Sequencing variant TCGA-AB-2830-03B-01W-0728-08 chr16:48244996 G>A maps to NM_032583.3 I490I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2898-03A-01W-0733-08 chr15:89401083 C>T maps to NM_013227.3 S1756S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2887-03A-01W-0732-08 chr11:108009743 T>G maps to NM_000019.3 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-3009-03A-01D-0739-09 chr12:50452779 C>G maps to NM_020039.2 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2973-03A-01D-0739-09 chr10:90695108 C>T maps to NM_001141945.1 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2936-03A-01W-0745-08 chr19:8808550 G>A maps to NM_178525.3 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2819-03B-01W-0728-08 chr5:156920097 G>T maps to ENST00000430702 I599I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2913-03A-01W-0732-08 chr3:64532571 A>T maps to NM_182920.1 I1642I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2862-03B-01W-0728-08 chr3:123071311 C>T maps to NM_183357.2 A417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2832-03B-01W-0728-08 chr15:73045152 A>G maps to NM_031284.4 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2854-03B-01W-0728-08 chr8:26627860 G>A maps to ENST00000356368 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2911-03A-01W-0732-08 chr11:67049290 A>G did not map to a codon.
Sequencing variant TCGA-AB-2912-03A-01W-0732-08 chr1:244580928 C>T did not map to a codon.
Sequencing variant TCGA-AB-3001-03A-01D-0739-09 chr23:147891442 G>A did not map to a codon.
Sequencing variant TCGA-AB-2992-03A-01D-0739-09 chr15:86790956 G>T maps to NM_152336.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2964-03A-01D-0739-09 chr1:110561262 C>T maps to NM_006621.4 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2830-03B-01W-0728-08 chr23:129283540 G>A did not map to a codon.
Sequencing variant TCGA-AB-2915-03A-01W-0745-08 chr10:71883241 C>A maps to NM_032797.5 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2862-03B-01W-0728-08 chr15:86118412 G>A maps to NM_006738.4 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2895-03A-01W-0733-08 chr19:49965891 G>A maps to NM_153329.3 R326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2899-03A-01W-0733-08 chr23:111003072 C>T did not map to a codon.
Sequencing variant TCGA-AB-2935-03A-01W-0755-09 chr10:45938938 C>T maps to NM_000698.2 F509F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2913-03A-01W-0732-08 chr15:85401205 G>A maps to NM_020778.4 E1281E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2992-03A-01D-0739-09 chr23:112058653 A>T did not map to a codon.
Sequencing variant TCGA-AB-2889-03A-01W-0732-08 chr4:114275764 C>T maps to NM_001148.4 F1997F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-3009-03A-01D-0739-09 chr10:61926580 C>A did not map to a codon.
Sequencing variant TCGA-AB-2990-03A-01D-0739-09 chr19:4186440 C>T maps to NM_133475.1 R7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2900-03A-01W-0733-08 chr5:55455692 C>T maps to NM_024669.2 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2903-03A-01W-0761-09 chr2:224640647 G>A maps to NM_001039569.1 Y87Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2889-03A-01W-0732-08 chr15:29398976 C>A maps to NM_005503.3 T624T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2847-03B-01W-0728-08 chr1:228285058 C>T maps to NM_001024228.1 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2862-03B-01W-0728-08 chr20:47589697 G>A maps to NM_006420.2 V514V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-3002-03A-01D-0739-09 chr1:155922485 G>T maps to NM_001162383.1 G639G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2991-03A-01D-0739-09 chr12:46254718 C>T maps to NM_152641.2 Q1637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2874-03A-01W-0732-08 chr10:23319671 C>A maps to NM_173081.3 T731T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2964-03A-01D-0739-09 chr23:3021840 G>A did not map to a codon.
Sequencing variant TCGA-AB-2923-03A-01W-0745-08 chr23:15306083 G>A did not map to a codon.
Sequencing variant TCGA-AB-2864-03D-01W-0755-09 chr7:95115471 T>G did not map to a codon.
Sequencing variant TCGA-AB-2980-03A-01D-0739-09 chr3:130737521 G>A maps to ENST00000514044 T447T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2821-03B-01W-0728-08 chr20:31022711 C>T maps to ENST00000375687 Q733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2907-03A-01D-0739-09 chr20:31024757 C>T maps to ENST00000375687 R1415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2927-03A-01W-0755-09 chr20:31022233 G>T did not map to a codon.
Sequencing variant TCGA-AB-3002-03A-01D-0739-09 chr2:234172657 C>T maps to ENST00000392018 D112D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2830-03B-01W-0728-08 chr23:138813875 G>A did not map to a codon.
Sequencing variant TCGA-AB-2972-03A-01D-0739-09 chr23:119505056 T>C did not map to a codon.
Sequencing variant TCGA-AB-2865-03B-01W-0728-08 chr23:152825263 G>A did not map to a codon.
Sequencing variant TCGA-AB-2910-03A-01W-0745-08 chr23:152814258 G>T did not map to a codon.
Sequencing variant TCGA-AB-2978-03A-01D-0739-09 chr23:40456844 C>T did not map to a codon.
Sequencing variant TCGA-AB-3006-03A-01D-0739-09 chr18:77013481 T>A maps to NM_198531.3 G403G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-3006-03A-01D-0739-09 chr12:58025849 G>A maps to NM_001478.3 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2861-03B-01W-0728-08 chr1:161143510 C>T maps to NM_003779.3 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2857-03B-01W-0728-08 chr21:30714965 C>A maps to NM_206866.1 R675R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2862-03B-01W-0728-08 chr1:94048127 G>A maps to NM_003567.2 G472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2887-03A-01W-0732-08 chr14:96707222 G>A maps to NM_000623.3 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2971-03A-01D-0739-09 chr6:55638912 G>A maps to NM_021073.2 R321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2963-03A-01D-0739-09 chr10:43289316 C>A maps to NM_014753.3 T369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2976-03A-01D-0739-09 chr3:112999442 C>T maps to ENST00000273395 G748G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2876-03A-01W-0732-08 chr20:31601735 C>T maps to NM_025227.1 H143H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2929-03A-01W-0732-08 chr23:154305489 C>T did not map to a codon.
Sequencing variant TCGA-AB-2888-03A-01W-0732-08 chr11:66108790 G>A maps to NM_001024957.1 R82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2876-03A-01W-0732-08 chr23:135574279 C>T did not map to a codon.
Sequencing variant TCGA-AB-2887-03A-01W-0732-08 chr23:79988963 T>C did not map to a codon.
Sequencing variant TCGA-AB-2994-03A-01D-0739-09 chr1:92612780 T>A maps to NM_183242.3 I325I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-3001-03A-01D-0739-09 chr10:115904369 G>A maps to NM_018017.2 G369G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2828-03C-01W-0761-09 chr12:27066474 C>A maps to NM_018164.2 G574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2984-03A-01D-0739-09 chr19:17386608 G>T did not map to a codon.
Sequencing variant TCGA-AB-2802-03B-01W-0728-08 chr20:35240438 C>T maps to NM_018840.4 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2807-03D-01W-0755-09 chr20:20079445 C>T maps to ENST00000389655 R283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2828-03C-01W-0761-09 chr2:44931440 G>A maps to NM_024766.3 E132E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2894-03A-01W-0733-08 chr2:210940455 C>G maps to NM_152519.2 L525L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AB-2915-03A-01W-0745-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AB-2818-03B-01W-0728-08 chr9:123724994 C>A maps to NM_001735.2 G1486G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2838-03A-01W-0726-08 chr6:151775781 C>T maps to NM_024573.1 H47H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2938-03A-01W-0732-08 chr7:5942326 C>T maps to NM_015622.5 D158D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2803-03B-01W-0728-08 chr7:150028045 C>T maps to NM_138434.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2915-03A-01W-0745-08 chr9:117396073 G>A maps to ENST00000374049 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2891-03A-01W-0733-08 chr9:135698682 C>T maps to NM_152572.2 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2972-03A-01D-0739-09 chr19:13370430 C>T maps to NM_023035.2 V1449V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2904-03A-01W-0732-08 chr17:48673939 C>T maps to NM_018896.3 S999S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2943-03A-01W-0745-08 chr3:54930838 C>A maps to NM_018398.2 Y770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2861-03B-01W-0728-08 chr17:65040805 C>T maps to NM_000727.3 R10R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2858-03D-01W-0755-09 chr17:65026861 C>T maps to NM_014405.3 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2904-03A-01W-0732-08 chr2:27466085 C>T maps to NM_004341.3 L2167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2882-03A-01W-0761-09 chr3:62484929 C>G maps to ENST00000383709 R871R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2990-03A-01D-0739-09 chr16:71419499 C>T maps to NM_001740.4 D216D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2972-03A-01D-0739-09 chr7:134613517 A>C maps to NM_033138.3 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2936-03A-01W-0745-08 chr5:110710561 C>T maps to NM_001744.4 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2938-03A-01W-0732-08 chr9:138714499 T>C maps to ENST00000409386 P680P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-3006-03A-01D-0739-09 chr2:85628971 C>G maps to NM_001747.2 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2964-03A-01D-0739-09 chr23:110507006 C>T did not map to a codon.
Sequencing variant TCGA-AB-2845-03D-01W-0755-09 chr12:30906626 C>T maps to NM_001002259.1 W24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2938-03A-01W-0732-08 chr15:44695121 G>A maps to NM_138423.3 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2833-03B-01W-0728-08 chr16:67070607 C>T maps to NM_022845.2 R78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2914-03A-01W-0732-08 chr11:119148874 G>C did not map to a codon.
Sequencing variant TCGA-AB-2978-03A-01D-0739-09 chr11:119168129 G>A maps to NM_005188.2 T730T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2922-03A-01W-0745-08 chr12:54651312 C>T maps to NM_012117.2 W41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2991-03A-01D-0739-09 chr7:128451963 G>A maps to NM_022742.3 R713R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2912-03A-01W-0732-08 chr15:74536465 C>T maps to ENST00000321288 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2863-03D-01W-0755-09 chr11:93127746 A>G maps to NM_181645.3 T388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2916-03A-01W-0732-08 chr1:158300844 C>T maps to NM_001764.2 Q23Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2869-03A-01W-0761-09 chr10:73461780 G>T maps to ENST00000398860 V805V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2993-03A-01D-0739-09 chr14:23518425 G>T maps to NM_022478.3 Y590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2978-03A-01D-0739-09 chr19:45184538 C>A maps to NM_020219.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-3000-03A-01D-0739-09 chr19:33793145 C>A maps to NM_004364.3 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2959-03A-01W-0733-08 chr14:23586707 C>A maps to NM_001805.2 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-3005-03A-01D-0739-09 chr3:48694470 C>T maps to NM_001407.2 Q1353Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2864-03D-01W-0755-09 chr20:3766878 C>T maps to NM_001810.5 W84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2812-03B-01W-0728-08 chr2:201994827 G>A maps to NM_001127183.1 E80E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2955-03A-01W-0733-08 chr1:154543958 G>A maps to NM_000748.2 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-3009-03A-01D-0739-09 chr19:19650500 C>T maps to NM_153221.2 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2860-03B-01W-0728-08 chr7:73790977 C>T maps to NM_003388.4 I749I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-3002-03A-01D-0739-09 chr9:17226282 C>T maps to NM_017738.2 Q178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-3009-03A-01D-0739-09 chr6:75860980 G>A maps to ENST00000322507 V1341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2857-03B-01W-0728-08 chr4:109820308 C>T did not map to a codon.
Sequencing variant TCGA-AB-2936-03A-01W-0745-08 chr19:10088362 C>T maps to NM_015719.3 E1011E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2968-03A-01D-0739-09 chr8:146076708 C>G maps to NM_001081003.1 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2857-03B-01W-0728-08 chr17:14110286 C>T maps to NM_001303.3 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2927-03A-01W-0755-09 chr16:84906114 G>A did not map to a codon.
Sequencing variant TCGA-AB-2862-03B-01W-0728-08 chr17:61950047 G>A maps to NM_020991.3 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2820-03B-01W-0728-08 chr8:3200834 A>T maps to NM_033225.5 G1204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2847-03B-01W-0728-08 chr3:39186565 C>T maps to NM_033027.3 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-3009-03A-01D-0739-09 chr16:67660468 C>T maps to NM_006565.3 R457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2872-03A-01W-0732-08 chr10:68040230 A>T maps to NM_013266.2 I627I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2807-03D-01W-0755-09 chr1:112997102 G>A maps to NM_018704.2 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2906-03A-01D-0739-09 chr10:16870962 C>T maps to NM_001081.3 T3535T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2898-03A-01W-0733-08 chr17:55962592 C>T maps to NM_017949.1 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2946-03A-01W-0755-09 chr17:55962640 G>A maps to NM_017949.1 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2926-03A-01W-0732-08 chr4:76943893 T>C maps to NM_001565.2 E46E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2927-03A-01W-0755-09 chr23:23953459 C>T did not map to a codon.
Sequencing variant TCGA-AB-2905-03A-01D-0739-09 chr23:37665661 G>A did not map to a codon.
Sequencing variant TCGA-AB-2934-03A-01W-0755-09 chr2:172411096 G>T maps to NM_024843.3 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-3012-03A-01D-0739-09 chr23:83128704 C>A did not map to a codon.
Sequencing variant TCGA-AB-2908-03A-01W-0745-08 chr19:41630693 C>T maps to NM_000774.3 A345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2927-03A-01W-0755-09 chr11:61503095 C>A maps to NM_006133.2 R398R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2976-03A-01D-0739-09 chr7:6461399 C>T maps to NM_139179.3 V392V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2927-03A-01W-0755-09 chr9:121971019 G>A maps to NM_014618.2 P374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-3007-03A-01D-0739-09 chr2:74605336 G>A maps to NM_004082.4 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2976-03A-01D-0739-09 chr14:53529749 C>T maps to NM_001160148.1 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-3002-03A-01D-0739-09 chr2:15757365 A>G did not map to a codon.
Sequencing variant TCGA-AB-2904-03A-01W-0732-08 chr12:31245811 C>T maps to NM_030653.3 Y425Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2926-03A-01W-0732-08 chr22:38894088 C>T did not map to a codon.
Sequencing variant TCGA-AB-3002-03A-01D-0739-09 chr5:176940352 C>T did not map to a codon.
Sequencing variant TCGA-AB-2926-03A-01W-0732-08 chr23:23018295 C>T did not map to a codon.
Sequencing variant TCGA-AB-2943-03A-01W-0745-08 chr10:12154954 T>G maps to NM_018706.5 V737V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2917-03A-01W-0732-08 chr23:96684725 C>T did not map to a codon.
Sequencing variant TCGA-AB-2906-03A-01D-0739-09 chr1:35370195 G>A maps to NM_001080418.1 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2810-03B-01W-0728-08 chr23:31854904 G>A did not map to a codon.
Sequencing variant TCGA-AB-2918-03A-01W-0745-08 chr5:13841908 A>G maps to NM_001369.2 L1792L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2995-03A-01D-0739-09 chr17:11572784 C>T maps to NM_001372.3 T1009T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2805-03B-01W-0728-08 chr9:34506775 C>T maps to NM_012144.2 D405D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2966-03A-01D-0739-09 chr16:4500469 G>A maps to NM_005147.4 T437T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2822-03D-01W-0755-09 chr2:25467207 C>T did not map to a codon.
Sequencing variant TCGA-AB-2839-03B-01W-0728-08 chr2:25468132 G>A maps to NM_175629.1 Q515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2861-03B-01W-0728-08 chr2:25467031 G>A maps to NM_175629.1 Q615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2869-03A-01W-0761-09 chr2:25468909 G>A maps to NM_175629.1 Q485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2891-03A-01W-0733-08 chr2:25467021 A>G did not map to a codon.
Sequencing variant TCGA-AB-2898-03A-01W-0733-08 chr2:25459802 A>C did not map to a codon.
Sequencing variant TCGA-AB-2928-03A-01W-0745-08 chr2:25470515 G>A maps to NM_175629.1 R320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2967-03A-01D-0739-09 chr2:25468162 C>A maps to NM_175629.1 E505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2968-03A-01D-0739-09 chr2:25469028 C>A maps to NM_175629.1 E477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2895-03A-01W-0733-08 chr5:169125453 G>A did not map to a codon.
Sequencing variant TCGA-AB-2915-03A-01W-0745-08 chr19:2216683 G>C maps to ENST00000221482 P776P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2876-03A-01W-0732-08 chr11:66249799 C>T maps to NM_005700.3 Y43Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2875-03A-01W-0732-08 chr11:113281640 G>A maps to ENST00000355319 G382G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2914-03A-01W-0732-08 chr11:113287657 G>A maps to ENST00000355319 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2993-03A-01D-0739-09 chr21:41414444 A>G maps to NM_001389.3 L1847L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2952-03A-01W-0733-08 chr11:117301645 G>A maps to NM_020693.2 H1886H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2932-03A-01W-0745-08 chr18:29100842 T>G maps to NM_001943.3 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2945-03A-01W-0733-08 chr11:58949356 G>A maps to NM_015177.1 K119K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2849-03B-01W-0728-08 chr15:45440165 T>A maps to NM_175940.1 I871I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2887-03A-01W-0732-08 chr11:103039544 T>C maps to NM_001080463.1 D1608D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2828-03C-01W-0761-09 chr2:71797453 C>T maps to NM_001130987.1 V1025V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-3000-03A-01D-0739-09 chr2:71795375 C>T maps to NM_001130987.1 D924D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2971-03A-01D-0739-09 chr11:19251104 C>A maps to NM_024680.2 E597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2822-03D-01W-0755-09 chr5:83402505 C>T maps to NM_005711.3 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2876-03A-01W-0732-08 chr11:85961446 C>A maps to ENST00000351625 S75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2913-03A-01W-0732-08 chr19:41306983 G>A maps to NM_053046.2 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2950-03A-01W-0733-08 chr11:64627707 C>T maps to NM_006795.2 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2819-03B-01W-0728-08 chr3:184910352 T>C maps to NM_001966.3 P611P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2968-03A-01D-0739-09 chr12:53413722 C>G maps to ENST00000438209 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2871-03A-01W-0732-08 chr23:129205023 C>T did not map to a codon.
Sequencing variant TCGA-AB-2854-03B-01W-0728-08 chr11:34515065 G>A maps to NM_198381.1 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2964-03A-01D-0739-09 chr7:73452037 G>A maps to ENST00000358929 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2869-03A-01W-0761-09 chr4:111397707 C>T maps to NM_001977.3 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2802-03B-01W-0728-08 chr12:132466884 G>A maps to ENST00000333577 Q633Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2898-03A-01W-0733-08 chr2:46602889 C>T maps to NM_001430.4 Y316Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2827-03B-01W-0728-08 chr1:38227575 G>A maps to NM_001099439.1 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2915-03A-01W-0745-08 chr6:93967200 T>C maps to NM_004440.3 G717G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2906-03A-01D-0739-09 chr3:134873070 C>T maps to NM_004441.4 Q459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2881-03A-01W-0732-08 chr5:54281093 C>T maps to NM_007036.4 Q84Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-3012-03A-01D-0739-09 chr22:29688595 G>T did not map to a codon.
Sequencing variant TCGA-AB-2872-03A-01W-0732-08 chr15:41482301 G>A maps to NM_152596.2 R239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2968-03A-01D-0739-09 chr6:592580 C>G maps to NM_018303.4 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2865-03B-01W-0728-08 chr7:148506161 C>T did not map to a codon.
Sequencing variant TCGA-AB-2816-03B-01W-0728-08 chr12:50282961 G>C maps to NM_012306.2 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2897-03A-01W-0733-08 chr13:107822901 G>A maps to NM_001080396.2 A440A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2863-03D-01W-0755-09 chr2:75720721 T>C maps to NM_032181.2 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2898-03A-01W-0733-08 chr4:2698283 G>A maps to ENST00000324666 T866T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2939-03A-01W-0745-08 chr23:34150072 G>A did not map to a codon.
Sequencing variant TCGA-AB-2955-03A-01W-0733-08 chr23:34150173 G>A did not map to a codon.
Sequencing variant TCGA-AB-2888-03A-01W-0732-08 chr23:34962507 C>T did not map to a codon.
Sequencing variant TCGA-AB-2967-03A-01D-0739-09 chr16:30037135 G>A maps to NM_031478.4 R151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2963-03A-01D-0739-09 chr1:93309545 C>T maps to NM_001006605.3 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2923-03A-01W-0745-08 chr8:87519293 A>G maps to NM_016033.2 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2946-03A-01W-0755-09 chr5:7867320 A>G maps to NM_024091.3 S292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2813-03B-01W-0728-08 chr11:92532289 G>T maps to ENST00000298047 T2037T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-3002-03A-01D-0739-09 chr5:127697500 G>A maps to NM_001999.3 N823N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2968-03A-01D-0739-09 chr7:5540408 G>A maps to ENST00000312577 S497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2977-03A-01D-0739-09 chr5:15936889 C>T maps to NM_012304.3 I357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2875-03A-01W-0732-08 chr19:40433434 G>A maps to NM_003890.2 Y278Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2950-03A-01W-0733-08 chr19:40408296 C>T maps to NM_003890.2 A1514A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2810-03B-01W-0728-08 chr5:141029102 C>T maps to ENST00000354789 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-3009-03A-01D-0739-09 chr19:35843149 G>A maps to NM_005303.2 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2808-03D-01W-0755-09 chr6:76022882 G>A maps to NM_015687.2 R889*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2812-03B-01W-0728-08 chr12:49315952 C>A maps to NM_016594.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2913-03A-01W-0732-08 chr19:18652579 C>T maps to NM_012181.3 E67E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2907-03A-01D-0739-09 chr9:108363629 G>T did not map to a codon.
Sequencing variant TCGA-AB-2998-03A-01D-0739-09 chr1:152281733 G>A maps to NM_002016.1 D1876D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2868-03B-01W-0728-08 chr8:142486213 C>T maps to NM_207414.2 K493K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2807-03D-01W-0755-09 chr7:128480713 C>T maps to NM_001458.4 Y554Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2877-03A-01W-0732-08 chr14:86088112 C>T maps to NM_013231.4 H85H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2943-03A-01W-0745-08 chr13:29001447 G>C maps to NM_002019.4 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2863-03D-01W-0755-09 chr2:216238071 C>A maps to NM_212482.1 E2074*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2805-03B-01W-0728-08 chr19:52249272 G>A maps to NM_002029.3 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2860-03B-01W-0728-08 chr4:79188549 C>T maps to NM_025074.6 C315C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2935-03A-01W-0755-09 chr13:39452969 C>T maps to NM_207361.4 D2954D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2972-03A-01D-0739-09 chr11:65161098 G>A maps to NM_031904.3 E103E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2854-03B-01W-0728-08 chr4:48567708 C>T did not map to a codon.
Sequencing variant TCGA-AB-2989-03A-01D-0739-09 chr15:27772759 G>A maps to NM_033223.4 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2817-03B-01W-0728-08 chr4:174219439 A>G maps to NM_017423.2 E380E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2895-03A-01W-0733-08 chr17:9830017 G>A maps to NM_201433.1 C318C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2976-03A-01D-0739-09 chr1:153791328 G>A maps to NM_020699.2 R179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-3005-03A-01D-0739-09 chr22:38209531 C>T maps to NM_001171690.1 D190D. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AB-3009-03A-01D-0739-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AB-3009-03A-01D-0739-09 chr20:34022054 A>T maps to ENST00000374375 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2999-03A-01D-0739-09 chr11:76982211 C>T maps to ENST00000376217 W121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2808-03D-01W-0755-09 chr1:35260716 G>A maps to NM_002060.2 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2917-03A-01W-0732-08 chr1:35251008 C>T maps to NM_001005752.1 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2813-03B-01W-0728-08 chr12:102179964 G>A maps to NM_024312.4 H132H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2869-03A-01W-0761-09 chr4:176573081 G>A maps to NM_005277.3 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2952-03A-01W-0733-08 chr23:136113703 C>T did not map to a codon.
Sequencing variant TCGA-AB-2849-03B-01W-0728-08 chr23:135427147 T>A did not map to a codon.
Sequencing variant TCGA-AB-2877-03A-01W-0732-08 chr23:135431545 C>T did not map to a codon.
Sequencing variant TCGA-AB-2937-03A-01W-0732-08 chr6:47681800 C>T maps to NM_153838.3 Q274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2888-03A-01W-0732-08 chr13:99947481 A>G maps to NM_004951.4 F306F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2917-03A-01W-0732-08 chr4:8588897 G>A maps to NM_080819.2 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2810-03B-01W-0728-08 chr1:101004926 C>A maps to NM_022049.2 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2900-03A-01W-0733-08 chr2:11741045 C>T maps to NM_014668.3 F818F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2950-03A-01W-0733-08 chr10:87407081 G>T maps to NM_017551.2 Y690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2967-03A-01D-0739-09 chr12:66838484 G>A maps to ENST00000359742 D522D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2802-03B-01W-0728-08 chr3:7503315 T>A maps to NM_181874.2 P474P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2915-03A-01W-0745-08 chr4:106638784 G>A maps to NM_001031720.2 K5K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2812-03B-01W-0728-08 chr12:42512849 T>C maps to NM_173601.1 Q146Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2830-03B-01W-0728-08 chr23:2793883 G>A did not map to a codon.
Sequencing variant TCGA-AB-2882-03A-01W-0761-09 chr20:7866397 C>T maps to NM_017545.2 K309K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2966-03A-01D-0739-09 chr23:153230155 G>A did not map to a codon.
Sequencing variant TCGA-AB-2870-03A-01W-0732-08 chr15:73624518 G>A maps to NM_005477.2 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2938-03A-01W-0732-08 chr1:156713595 C>T maps to NM_001126050.1 E204E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2901-03A-01W-0733-08 chr7:43591888 G>A maps to NM_015052.3 A1488A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2914-03A-01W-0732-08 chr1:228612762 C>T maps to NM_003493.2 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2929-03A-01W-0732-08 chr6:12125883 G>A maps to NM_002114.2 S1952S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-3002-03A-01D-0739-09 chr2:234750540 G>A maps to NM_018410.3 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2985-03A-01D-0739-09 chr10:71017129 C>A maps to NM_025130.3 T660T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-3008-03A-01D-0739-09 chr1:186094772 G>A maps to NM_031935.2 T4179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2860-03B-01W-0728-08 chr4:11401017 C>T maps to NM_005114.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2835-03B-01W-0728-08 chr5:132431895 T>A maps to NM_002154.3 L586*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AB-2999-03A-01D-0739-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AB-2994-03A-01D-0739-09 chr16:70977789 G>A maps to NM_032821.2 V2197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-3005-03A-01D-0739-09 chr11:68704309 C>T maps to NM_002180.2 R788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2996-03A-01D-0739-09 chr1:18661496 C>T maps to NM_032880.4 N139N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2908-03A-01W-0745-08 chr17:37922153 G>A maps to NM_012481.3 C473C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2899-03A-01W-0733-08 chr12:56420652 C>T maps to NM_022465.3 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2906-03A-01D-0739-09 chr3:57131718 G>C maps to NM_017563.3 S671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2979-03A-01D-0739-09 chr11:2182072 G>A maps to NM_001042376.2 C43C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2996-03A-01D-0739-09 chr10:15658523 G>A maps to NM_003638.1 V478V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2926-03A-01W-0732-08 chr2:187487078 T>A maps to NM_002210.3 Y110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2881-03A-01W-0732-08 chr3:124527913 G>A maps to NM_002213.3 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2929-03A-01W-0732-08 chr10:7791218 C>T maps to NM_002216.2 N921N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2822-03D-01W-0755-09 chr6:33657120 G>A maps to ENST00000374316 A2267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2827-03B-01W-0728-08 chr9:711980 C>G maps to NM_015158.2 A405A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-3008-03A-01D-0739-09 chr3:20164250 G>A maps to NM_003884.4 E456E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2844-03B-01W-0728-08 chr12:5020810 C>T maps to NM_000217.2 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2979-03A-01D-0739-09 chr1:111216735 C>T maps to NM_002232.3 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2930-03A-01W-0761-09 chr12:5154833 C>A maps to NM_002234.2 T507T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2934-03A-01W-0755-09 chr7:150649893 T>G maps to NM_000238.2 A392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2820-03B-01W-0728-08 chr8:140630862 G>T maps to NM_016601.2 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2905-03A-01D-0739-09 chr20:62038563 G>T maps to NM_172107.2 G684G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-3002-03A-01D-0739-09 chr20:62044801 C>T maps to ENST00000370222 R560R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2910-03A-01W-0745-08 chr8:36666295 G>A maps to NM_001031836.2 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2912-03A-01W-0732-08 chr8:36641946 C>T maps to NM_001031836.2 R7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2927-03A-01W-0755-09 chr8:36780101 G>A maps to NM_001031836.2 T897T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2842-03A-01W-0726-08 chr1:23405609 A>G maps to NM_001009999.2 P665P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2806-03B-01W-0728-08 chr23:44918513 C>A did not map to a codon.
Sequencing variant TCGA-AB-2867-03B-01W-0728-08 chr23:44922999 C>T did not map to a codon.
Sequencing variant TCGA-AB-2883-03A-01W-0732-08 chr23:44969322 G>A did not map to a codon.
Sequencing variant TCGA-AB-2912-03A-01W-0732-08 chr4:55964953 C>T maps to NM_002253.2 T761T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-3009-03A-01D-0739-09 chr17:44108922 C>T maps to NM_015443.3 A1079A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2862-03B-01W-0728-08 chr15:52885894 A>G maps to NM_019600.2 I896I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2886-03A-01W-0732-08 chr9:100077176 T>C maps to ENST00000375206 T431T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2820-03B-01W-0728-08 chr19:18368586 G>T maps to NM_001145304.1 A1169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2914-03A-01W-0732-08 chr17:4905791 C>T maps to NM_006612.5 R155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2955-03A-01W-0733-08 chr23:86773291 T>C did not map to a codon.
Sequencing variant TCGA-AB-2853-03D-01W-0755-09 chr4:39114765 G>A maps to NM_015990.4 T651T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2992-03A-01D-0739-09 chr19:51480907 G>A maps to NM_005046.2 Q216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2904-03A-01W-0732-08 chr17:39681181 A>G maps to NM_002276.4 D191D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2828-03C-01W-0761-09 chr12:53045803 G>A maps to NM_000423.2 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2857-03B-01W-0728-08 chr17:39577725 G>A maps to NM_003770.4 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2807-03D-01W-0755-09 chr12:52910545 G>T maps to NM_000424.3 A438A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2955-03A-01W-0733-08 chr12:52885484 T>C maps to NM_005554.3 E192E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2802-03B-01W-0728-08 chr12:52964547 G>A maps to NM_175053.3 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2857-03B-01W-0728-08 chr12:52827851 G>A maps to ENST00000252245 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2939-03A-01W-0745-08 chr12:53097122 C>T maps to NM_175078.2 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2841-03B-01W-0728-08 chr12:53217984 G>A maps to NM_175834.2 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2931-03A-01W-0745-08 chr21:46020571 C>T maps to ENST00000380102 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2807-03D-01W-0755-09 chr18:7036045 G>T maps to NM_005559.2 Y593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2996-03A-01D-0739-09 chr1:183085910 T>C maps to NM_002293.3 P479P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2914-03A-01W-0732-08 chr23:64749614 C>T did not map to a codon.
Sequencing variant TCGA-AB-2996-03A-01D-0739-09 chr1:152785066 G>T maps to NM_178349.1 G49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2895-03A-01W-0733-08 chr11:36250883 C>T maps to NM_174902.2 G325G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2950-03A-01W-0733-08 chr2:48936145 G>A maps to NM_000233.3 N207N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2939-03A-01W-0745-08 chr4:54364819 G>A maps to NM_001126328.1 D322D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2906-03A-01D-0739-09 chr8:12583331 A>G maps to NM_152271.3 S689S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2807-03D-01W-0755-09 chr6:160998166 C>T did not map to a codon.
Sequencing variant TCGA-AB-2857-03B-01W-0728-08 chr10:85994069 G>A maps to NM_015613.2 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2847-03B-01W-0728-08 chr2:141474287 C>T maps to NM_018557.2 L1952L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2905-03A-01D-0739-09 chr2:141083355 T>C maps to NM_018557.2 S4105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2905-03A-01D-0739-09 chr11:46905471 G>A maps to ENST00000256991 I899I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2872-03A-01W-0732-08 chr7:127669226 G>A maps to NM_022143.4 T489T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2941-03A-01W-0745-08 chr7:127669172 G>A maps to NM_022143.4 P507P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2966-03A-01D-0739-09 chr1:70614234 C>T maps to NM_017768.4 T546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-3005-03A-01D-0739-09 chr1:3700617 G>A maps to NM_020710.2 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2970-03A-01D-0739-09 chr1:204588351 G>A maps to NM_201630.1 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-3001-03A-01D-0739-09 chr11:24759848 G>C did not map to a codon.
Sequencing variant TCGA-AB-2920-03A-01W-0732-08 chr2:95715339 C>T maps to NM_002371.2 H92H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2922-03A-01W-0745-08 chr5:71495655 C>A maps to NM_005909.3 T2158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2915-03A-01W-0745-08 chr2:210561003 C>T maps to NM_002374.3 D1370D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2919-03A-01W-0745-08 chr23:20033424 C>T did not map to a codon.
Sequencing variant TCGA-AB-2818-03B-01W-0728-08 chr5:179676060 C>T maps to NM_002752.4 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2830-03B-01W-0728-08 chr15:42104228 G>A maps to NM_001128608.1 K134K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2906-03A-01D-0739-09 chr3:186937933 C>T maps to NM_001879.5 K675K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2818-03B-01W-0728-08 chr6:42981062 G>A maps to NM_014623.2 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2822-03D-01W-0755-09 chr23:70356167 G>A did not map to a codon.
Sequencing variant TCGA-AB-2917-03A-01W-0732-08 chr23:70347216 C>T did not map to a codon.
Sequencing variant TCGA-AB-2976-03A-01D-0739-09 chr23:40531147 T>C did not map to a codon.
Sequencing variant TCGA-AB-2895-03A-01W-0733-08 chr17:38189623 G>T maps to NM_014815.3 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2999-03A-01D-0739-09 chr15:66190367 G>A maps to NM_032445.2 Y1013Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2810-03B-01W-0728-08 chr19:42838271 G>A maps to ENST00000251268 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2898-03A-01W-0733-08 chr19:42873052 C>T maps to ENST00000251268 D2180D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2876-03A-01W-0732-08 chr18:48702765 T>C maps to NM_016626.4 P645P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2905-03A-01D-0739-09 chr3:127414006 C>T maps to NM_007283.5 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2849-03B-01W-0728-08 chr22:38323712 C>A maps to NM_033386.2 G587G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2956-03A-01W-0733-08 chr10:89268198 C>T maps to NM_004897.4 H248H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2996-03A-01D-0739-09 chr10:28023574 G>C maps to NM_173576.2 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2940-03A-01W-0733-08 chr7:151874160 C>A maps to ENST00000355193 E2793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2919-03A-01W-0745-08 chr9:13224489 C>T maps to ENST00000319217 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2819-03B-01W-0728-08 chr2:48027539 C>T maps to NM_000179.2 S806S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2970-03A-01D-0739-09 chr8:15978071 G>A maps to ENST00000445506 H377H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2885-03A-01W-0732-08 chr23:63574711 C>T did not map to a codon.
Sequencing variant TCGA-AB-2971-03A-01D-0739-09 chr23:63488601 C>T did not map to a codon.
Sequencing variant TCGA-AB-2859-03B-01W-0728-08 chr8:17541959 C>T maps to NM_001001924.2 L905L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2904-03A-01W-0732-08 chr19:9076507 G>A maps to NM_024690.2 S3646S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2915-03A-01W-0745-08 chr19:9060043 G>A maps to NM_024690.2 S9134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2997-03A-01D-0739-09 chr11:1272707 C>T maps to ENST00000447027 T4869T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2889-03A-01W-0732-08 chr23:3241844 A>C did not map to a codon.
Sequencing variant TCGA-AB-2997-03A-01D-0739-09 chr20:42343910 G>A maps to NM_002466.2 T654T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2847-03B-01W-0728-08 chr1:203139506 C>T maps to NM_004997.2 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2919-03A-01W-0745-08 chr1:109839465 G>A maps to NM_001010985.2 N223N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2843-03B-01W-0728-08 chr1:40363613 T>A maps to NM_001033082.2 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2849-03B-01W-0728-08 chr12:81102639 G>A maps to NM_002469.2 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2822-03D-01W-0755-09 chr17:10360863 G>A maps to NM_017533.2 D590D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2865-03B-01W-0728-08 chr17:10355545 G>A maps to NM_017533.2 I1150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2955-03A-01W-0733-08 chr14:23874853 G>C maps to NM_002471.3 Y109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2898-03A-01W-0733-08 chr13:109379888 C>T maps to NM_015011.1 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2974-03A-01D-0739-09 chr22:26219598 G>A maps to ENST00000407587 T885T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-3002-03A-01D-0739-09 chr19:8606788 C>T did not map to a codon.
Sequencing variant TCGA-AB-2886-03A-01W-0732-08 chr18:47369718 G>A maps to NM_001080467.2 P1501P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2865-03B-01W-0728-08 chr1:171605484 G>T maps to NM_000261.1 Y365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2976-03A-01D-0739-09 chr1:171621553 C>T maps to NM_000261.1 Q66Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2865-03B-01W-0728-08 chr1:24383988 G>A maps to ENST00000330966 T1396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2959-03A-01W-0733-08 chr1:24432513 G>A maps to ENST00000330966 R153R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2915-03A-01W-0745-08 chr4:140270696 G>A maps to NM_057175.3 W258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2950-03A-01W-0733-08 chr3:175165095 G>A maps to NM_207015.2 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2870-03A-01W-0732-08 chr16:5078915 G>C maps to NM_016256.3 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2867-03B-01W-0728-08 chr13:101712313 C>T maps to NM_052867.2 Q1587Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2996-03A-01D-0739-09 chr13:102047641 G>A maps to NM_052867.2 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2983-03A-01D-0739-09 chr19:46417669 C>T maps to NM_001029861.2 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-3009-03A-01D-0739-09 chr1:201618122 C>T maps to ENST00000367296 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2849-03B-01W-0728-08 chr11:20075634 C>T maps to ENST00000396087 P1520P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2955-03A-01W-0733-08 chr2:15415892 T>C maps to NM_015909.2 A1813A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2822-03D-01W-0755-09 chr4:17816952 C>T maps to NM_022346.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-3002-03A-01D-0739-09 chr19:55418013 C>T maps to NM_004829.5 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2932-03A-01W-0745-08 chr11:20959372 C>A maps to NM_006157.3 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2906-03A-01D-0739-09 chr1:156642554 G>A maps to NM_006617.1 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2940-03A-01W-0733-08 chr17:7228736 C>T maps to NM_032442.2 G474G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-3009-03A-01D-0739-09 chr17:29562980 C>T maps to NM_001042492.2 R1306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2812-03B-01W-0728-08 chr10:115664655 T>C maps to NM_198514.3 P595P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2809-03D-01W-0755-09 chr14:51224225 T>C maps to NM_020921.3 E1174E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2813-03B-01W-0728-08 chr23:118723958 G>A did not map to a codon.
Sequencing variant TCGA-AB-2849-03B-01W-0728-08 chr2:32477644 G>A maps to NM_021209.4 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-3011-03A-01D-0739-09 chr23:70511696 C>A did not map to a codon.
Sequencing variant TCGA-AB-3005-03A-01D-0739-09 chr1:145273365 C>T maps to ENST00000454606 R86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-3005-03A-01D-0739-09 chr23:105178381 T>C did not map to a codon.
Sequencing variant TCGA-AB-2829-03B-01W-0728-08 chr15:88670419 G>A maps to NM_001012338.1 T422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2994-03A-01D-0739-09 chr16:1836556 C>T maps to NM_012225.2 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2936-03A-01W-0745-08 chr23:101624924 G>A did not map to a codon.
Sequencing variant TCGA-AB-2807-03D-01W-0755-09 chr23:102335540 C>T did not map to a codon.
Sequencing variant TCGA-AB-2998-03A-01D-0739-09 chr23:41334034 C>T did not map to a codon.
Sequencing variant TCGA-AB-2838-03A-01W-0726-08 chr10:50966566 G>A maps to NM_018245.2 V24V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2899-03A-01W-0733-08 chr6:47776044 C>T maps to ENST00000489301 I304I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2870-03A-01W-0732-08 chr11:58035231 G>A maps to NM_207374.3 N33N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2806-03B-01W-0728-08 chr23:130678938 C>T did not map to a codon.
Sequencing variant TCGA-AB-2813-03B-01W-0728-08 chr23:130678090 T>C did not map to a codon.
Sequencing variant TCGA-AB-3011-03A-01D-0739-09 chr1:247921141 G>A maps to NM_012353.2 C189C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2867-03B-01W-0728-08 chr1:248367135 T>A maps to NM_001004689.1 L256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2916-03A-01W-0732-08 chr1:248756298 G>T maps to NM_001004693.1 Y257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2927-03A-01W-0755-09 chr11:55433283 G>A maps to NM_001004704.1 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2914-03A-01W-0732-08 chr11:5510839 G>T maps to NM_001005163.2 E302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2964-03A-01D-0739-09 chr11:6816372 C>T maps to NM_003696.2 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2929-03A-01W-0732-08 chr11:124412935 G>A maps to NM_001005195.1 D205D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2821-03B-01W-0728-08 chr11:55873033 C>T maps to NM_001005200.1 N172N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2838-03A-01W-0726-08 chr1:17418972 G>A maps to NM_007365.2 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2992-03A-01D-0739-09 chr14:20818768 A>T maps to NM_005484.3 R150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2930-03A-01W-0761-09 chr11:66638942 G>A maps to NM_022172.2 N110N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2872-03A-01W-0732-08 chr23:91133088 C>T did not map to a codon.
Sequencing variant TCGA-AB-2819-03B-01W-0728-08 chr23:99662491 G>A did not map to a codon.
Sequencing variant TCGA-AB-2864-03D-01W-0755-09 chr5:140264045 G>A maps to NM_018904.2 A731A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2894-03A-01W-0733-08 chr5:140208674 T>C maps to NM_018909.2 H333H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2984-03A-01D-0739-09 chr5:140209868 G>A maps to NM_018909.2 A731A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2907-03A-01D-0739-09 chr5:140432818 C>A maps to NM_013340.2 T588T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2871-03A-01W-0732-08 chr5:140589777 C>T maps to NM_018932.3 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2996-03A-01D-0739-09 chr5:140719341 C>T maps to NM_018915.2 D268D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2998-03A-01D-0739-09 chr5:140782842 C>T maps to NM_018921.2 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2846-03B-01W-0728-08 chr5:149324043 G>A maps to NM_000440.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2804-03B-01W-0728-08 chr23:133527978 G>T did not map to a codon.
Sequencing variant TCGA-AB-2959-03A-01W-0733-08 chr23:133547851 G>T did not map to a codon.
Sequencing variant TCGA-AB-2976-03A-01D-0739-09 chr23:133547991 G>A did not map to a codon.
Sequencing variant TCGA-AB-3009-03A-01D-0739-09 chr23:133551223 G>T did not map to a codon.
Sequencing variant TCGA-AB-2832-03B-01W-0728-08 chr16:81161615 C>A maps to NM_052892.3 V2033V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2998-03A-01D-0739-09 chr16:81241124 G>A maps to NM_052892.3 D292D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2923-03A-01W-0745-08 chr10:102048167 C>T maps to NM_016112.2 T801T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2979-03A-01D-0739-09 chr6:51524180 G>C maps to NM_138694.3 L3581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2904-03A-01W-0732-08 chr1:6531118 C>T maps to NM_198681.2 E518E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2922-03A-01W-0745-08 chr6:161135859 C>T maps to NM_000301.3 D194D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2998-03A-01D-0739-09 chr15:90209104 G>T maps to NM_002666.4 V426V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-3006-03A-01D-0739-09 chr23:153691780 C>T did not map to a codon.
Sequencing variant TCGA-AB-2838-03A-01W-0726-08 chr3:48451926 G>A maps to NM_001130082.1 D1819D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2994-03A-01D-0739-09 chr9:140358839 G>A maps to NM_001098537.1 A1036A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2843-03B-01W-0728-08 chr22:42998991 A>G maps to ENST00000415122 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2908-03A-01W-0745-08 chr14:50118022 G>T maps to NM_002692.3 V428V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2807-03D-01W-0755-09 chr19:1090935 C>A maps to NM_002695.3 E134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2986-03A-01D-0739-09 chr7:39379314 C>T maps to NM_007252.3 Q196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2904-03A-01W-0732-08 chr5:64875361 T>G maps to NM_015342.2 S424S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2943-03A-01W-0745-08 chr1:12884982 C>T maps to NM_001146344.1 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2927-03A-01W-0755-09 chr1:203452869 C>A maps to NM_201348.1 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2858-03D-01W-0755-09 chr10:72360181 G>A maps to NM_005041.4 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2943-03A-01W-0745-08 chr3:64085284 G>A maps to NM_198859.3 G659G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2978-03A-01D-0739-09 chr1:57161722 C>T maps to NM_006252.3 R227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2927-03A-01W-0755-09 chr14:30093423 G>A maps to NM_002742.2 I613I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2968-03A-01D-0739-09 chr19:36303650 C>T maps to NM_021232.1 W95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2849-03B-01W-0728-08 chr6:4049338 T>C maps to NM_003913.4 Y675Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2955-03A-01W-0733-08 chr6:4057321 C>G maps to NM_003913.4 T878T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2976-03A-01D-0739-09 chr12:53839827 C>T maps to NM_018457.3 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2964-03A-01D-0739-09 chr16:2763664 G>C maps to NM_031948.3 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2939-03A-01W-0745-08 chr6:84234377 C>T maps to NM_153362.2 N406N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2818-03B-01W-0728-08 chr8:18725296 C>G maps to ENST00000440756 V507V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2974-03A-01D-0739-09 chr19:43237056 G>A maps to NM_021016.3 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2865-03B-01W-0728-08 chr19:43772023 C>T maps to NM_002784.3 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2968-03A-01D-0739-09 chr9:98229497 G>A maps to NM_000264.3 Y820Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2890-03A-01W-0732-08 chr9:8376657 A>G maps to NM_002839.3 L1485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2914-03A-01W-0732-08 chr11:48158723 C>T maps to NM_002843.3 D681D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2898-03A-01W-0733-08 chr2:220166868 A>C maps to NM_002846.3 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2971-03A-01D-0739-09 chr7:157396753 C>T maps to NM_002847.3 R786R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2864-03D-01W-0755-09 chr12:9311060 A>G maps to NM_002864.2 N1083N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2966-03A-01D-0739-09 chr22:23492293 C>T maps to NM_004914.2 H104H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2975-03A-01D-0739-09 chr8:117868934 A>T maps to NM_006265.2 L255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2986-03A-01D-0739-09 chr8:117869559 C>A maps to NM_006265.2 E212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2927-03A-01W-0755-09 chr14:102700053 G>A maps to NM_014226.1 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2858-03D-01W-0755-09 chr4:160243596 G>T maps to NM_014247.2 E157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2986-03A-01D-0739-09 chr23:106310913 A>C did not map to a codon.
Sequencing variant TCGA-AB-2971-03A-01D-0739-09 chr2:238742983 A>G maps to NM_001080504.2 L1033L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2907-03A-01D-0739-09 chr4:155749092 C>T maps to NM_144979.3 S492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2901-03A-01W-0733-08 chr2:161133831 C>T maps to NM_016836.3 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-3002-03A-01D-0739-09 chr23:135961573 C>A did not map to a codon.
Sequencing variant TCGA-AB-2805-03B-01W-0728-08 chr7:103151447 A>G maps to ENST00000428762 N2708N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2869-03A-01W-0761-09 chr1:8526071 G>A maps to NM_012102.3 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2973-03A-01D-0739-09 chr10:43600499 G>T maps to NM_020975.4 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2838-03A-01W-0726-08 chr13:34409284 G>A maps to NM_002915.3 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2819-03B-01W-0728-08 chr23:109697078 C>A did not map to a codon.
Sequencing variant TCGA-AB-2966-03A-01D-0739-09 chr1:182616019 C>T maps to NM_033345.2 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2880-03A-01W-0732-08 chr17:74467768 G>A maps to NM_024599.5 F839F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2867-03B-01W-0728-08 chr22:45813581 G>A maps to NM_015653.3 Q98Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2977-03A-01D-0739-09 chr11:66103115 G>A maps to NM_004292.2 D140D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2891-03A-01W-0733-08 chr23:106145380 G>A did not map to a codon.
Sequencing variant TCGA-AB-2986-03A-01D-0739-09 chr14:21025165 C>T maps to NM_001110361.1 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2905-03A-01D-0739-09 chr15:59368278 C>T maps to ENST00000434298 Q605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2827-03B-01W-0728-08 chr17:74158050 G>A maps to NM_052916.2 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-3002-03A-01D-0739-09 chr8:10469264 G>A maps to NM_178857.5 S781S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2983-03A-01D-0739-09 chr11:8705619 C>T maps to NM_000990.4 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2923-03A-01W-0745-08 chr6:34392506 C>T maps to NM_001014.3 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2912-03A-01W-0732-08 chr23:83320022 G>A did not map to a codon.
Sequencing variant TCGA-AB-2859-03B-01W-0728-08 chr6:7230590 C>G maps to NM_001003699.3 T753T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2805-03B-01W-0728-08 chr21:36231782 G>A maps to NM_001754.4 R201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2890-03A-01W-0732-08 chr21:36231782 G>A maps to NM_001754.4 R201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2907-03A-01D-0739-09 chr21:36231876 T>G did not map to a codon.
Sequencing variant TCGA-AB-2927-03A-01W-0755-09 chr21:36231782 G>A maps to NM_001754.4 R201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2936-03A-01W-0745-08 chr21:36171606 G>A maps to NM_001754.4 R320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2978-03A-01D-0739-09 chr21:36231782 G>A maps to NM_001754.4 R201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2821-03B-01W-0728-08 chr8:93026824 G>A maps to NM_175634.2 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2881-03A-01W-0732-08 chr8:93004053 G>T maps to NM_175634.2 C268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2851-03B-01W-0728-08 chr19:39039014 C>T maps to NM_000540.2 Y4079Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2855-03B-01W-0728-08 chr23:134989143 G>A did not map to a codon.
Sequencing variant TCGA-AB-2889-03A-01W-0732-08 chr16:51174458 C>T maps to ENST00000251020 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2939-03A-01W-0745-08 chr7:12644245 A>C maps to NM_001112706.2 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2804-03B-01W-0728-08 chr23:18264754 G>A did not map to a codon.
Sequencing variant TCGA-AB-2830-03B-01W-0728-08 chr23:18343049 C>A did not map to a codon.
Sequencing variant TCGA-AB-2806-03B-01W-0728-08 chr8:144891738 G>C maps to NM_182706.3 A560A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2959-03A-01W-0733-08 chr11:9100946 G>A maps to ENST00000457346 D122D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2970-03A-01D-0739-09 chr6:35212478 C>T maps to ENST00000394681 R780R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2981-03A-01D-0739-09 chr14:50262634 A>G maps to NM_004713.3 S831S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2976-03A-01D-0739-09 chr15:74706984 C>T maps to NM_003612.3 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2844-03B-01W-0728-08 chr3:101136587 G>A maps to NM_020654.3 R111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2999-03A-01D-0739-09 chr7:55902219 C>T maps to NM_207366.2 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2878-03A-01W-0732-08 chr14:94933657 G>A maps to NM_175739.3 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2966-03A-01D-0739-09 chr10:104489529 G>A maps to NM_178858.4 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2838-03A-01W-0726-08 chr1:154938213 C>G maps to NM_001130040.1 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2814-03D-01W-0755-09 chr23:9862448 C>A did not map to a codon.
Sequencing variant TCGA-AB-2964-03A-01D-0739-09 chr23:9900371 C>T did not map to a codon.
Sequencing variant TCGA-AB-2847-03B-01W-0728-08 chr16:56933507 C>T maps to NM_000339.2 N909N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2993-03A-01D-0739-09 chr13:99378391 C>T maps to NM_005073.3 W77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2939-03A-01W-0745-08 chr2:230910901 G>A maps to NM_152527.4 R314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-3005-03A-01D-0739-09 chr17:4843184 G>C maps to NM_003562.4 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2912-03A-01W-0732-08 chr17:8198092 G>A maps to NM_201520.1 C11C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2905-03A-01D-0739-09 chr5:149357811 T>C maps to NM_000112.3 N199N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2865-03B-01W-0728-08 chr7:107431675 C>T maps to NM_000111.2 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2899-03A-01W-0733-08 chr4:9998562 G>A maps to NM_020041.2 Y84Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2839-03B-01W-0728-08 chr12:56631036 G>T maps to NM_001135195.1 V464V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2924-03A-01W-0745-08 chr5:33984526 C>T maps to NM_016180.3 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2949-03A-01W-0733-08 chr2:220505321 G>A did not map to a codon.
Sequencing variant TCGA-AB-2853-03D-01W-0755-09 chr5:101834476 G>A maps to NM_173488.3 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2983-03A-01D-0739-09 chr12:56581078 A>G maps to NM_003075.3 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2822-03D-01W-0755-09 chr23:53436077 G>C did not map to a codon.
Sequencing variant TCGA-AB-2824-03B-01W-0728-08 chr23:53426625 C>T did not map to a codon.
Sequencing variant TCGA-AB-2844-03B-01W-0728-08 chr23:53441940 C>T did not map to a codon.
Sequencing variant TCGA-AB-2858-03D-01W-0755-09 chr23:53409231 T>C did not map to a codon.
Sequencing variant TCGA-AB-2900-03A-01W-0733-08 chr23:53423536 C>A did not map to a codon.
Sequencing variant TCGA-AB-2963-03A-01D-0739-09 chr23:53426616 A>T did not map to a codon.
Sequencing variant TCGA-AB-2851-03B-01W-0728-08 chr10:112342355 A>T maps to NM_005445.3 R254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2950-03A-01W-0733-08 chr10:112360889 T>C did not map to a codon.
Sequencing variant TCGA-AB-2876-03A-01W-0732-08 chr18:2763717 T>C maps to NM_015295.2 D1550D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2938-03A-01W-0732-08 chr4:186544674 G>A maps to ENST00000355634 S732S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2872-03A-01W-0732-08 chr6:34508851 C>T maps to NM_012391.1 K181K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2870-03A-01W-0732-08 chr2:220343887 C>T maps to NM_005876.4 R1684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2899-03A-01W-0733-08 chr2:220344733 G>C maps to NM_005876.4 R1738R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2849-03B-01W-0728-08 chr1:16260237 G>A maps to NM_015001.2 W2501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2900-03A-01W-0733-08 chr14:65237712 C>A maps to ENST00000389723 R1900R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2988-03A-01D-0739-09 chr15:42168392 G>A maps to ENST00000320955 N1347N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2927-03A-01W-0755-09 chr23:38016253 C>T did not map to a codon.
Sequencing variant TCGA-AB-2984-03A-01D-0739-09 chr1:24995946 T>A maps to NM_005839.3 P691P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2927-03A-01W-0755-09 chr15:92977521 C>T maps to NM_006011.3 D69D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2850-03B-01W-0728-08 chr23:123224614 G>A did not map to a codon.
Sequencing variant TCGA-AB-2871-03A-01W-0732-08 chr23:123191827 G>A did not map to a codon.
Sequencing variant TCGA-AB-2913-03A-01W-0732-08 chr23:123200287 T>C did not map to a codon.
Sequencing variant TCGA-AB-2964-03A-01D-0739-09 chr23:123205040 C>T did not map to a codon.
Sequencing variant TCGA-AB-2972-03A-01D-0739-09 chr23:123197715 C>T did not map to a codon.
Sequencing variant TCGA-AB-2978-03A-01D-0739-09 chr23:123220475 C>T did not map to a codon.
Sequencing variant TCGA-AB-2916-03A-01W-0732-08 chr5:172745041 G>A maps to NM_003714.2 H239H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2963-03A-01D-0739-09 chr5:172745086 C>T maps to NM_003714.2 E224E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2964-03A-01D-0739-09 chr5:172744951 G>A maps to NM_003714.2 N269N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2809-03D-01W-0755-09 chr7:89856314 C>T maps to NM_152999.3 R175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2908-03A-01W-0745-08 chr5:146752755 C>T maps to NM_001112724.1 R268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2916-03A-01W-0732-08 chr2:168997251 C>T maps to NM_013233.2 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-3007-03A-01D-0739-09 chr11:59559688 G>T did not map to a codon.
Sequencing variant TCGA-AB-2982-03A-01D-0739-09 chr3:33194314 G>A maps to NM_015551.1 H603H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-3009-03A-01D-0739-09 chr1:149877520 G>A maps to NM_014849.3 I652I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2821-03B-01W-0728-08 chr6:33409386 C>T maps to NM_006772.2 P715P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2914-03A-01W-0732-08 chr6:33391287 C>T maps to NM_006772.2 Y34Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2810-03B-01W-0728-08 chr19:48878945 C>T maps to NM_012451.3 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2921-03A-01W-0755-09 chr4:119952551 G>A maps to NM_133477.2 Q874Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2929-03A-01W-0732-08 chr1:110019499 G>A maps to NM_001040709.1 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2978-03A-01D-0739-09 chr23:99936231 C>T did not map to a codon.
Sequencing variant TCGA-AB-2929-03A-01W-0732-08 chr23:37935910 G>A did not map to a codon.
Sequencing variant TCGA-AB-2964-03A-01D-0739-09 chr4:104510898 A>G maps to NM_001059.2 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2853-03D-01W-0755-09 chr17:61498205 C>T maps to ENST00000389520 A1631A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2955-03A-01W-0733-08 chr1:6636674 A>G maps to NM_138697.3 G487G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2803-03B-01W-0728-08 chr7:141672553 C>G maps to NM_176817.4 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2830-03B-01W-0728-08 chr23:106069436 T>A did not map to a codon.
Sequencing variant TCGA-AB-2915-03A-01W-0745-08 chr23:102884906 G>A did not map to a codon.
Sequencing variant TCGA-AB-2890-03A-01W-0732-08 chr23:102864441 A>G did not map to a codon.
Sequencing variant TCGA-AB-2941-03A-01W-0745-08 chr23:102864441 A>G did not map to a codon.
Sequencing variant TCGA-AB-3000-03A-01D-0739-09 chr23:102864441 A>G did not map to a codon.
Sequencing variant TCGA-AB-2899-03A-01W-0733-08 chr23:101396170 C>T did not map to a codon.
Sequencing variant TCGA-AB-2936-03A-01W-0745-08 chr23:101396080 C>A did not map to a codon.
Sequencing variant TCGA-AB-2862-03B-01W-0728-08 chr23:13680762 A>G did not map to a codon.
Sequencing variant TCGA-AB-2865-03B-01W-0728-08 chr4:106157937 C>T maps to ENST00000513237 Q968*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2876-03A-01W-0732-08 chr4:106156539 C>T maps to ENST00000513237 Q502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2879-03A-01W-0732-08 chr4:106164777 C>T maps to ENST00000513237 R1237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2908-03A-01W-0745-08 chr4:106164777 C>T maps to ENST00000513237 R1237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2923-03A-01W-0745-08 chr4:106156746 C>T maps to ENST00000513237 R571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2964-03A-01D-0739-09 chr4:106157844 C>T maps to ENST00000513237 Q937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2978-03A-01D-0739-09 chr4:106196212 C>T maps to ENST00000513237 R1537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-3006-03A-01D-0739-09 chr4:106193891 C>T maps to ENST00000513237 R1473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2827-03B-01W-0728-08 chr17:80320076 C>G maps to NM_207459.3 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2859-03B-01W-0728-08 chr23:132351105 G>A did not map to a codon.
Sequencing variant TCGA-AB-2820-03B-01W-0728-08 chr15:43525774 G>A maps to NM_201631.3 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2816-03B-01W-0728-08 chr20:2384302 C>T maps to NM_198994.2 F390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2871-03A-01W-0732-08 chr1:36767159 C>T maps to NM_005119.3 R837*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2988-03A-01D-0739-09 chr23:153557893 C>T did not map to a codon.
Sequencing variant TCGA-AB-2839-03B-01W-0728-08 chr15:83784621 C>T maps to NM_023003.3 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2827-03B-01W-0728-08 chr13:114193793 C>T maps to NM_017905.4 F554F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2913-03A-01W-0732-08 chr17:72791223 G>A maps to NM_017728.3 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2923-03A-01W-0745-08 chr17:72791744 C>T maps to NM_017728.3 R204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-3007-03A-01D-0739-09 chr2:216964916 C>T maps to NM_138390.3 Y182Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2846-03B-01W-0728-08 chr23:34657407 C>T did not map to a codon.
Sequencing variant TCGA-AB-2814-03D-01W-0755-09 chr21:19666639 G>A maps to NM_002772.2 G811G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2976-03A-01D-0739-09 chr1:175348814 G>A maps to NM_003285.2 L612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2913-03A-01W-0732-08 chr16:52479986 A>T maps to ENST00000407228 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2829-03B-01W-0728-08 chr17:7577608 C>T did not map to a codon.
Sequencing variant TCGA-AB-2838-03A-01W-0726-08 chr17:7579311 C>T maps to NM_001126112.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2868-03B-01W-0728-08 chr17:7578554 C>T did not map to a codon.
Sequencing variant TCGA-AB-2908-03A-01W-0745-08 chr17:7576896 G>A maps to NM_001126112.1 Q317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2929-03A-01W-0732-08 chr11:18044465 C>A maps to ENST00000341556 G347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2819-03B-01W-0728-08 chr3:185643272 G>A maps to NM_004593.2 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2916-03A-01W-0732-08 chr15:64686315 T>C did not map to a codon.
Sequencing variant TCGA-AB-2930-03A-01W-0761-09 chr23:54956610 G>A did not map to a codon.
Sequencing variant TCGA-AB-2833-03B-01W-0728-08 chr11:65715565 C>T maps to NM_152762.2 F366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2895-03A-01W-0733-08 chr11:76506896 G>A maps to NM_015516.3 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2820-03B-01W-0728-08 chr7:138853104 G>T maps to NM_024926.2 G323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2910-03A-01W-0745-08 chr21:38538289 C>T maps to NM_003316.3 S1258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2905-03A-01D-0739-09 chr14:76232531 A>G maps to NM_015072.4 R612R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2805-03B-01W-0728-08 chr2:179442195 G>A maps to NM_133378.4 L20388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2977-03A-01D-0739-09 chr2:179402120 C>T maps to NM_133378.4 Q30703Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2915-03A-01W-0745-08 chr3:138037000 G>A maps to ENST00000333911 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2978-03A-01D-0739-09 chr19:36234764 G>T maps to ENST00000412391 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2959-03A-01W-0733-08 chr2:170917883 C>T maps to ENST00000442603 C1679C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2985-03A-01D-0739-09 chr9:114676926 T>C maps to NM_003358.1 Y47Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2963-03A-01D-0739-09 chr10:73053674 G>A maps to NM_170744.3 T720T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2877-03A-01W-0732-08 chr23:47104802 T>A did not map to a codon.
Sequencing variant TCGA-AB-2898-03A-01W-0733-08 chr1:55589118 C>T did not map to a codon.
Sequencing variant TCGA-AB-2826-03B-01W-0728-08 chr2:61447537 G>A maps to NM_014709.3 R2652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2827-03B-01W-0728-08 chr17:76825030 G>A maps to NM_025090.3 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-3006-03A-01D-0739-09 chr12:95926871 A>G maps to NM_032147.2 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2943-03A-01W-0745-08 chr1:22033075 C>A maps to NM_032236.5 E699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-3001-03A-01D-0739-09 chr23:41010295 G>A did not map to a codon.
Sequencing variant TCGA-AB-2822-03D-01W-0755-09 chr1:7913479 G>A maps to NM_021995.2 N4N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2861-03B-01W-0728-08 chr6:31752210 G>A maps to NM_006295.2 F512F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2920-03A-01W-0732-08 chr6:30886616 G>A maps to NM_001167734.1 V363V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2922-03A-01W-0745-08 chr5:82833057 T>C maps to NM_004385.4 N1412N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2844-03B-01W-0728-08 chr19:50498515 C>T maps to NM_016440.3 K232K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2966-03A-01D-0739-09 chr10:28824555 C>T maps to NM_016628.3 D48D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-3001-03A-01D-0739-09 chr10:28905291 G>A did not map to a codon.
Sequencing variant TCGA-AB-2937-03A-01W-0732-08 chr7:71130528 G>A maps to NM_022479.1 W405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2936-03A-01W-0745-08 chr1:241912981 G>C maps to NM_144625.4 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2915-03A-01W-0745-08 chr23:54334367 C>T did not map to a codon.
Sequencing variant TCGA-AB-2913-03A-01W-0732-08 chr11:32417801 C>G did not map to a codon.
Sequencing variant TCGA-AB-2970-03A-01D-0739-09 chr11:32413610 C>T did not map to a codon.
Sequencing variant TCGA-AB-2980-03A-01D-0739-09 chr3:39225926 T>C maps to NM_194293.2 P1670P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2935-03A-01W-0755-09 chr23:119387297 A>C did not map to a codon.
Sequencing variant TCGA-AB-2959-03A-01W-0733-08 chr23:119387499 T>A did not map to a codon.
Sequencing variant TCGA-AB-2972-03A-01D-0739-09 chr16:88688689 C>T maps to ENST00000452588 R545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2994-03A-01D-0739-09 chr2:112994153 G>A maps to NM_032494.2 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2981-03A-01D-0739-09 chr5:850654 C>T maps to NM_024786.2 K21K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2861-03B-01W-0728-08 chr3:44674060 C>T maps to NM_006991.3 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2921-03A-01W-0755-09 chr23:152611032 A>G did not map to a codon.
Sequencing variant TCGA-AB-2994-03A-01D-0739-09 chr8:146003441 G>A maps to NM_030580.3 Y68Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2923-03A-01W-0745-08 chr19:37618610 C>T maps to NM_144689.3 R240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2857-03B-01W-0728-08 chr19:50549970 T>G maps to NM_015428.1 P757P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2915-03A-01W-0745-08 chr1:182027085 A>C maps to NM_001009992.1 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2977-03A-01D-0739-09 chr4:437877 T>C maps to NM_133474.2 Q126Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2964-03A-01D-0739-09 chr23:134428052 T>C did not map to a codon.
Sequencing variant TCGA-AB-2858-03D-01W-0755-09 chr7:99654637 C>T maps to NM_145914.2 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AB-2930-03A-01W-0761-09 chr19:56734092 T>C maps to NM_024303.1 L202L. Only missense variants will be evaluated by CHASM.
