps to ENST00000263528 Q43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKM-01A-11D-A42Y-10 chr15:79284127 G>T maps to NM_002891.4 G1028G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A8S2-01A-11D-A435-10 chr15:38800148 G>T maps to NM_005739.3 Y340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A9SE-01A-21D-A435-10 chr2:33783347 G>T maps to NM_170672.2 A550A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A9T9-01A-11D-A435-10 chr22:29709862 G>T maps to NM_006477.3 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-AA4L-01A-11D-A435-10 chr10:45486406 T>C maps to NM_032023.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr1:206681028 G>T maps to NM_182663.2 E32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFZ-01A-11D-A42Y-10 chr13:48947558 C>A maps to NM_000321.2 I382I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF4-01A-11D-A42Y-10 chr23:47030581 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAGI-01A-11D-A42Y-10 chr23:47039330 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAH0-01A-11D-A42Y-10 chr23:47030581 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAL5-01A-11D-A42Y-10 chr23:47030581 G>T did not map to a codon.
Sequencing variant TCGA-2G-AALF-01A-11D-A42Y-10 chr23:47030578 G>T did not map to a codon.
Sequencing variant TCGA-SB-A76C-01A-11D-A435-10 chr8:94746361 G>T maps to NM_203390.2 P759P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A89B-01A-11D-A435-10 chr3:51429279 G>T maps to NM_013286.4 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKD-01A-31D-A42Y-10 chr23:48434993 T>G did not map to a codon.
Sequencing variant TCGA-WZ-A7V3-01A-11D-A435-10 chr23:48434940 G>T did not map to a codon.
Sequencing variant TCGA-ZM-AA06-01A-12D-A435-10 chr23:48434993 T>G did not map to a codon.
Sequencing variant TCGA-2G-AAGM-01A-11D-A42Y-10 chr7:155473368 G>T maps to NM_053043.2 G112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0B-01A-11D-A435-10 chr7:155556645 G>T maps to NM_053043.2 G1040G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A89B-01A-11D-A435-10 chr11:66411185 T>A maps to NM_001198845.1 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFN-01A-31D-A42Y-10 chr4:155718041 C>T maps to NM_144979.3 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AE-01A-11D-A435-10 chr4:155720330 C>T maps to NM_144979.3 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84W-01A-11D-A435-10 chr11:66436559 G>A maps to NM_031492.2 Y205Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGJ-01A-11D-A42Y-10 chr15:65043816 G>A maps to NM_194272.1 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H5-01A-11D-A435-10 chr11:32119922 C>A maps to NM_002901.2 S159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHL-01A-11D-A42Y-10 chr11:63682722 G>T maps to NM_173587.3 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOJ-01A-12D-A435-10 chr19:1496339 G>A maps to ENST00000395479 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANI-01A-11D-A435-10 chr20:30064433 C>T maps to NM_014012.4 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1H-01A-11D-A435-10 chr7:150069136 C>T maps to NM_001099695.1 C326C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X3-A8G4-01A-11D-A435-10 chr7:150069589 G>T maps to NM_001099695.1 A477A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr23:17047744 G>A did not map to a codon.
Sequencing variant TCGA-YU-A90Q-01A-11D-A435-10 chr23:17072944 C>T did not map to a codon.
Sequencing variant TCGA-2G-AAGK-01A-11D-A42Y-10 chr10:43604575 C>T maps to NM_020975.4 G387G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90Y-01A-11D-A435-10 chr6:111714086 T>C maps to NM_002912.3 E218E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A9SE-01A-21D-A435-10 chr19:1827047 T>G maps to NM_020695.3 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGN-01A-11D-A42Y-10 chr9:136277899 G>T maps to NM_020385.2 G238G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALF-01A-11D-A42Y-10 chr22:32589087 G>A maps to NM_001098527.2 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0F-01A-21D-A435-10 chr1:176175757 G>T maps to NM_022457.5 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF8-01A-11D-A42Y-10 chr23:109694902 C>T did not map to a codon.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr23:109695093 G>A did not map to a codon.
Sequencing variant TCGA-VF-A8AC-01A-11D-A435-10 chr23:109694019 G>T did not map to a codon.
Sequencing variant TCGA-2G-AALG-01A-11D-A42Y-10 chr1:183816713 G>A maps to NM_015149.3 Q86Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFH-01A-12D-A42Y-10 chr23:46951544 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAGN-01A-11D-A42Y-10 chr2:88125233 T>C maps to NM_001078170.2 K5K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA06-01A-12D-A435-10 chr2:88125233 T>C maps to NM_001078170.2 K5K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGA-01A-11D-A42Y-10 chr4:3319117 C>T maps to NM_198229.2 D407D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGK-01A-11D-A42Y-10 chr5:176798510 T>C maps to ENST00000398128 H474H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALX-01A-11D-A42Y-10 chr1:163043411 G>A maps to NM_001102445.2 E223E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG6-01A-11D-A42Y-10 chr1:240975326 G>A maps to ENST00000407727 Q325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGI-01A-11D-A42Y-10 chr16:108512 G>T maps to NM_022450.3 Y798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AA-01A-11D-A435-10 chr16:108652 G>A maps to NM_022450.3 L752L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGJ-01A-11D-A42Y-10 chr7:151188047 G>C maps to NM_005614.3 Y35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHG-01A-11D-A42Y-10 chr3:49399926 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAH0-01A-11D-A42Y-10 chr5:95067646 G>A maps to NM_014899.3 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGY-01A-11D-A42Y-10 chr12:122231058 G>T maps to NM_019034.2 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFG-01A-11D-A42Y-10 chr17:30536464 G>T did not map to a codon.
Sequencing variant TCGA-2G-AALW-01A-11D-A42Y-10 chr23:119249676 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAH2-01A-11D-A42Y-10 chr19:33517426 G>A maps to NM_033103.4 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AD-01A-11D-A435-10 chr23:53455229 G>T did not map to a codon.
Sequencing variant TCGA-YU-A90P-01A-11D-A435-10 chr23:53457698 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAG3-01A-11D-A42Y-10 chr12:123968737 G>T maps to NM_178314.3 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W4-A7U2-01A-11D-A435-10 chr22:20457059 C>G maps to NM_015672.1 V1414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-W4-A7U2-01A-11D-A435-10 chr22:20457203 G>A maps to NM_015672.1 G1366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALZ-01A-11D-A42Y-10 chr11:66100213 G>T maps to NM_004292.2 R629R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AAAL-01A-11D-A435-10 chr1:40661432 G>T maps to NM_012421.3 E202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90Q-01A-11D-A435-10 chr23:73811754 T>G did not map to a codon.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr16:67683477 C>A maps to NM_001013838.1 G625G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SO-A8JP-01A-11D-A435-10 chr2:3605787 G>T maps to NM_002936.3 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALG-01A-11D-A42Y-10 chr2:86849820 G>C maps to NM_005667.3 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFL-01A-21D-A42Y-10 chr23:119005137 T>C did not map to a codon.
Sequencing variant TCGA-2G-AAH4-01A-12D-A42Y-10 chr23:105937557 C>T did not map to a codon.
Sequencing variant TCGA-2G-AAHP-01A-12D-A42Y-10 chr17:78321500 C>T maps to NM_020914.4 H3171H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHL-01A-11D-A42Y-10 chr11:119206596 C>G maps to NM_032015.3 T255T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-WZ-A8D5-01A-11D-A435-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-ZM-AA0H-01A-11D-A435-10 chr16:2312408 G>T maps to NM_080594.2 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFL-01A-21D-A42Y-10 chr16:4848587 G>T maps to NM_024589.1 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H5-01A-11D-A435-10 chr16:4848605 G>A maps to NM_024589.1 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A89B-01A-11D-A435-10 chr15:60849112 C>T maps to NM_134260.2 Q78Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H5-01A-11D-A435-10 chr1:151783857 C>A maps to ENST00000392697 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGG-01A-11D-A42Y-10 chr8:10466033 C>T maps to NM_178857.5 G1858G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH3-01A-11D-A42Y-10 chr8:10465178 A>T maps to NM_178857.5 P2143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X3-A8G4-01A-11D-A435-10 chr8:10468934 C>A maps to NM_178857.5 G891G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGC-01A-21D-A42Y-10 chr23:38146263 C>G did not map to a codon.
Sequencing variant TCGA-XE-A8H5-01A-11D-A435-10 chr23:38186592 C>T did not map to a codon.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr14:21756200 G>T maps to NM_020366.3 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-AA61-01A-11D-A435-10 chr16:53682979 G>T maps to NM_015272.2 R734R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGC-01A-21D-A42Y-10 chr19:17972940 G>A maps to NM_000980.2 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANI-01A-11D-A435-10 chr1:6253101 G>A maps to NM_000983.3 Q44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHG-01A-11D-A42Y-10 chr12:120637137 G>A maps to NM_053275.3 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2X-A9D5-01A-11D-A435-10 chr12:120634653 A>T maps to NM_053275.3 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALN-01A-11D-A42Y-10 chr3:128344481 G>A maps to NM_002950.3 F430F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG6-01A-11D-A42Y-10 chr11:64135944 G>T maps to NM_003942.2 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALF-01A-11D-A42Y-10 chr23:83361423 A>G did not map to a codon.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr23:83360832 G>A did not map to a codon.
Sequencing variant TCGA-YU-A90Q-01A-11D-A435-10 chr16:66956207 G>T maps to NM_004165.2 S233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGK-01A-11D-A42Y-10 chr11:14380338 G>T maps to NM_012250.5 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF1-01A-11D-A42Y-10 chr20:17640066 G>T maps to ENST00000377813 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGN-01A-11D-A42Y-10 chr20:17639826 G>A maps to ENST00000377813 A442A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG6-01A-11D-A42Y-10 chr6:7231406 C>T maps to NM_001003699.3 S1025S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0E-01A-12D-A435-10 chr21:45222242 T>A maps to NM_003683.5 R366R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALG-01A-11D-A42Y-10 chr10:99133413 G>T maps to NM_015179.3 G648G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALZ-01A-11D-A42Y-10 chr10:99126539 C>T maps to NM_015179.3 E1058E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM3-01A-11D-A435-10 chr10:99126539 C>T maps to NM_015179.3 E1058E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2X-A9D6-01A-11D-A435-10 chr10:99133625 G>A maps to NM_015179.3 S608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANV-01A-11D-A435-10 chr10:99126539 C>T maps to NM_015179.3 E1058E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V3-01A-11D-A435-10 chr7:5983085 G>A maps to NM_173565.3 Q543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0B-01A-11D-A435-10 chr1:38078477 C>T maps to NM_001038633.2 Q247Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFI-01A-21D-A42Y-10 chr10:63957723 C>T maps to NM_145307.2 R591R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFH-01A-12D-A42Y-10 chr11:63488320 G>T maps to ENST00000377819 E783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V5-01A-11D-A435-10 chr17:1840548 G>T maps to NM_178568.2 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0H-01A-11D-A435-10 chr5:179036459 G>T maps to NM_025158.3 V689V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SB-A6J6-01A-11D-A435-10 chr4:71659589 C>T maps to NM_001037442.2 Q476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOL-01A-11D-A435-10 chr17:42393854 G>T maps to NM_001144825.1 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGZ-01A-11D-A42Y-10 chr6:45390456 G>A maps to ENST00000359524 Q130Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2X-A9D5-01A-11D-A435-10 chr6:45390444 A>G maps to ENST00000359524 Q126Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG0-01A-11D-A42Y-10 chr1:155292769 A>C maps to NM_001105203.1 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG6-01A-11D-A42Y-10 chr1:155292769 A>C maps to NM_001105203.1 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOL-01A-11D-A435-10 chr1:155292769 A>C maps to NM_001105203.1 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHC-01A-11D-A42Y-10 chr9:35548532 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAHN-01A-11D-A42Y-10 chr19:38976838 G>T maps to NM_000540.2 L1848L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKD-01A-31D-A42Y-10 chr19:38986923 G>T maps to NM_000540.2 T2206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANJ-01A-11D-A435-10 chr19:38958373 G>T maps to NM_000540.2 V1101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALX-01A-11D-A42Y-10 chr1:33295579 G>T maps to NM_022753.2 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAL5-01A-11D-A42Y-10 chr19:5667166 T>C maps to ENST00000433404 P815P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFN-01A-31D-A42Y-10 chr23:134993828 G>C did not map to a codon.
Sequencing variant TCGA-2G-AAH3-01A-11D-A42Y-10 chr18:76754582 C>T maps to NM_171999.2 S864S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X3-A8G4-01A-11D-A435-10 chr17:48195665 C>T maps to NM_174920.2 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr17:26712057 G>T did not map to a codon.
Sequencing variant TCGA-2G-AALP-01A-12D-A42Y-10 chr12:56154394 C>T maps to NM_033082.3 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALN-01A-11D-A42Y-10 chr11:65733918 G>A maps to NM_005146.4 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHA-01A-11D-A42Y-10 chr23:128926626 G>T did not map to a codon.
Sequencing variant TCGA-XY-A8S2-01A-11D-A435-10 chr23:128925039 G>A did not map to a codon.
Sequencing variant TCGA-2G-AALY-01A-11D-A42Y-10 chr23:23802157 T>A did not map to a codon.
Sequencing variant TCGA-2G-AALR-01A-21D-A42Y-10 chr23:84349178 T>G did not map to a codon.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr23:84362714 G>T did not map to a codon.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr23:84363308 G>T did not map to a codon.
Sequencing variant TCGA-2G-AALS-01A-12D-A42Y-10 chr19:50156723 G>A maps to NM_021228.2 E1026E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JW-01A-11D-A435-10 chr19:50149823 G>A maps to NM_021228.2 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-AA61-01A-11D-A435-10 chr19:50148668 G>A did not map to a codon.
Sequencing variant TCGA-ZM-AA0B-01A-11D-A435-10 chr9:127783011 T>G maps to NM_173690.4 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGV-01A-11D-A42Y-10 chr3:47462211 G>T maps to NM_012235.2 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGW-01A-11D-A42Y-10 chr3:47459291 C>T maps to NM_012235.2 V824V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2X-A9D5-01A-11D-A435-10 chr3:47455364 A>G maps to NM_012235.2 S1273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH2-01A-11D-A42Y-10 chr8:27779325 C>T maps to NM_173833.5 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHP-01A-12D-A42Y-10 chr13:78142454 G>T maps to NM_144777.2 E129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALP-01A-12D-A42Y-10 chr2:224463778 G>A maps to NM_003469.4 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A8S2-01A-11D-A435-10 chr11:62012169 G>T maps to NM_006551.3 *91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGO-01A-11D-A42Y-10 chr11:62038533 G>T maps to NM_002411.2 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALZ-01A-11D-A42Y-10 chr2:239006908 C>T maps to NM_016510.4 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOJ-01A-12D-A435-10 chr1:41514363 G>T maps to NM_001031694.2 S425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHN-01A-11D-A42Y-10 chr2:167328933 G>A maps to NM_002976.2 Y155Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAL5-01A-11D-A42Y-10 chr12:6457128 A>G maps to NM_001159576.1 P699P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHC-01A-11D-A42Y-10 chr1:1223347 C>T maps to NM_001130413.2 Y433Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr1:1221415 G>A maps to NM_001130413.2 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A912-01A-11D-A435-10 chr8:144874950 G>T maps to NM_182706.3 P1368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2X-A9D5-01A-11D-A435-10 chr17:45915295 G>A maps to NM_138355.3 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-AA4L-01A-11D-A435-10 chr20:644428 G>T maps to NM_033129.3 C270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGO-01A-11D-A42Y-10 chr4:76882373 G>A maps to NM_018115.2 H423H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHP-01A-12D-A42Y-10 chr4:76903124 G>T maps to NM_018115.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGK-01A-11D-A42Y-10 chr22:21997331 G>A maps to NM_022044.2 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H5-01A-11D-A435-10 chr5:256507 C>T maps to NM_004168.2 T656T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A9SE-01A-21D-A435-10 chr5:228448 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAGV-01A-11D-A42Y-10 chr7:4188934 G>T maps to NM_152744.3 E1489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALR-01A-21D-A42Y-10 chr17:71387577 C>T did not map to a codon.
Sequencing variant TCGA-XE-AANI-01A-11D-A435-10 chr15:85234839 G>T maps to NM_014300.2 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF4-01A-11D-A42Y-10 chr9:139360564 A>G maps to NM_014866.1 N1384N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGS-01A-11D-A42Y-10 chr9:139355645 G>A maps to NM_014866.1 H1658H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A6IS-01A-11D-A435-10 chr4:83763614 C>T maps to ENST00000505472 P913P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AD-01A-11D-A435-10 chr6:108214782 G>C maps to NM_007214.4 S526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr4:25769162 G>T maps to NM_015187.3 I943I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2X-A9D5-01A-11D-A435-10 chr3:52475646 G>T maps to NM_020163.1 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG0-01A-11D-A42Y-10 chr9:91994110 G>T maps to NM_006378.3 P699P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-2G-AALX-01A-11D-A42Y-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-2G-AALP-01A-12D-A42Y-10 chr3:122645324 G>A maps to NM_001031702.2 G350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr15:48058772 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAGG-01A-11D-A42Y-10 chr17:7466635 G>A maps to ENST00000321337 E81E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGS-01A-11D-A42Y-10 chr17:7466635 G>A maps to ENST00000321337 E81E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SB-A6J6-01A-11D-A435-10 chr17:7466635 G>A maps to ENST00000321337 E81E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V4-01A-11D-A435-10 chr17:7466635 G>A maps to ENST00000321337 E81E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFN-01A-31D-A42Y-10 chr23:118774679 C>G did not map to a codon.
Sequencing variant TCGA-2G-AALN-01A-11D-A42Y-10 chr15:44085842 T>C maps to ENST00000409960 H62H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG3-01A-11D-A42Y-10 chr6:122773071 G>T maps to NM_020755.2 C240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKG-01A-11D-A42Y-10 chr14:94756509 G>A maps to NM_001100607.1 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A8S2-01A-11D-A435-10 chr14:94933615 C>T maps to NM_175739.3 E262E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A8S3-01B-11D-A435-10 chr6:2955760 G>T maps to ENST00000316782 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGS-01A-11D-A42Y-10 chr2:224866575 C>T maps to NM_001136530.1 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH2-01A-11D-A42Y-10 chr18:42529988 C>T maps to NM_015559.2 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH8-01A-11D-A42Y-10 chr18:42531522 G>T maps to NM_015559.2 E740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGY-01A-11D-A42Y-10 chr16:30992479 C>T maps to NM_014712.1 Y1597Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1G-01A-11D-A435-10 chr16:30974775 T>C maps to NM_014712.1 Y180Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALF-01A-11D-A42Y-10 chr4:140432972 G>T maps to NM_030648.2 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA06-01A-12D-A435-10 chr9:135203903 G>T maps to ENST00000372169 I1027I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGM-01A-11D-A42Y-10 chr1:38442579 G>T maps to NM_006802.2 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOF-01A-11D-A435-10 chr2:73215426 G>T maps to NM_144579.2 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AE-01A-11D-A435-10 chr8:8234016 C>T maps to NM_001080826.1 Q634Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SB-A76C-01A-11D-A435-10 chr17:26941124 G>T maps to NM_001174103.1 R19R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM4-01A-11D-A435-10 chr22:25255729 G>T maps to NM_001039948.2 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHP-01A-12D-A42Y-10 chr17:2266156 C>T maps to NM_014853.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGV-01A-11D-A42Y-10 chr5:64966158 G>A maps to NM_019072.2 Q277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A8D5-01A-11D-A435-10 chr5:65008802 G>T maps to NM_019072.2 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SO-A8JP-01A-11D-A435-10 chr16:28877474 A>C maps to NM_001145795.1 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA05-01A-12D-A435-10 chr16:28883694 C>T maps to NM_001145795.1 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr12:111886036 G>T maps to NM_005475.2 S553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOL-01A-11D-A435-10 chr1:156783684 C>T maps to NM_001161441.1 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKO-01A-11D-A42Y-10 chr22:38044406 G>T maps to NM_018957.3 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANR-01A-11D-A435-10 chr4:2826351 G>T maps to NM_001145856.1 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF1-01A-11D-A42Y-10 chr19:4362648 G>T maps to NM_003025.2 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG3-01A-11D-A42Y-10 chr11:70653200 G>A maps to ENST00000338508 Y524Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGC-01A-21D-A42Y-10 chr11:70332653 G>T maps to ENST00000338508 Y1242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHG-01A-11D-A42Y-10 chr11:70653167 G>T maps to ENST00000338508 V535V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH4-01A-12D-A42Y-10 chr22:51117452 C>T maps to NM_001080420.1 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO6-01A-31D-A435-10 chr22:51169199 C>A maps to NM_001080420.1 P1568P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AC-01A-11D-A435-10 chr9:38068264 G>T maps to NM_003028.2 R126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr17:7533537 G>T maps to NM_001040.3 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALZ-01A-11D-A42Y-10 chr19:41094563 T>C maps to NM_138392.3 S457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFZ-01A-11D-A42Y-10 chr10:112724385 G>T maps to NM_007373.3 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO6-01A-31D-A435-10 chr5:132161736 G>T maps to NM_001172700.1 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA05-01A-12D-A435-10 chr23:9863375 T>G did not map to a codon.
Sequencing variant TCGA-2G-AAF8-01A-11D-A42Y-10 chr4:77676328 G>T maps to NM_020859.3 E1565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALZ-01A-11D-A42Y-10 chr23:50438917 G>T did not map to a codon.
Sequencing variant TCGA-SN-A84W-01A-11D-A435-10 chr3:164777692 T>C maps to NM_001041.3 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1G-01A-11D-A435-10 chr11:124517335 G>A maps to NM_170601.3 I297I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO6-01A-31D-A435-10 chr11:124518071 C>A did not map to a codon.
Sequencing variant TCGA-XY-A8S3-01B-11D-A435-10 chr20:3677792 G>T maps to NM_023068.3 A773A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGT-01A-11D-A42Y-10 chr19:51919247 G>A maps to NM_033130.4 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H4-01A-31D-A435-10 chr19:51630548 G>A maps to NM_014441.2 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHT-01A-11D-A42Y-10 chr9:34637552 G>A maps to NM_005866.2 Q48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG7-01A-11D-A42Y-10 chr11:116746686 G>T maps to ENST00000445177 I371I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANJ-01A-11D-A435-10 chr11:116718215 G>A maps to ENST00000445177 Q1303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-AA4L-01A-11D-A435-10 chr5:138283065 G>A maps to ENST00000509534 Q383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH0-01A-11D-A42Y-10 chr20:1876143 G>T maps to ENST00000400068 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHL-01A-11D-A42Y-10 chr20:1615979 C>T maps to NM_018556.3 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0N-01A-21D-A435-10 chr20:1610929 C>T maps to NM_018556.3 A368A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90P-01A-11D-A435-10 chr10:69676304 G>T maps to NM_012238.4 V733V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X3-A8G4-01A-11D-A435-10 chr19:4179129 G>A maps to NM_016539.2 D116D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANJ-01A-11D-A435-10 chr1:2160972 G>T maps to NM_003036.3 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGW-01A-11D-A42Y-10 chr6:31931718 C>T maps to NM_006929.4 A559A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHA-01A-11D-A42Y-10 chr1:160465887 G>T maps to NM_001184714.1 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH2-01A-11D-A42Y-10 chr5:127485690 G>T maps to NM_001046.2 E670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0F-01A-21D-A435-10 chr5:127420308 G>T maps to NM_001046.2 V221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKG-01A-11D-A42Y-10 chr16:56913027 A>T maps to NM_000339.2 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1I-01A-11D-A435-10 chr16:56906330 C>A maps to NM_000339.2 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGO-01A-11D-A42Y-10 chr15:34549911 G>T maps to NM_133647.1 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr7:100458782 G>A maps to NM_020246.2 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V3-01A-11D-A435-10 chr7:100458761 G>T maps to NM_020246.2 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGA-01A-11D-A42Y-10 chr7:135406262 C>T maps to NM_012450.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr18:43248364 G>A maps to NM_007163.3 L653L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGW-01A-11D-A42Y-10 chr11:60718891 C>T maps to NM_016582.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALR-01A-21D-A42Y-10 chr17:80195737 G>A maps to NM_001042423.1 A364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGE-01A-21D-A42Y-10 chr17:66270086 G>T maps to NM_004694.4 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0N-01A-21D-A435-10 chr8:20005147 G>A maps to NM_001135691.2 I432I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGG-01A-11D-A42Y-10 chr2:113414818 G>T did not map to a codon.
Sequencing variant TCGA-SN-A6IS-01A-11D-A435-10 chr8:42329668 G>T maps to NM_006749.3 Y80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGF-01A-31D-A42Y-10 chr11:64367947 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAH4-01A-12D-A42Y-10 chr3:38317787 G>T maps to NM_004256.3 V416V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SB-A6J6-01A-11D-A435-10 chr6:110752415 C>T maps to NM_033125.2 P493P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHC-01A-11D-A42Y-10 chr5:131630458 T>C maps to NM_003059.2 C50C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr5:131676373 C>T maps to NM_003059.2 Q521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGG-01A-11D-A42Y-10 chr23:129474304 C>T did not map to a codon.
Sequencing variant TCGA-2G-AAGW-01A-11D-A42Y-10 chr6:46623641 C>A maps to NM_004277.3 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALG-01A-11D-A42Y-10 chr14:100758775 C>T maps to NM_001039355.1 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHN-01A-11D-A42Y-10 chr23:118603653 G>T did not map to a codon.
Sequencing variant TCGA-XE-AAOD-01A-11D-A435-10 chr23:118602490 G>A did not map to a codon.
Sequencing variant TCGA-ZM-AA05-01A-12D-A435-10 chr6:35960388 A>G maps to NM_052961.3 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALR-01A-21D-A42Y-10 chr19:17598308 G>C maps to NM_198580.1 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X3-A8G4-01A-11D-A435-10 chr19:17597497 C>T maps to NM_198580.1 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO6-01A-31D-A435-10 chr19:17581366 G>A maps to NM_198580.1 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A6IS-01A-11D-A435-10 chr10:73121734 G>T maps to NM_018344.5 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SB-A6J6-01A-11D-A435-10 chr20:45362412 C>T maps to NM_030777.3 G522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG6-01A-11D-A42Y-10 chr12:7982478 G>A maps to NM_153449.2 C155C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALR-01A-21D-A42Y-10 chr12:7982385 T>G maps to NM_153449.2 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALR-01A-21D-A42Y-10 chr12:8083899 G>T maps to NM_006931.2 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOJ-01A-12D-A435-10 chr20:62374110 C>A maps to NM_020062.3 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH2-01A-11D-A42Y-10 chr1:9101769 G>A maps to NM_001135585.1 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHP-01A-12D-A42Y-10 chr9:136340190 G>A maps to NM_017585.3 C273C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2X-A9D6-01A-11D-A435-10 chr9:136342252 G>T maps to NM_017585.3 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALY-01A-11D-A42Y-10 chr9:130160365 C>T maps to NM_014580.3 C134C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84W-01A-11D-A435-10 chr1:211751851 G>A maps to NM_021194.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr1:26368221 G>T maps to NM_001004434.1 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANJ-01A-11D-A435-10 chr9:140128919 C>A maps to NM_080877.2 G382G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANR-01A-11D-A435-10 chr9:140128576 G>T maps to NM_080877.2 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94D-01A-11D-A435-10 chr1:67519690 C>T maps to NM_015139.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFG-01A-11D-A42Y-10 chr11:124951661 G>T maps to NM_198277.2 E249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHT-01A-11D-A42Y-10 chr11:124955358 C>T maps to NM_198277.2 T439T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGI-01A-11D-A42Y-10 chr7:140064287 G>A maps to NM_207113.1 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFO-01A-31D-A42Y-10 chr17:79257225 G>T maps to NM_001037984.1 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AB-01A-31D-A435-10 chr2:165793939 C>G did not map to a codon.
Sequencing variant TCGA-2G-AALR-01A-21D-A42Y-10 chr16:58713787 G>A maps to NM_018231.1 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALR-01A-21D-A42Y-10 chr16:84075678 G>T maps to NM_001080442.1 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFL-01A-21D-A42Y-10 chr17:70645039 C>A maps to NM_001159770.1 V284V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOF-01A-11D-A435-10 chr11:47436632 G>T maps to NM_001128225.2 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0H-01A-11D-A435-10 chr18:33696733 C>T maps to NM_012319.3 K456K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALF-01A-11D-A42Y-10 chr17:19618515 C>T maps to NM_152908.3 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90S-01A-11D-A435-10 chr5:139747090 G>T maps to ENST00000507527 L724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0B-01A-11D-A435-10 chr23:115568987 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAGP-01A-11D-A42Y-10 chr5:1216726 G>T maps to NM_001003841.2 S314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-AA4L-01A-11D-A435-10 chr3:45814059 G>T maps to NM_020208.3 Y210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALS-01A-12D-A42Y-10 chr17:28548796 C>T maps to ENST00000394821 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALG-01A-11D-A42Y-10 chr23:152960295 G>A did not map to a codon.
Sequencing variant TCGA-2G-AAHC-01A-11D-A42Y-10 chr23:70149797 C>T did not map to a codon.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr23:70146766 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAGY-01A-11D-A42Y-10 chr14:70633870 T>C maps to NM_183002.1 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO6-01A-31D-A435-10 chr16:2079696 C>T maps to ENST00000191922 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0H-01A-11D-A435-10 chr16:2086856 C>G maps to ENST00000191922 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH3-01A-11D-A42Y-10 chr15:92671631 T>C maps to NM_013272.3 C475C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X3-A8G4-01A-11D-A435-10 chr17:33749876 T>C maps to NM_018042.3 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOC-01A-11D-A435-10 chr17:33749876 T>C maps to NM_018042.3 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGW-01A-11D-A42Y-10 chr17:33591733 A>T maps to NM_144975.3 T557T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGV-01A-11D-A42Y-10 chr10:98781010 G>T maps to NM_003061.2 C914*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0H-01A-11D-A435-10 chr3:164905990 T>C maps to NM_014926.2 G876G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr23:142717463 G>T did not map to a codon.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr3:57857387 G>T maps to ENST00000428312 G404G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1H-01A-11D-A435-10 chr15:59192107 T>C maps to NM_024755.2 Q206Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALO-01A-12D-A42Y-10 chr18:48586286 G>T did not map to a codon.
Sequencing variant TCGA-2G-AALX-01A-11D-A42Y-10 chr18:46476632 G>A maps to NM_005904.3 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0D-01A-11D-A435-10 chr23:128625995 G>A did not map to a codon.
Sequencing variant TCGA-2G-AAHL-01A-11D-A42Y-10 chr17:38798745 G>T maps to NM_003079.4 Y39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0E-01A-12D-A435-10 chr18:2705753 C>T maps to NM_015295.2 G635G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGZ-01A-11D-A42Y-10 chr16:18844389 G>A maps to ENST00000389467 D2888D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHT-01A-11D-A42Y-10 chr17:1968953 G>T maps to NM_017575.4 G1285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A9T9-01A-11D-A435-10 chr17:1964854 C>A maps to NM_017575.4 V1397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAEX-01A-11D-A42Y-10 chr11:6411971 T>G maps to NM_000543.4 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA05-01A-12D-A435-10 chr6:109764879 A>G maps to NM_003080.2 G348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALR-01A-21D-A42Y-10 chr16:68398786 C>T maps to NM_018667.3 G474G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2X-A9D6-01A-11D-A435-10 chr16:68395598 G>T maps to NM_018667.3 G591G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF8-01A-11D-A42Y-10 chr2:130910945 G>T maps to NM_017951.4 P696P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG6-01A-11D-A42Y-10 chr2:130913639 G>A maps to NM_017951.4 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V3-01A-11D-A435-10 chr2:130910187 A>G maps to NM_017951.4 Y847Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94D-01A-11D-A435-10 chr23:21995230 G>C did not map to a codon.
Sequencing variant TCGA-SB-A76C-01A-11D-A435-10 chr1:214491482 G>T did not map to a codon.
Sequencing variant TCGA-YU-A90Q-01A-11D-A435-10 chr1:246670510 C>T maps to NM_001167740.1 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AB-01A-31D-A435-10 chr1:227947186 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAF1-01A-11D-A42Y-10 chr5:121758671 G>A maps to ENST00000379533 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr7:127714712 G>T maps to NM_014390.2 E647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAL7-01A-11D-A42Y-10 chr2:241979570 C>T maps to NM_001080437.1 C375C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG6-01A-11D-A42Y-10 chr20:2442425 C>T maps to ENST00000339610 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANI-01A-11D-A435-10 chr20:2443297 A>G maps to ENST00000339610 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A6IS-01A-11D-A435-10 chr20:16721613 G>T maps to NM_198220.2 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AAAL-01A-11D-A435-10 chr8:51449299 C>T maps to NM_018967.2 C204C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A9T9-01A-11D-A435-10 chr7:17836516 G>T maps to ENST00000417048 C901*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALX-01A-11D-A42Y-10 chr2:27598735 G>T maps to NM_014748.2 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr1:151665437 G>T maps to ENST00000458013 E481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH4-01A-12D-A42Y-10 chr17:76354723 C>T maps to NM_003955.3 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94D-01A-11D-A435-10 chr14:55509765 G>T maps to NM_199421.1 E3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2X-A9D6-01A-11D-A435-10 chr16:602369 C>T maps to NM_005632.2 S859S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0D-01A-11D-A435-10 chr11:121466452 C>A maps to NM_003105.5 C1497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFO-01A-31D-A42Y-10 chr20:62680647 G>A maps to NM_018419.2 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAL7-01A-11D-A42Y-10 chr11:16068173 C>T maps to NM_001145819.1 A516A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90Y-01A-11D-A435-10 chr16:1032206 G>A maps to NM_014587.3 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A8S2-01A-11D-A435-10 chr2:231174674 G>T maps to NM_007237.4 G699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANR-01A-11D-A435-10 chr17:26905513 G>T maps to NM_006461.3 R1077R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A8S2-01A-11D-A435-10 chr17:49124779 G>A maps to ENST00000376407 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAEX-01A-11D-A42Y-10 chr23:52825638 G>A did not map to a codon.
Sequencing variant TCGA-XE-A9SE-01A-21D-A435-10 chr16:89763951 G>T maps to NM_152339.3 Y355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG9-01A-11D-A42Y-10 chr12:49908382 G>T maps to NM_023071.3 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANR-01A-11D-A435-10 chr4:177248365 G>A maps to NM_021928.3 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGW-01A-11D-A42Y-10 chr2:29063246 G>T maps to NM_182756.3 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H1-01A-11D-A435-10 chr2:220342105 C>T maps to NM_005876.4 T1556T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGN-01A-11D-A42Y-10 chr17:7324623 A>C maps to NM_199339.2 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG7-01A-11D-A42Y-10 chr1:16254717 G>A maps to NM_015001.2 W661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKO-01A-11D-A42Y-10 chr1:16258923 A>G maps to NM_015001.2 V2063V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84Y-01A-11D-A435-10 chr1:16265331 G>T maps to NM_015001.2 A3608A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A912-01A-11D-A435-10 chr1:16174548 G>T did not map to a codon.
Sequencing variant TCGA-SB-A6J6-01A-11D-A435-10 chr13:46288212 C>T maps to NM_152719.1 D351D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGP-01A-11D-A42Y-10 chr15:44955775 G>T maps to NM_025137.3 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr17:74382928 G>T maps to NM_182965.2 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H1-01A-11D-A435-10 chr19:49131955 C>A maps to NM_020126.3 G297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGK-01A-11D-A42Y-10 chr23:57162582 T>C did not map to a codon.
Sequencing variant TCGA-SN-A6IS-01A-11D-A435-10 chr23:57162582 T>C did not map to a codon.
Sequencing variant TCGA-SN-A84W-01A-11D-A435-10 chr23:57162582 T>C did not map to a codon.
Sequencing variant TCGA-2G-AAHG-01A-11D-A42Y-10 chr23:57146614 T>C did not map to a codon.
Sequencing variant TCGA-WZ-A8D5-01A-11D-A435-10 chr23:57146614 T>C did not map to a codon.
Sequencing variant TCGA-2G-AAGA-01A-11D-A42Y-10 chr23:57020932 T>C did not map to a codon.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr23:62570275 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAG6-01A-11D-A42Y-10 chr16:89925691 A>G maps to NM_032451.1 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X3-A8G4-01A-11D-A435-10 chr17:4352589 G>T maps to NM_182538.4 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA06-01A-12D-A435-10 chr1:32259794 G>T maps to NM_144569.4 P771P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90S-01A-11D-A435-10 chr17:47688678 G>A maps to NM_003563.3 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-AA4L-01A-11D-A435-10 chr2:65541090 G>T maps to NM_181784.2 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFG-01A-11D-A42Y-10 chr1:153005015 C>T maps to NM_003125.2 C65C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A6IS-01A-11D-A435-10 chr12:56862910 A>G maps to NM_207344.3 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V3-01A-11D-A435-10 chr16:1828457 G>A maps to NM_080861.3 C94C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94I-01A-11D-A435-10 chr1:158605701 C>T did not map to a codon.
Sequencing variant TCGA-SN-A84W-01A-11D-A435-10 chr9:131337576 G>T maps to NM_001130438.2 E202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A9T9-01A-11D-A435-10 chr14:65260085 C>T maps to ENST00000389723 L769L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGK-01A-11D-A42Y-10 chr11:66468011 G>A maps to NM_006946.2 G1186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGY-01A-11D-A42Y-10 chr15:42175408 G>A maps to ENST00000320955 T559T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A8D5-01A-11D-A435-10 chr20:13107266 G>T maps to NM_018327.2 S394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84Y-01A-11D-A435-10 chr5:79616894 C>G maps to NM_032567.3 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGS-01A-11D-A42Y-10 chr15:45980602 G>T did not map to a codon.
Sequencing variant TCGA-YU-A94I-01A-11D-A435-10 chr5:179251213 G>T maps to NM_003900.4 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFJ-01A-11D-A42Y-10 chr16:30748507 A>T maps to NM_006662.2 K2383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGI-01A-11D-A42Y-10 chr16:30732774 C>A maps to NM_006662.2 P1173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANI-01A-11D-A435-10 chr16:30723653 G>A maps to NM_006662.2 L629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFG-01A-11D-A42Y-10 chr22:42293165 G>T did not map to a codon.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr22:42289197 C>T maps to NM_004599.2 C762C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH0-01A-11D-A42Y-10 chr5:112228536 G>T maps to ENST00000391338 E401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SB-A6J6-01A-11D-A435-10 chr5:112228214 C>T maps to ENST00000391338 N293N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr5:112228214 C>T maps to ENST00000391338 N293N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1G-01A-11D-A435-10 chr17:74037022 G>T maps to NM_014230.2 R521R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGO-01A-11D-A42Y-10 chr7:104844186 C>T maps to ENST00000336613 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF6-01A-11D-A42Y-10 chr23:153046775 G>T did not map to a codon.
Sequencing variant TCGA-XE-AAOJ-01A-12D-A435-10 chr1:24996015 G>A maps to NM_005839.3 P714P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGO-01A-11D-A42Y-10 chr16:2819138 C>T maps to NM_016333.3 S2625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALN-01A-11D-A42Y-10 chr16:2819138 C>T maps to NM_016333.3 S2625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANI-01A-11D-A435-10 chr16:2819138 C>T maps to NM_016333.3 S2625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALN-01A-11D-A42Y-10 chr19:18544012 C>T maps to NM_032627.3 N327N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM4-01A-11D-A435-10 chr7:149522447 G>A maps to NM_198455.2 P4698P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANJ-01A-11D-A435-10 chr7:149500590 G>T maps to NM_198455.2 L2665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO3-01A-11D-A435-10 chr7:149486701 C>T maps to NM_198455.2 C1493C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFO-01A-31D-A42Y-10 chr6:7313284 G>T maps to ENST00000474597 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG0-01A-11D-A42Y-10 chr11:130068299 C>T maps to NM_021978.3 D519D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA05-01A-12D-A435-10 chr1:77334300 A>G maps to NM_030965.1 Q45Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr12:22354746 G>T maps to NM_003034.3 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALY-01A-11D-A42Y-10 chr18:44260337 G>A maps to NM_013305.4 D266D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84Y-01A-11D-A435-10 chr3:52545760 G>T maps to NM_015136.2 L961L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGV-01A-11D-A42Y-10 chr12:57642941 C>T maps to NM_145064.1 E72E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALR-01A-21D-A42Y-10 chr23:123184102 G>T did not map to a codon.
Sequencing variant TCGA-XE-AAO3-01A-11D-A435-10 chr23:123191754 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAGM-01A-11D-A42Y-10 chr7:74306638 C>G did not map to a codon.
Sequencing variant TCGA-2G-AALO-01A-12D-A42Y-10 chr23:67940200 G>C did not map to a codon.
Sequencing variant TCGA-4K-AA1G-01A-11D-A435-10 chr23:67940200 G>C did not map to a codon.
Sequencing variant TCGA-2G-AALX-01A-11D-A42Y-10 chr2:120005328 C>T maps to NM_182915.2 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A8S2-01A-11D-A435-10 chr11:3877620 G>T maps to NM_003156.3 E41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AB-01A-31D-A435-10 chr7:43622931 G>A maps to NM_004760.2 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A8S2-01A-11D-A435-10 chr7:23776555 G>T maps to NM_031414.3 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM3-01A-11D-A435-10 chr11:8474399 C>T maps to NM_030906.2 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90P-01A-11D-A435-10 chr20:2083850 G>T maps to NM_080836.3 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr2:219540115 C>A maps to NM_015690.3 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH4-01A-12D-A42Y-10 chr13:39542578 G>T maps to NM_145286.2 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A8D5-01A-11D-A435-10 chr13:39542625 G>T maps to NM_145286.2 R188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA06-01A-12D-A435-10 chr13:39544324 G>T maps to NM_145286.2 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr15:74476263 A>G maps to ENST00000449139 H450H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG5-01A-11D-A42Y-10 chr2:202344879 C>T maps to NM_018571.5 D413D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANV-01A-11D-A435-10 chr2:202344885 C>T maps to NM_018571.5 Y415Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOF-01A-11D-A435-10 chr2:37094973 A>G maps to NM_003162.2 Y510Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A9SE-01A-21D-A435-10 chr23:7171291 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAFY-01A-11D-A42Y-10 chr11:125482642 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAGE-01A-21D-A42Y-10 chr4:4421778 G>T maps to NM_016930.2 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOL-01A-11D-A435-10 chr16:28619840 G>T maps to NM_177529.1 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFL-01A-21D-A42Y-10 chr14:21830429 A>G maps to NM_007192.3 Y573Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGE-01A-21D-A42Y-10 chr19:39964104 C>T maps to NM_003169.3 S812S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr19:39965023 G>A maps to NM_003169.3 P934P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H4-01A-31D-A435-10 chr17:27010744 G>T maps to NM_003170.3 E714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H4-01A-31D-A435-10 chr17:27015152 G>T maps to NM_003170.3 L1017L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO3-01A-11D-A435-10 chr17:27028471 A>G maps to NM_003170.3 A1670A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO4-01A-11D-A435-10 chr23:48564673 G>T did not map to a codon.
Sequencing variant TCGA-WZ-A7V3-01A-11D-A435-10 chr15:91810816 G>T maps to NM_014848.4 G384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A8D5-01A-11D-A435-10 chr8:110587803 C>T maps to NM_001099744.1 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A89B-01A-11D-A435-10 chr6:10928664 T>C maps to NM_001040274.2 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGM-01A-11D-A42Y-10 chr19:46355580 G>T maps to NM_004819.2 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO3-01A-11D-A435-10 chr19:46332316 G>T maps to NM_004819.2 A632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGI-01A-11D-A42Y-10 chr23:47478984 G>A did not map to a codon.
Sequencing variant TCGA-2G-AAGI-01A-11D-A42Y-10 chr22:33265024 G>T maps to NM_003490.3 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA06-01A-12D-A435-10 chr22:32923914 T>G maps to NM_003490.3 P436P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO3-01A-11D-A435-10 chr6:86346825 C>T maps to NM_006372.4 E175E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALS-01A-12D-A42Y-10 chr6:152589279 G>C maps to NM_182961.2 A6242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90Y-01A-11D-A435-10 chr6:152631004 G>A maps to NM_182961.2 Q5723*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF4-01A-11D-A42Y-10 chr14:64675555 C>A maps to NM_182914.2 S6094S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0D-01A-11D-A435-10 chr14:64626068 G>T maps to NM_182914.2 E5335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84X-01A-11D-A435-10 chr15:99666939 G>T maps to ENST00000336292 G316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94I-01A-11D-A435-10 chr19:51135703 T>A maps to NM_001160329.1 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A912-01A-11D-A435-10 chr11:85415905 G>T maps to ENST00000359152 R1603R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90Y-01A-11D-A435-10 chr23:99956556 G>T did not map to a codon.
Sequencing variant TCGA-YU-AA61-01A-11D-A435-10 chr23:99945111 C>A did not map to a codon.
Sequencing variant TCGA-S6-A8JW-01A-11D-A435-10 chr23:37966001 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAEX-01A-11D-A42Y-10 chr11:64895913 G>T maps to NM_172230.2 P598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94I-01A-11D-A435-10 chr11:64897840 G>T maps to NM_172230.2 G372G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr22:39826223 G>A maps to NM_006116.2 P504P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGT-01A-11D-A42Y-10 chr23:30870898 G>A did not map to a codon.
Sequencing variant TCGA-2G-AAF8-01A-11D-A42Y-10 chr2:10059214 C>T maps to NM_005680.2 D439D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALG-01A-11D-A42Y-10 chr16:84213857 C>T maps to NM_005679.2 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFY-01A-11D-A42Y-10 chr10:8006559 C>T maps to NM_031923.2 Q363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGV-01A-11D-A42Y-10 chr7:99705015 A>G maps to ENST00000472509 P686P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JY-01A-11D-A435-10 chr23:100533045 C>T did not map to a codon.
Sequencing variant TCGA-YU-A94I-01A-11D-A435-10 chr23:77393364 C>T did not map to a codon.
Sequencing variant TCGA-2G-AAFZ-01A-11D-A42Y-10 chr2:159992708 C>G maps to NM_033394.2 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGA-01A-11D-A42Y-10 chr17:61498458 C>T maps to ENST00000389520 R1716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84X-01A-11D-A435-10 chr17:61489047 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAGM-01A-11D-A42Y-10 chr2:162087614 C>T maps to NM_004180.2 C218C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHG-01A-11D-A42Y-10 chr16:29998787 G>A maps to NM_016151.2 A1065A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALT-01A-11D-A42Y-10 chr12:118590214 C>A did not map to a codon.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr15:102264362 G>T maps to NM_152334.2 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKM-01A-11D-A42Y-10 chr1:1269177 C>T maps to NM_152228.1 A631A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKD-01A-31D-A42Y-10 chr12:11244877 A>G did not map to a codon.
Sequencing variant TCGA-2G-AAM3-01A-11D-A435-10 chr8:125520717 T>C maps to NM_032026.3 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H5-01A-11D-A435-10 chr8:125520902 G>C maps to NM_032026.3 S139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SO-A8JP-01A-11D-A435-10 chr3:10318067 G>T maps to NM_014760.3 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JX-01A-11D-A435-10 chr23:153640237 G>T did not map to a codon.
Sequencing variant TCGA-W4-A7U2-01A-11D-A435-10 chr23:153648386 T>C did not map to a codon.
Sequencing variant TCGA-WZ-A7V5-01A-11D-A435-10 chr12:72266783 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAGN-01A-11D-A42Y-10 chr23:48418341 G>T did not map to a codon.
Sequencing variant TCGA-4K-AAAL-01A-11D-A435-10 chr17:28887160 T>C maps to NM_015594.2 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90W-01A-11D-A435-10 chr17:28890346 A>G maps to NM_015594.2 Q119Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGY-01A-11D-A42Y-10 chr6:170871015 G>A maps to NM_003194.4 Q64Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALY-01A-11D-A42Y-10 chr6:170871015 G>A maps to NM_003194.4 Q64Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90P-01A-11D-A435-10 chr6:170871003 G>A maps to NM_003194.4 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0D-01A-11D-A435-10 chr6:170871003 G>A maps to NM_003194.4 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0F-01A-21D-A435-10 chr6:170871033 G>A maps to NM_003194.4 Q70Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SO-A8JP-01A-11D-A435-10 chr11:67399114 G>T maps to NM_005995.4 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANI-01A-11D-A435-10 chr6:85473884 T>A maps to NM_001080508.1 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGT-01A-11D-A42Y-10 chr19:3600389 G>T maps to NM_201636.2 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A8S3-01B-11D-A435-10 chr20:62701154 G>T maps to NM_003195.4 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGG-01A-11D-A42Y-10 chr23:13681575 C>T did not map to a codon.
Sequencing variant TCGA-XY-A8S3-01B-11D-A435-10 chr16:2825542 C>T maps to NM_207013.1 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG7-01A-11D-A42Y-10 chr10:133106528 C>T maps to NM_174937.3 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JX-01A-11D-A435-10 chr10:133058642 G>A maps to NM_174937.3 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF6-01A-11D-A42Y-10 chr22:42608227 T>C maps to NM_005650.1 G1028G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGO-01A-11D-A42Y-10 chr10:114925529 C>A maps to NM_030756.4 P530P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFZ-01A-11D-A42Y-10 chr20:61488883 T>C maps to NM_006602.2 E367E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF1-01A-11D-A42Y-10 chr1:152082980 C>T maps to NM_007113.2 Q904Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGM-01A-11D-A42Y-10 chr11:67818020 G>T maps to NM_006019.3 V768V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr11:67818093 G>T maps to NM_006019.3 G793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOC-01A-11D-A435-10 chr11:67817182 G>A maps to NM_006019.3 L647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAL5-01A-11D-A42Y-10 chr5:149767637 G>A maps to ENST00000451292 Q1048Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALW-01A-11D-A42Y-10 chr6:167789493 G>T maps to NM_004610.3 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOL-01A-11D-A435-10 chr1:45271710 G>A maps to NM_001013632.2 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFH-01A-12D-A42Y-10 chr14:104481100 C>T maps to NM_153046.2 Q716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr1:151751707 G>A maps to NM_001083965.1 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG7-01A-11D-A42Y-10 chr6:35445112 C>T maps to ENST00000357281 Q226Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA05-01A-12D-A435-10 chr19:14675086 C>A maps to ENST00000436007 R174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF1-01A-11D-A42Y-10 chr11:120989052 T>C maps to NM_005422.2 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF4-01A-11D-A42Y-10 chr11:120996447 G>T maps to NM_005422.2 V547V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOB-01A-11D-A435-10 chr11:121061448 G>T maps to NM_005422.2 T2134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr16:1559885 G>A maps to NM_016111.3 L821L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGI-01A-11D-A42Y-10 chr10:70332382 C>G maps to NM_030625.2 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A9SE-01A-21D-A435-10 chr10:70333542 C>G maps to NM_030625.2 S483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKO-01A-11D-A42Y-10 chr23:104464814 C>T did not map to a codon.
Sequencing variant TCGA-2G-AAL7-01A-11D-A42Y-10 chr23:104463846 C>T did not map to a codon.
Sequencing variant TCGA-2G-AAFV-01A-11D-A42Y-10 chr3:51737953 G>T maps to NM_015926.4 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94D-01A-11D-A435-10 chr6:50740417 A>C maps to NM_172238.3 T400T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALF-01A-11D-A42Y-10 chr1:36054039 G>A maps to NM_178548.3 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A9SE-01A-21D-A435-10 chr23:48900700 C>T did not map to a codon.
Sequencing variant TCGA-2G-AAGO-01A-11D-A42Y-10 chr16:31484849 T>C maps to NM_001042454.2 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGN-01A-11D-A42Y-10 chr15:43571976 C>A maps to NM_052955.2 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGE-01A-21D-A42Y-10 chr16:67876780 G>A maps to NM_020457.2 Q108Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALN-01A-11D-A42Y-10 chr2:242573037 T>C maps to NM_015963.5 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG9-01A-11D-A42Y-10 chr20:23028596 C>A maps to NM_000361.2 S515S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM4-01A-11D-A435-10 chr20:23028533 G>T maps to NM_000361.2 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOD-01A-11D-A435-10 chr23:122747910 G>T did not map to a codon.
Sequencing variant TCGA-XY-A89B-01A-11D-A435-10 chr22:29916093 C>G did not map to a codon.
Sequencing variant TCGA-2G-AALP-01A-12D-A42Y-10 chr6:155450816 G>T maps to ENST00000456144 E154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V5-01A-11D-A435-10 chr8:144681320 G>A maps to NM_032862.4 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALS-01A-12D-A42Y-10 chr12:56814370 C>T maps to NM_003920.3 R1070R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALS-01A-12D-A42Y-10 chr12:56817447 C>T maps to NM_003920.3 E670E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90Q-01A-11D-A435-10 chr12:56817447 C>T maps to NM_003920.3 E670E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAEX-01A-11D-A42Y-10 chr10:51592584 T>C maps to NM_006327.2 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFY-01A-11D-A42Y-10 chr19:7998430 G>A maps to NM_006351.3 H236H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFL-01A-21D-A42Y-10 chr19:39971460 C>T maps to NM_001001563.1 R93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOD-01A-11D-A435-10 chr11:126162382 C>T maps to NM_148910.2 Q27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1G-01A-11D-A435-10 chr19:3747806 G>T maps to NM_014428.1 E813*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF1-01A-11D-A42Y-10 chr3:53264544 G>C maps to ENST00000423516 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AC-01A-11D-A435-10 chr23:153540935 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAEW-01A-11D-A42Y-10 chr15:70346958 G>A maps to NM_005078.2 G551G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H4-01A-31D-A435-10 chr15:62994393 G>T maps to NM_015059.2 G634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94I-01A-11D-A435-10 chr9:120475854 C>T maps to NM_138554.3 F483F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JY-01A-11D-A435-10 chr23:12904183 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAG5-01A-11D-A42Y-10 chr10:102891432 C>T maps to NM_005521.3 Y45Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1G-01A-11D-A435-10 chr2:74743243 G>T maps to NM_016170.4 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFZ-01A-11D-A42Y-10 chr13:100192990 G>T maps to NM_004800.1 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOJ-01A-12D-A435-10 chr19:54668248 C>T maps to NM_001145303.1 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84X-01A-11D-A435-10 chr12:94976044 C>T maps to NM_020698.2 E116E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH2-01A-11D-A42Y-10 chr19:10946840 G>T maps to NM_006858.2 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X3-A8G4-01A-11D-A435-10 chr19:10943838 G>T maps to NM_006858.2 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H4-01A-31D-A435-10 chr16:69377513 G>T maps to NM_144676.3 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALN-01A-11D-A42Y-10 chr17:8079144 G>T maps to NM_032354.3 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-AA4L-01A-11D-A435-10 chr11:60689300 G>T maps to NM_024092.2 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr12:130184359 C>T maps to NM_133448.2 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SO-A8JP-01A-11D-A435-10 chr12:130184605 G>A maps to NM_133448.2 C239C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGY-01A-11D-A42Y-10 chr17:32964257 C>T maps to NM_207313.1 Y654Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGF-01A-31D-A42Y-10 chr4:159161569 G>T maps to NM_018342.4 G268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-AA61-01A-11D-A435-10 chr4:947054 G>T maps to NM_032326.2 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGS-01A-11D-A42Y-10 chr7:150489161 G>T maps to NM_014020.3 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG3-01A-11D-A42Y-10 chr2:103380803 C>G maps to NM_144632.3 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94D-01A-11D-A435-10 chr2:103380824 C>A maps to NM_144632.3 Y90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGN-01A-11D-A42Y-10 chr23:148690470 C>T did not map to a codon.
Sequencing variant TCGA-XE-AAOJ-01A-12D-A435-10 chr19:55889030 C>T maps to NM_139172.1 C55C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SO-A8JP-01A-11D-A435-10 chr6:130762742 G>T maps to NM_052913.2 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKL-01A-11D-A42Y-10 chr16:75590078 G>T maps to NM_001077416.1 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGF-01A-31D-A42Y-10 chr6:75994278 G>T maps to NM_018247.3 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90Q-01A-11D-A435-10 chr14:20928915 C>A maps to NM_001100814.1 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO4-01A-11D-A435-10 chr6:44114584 G>T maps to NM_018426.1 E262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG9-01A-11D-A42Y-10 chr8:125384233 G>T maps to NM_194291.2 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr1:16069670 G>A maps to NM_001013641.1 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr19:55739751 G>T maps to NM_173804.4 Y35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AE-01A-11D-A435-10 chr19:4292622 T>C maps to NM_144615.2 K274K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO3-01A-11D-A435-10 chr19:4292841 C>G maps to NM_144615.2 G201G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-XE-AAO4-01A-11D-A435-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-XE-AAO4-01A-11D-A435-10 chr9:100325014 G>T maps to ENST00000395208 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAEW-01A-11D-A42Y-10 chr17:42266737 T>G maps to NM_001076674.1 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0E-01A-12D-A435-10 chr11:57505457 G>A maps to NM_015959.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGJ-01A-11D-A42Y-10 chr20:8000251 A>C maps to NM_021156.2 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGX-01A-11D-A42Y-10 chr20:8000251 A>C maps to NM_021156.2 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AD-01A-11D-A435-10 chr20:8000251 A>C maps to NM_021156.2 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM3-01A-11D-A435-10 chr9:117846506 G>T maps to NM_002160.2 V704V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X3-A8G4-01A-11D-A435-10 chr8:22880438 C>T maps to NM_003842.4 P356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF1-01A-11D-A42Y-10 chr18:60036583 T>C maps to NM_003839.2 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOF-01A-11D-A435-10 chr20:62328828 C>T maps to NM_003823.2 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0E-01A-12D-A435-10 chr17:7460570 G>T maps to NM_003809.2 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGM-01A-11D-A42Y-10 chr3:170856033 C>A maps to NM_015028.2 L518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGY-01A-11D-A42Y-10 chr5:150436452 C>T maps to NM_006058.3 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A8S2-01A-11D-A435-10 chr5:150444638 C>T maps to NM_006058.3 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0F-01A-21D-A435-10 chr4:2749516 G>A maps to NM_024309.3 C144C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-AA61-01A-11D-A435-10 chr8:9627762 A>G maps to NM_003747.2 R1296R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF8-01A-11D-A42Y-10 chr19:12816531 G>C maps to NM_001136196.1 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr1:175328772 G>A maps to NM_003285.2 Y983Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGW-01A-11D-A42Y-10 chr7:5410780 C>T maps to NM_001080495.2 P1148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0B-01A-11D-A435-10 chr7:5352832 G>A maps to NM_001080495.2 S2563S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGA-01A-11D-A42Y-10 chr16:24826528 C>T maps to NM_014494.2 N1578N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AAAL-01A-11D-A435-10 chr17:76063991 A>G maps to NM_001142640.1 K919K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SO-A8JP-01A-11D-A435-10 chr17:76047437 C>T maps to NM_001142640.1 T765T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOD-01A-11D-A435-10 chr17:76047437 C>T maps to NM_001142640.1 T765T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGG-01A-11D-A42Y-10 chr7:47474984 C>T maps to NM_022748.11 W73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG5-01A-11D-A42Y-10 chr6:32037570 C>T maps to ENST00000375244 L1782L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr17:48941030 A>G maps to NM_005749.2 D116D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0H-01A-11D-A435-10 chr1:179851684 T>G maps to ENST00000398836 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKL-01A-11D-A42Y-10 chr9:132565664 C>T maps to NM_014506.1 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALS-01A-12D-A42Y-10 chr8:59728031 A>G maps to NM_014729.2 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A8D5-01A-11D-A435-10 chr20:42694569 A>G maps to ENST00000348077 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94I-01A-11D-A435-10 chr3:189586469 C>A maps to NM_003722.4 S365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94I-01A-11D-A435-10 chr1:3607507 G>T maps to NM_001126240.1 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AB-01A-31D-A435-10 chr12:113714755 C>T maps to NM_001143819.1 D397D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALP-01A-12D-A42Y-10 chr11:68830458 G>T did not map to a codon.
Sequencing variant TCGA-YU-A90W-01A-11D-A435-10 chr1:186283153 C>T maps to NM_003292.2 V2347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG7-01A-11D-A42Y-10 chr13:20025335 A>G maps to NM_199254.2 H257H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGI-01A-11D-A42Y-10 chr13:20025335 A>G maps to NM_199254.2 H257H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAEX-01A-11D-A42Y-10 chr12:112579947 T>G maps to NM_006700.2 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALQ-01A-12D-A42Y-10 chr12:112579947 T>G maps to NM_006700.2 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH8-01A-11D-A42Y-10 chr3:129695839 G>A maps to NM_007117.3 E170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANJ-01A-11D-A435-10 chr3:129695839 G>A maps to NM_007117.3 E170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFN-01A-31D-A42Y-10 chr13:50590788 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAG6-01A-11D-A42Y-10 chr13:50588548 A>G did not map to a codon.
Sequencing variant TCGA-XE-AAO4-01A-11D-A435-10 chr13:50589359 G>T did not map to a codon.
Sequencing variant TCGA-YU-A90P-01A-11D-A435-10 chr5:64906829 G>C maps to NM_001656.3 S229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFI-01A-21D-A42Y-10 chr7:138239516 C>T maps to NM_015905.2 Q446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG8-01A-31D-A42Y-10 chr11:119998157 C>A maps to NM_012101.3 V340V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALO-01A-12D-A42Y-10 chr1:155156380 G>T maps to NM_025058.3 S665S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGG-01A-11D-A42Y-10 chr11:5699637 G>A maps to NM_033034.2 N180N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGK-01A-11D-A42Y-10 chr11:5631467 G>T maps to NM_001003819.3 V317V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0E-01A-12D-A435-10 chr1:231299689 G>T maps to NM_001004342.3 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAL7-01A-11D-A42Y-10 chr3:32915368 C>T maps to NM_001039111.1 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFI-01A-21D-A42Y-10 chr5:14507270 G>T maps to NM_007118.2 G2885*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFV-01A-11D-A42Y-10 chr2:230668943 C>G did not map to a codon.
Sequencing variant TCGA-2G-AAFZ-01A-11D-A42Y-10 chr2:230650471 C>T did not map to a codon.
Sequencing variant TCGA-2G-AAGF-01A-31D-A42Y-10 chr7:100466177 C>A maps to NM_003302.2 S142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG9-01A-11D-A42Y-10 chr14:104001088 C>T maps to ENST00000299201 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH2-01A-11D-A42Y-10 chr22:46749662 G>C did not map to a codon.
Sequencing variant TCGA-2G-AALQ-01A-12D-A42Y-10 chr22:46731699 C>T maps to NM_018006.4 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANI-01A-11D-A435-10 chr8:72987611 A>T maps to NM_007332.2 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGZ-01A-11D-A42Y-10 chr20:33609142 A>G maps to NM_015638.2 P356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOL-01A-11D-A435-10 chr5:135692523 C>T maps to NM_020389.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM4-01A-11D-A435-10 chr11:2436202 C>T maps to ENST00000452833 W520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFO-01A-31D-A42Y-10 chr9:77359050 G>T maps to NM_017662.4 A1698A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG0-01A-11D-A42Y-10 chr8:116599270 G>T maps to NM_014112.2 S886*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANI-01A-11D-A435-10 chr12:110230495 C>T maps to NM_021625.4 G595G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X3-A8G4-01A-11D-A435-10 chr7:142606734 G>T maps to NM_019841.4 R606R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFM-01A-11D-A42Y-10 chr7:98601960 G>A maps to ENST00000359863 S3472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0E-01A-12D-A435-10 chr7:98507791 C>A maps to ENST00000359863 P488P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHC-01A-11D-A42Y-10 chr16:2106706 G>T maps to NM_000548.3 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALX-01A-11D-A42Y-10 chr23:106957875 T>C did not map to a codon.
Sequencing variant TCGA-2G-AAG3-01A-11D-A42Y-10 chr3:12544860 G>T maps to NM_025265.3 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF1-01A-11D-A42Y-10 chr14:81534630 G>T maps to NM_000369.2 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF8-01A-11D-A42Y-10 chr14:81422035 G>A maps to NM_000369.2 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr19:50251404 G>A maps to NM_021733.1 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A8D5-01A-11D-A435-10 chr17:79612647 C>T maps to NM_031945.3 Q223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFG-01A-11D-A42Y-10 chr11:864453 G>T maps to ENST00000409531 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH3-01A-11D-A42Y-10 chr23:53111841 G>T did not map to a codon.
Sequencing variant TCGA-YU-A90S-01A-11D-A435-10 chr23:53111999 A>G did not map to a codon.
Sequencing variant TCGA-2G-AAF1-01A-11D-A42Y-10 chr6:116574166 G>T maps to ENST00000368611 G385G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H5-01A-11D-A435-10 chr11:113233142 C>T maps to NM_017868.3 S545S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A8S3-01B-11D-A435-10 chr3:180320159 G>T maps to NM_133462.3 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGS-01A-11D-A42Y-10 chr11:43465664 G>A maps to NM_018259.5 G857G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH0-01A-11D-A42Y-10 chr15:99740252 T>C maps to NM_022905.4 Q210Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALS-01A-12D-A42Y-10 chr1:156551834 G>T maps to NM_001105669.2 E227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0H-01A-11D-A435-10 chr21:38468892 C>T maps to NM_003316.3 Y265Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84W-01A-11D-A435-10 chr5:94803685 G>T maps to NM_014639.3 R1502R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH8-01A-11D-A42Y-10 chr22:46685355 C>A maps to NM_017931.2 C380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SO-A8JP-01A-11D-A435-10 chr14:91252655 A>G maps to NM_001010854.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94D-01A-11D-A435-10 chr14:71109247 G>T maps to NM_015351.1 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGE-01A-21D-A42Y-10 chr1:1132854 C>T maps to NM_001130045.1 G550G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALR-01A-21D-A42Y-10 chr22:43579062 C>T maps to NM_015140.3 Q90Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGN-01A-11D-A42Y-10 chr15:90793910 G>T maps to ENST00000438251 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFI-01A-21D-A42Y-10 chr6:167754660 A>T maps to NM_031949.4 R425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90W-01A-11D-A435-10 chr2:219612367 G>T maps to NM_014640.4 R766R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFV-01A-11D-A42Y-10 chr2:179490018 G>A maps to NM_133378.4 H12275H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0N-01A-21D-A435-10 chr19:54941999 C>T maps to ENST00000391739 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SB-A76C-01A-11D-A435-10 chr17:72218736 C>A maps to NM_032646.5 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANR-01A-11D-A435-10 chr12:49580191 A>G maps to NM_006009.2 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H4-01A-31D-A435-10 chr13:19751291 T>C maps to NM_006001.1 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGS-01A-11D-A42Y-10 chr6:30691667 G>T maps to NM_178014.2 G277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGE-01A-21D-A42Y-10 chr15:43678500 G>T maps to ENST00000399460 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SO-A8JP-01A-11D-A435-10 chr22:50656422 A>C maps to NM_020461.3 G1764G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOC-01A-11D-A435-10 chr1:151546804 G>A maps to NM_020127.2 E218E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFJ-01A-11D-A42Y-10 chr8:15517059 A>G maps to NM_006765.2 K157K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHN-01A-11D-A42Y-10 chr3:52264020 C>T maps to ENST00000494383 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94D-01A-11D-A435-10 chr4:48115253 C>T maps to NM_003328.2 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90Y-01A-11D-A435-10 chr6:139569007 G>A maps to ENST00000358430 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOD-01A-11D-A435-10 chr6:7883445 C>T maps to NM_030810.3 E410E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALG-01A-11D-A42Y-10 chr22:19885585 G>A maps to NM_006440.3 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2X-A9D6-01A-11D-A435-10 chr22:50965053 G>A maps to ENST00000395681 C293C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFY-01A-11D-A42Y-10 chr15:41865665 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAH8-01A-11D-A42Y-10 chr19:36233571 C>T maps to NM_144987.2 W179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84W-01A-11D-A435-10 chr19:56180495 G>T maps to NM_007279.2 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANI-01A-11D-A435-10 chr15:70976694 C>T maps to NM_018003.2 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALX-01A-11D-A42Y-10 chr13:99853188 G>T maps to NM_001144072.1 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOB-01A-11D-A435-10 chr11:122526900 G>A maps to NM_032873.4 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFH-01A-12D-A42Y-10 chr17:16285478 C>G maps to NM_018955.2 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr12:125398023 G>A maps to NM_021009.5 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO3-01A-11D-A435-10 chr3:23848777 G>T maps to NM_003341.3 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr16:1370229 C>T maps to NM_194259.1 C93C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH3-01A-11D-A42Y-10 chr23:142967559 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAFG-01A-11D-A42Y-10 chr12:109972568 G>T maps to NM_183415.1 T1063T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG9-01A-11D-A42Y-10 chr16:23569547 C>T maps to ENST00000219638 F325F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF8-01A-11D-A42Y-10 chr15:74744663 C>T maps to NM_201265.1 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFH-01A-12D-A42Y-10 chr16:4925275 G>A maps to NM_016936.3 G955G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A912-01A-11D-A435-10 chr16:4903070 C>G maps to NM_016936.3 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALT-01A-11D-A42Y-10 chr2:170684526 C>T maps to ENST00000442603 C170C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFH-01A-12D-A42Y-10 chr1:19483406 G>A maps to ENST00000375267 Q1925*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG7-01A-11D-A42Y-10 chr1:26624521 G>T maps to NM_183008.2 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKL-01A-11D-A42Y-10 chr1:26608903 A>G maps to NM_183008.2 P483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X3-A8G4-01A-11D-A435-10 chr9:134404414 G>A maps to NM_031432.2 D173D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A6IS-01A-11D-A435-10 chr4:186324767 T>C maps to NM_018359.3 G401G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V5-01A-11D-A435-10 chr6:150390211 G>T did not map to a codon.
Sequencing variant TCGA-SN-A84Y-01A-11D-A435-10 chr12:132398926 C>T maps to NM_003565.2 C426C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-AA61-01A-11D-A435-10 chr12:132403797 G>A maps to NM_003565.2 L851L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr21:43547247 G>T maps to NM_173568.3 G1270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFM-01A-11D-A42Y-10 chr17:73832672 G>T maps to ENST00000412096 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFM-01A-11D-A42Y-10 chr11:67770592 C>A maps to NM_030930.2 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGE-01A-21D-A42Y-10 chr11:67763106 A>G maps to NM_030930.2 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOJ-01A-12D-A435-10 chr11:67763106 A>G maps to NM_030930.2 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA05-01A-12D-A435-10 chr11:67763106 A>G maps to NM_030930.2 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SB-A6J6-01A-11D-A435-10 chr17:73808666 G>T did not map to a codon.
Sequencing variant TCGA-XE-A9SE-01A-21D-A435-10 chr17:73812896 C>T maps to NM_001080419.1 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0N-01A-21D-A435-10 chr16:1417323 C>T maps to ENST00000508903 A605A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOJ-01A-12D-A435-10 chr7:48139312 G>T maps to NM_003364.2 E31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGV-01A-11D-A42Y-10 chr23:74519637 A>G did not map to a codon.
Sequencing variant TCGA-XE-AANJ-01A-11D-A435-10 chr20:33891796 T>A maps to NM_018244.4 K281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALW-01A-11D-A42Y-10 chr7:43917156 C>T maps to NM_001077663.1 R635R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H5-01A-11D-A435-10 chr16:84797755 T>C maps to NM_005153.2 G573G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG9-01A-11D-A42Y-10 chr23:47092515 G>T did not map to a codon.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr3:49146486 G>T maps to ENST00000434032 G1388G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X3-A8G4-01A-11D-A435-10 chr3:49154691 G>T maps to ENST00000434032 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AE-01A-11D-A435-10 chr15:63852124 A>G maps to NM_006537.2 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG7-01A-11D-A42Y-10 chr17:58303400 G>A maps to NM_032582.3 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V5-01A-11D-A435-10 chr17:58343351 G>T maps to NM_032582.3 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALZ-01A-11D-A42Y-10 chr2:61610447 G>T maps to NM_014709.3 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFM-01A-11D-A42Y-10 chr17:76799978 G>T maps to NM_025090.3 P766P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKG-01A-11D-A42Y-10 chr17:76810499 G>A maps to NM_025090.3 Y386Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JX-01A-11D-A435-10 chr17:76799993 C>T maps to NM_025090.3 L761L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr2:85843582 C>T maps to NM_006590.2 R89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JY-01A-11D-A435-10 chr2:234394245 C>T maps to NM_018218.2 K1156K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAL7-01A-11D-A42Y-10 chr12:6965260 C>T maps to NM_001098536.1 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFG-01A-11D-A42Y-10 chr15:50733582 G>T maps to NM_005154.3 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGE-01A-21D-A42Y-10 chr24:14952389 C>T did not map to a codon.
Sequencing variant TCGA-2G-AAHA-01A-11D-A42Y-10 chr24:14952958 G>T did not map to a codon.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr24:14902337 A>G did not map to a codon.
Sequencing variant TCGA-2G-AAEX-01A-11D-A42Y-10 chr17:49338190 G>A maps to NM_016001.2 E82E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84W-01A-11D-A435-10 chr12:101763602 G>A maps to NM_014503.2 L2163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V5-01A-11D-A435-10 chr6:145148507 G>A maps to NM_007124.2 W3173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90Y-01A-11D-A435-10 chr6:144780095 C>T maps to NM_007124.2 S825S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALW-01A-11D-A42Y-10 chr24:15478189 C>A did not map to a codon.
Sequencing variant TCGA-2G-AAG3-01A-11D-A42Y-10 chr6:30890753 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAGX-01A-11D-A42Y-10 chr16:4432542 A>C maps to NM_138440.2 T555T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGF-01A-31D-A42Y-10 chr16:77822665 C>T maps to NM_020927.1 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr2:71148282 G>T maps to NM_012476.2 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90P-01A-11D-A435-10 chr9:35059087 T>C maps to NM_007126.3 R711R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALX-01A-11D-A42Y-10 chr23:7811809 G>C did not map to a codon.
Sequencing variant TCGA-2G-AAHG-01A-11D-A42Y-10 chr23:8434339 G>A did not map to a codon.
Sequencing variant TCGA-XY-A8S2-01A-11D-A435-10 chr6:43738964 C>T maps to NM_001025366.2 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOJ-01A-12D-A435-10 chr11:64003784 C>T maps to NM_003377.3 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A9T9-01A-11D-A435-10 chr11:64005047 A>C maps to NM_003377.3 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SB-A6J6-01A-11D-A435-10 chr10:135051633 G>T maps to NM_014468.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFZ-01A-11D-A42Y-10 chr7:100807776 G>T maps to NM_003378.3 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A9SE-01A-21D-A435-10 chr3:10191523 G>T maps to NM_000551.2 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANI-01A-11D-A435-10 chr3:38035876 G>T maps to NM_015873.3 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFL-01A-21D-A42Y-10 chr17:4689635 G>T maps to NM_182566.2 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGT-01A-11D-A42Y-10 chr22:24095308 G>T maps to ENST00000405618 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH3-01A-11D-A42Y-10 chr15:62254065 G>T maps to NM_020821.2 A1210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AAAL-01A-11D-A435-10 chr15:62199516 G>T maps to NM_020821.2 T3017T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90P-01A-11D-A435-10 chr15:62204117 G>T maps to NM_020821.2 S2879*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0B-01A-11D-A435-10 chr1:12304671 G>T maps to NM_015378.2 E149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH3-01A-11D-A42Y-10 chr20:2843983 C>G maps to NM_022575.2 Y472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG9-01A-11D-A42Y-10 chr11:134114844 G>T maps to NM_052875.3 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2X-A9D5-01A-11D-A435-10 chr11:134114859 G>T maps to NM_052875.3 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AA-01A-11D-A435-10 chr12:122723202 G>A maps to NM_022916.4 C411C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO3-01A-11D-A435-10 chr7:38902195 G>T maps to NM_014396.3 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0H-01A-11D-A435-10 chr18:61067302 C>T maps to NM_004869.3 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94D-01A-11D-A435-10 chr2:64160839 G>T maps to NM_016516.2 S569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALS-01A-12D-A42Y-10 chr1:151156790 A>T did not map to a codon.
Sequencing variant TCGA-ZM-AA0F-01A-21D-A435-10 chr2:58316776 G>T maps to NM_001130480.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFM-01A-11D-A42Y-10 chr23:65253546 C>A did not map to a codon.
Sequencing variant TCGA-2G-AAGV-01A-11D-A42Y-10 chr1:159824641 G>A maps to NM_001013661.1 C382C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG0-01A-11D-A42Y-10 chr20:25060100 G>T maps to NM_014588.4 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALN-01A-11D-A42Y-10 chr14:68118104 A>G maps to NM_006370.2 H232H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGP-01A-11D-A42Y-10 chr7:49815585 G>C maps to NM_198570.3 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF4-01A-11D-A42Y-10 chr11:61042027 G>A maps to NM_152718.2 Y508Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM3-01A-11D-A435-10 chr12:6127717 G>A maps to NM_000552.3 D1622D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFI-01A-21D-A42Y-10 chr1:27736342 G>A maps to NM_006990.2 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84Y-01A-11D-A435-10 chr1:27736267 C>T maps to NM_006990.2 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFY-01A-11D-A42Y-10 chr12:14947585 A>G maps to NM_016312.2 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFZ-01A-11D-A42Y-10 chr12:14947585 A>G maps to NM_016312.2 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALN-01A-11D-A42Y-10 chr12:14947585 A>G maps to NM_016312.2 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM4-01A-11D-A435-10 chr12:14947585 A>G maps to NM_016312.2 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H5-01A-11D-A435-10 chr12:14941900 A>G maps to NM_016312.2 P492P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H5-01A-11D-A435-10 chr12:14941933 A>G maps to NM_016312.2 G481G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90S-01A-11D-A435-10 chr16:737361 G>T maps to ENST00000248142 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SO-A8JP-01A-11D-A435-10 chr2:20113318 T>C maps to NM_001006657.1 *1182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM3-01A-11D-A435-10 chr21:44273834 C>T maps to NM_018669.4 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGA-01A-11D-A42Y-10 chr23:48935721 G>C did not map to a codon.
Sequencing variant TCGA-2G-AAGC-01A-21D-A42Y-10 chr9:137007544 G>A did not map to a codon.
Sequencing variant TCGA-4K-AAAL-01A-11D-A435-10 chr3:113115370 G>A maps to NM_001164496.1 A591A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO6-01A-31D-A435-10 chr3:113115496 T>C maps to NM_001164496.1 K549K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGF-01A-31D-A42Y-10 chr19:36577592 G>T maps to NM_001083961.1 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFG-01A-11D-A42Y-10 chr1:85573832 G>T maps to NM_145172.3 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFN-01A-31D-A42Y-10 chr1:85573730 G>A maps to NM_145172.3 W523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AE-01A-11D-A435-10 chr15:44134648 G>T maps to NM_024908.3 E257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOL-01A-11D-A435-10 chr16:705433 C>A maps to NM_145294.4 R562R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGA-01A-11D-A42Y-10 chr1:27632717 T>G maps to ENST00000319394 G626G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHL-01A-11D-A42Y-10 chr4:6293695 C>T maps to NM_006005.3 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH0-01A-11D-A42Y-10 chr7:5266966 G>T maps to NM_015610.3 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90Q-01A-11D-A435-10 chr8:134232842 C>T maps to NM_003882.2 C123C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H4-01A-31D-A435-10 chr12:994307 A>G maps to NM_001184985.1 A1706A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGJ-01A-11D-A42Y-10 chr9:95947606 T>A maps to ENST00000297954 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGY-01A-11D-A42Y-10 chr9:96055380 C>A maps to ENST00000297954 S1915S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0D-01A-11D-A435-10 chr9:96024343 C>T maps to ENST00000297954 A1105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1H-01A-11D-A435-10 chr23:54263898 G>T did not map to a codon.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr23:54285765 T>C did not map to a codon.
Sequencing variant TCGA-WZ-A7V5-01A-11D-A435-10 chr23:54265468 C>T did not map to a codon.
Sequencing variant TCGA-XE-A8H4-01A-31D-A435-10 chr23:54320995 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAFZ-01A-11D-A42Y-10 chr3:55504143 G>A maps to NM_003392.3 I373I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAL7-01A-11D-A42Y-10 chr1:228112985 G>A maps to NM_003395.2 Y110Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALP-01A-12D-A42Y-10 chr17:7606660 T>C maps to NM_018081.2 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A8S2-01A-11D-A435-10 chr6:2770514 G>A maps to NM_020135.2 A392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr5:167719172 C>T maps to NM_001161661.1 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHL-01A-11D-A42Y-10 chr23:10098005 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAGC-01A-21D-A42Y-10 chr23:2700163 G>A did not map to a codon.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr23:123040894 G>T did not map to a codon.
Sequencing variant TCGA-SB-A6J6-01A-11D-A435-10 chr8:71646626 G>T maps to NM_001011720.1 E364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOD-01A-11D-A435-10 chr23:128886307 A>G did not map to a codon.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr6:43519112 G>T maps to NM_020750.2 S550S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG6-01A-11D-A42Y-10 chr1:180756958 A>G maps to NM_004736.3 K64K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGO-01A-11D-A42Y-10 chr7:152357796 G>T maps to NM_005431.1 S37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOC-01A-11D-A435-10 chr14:104169620 G>T maps to NM_005432.3 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALO-01A-12D-A42Y-10 chr2:216990648 G>T maps to NM_021141.3 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A8D5-01A-11D-A435-10 chr16:17228330 G>A maps to NM_022166.3 R676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2X-A9D6-01A-11D-A435-10 chr17:48431835 G>T maps to NM_022167.2 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF8-01A-11D-A42Y-10 chr12:42631961 G>T maps to NM_001190979.1 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH3-01A-11D-A42Y-10 chr14:75230978 G>T maps to NM_019589.2 E263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGI-01A-11D-A42Y-10 chr4:69202913 C>T maps to NM_001031732.2 E238E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALF-01A-11D-A42Y-10 chr20:61833917 G>A maps to NM_017798.3 Y458Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGO-01A-11D-A42Y-10 chr8:64099414 A>G maps to ENST00000339066 K281K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A94I-01A-11D-A435-10 chr22:32352742 C>T maps to NM_003405.3 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFJ-01A-11D-A42Y-10 chr2:9725474 C>G did not map to a codon.
Sequencing variant TCGA-ZM-AA0H-01A-11D-A435-10 chr2:9727623 G>A maps to NM_006826.2 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKG-01A-11D-A42Y-10 chr7:100331728 A>G did not map to a codon.
Sequencing variant TCGA-2G-AAKD-01A-31D-A42Y-10 chr3:167034804 G>A maps to ENST00000307529 V394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84Y-01A-11D-A435-10 chr23:2406763 T>C did not map to a codon.
Sequencing variant TCGA-SN-A84X-01A-11D-A435-10 chr14:64989757 G>A maps to NM_001123329.1 R512R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H4-01A-31D-A435-10 chr14:64998613 G>T maps to NM_014950.2 *645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALY-01A-11D-A42Y-10 chr3:101373561 G>T maps to NM_014415.3 G765G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHP-01A-12D-A42Y-10 chr11:62520425 G>T maps to NM_024784.3 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A8S2-01A-11D-A435-10 chr1:173839875 G>A maps to NM_001122770.1 K171K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANV-01A-11D-A435-10 chr17:7366299 G>T maps to NM_020899.3 Y667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr9:129596182 G>A maps to NM_014007.3 E465E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFN-01A-31D-A42Y-10 chr20:62421957 G>T maps to NM_025224.2 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFM-01A-11D-A42Y-10 chr19:4054918 C>T maps to NM_015898.2 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AC-01A-11D-A435-10 chr1:33099657 T>C maps to NM_178547.2 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H1-01A-11D-A435-10 chr6:33423521 G>A maps to NM_152735.3 E215E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG6-01A-11D-A42Y-10 chr23:64722642 A>C did not map to a codon.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr16:88664701 G>T maps to ENST00000452588 G293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKG-01A-11D-A42Y-10 chr22:41742034 C>T maps to ENST00000351589 Y512Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A8S2-01A-11D-A435-10 chr7:129664140 G>T maps to NM_016478.3 R328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A8D5-01A-11D-A435-10 chr16:87451242 C>T maps to NM_015144.2 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGG-01A-11D-A42Y-10 chr16:67428727 C>T maps to NM_013304.2 P433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG3-01A-11D-A42Y-10 chr5:840703 G>A maps to NM_024786.2 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALS-01A-12D-A42Y-10 chr11:19174228 G>T maps to NM_019028.2 E291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALN-01A-11D-A42Y-10 chr23:74698771 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAM3-01A-11D-A435-10 chr12:77209654 G>A maps to NM_015336.2 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2X-A9D6-01A-11D-A435-10 chr11:66313360 C>T maps to NM_207340.1 V38V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA05-01A-12D-A435-10 chr11:66307128 G>T maps to NM_207340.1 C242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A8D5-01A-11D-A435-10 chr22:20128207 G>T maps to NM_013373.3 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AAAL-01A-11D-A435-10 chr10:31803541 G>T maps to NM_001174096.1 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHL-01A-11D-A42Y-10 chr12:72028577 T>A maps to NM_144982.4 K756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84Y-01A-11D-A435-10 chr16:72821623 G>A maps to NM_006885.3 G3517G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGI-01A-11D-A42Y-10 chr8:77775450 T>A maps to NM_024721.4 P3167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGS-01A-11D-A42Y-10 chr8:77617507 G>A maps to NM_024721.4 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V5-01A-11D-A435-10 chr19:38125921 G>T maps to NM_014898.2 S507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH4-01A-12D-A42Y-10 chr4:188924032 G>A maps to NM_174900.3 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGJ-01A-11D-A42Y-10 chr8:106813719 A>T maps to NM_012082.3 I470I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90Y-01A-11D-A435-10 chr19:3831688 G>T maps to NM_015174.1 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKO-01A-11D-A42Y-10 chr23:24228772 C>T did not map to a codon.
Sequencing variant TCGA-2G-AAGS-01A-11D-A42Y-10 chr24:2829679 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAGT-01A-11D-A42Y-10 chr24:2829597 C>T did not map to a codon.
Sequencing variant TCGA-2G-AAFV-01A-11D-A42Y-10 chr15:41104994 C>T maps to NM_001077268.1 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A6IS-01A-11D-A435-10 chr10:99504636 G>T maps to NM_001002261.3 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFZ-01A-11D-A42Y-10 chr20:62364704 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAG3-01A-11D-A42Y-10 chr8:124267670 A>G maps to NM_007222.3 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFZ-01A-11D-A42Y-10 chr23:70472908 A>G did not map to a codon.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr23:70470505 C>T did not map to a codon.
Sequencing variant TCGA-YU-A94D-01A-11D-A435-10 chr1:35486069 T>C did not map to a codon.
Sequencing variant TCGA-2G-AAGP-01A-11D-A42Y-10 chr20:45874863 G>A maps to ENST00000471951 G725G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGP-01A-11D-A42Y-10 chr19:19823096 C>T maps to NM_021030.2 G331G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALX-01A-11D-A42Y-10 chr11:9519220 G>T did not map to a codon.
Sequencing variant TCGA-ZM-AA06-01A-12D-A435-10 chr19:36727686 C>T maps to NM_007145.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGP-01A-11D-A42Y-10 chr23:47847943 G>T did not map to a codon.
Sequencing variant TCGA-2G-AALR-01A-21D-A42Y-10 chr23:152110347 C>A did not map to a codon.
Sequencing variant TCGA-2G-AAFN-01A-31D-A42Y-10 chr19:22157460 C>T maps to NM_007153.3 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr19:22156902 C>T maps to NM_007153.3 K311K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF8-01A-11D-A42Y-10 chr20:52192818 C>T maps to NM_006526.2 G828G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOJ-01A-12D-A435-10 chr20:52199326 G>T maps to NM_006526.2 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-AA4L-01A-11D-A435-10 chr20:52198197 G>A maps to NM_006526.2 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V3-01A-11D-A435-10 chr19:44778516 G>T maps to NM_181756.1 V568V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANJ-01A-11D-A435-10 chr19:44778237 T>C maps to NM_181756.1 T475T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO4-01A-11D-A435-10 chr19:44778738 T>C maps to NM_181756.1 H642H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANI-01A-11D-A435-10 chr18:74637143 G>T did not map to a codon.
Sequencing variant TCGA-WZ-A7V5-01A-11D-A435-10 chr7:64389257 G>T maps to NM_021148.2 E518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALR-01A-21D-A42Y-10 chr23:152612976 C>T did not map to a codon.
Sequencing variant TCGA-ZM-AA0H-01A-11D-A435-10 chr16:89789842 C>G maps to NM_001113525.1 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AD-01A-11D-A435-10 chr22:22842205 T>A maps to NM_080764.2 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0H-01A-11D-A435-10 chr19:44352550 G>T maps to NM_181845.1 E600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOB-01A-11D-A435-10 chr19:9268705 G>T maps to NM_020933.4 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr16:58031251 C>T maps to NM_020807.1 P306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AC-01A-11D-A435-10 chr20:32379154 G>T maps to ENST00000375200 A799A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AAAL-01A-11D-A435-10 chr20:2464082 G>A maps to NM_024325.4 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGA-01A-11D-A42Y-10 chr5:176449807 G>T maps to ENST00000503039 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A8D5-01A-11D-A435-10 chr19:7585210 G>T maps to NM_018083.4 A361A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-2G-AALZ-01A-11D-A42Y-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-2G-AALZ-01A-11D-A42Y-10 chr12:6777082 G>A maps to NM_001135734.1 Q511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALY-01A-11D-A42Y-10 chr18:32949291 G>T maps to NM_145756.2 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGM-01A-11D-A42Y-10 chr7:148851347 G>T maps to NM_170686.2 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGY-01A-11D-A42Y-10 chr7:148876751 T>G maps to NM_170686.2 G596G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALP-01A-12D-A42Y-10 chr7:148876751 T>G maps to NM_170686.2 G596G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A9T9-01A-11D-A435-10 chr18:72775487 A>G maps to NM_017757.2 G1937G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84X-01A-11D-A435-10 chr23:47308135 G>T did not map to a codon.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr23:47315339 G>A did not map to a codon.
Sequencing variant TCGA-2G-AAG8-01A-31D-A42Y-10 chr16:49670953 C>A maps to NM_015069.2 S703S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHL-01A-11D-A42Y-10 chr16:49671202 G>T maps to NM_015069.2 L620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAOD-01A-11D-A435-10 chr7:148801462 G>T maps to NM_001001661.2 C500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA06-01A-12D-A435-10 chr19:21991245 A>G maps to NM_003423.2 T531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-A8H5-01A-11D-A435-10 chr19:52550106 C>T maps to NM_014650.2 Q5Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AD-01A-11D-A435-10 chr19:11978337 G>T maps to NM_152262.2 E152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFI-01A-21D-A42Y-10 chr1:247464564 C>T maps to NM_032752.1 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGE-01A-21D-A42Y-10 chr1:247492679 G>A maps to NM_032752.1 C67C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84Y-01A-11D-A435-10 chr19:58868527 G>T maps to NM_198458.1 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AALR-01A-21D-A42Y-10 chr3:44762584 A>G maps to NM_033210.4 E92E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFJ-01A-11D-A42Y-10 chr10:77159835 A>C maps to NM_032772.4 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAL5-01A-11D-A42Y-10 chr10:77159541 C>T maps to NM_032772.4 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFO-01A-31D-A42Y-10 chr20:62594603 G>T maps to NM_020713.1 A604A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH4-01A-12D-A42Y-10 chr20:62594729 G>A maps to NM_020713.1 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANV-01A-11D-A435-10 chr19:56113900 G>A maps to NM_153219.2 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1H-01A-11D-A435-10 chr19:42729229 A>G maps to NM_133444.1 K225K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO4-01A-11D-A435-10 chr19:31040044 C>A maps to NM_014717.1 S1173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr19:9452579 A>G maps to NM_032497.1 Q151Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90S-01A-11D-A435-10 chr19:56090219 C>G maps to NM_152600.2 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKH-01A-11D-A42Y-10 chr19:52519422 A>G maps to NM_025040.3 C476C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-A90S-01A-11D-A435-10 chr3:40573807 G>T maps to NM_001098414.1 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHL-01A-11D-A42Y-10 chr16:30794397 G>T maps to NM_001080417.1 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGG-01A-11D-A42Y-10 chr23:47919585 A>T did not map to a codon.
Sequencing variant TCGA-YU-A94D-01A-11D-A435-10 chr23:22291677 A>G did not map to a codon.
Sequencing variant TCGA-XY-A8S3-01B-11D-A435-10 chr16:31092942 T>C maps to NM_014699.3 C1766C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SB-A76C-01A-11D-A435-10 chr19:52394803 C>T maps to NM_023074.3 E195E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84W-01A-11D-A435-10 chr19:11616496 G>T maps to NM_138783.3 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZM-AA0B-01A-11D-A435-10 chr19:11597956 G>A maps to NM_138783.3 C396C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANJ-01A-11D-A435-10 chr19:58232943 G>T maps to ENST00000335820 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGT-01A-11D-A42Y-10 chr1:249142348 C>T maps to NM_024836.1 F292F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAFH-01A-12D-A42Y-10 chr19:22363735 T>G maps to NM_001001411.2 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAH2-01A-11D-A42Y-10 chr19:22363171 G>A maps to NM_001001411.2 Y449Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAKL-01A-11D-A42Y-10 chr19:22363171 G>A maps to NM_001001411.2 Y449Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANJ-01A-11D-A435-10 chr19:22363171 G>A maps to NM_001001411.2 Y449Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANV-01A-11D-A435-10 chr19:22363171 G>A maps to NM_001001411.2 Y449Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1H-01A-11D-A435-10 chr1:249148142 C>T maps to NM_001136036.2 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAG5-01A-11D-A42Y-10 chr1:120165429 G>T maps to NM_001080470.1 R512R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YU-AA4L-01A-11D-A435-10 chr22:24087225 A>G maps to NM_021916.2 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AE-01A-11D-A435-10 chr23:84510317 G>T did not map to a codon.
Sequencing variant TCGA-2G-AALT-01A-11D-A42Y-10 chr22:20759904 G>A maps to NM_003426.2 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AB-01A-31D-A435-10 chr22:20760069 G>T maps to NM_003426.2 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AB-01A-31D-A435-10 chr22:20760417 C>T maps to NM_003426.2 C365C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SB-A76C-01A-11D-A435-10 chr19:12089264 G>T maps to NM_001012753.1 E179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAHL-01A-11D-A42Y-10 chr16:30566958 G>T maps to NM_033410.3 C261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGT-01A-11D-A42Y-10 chr19:57984887 G>T maps to NM_001024596.2 C408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SB-A76C-01A-11D-A435-10 chr19:58265467 G>T maps to NM_173632.3 E324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A6IS-01A-11D-A435-10 chr7:149153032 G>A maps to ENST00000440594 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGJ-01A-11D-A42Y-10 chr16:30594138 G>T maps to NM_152458.6 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4K-AA1H-01A-11D-A435-10 chr7:148769128 G>A maps to NM_152411.3 C245C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8AD-01A-11D-A435-10 chr19:35454539 G>T maps to NM_175872.4 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr3:113956063 G>T did not map to a codon.
Sequencing variant TCGA-XY-A89B-01A-11D-A435-10 chr19:53050832 A>G maps to NM_001039886.3 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A8S3-01B-11D-A435-10 chr23:47705715 G>T did not map to a codon.
Sequencing variant TCGA-2G-AAG7-01A-11D-A42Y-10 chr19:11833769 T>C maps to NM_001080493.2 K193K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WZ-A7V3-01A-11D-A435-10 chr4:146823704 G>A maps to ENST00000508784 R236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S6-A8JX-01A-11D-A435-10 chr19:21132801 C>A maps to NM_003429.4 P494P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VF-A8A8-01A-11D-A435-10 chr7:149543303 C>T maps to NM_001099220.1 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGZ-01A-11D-A42Y-10 chr19:52887145 A>T maps to NM_001145434.1 K105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84Y-01A-11D-A435-10 chr11:64884375 G>T maps to NM_014205.2 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAF1-01A-11D-A42Y-10 chr19:5455600 G>A maps to NM_181710.3 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SN-A84Y-01A-11D-A435-10 chr11:60640736 G>T maps to NM_207341.2 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AANR-01A-11D-A435-10 chr17:38028692 G>T maps to NM_199321.2 E193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAGA-01A-11D-A42Y-10 chr16:3142731 G>T maps to NM_032805.1 C14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XE-AAO4-01A-11D-A435-10 chr19:58846206 G>A maps to NM_181846.2 W13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2G-AAM3-01A-11D-A435-10 chr19:13915705 C>A maps to NM_023072.2 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XY-A8S2-01A-11D-A435-10 chr23:57936053 G>A did not map to a codon.
Sequencing variant TCGA-2G-AAHP-01A-12D-A42Y-10 chr23:57618620 T>C did not map to a codon.
Sequencing variant TCGA-2G-AAFO-01A-31D-A42Y-10 chr3:126180458 G>T maps to NM_025112.4 P682P. Only missense variants will be evaluated by CHASM.
